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Vasectomy (2015)

Using aua guidelines.

This AUA guideline is provided free of use to the general public for academic and research purposes. However, any person or company accessing AUA guidelines for promotional or commercial use must obtain a licensed copy. To obtain the licensable copy of this guideline, please contact Keith Price at [email protected] .

To cite this guideline: Sharlip ID, Belker AM, Honig S et al: Vasectomy: AUA guideline. J Urol 2012; 188: 2482.

Published 2012; Amended 2015

The purpose of this clinical guideline is to provide guidance to clinicians who offer vasectomy services. This guidance covers pre-operative evaluation and consultation of prospective vasectomy patients; techniques for local anesthesia, isolation of the vas deferens and occlusion of the vas deferens during vasectomy; post-operative follow-up; post-vasectomy semen analysis (PVSA) and potential complications and consequences of vasectomy.

Guideline as it appears in The Journal of Urology ® [pdf]

Unabridged version of this Guideline [pdf]

Panel Members

Ira D. Sharlip, Arnold M. Belker, Stanton Honig, Michel Labrecque, Joel L. Marmar, Lawrence S. Ross, Jay I. Sandlow, David C. Sokal

Executive Summary

Note to the reader:.

Please note that this Guideline was edited in 2015 to include additional information related to vasectomy and the risk of prostate cancer.

The purpose of this Guideline is to provide guidance to clinicians who offer vasectomy services. This guidance covers pre-operative evaluation and consultation of prospective vasectomy patients; techniques for local anesthesia, isolation of the vas deferens and occlusion of the vas deferens during vasectomy; post-operative follow-up; post-vasectomy semen analysis (PVSA) and potential complications and consequences of vasectomy.

A systematic review of the literature using the MEDLINE and POPLINE databases (search dates January 1949 to August 2011) was conducted to identify peer-reviewed publications relevant to vasectomy. The search identified almost 2,000 titles and abstracts. Almost 900 articles were retrieved for full-text review. These yielded an evidence base of 275 articles after application of inclusion and exclusion criteria. These publications were used to create the evidence-based portion of the Guideline. When sufficient evidence existed, the body of evidence for a particular treatment was assigned a strength rating of A (high), B (moderate) or C (low). Additional information is provided as Clinical Principles and Expert Opinion when insufficient evidence existed.

Guideline Statements

1. A preoperative interactive consultation should be conducted, preferably in person. If an in-person consultation is not possible, then preoperative consultation by telephone or electronic communication is an acceptable alternative. Expert Opinion

2. The minimum and necessary concepts that should be discussed in a preoperative vasectomy consultation include the following: Expert Opinion

  • Vasectomy is intended to be a permanent form of contraception.
  • Vasectomy does not produce immediate sterility.
  • Following vasectomy, another form of contraception is required until vas occlusion is confirmed by post- vasectomy semen analysis (PVSA).
  • Even after vas occlusion is confirmed, vasectomy is not 100% reliable in preventing pregnancy.
  • The risk of pregnancy after vasectomy is approximately 1 in 2,000 for men who have post-vasectomy azoospermia or PVSA showing rare non-motile sperm (RNMS).
  • Repeat vasectomy is necessary in ≤1% of vasectomies, provided that a technique for vas occlusion known to have a low occlusive failure rate has been used.
  • Patients should refrain from ejaculation for approximately one week after vasectomy.
  • Options for fertility after vasectomy include vasectomy reversal and sperm retrieval with in vitro fertilization. These options are not always successful, and they may be expensive.
  • The rates of surgical complications such as symptomatic hematoma and infection are 1-2%. These rates vary with the surgeon's experience and the criteria used to diagnose these conditions.
  • Chronic scrotal pain associated with negative impact on quality of life occurs after vasectomy in about 1-2% of men. Few of these men require additional surgery.
  • Other permanent and non-permanent alternatives to vasectomy are available.

3. Clinicians do not need to routinely discuss prostate cancer, coronary heart disease, stroke, hypertension, dementia or testicular cancer in pre-vasectomy counseling of patients because vasectomy is not a risk factor for these conditions. Standard (Evidence Strength Grade B)

4. Prophylactic antimicrobials are not indicated for routine vasectomy unless the patient presents a high risk of infection. Recommendation (Evidence Strength Grade C)

5. Vasectomy should be performed with local anesthesia with or without oral sedation. If the patient declines local anesthesia or if the surgeon believes that local anesthesia with or without oral sedation will not be adequate for a particular patient, then vasectomy may be performed with intravenous sedation or general anesthesia. Expert Opinion

6. Isolation of the vas should be performed using a minimally-invasive vasectomy (MIV) technique such as the no-scalpel vasectomy (NSV) technique or other MIV technique. Standard (Evidence Strength Grade B)

7. The ends of the vas should be occluded by one of three divisional methods:

  • Mucosal cautery (MC) with fascial interposition (FI) and without ligatures or clips applied on the vas;
  • MC without FI and without ligatures or clips applied on the vas;
  • Open ended vasectomy leaving the testicular end of the vas unoccluded, using MC on the abdominal end and FI; OR by the non-divisional method of extended electrocautery. Recommendation (Evidence Strength Grade C)

8. The divided vas may be occluded by ligatures or clips applied to the ends of the vas, with or without FI and with or without excision of a short segment of the vas, by surgeons whose personal training and/or experience enable them to consistently obtain satisfactory results with such methods. Option  (Evidence Strength Grade C)

9. Routine histologic examination of the excised vas segments is not required. Expert Opinion

10. Men or their partners should use other contraceptive methods until vasectomy success is confirmed by PVSA. Clinical Principle

11. To evaluate sperm motility, a fresh, uncentrifuged semen sample should be examined within two hours after ejaculation.  Expert Opinion

12. Patients may stop using other methods of contraception when examination of one well-mixed, uncentrifuged, fresh post-vasectomy semen specimen shows azoospermia or only rare non-motile sperm (RNMS or ≤ 100,000 non-motile sperm/mL). Recommendation (Evidence Strength Grade C)

13. Eight to sixteen weeks after vasectomy is the appropriate time range for the first PVSA. The choice of time to do the first PVSA should be left to the judgment of the surgeon. Option (Evidence Strength Grade C)

14. Vasectomy should be considered a failure if any motile sperm are seen on PVSA at six months after vasectomy, in which case repeat vasectomy should be considered. Expert Opinion

15. If > 100,000 non-motile sperm/mL persist beyond six months after vasectomy, then trends of serial PVSAs and clinical judgment should be used to decide whether the vasectomy is a failure and whether repeat vasectomy should be considered. Expert Opinion

The purpose of this Guideline is to provide guidance to clinicians who offer vasectomy services. The Guideline covers pre-vasectomy evaluation and consultation of prospective vasectomy patients; techniques for local anesthesia, isolation of the vas deferens and occlusion of the vas deferens during vasectomy; post-operative follow-up; post-vasectomy semen analysis (PVSA) to verify sterility and potential complications and consequences of vasectomy. Currently, the practice of vasectomy is characterized by wide variation in pre-operative counseling, surgical technique and post-operative follow-up. The intent of this Guideline is to provide a set of approaches and procedures that maximizes successful vasectomy outcomes and minimizes failure and other adverse events.

The strategies and approaches recommended in this document were derived from evidence-based and consensus-based processes. There is a continually expanding literature on vasectomy. The Panel  notes that this document constitutes a clinical approach to the practice of vasectomy. This Guideline is not intended to replace the judgment of an individual clinician faced with a particular patient. As the science relevant to vasectomy evolves and improves, the strategies presented here will require updating to remain consistent with the highest standards of clinical care.

Methodology

Process for Literature Selection . A systematic review was conducted to identify published articles relevant to key questions specified by the Panel (See Appendix C). The key questions focused on identifying necessary elements of pre-operative evaluation and consultation, optimal procedures for anesthetic administration, the least traumatic and most effective procedures for isolation of the vas deferens, the most effective procedures for occluding the vas deferens, the complications and consequences of vasectomy and the necessary components of post-operative follow-up, including semen analysis to verify sterility.

Literature searches were performed using the MEDLINE® and POPLINE® databases from January 1949 to August 2011 with the goal of identifying literature broadly relevant to the practice of vasectomy. This literature included studies that focused on the prevalence of vasectomy; the demographics of patients and couples who chose vasectomy; vasectomy operative techniques, including techniques for vas isolation and vas occlusion and associated failure rates; short-term and long-term complications of vasectomy, other outcomes potentially associated with vasectomy (e.g., coronary heart disease, stroke, prostate and testicular cancer, sexual outcomes, psychosocial outcomes) and PVSA procedures and timing. Inclusion criteria for operative procedures were conventional vasectomy (CV) and minimally-invasive vasectomy (MIV), including the no-scalpel vasectomy (NSV) technique. All methods for occluding the vas were included. The following topics were excluded from the scope of the review: laparoscopic vasectomy, vasectomy reversal, post-vasectomy options for pregnancy, treatment of post-vasectomy pain syndrome, examination of antibodies to antigens other than sperm post-vasectomy and techniques for teaching vasectomy. Articles on antibiotic prophylaxis also were excluded as the topic of antibiotic prophylaxis in surgical procedures without entering the urinary tract is covered in an AUA Best Practice Policy [pdf] . All settings and all ages of vasectomy patients were included. All study designs were included except for single-group cohort studies on immediate post-operative complications with fewer than 500 participants. Review article references were checked to ensure inclusion of all possibly relevant studies. Multiple reports on the same patient group were carefully examined to ensure exclusion of redundant information.

Nearly 2,000 citations were reviewed by title and/or abstract. After application of inclusion and exclusion criteria, 275 articles were chosen to form the evidence base of this Guideline. Data were extracted on study design (e.g., randomized controlled trial, comparative observational study, case-series); pre-operative, operative and post-operative parameters; complications and other consequences of vasectomy (e.g., patient satisfaction, patient regret) and vasectomy effectiveness and failure rates.

Quality of Individual Studies and Determination of Evidence Strength . Quality of individual studies that were randomized controlled trials (RCTs) or comparative observational studies was assessed using the Cochrane Risk of Bias tool. 1 Since there is no widely-accepted quality assessment tool for single-cohort observational studies, the quality of these studies was not assessed.

The categorization of evidence strength is conceptually distinct from the quality of individual studies. Evidence strength refers to the body of evidence available for a particular question and includes consideration of study design; individual study quality; the consistency of findings across studies; the adequacy of sample sizes and the generalizability of samples, settings and treatments for the purposes of the Guideline. The AUA categorizes body of evidence strength (ES) as Grade A (well-conducted RCTs or exceptionally strong observational studies), Grade B (RCTs with some weaknesses of procedure or generalizability or generally strong observational studies) or Grade C (observational studies that are inconsistent, have small sample sizes, or have other problems that potentially confound interpretation of data).

AUA Nomenclature: Linking Statement Type to Evidence Strength . The AUA nomenclature system explicitly links statement type to body of evidence strength and the Panel's judgment regarding the balance between benefits and risks/burdens (see Table 2). 2 Standards are directive statements that an action should (benefits outweigh risks/burdens) or should not (risks/burdens outweigh benefits) be undertaken based on Grade A or Grade B evidence. Recommendations are directive statements that an action should (benefits outweigh risks/burdens) or should not (risks/burdens outweigh benefits) be undertaken based on Grade C evidence. Options are non-directive statements that leave the decision to take an action up to the individual clinician and patient because the balance between benefits and risks/burdens appears relatively equal or appears unclear; Options may be supported by Grade A, B or C evidence. For some clinical issues, there was little or no evidence from which to construct evidence-based statements. Where gaps in the evidence existed, the Panel provides guidance in the form of Clinical Principles or Expert Opinion with consensus achieved using a modified Delphi technique if differences of opinion existed among Panel members. 3 A Clinical Principle is a statement about a component of clinical care that is widely agreed upon by urologists or other clinicians for which there may or may not be evidence in the medical literature. Expert Opinion refers to a statement, achieved by consensus of the Panel, that is based on members' clinical training, experience, knowledge and judgment and for which there is no evidence.

Panel Selection and Peer Review Process . The Vasectomy Panel was created in 2008 by the American Urological Association Education and Research, Inc. (AUA). The Practice Guidelines Committee (PGC) of the AUA selected the Panel Chair and Vice Chair who in turn appointed the additional panel members, all of whom have specific expertise with regard to vasectomy.

The AUA conducted an extensive peer review process. The initial draft of this Guideline was distributed to 72 peer reviewers; 55 responded with comments. The panel reviewed and discussed all submitted comments and revised the draft as needed. Since the changes were substantial, a second draft was circulated to 64 peer reviewers. The panel reviewed and discussed all submitted comments in response to this second round of peer review and again revised the document. Once finalized, the Guideline was submitted for approval to the PGC. It was then submitted to the AUA Board of Directors for final approval.  Funding of the panel was provided by the AUA. Panel members received no remuneration for their work.

The Practice of Vasectomy

The importance of vasectomy.

Vasectomy is the most common non-diagnostic operation performed by urologists in the United States (US). Estimates of the number of vasectomies performed annually in the US vary depending on survey type. Data from the National Study of Family Growth in which only married couples were polled indicate a range from 175,000 to 354,000. 4 In a physician survey, an estimated 526,501 vasectomies were performed in the US in 2002. 5 This number seems to have been approximately stable for the previous decade. More than 75% of vasectomies in the US are done by urologists, and about 90% of urology practices in the US perform vasectomy. 5-6

In 2002, data collected in the US show that vasectomy was used by 5.7% of men ages 15-44 and that this represents the fourth most commonly-used contraceptive method. The first three were condoms, used by 29.5% of men, oral contraceptives for women used by 25.6% of couples and tubal ligation used by 8.1% of couples. 7 Compared to tubal ligation , which is also a method of permanent contraception, vasectomy is equally effective in preventing pregnancy; however, vasectomy is simpler, faster, safer and less expensive. Vasectomy is one of the most cost-effective of all methods of contraception; its cost is about one-fourth of the cost of tuba lligation. 8 Vasectomy requires less time off work, requires only local rather than general anesthesia and is usually performed in a doctor's office or clinic. The potential complications of vasectomy are less serious than those of tubal ligation.

Despite the clear advantages of vasectomy, prevalence data for 1998-2002 show that tubal ligation was performed about two to three times more often than vasectomy. 4 Among all women in 2002, married and unmarried, ages 15 to 44 years in the United States, only 5.7% relied on vasectomy for contraception compared to 16.7% who relied on tubal ligation. 9 Even among married women and married men who desire permanent contraception, in the US the prevalence of tubal ligation has exceeded the prevalence of vasectomy. 10

Worldwide, the discrepancy between vasectomy and tubal ligation is even more marked than in the US. Data compiled in 2008 by the Population Division of the Department of Economic and Social Affairs of the United Nations show that 33 million married women ages 15-49 relied on vasectomy for contraception compared to 225 million who relied on tubal ligation. 11 There are only eight nations in which vasectomy use is equal to or more frequent than tubal ligation for contraception – Korea, Canada, the United Kingdom, New Zealand, Bhutan, the Netherlands, Denmark and Austria ( World Contraceptive Use 2011 ).

Given that vasectomy and tubal ligation  have equivalent contraceptive effectiveness and that vasectomy enjoys advantages compared to tubal sterilization of lower cost, less pain, greater safety and faster recovery, vasectomy should be considered for permanent contraception much more frequently than is the current practice in the United States and most nations of the world.

Preoperative Practice

Background Information About Who Chooses Vasectomy and Why

Reasons for Choosing Vasectomy. Several studies have addressed the reasons that men or their partners choose vasectomy. 10, 12-16 The decision for a partner to undergo a sterilization procedure usually is initiated by the female partner. The decision about which partner undergoes a sterilization procedure often is based on information obtained by one of the partners from medical professionals or from friends. Dissatisfaction with or failure of other contraceptive methods may prompt one or both partners to consider surgical sterilization for one of them. In the US, couples with higher numbers of children, higher educational levels and Caucasian ethnicity are more likely to choose vasectomy. 10

One study surveyed 400 couples regarding their choice of sterilization. Vasectomy was chosen when it was believed to be "easier" than tubal ligation, the physician recommended a vasectomy, there was effective couple communication and the previous method of contraception involved the use of condoms. The use of an intrauterine device (IUD) and the use of coitus interruptus were associated with the selection of tubal ligation. More people known by the wife to be satisfied with either vasectomy or tubal ligation predicted the choice of either vasectomy or tubal occlusion. 12

An additional study looked at 84 couples in Scotland who selected vasectomy for contraception. In 46% of couples, both spouses were willing to be sterilized, whereas 23% of men requested vasectomy because their wives were unwilling to be sterilized and 24% of men insisted on vasectomy as their contribution to the partnership. The remaining couples gave medical reasons contraindicating a tubal ligation. The main influences for making the choice of vasectomy were favorable reports from other men (40%) and recommendations by general practitioners (21%). 13

One group examined the psychological correlates of vasectomy in 74 men seeking vasectomy at a urology clinic in a tertiary care teaching hospital in the mid-western US. Half of the men had contemplated vasectomy for one year or less and 85% had a high level of certainty regarding their decision. Ninety-one percent of men indicated that their wives or partners were involved in the decision and 90% indicated that their wives or partners were very certain about the decision (data were not collected from the partners). Mean anxiety level was 3.5 out of 10 (10 was the highest possible anxiety level). The most common reasons for anxiety were anticipated pain (27%) and fear of the unknown (23%). Finality of the procedure was a source of anxiety in only 5%. Fifteen percent of men indicated they understood that vasectomy was not reversible, while 30% believed that it was reversible. 14

One group reported on 719 men undergoing vasectomy compared to similar men identified from a national practice-based survey. The most common reason for choosing vasectomy over other dependably reversible methods of contraception was that vasectomy was perceived as the most secure way of avoiding pregnancy (50% of respondents). Twenty-two percent of respondents stated that the main reason was that they or their partners disliked other contraceptive measures, and 7% reported the reason was a recent unplanned pregnancy or pregnancy scare. Sixty-two percent of men responded that they chose male sterilization over tubal ligation because it was safer and simpler; an additional 14% stated it was their turn to take responsibility for contraception. Health care providers (31%) were the most commonly reported source of information that helped in the decision-making process, followed by wives/partners (25%) and friends (23%). 15

Characteristics of Patients and Couples Who Chose Vasectomy. Several studies examined the characteristics of men or their partners who choose vasectomy. 14, 15, 17-19 One such study examined data from the 1991 National Survey of Men and focused on a subset of 1,671 married men aged 20 to 39 years. Eleven and a half percent of men previously had a vasectomy and 12.6% of women had undergone a tubal ligation. Characteristics that were significantly (p<0.05) associated with choosing a vasectomy were older husband's age, white race of either spouse, living in the western US, smaller number of pregnancies in the current marriage, longer duration of marriage, prior failure with a male method of contraception and wife without religious affiliation. The husband's religion had no effect on the choice of vasectomy. 17

In a large case control study on the relationship of vasectomy and prostate cancer from New Zealand, the demographic characteristics of 1,261 men or their partners who chose a vasectomy were examined. 18 Significant predictors for vasectomy included advanced vocational qualifications, non-Catholic men and men who had fathered one to five children compared with men who had no children. Men with greater numbers of marriages and with more highly-educated wives were significantly more likely to have had a vasectomy (p<0.05). After adjusting for age, the following characteristics were not significant predictors (p>0.05) for vasectomy: socioeconomic status, geographic region of residence and age at first marriage. 18

Additional reporting included characteristics of men undergoing vasectomy compared to a comparison group. Men undergoing vasectomy differed from the comparison group as follows: a higher percentage were married or cohabitating (91% vs 62% in the general US population), a higher proportion of non-Hispanic whites (87% vs 75%) and a greater percentage of vasectomized men had a bachelor's degree (48% vs 25%). The response rate for this survey was low: only 21% of eligible practices provided data. 15

One study examined the use of vasectomy in the 2002 National Survey of Family Growth, a nationally representative survey of US residents ages 15-44 years. They evaluated differences between groups of patients in which the man did and did not have a vasectomy. For men between 30-45 years of age, white race, ever being married, older age, and increasing number of offspring were associated with increased utilization of vasectomy. 16

An additional study also examined data from male participants in the 2002 National Survey of Family Growth. They found that 13.3% of married men reported having had a vasectomy and 13.8% reported tubal sterilization in their partners. It is notable that tubal sterilization was reported by 21.3% of married women participants of the same ages in the 2002 National Survey of Family Growth. The likelihood of vasectomy increased with older age and greater number of biological children, non-Hispanic white ethnicity and having ever gone to a family planning clinic. Tubal ligation as the contraceptive method was more likely among partners of men who had not attended college, those of older age and those with live births. 10

General Guideline Statements

Guideline statement 1.

A preoperative interactive consultation should be conducted, preferably in person. If an in-person consultation is not possible, then preoperative consultation by telephone or electronic communication is an acceptable alternative. Expert Opinion

There should be a consultation with the patient prior to vasectomy. Similar to any surgical procedure, vasectomy requires an interactive discussion regarding risks, benefits and alternatives. Patients selecting vasectomy are choosing to make a permanent change in their fertility status. Some patients later regret this decision.  Therefore, a thoughtful preoperative discussion is important. The goal of this discussion is to ensure that the patient has appropriate expectations regarding the preoperative, operative and post-operative consequences of the vasectomy choice. A face-to-face discussion is not necessary if the distance between the patient and surgeon or other factors preclude an in-person meeting, but the consultation setting should allow the surgeon to take the patient's reproductive and medical history; the patient to ask questions of the surgeon and receive answers and the surgeon to provide pre-operative, operative and post-operative information relevant to the patient's decision.

Some men need help making the decision to have a vasectomy. The needs for support in making this decision were examined. 20 Forty-eight percent of men reported that the decision to undergo vasectomy was easy; 45% felt that the decision was difficult. Decisional difficulty was associated with the permanence of the procedure, risk of death of a child, fear of the unknown, fear of pain during the procedure and uncertainty about the effectiveness of the procedure. Physicians perceived that the factors that made the decision difficult for patients were fear of pain during the procedure, permanence of the procedure and fear of complications. The consultation procedure should be sufficient to allow the patient to address these kinds of concerns with the surgeon.

The surgeon performing vasectomy should obtain a general medical history, with particular emphasis on bleeding diatheses and other possible contraindications to surgery. For example, if a patient requires chronic anticoagulation and the risks of stopping anticoagulation are significant, then the surgeon and patient should consider alternative methods of family planning.

A physical exam of the genitalia should be performed prior to vasectomy. This exam may be performed immediately before the operative procedure if the preoperative consultation was not conducted in person. Physical examination at the time of in-person preoperative consultation is highly desirable because it may  identify genital pathology, such as a testis tumor or undescended testis, which would contraindicate routine bilateral vasectomy. In addition, physical examination may identify patients who are not good candidates for local anesthesia because of unusual scrotal sensitivity, patients who are too uncomfortable or too anxious to tolerate vasectomy under local anesthesia or patients whose vasa are especially difficult to palpate. It is preferable to do this examination far enough in advance of the vasectomy to allow the surgeon to plan for oral or other sedation if necessary. If preoperative counseling cannot be done in person, the preoperative physical examination may be delayed to a later date or to the day of surgery if necessary.

Guideline Statement 2

The minimum and necessary concepts that should be discussed in a preoperative vasectomy consultation include the following: Expert Opinion

Vasectomy as a permanent form of contraception. It is important for patients to understand that vasectomy is intended to be a permanent form of contraception. For this reason, the surgeon should be sure that the patient's request for vasectomy is soundly reasoned and not made precipitously. Some states require a delay or cool-down period between signing a consent form for vasectomy and the surgical date. The experience of the Panel members is that almost all men who request vasectomy have given the procedure serious thought for months or years, making a cool-down period superfluous in most cases. Nevertheless, state requirements must be observed.

Vasectomy does not produce immediate sterility. All patients have motile sperm in the ejaculate after vasectomy for some period of time. Other methods of contraception should be utilized until azoospermia or rare non-motile sperm (RNMS, ≤100,000 non-motile sperm/mL) is achieved. The time from vasectomy to azoospermia or RNMS can vary from weeks to months based on multiple factors, including frequency of ejaculation, patient age, surgical technique and variations in the anatomy of the vasal ampullae and/or seminal vesicles (for detailed discussion, see Section 6: Postoperative Practice). PVSA showing azoospermia or RNMS is necessary for the surgeon to be able to tell the patient if he can rely on his vasectomy for contraception.

A patient can be considered to be sterile if the PVSA shows azoospermia or RNMS. Patients whose post-operative semen analyses do not meet these criteria may eventually require a repeat vasectomy to assure occlusive effectiveness. This possibility should be mentioned in the preoperative visit.

Another form of contraception is required until vas occlusion is confirmed after vasectomy. Sperm that are left in the male reproductive system distal to the vasectomy site may retain the ability to fertilize an ovum. 21-24 Another form of contraception should be used routinely until PVSA shows azoospermia or RNMS.

Risk of pregnancy after vasectomy. Vasectomy is not 100% reliable in preventing pregnancy even after vas occlusion is confirmed by PVSA. There is a very small but finite risk of pregnancy after vasectomy even if the PVSA demonstrates azoospermia. The pregnancy rate in partners of men who have documented azoospermia after a vasectomy is about 1 in 2,000. 25-29 At the Elliot Smith Clinic in the UK, about three-fourths of 16,796 vasectomies were performed with mucosal cautery (MC) and the remainder were performed with ligation, excision and folding back. This Clinic reported a risk of about 1 in 2,800 after documented azoospermia on two consecutive semen analyses. 25-27 Marie Stopes International, which used nondivisional extended electrocautery, reported that approximately 1 in 2,500 vasectomies resulted in pregnancy after confirmation of azoospermia on two consecutive samples. 29   Alderman et al. (1988), who used ligation and excision for vas occlusion, reported four pregnancies among 5,331 men who completed the recommended PVSA regimen, giving a rate of about 1 in 1,300. 28   However, in other studies using ligation and excision without fascial interposition (FI), the risk of pregnancy has been reported to range from 1 in 30030 to 1 in 66. 31

Need for repeat vasectomy/risk of failure.  The possible need for repeat vasectomy, although rare, should be discussed with the patient in the preoperative visit. Vasectomy failure is defined as failure to achieve azoopsermia or RNMS or the occurrence of pregnancy. The patient may be told that the risk of vasectomy failure requiring repeat vasectomy is less than 1% if a technique of vas occlusion known to have a low occlusive failure rate was used during vasectomy (see Discussion under Guideline Statements 7 and 8  regarding occlusive failure rates). 15, 26, 29, 32-47

Patients should refrain from ejaculation for approximately one week after vasectomy. There is considerable variability among vasectomy surgeons regarding the suggested period of sexual abstinence following vasectomy. The opinion of the Panel is that patients should refrain from ejaculation for approximately one week after vasectomy to allow the surgical sites to heal and to allow for development of luminal occlusion of the vas after methods that use MC for vasal occlusion.

Patients who notice hematospermia during the first month or two after vasectomy may be reassured that this will resolve spontaneously and has no clinical significance.

Options for fertility after vasectomy.  Vasectomy reversal, sperm retrieval combined with in vitro fertilization (IVF) and/or intracytoplasmic sperm injection (ICSI) or cryopreserved sperm obtained before vasectomy, if available, may be used to achieve fertility after vasectomy. 48 With these techniques, the chance for pregnancy varies with individual patient conditions and circumstances such as the age of the female partner, the number of years between a vasectomy and its reversal and the number of actively motile sperm after thawing of a cryopreserved specimen. In general, pregnancy with live birth occurs in approximately one of two couples who attempt these techniques. This pregnancy rate is less than the pregnancy rate in couples in whom the male partner has not had a vasectomy. In addition, these reproductive techniques may be expensive.

Symptomatic hematoma and infection rates. Many studies with sample sizes >500 patients reported rates of immediate post-operative local complications; 37, 49-59 rates of hematoma and infection were 1 to 2% in most series. There is some evidence that rates are lowest among urologists compared to family physicians and general surgeons. 50 It is important to note that in this group of studies the method of vas isolation and occlusion often was not reported, making it unclear if surgical technique was related to complication rate. Although these studies were consistent in their findings, they were observational and largely retrospective, and, therefore, present an unknown risk of under-reporting. In addition to these reports of post-operative hematoma and infection in studies with sample sizes > 500 patients, there are very rare case reports of Fournier's gangrene after vasectomy 60-64 including one patient in Europe who died. 62 The opinion of the Panel is that patients should be counseled that the risk of hematoma and wound infection after vasectomy is approximately 1-2%.

Chronic scrotal pain. Rarely, some men complain of persistent unilateral or bilateral scrotal pain after vasectomy. The medical literature on post-vasectomy pain is comprised of poor-quality studies characterized by small sample sizes, failure to report inclusion criteria, failure to use validated pain measures, high non-response rates, poorly-specified definitions of outcomes, highly variable rates and lack of clarity regarding whether active or passive surveillance was used to determine chronic pain rates. The opinion of the Panel is that the most important information for patient counseling is the risk of chronic scrotal pain which is severe enough to cause the patient to seek medical attention and/or to interfere with quality of life. The most robust study of this indicates a 0.9% rate of such a pain seven months after the surgery. 65 Only three studies reported follow-up of three years or more regarding severe chronic scrotal pain after vasectomy. One group reported in a single-group retrospective study that at 4.8 years of follow-up, 2.2% of vasectomized men reported chronic scrotal pain sufficient to exert an adverse impact on quality of life. 66 An additional group reported in a prospective single-cohort design with four years of follow-up that 5% of vasectomized men sought medical attention because of testicular pain. 67 In the sole comparative study, at 3.9 years of follow-up 6.0% of vasectomized men reported pain severe enough to motivate the seeking of medical care compared to 2.0% of non-vasectomized men. 68 The opinion of the Panel is that chronic scrotal pain severe enough to interfere with quality of life occurs in 1-2% of men after vasectomy.  Medical or surgical therapy is usually, but not always, effective in improving this chronic pain. Few men require surgical treatment for chronic scrotal pain that may occur after vasectomy.

Permanent and non-permanent vasectomy alternatives. As with any surgical procedure, alternatives to vasectomy should be discussed. Benefits and risks of other permanent methods of contraception, (e.g., tubal sterilization) and/or non-permanent options for the patient (e.g., barrier methods) and partner (e.g., oral or injectable contraceptives and barrier methods) should be reviewed.

Additional relevant information. During the preoperative consultation, it is important to discuss the reproductive status of the patient's female partner. If the chance for pregnancy in the female partner is poor, the need for vasectomy may be less than the couple initially expected. In addition, if the female partner is pregnant at the time of the preoperative consultation, the couple may be advised to consider delaying the vasectomy until after delivery to avoid regret about vasectomy, which might occur if the pregnancy is lost unexpectedly.

Clinicians also should provide verbal and/or written instructions regarding post-operative care. The patient should wear supportive undergarments immediately after the procedure to reduce pain caused by tension on the spermatic cord. This support should be continued until the patient is comfortable without it. Mild swelling and pain are common for a few days. The patient should take oral pain medication as recommended by his physician.

Application of cold temperatures to the scrotum post-operatively is optional. In general, the patient should keep the surgical site clean and dry, but showers may be permitted the day after the surgery including gentle washing of the surgical site(s) with soap and water. Swimming or bathing in a tub of water should be avoided for three to five days.

In the absence of bothersome discomfort, patients may return to non-physical work on the day of or the day after vasectomy. The patient should be provided access to the doctor or his or her staff and should be instructed to call in the event of unusually severe pain, excessive bleeding or drainage, excessive swelling, redness, fever or any other problem that concerns the patient. Physical work or physical recreational activity may be resumed when permitted by pain tolerance.

Guideline Statement 3

Clinicians do not need to routinely discuss prostate cancer, coronary heart disease, stroke, hypertension, dementia or testicular cancer in pre-vasectomy counseling of patients because vasectomy is not a risk factor for these conditions. Standard

(Evidence strength – Grade B; Risk/burdens outweigh benefits) . The studies reviewed below under each disease state constitute Grade B evidence strength. Findings for each subgroup of studies were statistically and/or conceptually consistent, and any sources of bias were likely to result in increased reports of the disease state among vasectomized men compared to non-vasectomized men. Overall, there was no evidence that vasectomy constituted a risk factor for any of the listed conditions. The opinion of the Panel is that discussion of these disease states is not necessary as part of prevasectomy counseling.

Coronary heart disease (CHD). Three case-control studies 69-71 and ten comparative observational studies 72-81 examined a possible association between history of vasectomy and coronary heart disease (CHD). A variety of CHD measures were reported (e.g., new diagnosis of CHD, CHD-related hospitalizations, angina, ischemic heart disease, myocardial infarctions), limiting the feasibility of pooling outcomes across studies. Twelve of fourteen studies reported no significant differences between vasectomized and non-vasectomized men in diagnosis of CHD, CHD symptoms, non-fatal myocardial infarction or fatal myocardial infarction. One study reported lower rates of ischemic heart disease among vasectomized men compared to non-vasectomized men (OR 0.7, 95% confidence interval 0.6-1.0). 80 Only one study reported that vasectomized men were at higher risk of angina and CHD-related hospitalization than were non-vasectomized men;76 however, the findings from this study lack certainty because of the very small number of reported events in both groups. No study reported a significant relationship between years since vasectomy and CHD events, new diagnosis or prevalence when these studies controlled for key confounders such as age. The single study that reported on men with CHD risk factors (e.g., advanced age, cigarette smoking, elevated cholesterol, hypertension, family history) also found no significant relationship with vasectomy status. 71 Overall, the body of evidence indicates that there is no association between CHD and vasectomy.

Stroke . Five comparative cohort studies evaluated the relationship between vasectomy and stroke. 72-75, 80 There were no significant differences in incidence or fatality rates between vasectomized and non-vasectomized men. There also was no relationship between time since vasectomy and risk of stroke. 72-74

Primary progressive aphasia (PPA) and other forms of dementia . Only one small study has reported a potential link between vasectomy and dementia. 82 This study reported that vasectomy may be a risk factor for PPA, a rare type of dementia. This small case control study has uncertain significance. Anti-sperm antibodies, which are the putative link between vasectomy and PPA, were not found to be associated with dementia or language ability in a more recent study. 83 Further, a large epidemiologic study found no association between a history of vasectomy and several immune-related diseases. 84 Other large epidemiologic studies of vasectomy have not looked specifically for evidence that vasectomy is a risk factor for dementia; nonetheless, there is no evidence (other than one small study 82 of uncertain significance) that identifies an association between vasectomy and dementia. The opinion of the Panel is that clinicians do not need to routinely discuss PPA or other forms of dementia in pre-vasectomy counseling of patients because there is no convincing evidence that such a relationship exists.

Hypertension. Four comparative cohort studies examined the relationship between vasectomy and hypertension. 76, 79, 80, 85 Three studies reported no significant difference in frequency of hypertension in vasectomized men compared to non-vasectomized men. 79, 80, 85 One study reported that vasectomized men were at lower risk for the development of hypertension and for the utilization of diuretics and betablockers than were non-vasectomized men. 76

Prostate cancer. Fourteen papers reporting on ten comparative cohort studies were retrieved in the literature search. 73, 77, 86-97 Reports on only three studies indicated a statistically significant relationship between vasectomy and prostate cancer. 87, 91, 96, 97 A meta-analysis of 7 cohort studies that met criteria for pooling was performed to further delineate the possible association of vasectomy and prostate cancer (Coulson 1993; Giovannucci Tosteson 1992, 1993; Hiatt 1994; Lynge 2002; Romero 2012; Sidney 1987, 1991; Siddiqui 2014). 87-89 92-97 This analysis indicated that the relative risk of prostate cancer in vasectomized versus nonvasectomized men was statistically indistinguishable (Relative risk (RR) 1.07; 95% confidence interval (CI) 0.94 to 1.23, p=0.29). Twenty case-control studies were identified that evaluated the association of vasectomy and prostate cancer (Cossack 2014; Cox 2002; Emard 2001; Ganesh 2011; Hayes 1993; Hennis 2013; Holt 2008; Honda 1988; Hsing 1994; John 1995; Lesko 1999; Mazdak 2012; Mettlin 1990; Patel 2005; Platz 1997; Rosenberg 1990, 1994; Schwingle 2009; Stanford 1999; Zhu 1996); 98-116 only four studies reported a statistically significant odds ratio for this relationship (Emard 2001; one of three control groups reported by Hsing 1994; Mettlin 1990; Rosenberg 1990). A meta-analysis of 13 case-control studies that met inclusion criteria for pooling 98, 102, 104, 105, 107, 108, 110-112, 114-116 indicated that vasectomy was not statistically significantly associated with prostate cancer (pooled odds ratio – 1.7; 95% CI 0.98 to 1.16; p=0.12). The Panel concluded based on the results of the two meta-analyses that vasectomy is not associated with prostate cancer.

Of this group of 30 studies, fourteen reported an analysis that focused on whether age at vasectomy conferred differential risk of prostate cancer. Ten studies reported no relationship between age at vasectomy and prostate cancer (Hayes 1993; Holt 2008; John 1995; Lesko 1990; Mettlin 1990; Rosenberg 1994; Schwingl 2009; Sidney 1987, 1991; Stanford 1999; Zhu 1996); 92, 93, 98, 102, 104, 107, 108, 110, 114-116 four reported at least one significant statistical test (Patel 2005; Platz 1997; Lynge 2002; Rohrmann 2005). 89, 91, 111, 112 Eighteen studies analyzed whether years since vasectomy conferred differential prostate cancer risk. Thirteen studies concluded there was no relationship between years since vasectomy and prostate cancer; 89, 92, 93, 98, 104, 105, 107, 108, 110, 114-116 five studies reported at least one statistically significant finding (Emard 2001; Giovannucci Tosteson 1992, 1993; Rohrmann 2005; Rosenberg 1990; Siddiqui 2014 ). 87, 91, 96, 97, 100, 113 Thirteen studies reported an analysis based on prostate cancer stage. Nine studies reported no association between vasectomy and prostate cancer stage or grade; 98, 102, 104, 107, 108, 114-116 four studies reported at least one statistically significant finding. 91, 96, 113, 106 These subgroup analyses were not appropriate for meta-analysis given different data breakdowns across studies (i.e., different age breakdowns, years since vasectomy, and different methods of specifying prostate cancer lethality or stage) and the small sample sizes in some subgroups. Given the overwhelming majority of negative findings from these sub-analyses, however, the Panel interpreted these data to indicate that there is no association between age at vasectomy or years since vasectomy with differential prostate cancer risk, and that vasectomy does not predispose men to develop advanced or lethal prostate cancer.

Two older meta-analyses evaluated essentially the same set of studies retrieved by the panel's literature review. One such study reported an RR of 1.22 (95% CI of 0.90-1.64) for pooled cohort studies, an RR of 1.14 (CI 0.93-1.39) for pooled population-based case control studies and an RR of 1.92 (CI 1.37-2.67) for hospital-based case-control studies. 94 These estimates were characterized, however, by significant unexplained heterogeneity. One group pooled findings across study designs and reported an RR of 1.23 (95% CI 1.01-1.49). 95 These authors also reported the presence of significant unexplained heterogeneity. The authors of these two meta-analyses concluded that the statistical differences could be explained by high risk of selection bias.

Testicular Cancer. Four case-control studies 98, 118-120 and seven comparative observational studies 73, 77, 89, 90, 94, 121, 122 investigated whether there is an association between vasectomy and testicular cancer. A meta-analysis conducted as part of the Panel's literature review for the case-control studies indicated no significant difference between groups in terms of the odds of being diagnosed with testicular cancer for vasectomized men compared with non-vasectomized men (Odds ratio (OR) 1.18; 95% CI 0.93-1.49). Outcomes reporting differences across comparative observational studies did not permit a pooled analysis, but all seven studies reported non-significant differences between vasectomized and non-vasectomized men, and in the three studies that reported incidence by group, 73, 90, 94 incidence rates ranged from 0.02% to 0.11% across both groups. There was no association between history of vasectomy and testicular cancer stratified by years since vasectomy. 90, 98

Death . There is only one reported death, which was not in the United States, due to vasectomy. 62 Because the risk of death is very close to zero, the opinion of the Panel is that death due to vasectomy does not need to be discussed in preoperative counseling.

Guideline Statement 4

Prophylactic antimicrobials are not indicated for routine vasectomy unless the patient presents a high risk of infection. Recommendation

(Evidence strength – Grade C; Risks/burdens outweigh benefits). The AUA Best Practice Policy on Urologic Surgery Antimicrobial Prophylaxis [pdf] recommends that prophylactic antibiotics for open and laparoscopic surgery (including genital surgery) performed without entering the urinary tract are indicated only if risk factors are present. Risk factors include advanced age, anatomic anomalies of the urinary tract, poor nutritional status, smoking, chronic corticosteroid use, immunodeficiency, distant co-existent infection and prolonged hospitalization. The Panel affirms this recommendation and believes that diabetes is also a risk factor for post-operative infection. The opinion of the Panel is that the presence of one or more of these infection risk factors does not necessarily require the use of antimicrobial prophylaxis. When operating on certain patients who present with comorbidities associated with a particularly high risk of infection, the surgeon should consider the use of prophylactic antimicrobials.

Additional Points for Preoperative Practice

The minimum age requirement for vasectomy is the legal age of consent in the prevailing legal jurisdiction in which the procedure is performed. The prospective vasectomy patient must, at a minimum, be the legal age of consent according to relevant legal statutes. In addition, each surgeon should exercise clinical judgment to determine the appropriateness of performing a vasectomy on a particular patient. The patient's age, the number of children that the patient has and other factors that the surgeon's experience indicate may be associated with successful outcomes (e.g., patient satisfaction, absence of regret) should be taken into account in making this decision.

In the US, there is no requirement for spousal or partner involvement in preoperative consultation, but patients should be advised that partner or spousal involvement is desirable. Any consenting adult male may proceed with a vasectomy without consultation with his partner unless local laws stipulate otherwise. However, because the prospective vasectomy patient's decision affects the fertility options for both him and his partner or spouse, it is optimal that his partner should be included in the preoperative consultation and decision-making process.

Preoperative laboratory tests are not required for vasectomy patients unless the patient's medical history suggests that laboratory work may be necessary to assess the patient's suitability for the vasectomy procedure. In particular, preoperative coagulation tests should be considered if the patient has a history of liver disease, bleeding diatheses or is taking anticoagulants.

Absence from work. A low-quality, limited amount of literature was available to address how much time men typically take off from work after vasectomy. 25, 26, 52, 53, 123-135 Time off from work appears to be based on several factors, including type of job, day of the week of the procedure and patient preference. Many men took no time off work after vasectomy; others were absent from one to three days and sometimes more. For men who reported no time out of work, it was generally unclear if scheduled time off following the procedure had been pre-arranged prior to the vasectomy. Time lost from work varied considerably, and there may be cultural and financial reasons that explain the disparities. Insufficient information was provided to explore this hypothesis, however.

Additional Long-term Postoperative Complications and Outcomes:

Epididymitis . Rates of epididymitis varied across studies. Some variability is likely the result of different definitions used for epididymitis. For example, most studies did not differentiate between infectious epididymitis and non-infectious "congestive" epididymitis. Bacterial epididymitis is often confused with pain caused by distention of the epididymal tubule due to back pressure below the vasectomy site or by epididymal sperm granuloma. Nevertheless, across the 36 available studies, rates of epididymitis were generally low. Fourteen studies reported rates ≤ 1 percent. 33, 40, 55, 57, 128, 136-143 Most of the remaining studies reported rates ≤ 3 percent. 30, 32, 46, 144-151  True bacterial epididymitis post-vasectomy was rare and ranged up to 1.5% in the available studies. 137, 138, 148 The majority of studies compared vasectomy techniques, rather than using unvasectomized men for controls. The lack of an unvasectomized control group does not allow for a true estimate of the rate of these complications among vasectomized men; the rates presented here may be over-estimations.

Sperm granuloma . The rate of formation of a symptomatic nodule (presumed to be a sperm granuloma or a suture granuloma if a ligature was used to occlude the transected testicular end of the vas) varies based on technique, but in the overwhelming majority of available studies it was diagnosed at rates < 5% and was rarely symptomatic. 33, 35-37, 39, 50, 55, 106, 136, 137, 139, 141, 142, 145, 150, 152-161 The occurrence of an asymptomatic inflammatory nodule at the vasectomy site is probably common, and this is not considered a complication of vasectomy. The true rate of nodule formation at the vasectomy site has not been identified. Some of these nodules, whether they are histological sperm granulomata or not, are initially painful but the acute pain spontaneously resolves in two to three months or less in most cases. Treatment for a painful nodule at the vasectomy site is symptomatic therapy with anti-inflammatory agents and analgesics if needed. Persistent pain at the vasectomy site is rare and may respond to excision and repeat vasectomy.

Psychosocial outcomes . Relatively few studies examined psychological outcomes among vasectomized men. There is a paucity of high-quality, comparative observational studies reporting outcomes measured with validated instruments. In particular, data with applicability to men in the US or in other developed countries are sparse. Outcomes may vary by year of the study, geographic location, measurement tools used, selection of the study population, length of follow-up and other variables. It is thus impossible to draw firm conclusions on the effect of vasectomy on psychological function. 125, 162-164

Sexual outcomes . Although there is a large number of studies examining sexual outcomes after vasectomy, 45, 51, 53, 55, 59, 60, 123-126, 131, 134-136, 138, 144, 149, 152, 165-181 there are few studies with a comparison group and few studies that report data before and after the procedure. Thus, it is difficult to attribute changes in sexual satisfaction or function to the vasectomy itself. Outcomes relating to sexual function were heterogeneous, often poorly defined, and were usually assessed with instruments that were not validated.

Despite the relatively weak study designs, the available data with regard to sexual outcomes of vasectomy were consistent. Men generally resumed intercourse within two weeks of vasectomy. There was an increase in frequency or improvement in sexual satisfaction in half or more of patients and a decrease in frequency of intercourse and in sexual habits in only 5% of men across studies. A recent large population-based study confirmed the lack of sexual problems in men following vasectomy. 182 Overall, it appears that for the vast majority of men who undergo vasectomy, there are no negative effects on sexual function. Many patients are concerned that vasectomy may cause changes in sexual function such as erectile dysfunction, reduced or absent orgasmic sensation, decreased ejaculate volume, reduced sexual interest, decreased genital sensation and/or diminished sexual pleasure. Patients may be reassured that there is no evidence that any of these problems are caused by vasectomy.

Dissatisfaction and regret . Rates of dissatisfaction with vasectomy and/or regret at having undergone the procedure were in the range of 1-2% across a large number of studies, settings, and techniques. 51, 59, 66, 124, 125, 127, 134, 135, 137, 145, 147, 157, 167-169, 173, 175-178, 180, 181, 183-186 Eighty to 100% of vasectomized men would recommend the procedure to others. In the few studies that assessed reasons for dissatisfaction or regret, the most commonly reported reason was the desire for more children. 127, 185 These data highlight the importance of thoughtful pre-vasectomy counseling.

Endocrine outcomes . The literature review revealed no evidence of significant effects of vasectomy on testosterone, follicle-stimulating hormone (FSH), luteinizing hormone (LH), lipids (e.g., serum total cholesterol, low-density lipoproteins, high-density lipoproteins, triglycerides) or bone mineral density 187-194 at follow-up durations ranging from one to 21 years. 

Urolithiasis . One low-quality study reported on urolithiasis rates of vasectomized compared to non-vasectomized men. 195 The odds ratio of urolithiasis in vasectomized versus nonvasectomized men < 45 years of age was 1.9 (95% CI, 1.2-3.1); the OR was not statistically significant for men > 45 years of age. The OR was highest in men zero to four years post- vasectomy, compared to men without vasectomy. 195 In the absence of more definitive data or other confirmatory studies, it remains unclear whether there is a relation between vasectomy and urolithiasis.

Immunologic outcomes . A limited literature was available on the incidence and relevance of anti-sperm antibodies (ASAs) post-vasectomy. 196-208 Most studies are based on measurement techniques which are no longer used. ASAs were rarely present prior to vasectomy and a number of studies demonstrated the appearance of sperm agglutinins and/or immobilizing antibodies in serum after vasectomy. 201-204, 207, 209 Few of these studies correlated the presence or titer of such antibodies with pregnancy outcome after vasectomy reversal. One such study showed the presence of such antibodies in the seminal plasma of only 4% of men after vasectomy and the appearance of sperm agglutinins in the seminal plasma of 10 of 29 men after vasectomy reversal. 208 An additional study also showed that pregnancy occurred in the wives of 11 of 13 men without seminal plasma sperm agglutinins after vasovasostomy compared to only 1 of 7 men with seminal plasma sperm agglutinins. 206 To the contrary, one study showed no statistically significant difference in the level of serum sperm agglutinating or immobilizing antibodies one year after vasectomy reversal between 17 men whose partners had become pregnant and 18 men whose partners had not yet become pregnant. 209 These investigators found low to moderate titers of immobilizing or agglutinating antisperm antibodies in the seminal plasma of 5 of 25 men one year after vasectomy reversal; one of these five men had established a pregnancy. Studies pertaining to the influence of antisperm antibodies on pregnancy rates after vasectomy reversal are rare. The precise prevalence of impaired fertility due to anti-sperm antibodies is unknown.

In a review of this topic, one study concluded that the most rigorous studies have not proven a cause and effect between abnormal immune parameters, such as the presence of antisperm antibodies, and impaired fertility and noted that there is wide variation and inconsistency regarding this association, depending upon which test(s) are employed, the study methodology used and the patient population under study. 201 That same study also concluded that there is no universal agreement regarding which method of anti-sperm antibody test should be used or the proper treatment if anti-sperm antibodies (ASA) are detected. The opinion of the Panel is that, after vasectomy, impaired fertility due to anti-sperm antibodies is infrequent and that the presence of serum antisperm antibodies should not be considered a deterrent to vasectomy reversal.

Testicular changes after vasectomy . Data are sparse on the effect of vasectomy on testicular histology and on pathologic changes following vasectomy. The available studies suggest that there may be significant post-vasectomy pathological changes in testes. 211, 212 Electron microscopy revealed that interstitial fibrosis was present in the testis of 23% (p<0.01) of men following vasectomy and that there was a significant correlation (p<0.01) between these changes and fertility in men who underwent a successful vasectomy reversal as defined by sperm in the ejaculate. 211 These testicular changes were not associated with antisperm antibody status as measured by the indirect immunobead assay. 212

Death as a result of vasectomy . The literature review found no reports of death as a result of vasectomy in contemporary American urological practice. There is one report of death after vasectomy due to Fournier's gangrene. This case occurred in Europe and was reported in 1992. 62 In addition, a large cohort study did not show any association between overall mortality and vasectomy. 97

Techniques for Local Anesthesia

Guideline statement 5.

Vasectomy should be performed with local anesthesia with or without oral sedation. If the patient declines local anesthesia or if the surgeon believes that local anesthesia with or without oral sedation will not be adequate for a particular patient, then vasectomy may be performed with intravenous sedation or general anesthesia. Expert Opinion

Vasectomy can be safely performed in almost all patients using local anesthesia alone. Occasionally adjunctive oral or intravenous sedation may be optimal or necessary for the few patients who are unable to tolerate vasectomy under local anesthesia alone. For the rare patient in whom preoperative examination suggests that vas isolation will be particularly difficult and in whom oral or intravenous sedation is unlikely to be sufficient for patient comfort, general anesthesia may be necessary. Direct topical application of anesthetic cream at the vasectomy site in addition to standard injection of local anesthesia also may be used. Several small studies have shown that topical application of anesthetic cream before local injection of anesthetic may reduce pain associated with injection of local anesthetic agents. 213-215 One additional study showed no decrease in intraoperative pain when topical anesthetic cream was used. 216 The opinion of the Panel is that there is uncertainty regarding whether the topical application of anesthetic cream reliably reduces pain; the decision regarding the use of anesthetic cream should be left to the judgment of the individual practitioner. The topical cream should be applied by a health care professional rather than by the patient to prevent excessive application and risk of toxicity.

Practitioners are cautioned that topical anesthetic cream should not be the sole source of local anesthesia for the performance of vasectomy. Infiltration of local anesthetic agent into the skin and perivasal tissue is always necessary prior to performance of a vasectomy, regardless of whether topical anesthetic cream is used.

Other Important Points of Technique for Local Anesthesia.

Needle size . In the opinion of the Panel, the smallest available needle should be used for the injection of local anesthesia because small gauge needles typically produce less pain than larger gauge needles. In the Panel's experience, the optimal range of needle sizes is 25 to 32 gauge. One study evaluated patient visual analog scale (VAS) scores in response to blinded forearm intradermal injection with 25 gauge vs. 30 gauge needles. 217 Mean VAS score was 32mm for the 25 gauge needle compared to 25mm for the 30 gauge needle. Although this difference was statistically significant (p<0.05), it is not clear that the difference represents a clinically-meaningful difference in patient pain experience. However, these data do indicate that the pain associated with needle diameters in this range is minor. These data are in agreement with the Panel's opinion that needles between 25 and 32 gauge should be utilized for local infiltration and spermatic cord block to minimize patient pain. Patients may be told that the anesthetic often takes effect within one to three seconds. The majority of members of the panel feel that the use of 30 or 32 gauge needles for injection of the local anesthetic is associated with less pain than occurs with the use of larger needles.

Pneumatic injector . A pneumatic injector, also known as a jet or no needle device, has been used to deliver anesthetic agent transcutaneously. However, it is not clear that intra-operative pain is reduced by this technique compared to standard injection technique. In one study, the mean VAS score for initial pain after pneumatic injections was 15.6 mm compared to 21.2 mm with needle injection (on a 0 to 100 mm scale). This difference was statistically significant (p=0.029) but may not be clinically meaningful given that VAS scores were low for both techniques. 218 Furthermore, the pain during the remainder of the procedure was 16.8 mm versus 18.6 mm respectively. 218 These differences were not statistically significant. 

In a separate cohort study, the mean VAS scores were reported for three separate procedures: 33 mm for local infiltration, 22 mm for no-needle pneumatic injector and 17 mm for local infiltration and cord block. The VAS score differences for the initial injection were significantly different between local infiltration and local infiltration with cord block and between local infiltration and pneumatic injection, but there were no differences for the VAS scores during the remainder of the procedure. 219 Overall, the opinion of the Panel is that it is unclear whether use of a pneumatic injector reliably reduces pain to a clinically significant extent; this decision is left to the judgment of the individual practitioner. Pneumatic injection may be especially suitable for needle-phobic men.

Addition of buffer, epinephrine or corticosteroids to the local anesthetic agent or a topical cutaneous spray . There are insufficient data to know whether addition of buffer, epinephrine or corticosteroids to the local anesthetic agent or topical cutaneous spray reduces pain during vasectomy or reduces postoperative inflammation. Therefore, the addition of these agents is not endorsed by the Panel. Buffers have been added to local anesthetic agents to reduce pain during intradermal injections of various types but not specifically for vasectomy. For example, commercially available xylocaine 1% is buffered to a pH of 6.7 (range 5.5-7.2). 220 In a blinded study, VAS scores for buffered solutions were 18.3 mm and for fresh solutions were 23.5 mm (p=0.05). 221 Although VAS scores were lower for buffered solutions, the difference may not be clinically significant. In the absence of data obtained specifically for vasectomy, the Panel does not endorse the addition of these substances to anesthetic agents.

Vas Isolation

Background Information About Vas Isolation

Vas Isolation Techniques.  There are two key surgical steps in performing vasectomy: 1) isolation of the vas and 2) occlusion of the vas. The risks of intraoperative and early postoperative pain, bleeding and infection are related mainly to the method of vas isolation. The success and failure rates of vasectomy are related to the method of vas occlusion (see next section titled Vas Occlusion Techniques).  Methods of vas isolation include Conventional Vasectomy (CV) and Minimally-Invasive Vasectomy (MIV), which includes no-scalpel vasectomy (NSV). For definitions, see Table 3 above.

Conventional Vasectomy (CV) . CV technique was the most common technique before the introduction of MIV techniques and special vasectomy instruments. CV is performed by making either one midline incision or bilateral scrotal incisions using a scalpel. Incisions are usually from 1.5 - 3 cm. No special instruments are used during CV, and the vas usually is grasped with a towel clip or an Allis forceps. During CV, the area of scrotal dissection usually is much larger than occurs with MIV techniques.

No-Scalpel Vasectomy (NSV) . The no-scalpel vasectomy technique was developed in 1974 in China by Dr. Li Shunqiang to make vasectomy a more acceptable method of contraception. The NSV isolation technique was the first minimally-invasive technique for vasectomy and is described in detail in text and with diagrams by Li et al. (1991). 222 An excellent description of NSV technique also can be found in training materials prepared by EngenderHealth 223 . Note that the NSV technique is a method of vas isolation and does not specify a method of vas occlusion. For a detailed description of the NSV technique, see Appendix A.

Strictly speaking, to be called a Li no-scalpel vas isolation technique, all of the following surgical steps must be observed:

  • Use vas ring clamp and vas dissector, both of which have been specially designed for no-scalpel vasectomy
  • Apply the vas ring clamp around the vas, perivasal tissue and overlying skin before making the skin opening
  • Create a skin opening of ≤10 mm by piercing the skin with the vas dissector followed by spreading the tissue overlying the vas with the vas dissector to expose the bare anterior wall of the vas
  • Pierce the bare vas with one tip of the vas dissector
  • Then use a supination maneuver to elevate the vas above the skin opening
  • Re-grasp a partial thickness of the vas with the vas ring clamp rather than encircling the vas with the ring clamp
  • Complete the posterior dissection with the vas dissector to isolate the vas from surrounding perivasal tissue and vessels
  • Divide the vas, with or without excision of a vas segment, and then occlude the vas with the surgeon's preferred technique for vas occlusion
  • Leave the skin opening unsutured except in rare cases that may require a skin suture

If all of these specific steps are not used, then the vasectomy should be called a minimally-invasive vasectomy (MIV) rather than a no-scalpel vas isolation technique. As an example, if the only difference is creation of a skin opening ≤10 mm with a scalpel before applying the vas ring clamp around the vas, the technique is labeled as an MIV technique because each exact step of the NSV technique was not used. 211

When difficulty in isolating the vas is encountered or anticipated, as may be expected with a history of surgery for testicular maldescent or perivasal scarring from a previous operative procedure, a larger incision similar to the incision typically used for CV may be needed. Even in these more difficult vasectomies, the vas ring clamp and vas dissector facilitate the procedure and minimize tissue dissection.

Minimally-Invasive Vasectomy (MIV) . The term "minimally invasive vasectomy" includes any vas isolation procedure, including the NSV technique, which incorporates two key surgical principles. 39, 224

1. Small (≤10 mm) openings in the scrotal skin, either as a single midline opening or as bilateral openings

2. Minimal dissection of the vas and perivasal tissues, which is facilitated by using a vas ring clamp and vas dissector or similar special instruments

The three finger technique described in Appendix A for immobilizing the vas or for making the skin opening has been modified slightly by various surgeons using MIV techniques other than the strict NSV technique. These variations include the use of the thumb rather than the middle finger behind the scrotum and other modifications of finger placement, bilateral skin openings or scrotal skin opening(s) made before grasping the vas with the vas ring clamp. 

MIV isolation techniques utilize either an open access approach or a closed access approach. In the open access approach, the skin opening(s) are made before the vas ring clamp or similar instrument is applied to the vas. In the closed access approach, the vas ring clamp or similar instrument is applied around the vas, perivasal tissue and overlying skin before the skin opening(s) is (are) made. The vas ring clamp and vas dissector are not required to perform MIV but are always very helpful. 126 Other small or specially designed instruments may be used successfully to isolate the vas. 39, 126, 224 Open access is sometimes necessary for men with thick scrotal skin or other anatomy that makes closed access difficult or impossible.

Other Important Points of Surgical Technique .

Single midline or bilateral incisions . The use of one midline or bilateral scrotal skin openings should be based on the surgeon's preference. One large observational study (N=1,800) compared single incision to double incision procedures. Fewer adverse events were reported with a single incision and the procedure time was reduced, but no statistical testing was performed. 225 The Panel opinion is that there is no clear advantage to making one or two skin openings. The choice between midline and bilateral incisions should be left to the clinical judgment of the surgeon performing vasectomy.

Site of incision(s) . For a midline approach, the scrotal skin opening should be made just below the penoscrotal junction or midway between the penoscrotal junction and the top of the testes. For a lateral approach, some experts recommend that the scrotal skin opening should be made at the level of the penoscrotal junction or higher.Scrotal skin openings for vasectomy should be positioned to provide access to the straight portion of the vas. Higher openings allow better access to the straight portion of the vas, make it easier to perform mucosal cautery and create longer vas remnants on the testicular side of the vasectomy. The opinion of the Panel is that occlusion of the vas is more easily performed in the straight portion than in the convoluted portion of the vas. In addition, occlusion of the vas in its straight portion may facilitate the performance of the anastomosis during vasovasostomy if reversal of the vasectomy is requested later.

Insuring that one vas is not occluded twice . For a single-incision vasectomy, the surgeon should ensure that the same vas is not isolated and occluded in two locations, leaving the other vas unoccluded. A gentle tug on each vas during isolation will cause the ipsilateral testis to move. 226

Guideline Statement 6

Isolation of the vas should be performed using a minimally-invasive vasectomy (MIV) technique such as the no-scalpel vasectomy (NSV) technique or other MIV technique. Standard

(Evidence strength – Grade B; Benefits outweigh risks/burdens) . No-Scalpel Vas Isolation Technique. The available evidence indicates that a minimally-invasive vas isolation procedure results in less discomfort during the procedure and in fewer postoperative complications. One large randomized controlled trial, 59 one comparative study, 227 one observational study, 222 and two systematic reviews 228, 229 concluded that the NSV technique of vas isolation has fewer early postoperative complications than CV. The randomized trial was a multi-center study at eight sites and included 1,429 men. 59 One study found significantly fewer hematomas and infections, significantly less pain and a more rapid resumption of sexual activity among men who had an NSV procedure. The comparative study included 1,203 vasectomies. 227 While not a randomized trial, the 28 surgeons in the study were all experienced and had participated in previous vasectomy "festivals" in Thailand. One study found that the men who had the NSV technique had significantly fewer hematomas and infections, with an overall complication rate of 0.4/100 procedures for the NSV technique compared with 3.1/100 for conventional vasectomy (p<0.001). This study found that NSV took less time than CV. 227

Other MIV Techniques . Reports on other MIV techniques have proposed special instruments other than the vas ring clamp and vas dissector 39, 123, 126, 224 or alternative ways to use the vas ring clamp and vas dissector. 231 The rate of intraoperative and early postoperative complications appear similar to those of the NSV technique. 39, 123, 126, 224, 230

When any MIV technique is used, the skin opening may be closed with a suture or left open at the end of the procedure. With a skin opening of ≤ 10 mm, sutures are usually not needed for wound closure. The choice of suturing the skin or leaving it open should be based on individual operative conditions and the surgeon's experience.

The body of evidence showing the superiority of MIV techniques (reduced intraoperative discomfort and reduced postoperative complications) compared to conventional vasectomy techniques is given Grade B for strength of evidence because it is comprised of a good quality RCT and several systematic reviews in addition to a body of observational studies. Overall, the findings across reports were consistent. It is the strong opinion of the Panel members that isolation of the vas with an MIV technique is superior to CV isolation procedures.

Vas Occlusion

Background Information about Vas Occlusion

In the US, virtually all techniques of vasectomy use complete division of the vas with or without excision of a segment of the vas. Following division of the vas, the divided vasal ends may be separated by one of several techniques and/or the flow of fluid and sperm within the vas lumen may be blocked by one of several methods. There is only one technique of vas occlusion, non-divisional extended electrocautery or the Marie Stopes International technique (see below), which does not use division of the vas. This technique is rarely, if ever, used in the United States. Therefore, in this guideline, vas occlusion means that the vas has been completely divided with or without excision of a vas segment, unless otherwise noted. Further, in this document, division/excision (D/E) means that the vas is divided and that a segment may or may not be excised. The panel found no consistent evidence indicating that division with excision of a short vas segment (< 4 cm) is preferable to division without excision of a vas segment.

Vasectomy effectiveness can be defined as either contraceptive effectiveness , which is the absence of pregnancy, or occlusive effectiveness , which is demonstrated by the finding on PVSA of azoospermia or of RNMS, as defined in a subsequent section of this Guideline. For definitions, see Table 4.

The most commonly utilized vasectomy occlusion techniques are the following:

Fascial interposition (FI) is the technique of placing a layer of the internal spermatic fascia between the two divided ends of the vas. The fascial layer may be placed over the testicular or the abdominal end. Typically it is combined with other techniques such as ligation and excision or mucosal cautery.

Ligation means occlusion of the vas with ligatures with division/excision of the vas between the occluded points and with or without FI. The number of ligatures on each end of the divided vas varies between one (most common) and three. The length of the vas segment excised is most commonly approximately 1 cm but varies between 0 and 5 cm.

Clips means occlusion of the vas with clips with division/excision of the vas between the occluded points and with or without FI. The number of clips placed on each end of the divided vas is usually one or two but may be more. The length of the vas segment excised is most commonly approximately 1 cm.

Folding back is the technique of folding and suturing each divided vas end on itself to prevent the two cut ends from facing each other.

Mucosal cautery (MC) is the technique of applying thermal or electrical cautery to the mucosa of the cut ends of the vas to destroy the vasal mucosa while avoiding or minimizing damage to muscle layers. The goal of MC is to create a plug of scar tissue which occludes the vas lumen. The length of the cauterized segment varies from a few mm to 1.5 cm. MC may be combined with excision of a vas segment, folding back or FI. Cauterizing the mucosa while simultaneously limiting cautery damage to the muscular layer of the vas prevents sloughing of the cauterized portion of the vas, which could occur if its full thickness is destroyed by cautery. 

Non-divisional extended electrocautery technique of vas occlusion (Marie Stopes International technique) consists of electrocoagulation of the full thickness of the anterior wall and a partial thickness of the posterior wall of the vas for a length of approximately 2.5 to 3 cm without dividing the vas. 29, 153 It is the only technique which does not completely divide the vas. It uses monopolar electrocautery delivered by a Hyfrecator through a reusable needle. The technique was developed by Marie Stopes International in London (United Kingdom) as a vasectomy technique that could be easily disseminated, particularly in Third World conditions. 153

Open-ended vasectomy is the technique of leaving the testicular end of the divided vas unoccluded while occluding the abdominal end. The hypothetical aims of this technique are 1) to prevent or reduce post-vasectomy pain by decreasing back pressure in the epididymis 46 and 2) to allow the formation of a sperm granuloma at the transected testicular end of the vas, which some experts speculate might increase the chance of success of vasectomy reversal. 46, 150 When open-ended vasectomy is performed, FI is used to prevent recanalization.

Challenges in Interpreting the Evidence. The Panel undertook review of the vas occlusion literature with the goal of identifying with a high level of certainty specific techniques that consistently produce occlusive effectiveness. However, the vas occlusion literature suffers from serious methodological flaws that reduce certainty regarding conclusions about the relative efficacy of various occlusion techniques. These flaws include failure to identify whether enrollment is comprised of consecutive or selected patients; failure to obtain at least one PVSA in large percentages of vasectomized men, resulting in incomplete information regarding vasectomy outcomes; lack of information about follow-up protocols; unclear criteria for vasectomy failure; wide variations in follow-up duration; very short periods of follow-up duration and, possibly, failure to report series that had high failure rates. Two reports showed uncertain significance. 25, 45 One reported on a series of 14,047 vasectomies among which six men reported late recanalization with pregnancy. It is not clear from this report exactly how many couples were followed for pregnancy occurrence. In the absence of this information, it is not possible to conclude with certainty that the pregnancy failure rate is 6 in 14,047; the pregnancy failure rate may be higher if pregnancy data were not available for all patients. The other study reported no cases of sperm persistence and no pregnancies in 6,248 vasectomy patients. Because the number of patients who were followed and the timing of follow-up are not detailed in this paper, it is not possible to know whether successful vasectomy occurred in 6,248 men or in some number less than 6,248. Methodologically strong studies of occlusion technique effectiveness that would result in a high level of certainty regarding findings are characterized by the following:

  • Randomized controlled trial procedures
  • Enrollment of consecutive patients
  • Clearly described technique of vas occlusion
  • Standardized PVSA protocol
  • Clearly described criteria for PVSA failure
  • PVSA data on all patients for a minimum of six months post-vasectomy
  • Follow-up regarding pregnancy for a minimum of one year after vasectomy
  • Studies with sufficient sample size to allow precise estimation of effects

None of the studies reviewed by the Panel met all of these criteria, and only three studies met a majority of these criteria. This resulted in assigning Grade C as the strength of evidence for the body of literature on the efficacy of vas occlusion. Given the limited certainty associated with the use of Grade C evidence, the Panel focused on identifying methods of vas occlusion that produce consistent findings, including acceptably low failure rates, across multiple studies with large numbers of patients.  Four methods of vas occlusion that appear to be consistently reliable with regard to contraceptive and occlusive effectiveness were identified: (1) MC with FI and without the use of ligatures or clips on the vas; (2) MC without FI and without the use of ligatures or clips on the vas; (3) open ended vasectomy leaving the testicular end unoccluded while using MC of the abdominal end of the vas with FI; and (4) the Marie Stopes International method of vasectomy with extended non-divisional electrocautery of the vas. Based on this analysis of the literature, the Recommendations below were created. The Panel acknowledges that, in creating an evidence-based guideline, these Recommendations are necessarily based on the data that are available in the medical literature. The panel recognizes that there may be other techniques of vas occlusion that are reliable in producing occlusive effectiveness, even though detailed reports of the results of such occlusive methods have not been published.

Guideline Statement 7

The ends of the vas should be occluded by one of three divisional methods:

  • Open ended vasectomy leaving the testicular end of the vas unoccluded, using MC on the abdominal end and FI;

OR by the non-divisional method of extended electrocautery. Recommendation

(Body of Evidence Strength – Grade C; Benefits outweigh risks/burdens) . Reliable Techniques of Vas Occlusion. The Panel chose to define the acceptable rate of vas occlusion failure as ≤ 1%. In researching the results of vas occlusion techniques, 89 study arms reporting on 126,821 patients were found (see Table 5 below; see text under Discussion sections for citations). Failure of vas occlusion was reported in most of these studies as failure to achieve azoospermia or in a few studies as failure to achieve azoospermia or RNMS.

The opinion of the Panel is that, for a method of vas occlusion to be recommended, it should have occlusive failure rates which are consistently ≤1% in large numbers of patients across studies conducted by different surgeons. Three divisional techniques that fit these criteria were identified and are recommended by the Panel: (1) MC with FI and without ligatures or clips applied on the vas; (2) MC without FI and without ligatures or clips applied on the vas; and (3) open ended vasectomy leaving the testicular end of the vas unoccluded, using MC on the abdominal end and interposing fascia between the ends. One non-divisional technique also is recommended:  non-divisional extended electrocautery.

Figure 1: Definitions and Diagrams

Mucosal cautery with fascial interposition.

Thirteen study arms evaluated MC of both vas ends and FI to occlude the vas in approximately 18,456 patients. 33, 35-37, 39-41, 43-45, 47, 231, 232 In nine study arms FI was performed over the abdominal end, in two study arms FI was performed over the testicular end, and in two study arms the end was not specified. Failure rates for this technique ranged from 0.0% to 0.55%, with most study arms reporting rates of 0.0% failure. Although the majority of these data were from non-randomized observational designs, one study arm was from a high-quality observational study 231 that reported an occlusive failure rate of 0.0% and one technical failure associated with a missed vas. Additional support for the efficacy of MC of both vas ends and FI is provided by Labrecque (2006), 233 which is a secondary analysis of PVSA data from Barone (2004). 231 This paper reported 0% recanalizations with use of this technique. Given the large number of patients evaluated, the overall consistently low failure rates and the low failure rate from the single high-quality study, the panel judged that this vas occlusion technique is likely to be consistently effective.

Figure 2: Mucosal cautery with fascial interposition.

Mucosal cautery without fascial interposition.

Six study arms (Barone 2004 – 2 arms; Coffman 1974; O'Brien 1995; Philp 1984; Shapiro 1979) evaluated MC of both vas ends but without FI to occlude the vas in approximately 13,851 patients. 26, 32, 42, 46, 231 Failure rates for this technique ranged from 0.0% to approximately 1.0%. Four of the six study arms were from non-randomized observational designs, but two arms were from Barone (2004), the high-quality observational study; these two arms reported an overall failure rate of 1.0% It should be noted that the failures in Barone (2004) all occurred in the Brazil arm which is the only arm of the six discussed here that used division without excision. All of the other study arms both divided the vas and excised a segment. Given the relatively large number of patients evaluated, the consistently low failure rates and the low failure rate from the single high-quality study, the panel judged that MC without FI also is likely to be consistently effective.

Figure 3: MC without FI

Open ended method leaving the testicular end unoccluded with mucosal cautery of the abdominal end and FI.

Four study arms 38, 41, 158, 231 evaluated approximately 4,600 men with an open ended method in which the testicular end was left unoccluded, the abdominal end was occluded with MC and FI was performed. Failure rates ranged from 0.0% to 0.50%. One of the three study arms was from Barone (2004), the high-quality observational study, and reported a failure rate of 0.0%.212231 Additional support for leaving the testicular end open, applying MC to the abdominal end and performing FI is provided by Labrecque et al. (2006), which is a secondary analysis of PVSA data from Barone (2004). 214, 233 Labrecque (2006) reported 0% recanalizations with use of this technique. Because of the low failure rates, including the low failure rate from the high-quality study arm, the panel judged that this technique also is consistently effective.

With regard to the same technique of open ended vasectomy with MC but without FI, only two study arms were found. Both study arms were from the same study evaluated a total of 171 patients and reported failure rates of 4.73% and 4.35% in the two arms of the study. 46 The panel judged that, given the available evidence, uncertainty remains regarding the efficacy of open ended vasectomy with MC to occlude the abdominal end without FI. Therefore, the panel does not advocate the omission of FI in performing open ended vasectomy with MC.

Figure 4: Testicular end open, abdominal end cauterized with FI

Non-divisional vasectomy with extended electrocautery (Marie Stopes technique).

One paper reports the findings from a 10-year period at the Marie-Stopes Clinic during which 45,123 vasectomies were performed at more than 20 centers by up to 30 clinicians. PVSAs were obtained on 41,814 patients and revealed 267 early failures (a failure rate of 0.64%) defined as patients whose PVSAs continued to show the presence of sperm and required reoperation. 29   Failure rates ranged from 0.28% to 1.3% across centers that used this method. Given the consistency of low failure rates across many centers and many clinicians as well as the very large number of patients, the panel interpreted these data to indicate that non-divisional vasectomy with extended electrocautery of the vas also is consistently effective.

Figure 5: MSI

Guideline Statement 8

The divided vas may be occluded by ligatures or clips applied to the ends of the vas, with or without FI and with or without excision of a short segment of the vas, by surgeons whose personal training and/or experience enable them to consistently obtain satisfactory results with such methods. Option

(Body of Evidence Strength – Grade C; Balance between benefits and risks/burdens uncertain) . The Panel has defined consistently satisfactory results as an occlusive failure rate of 1% or less and has focused occlusive technique recommendations on techniques that produce consistently satisfactory results across multiple surgeons and large numbers of patients. The Panel is aware, however, that large numbers of surgeons in the US and elsewhere occlude the vas using ligatures or clips. The available literature reporting on these techniques is characterized by great variability in failure rates, with single surgeons from single institutions reporting satisfactory results (i.e., ≤1.0% failure) and others reporting unacceptably high failure rates. In addition, many studies, including more than half of those that reported on the use of ligation, were published more than 30 years ago and may not reflect the skill level of current surgeons.

This highly-variable literature is reviewed in the paragraphs below. The Panel interpreted these data to mean, overall, that the balance between benefits and risks/burdens for these techniques is uncertain. However, individual surgeons who have the training and/or experience that produce consistently satisfactory failure rates of 1% or less are justified in using these techniques.

Occlusion of both vasal ends with ligatures without FI.

Thirty-one study arms evaluated occlusion by ligatures of both ends of the vas without FI. 23, 26, 28, 31, 35, 36, 43, 47, 131, 137, 138, 140, 141, 143, 145, 147, 149, 155, 160, 184, 234-242 Failure rates ranged from 0.0% to 13.79%. Specifically, twelve studies reported failure rates of 1.0% or less (including four studies from the US, one from Canada, three from the UK, two from India, one from Australia and one from Brazil). Six studies reported failure rates between 1.0 and 2.0% (including two studies from the US, one from Canada, one from Thailand, one from El Salvador and one from China). Thirteen studies reported rates higher than 2.0%, including five studies that reported rates higher than 5.0% (comprised of one study from the US, two from Mexico, one from the UK and one from Finland). Two of the three highest failure rates were reported in high-quality studies. The only randomized trial reported a failure rate of 12.74%. 241 A single-group design with more methodological rigor than most studies (e.g., a clear and complete follow-up protocol and all patients accounted for) reported a failure rate of 11.5%. 242 One study reported that in the only randomized controlled trial, the early recanalization rate for this technique was 25.0% with approximately half of these patients eventually achieving a successful vasectomy after delayed occlusion was detected. 233

The panel interpreted this wide range of failure rates to mean, overall, that the balance between benefits and risks/burdens of this technique is uncertain. Nevertheless, the Panel recognizes that some surgeons achieve consistently satisfactory results with this technique.

Figure 6: Ligation both ends without FI

Occlusion of both vasal ends with ligatures and FI.

Nine study arms evaluated the use of ligatures on both ends of the vas in combination with FI. Six study arms reported failure rates of less than 1.0% (including one UK study, one study from Denmark, one study from Africa, one study from the US and one study from New Zealand); five of these six studies reported 0.0% failure rates. The remaining studies reported failure rates of 1.11%, 1.98%, and 5.85%. The high rate of 5.85% was reported in the only RCT among the included studies. 241 Because the highest quality study also reported the highest failure rate, the Panel interpreted these data to mean that the balance between benefits and risks/burdens for this technique is uncertain but that some surgeons achieve consistently satisfactory results.

Figure 7: Ligation both ends with FI

Occlusion of both vasal ends with clips without FI.

Seven study arms used clips on both ends of the vas without FI. 38, 40, 132, 141, 156, 243 These studies reported failure rates ranging from 0.0% to 8.67%. Four studies reported failure rates less than 1.0% (including three US studies and one Canadian study), one US study reported a failure rate of 1.18%, and the remaining studies (both from Canada) reported failure rates of 5.42% and 8.67%. Again, the Panel interpreted this wide range of failure rates to indicate that, overall, the balance between benefits and risks/burdens of this technique is uncertain but that some surgeons achieve consistently satisfactory results.

The literature review identified only one study that combined clips with FI; 0.0% occlusive failures were reported in 1,073 patients. 244 Given the lack of additional studies using this technique, the reliability of clips combined with FI across surgeons and centers is not known. The opinion of the Panel, however, is that vas occlusion by clips and FI is unlikely to produce higher occlusive failure rates than vas occlusion by clips alone.

Figure 8: Clip Both ends without FI

Other Occlusive Techniques . Numerous other occlusive techniques or combinations of occlusive techniques with adjunctive methods have been reported (see Table 5), but insufficient evidence was retrieved to address whether these other techniques with or without adjunctive methods produced consistently satisfactory results. In many cases, a particular technique was reported in only a single study by a single surgeon, making it unclear if results would replicate and generalize to other surgeons and settings.

Adjunctive Techniques for Vas Occlusion . The literature was also examined to determine whether adjunctive techniques for vas occlusion are associated with consistently lower failure rates. Insufficient evidence was found to draw conclusions with regard to the techniques of folding back, irrigation of the abdominal end of the divided vas, excision of different lengths of vas segments and FI over the abdominal end compared to FI over the testicular end. With regard to folding back of the vas on itself as a method to separate the ends of the divided vas, the available studies used a variety of occlusive techniques in addition to folding back, making it unclear whether folding back affected failure rates. 23, 47, 143, 147, 149, 150, 160, 234 Due to these inconclusive reports, the Panel cannot make a recommendation for or against folding back as an adjunctive technique for vasectomy. Similarly, it is not clear whether irrigation of the abdominal end of the vas with various solutions enhances sperm clearance rates. 245-250

There also is insufficient evidence to establish the optimal length of vas which should be excised, if any. Although failure is very rare with any occlusive technique when a 5 cm or larger vas segment is excised, 234, 236 excising such a long segment requires more extensive dissection of the spermatic cord. The extended dissection may be associated with a higher risk of surgical complications, may make vasectomy reversal more difficult to perform and may make vasectomy reversal less likely to be successful. Most surgeons excise a segment of the vas that ranges from 0.5 to 2.0 cm; the Panel believes that 1.0 cm is an adequate length. In addition, based on the available evidence, there do not appear to be differences in effectiveness when FI is performed over the testicular vs. the abdominal end.

Guideline Statement 9

Routine histologic examination of the excised vas segments is not required. Expert Opinion

Although there is no evidence for or against routine histologic examination of excised vas segments, the American Urological Association recommended in 1998 and reaffirmed in 2003 and again in 2007 "that physicians in practice and residency training programs no longer require histologic confirmation of the vas deferens as a measurement of vasectomy success" because the PVSA is the determinant of success of the procedure. The panel agrees with the lack of value of histologic examination of resected vas deferens segments as a determinant of success of the vasectomy. At the discretion of the surgeon, it may be helpful to send excised tissues for histological evaluation for confirmation of vasal tissue.

Post-Operative Practice

Background information about patient follow-up and post-vasectomy semen analysis.

PVSA is used to confirm the effectiveness of a vasectomy postoperatively (for definitions, see Table 6). Vasectomy effectiveness can be defined as either contraceptive effectiveness or occlusive effectiveness. The standard definition of contraceptive effectiveness is the absence of pregnancy. The standard definition of occlusive effectiveness is post-vasectomy azoospermia. However, some men fail to achieve azoospermia after vasectomy yet never father a pregnancy. For example, one study found sperm in the semen of 18 of 186 (9.7%) men prior to vasectomy reversal. 251 The average time since vasectomy was 10.7 years and no pregnancies occurred in the partners of these 18 men. Thus the definition of occlusive effectiveness should not be restricted to azoospermia but should include those men whose PVSAs show rare non-motile sperm (RNMS, or ≤100,000 non-motile sperm/mL) and no sperm motility.

Vasectomy failure. Vasectomy failure is the occurrence of pregnancy or failure to achieve azoospermia or RNMS after a reasonable period of time following vasectomy. Vasectomy failure may be a technical failure resulting from a surgical error such as occluding one vas twice without occluding the other vas or failure to identify the very rare situation of vas duplication on one side. Technical failure is characterized by persistently normal or nearly normal motile sperm counts and sperm motility after vasectomy. Vasectomy failure also may result from recanalization at the vasectomy site.

Recanalization following vasectomy should be suspected if motile sperm or rising sperm concentrations are seen after a routine PVSA has shown azoospermia or RNMS. Recanalization can be either transient or persistent based on the results of serial PVSAs. It is impossible to know the true incidence of late recanalization because PVSA is rarely repeated after a PVSA shows azoospermia or RNMS. Pregnancy due to recanalization is estimated to occur after approximately 1 in 2000 vasectomies or less often. 25-29 The incidence of recanalization is very likely greater than the reported rate of pregnancy after post-vasectomy azoospermia because not all recanalizations result in pregnancy.

PVSA Principles. Controversies in the timing, technique, reporting and significance of PVSA include the following:

  • When the first PVSA should be done
  • Number of PVSAs that should be done
  • Necessity for the PVSA to be performed on a fresh specimen
  • Necessity for centrifugation of the specimen
  • Reliability of PVSAs sent for analysis by mail
  • Reliability of PVSA home test kits
  • Criteria of vasectomy success defined by absolute azoospermia or the presence of RNMS
  • Volume of semen that should be examined
  • Number of semen aliquots that should be examined
  • Number of high power fields that should be examined

The aim of a PVSA is to confirm occlusive effectiveness and to advise a patient that he can safely rely on his vasectomy for contraceptive purposes. Practical principles relevant to PVSA are as follows:

  • The PVSA protocol should be as simple as possible to encourage patient compliance.
  • The PVSA should allow for confirmation of occlusive effectiveness as soon as possible after vasectomy while simultaneously minimizing the number of PVSAs required to document occlusive effectiveness.
  • The PVSA protocol should confirm occlusive effectiveness with the highest possible level of certainty.
  • Patients should be informed that post-vasectomy pregnancies are rare but have been documented even after multiple serial PVSAs reveal azoospermia.

Considering these principles, a vasectomy should be considered successful as soon as a PVSA confirms that the risk of pregnancy is sufficiently low to allow the patient to rely on the vasectomy alone for contraception. Conversely, a vasectomy should be considered a failure – or not yet a success – when a man needs to use another contraceptive method or needs to repeat the surgical procedure before relying on his vasectomy.

Sperm Clearance After Vasectomy. Sperm clearance after vasectomy is time dependent with both large inter-individual variations as well as variability across published reports, including those that used the same vas occlusion technique. Inter-individual variation may result from differences in reproductive anatomy and possibly patient age. Sperm may persist in the ejaculate for many months after vasectomy. Such persistence may be due to residual sperm in the seminal vesicles or ampullae of the vasa, 252 recanalization, or, very rarely, a failure to have performed the vasectomy on one vas. The main reason for the presence of non-motile sperm is probably that residual sperm in the seminal vesicles or ampullae of the vasa are slowly released from the reproductive tract. 252 There are wide variations in the clearance of residual sperm in the seminal vesicles or ampullae of the vasa among men due to inter-individual differences in the anatomy of these structures. 252 However, in most men, either no sperm or only small numbers of non-motile residual sperm in the PVSA are seen at three months or later after vasectomy. Nevertheless, some men have continued to have sperm or sperm parts in the semen which have been found for as long as 31 years post-vasectomy. 251, 253

With regard to age, several studies have suggested that sperm clearance may take longer in older men compared to younger men. 10, 15, 235, 254, 255 For example, Marshall and Lyon (1972) reported that younger patients may achieve azoospermia with fewer ejaculations than older patients. 256 Marwood (1979) reported that the frequency of ejaculation affected time to azoospermia more in older than in younger men, with a frequency of three times a week associated with rapid clearance regardless of age. 257

The published literature also contains mixed results regarding the relationship between sperm clearance and number of ejaculations. After 10 ejaculations, rates of azoospermia ranged from 43% to 50%. 34, 232, 258 After 12 ejaculations, rates of azoospermia have been reported as 66% 256 and 88%. 259 However, one study with relatively complete follow up showed that only 44% of patients were azoospermic after 20 ejaculations. 242 Many practitioners recommend that the first PVSA should be done after 20 ejaculations. The opinion of the Panel is that rates of azoospermia related to number of post-vasectomy ejaculations are too variable to be useful in determining when to do the first PVSA.

Variability across published reports in sperm clearance rates may result from surgical technique used to occlude the vas; differences in criteria for vasectomy success (e.g., one, two or three azoospermic specimens); variations in PVSA laboratory techniques and reporting; small sample sizes in some studies and varying time points at which PVSA was performed.  In addition, in many studies, although patients were instructed to report at specific intervals post-vasectomy, some report at later intervals. This inconsistency between requested PVSA timing and actual PVSA timing creates uncertainty regarding true sperm clearance rates because not all articles clearly indicate when patients actually returned for PVSAs. In addition, in most studies about a third of patients do not return for the requested PVSAs. 260 The lack of complete follow-up data also creates uncertainty regarding true sperm clearance rates.

Another source of variation in the proportion of men achieving azoospermia is variation in the laboratory techniques used for PVSA and for reporting of PVSA results. Rigorous semen examination including centrifugation and examination of hundreds of microscopic fields is likely to find more sperm than less rigorous laboratory techniques. If the physician sends PVSA specimens to a commercial laboratory, the physician should request that the laboratory perform the PVSA without centrifugation because centrifugation may reduce or eliminate sperm motility (see below). The physician should also request the laboratory to report both the presence or absence of sperm and the presence or absence of sperm motility. If only non-motile sperm are present, the physician should request the laboratory to report the number of non-motile sperm per mL. If no sperm are found in the uncentrifuged specimen, then ideally the laboratory should report that the presence of sperm is "below the limit of detection," although most laboratories report "azoospermia" in this situation.

Clearance of motile sperm. Clearance of motile sperm is much more rapid than clearance of non-motile sperm. Older studies suggest all motile sperm disappear within three weeks after vasectomy. 261, 262 More recent studies confirm that when MC and FI are combined to occlude the vas, essentially all motile sperm have disappeared by five to six weeks 233 with only 1% of men continuing to show motile sperm. 258 At 7 to 14 weeks, this proportion drops to 0.4% and by more than 14 weeks post-vasectomy, no motile sperm were observed. 258

Numerous studies have reported the reappearance of nonmotile sperm 28, 263-265 and even motile sperm 22, 28, 35, 42, 256, 263, 266 after azoospermia was confirmed, with most studies reporting this phenomenon in small numbers of patients (i.e., < 1%). However, it should be noted that many patients in these studies did not return for PVSAs or did not return for a second PVSA when requested, making the true rates of sperm reappearance (both motile and non-motile) unclear.

PVSA Analytic Techniques: Centrifugation of semen samples for PVSA is unnecessary. Laboratory techniques, especially centrifugation, influence the presence or absence of azoospermia observed in a PVSA. Over the past two decades, data suggest that centrifugation leads to the identification of more men with small numbers of sperm. This means that correspondingly fewer men are reported with azoospermia, leading to increased follow-up testing and more repeat vasectomies, some of which may not be necessary. 267

The British Andrology Society and the 1992 (3rd edition) and 1999 (4th edition) of the World Health Organization laboratory manual for the examination of human semen and sperm-cervical mucus interaction specifically recommended centrifugation of azoospermic semen samples as part of the routine post-vasectomy semen analysis. 268 However, centrifugation is not necessary to confirm that only rare non-motile sperm are present. The 2010 (5th edition) WHO laboratory manual for the examination and processing of human semen suggests relying on careful examination of an uncentrifuged specimen, similar to a recently PVSA protocol proposed by Korthorst (2009). 244, 269 The 2010 (5th edition) WHO laboratory manual states in Section 2.10.3, page 46, "When motile spermatozoa are sought (e.g., in a post-vasectomy semen sample), diluting the specimen in fixative or high-speed centrifugation of spermatozoa must be avoided." 269 One group examined uncentrifuged azoospermic semen specimens compared with centrifuged specimens (n=2,014 samples) and concluded that uncentrifuged semen analysis is a reliable method of identifying samples with > 100,000 sperm/ml. 270 The sensitivity of the uncentrifuged sample was 99.3% and the negative predictive value was 99.8%.

Because centrifugation may interfere with sperm motility 269 and clinically relevant numbers of sperm can be identified without centrifugation, a surgeon should request a clinical laboratory not to perform centrifugation for a PVSA.

Office examination of uncentrifuged post vasectomy semen samples. In the US, CDC regulations implementing the 1988 Clinical Laboratory Improvement Act (CLIA) (42 CFR 493.19) distinguish provider-performed microscopy (PPM) analysis from that in laboratories performing tests of high complexity. These regulations allow for semen analysis in a doctor's office, i.e., "provider performed microscopy," as long as the reported result is qualitative, i.e., "limited to the presence or absence of sperm and detection of motility." Thus US physicians are permitted to conduct PVSA in their offices, but they are not allowed to determine sperm concentration unless the office laboratory has a high-complexity level of CLIA certification. There is now interest in developing a method of estimating the number of sperm per mL of semen from the number of sperm per Hpf found in a PVSA. Such a method would allow vasectomy surgeons to correlate the number of sperm per Hpf in PVSAs which do not show azoospermia to various concentrations of sperm/mL.

Self-PVSA Testing. A self-PVSA home test has been approved by the FDA and is available for clinical use. This test is sensitive to sperm counts >250,000/ml, 271 but the test does not assess for sperm motility. If two tests are performed and both are negative, then the negative predictive value of a sperm count >250,000 sperm/mL is 99.9%. However, the 250,000 sperm/mL cut-off is significantly higher than the cut-off most commonly used to declare a man sterile after vasectomy. The most commonly used cut-off in the literature and the definition of vasectomy success used in this guideline is ≤100,000 non-motile sperm/mL. Furthermore, no other studies have shown that clearing men at this cut-off without evaluating for motility is reliable enough to recommend discontinuation of contraception, and no studies have followed patients who used the test to assess for the risk of unanticipated pregnancy. In addition, it has been suggested that a home PVSA test might increase patient compliance with PVSA instructions, but improved patient compliance has not yet been studied or proven.

Because the test results are read by the patient, the surgeon must instruct the patient on all aspects of the test prior to its use. To avoid potential legal problems, careful instruction is essential to ensure that the patient will use the test in a valid manner. The disclosures must include how to set up the test, how to read the final result and the relative risks of pregnancy. Given this requirement and the lack of long-term follow-up data on patients who have used the test, the opinion of the Panel at this time is that, although this test may have potential value that may be proven in the future, there are insufficient data for the panel to come to a conclusion regarding its use in clinical practice.

Guideline Statement 10

Men or their partners should use other contraceptive methods until vasectomy success is confirmed by PVSA. Clinical Principle

During the first few weeks after vasectomy, sperm that are left in the male reproductive system on the abdominal side of the vasectomy site may retain the ability to fertilize an ovum. 258, 261, 262 Semen analysis after vasectomy is very strongly advised because it provides assurance for the patient and his partner that the risk of future pregnancy is very low, and it provides a continuing measure of quality control for the physician.

Guideline Statement 11

To evaluate sperm motility, a fresh uncentrifuged semen sample should be examined within two hours after ejaculation.  Expert Opinion

WHO guidelines (2010) recommend that semen analysis to assess motility should be done within 60 minutes of ejaculation when the semen sample is provided in the laboratory facility. 269 If a man is unable to ejaculate at the clinic, then delivery of a semen sample to the laboratory should be within one hour of ejaculation so that the motility assessment can occur during the second hour after ejaculation. Semen samples should be transported at ambient temperatures, i.e. between 20° and 37°C. In most semen samples, sperm motility does not decrease between one and two hours post-ejaculation. 272

Some clinicians recommend for convenience and compliance reasons, that PVSA specimens can be sent by mail (following regulations regarding shipping biohazards). This approach is adequate to assess only the presence or absence of sperm. Motility cannot be evaluated reliably in a semen sample produced more than two hours before microscopic examination.

Guideline Statement 12

Patients may stop using other methods of contraception when examination of one well-mixed, uncentrifuged fresh post-vasectomy semen specimen shows azoospermia or only rare non-motile sperm (RNMS or ≤ 100,000 non-motile sperm/mL). Recommendation

(Evidence Strength – Grade C; Benefits outweigh risks/burdens) . Both azoospermia and RNMS are acceptable criteria for vasectomy success. The definition of RNMS used in the medical literature has varied from more than 0 to less than 1 million/mL, but the most commonly used definition of RNMS is ≤100,000 per mL. 268, 273

Several studies show that the risk of pregnancy associated with the presence of ≤100,000 non-motile sperm/Hpf is very low and similar to the risk when sperm are absent. Absence of sperm motility appears to be a robust criterion to indicate occlusive effectiveness. One group reported routine testing of men at three to four weeks after vasectomy using MC and FI and provided clearance based on the absence of motile sperm. 258 Among 3,178 vasectomized men, two pregnancies were documented. One man had an apparent late recanalization; the other had not returned for a PVSA. This pregnancy rate is not significantly different from the risk of about 1 in 2,000 after documented azoospermia on two consecutive semen analyses, based on data from the Elliot Smith Clinic, 25-27 from Marie Stopes International, 29 and from large case series reports. 28 Even in men with some motile sperm, risk of pregnancy appears to be low if the concentration of motile and non-motile sperm is ≤100,000/mL. In a WHO study of a hormonal male contraceptive, 8.1 pregnancies/100 person-years were observed in men with 100,000 to 3 million sperm/ml (motile and nonmotile) and 0 pregnancies/100 person-years in men with 0 to 100,000 sperm/ml (motile and nonmotile). 274 Contraceptive failure (pregnancy) after declaration of vasectomy success is a rare event despite the reappearance of nonmotile sperm, 42,251,265,275 and even motile sperm 22, 35, 266 after azoospermia was confirmed.

Philp et al. (1984) proposed a method for defining when a patient who has persistence of small numbers of non-motile sperm in the PVSA can rely on vasectomy alone for contraception. 25 They analyzed data from 16,796 patients at the Elliot Smith Clinic in Oxford (United Kingdom). About 4,500 vasectomies were performed with ligation and excision between 1970 and 1974, and about 12,300 vasectomies were performed with MC but not FI after 1974. This group used the term "special clearance" to determine when a man whose PVSA showed RNMS could be informed that he is sterile. They defined three criteria for "special clearance:" (1) a level of 10,000 sperm/mL or less in two consecutive semen exams, (2) no motile sperm and (3) at least seven months post-vasectomy. However, the method of semen analysis at the Elliot Smith Clinic has not been reported, except for the information that patients provided semen samples by mail, which precludes an examination for motility. Nonetheless, subsequent reports from this clinic have confirmed a lack of pregnancies among men with only rare sperm. 27, 42

Korthorst et al. (2009) reported prospective findings from 1,073 men who underwent vas occlusion by clips and FI. 244 Using the threshold of <100,000 non-motile sperm/mL in accordance with the recommendations of the Dutch Urological Association, 273 men were cleared if they met this criterion in a single sample at 12 weeks or later. No pregnancies were reported among 481 men who had < 100,000 non-motile sperm, with a median follow-up of 14 months. Based on data from an additional study, most recanalizations occur during the first year post-vasectomy. 276 Therefore, such results would seem unlikely to change with longer follow-up.

The opinion of the Panel is that both azoospermia and ≤100,000 non-motile sperm/mL are reliable indicators of vasectomy success.

Guideline Statement 13

Eight to sixteen weeks after vasectomy is the appropriate time range for the first PVSA. The choice of time to do the first PVSA should be left to the judgment of the surgeon. Option

(Evidence strength – Grade C; benefits and risks/burdens balanced) . The choice of time to do the first PVSA should be left to the judgment of the surgeon. It is desirable to select a time for the first PVSA that will minimize the number of PVSAs needed to establish that azoospermia or RNMS has been achieved but still allow men to abandon other forms of contraception as soon as possible after vasectomy. The longer the time period before the first PVSA, the better the chance that the PVSA will show azoospermia or RNMS but the longer the time that the patient must use another method of contraception. Motile sperm disappear within a few weeks after successful vasectomy. 233, 258, 261, 262 Performing the first PVSA earlier than 12 weeks may allow some men to rely on their vasectomy for contraception sooner than if the first PVSA is done at 12 weeks or later. However, if the first PVSA is performed before 12 weeks post-vasectomy, more men will have to submit additional samples for PVSA to confirm the success of the procedure if the initial sample contains motile sperm or >100,000 non-motile sperm/ml.

While rates of sperm clearance vary across studies, including studies that used the same vas occlusion technique, the available literature indicates that, in general, the proportion of men who achieve azoospermia or RNMS after vasectomy increases with time. Eleven study arms from nine studies reported rates of azoospermia at eight weeks post-vasectomy. 23, 35, 37, 138, 170, 241, 277-279 Azoospermia rates ranged from 30.0% to 88.5% with six studies reporting rates above 80%.

Sixteen study arms reported azoospermia rates at 12 weeks post-vasectomy. 23, 35, 37, 138, 231, 237, 241, 242, 246, 263, 264, 277-279 Rates ranged from 48.0% to 99.0% with eight study arms reporting rates of 90.0% or above and ten study arms reporting rates of 80.0% or above. The lowest rate of 48.0% was reported in the randomized controlled trial 242 in a group of men who underwent vas occlusion by ligation (value estimated from Kaplan-Meier graph). 

Thirteen study arms reported azoospermia rates at six months post-vasectomy. 23, 131, 137, 138, 144, 231, 235, 239, 241, 242, 279, 280 Rates ranged from 61.5% to 99.6% with five study arms reporting rates of 90.0% or above and ten study arms reporting rates of 80.0% or above. The low rate of 61.5% was reported by Barnes (1973) in a group of men who underwent vas occlusion by ligation. 137

Given the potential confounders to interpretation discussed in the Vas Occlusion section of this Guideline, it is not clear if vas occlusion technique affects the rate of achieving azoospermia. Of the six studies that reported azoospermia rates above 80% at eight weeks, four used ligation, one used MC and FI and one used ligation and FI. It is worth noting, however, that the methodologically strongest study in this group (the Sokal 2004 RCT) reported relatively low rates of 30.0% and 48.0% at eight weeks (estimated from Kaplan-Meier graphs) in patients who underwent vas occlusion by ligation without and with FI, respectively, with the higher rate in the group that had FI.

Similarly, of the eight study arms reporting azoospermia rates of 90.0% or above at 12 weeks, one used MC and clips, one used MC and suturing of the testicular end, three used ligation of both ends, one used MC and FI, one used ligation of both ends and FI and one reported on a mixed group of techniques (Barone 2004; MC with or without FI and MC only). 231 Of the five study arms reporting azoospermia rates of 90.0% or higher at six months, three used ligation, one used ligation of both ends and FI, and the third study reported on mixed techniques (Barone 2004). 231

Additional useful information regarding the potential influence of vas occlusion technique is provided by Labrecque et al. (2006), which is a secondary analysis of serial PVSA data from Barone (2004) and Sokal (2004). 234 The authors document the presence of motile sperm and note that when thermal MC and FI were used, all motile sperm cleared by six weeks post-vasectomy. When mucosal electrocautery without FI was used, all motile sperm cleared by 10 weeks post-vasectomy. When ligation alone was used, 5 to 10% of tested men continued to exhibit motile sperm at periods up to 26 weeks post-vasectomy. When FI was combined with ligation, 1 to 4% of men continued to exhibit motile sperm at up to 26 weeks post-vasectomy.

Because the majority of studies reporting azoospermia rates at 12 weeks post-vasectomy indicated that 80% or more of men had achieved this goal, the Panel interpreted these data to indicate that at 12 weeks most men will be azoospermic or will meet the RNMS criterion. In addition, it was found that a 12-week time period was a more reliable parameter for vasectomy success than a specific number of ejaculations (e.g., 20). 242 WHO incorporated this finding in its 2004 guideline and now recommends a waiting period of three months. 281 With regard to the influence of vas occlusion technique on the time to achieve azoospermia or RNMS, the Panel notes that one study 233 demonstrated that the fastest motile sperm clearance rates occurred when MC was combined with FI, and the slowest rates occurred when ligation was used. This study provides additional information that may be considered by the surgeon in the decision regarding when to request the first PVSA.

Guideline Statement 14

Vasectomy should be considered a failure if any motile sperm are seen on PVSA at six months after vasectomy, in which case repeat vasectomy should be considered. Expert Opinion

When the vas is successfully occluded, motile sperm disappear by a few weeks after vasectomy. 233, 258, 261, 262 The presence of motile sperm at 6 to 12 weeks after vasectomy indicates that recanalization has occurred or that there was a technical failure in vas occlusion. However, vasectomy should not be repeated immediately if motile sperm are found on PVSA prior to six months after vasectomy. Additional PVSAs should be performed at intervals of four to six weeks for up to six months after vasectomy for further evaluation. Motile sperm may represent a risk of pregnancy and indicate the need for continued use of another contraceptive method, further PVSA testing and, if persistent, repeat vasectomy. However, approximately 30% to 50% of men with recanalization eventually achieve azoospermia or RNMS over a period of six months after vasectomy due to fibrosis of the vas and occlusion of the recanalization. 22, 241 These men continue to have effective occlusion on long term follow-up. 22 Therefore, the decision to repeat the vasectomy should not rely on a single semen analysis showing motile sperm within six months after vasectomy. Repeat vasectomy should be done if the number of motile sperm increases in subsequent semen analyses or if motile sperm persist for >6 months after vasectomy. There are no data to suggest that delayed occlusive success occurs in men who still have any motile sperm in a PVSA at six months after vasectomy.

Guideline Statement 15

If > 100,000 non-motile sperm/mL persist beyond six months after vasectomy, then trends of serial PVSAs and clinical judgment should be used to decide whether the vasectomy is a failure and whether repeat vasectomy should be considered. Expert Opinion

If non-motile sperm are present on the first PVSA in the surgeon's office, one or more repeat PVSAs should be performed in the surgeon's office laboratory to determine if azoospermia develops over time. If azoospermia is not achieved by six months after vasectomy, then a PVSA should be performed in a laboratory approved for high complexity semen testing. If the PVSA shows ≤100,000 non-motile sperm/mL and no motile sperm, then the couple may stop using other methods of contraception.

If the PVSA shows > 100,000 non-motile sperm/mL or any motile sperm, then further PVSA monitoring or repeat vasectomy may be considered. The Panel's opinion is that the decision to consider vasectomy a failure if >100,000 non-motile sperm/mL persist should be based on clinical judgment that includes the trend of sperm counts, the patient's preferences and the patient's tolerance for the risk of pregnancy.

Additional Important Points of Postoperative Practice.

After completion of a vasectomy, physicians should consider giving men a specific appointment for the first PVSA to improve compliance with follow-up. Based on 46 published studies reviewed in 49 papers, a median of 78% (range 33-100%) of men return for a single PVSA and a median of 73% (range 21-100%) are fully compliant with PVSA study protocols. 13, 22-28, 30, 34, 35, 37, 38, 52, 131, 134, 137, 138, 142, 144, 170, 181, 231, 232, 235, 237, 242, 243, 253, 256-265, 277, 280, 282-288 Compliance rates varied greatly across studies and might be lower in clinical practice than in published studies. In the largest cohorts that appear typical of North American vasectomy practice, only about two thirds of men (between 55% and 71%) return for at least one PVSA. 28, 30, 38, 243, 260, 288

The number of tests requested (one or two) and the time at which samples were requested (one to two months vs. three to four months) do not appear to make a significant difference in compliance rates. When the second test was requested at three to four months post vasectomy, rates of full compliance were decreased somewhat compared to protocols where two tests were ordered within two months. 289

One randomized controlled trial including 228 men evaluated the effectiveness of scheduling an appointment for the first PVSA versus simply asking men to return at two months post-vasectomy. In the appointment group 84% of men returned for semen analysis versus 65% in the no appointment group. 290 The Panel suggests that the practice of scheduling a follow-up PVSA appointment should be left to the judgment of the individual clinician.

A postoperative visit with the surgeon specifically for physical examination of the scrotum is not routinely necessary. The results of the PVSA and/or the need for one or more additional PVSAs can be conveyed by telephone or other modes of communication. When giving PVSA results, men should be reminded that no contraceptive method, including vasectomy, is 100% effective. At this time, patients should be informed that there is always a remote risk of pregnancy even if azoospermia has been achieved. Each patient should know that if his partner becomes pregnant, he may have experienced a rare vasectomy failure and should return to his surgeon for a semen analysis. Even if a PVSA at such a time reveals azoospermia, a transient recanalization may have occurred with the subsequent disappearance of sperm from the semen, as shown by DNA studies on parents and the child in such situations. 291

Most men whose partners become pregnant after vasectomy have motile sperm in the semen, but some are found to be azoospermic on multiple examinations following identification of the pregnancy. If a man reports that his wife has become pregnant and his semen analysis reveals azoospermia, then the physician should inform him that the pregnancy could have been due to a transient recanalization despite the semen analysis results. A number of case reports have confirmed paternity based on genetic testing even though the men previously had multiple semen analyses showing azoospermia, i.e., sperm counts below the limit of detection. 291-293 Patients may be informed that genetic analysis to document paternity is available.

Future Research

One benefit of a systematic review is to illuminate deficits in the scientific knowledge base, the amelioration of which would move the field forward and allow for advances in clinical care. The Panel identified the following areas for future research efforts.

Preoperative Evaluation and Counseling

  • Identification of the information most important to patients and partners during and after the decision-making process and, in particular, the type of information and information presentation that is most effective to gain the patient's attention, maximize understanding and minimize post-procedure regret and dissatisfaction. One recent study addressed the value of a patient decision aid before and after the procedure and concluded that it was helpful in both a comprehensive and an abridged version. 294
  • The percentages of couples who select vasectomy vs. tubal ligation when fully informed regarding both options. This information is central to understand the extent to which the relative under-utilization of vasectomy in the US is a function of lack of understanding of the procedure.
  • The selection of vasectomy or tubal occlusion depending upon whether the patient/couple sees a gynecologist or urologist first.
  • Whether rates of dissatisfaction and/or regret are related to the inclusion of the spouse or partner in the preoperative counseling process.
  • Do men and partners of men considering vasectomy believe that vasectomy is a family or an individual decision?
  • Pain levels (measured with visual analog scales) associated with the use of smaller gauge vs. larger gauge needles for local anesthesia administration, with the use of a mini-needle technique (30-32 gauge needle with 3 cc xylocaine) compared to the Li anesthetic block technique (25-27 gauge needle with 10 cc xylocaine) and the use of mini-needles compared to jet injection.
  • Whether or not topical anesthetic cream application before injection of local anesthetic reduces the amount of pain (measured by a visual analog score). If the pain of local anesthetic injection is reduced, the extent to which topical anesthetic cream before local anesthetic injection reduces the pain of injection as well as the pain of the vasectomy.
  • Pain level during local anesthesia administration as opposed to during the vasectomy procedure itself.
  • Whether or not application of a topical cutaneous spray such as ethyl chloride, cocaine or other products prior to injection of local anesthetic reduces the pain of injection.
  • Whether pain is reduced when an NSV or MIV vas isolation technique is used compared to a conventional technique.
  • Intraoperative and post-operative pain levels and surgical complications (e.g., at one, two and four weeks) with an MIV technique compared to a conventional vasectomy.
  • The incidence of failed vasectomy with use of a single midline incision compared to bilateral incisions.
  • Information regarding how the technical skills required to perform NSV are learned and translated into practice and to what extent practitioners reporting that they perform NSV are adhering to each of the requirements of the technique.
  • The incidence of early post-vasectomy scrotal hematoma and abscess formation according to the method of vas isolation.
  • Methodologically robust (e.g., well-designed prospective observational studies and RCTs) are needed of large cohorts in developed countriesthat compare occlusive techniques with regard to surgical complication rates, post-vasectomy pain and occlusive and contraceptive effectiveness at short-, medium- and long-term follow up points.
  • Evaluation of the effectiveness of thermal cautery vs. electrocautery for vas occlusion.
  • RCTs to evaluate the occlusive effectiveness and complication rates associated with cautery and FI vs. cautery alone, open versus closed testicular end with FI and cautery of the abdominal side and complications including anti-sperm antibodies.
  • Reliable techniques for applying cautery to the vasal mucosa and avoid damage to the vasal muscularis.
  • Information regarding the potential value and possible complications from the addition of folding back to any technique.
  • Whether postoperative bleeding complications are more common if FI is performed than if FI is not performed.
  • The development of percutaneous occlusion techniques.

Post-Vasectomy Follow-up

  • More rigorous study of the prevalence of azoospermia and RNMS related to the method of vas occlusion at various time intervals after vasectomy (e.g., at weeks 6, 9, 12, 16, 20 and 24).
  • Study of why some men have RNMS for substantial intervals post-vasectomy (e.g., three, six, nine months) while others do not.
  • Information about the prevalence of paternity at various post-vasectomy time intervals as long as 5 to 10 years.
  • Contraceptive effectiveness at different PVSA thresholds (including varying levels of RNMS).
  • Whether the PVSA thresholds of commercially available home test kits are sufficient to ensure contraceptive effectiveness.
  • How couples who desire to have more children after a vasectomy choose between vasectomy reversal and sperm retrieval with IVF/ICSI and the percentage of couples choosing each technique.
  • Comparisons of PVSA results when the analysis is done by physicians in office laboratories certified for provider performed microscopy compared to results of commercial laboratories certified for high complexity testing.
  • Comparison of the number of sperm/HPF between standard light microsopy and phase contrast microsopy.
  • Patient preferences for the timing of PVSA with regard to achieving earlier clearance vs. the need for more than one PVSA.
  • Investigations of post-vasectomy testicular changes (i.e., histologic changes in the seminiferous tubules and in spermatogenesis, electron microscopic changes of interstitial fibrosis) and how they may correlate with both post-vasectomy antisperm antibody status and with vasectomy reversal outcomes.
  • The incidence of serum antisperm antibodies as determined by immunoglobulin A, G and M testing after vasectomy and how they affect fertility rates after vasectomy reversal and after sperm retrieval with IVF/ICSI (including sperm surface antibody studies in seminal plasma after vasectomy reversal).

Complications

  • Methodologically rigorous studies to provide accurate rates of early post-vasectomy hematoma, wound infection and scrotal abscess formation.
  • Studies that distinguish between post-vasectomy pain due to epididymal congestion or epididymal sperm granuloma (resulting from rupture of the epididymal tubule caused by back pressure below the level of the vasectomy) vs. pain due to true bacterial epididymitis.
  • Studies of various imaging modalities that allow the accurate diagnosis of the cause of post-vasectomy epididymal pain.
  • Incidence of chronic post-vasectomy pain according to standardized scales starting at three to six months and continuing until up to three to five years post-vasectomy.
  • Incidence of chronic pain of differing severity, the percentage of patients who feel that their quality of life has been impacted by the pain, the percentage of patients who seek medical help for relief of such pain, the percentage who undergo some type of surgical procedure for pain relief and the success rate of the various procedures for relieving the pain.

Tools and Resources

Abbreviations.

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  • Chawla A, Bowles B and Zini A: Vasectomy follow-up: clinical significance of rare nonmotile sperm in postoperative semen analysis. Urology 2004; 64: 1212.
  • Korthorst RA, Consten D and Van Roijen HJ: Clearance after vasectomy with a single semen sample containing < than 100 000 immotile sperm/mL: analysis of 1073 patients. BJU Int 2010; 10511 .
  • Berthelsen JG: Peroperative irrigation of the vas deferens during vasectomy. Scand J Urol Nephrol 1976; 10: 100.
  • Eisner B, Schuster T, Rodgers P et al: A randomized clinical trial of the effect of intraoperative saline perfusion on postvasectomy azoospermia. Ann Fam Med 2004; 2: 221.
  • Gandrup P, Berthelsen JG and Nielsen OS: Irrigation During Vasectomy: A comparison between sterile water and the spermicide euflavine. J Urol 1982; 127: 60.
  • Leungwattanakij S, Lertsuwannaroj A and Ratana-Olarn K: Irrigation of the distal vas deferens during vasectomy: does it accelerate the post-vasectomy sperm-free rate? Int J Androl 2001; 24: 241.
  • Mason RG, Dodds L and Swami SK: Sterile water irrigation of the distal vas deferens at vasectomy: does it accelerate clearance of sperm? A prospective randomized trial. Urology 2002; 59: 424.
  • Pearce I, Adeyoju A, Bhatt RI et al: The effect of perioperative distal vasal lavage on subsequent semen analysis after vasectomy: a prospective randomized controlled trial. BJU Int 2002; 90: 282.
  • Lemack GE and Goldstein M: Presence of sperm in the pre-vasectomy reversal semen analysis: incidence and implications. J Urol 1996; 155: 167.
  • Schiff J, Chan P, Li PS et al: Outcome and late failures compared in 4 techniques of microsurgical vasoepididymostomy in 153 consecutive men. J Urol 2005; 174: 651.
  • Freund MJ and Couture M: The presence of spermatozoa in the semen of vasectomized men. Journal of Andrology 1982; 3: 313.
  • Arango Toro O, Andolz Peitivi P, Lladó Carbonell C et al: Post-vasectomy semen in 313 males. Statistical analysis, medical aspects, legal implications. Arch Esp Urol 1993; 46: 29.
  • Spencer B and Charlesworth D: Factors determining the rate of disappearance of sperm from the ejaculate after vasectomy. Br J Surg 1976; 63: 477.
  • Marshall S and Lyon RP: Variability of sperm disappearance from the ejaculate after vasectomy. J Urol 1972; 107: 815.
  • Marwood RP and Beral V: Disappearance of spermatozoa from ejaculate after vasectomy. Br Med J 1979; 1: 87.
  • Edwards IS: Earlier testing after vasectomy, based on the absence of motile sperm. Fertil Steril 1993; 59: 431.
  • Smucker DR, Mayhew HE, Nordlund DJ et al: Postvasectomy semen analysis: why do patients don't follw-up. JABFP 1991; 4: 5.
  • Belker AM, Sexter MS, Sweitzer SJ et al: The high rate of noncompliance for post-vasectomy semen examination: medical and legal considerations. J Urol 1990; 144: 284.
  • Bedford JM and Zelikovsky G: Viability of spermatozoa in the human ejaculate after vasectomy. Fertil Steril 1979; 32: 460.
  • Jouannet P and David G: Evolution of the properties of semen immediately following vasectomy. Fertil Steril 1978; 29: 435.
  • Alderman PM: General and anomalous sperm disappearance characteristics found in a large vasectomy series. Fertil Steril 1989; 51: 859.
  • De Knijff DW, Vrijhof HJ, Arends J et al: Persistence or reappearance of nonmotile sperm after vasectomy: does it have clinical consequences? Fertil Steril 1997; 67: 332.
  • Smith AG, Crooks J, Singh NP et al: Is the timing of post-vasectomy seminal analysis important? Br J Urol 1998; 81: 458.
  • Sherlock DJ and Holl-Allen RT: Delayed spontaneous recanalization of the vas deferens. Br J Surg 1984; 71: 532.
  • Benger JR, Swami SK and Gingell JC: Persistent spermatozoa after vasectomy: a survey of British urologists. Br J Urol 1995; 76: 376.
  • Hancock P and McLaughlin E: British Andrology Society guidelines for the assessment of post vasectomy semen samples (2002). J Clin Pathol 2002; 55: 812.
  • World Health Organization: WHO laboratory manual for the Examiniation and processing of human semen: 5th Edition. World Health Organization 2010.
  • Steward B, Hays M and Sokal D: Diagnostic Accuracy of an Initial Azoospermic Reading Compared With Results of Post-Centrifugation Semen Analysis After Vasectomy. J Urol 2008; 180: 2119.
  • Klotz KL, Coppola MA, Labrecque M et al: Clinical and Consumer Trial Performance of a Sensitive Immunodiagnostic Home Test That Qualitatively Detects Low Concentrations of Sperm Following Vasectomy. J Urol 2008; 180: 2569.
  • Shulte RT, Keller LM, Hiner MR et al: Temporal Decreases in Sperm Motility: Which Patients Should Have Motility Checked at Both 1 and 2 Hours After Collection? Journal of Andrology 2008; 29: 558.
  • Dohle GR, Meuleman EJ, Hoekstra JW et al: Revised guideline 'Vasectomy' from the Dutch Urological Association. Ned Tijdschr Geneeskd 2005; 149: 2728.
  • World Health Organization Task Force on Methods for the Regulation of Male Fertility: Contraceptive efficacy of testosterone-induced azoospermia and oligozoospermia in normal men. Fertil Steril 1996; 65: 821.
  • Lindsay KS, Floyd I and Swan R: Classification of asoozpermic samples. Lancet 1995; 345: 1642.
  • Haldar N, Cranston D, Turner E et al: How reliable is a vasectomy? Long-term follow-up of vasectomised men. Lancet 2000; 356: 43.
  • Dhar NB, Bhatt A and Jones JS: Determining the success of vasectomy. BJU Int 2006; 97: 773.
  • Lehtonen T: Vasectomy for Voluntary Male Sterilisation. Sc J Urol Neph 1975; 9: 174.
  • Sivanesaratnam V: Onset of azoospermia after vasectomy. N Z Med J 1985; 98: 331.
  • Chan J, Anderson R and Glasier A: Post-vasectomy semen analysis: unnecessary delay or belt and braces?. Br J Fam Plan 1997; 23: 77.
  • World Health Organization: Selected Practice Recommendations for Contraceptive Use (recommendation #15). Geneva: Department of Reproductive Health and Research Family and Community Health 2004.
  • Bradshaw HD, Rosario DJ, James MJ et al: Review of currect practice to establish success after vasectomy. Br Sur J 2001; 88: 290.
  • Christensen RE and Maples DC, Jr.: Postvasectomy semen analysis: are men following up? J Am Board Fam Pract 2005; 18: 44.
  • Corea M, Campagnone J and Sigman M: The diagnosis of azoospermia depends on the force of centrifugation. Fertil Steril 2005; 83: 920.
  • Eisner BH, Schuster TG, Smith GD et al: Monitoring for azoospermia following vasectomy: time course and patient compliance. Fertil Steril 2001; 76: S187.
  • Katsoulis IE and Walker SR: Vasectomy management in Morecambe Bay NHS Trust. Ann R Coll Surg Engl 2005; 87: 131.
  • Lewis EL, Brazil CK and Overstreet JW: Human sperm function in the ejaculate following vasectomy. Fertil Steril 1984; 42: 895.
  • Maatman TJ, Aldrin L and Carothers GG: Patient noncompliance after vasectomy. Fertil Steril 1997; 68: 552.
  • Griffin T, Tooher R, Nowakowski K et al: Post-vasectomy testing to confirm sterility: a systematic review. Australian Safety and Efficacy Register of New Interventional Procedures-Surgical 2003: i.
  • Dhar NB, Jones JS, Bhatt A et al: A prospective evaluation of the impact of scheduled follow-up appointments with compliance rates after vasectomy. BJUI 2007; 99: 1094.
  • Smith JC, Cranston D, O'Brien T et al: Fatherhood without apparent spermatozoa after vasectomy. Lancet 1994; 344: 30.
  • Thomson JA, Lincoln PJ and Mortimer P: Paternity by a seemingly infertile vasectomised man. BMJ 1993; 307: 299.
  • Lucon M, Lucon AM, Pasqualoto FF et al: Paternity after vasectomy with two previous semen analyses without spermatozoa. Sao Paul Med J 2007; 125: 122.
  • Labrecque M, Paunescu C, Plesu I et al: Evaluation of the effect of a patient decision aid about vasectomy on the decision-making process: a randomized trial. Contraception 2010; 82: 556.

This document was written by the Vasectomy Guideline Panel of the American Urological Association Education and Research, Inc., which was created in 2008. The Practice Guidelines Committee (PGC) of the AUA selected the panel chair and co-chair. Panel members were selected by the chair and co-chair. Membership of the panel included urologists, family medicine physicians, and other clinicians with specific expertise on vasectomy techniques. The mission of the committee was to develop recommendations that are evidence-based or consensus-based, depending on Panel processes and available data, for optimal clinical practices in the surgical technique of vasectomy. Funding of the committee was provided by the AUA; committee members received no remuneration for their work. Each member of the committee provides an ongoing conflict of interest disclosure to the AUA. While these guidelines do not necessarily establish the standard of care, AUA seeks to recommend and to encourage compliance by practitioners with current best practices related to the condition being treated. As medical knowledge expands and technology advances, the guidelines will change. Today, these evidence based guideline statements represent not absolute mandates but provisional proposals for treatment under the specific conditions described in each document. For all these reasons, the guidelines do not pre-empt physician judgment in individual cases. Treating physicians must take into account variations in resources, and patient tolerances, needs, and preferences. Conformance with any clinical guideline does not guarantee a successful outcome. These guidelines are not intended to provide legal advice about vasectomy. Although guidelines are intended to encourage best practices and potentially encompass available technologies with sufficient data as of close of the literature review, they are necessarily time-limited. Guidelines cannot include evaluation of all data on emerging technologies or management, including those that are FDA-approved, which may immediately come to represent accepted clinical practices. For this reason, the AUA does not regard technologies or management which are too new to be addressed by these guidelines as necessarily experimental or investigational. The complete evidence report may be requested through AUA.

IMAGES

  1. Vasectomy: What You Should Know

    visit for vasectomy evaluation icd 10

  2. Vasectomy

    visit for vasectomy evaluation icd 10

  3. ICD-10-CM Diagnosis Code Z98.52

    visit for vasectomy evaluation icd 10

  4. Overview of Vasectomy and Possible Side Effects

    visit for vasectomy evaluation icd 10

  5. Vasectomy: What to Expect, Effectiveness & Healing Time

    visit for vasectomy evaluation icd 10

  6. Vasectomy Procedure, Effects, Risks, Effectiveness, and More

    visit for vasectomy evaluation icd 10

COMMENTS

  1. PDF Coding For Vasectomies

    ICD-10 Diagnosis Codes. Z30.0 Encounter for general counseling and advice on contraception Z30.8 Encounter for other contraceptive management (applicable to post-vasectomy sperm count) Z30.09 Encounter for other general counseling and advice on contraception. Z30.2.

  2. 2024 ICD-10-CM Diagnosis Code Z30.2

    Z30.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2024 edition of ICD-10-CM Z30.2 became effective on October 1, 2023. This is the American ICD-10-CM version of Z30.2 - other international versions of ICD-10 Z30.2 may differ. Z codes represent reasons for encounters. A ...

  3. Trust These 6 Tips for Successful Vasectomy Coding : Coding Tips

    Code Z30.2 is appropriate for confirmed surgery; Z30.09 applies when the patient is unsure they want to have the vasectomy during discussion at the preoperative visit. "It is helpful to note that despite being a 'Z' code, it is acceptable as a primary diagnosis code per ICD-10-CM," says Piaskowski. 4.

  4. Focus on 5 Steps for Successful Vasectomy Coding

    Note that some payers link ICD-9 code V25.09 with only female patients and therefore, may deny payment if used for a vasectomy office evaluation. In these cases, use V25.2 for both the visit and the vasectomy itself. Nevertheless, be sure to check the coding with your payer. 4. Verify Coverage Before Surgery

  5. ICD-10-CM Diagnosis Code Z30.2

    Encounter for contraceptive management. ( Z30) Z30.2 is a billable diagnosis code used to specify a medical diagnosis of encounter for sterilization. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024. The code is exempt from present on admission ...

  6. 2024 ICD-10-CM Diagnosis Code Z98.52: Vasectomy status

    Vasectomy status. Z98.52 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2024 edition of ICD-10-CM Z98.52 became effective on October 1, 2023. This is the American ICD-10-CM version of Z98.52 - other international versions of ICD-10 Z98.52 may differ.

  7. Follow These 4 Steps for Quick

    Use code 55250 for any open vasectomy, standard or non-scalp and code 55559 when the urologist performs the surgery laparoscopically. For either type of approach, submit diagnosis Z30.2. 3. Report the Surgical Tray. When finalizing the claim, don't forget to report the surgical tray and supplies.

  8. Coding for Vasectomy

    Share on Facebook; Share on Twitter; Send via email; Coding for Vasectomy. June 15, 2023. CPT and ICD-10 procedure and other codes to use for documentation and billing of a vasectomy procedure.

  9. Vasectomy Guideline

    The purpose of this clinical guideline is to provide guidance to clinicians who offer vasectomy services. This guidance covers pre-operative evaluation and consultation of prospective vasectomy patients; techniques for local anesthesia, isolation of the vas deferens and occlusion of the vas deferens during vasectomy; post-operative follow-up; post-vasectomy semen analysis (PVSA) and potential ...

  10. Z98.52

    ICD-10-CM Code. Z98.52. Z98.52 is a valid billable ICD-10 diagnosis code for Vasectomy status . It is found in the 2024 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2023 - Sep 30, 2024 . Z98.52 is exempt from POA reporting ( Present On Admission).

  11. 2024 ICD-10-CM Diagnosis Code Z02.89: Encounter for other

    Z02.89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2024 edition of ICD-10-CM Z02.89 became effective on October 1, 2023. This is the American ICD-10-CM version of Z02.89 - other international versions of ICD-10 Z02.89 may differ. Applicable To.

  12. New Patient Visit About Vasectomy Can Be Moderate MDM

    This is a new problem since the patient has not seen your physician before, and the situation requires additional work-up (the vasectomy procedure). Combining these factors brings you to moderate complexity medical decision-making (MDM), which can support a level-four E/M code, such as 99214 (Office or other outpatient visit for the evaluation ...

  13. 2024 ICD-10-CM Diagnosis Code Z30.09

    Note. Z codes represent reasons for encounters. A corresponding procedure code must accompany a Z code if a procedure is performed. Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00-Y89 are recorded as 'diagnoses' or 'problems'.This can arise in two main ways:

  14. ICD-10-CM Diagnosis Code Z98.52

    Z98.52 is a billable diagnosis code used to specify a medical diagnosis of vasectomy status. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute ...

  15. Dx for male sterilization consultation

    I explained that this was just the initial visit (consultation) and the consent form will be submitted with the claim for the procedure, CPT 55250. The rep. said DX Z30.2 is inappropriate for this visit or consultation and should only be used with the procedure, CPT 55250. What would be the appropriate DX code then?

  16. Post Vasectomy Infertility

    Question and Answer about Post Vasectomy Infertility. ... Diagnostic evaluation of sexual dysfunction in the male partner in the setting of infertility: a committee opinion (2023) ... My staff is telling me that I am getting reimbursed for the first sonogram and OB visit (using ICD 10 code for pregnancy of uncertain viability - O36.80X0.

  17. 2024 ICD-10-CM Diagnosis Code Z13.6

    Z13.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2024 edition of ICD-10-CM Z13.6 became effective on October 1, 2023. This is the American ICD-10-CM version of Z13.6 - other international versions of ICD-10 Z13.6 may differ. Z codes represent reasons for encounters. A ...

  18. ICD-10 Code for Vasectomy status- Z98.52- Codify by AAPC

    Codes. ICD-10. ICD-10-CM Codes. Factors influencing health status and contact with health services. Persons with potential health hazards related to family and personal history and certain conditions influencing health status. Other postprocedural states (Z98) Vasectomy status (Z98.52) Z98.51. Z98.52.

  19. MEDA 165: MODULE 3A E/M Flashcards

    A 53 year old patient presents for an initial office visit to discuss surgical vasectomy for sterilization. The history and examination are detailed and the MDM is of low complexity. A new patient a 10 year old boy is brought in by his father for a knee injury sustained in a hockey game. The knee is swollen and the patient is in apparent pain.

  20. 2024 ICD-10-CM Diagnosis Code Z04.9

    Z04.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Encounter for examination and observation for unsp reason The 2024 edition of ICD-10-CM Z04.9 became effective on October 1, 2023.

  21. DOCX CodingforVasectomiesICD9.docx.docx

    ICD-10 Diagnosis Codes. Z30. 0. Encounter for general counseling and advice on contraception ... Encounter Vasectomy, unilateral or bilateral (separate procedure), including postoperative ... elsewhere) G0027. Semen analysis; presence and/or motility of sperm excluding Huhner (if performing in. clinic/office) Evaluation and Management (E/M ...

  22. Coding for Contraceptive Procedures and Devices

    Vasectomy has a low risk of problems and can usually be performed in an outpatient setting under local anesthesia." ... but you should be able to separately bill an office visit evaluation and management or consultation for a pre-vasectomy visit, ... ICD-10-CM Codes for Contraceptive Services.

  23. Search Page 1/1: VASECTOMY CONSULTATION

    Male infertility. vasectomy status (Z98.52) ICD-10-CM Diagnosis Code Z92.89 [convert to ICD-9-CM]