Regulatory Significance 5/10

UK Guidelines for Post-Vasectomy Semen Analysis Under ISO 15189 Accreditation

These 2016 joint guidelines from the Association of Biomedical Andrologists, British Andrology Society, and BAUS establish standardised procedures for post-vasectomy semen analysis, including timing, sample handling, clearance thresholds, and the special clearance cutoff of fewer than 100,000 non-motile sperm per millilitre. The guidelines are designed to support accredited laboratory services under ISO 15189 and replace the 2002 BAS recommendations.

The original study

2016 Laboratory guidelines for postvasectomy semen analysis: Association of Biomedical Andrologists, the British Andrology Society and the British Association of Urological Surgeons.

Authors
Hancock P, Woodward BJ, Muneer A, Kirkman-Brown JC
Journal
Journal of clinical pathology
Type
Guideline, Journal Article
PMID
27083211
Read the original study →

Original abstract

Post-vasectomy semen analysis (PVSA) is the procedure used to establish whether sperm are present in the semen following a vasectomy. PVSA is presently carried out by a wide variety of individuals, ranging from doctors and nurses in general practitioner (GP) surgeries to specialist scientists in andrology laboratories, with highly variable results.Key recommendations are that: (1) PVSA should take place a minimum of 12 weeks after surgery and after a minimum of 20 ejaculations. (2) Laboratories should routinely examine samples within 4 h of production if assessing for the presence of sperm. If non-motile sperm are observed, further samples must be examined within 1 h of production. (3) Assessment of a single sample is acceptable to confirm vasectomy success if all recommendations and laboratory methodology are met and no sperm are observed. Clearance can then be given. (4) The level for special clearance should be <100 000/mL non-motile sperm. Special clearance cannot be provided if any motile sperm are observed and should only be given after assessment of two samples in full accordance with the methods contained within these guidelines. Surgeons are responsible both preoperatively and postoperatively for the counselling of patients and their partners regarding complications and the possibility of late recanalisation after clearance. These 2016 guidelines replace the 2002 British Andrology Society (BAS) laboratory guidelines and should be regarded as definitive for the UK in the provision of a quality PVSA service, accredited to ISO 15189:2012, as overseen by the United Kingdom Accreditation Service (UKAS).