American Society of Hirudotherapy

Medicinal Leech Therapy in Urology: A PRISMA-Compliant Systematic Review

Systematic review published in African journal of urology : the official journal of the Pan African Urological Surgeons' Association (PAUSA) (2023)

Last Updated: November 1, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportClinical LiteratureBattin A, Hobeika N, Zdilla M · African journal of urology : the official journal of the Pan African Urological Surgeons' Association (PAUSA), 2023

Abstract

PURPOSE: To systematically review cases of medicinal leech therapy, otherwise known as hirudotherapy or leeching, in the context of urology. METHODS: A systematic review of cases in MEDLINE / PubMed was performed in accordance with PRISMA guidelines. RESULTS: Of 46 search results, 10 articles detailing 12 unique cases of medicinal leech therapy used in the urological context were included. Leeching was conducted in 9 of 12 cases (75%) for the management of congested blood occurring in four cases post penile replantation, two cases of postoperative scrotal hematoma, two cases of venous congestion of the glans post neonatal bladder exstrophy repair, and one case of refractory priapism. Leeching in the remaining three cases was for the management of penoscrotal edema in patients with hormone refractory prostate carcinoma treated with radical radiation therapy. All 12 cases (100%) reported clinical improvement from leech therapy. Venous congestion / hematoma cases noted decreased displaced blood volume. The patient experiencing priapism reported decreased pain despite the persistence of cavernosal swelling. The three cases of penoscrotal edema reported significant decreases in swelling due to serous fluid drainage from leech puncture sites. No complications or side effects were reported in the nine adult patients. The three postoperative neonatal patients all required some form of blood product throughout treatment. CONCLUSIONS: The systematic review of the cases, though limited in number, suggests that medicinal leech therapy is a favorable treatment option for individuals with varied urological pathologies and that leeching may improve post-surgical outcomes in the urological setting.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article

Summary

A PRISMA-compliant systematic review of 12 urological cases found medicinal leech therapy achieved clinical improvement in all 12, with nine treated for congested blood and three for penoscrotal edema.

Why This Matters for Hirudotherapy

This PRISMA-compliant systematic review compiled 12 unique cases of medicinal leech therapy across urological conditions, including venous congestion following penile replantation, postoperative scrotal hematoma, glans congestion after neonatal bladder exstrophy repair, refractory priapism, and radiation-related penoscrotal edema. All 12 cases reported clinical improvement, with no complications among the nine adult patients, though all three neonates required blood product support during treatment. The review specifically examines hirudotherapy applications and reported outcomes within a surgical subspecialty. However, the authors acknowledge that the included cases are limited in number, and the conclusions are correspondingly framed as suggestions—leech therapy 'may improve' outcomes and 'suggests' favorability—rather than as established efficacy findings.

Citation

Reference (Vancouver style)

Battin AO, Hobeika N, Zdilla MJ. Medicinal Leech Therapy in Urology: A PRISMA-Compliant Systematic Review. Afr J Urol. 2023;29:21. doi:10.1186/s12301-023-00351-9. PMID: 41684506

Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.

Added to ASH library: March 18, 2026 · Site last updated: November 1, 2026

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.