American Society of Hirudotherapy

Utilization of Leech Therapy after Rhinoplasty

Research article published in Plastic and reconstructive surgery (2022)

Last Updated: November 1, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportClinical LiteratureShtraks J, Peng G, Nassif P · Plastic and reconstructive surgery, 2022

Abstract

BACKGROUND: The use of medicinal leeches in modern reconstructive surgery is well-described. Leech therapy after rhinoplasty has not been previously well-characterized. METHODS: The medical records of all patients who underwent open rhinoplasty by a single surgeon over a 4-year period were reviewed. Patient demographics, including age, sex, medical comorbidities, number of previous rhinoplasty surgeries, time to utilization of leech therapy, adjunct therapies used, resolution of skin changes, and smoking status, were recorded. Operative reports were reviewed for pertinent information, including number of tip grafts used, graft materials used, and placement of septal extension grafts or "unicorn" grafts. RESULTS: Between April of 2016 and March of 2020, 545 patients underwent rhinoplasty performed by the senior author (P.S.N.). Of these patients, 39 (7.2 percent) underwent leech therapy postoperatively. The mean age of included patients was 47.4 years. Of the patients who required leech therapy, 34 (87.2 percent) had undergone revision rhinoplasty. The mean number of previous rhinoplasties was 3.4. The mean number of tip grafts used was 2.6. Thirty-three patients (84.6 percent) had either a traditional septal extension graft or unicorn graft placed. Nine patients (23.1 percent) were former smokers. Complete resolution of skin color changes was seen in 38 patients (97.4 percent). There were no major complications after leech therapy. CONCLUSIONS: Leech therapy is a useful tool for the rhinoplasty surgeon, particularly in the setting of complex revision rhinoplasty, in patients who have undergone multiple previous nasal surgical procedures, or in patients who require significant cartilage grafting to reconstruct the nasal tip or lengthen the nose. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.

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

Publication typeJournal Article
Indexed MeSH termsCartilageHumansLeechingMiddle AgedNasal SeptumNoseRetrospective StudiesRhinoplastyTreatment Outcome

Summary

A retrospective review of 545 rhinoplasty patients identified 39 (7.2%) who received postoperative leech therapy, with complete skin color resolution in 97.4% and no major complications, particularly after revision surgery or extensive cartilage grafting.

Why This Matters for Hirudotherapy

This study reports a single-surgeon experience with postoperative leech therapy following open rhinoplasty, in which 39 of 545 patients (7.2%) received leech treatment—predominantly after revision procedures (87.2%)—with complete resolution of adverse skin color changes observed in 97.4% and no major complications. This work is directly relevant to hirudotherapy, providing clinical outcome data on medicinal leech use in facial plastic surgery and reinforcing the established role of leech therapy in managing compromised tissue perfusion across reconstructive contexts. The findings reflect one surgeon's practice and patient population, provide no data on leech species, salivary secretome components, or pharmacologic mechanisms underlying the observed clinical effects, and do not establish optimal treatment protocols for broader application.

Citation

Reference (Vancouver style)

Shtraks JP, Peng GL, Nassif PS. Utilization of Leech Therapy after Rhinoplasty. Plast Reconstr Surg. 2022;149(6):1090e-1095e. doi:10.1097/PRS.0000000000009096. PMID: 35383721

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.