Американское общество гирудотерапии

Acute postoperative infection with Aeromonas hydrophila after using medical leeches for treatment of venous congestion

Case series published in Archives of Orthopaedic and Trauma Surgery (2010)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportБезопасность и инфекционный контрольКлинические исследованияSchnabl SM, Kunz C, Unglaub F et al. · Archives of orthopaedic and trauma surgery, 2010

Abstract

INTRODUCTION: Venous convulsion after reconstructive microsurgery procedures is one major complication a surgeon has to deal with. Today, especially in the field of reconstructive microsurgery, medicinal leech therapy enjoys a renaissance. The potential risks such as infections associated with leech therapy are generally underestimated and not sufficiently discussed in literature. METHOD/PATIENTS: We present five male patients with an average age of 47 years. All patients suffered from a trauma incident, which had to be treated as an emergency. Three patients showed, postoperatively, a venous congestion after the reconstructive procedures. Another two patients with flap reconstruction and flap training developed venous problems after 12 and 14 days. In all five cases, the indication was given to use medical leeches (Hirudo medicinalis). In all the patients, a local infection of the injured extremity could be regarded after beginning with the leech treatment. The treatment duration with medical leeches for postoperative venous congestion was an average of 6 days. RESULTS: The reconstructive procedures in all five cases were unfortunately unsuccessful as major local infections were observed. Microbiological analyses showed, in all cases, an infection with Aeromonas hydrophila. CONCLUSION: We recommend making a considered indication for leech therapy, to diagnose wound infections early and to think about prophylactic antibiotics in patients with leech application.

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

Publication typeJournal Article
Indexed MeSH termsAeromonas hydrophilaAnimalsGram-Negative Bacterial InfectionsHirudo medicinalisHumansLeechingMaleMicrosurgeryMiddle AgedPlastic Surgery ProceduresSurgical FlapsTreatment Failure

Резюме

Five patients receiving leech therapy after reconstructive microsurgery developed Aeromonas hydrophila infections leading to flap failure, underscoring the importance of antibiotic prophylaxis and early infection diagnosis.

Почему это важно для гирудотерапии

This report describes five male trauma patients who developed local infections with Aeromonas hydrophila following medical leech (Hirudo medicinalis) therapy for postoperative venous congestion after reconstructive microsurgery procedures. The findings are directly relevant to hirudotherapy practice, as all five reconstructive procedures were unsuccessful due to major local infections, leading the authors to recommend careful indication for leech therapy, early diagnosis of wound infections, and consideration of prophylactic antibiotics when leeches are applied. However, the report involves only five patients and the abstract provides limited detail on microbiological methodology, whether antibiotic prophylaxis was used initially, or comparative infection rates, restricting broader conclusions about infection risk magnitude or optimal prevention strategies.

Цитирование

Acute postoperative infection with Aeromonas hydrophila after using medical leeches for treatment of venous congestion.

Schnabl SM, Kunz C, Unglaub F et al. · Archives of orthopaedic and trauma surgery, 2010

Связанный клинический контекст

Добавлено в библиотеку ASH: May 26, 2026 · Последнее обновление сайта: June 18, 2026

Этот сайт предоставляет образовательную информацию и не является медицинской консультацией, диагнозом или рекомендацией по лечению. Гирудотерапия сопряжена с клинически значимыми рисками и должна проводиться только квалифицированными клиницистами в рамках институционально утверждённых протоколов. Разрешение FDA 510(k) для медицинских пиявок ограничено определёнными показаниями; обсуждения исследовательского и нелицензионного применения отмечены соответствующим образом. Для индивидуальных медицинских рекомендаций обратитесь к квалифицированному медицинскому специалисту.