Американское общество гирудотерапии

Implantable Doppler flow system: experience with 24 microvascular free-flap operations.

Research article published in Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery (2006)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportКлинические исследованияPryor et al. · Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 2006

Abstract

OBJECTIVES: Microvascular reconstruction requires postoperative monitoring to prevent vascular occlusion and flap failure. These methods require skilled personnel and can delay diagnosis and treatment of threatened flap failures. The Cook-Swartz implantable Doppler flow system provides continual feedback on vascular pedicle status, which in turn provides rapid assessment of minute-to-minute changes in flap vasculature that may allow intervention before total vascular occlusion and expeditious reexploration for threatened flap failure, possibly improving flap salvage. STUDY DESIGN AND SETTING: Charts of 24 patients with microvascular free-flap reconstruction and implantation of Doppler flow system at Mayo Clinic Rochester were retrospectively reviewed. Surgical technique and flap outcomes were evaluated. RESULTS: Microvascular reconstruction and implantation of Doppler flow system were successful in all patients. Complications were minimal, and postoperative monitoring system facilitated rapid reexploration when necessary. Flap viability was 96%. CONCLUSION: Doppler flow system is reliable for monitoring minute-to-minute changes in microvascular flap vascular status postoperatively, and allows rapid recognition of complications and facilitating reexploration. This is a valuable, easily mastered tool for microvascular reconstructive surgery. SIGNIFICANCE: May alter postoperative monitoring techniques of microvascular surgeons.

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

Publication typeJournal Article
Indexed MeSH termsAdolescentAdultAgedAged, 80 and overFemaleHead and Neck NeoplasmsHumansLaser-Doppler FlowmetryMaleMicrocirculationMiddle AgedMonitoring, Physiologic

Резюме

Microvascular reconstruction requires postoperative monitoring to prevent vascular occlusion and flap failure. These methods require skilled personnel and can delay diagnosis and treatment of threatened flap failures.

Почему это важно для гирудотерапии

This study retrospectively reviewed charts of 24 patients who underwent microvascular free-flap reconstruction with implantation of a Doppler flow system, evaluating surgical technique and flap outcomes. The implantable Doppler system provided continuous feedback on vascular pedicle status and facilitated rapid reexploration when necessary, with reported 96% flap viability and minimal complications. The study evaluates a mechanical postoperative monitoring technology for microvascular reconstruction. The abstract makes no mention of leeches, hirudotherapy, or any leech-related intervention, and its relevance to hirudotherapy or the leech secretome is entirely indirect, limited to the general clinical context of postoperative flap management.

Цитирование

Implantable Doppler flow system: experience with 24 microvascular free-flap operations.

Pryor et al. · Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 2006

Связанный клинический контекст

Узнайте, как это исследование связано с клинической практикой

Добавлено в библиотеку ASH: May 28, 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.