Американское общество гирудотерапии

Monitoring Breast Reconstruction Flaps Using Near-Infrared Spectroscopy Tissue Oximetry

Research article published in Plastic surgical nursing : official journal of the American Society of Plastic and Reconstructive Surgical Nurses (2024)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Observational studyРазработка лекарственных препаратовKumbasar DE et al. · Plastic surgical nursing : official journal of the American Society of Plastic and Reconstructive Surgical Nurses, 2024

Abstract

Free flap reconstruction is a common procedure with success rates greater than 99%. However, vascular complications may occur, resulting in flap failure. For this reason, early detection of vascular compromise is crucial for flap salvage. Vascular complications may be detected early by monitoring tissue oximetry parameter changes using near-infrared spectroscopy (NIRS). This method of noninvasive monitoring can evaluate changes in flap oxygenation levels caused by arterial and venous thrombosis before surgical reexploration. The goal of this study was to assess the validity of using NIRS oximetry for monitoring free flaps. We conducted a prospective cohort observational study of 10 patients undergoing breast reconstruction. We used the INVOS 7100 cerebral oximetry monitoring system (Medtronic, Dublin, Ireland) to provide 24-hr continuous postoperative monitoring of flap perfusion and compared the data with clinical assessment findings. The median patient age was 57 years (range = 41-61 years). Patients underwent immediate breast reconstruction with deep inferior epigastric perforator (DIEP) flap surgery (n = 4), delayed reconstruction with DIEP flap surgery (n = 4), transverse upper gracilis flap surgery (n = 1), and latissimus dorsi flap with lipofilling (n = 1). We successfully monitored all 10 flaps for 24 hr postoperatively. The overall flap survival rate was 100%. Findings of clinical examination, Doppler studies, and surgical outcome were consistent with NIRS monitoring. In conclusion, NIRS tissue oximetry could potentially provide a noninvasive method for effective postoperative monitoring of free flaps.

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

Publication typeJournal ArticleObservational Study
Indexed MeSH termsAdultCohort StudiesFemaleHumansMammaplastyMiddle AgedMonitoring, PhysiologicOximetryProspective StudiesSpectroscopy, Near-InfraredSurgical FlapsVictoria

Резюме

Free flap reconstruction is a common procedure with success rates greater than 99%.

Почему это важно для гирудотерапии

This prospective cohort observational study of 10 patients evaluated the use of near-infrared spectroscopy (NIRS) tissue oximetry for 24-hour continuous postoperative monitoring of free flaps in breast reconstruction, finding 100% flap survival and consistency between NIRS readings, clinical examination, Doppler studies, and surgical outcomes. The abstract notes that NIRS can evaluate changes in flap oxygenation caused by arterial and venous thrombosis before surgical reexploration. The study does not involve leeches, hirudotherapy, or any leech-derived agents. There is no direct relevance to ASH's domain; the study addresses a perfusion monitoring technology in flap surgery without any leech-related content.

Цитирование

Monitoring Breast Reconstruction Flaps Using Near-Infrared Spectroscopy Tissue Oximetry

Kumbasar DE et al. · Plastic surgical nursing : official journal of the American Society of Plastic and Reconstructive Surgical Nurses, 2024

Связанный клинический контекст

Узнайте, как это исследование связано с клинической практикой

Добавлено в библиотеку ASH: May 27, 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.