Anesthetic Protocol For Patients With Hereditary Hemorrhagic Telangiectasia Undergoing Enteroscopy For Angiodysplastic Lesions: A Case Report

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare genetic disorder that poses significant perioperative challenges due to the risk of bleeding. We report the case of a 47-year-old male with HHT undergoing double-balloon enteroscopy (DBE) for gastrointestinal angiodysplastic lesions. Preoperative preparation included detailed screening for anemia, coagulation status, and arteriovenous malformations (AVMs). Anesthetic considerations included airway management strategies to prevent and detect telangiectasia rupture, maintenance of hemodynamic stability, and post-procedural bleeding management. Intraoperative measures included careful intubation, hemodynamic monitoring, and mitigation of embolic risks. The procedure was completed successfully, managing over 100 lesions without incident. This case highlights the importance of personalized perioperative protocols, intraoperative vigilance, and post-operative care which are crucial for the successful management of patients with HHT. We present our HHT-specific anesthetic protocol from a hematology center to address the unique challenges of HHT in endoscopic clinics, contributing to safer outcomes for patients with this rare genetic disorder.

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Publication Details

Journal
University of Toronto Medical Journal
Published
2025-07-12
DOI
https://doi.org/10.33137/utmj.v102i2.43726
Primary Topic
Vascular Anomalies and Treatments
Type
article
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article

Anesthetic Protocol For Patients With Hereditary Hemorrhagic Telangiectasia Undergoing Enteroscopy For Angiodysplastic Lesions: A Case Report

Brian Yang, Janaka Perera, Michael J. Ricci, Wesla Pfeifer et al.
University of Toronto Medical Journal
Vascular Anomalies and Treatments
article

Anesthetic Protocol For Patients With Hereditary Hemorrhagic Telangiectasia Undergoing Enteroscopy For Angiodysplastic Lesions: A Case Report

Brian Yang, Janaka Perera, Michael J. Ricci, Wesla Pfeifer, Vetri Thangavelu
article en

Abstract

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare genetic disorder that poses significant perioperative challenges due to the risk of bleeding. We report the case of a 47-year-old male with HHT undergoing double-balloon enteroscopy (DBE) for gastrointestinal angiodysplastic lesions. Preoperative preparation included detailed screening for anemia, coagulation status, and arteriovenous malformations (AVMs). Anesthetic considerations included airway management strategies to prevent and detect telangiectasia rupture, maintenance of hemodynamic stability, and post-procedural bleeding management. Intraoperative measures included careful intubation, hemodynamic monitoring, and mitigation of embolic risks. The procedure was completed successfully, managing over 100 lesions without incident. This case highlights the importance of personalized perioperative protocols, intraoperative vigilance, and post-operative care which are crucial for the successful management of patients with HHT. We present our HHT-specific anesthetic protocol from a hematology center to address the unique challenges of HHT in endoscopic clinics, contributing to safer outcomes for patients with this rare genetic disorder.

University of Toronto Medical JournalVol. 102(2)
St. Michael's Hospital (CA), University of Toronto (CA), St Michael's Hospital (GB)
Openalex Percentile: Top 70%
Vascular Anomalies and Treatments
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