Angioscopy: Direct visualization of chronic venous occlusion, May-Thurner syndrome, and other applications in phlebology.


Journal

Journal of vascular surgery. Venous and lymphatic disorders
ISSN: 2213-3348
Titre abrégé: J Vasc Surg Venous Lymphat Disord
Pays: United States
ID NLM: 101607771

Informations de publication

Date de publication:
11 2019
Historique:
received: 15 01 2019
accepted: 03 05 2019
pubmed: 25 8 2019
medline: 14 7 2020
entrez: 25 8 2019
Statut: ppublish

Résumé

Angioscopy has been widely used in the diagnosis and management of vascular disorders and in particular in coronary artery disease. However, few applications have been developed in the diagnosis or management of venous disease. Endovenous angioscopy was performed to explore applications of this modality in phlebology. Procedures were performed in a sterile setting. Access was obtained by ultrasound guidance and a 9F introducer sheath. An 8.5F videoscope was used to visualize target veins. Continuous saline irrigation was used to displace blood and to clear the visual field. Fifteen procedures were performed. We describe diagnostic or interventional applications of endovenous angioscopy that include diagnosis and characterization of chronic venous occlusion, deployment of venous stents, angioscopy-guided thrombectomy, foam sclerotherapy, and endovenous laser ablation. Chronic venous occlusion was observed to be fibrotic rather than thrombotic. Endoscopic imaging of the venous system has great potential to improve access and to guide endovenous interventions. Chronic venous occlusion in post-thrombotic syndrome is a fibrotic process, and chronic venous fibrosis is a better description of the type of occlusion and should replace chronic venous thrombosis.

Sections du résumé

BACKGROUND
Angioscopy has been widely used in the diagnosis and management of vascular disorders and in particular in coronary artery disease. However, few applications have been developed in the diagnosis or management of venous disease.
METHODS
Endovenous angioscopy was performed to explore applications of this modality in phlebology. Procedures were performed in a sterile setting. Access was obtained by ultrasound guidance and a 9F introducer sheath. An 8.5F videoscope was used to visualize target veins. Continuous saline irrigation was used to displace blood and to clear the visual field.
RESULTS
Fifteen procedures were performed. We describe diagnostic or interventional applications of endovenous angioscopy that include diagnosis and characterization of chronic venous occlusion, deployment of venous stents, angioscopy-guided thrombectomy, foam sclerotherapy, and endovenous laser ablation. Chronic venous occlusion was observed to be fibrotic rather than thrombotic.
CONCLUSIONS
Endoscopic imaging of the venous system has great potential to improve access and to guide endovenous interventions. Chronic venous occlusion in post-thrombotic syndrome is a fibrotic process, and chronic venous fibrosis is a better description of the type of occlusion and should replace chronic venous thrombosis.

Identifiants

pubmed: 31444090
pii: S2213-333X(19)30349-X
doi: 10.1016/j.jvsv.2019.05.008
pii:
doi:

Types de publication

Journal Article Review Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

870-881

Informations de copyright

Copyright © 2019 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

Auteurs

Mina Kang (M)

Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.

Claudia Hurwitz (C)

Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.

Tom Exner (T)

Haematex Research Pty Ltd, St. Vincent's Hospital, Sydney, New South Wales, Australia.

Anes Yang (A)

Department of Dermatology, St. Vincent's Hospital, Sydney, New South Wales, Australia; Dermatology, Phlebology and Fluid Mechanics Research Laboratory, St. Vincent's Centre for Applied Medical Research, St. Vincent's Hospital, Sydney, New South Wales, Australia.

David Connor (D)

Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia; Dermatology, Phlebology and Fluid Mechanics Research Laboratory, St. Vincent's Centre for Applied Medical Research, St. Vincent's Hospital, Sydney, New South Wales, Australia.

Kurosh Parsi (K)

Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia; Department of Dermatology, St. Vincent's Hospital, Sydney, New South Wales, Australia; Dermatology, Phlebology and Fluid Mechanics Research Laboratory, St. Vincent's Centre for Applied Medical Research, St. Vincent's Hospital, Sydney, New South Wales, Australia. Electronic address: kurosh.parsi@svha.org.au.

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