Effect of Percutaneous Suction Thromboembolectomy on Improved Right Ventricular Function.
Female
Follow-Up Studies
Heart Ventricles
/ diagnostic imaging
Humans
Male
Middle Aged
Pulmonary Artery
/ diagnostic imaging
Pulmonary Embolism
/ diagnosis
Retrospective Studies
Suction
/ methods
Thrombectomy
/ methods
Tomography, X-Ray Computed
Treatment Outcome
Ventricular Function, Right
/ physiology
Embolectomy/instrumentation/methods
equipment design
pulmonary embolism/prevention & control/surgery/therapy
retrospective studies
thrombectomy/instrumentation/methods/mortality
thromboembolism/complications
treatment outcome
vascular access devices
ventricular function, right
Journal
Texas Heart Institute journal
ISSN: 1526-6702
Titre abrégé: Tex Heart Inst J
Pays: United States
ID NLM: 8214622
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
entrez:
26
6
2019
pubmed:
27
6
2019
medline:
18
12
2019
Statut:
epublish
Résumé
Venous thromboembolism is a leading cause of cardiovascular death. Historically, surgical intervention has been associated with high morbidity rates. Pharmacologic therapy alone can be inadequate for patients with substantial hemodynamic compromise, so minimally invasive procedures are being developed to reduce clot burden. We describe our initial experience with using the AngioVac system to remove thromboemboli percutaneously. We reviewed all suction thromboembolectomy procedures performed at our institution from March 2013 through August 2015. The main indications for the procedure were failed catheter-directed therapy, contraindication to thrombolysis, bleeding-related complications, and clot-in-transit phenomena. We collected details on patient characteristics, procedural indications, thrombus location, hemodynamic values, cardiac function, pharmacologic support, and survival to discharge from the hospital. The Wilcoxon signed-rank test was used for statistical analysis. Thirteen patients (mean age, 56 ± 15 yr; 10 men) underwent suction thromboembolectomy; 10 (77%) survived to hospital discharge. The median follow-up time was 74 days (interquartile range [IQR], 23-221 d). Preprocedurally, 8 patients (62%) had severe right ventricular dysfunction; afterwards, 11 (85%) had normal function or mild-to-moderate dysfunction, and only 2 (17%) had severe dysfunction (
Identifiants
pubmed: 31236075
doi: 10.14503/THIJ-17-6551
pmc: PMC6555294
doi:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
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