Risk of Mortality with Paclitaxel Drug-Coated Balloon in De Novo Coronary Artery Disease.


Journal

Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551

Informations de publication

Date de publication:
04 2020
Historique:
received: 14 01 2020
accepted: 14 01 2020
pubmed: 23 4 2020
medline: 27 10 2020
entrez: 23 4 2020
Statut: ppublish

Résumé

A recent meta-analysis showed increased mortality with paclitaxel drug-coated balloons (PCB) in peripheral arterial disease. With the absence of a definitive study evaluating the risk of mortality with PCB in de novo coronary artery disease, we performed a systematic review and critical appraisal of the literature analyzing this risk. In this review, we included 17 trials with a total of 1573 patients. Cardiac mortality was reported in 16 studies and all-cause mortality in 14 studies. Eleven studies had <12 months' follow-up; 6 had ≥12 months' follow-up. None of the studies was powered to evaluate any differences in mortality. The majority of the included studies have a Jadad scale ≤2. Ten of 17 studies had no mortality, 4 had numerically higher mortality with PCB, and 3 had lower or same mortality with PCB, when compared to drug-eluting stents. A standard meta-analysis cannot be performed, as most studies did not report hazard ratios or Kaplan-Meier survival plots on mortality. With the available literature, conclusions cannot be made in identifying the association of mortality with PCB in de novo coronary artery disease. There is an urgent need for well-designed studies with long-term follow-up for PCB in de novo coronary artery disease. A recent meta-analysis showed increased mortality with paclitaxel drug-coated balloon (PCB) in peripheries. No studies to date evaluate the risk of mortality with PCB in de novo coronary artery disease. In this systematic review and critical appraisal of literature, we outline why the risk cannot be elucidated from the available literature. A standard meta-analysis using inverse variance method would be incorrect to use, as mortality is a time-to-event data point, and only 1 out of 17 studies reported a Kaplan-Meier survival plot.

Identifiants

pubmed: 32317227
pii: S1553-8389(20)30021-X
doi: 10.1016/j.carrev.2020.01.012
pii:
doi:

Substances chimiques

Cardiovascular Agents 0
Coated Materials, Biocompatible 0
Paclitaxel P88XT4IS4D

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

549-555

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest

Auteurs

Charan Yerasi (C)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Brian C Case (BC)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Brian J Forrestal (BJ)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Paul Kolm (P)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Kazuhiro Dan (K)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Rebecca Torguson (R)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

William S Weintraub (WS)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Hector M Garcia-Garcia (HM)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America.

Ron Waksman (R)

Section of Interventional Cardiology, Medstar Washington Hospital Center, Washington, DC, United States of America. Electronic address: ron.waksman@medstar.net.

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Classifications MeSH