Vascular Quality Initiative Surveillance of Femoropopliteal Artery Paclitaxel Devices.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
13 12 2021
Historique:
received: 02 03 2021
revised: 12 08 2021
accepted: 17 08 2021
entrez: 10 12 2021
pubmed: 11 12 2021
medline: 1 4 2022
Statut: ppublish

Résumé

This study sought to determine the safety and efficacy of paclitaxel (PTX) devices in the treatment of peripheral artery disease involving the femoropopliteal artery. A meta-analysis of PTX devices for the treatment of femoropopliteal artery disease reported a mortality signal. This was a multicenter cohort study using an integrated clinical data surveillance system to conduct a prospective, propensity score-matched survival analysis of 2,456 patients in the Society for Vascular Surgery Vascular Quality Initiative from January 2017 to May 2020. The study compared PTX drug-coated balloon angioplasty versus percutaneous transluminal balloon angioplasty, PTX drug-eluting stents versus bare-metal stents, and any PTX device versus any non-PTX device. The primary outcome was 2-year survival. Secondary endpoints were successful ambulation and interventional success. Treatment with any PTX device versus any non-PTX device was associated with increased 2-year survival (89.5% vs 86.7%; HR: 0.79; 95% CI: 0.72-0.87; P = 0.004), improved interventional success (81.6% vs 77.6%; HR: 0.82; 95% CI: 0.74-0.91; P < 0.001), and higher rates of independent ambulation at 1 year (86.0% vs 83.4%; HR: 0.85; 95% CI: 0.79-0.91; P = 0.008). Treatment with PTX drug-coated balloon angioplasty was associated with improved survival at 2 years (88.9% vs 85.7%; HR: 0.77; 95% CI: 0.70-0.86; P = 0.005), while PTX drug-eluting stent therapy was associated with similar survival compared with bare-metal stent therapy (91.3% vs 89.6%; HR: 0.84; 95% CI: 0.70-1.01; P = 0.36). In this prospective, active surveillance of a national clinical registry, PTX-containing devices were associated with increased survival at 2 years and improved clinical outcomes at 1 year. (VQI DELTA Paclitaxel Device Safety Analysis [VQI-PTX]; NCT04110288).

Sections du résumé

OBJECTIVES
This study sought to determine the safety and efficacy of paclitaxel (PTX) devices in the treatment of peripheral artery disease involving the femoropopliteal artery.
BACKGROUND
A meta-analysis of PTX devices for the treatment of femoropopliteal artery disease reported a mortality signal.
METHODS
This was a multicenter cohort study using an integrated clinical data surveillance system to conduct a prospective, propensity score-matched survival analysis of 2,456 patients in the Society for Vascular Surgery Vascular Quality Initiative from January 2017 to May 2020. The study compared PTX drug-coated balloon angioplasty versus percutaneous transluminal balloon angioplasty, PTX drug-eluting stents versus bare-metal stents, and any PTX device versus any non-PTX device. The primary outcome was 2-year survival. Secondary endpoints were successful ambulation and interventional success.
RESULTS
Treatment with any PTX device versus any non-PTX device was associated with increased 2-year survival (89.5% vs 86.7%; HR: 0.79; 95% CI: 0.72-0.87; P = 0.004), improved interventional success (81.6% vs 77.6%; HR: 0.82; 95% CI: 0.74-0.91; P < 0.001), and higher rates of independent ambulation at 1 year (86.0% vs 83.4%; HR: 0.85; 95% CI: 0.79-0.91; P = 0.008). Treatment with PTX drug-coated balloon angioplasty was associated with improved survival at 2 years (88.9% vs 85.7%; HR: 0.77; 95% CI: 0.70-0.86; P = 0.005), while PTX drug-eluting stent therapy was associated with similar survival compared with bare-metal stent therapy (91.3% vs 89.6%; HR: 0.84; 95% CI: 0.70-1.01; P = 0.36).
CONCLUSIONS
In this prospective, active surveillance of a national clinical registry, PTX-containing devices were associated with increased survival at 2 years and improved clinical outcomes at 1 year. (VQI DELTA Paclitaxel Device Safety Analysis [VQI-PTX]; NCT04110288).

Identifiants

pubmed: 34887051
pii: S1936-8798(21)01656-3
doi: 10.1016/j.jcin.2021.08.058
pii:
doi:

Substances chimiques

Cardiovascular Agents 0
Paclitaxel P88XT4IS4D

Banques de données

ClinicalTrials.gov
['NCT04110288']

Types de publication

Journal Article Meta-Analysis Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

2598-2609

Subventions

Organisme : FDA HHS
ID : U01 FD004963
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures This research was supported through U.S. Food and Drug Administration research grant 1U01FD004963-01: Active Surveillance of Cardiovascular Devices: The Multi-Registry DELTA Network. Mr Smale is an employee of BD Peripheral Intervention. Dr Lottes was an employee of Cook Medical during the conduct of the study. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Daniel J Bertges (DJ)

Division of Vascular Surgery, University of Vermont Medical Center, Burlington, Vermont, USA. Electronic address: daniel.bertges@uvmhealth.org.

Jens Eldrup-Jorgensen (J)

Division of Vascular Surgery, Maine Medical Center, Portland, Maine, USA.

Susan Robbins (S)

Division of Cardiovascular Medicine, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.

Henry Ssemaganda (H)

Division of Cardiovascular Medicine, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.

Misti Malone (M)

Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Danica Marinac-Dabic (D)

Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Joshua Smale (J)

BD Peripheral Intervention, Tempe, Arizona, USA.

Aaron E Lottes (AE)

Weldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, USA.

Arjun Majithia (A)

Division of Cardiovascular Medicine, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.

Frederic S Resnic (FS)

Division of Cardiovascular Medicine, Lahey Hospital and Medical Center, Burlington, Massachusetts, USA.

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Classifications MeSH