Log in to save to my catalogue

24-Month Efficacy and Safety Results from Japanese Patients in the IMPERIAL Randomized Study of the...

24-Month Efficacy and Safety Results from Japanese Patients in the IMPERIAL Randomized Study of the...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8382620

24-Month Efficacy and Safety Results from Japanese Patients in the IMPERIAL Randomized Study of the Eluvia Drug-Eluting Stent and the Zilver PTX Drug-Coated Stent

About this item

Full title

24-Month Efficacy and Safety Results from Japanese Patients in the IMPERIAL Randomized Study of the Eluvia Drug-Eluting Stent and the Zilver PTX Drug-Coated Stent

Publisher

New York: Springer US

Journal title

Cardiovascular and interventional radiology, 2021-09, Vol.44 (9), p.1367-1374

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

Purpose
The purpose of the study is to report 24-month efficacy and safety results for the Japanese patient cohort in a prospective randomized controlled trial (RCT) of drug-eluting stent (DES) use for peripheral artery disease.
Materials and methods
Patients in the global IMPERIAL RCT had femoropopliteal lesions treated with either the Eluvia DES (Boston Scientific, Marlborough, MA, USA) or the Zilver PTX drug-coated stent (Cook Medical, Bloomington, IN, USA). At 24 months, assessments included duplex ultrasound imaging for core laboratory vessel patency measurement, target lesion revascularization (TLR) rates, and clinical outcome measures.
Results
The Japanese cohort included 84 patients (56 treated with Eluvia and 28 with Zilver PTX). The clinically driven TLR rates were 5.6% (3/54) and 18.5% (5/27) for patients treated with Eluvia and Zilver PTX, respectively (difference -13.0%, 95%CI -28.8, 2.9%;
p
 = 0.11). The Kaplan–Meier estimates for freedom from clinically driven TLR at 24 months were 94.3% for patients who received Eluvia and 80.4% for those who received Zilver PTX (log rank
p
 = 0.05), and for primary patency they were 88.5% and 80.4%, respectively (log rank
p
 = 0.28). Mortality rates were 5.6% (3/54) and 11.1% (3/27);
p
 = 0.39. Rutherford classification improved by at least one category without TLR for 91.8% (45/49) and 68.2% (15/22) of patients (
p 
= 0.03). Walking impairment score improvements were sustained over time.
Conclusion
The results at 24 months support the efficacy and safety of DES in Japanese patients, with sustained clinical improvements and numerically fewer reinterventions for those treated with Eluvia.
Clinical trial Registration
Clinicaltrials.gov identifier NCT02574481.
https://clinicaltrials.gov/ct2/show/NCT02574481
Level of Evidence
EBM Level III; cohort analysis of randomized trial....

Alternative Titles

Full title

24-Month Efficacy and Safety Results from Japanese Patients in the IMPERIAL Randomized Study of the Eluvia Drug-Eluting Stent and the Zilver PTX Drug-Coated Stent

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8382620

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8382620

Other Identifiers

ISSN

0174-1551

E-ISSN

1432-086X

DOI

10.1007/s00270-021-02901-6

How to access this item