J 2024

Complete Versus Culprit-Only Revascularization in Older Patients With ST-Segment-Elevation Myocardial Infarction: An Individual Patient Meta-Analysis

CAMPO, Gianluca; Felix BOHM; Thomas ENGSTROM; Pieter C SMITS; Islam Y ELGENDY et al.

Základní údaje

Originální název

Complete Versus Culprit-Only Revascularization in Older Patients With ST-Segment-Elevation Myocardial Infarction: An Individual Patient Meta-Analysis

Autoři

CAMPO, Gianluca; Felix BOHM; Thomas ENGSTROM; Pieter C SMITS; Islam Y ELGENDY; Gerry P MCCANN; David A WOOD; Matteo SERENELLI; Stefan JAMES; Dan Eik HOFSTEN; Klerk Bianca M BOXM-DE; Adrian BANNING; John A CAIRNS; Rita PAVASINI; Goran STANKOVIC; Petr KALA; Henning KELBAEK; Emanuele BARBATO; Ilija SRDANOVIC; Mohamed HAMZA; Amerjeet S BANNING; Simone BISCAGLIA a Shamir MEHTA

Vydání

Circulation, Philadelphia, Lippincott Williams Wilkins, 2024, 0009-7322

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30201 Cardiac and Cardiovascular systems

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 38.600

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14110/24:00138592

Organizační jednotka

Lékařská fakulta

EID Scopus

Klíčová slova anglicky

complete revascularization; meta-analysis; multivessel disease; myocardial infarction; older patients

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 23. 1. 2025 10:46, Mgr. Tereza Miškechová

Anotace

V originále

BACKGROUND:Complete revascularization is the standard treatment for patients with ST-segment-elevation myocardial infarction and multivessel disease. The FIRE trial (Functional Assessment in Elderly Myocardial Infarction Patients With Multivessel Disease) confirmed the benefit of complete revascularization in a population of older patients, but the follow-up is limited to 1 year. Therefore, the long-term benefit (>1 year) of this strategy in older patients is debated. To address this, an individual patient data meta-analysis was conducted in patients with ST-segment-elevation myocardial infarction >= 75 years of age enrolled in randomized clinical trials investigating complete versus culprit-only revascularization strategies. METHODS:PubMed, Embase, and the Cochrane database were systematically searched to identify randomized clinical trials comparing complete versus culprit-only revascularization. Individual patient-level data were collected from the relevant trials. The primary end point was death, myocardial infarction, or ischemia-driven revascularization. The secondary end point was cardiovascular death or myocardial infarction. RESULTS:Data from 7 randomized clinical trials encompassing 1733 patients (917 randomized to culprit-only and 816 to complete revascularization) were analyzed. The median age was 79 [interquartile range, 77-83] years. Of the patients, 595 (34%) were female. Follow-up ranged from a minimum of 6 months to a maximum of 6.2 years (median, 2.5 [interquartile range, 1-3.8] years). Complete revascularization reduced the primary end point up to 4 years (hazard ratio, 0.78 [95% CI, 0.63-0.96]) but not at the longest available follow-up (hazard ratio, 0.83 [95% CI, 0.69-1.01]). Complete revascularization significantly reduced the occurrence of cardiovascular death or myocardial infarction at the longest available follow-up (hazard ratio, 0.76 [95% CI, 0.58-0.99]). This was observed even when censoring the follow-up at each year. Long-term rate of death did not differ between complete and culprit-only revascularization arms. CONCLUSIONS:In this individual patient data meta-analysis of older patients with ST-segment-elevation myocardial infarction and multivessel disease, complete revascularization reduced the primary end point of death, myocardial infarction, or ischemia-driven revascularization up to 4 years. At the longest follow-up, complete revascularization reduced the composite of cardiovascular death or myocardial infarction but not the primary end point. REGISTRATION:URL: https://www.crd.york.ac.uk/prospero/; Unique identifier: CRD42022367898.