Abstrakt:
Background: The optimal timing of coronary intervention in patients
with non–ST-segment elevation acute coronary syndromes
(NSTE-ACSs) is a matter of debate. Conflicting results among published
studies partly relate to different risk profiles of the studied
populations.
Purpose: To do the most comprehensive meta-analysis of current
evidence on early versus delayed invasive treatment in NSTE-ACS.
Data Sources: MEDLINE, PubMed Central, and Google Scholar
databases; conference proceedings; ClinicalTrials.gov registry; and
Current Controlled Trials registry through May 2012.
Study Selection: Available randomized, controlled trials (RCTs) and
observational studies comparing early versus delayed intervention in
the NSTE-ACS population.
Data Extraction: Data were extracted for populations, interventions,
outcomes, and risk of bias. All-cause mortality was the prespecified
primary end point. The longest follow-up available in each
study was chosen. The odds ratio with 95% CI was the effect
measure.
Data Synthesis: Seven RCTs (5370 patients) and 4 observational
studies (77 499 patients) were included. Early intervention was less
than 20 hours after hospitalization or randomization for RCTs and
24 hours or less for observational studies. Meta-analysis of the
RCTs was inconclusive for a survival benefit associated with the
early invasive strategy (odds ratio, 0.83 [95% CI, 0.64 to 1.09];
P 0.180); a similar result emerged from the observational studies.
With early versus late intervention, the odds ratios in the RCTs
were 1.15 (CI, 0.65 to 2.01; P 0.63) and 0.76 (CI, 0.56 to 1.04;
P 0.090) for myocardial infarction and major bleeding during
follow-up, respectively.
Limitation: Current evidence from RCTs is limited by the small
overall sample size, low numbers of events in some trials, and
heterogeneity in the timing of intervention and in patient risk
profiles.
Conclusion: At present, there is insufficient evidence either in favor
of or against an early invasive approach in the NSTE-ACS population.
A more definitive RCT is warranted to guide clinical practice.
Primary Funding Source: None.