Outcomes in the ISCHEMIA Trial Based on Coronary Artery Disease and Ischemia Severity
Reynolds, Harmony R. ✉; Shaw, Leslee J.; Min, James K.; Page, Courtney B.; Berman, Daniel S.; Chaitman, Bernard R.; Picard, Michael H.; Kwong, Raymond Y.; O'Brien, Sean M.; Huang, Zhen; Mark, Daniel B.; Nath, Ranjit K.; Dwivedi, Sudhanshu K.; Smanio, Paola E. P.; Stone, Peter H.; Held, Claes; Keltai, Matyas [Keltai, Mátyás (Klinikai kardiológia), szerző] Semmelweis Egyetem; Bangalore, Sripal; Newman, Jonathan D.; Spertus, John A.; Stone, Gregg W.; Maron, David J.; Hochman, Judith S.
BACKGROUND: The ISCHEMIA trial (International Study of Comparative Health Effectiveness
With Medical and Invasive Approaches) postulated that patients with stable coronary
artery disease (CAD) and moderate or severe ischemia would benefit from revascularization.
We investigated the relationship between severity of CAD and ischemia and trial outcomes,
overall and by management strategy.METHODS: In total, 5179 patients with moderate
or severe ischemia were randomized to an initial invasive or conservative management
strategy. Blinded, core laboratory-interpreted coronary computed tomographic angiography
was used to assess anatomic eligibility for randomization. Extent and severity of
CAD were classified with the modified Duke Prognostic Index (n=2475, 48%). Ischemia
severity was interpreted by independent core laboratories (nuclear, echocardiography,
magnetic resonance imaging, exercise tolerance testing, n=5105, 99%). We compared
4-year event rates across subgroups defined by severity of ischemia and CAD. The primary
end point for this analysis was all-cause mortality. Secondary end points were myocardial
infarction (MI), cardiovascular death or MI, and the trial primary end point (cardiovascular
death, MI, or hospitalization for unstable angina, heart failure, or resuscitated
cardiac arrest).RESULTS: Relative to mild/no ischemia, neither moderate ischemia nor
severe ischemia was associated with increased mortality (moderate ischemia hazard
ratio [HR], 0.89 [95% CI, 0.61-1.30]; severe ischemia HR, 0.83 [95% CI, 0.57-1.21];
P=0.33). Nonfatal MI rates increased with worsening ischemia severity (HR for moderate
ischemia, 1.20 [95% CI, 0.86-1.69] versus mild/no ischemia; HR for severe ischemia,
1.37 [95% CI, 0.98-1.91]; P=0.04 for trend, P=NS after adjustment for CAD). Increasing
CAD severity was associated with death (HR, 2.72 [95% CI, 1.06-6.98]) and MI (HR,
3.78 [95% CI, 1.63-8.78]) for the most versus least severe CAD subgroup. Ischemia
severity did not identify a subgroup with treatment benefit on mortality, MI, the
trial primary end point, or cardiovascular death or MI. In the most severe CAD subgroup
(n=659), the 4-year rate of cardiovascular death or MI was lower in the invasive strategy
group (difference, 6.3% [95% CI, 0.2%-12.4%]), but 4-year all-cause mortality was
similar.CONCLUSIONS: Ischemia severity was not associated with increased risk after
adjustment for CAD severity. More severe CAD was associated with increased risk. Invasive
management did not lower all-cause mortality at 4 years in any ischemia or CAD subgroup.