TY - JOUR
T1 - Lack of benefit from percutaneous intervention of persistently occluded infarct arteries after the acute phase of myocardial infarction is time independent
T2 - Insights from occluded artery trial
AU - Menon, Venu
AU - Pearte, Camille A.
AU - Buller, Christopher E.
AU - Steg, Ph Gabriel
AU - Forman, Sandra A.
AU - White, Harvey D.
AU - Marino, Paolo N.
AU - Katritsis, Demosthenes G.
AU - Caramori, Paulo
AU - Lasevitch, Ricardo
AU - Loboz-Grudzien, Krystyna
AU - Zurakowski, Aleksander
AU - Lamas, Gervasio A.
AU - Hochman, Judith S.
N1 - Funding Information:
National Heart, Lung, and Blood Institute, National Institutes of Health (U01 HL062509, U01 HL062511).
PY - 2009/1
Y1 - 2009/1
N2 - Aims: The Occluded Artery Trial (OAT) (n = 2201) showed no benefit for routine percutaneous intervention (PCI) (n = 1101) over medical therapy (MED) (n = 1100) on the combined endpoint of death, myocardial infarction (MI), and class IV heart failure (congestive heart failure) in stable post-MI patients with late occluded infarct-related arteries (IRAs). We evaluated the potential for selective benefit with PCI over MED for patients enrolled early in OAT. Methods and results: We explored outcomes with PCI over MED in patients randomized to the ≤3 calendar days and ≤7 calendar days post-MI time windows. Earlier, times to randomization in OAT were associated with higher rates of the combined endpoint (adjusted HR 1.04/day: 99% CI 1.01-1.06; P < 0.001). The 48-month event rates for ≤3 days, ≤7 days post-MI enrolled patients were similar for PCI vs. MED for the combined and individual endpoints. There was no interaction between time to randomization defined as a continuous (P = 0.55) or categorical variable with a cut-point of 3 days (P = 0.98) or 7 days (P = 0.64) post-MI and treatment effect. Conclusion: Consistent with overall OAT findings, patients enrolled in the ≤3 day and ≤7 day post-MI time windows derived no benefit with PCI over MED with no interaction between time to randomization and treatment effect. Our findings do not support routine PCI of the occluded IRA in trial-eligible patients even in the earliest 24-72 h time window.
AB - Aims: The Occluded Artery Trial (OAT) (n = 2201) showed no benefit for routine percutaneous intervention (PCI) (n = 1101) over medical therapy (MED) (n = 1100) on the combined endpoint of death, myocardial infarction (MI), and class IV heart failure (congestive heart failure) in stable post-MI patients with late occluded infarct-related arteries (IRAs). We evaluated the potential for selective benefit with PCI over MED for patients enrolled early in OAT. Methods and results: We explored outcomes with PCI over MED in patients randomized to the ≤3 calendar days and ≤7 calendar days post-MI time windows. Earlier, times to randomization in OAT were associated with higher rates of the combined endpoint (adjusted HR 1.04/day: 99% CI 1.01-1.06; P < 0.001). The 48-month event rates for ≤3 days, ≤7 days post-MI enrolled patients were similar for PCI vs. MED for the combined and individual endpoints. There was no interaction between time to randomization defined as a continuous (P = 0.55) or categorical variable with a cut-point of 3 days (P = 0.98) or 7 days (P = 0.64) post-MI and treatment effect. Conclusion: Consistent with overall OAT findings, patients enrolled in the ≤3 day and ≤7 day post-MI time windows derived no benefit with PCI over MED with no interaction between time to randomization and treatment effect. Our findings do not support routine PCI of the occluded IRA in trial-eligible patients even in the earliest 24-72 h time window.
KW - Coronary artery disease
KW - Myocardial infarction
KW - Percutaneous intervention
UR - http://www.scopus.com/inward/record.url?scp=58449089587&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehn486
DO - 10.1093/eurheartj/ehn486
M3 - Article
SN - 0195-668X
VL - 30
SP - 183
EP - 191
JO - European Heart Journal
JF - European Heart Journal
IS - 2
ER -