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Predictors and clinical outcomes of use of angiotensin-converting-enzyme inhibitor in paients with acute myocardial infarction.
Korea Acute Myocardial infarction Registry Investigators
이장훈, 정명호, 안영근, 채성철, 김종현, 성인환, 김영조, 허승호, 최동훈, 홍택종, 윤정한, 류제영, 채제건, 김두일, 채인호, 구본권, 김병옥, 이내희, 황진용, 오석규, 조명찬, 김기식, 정경태, 이명용, 김종진, 정욱성, 장양수, 승기배, 박승정 외 KAMIR 연구자
BACKGROUND AND OBJECTIVES: Angiotensin-converting-enzyme inhibitors (ACE-Is) reduce major adverse cardiovascular events (MACE) among patients with myocardial infarction (MI). We investigated predictors and 6-month MACE of use of ACE-Is in the Korea Acute Myocardial Infarction Registry (KAMIR) patients. METHOD: Between November 2005 and January 2008, 10228 post-MI survivors (7337 males and 2891 females; mean age=64.1±12.5 year-old) who did not have any contraindications to ACE-Is/ARBs were analyzed. We considered hypotension (systolic blood pressure <90mmHg) and severe renal dysfunction (serum creatinine > 2.5 mg/dL in men or >2.0 mg/dL in women) as contraindications to ACE-Is. RESULTS: Of 10228 patients, 8370 were prescribed ACE-Is (66.4%) or ARBs (15.4%) and 1858 (18.2%) were prescribed neither ACE-Is nor ARBs at discharge. In multivariate analysis, history of hypertension (odds ratio [OR] 1.129, 95% confidence interval [CI] 1.003 to 1.270, p=0.044), ST elevation MI (OR 1.157, 95%CI 1.029 to 1.302, p=0.015), use of beta-blockers (OR 3.244, 95%CI 2.896 to 3.634, p<0.001), use of lipid-lowering drugs (OR 1.532, 95%CI 1.352 to 1.736, p<0.001), and renal dysfunction (serum creatinine >1.5mg/dl) (OR 1.292, 95%CI 1.049 to 1.591, p=0.016) were independent predictors of use of ACE-Is/ARBs at discharge. Compared with ARBs only group, males (OR 1.297, 95%CI 1.104 to 1.524, p=0.002), history of ischemic heart disease (OR 0.753, 95%CI 0.640 to 1.886, p=0.001), hypertension (OR 0.726, 95%CI 0.638 to 0.828, p<0.001), Killip class≥2 (OR 0.747, 95%CI 0.648 to 1.726, p<0.001), renal dysfunction (OR 0.679, 95%CI 0.560 to 0.825, p<0.001), and use of beta-blockers (OR 1.856, 95%CI 1.621 to 2.125, p<0.001) were independent predictors of use of ACE-Is. During 6 months follow-up, there was no significant difference in 6-month MACE including death, recurrent myocardial infarction, revascularization among three groups (neither: 4.9%, ACE inhibitors alone: 5.1%, ARBs alone: 5.4%, p=0.570). CONCLUSIONS: About one-fifth of post-MI patients with no contraindications to ACE-Is were not taking ACE-Is or ARBs at discharge. There was no significant difference in the short-term prognosis among ACE-I, ARBs, and neither treatment groups.


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