Gouya Ghazaleh, Reichardt Berthold, Ohrenberger Gerald, Wolzt Michael
Department of Clinical Pharmacology, Allgemeines Krankenhaus Wien, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Eur J Epidemiol. 2007;22(3):145-9. doi: 10.1007/s10654-006-9087-9. Epub 2007 Mar 14.
There is consensus that patients should be treated with antiplatelet agents, beta-blockers, ACE-inhibitors/ARBs, and lipid lowering drugs for secondary prevention after acute myocardial infarction (AMI), but this evidence-based pharmacotherapy is underutilized. A quality improvement program was conducted in the Austrian county of Burgenland to emphasize the importance of cardiovascular drug therapy at hospital discharge in patients with AMI. In this prospective cohort study 250 members of a regional health insurance company, Burgenländische Gebietskrankenkasse (BGKK), with AMI during the year 2003 were identified using BGKK database. Discharge prescriptions and pharmacy reimbursement data of all included patients were determined. Overall prescription rate for patients discharged from hospital after AMI (n = 207) was 86% for platelet aggregation inhibitors, 77% for ACE-inhibitors or ARBs, 72% for beta-blockers, and 68% for a lipid lowering agent including statins. The all-cause mortality rate during a mean follow-up period of 552 days was 20%. Hazard ratio (HR) for death of patients with maximum 2 medications vs. those receiving 3 or 4 medications was 2.23 (95% CI: 1.19-4.18; p = 0.012). These data demonstrate that use of evidence-based drug treatment for prevention of mortality in patients with AMI is associated with risk reduction and survival benefit. Continuous quality improvement initiatives serve to improve outcome after AMI.
目前已达成共识,急性心肌梗死(AMI)后患者应接受抗血小板药物、β受体阻滞剂、ACE抑制剂/ARB以及降脂药物治疗以进行二级预防,但这种基于证据的药物治疗未得到充分利用。奥地利布尔根兰州开展了一项质量改进项目,以强调AMI患者出院时心血管药物治疗的重要性。在这项前瞻性队列研究中,利用布尔根兰州地区健康保险公司(Burgenländische Gebietskrankenkasse,BGKK)的数据库,确定了2003年期间患有AMI的250名BGKK成员。确定了所有纳入患者的出院处方和药房报销数据。AMI后出院患者(n = 207)的血小板聚集抑制剂总体处方率为86%,ACE抑制剂或ARB为77%,β受体阻滞剂为72%,包括他汀类药物在内的降脂药物为68%。在平均552天的随访期内,全因死亡率为20%。最多服用2种药物的患者与服用3或4种药物的患者相比,死亡风险比(HR)为2.23(95%CI:1.19 - 4.18;p = 0.012)。这些数据表明,使用基于证据的药物治疗预防AMI患者死亡与降低风险和生存获益相关。持续的质量改进举措有助于改善AMI后的结局。