Emery Michael, López-Sendón José, Steg Philippe Gabriel, Anderson Frederick A, Dabbous Omar H, Scheuble Aliocha, Eagle Kim A
The University of Michigan Cardiovascular Center, Ann Arbor, MI 48109-0477, USA.
Am Heart J. 2006 Dec;152(6):1015-21. doi: 10.1016/j.ahj.2006.08.024.
Early beta-blocker (BB) therapy improves outcomes in ST-segment elevation myocardial infarction; however, limited data are available on its early use and its impact in non-ST-segment elevation myocardial infarction (NSTEMI).
We evaluated data from 7106 patients with NSTEMI, without contraindications to BBs, enrolled in the Global Registry of Acute Coronary Events between April 1999 and September 2004. Baseline characteristics, management, and outcomes were analyzed according to the use of oral (+/-intravenous) BB within 24 hours of presentation. Multivariable analysis was conducted adjusting for comorbidities using the Global Registry of Acute Coronary Events risk model (c statistic 0.83).
Beta-blocker therapy was initiated within the first 24 hours in 76% of patients with NSTEMI (79% with Killip class I vs 62% with class II/III; P < .001). Failure to initiate BBs within the first 24 hours was associated with lower rates of subsequent BB therapy (P < .001) and other evidence-based therapies. Early BB therapy was correlated with lower hospital mortality for NSTEMI patients (OR 0.58, 95% CI 0.42-0.81) and for those with Killip class II/III (OR 0.39, 95% CI 0.23-0.68) with a trend toward lower mortality in the Killip class I group (OR 0.77, 95% CI 0.49-1.21). At 6 months postdischarge, early BB use was associated with lower mortality in NSTEMI patients (OR 0.75, 95% CI 0.56-0.997) with a trend toward lower mortality in patients with Killip class I or II/III.
Many eligible patients do not receive early BB therapy. Treatment with early BBs may have a beneficial impact on hospital and 6-month mortality in all patients, including those presenting with heart failure.
早期使用β受体阻滞剂(BB)可改善ST段抬高型心肌梗死的预后;然而,关于其在非ST段抬高型心肌梗死(NSTEMI)中的早期使用及其影响的数据有限。
我们评估了1999年4月至2004年9月期间纳入全球急性冠状动脉事件注册研究的7106例无BB使用禁忌证的NSTEMI患者的数据。根据患者就诊后24小时内口服(±静脉注射)BB的情况分析基线特征、治疗及预后。使用全球急性冠状动脉事件注册研究风险模型(c统计量0.83)对合并症进行校正后进行多变量分析。
76%的NSTEMI患者在发病后24小时内开始使用BB治疗(Killip I级患者为79%,II/III级患者为62%;P <.001)。发病后24小时内未开始使用BB与后续BB治疗率较低(P <.001)及其他循证治疗相关。早期BB治疗与NSTEMI患者较低的院内死亡率相关(比值比0.58,95%置信区间0.42 - 0.81),Killip II/III级患者也是如此(比值比0.39,95%置信区间0.23 - 0.68),Killip I级组死亡率有降低趋势(比值比0.77,95%置信区间0.49 - 1.21)。出院后6个月时,早期使用BB与NSTEMI患者较低的死亡率相关(比值比0.75,95%置信区间0.56 - 0.997),Killip I级或II/III级患者死亡率有降低趋势。
许多符合条件的患者未接受早期BB治疗。早期使用BB治疗可能对所有患者,包括出现心力衰竭的患者的院内及6个月死亡率产生有益影响。