Go Alan S, Yang Jingrong, Gurwitz Jerry H, Hsu John, Lane Kimberly, Platt Richard
Division of Research, Kaiser Permanente of Northern California, Oakland, California, USA.
Am J Cardiol. 2007 Aug 15;100(4):690-6. doi: 10.1016/j.amjcard.2007.03.084. Epub 2007 Jun 26.
Placebo-controlled randomized trials have demonstrated the efficacy of selected beta blockers on outcomes in chronic heart failure (HF), but the relative effectiveness of different beta blockers in usual clinical care is poorly understood. We compared 12-month risk of rehospitalization for HF associated with receipt of different beta blockers in 7,883 adults hospitalized for HF within 2 large health plans between January 1, 2001 and December 31, 2002. Beta-blocker use was ascertained from electronic pharmacy databases and readmissions within 12 months were identified from hospital discharge databases. Extended Cox regression was used to examine the association between receipt of different beta blockers and risk of readmission for HF after adjustment for potential confounders. During follow-up, there were 3,234 person-years of exposure to beta blockers (39.3% atenolol, 42.0% metoprolol tartrate, 12.3% carvedilol, and 6.4% other). Crude 12-month rates of readmissions for HF were high overall (42.6 per 100 person-years). After adjustment for potential confounders, cumulative exposure to each beta blocker, and propensity to receive carvedilol compared with atenolol, adjusted risks of readmission were not significantly different for metoprolol tartrate (adjusted hazard ratio 0.95, 95% confidence interval 0.85 to 1.05) or for carvedilol (adjusted hazard ratio 0.92, 95% confidence interval 0.74 to 1.14). In conclusion, in a contemporary cohort of high-risk patients hospitalized with HF, we found that adjusted risks of rehospitalization for HF within 12 months were not significantly different in patients receiving atenolol, shorter-acting metoprolol tartrate, or carvedilol.
安慰剂对照随机试验已证明某些β受体阻滞剂对慢性心力衰竭(HF)患者预后的有效性,但不同β受体阻滞剂在常规临床治疗中的相对疗效尚不清楚。我们比较了2001年1月1日至2002年12月31日期间在2个大型医疗保健计划中因HF住院的7883名成年人接受不同β受体阻滞剂治疗后12个月内HF再住院风险。通过电子药房数据库确定β受体阻滞剂的使用情况,并从医院出院数据库中识别12个月内的再入院情况。使用扩展Cox回归分析在调整潜在混杂因素后,不同β受体阻滞剂的使用与HF再入院风险之间的关联。在随访期间,共有3234人年暴露于β受体阻滞剂(阿替洛尔占39.3%,酒石酸美托洛尔占42.0%,卡维地洛占12.3%,其他占6.4%)。HF的粗12个月再入院率总体较高(每100人年42.6例)。在调整潜在混杂因素、每种β受体阻滞剂的累积暴露量以及与阿替洛尔相比接受卡维地洛的倾向后,酒石酸美托洛尔(调整后风险比0.95,95%置信区间0.85至1.05)或卡维地洛(调整后风险比0.92,95%置信区间0.74至1.14)的调整后再入院风险无显著差异。总之,在当代一组因HF住院的高危患者中,我们发现接受阿替洛尔、短效酒石酸美托洛尔或卡维地洛治疗的患者12个月内HF再入院的调整后风险无显著差异。