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首页> 外文期刊>Cardiology >Tolerability of beta-Blocker Initiation and Titration with Bisoprolol and Carvedilol in Congestive Heart Failure - A Randomized Comparison.
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Tolerability of beta-Blocker Initiation and Titration with Bisoprolol and Carvedilol in Congestive Heart Failure - A Randomized Comparison.

机译:在充血性心力衰竭中使用β-阻滞剂引发和比索洛尔和卡维地洛滴定的耐受性-随机比较。

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In clinical trials beta-blockers (BB) are well tolerated in patients with systolic congestive heart failure (CHF). In contrast, in daily practice treatment initiation and titration appear to be more difficult and may differ in various BB - but systematic data are lacking. We randomized 87 patients with systolic CHF (mean age 70.1 +/- 10.6 years, 24% females, LVEF 0.28 +/- 0.10, NYHA III-IV 29%) to treatment with either bisoprolol or carvedilol, in order to assess and compare the maximally achievable number of patients on treatment with these BB and the maximally achieved dosage during a minimum of 2 months attendance at our out patient heart failure clinic. In those randomized to bisoprolol, mean dose at 2 months was 33% of target dose (3.1 +/- 2.6 mg ) and 41% at discharge. In those on carvedilol, the mean dose at 2 months was 27% of target dose (13.4 +/- 14.0 mg) and 32% at discharge. Thirty-nine and 40% of the bisoprolol and carvedilol treated patients, respectively, had stopped treatment at discharge. None of the figures differed significantly between the two treatment groups and no baseline parameter predicted BB tolerability. Thus, almost twice the number of unselected patients with systolic CHF attending a heart failure clinic focusing on systematic medical titration were intolerant to BB treatment and only a minority reached target dose treatment. The present data reveal no clear difference with respect to tolerability of carvedilol and bisoprolol, and no parameter predicts tolerability. Copyright 2004 S. Karger AG, Basel
机译:在临床试验中,收缩期充血性心力衰竭(CHF)患者对β受体阻滞剂(BB)的耐受性良好。相反,在日常操作中,治疗的开始和滴定似乎更加困难,并且在各种BB中可能有所不同-但缺乏系统的数据。我们将87例收缩期CHF患者(平均年龄70.1 +/- 10.6岁,女性24%,LVEF 0.28 +/- 0.10,NYHA III-IV 29%)随机分配至比索洛尔或卡维地洛治疗,以评估和比较在我们门诊患者的心力衰竭诊所就诊至少2个月内,使用这些BB治疗的最大患者数和达到的最大剂量。在随机分配比索洛尔的患者中,2个月的平均剂量为目标剂量的33%(3.1 +/- 2.6 mg),出院时为41%。在使用卡维地洛的患者中,2个月的平均剂量为目标剂量的27%(13.4 +/- 14.0 mg),出院时为32%。比索洛尔和卡维地洛治疗的患者中分别有39名和40%在出院时停止治疗。两个治疗组之间的数字均无显着差异,并且没有基线参数可预测BB耐受性。因此,在以系统性药物滴定为重点的心力衰竭门诊就诊的未选择的收缩期CHF患者中,几乎有两倍的患者无法接受BB治疗,只有少数达到目标剂量治疗。目前的数据显示卡维地洛和比索洛尔的耐受性没有明显差异,并且没有参数可预测耐受性。版权所有2004 S. Karger AG,巴塞尔

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