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射血分数降低的心力衰竭的加速和个体化治疗。

Accelerated and personalized therapy for heart failure with reduced ejection fraction.

机构信息

Department of Internal Medicine, School of Clinical Medicine, Hangzhou Normal University, Hangzhou 311121, China.

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK.

出版信息

Eur Heart J. 2022 Jul 14;43(27):2573-2587. doi: 10.1093/eurheartj/ehac210.

Abstract

AIMS

Previously, guidelines recommended initiating therapy in patients with heart failure and reduced ejection fraction (HFrEF) in a sequence that follows the chronological order in which trials were conducted, with cautious up-titration of each treatment. It remains unclear whether this historical approach is optimal and alternative approaches may improve patient outcomes.

METHODS AND RESULTS

The potential reductions in events that might result from (i) more rapid up-titration of therapies used in the conventional order (based on the chronology of the trials), and (ii) accelerated up-titration and using treatments in different orders than is conventional were modelled using data from six pivotal trials in HFrEF. Over the first 12 months from starting therapy, using a rapid up-titration schedule led to 23 fewer patients per 1000 patients experiencing the composite of heart failure hospitalization or cardiovascular death and seven fewer deaths from any cause. In addition to accelerating up-titration of treatments, optimized alternative ordering of the drugs used resulted in a further reduction of 24 patients experiencing the composite outcome and six fewer deaths at 12 months. The optimal alternative sequences included sodium-glucose cotransporter 2 inhibition and a mineralocorticoid receptor antagonist as the first two therapies.

CONCLUSION

Modelling of accelerated up-titration schedule and optimized ordering of treatment suggested that at least 14 deaths and 47 patients experiencing the composite outcome per 1000 treated might be prevented over the first 12 months after starting therapy. Standard treatment guidance may not lead to the best patient outcomes in HFrEF, though these findings should be tested in clinical trials.

摘要

目的

先前,指南建议按照试验进行的时间顺序,依次为射血分数降低的心力衰竭(HFrEF)患者启动治疗,谨慎逐步增加每种治疗的剂量。目前尚不清楚这种历史方法是否最优,替代方法是否可能改善患者结局。

方法和结果

使用来自 HFrEF 六项关键试验的数据,对(i)按照常规顺序(基于试验的时间顺序)更快地增加治疗药物的剂量,以及(ii)加速增加剂量并以非常规顺序使用治疗药物可能带来的事件减少量进行建模。在开始治疗后的前 12 个月内,采用快速滴定方案可使每 1000 名患者中发生心力衰竭住院或心血管死亡复合事件的患者减少 23 例,任何原因导致的死亡减少 7 例。除了加速治疗药物的滴定外,优化药物的替代使用顺序还可使 12 个月时发生复合结局的患者进一步减少 24 例,死亡人数减少 6 例。最佳替代顺序包括钠-葡萄糖共转运蛋白 2 抑制剂和盐皮质激素受体拮抗剂作为前两种治疗药物。

结论

加速滴定方案和治疗药物优化排序的建模表明,开始治疗后的前 12 个月内,每 1000 名治疗患者中至少可预防 14 例死亡和 47 例发生复合结局。标准治疗指南可能无法为 HFrEF 患者带来最佳结局,但这些发现应在临床试验中进行检验。

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