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Association between evidence-based medication at discharge and outcomes in patients with heart failure: a systematic review and meta-analysis

机译:心力衰竭患者的循证和结果之间的循证药物之间的关联:系统审查和荟萃分析

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To conduct a meta-analysis of observational studies assessing the association between dispensing evidence-based medications (EBMs) at discharge and outcomes, we extracted published studies in English from PubMed, Medline, and EMBASE from 2007 to early 2019. The EBMs included renin-angiotensin system inhibitors (RASIs), beta-blockers, and mineralocorticoid receptor antagonists (MRAs). The main outcomes of interest were all-cause death and heart failure (HF) readmission. Pooled hazard ratios (HRs) were calculated using random effect model from the adjusted HRs or relative risks (RRs) extracted from individual studies, stratified by HF patients with reduced ejection fraction (HFrEF), and preserved ejection fraction (HFpEF). Forty-three studies including a total number of 295,060 patients with an average follow-up time of 2.3 years were identified for systematic review. Dispensing RASI at discharge was independently associated with 30% and 25% lower risks of all-cause death and HF readmission respectively in HFrEF but has a moderate effect on reducing all-cause deaths (HR = 0.88, 95% CI: 0.81-0.95) in HFpEF. By contrast, dispensing beta-blockers at discharge was associated with 35% lower risk of all-cause deaths in HFrEF and has a weak association with borderline statistical significance on improving overall survival in HFpEF. Dispensing MRA at discharge was associated with 5% lower risk of all-cause death in HFrEF. This meta-analysis provides evidence to support RASIs and beta-blockers as primary pharmacotherapies for HF patients. Our findings suggest that the health professionals maintain use of RASIs and beta-blockers at discharge for potential survival improvement.
机译:为了对评估出院时配药循证药物(EBM)与预后之间关系的观察性研究进行荟萃分析,我们从2007年至2019年初的PubMed、Medline和EMBASE中提取了已发表的英文研究。EBMs包括肾素-血管紧张素系统抑制剂(RASI)、β受体阻滞剂和盐皮质激素受体拮抗剂(MRA)。主要的研究结果是全因死亡和心力衰竭(HF)再入院。使用随机效应模型计算合并危险比(HRs),该模型来自调整后的HRs或从个体研究中提取的相对风险(RRs),按射血分数降低(HFrEF)和射血分数保留(HFpEF)的心衰患者分层。共有43项研究(包括295060名患者,平均随访时间为2.3年)被确定为系统评价。出院时配发RASI与HFrEF患者全因死亡和HF再入院风险分别降低30%和25%独立相关,但对减少HFpEF患者全因死亡(HR=0.88,95%CI:0.81-0.95)有中度效果。相比之下,出院时服用β受体阻滞剂与HFrEF全因死亡风险降低35%相关,与改善HFpEF总体生存率的临界统计显著性相关性较弱。出院时进行MRA与HFrEF全因死亡风险降低5%相关。这项荟萃分析为支持RASIs和β受体阻滞剂作为心衰患者的主要药物治疗提供了证据。我们的研究结果表明,卫生专业人员在出院时继续使用RASIs和β受体阻滞剂,以提高潜在的生存率。

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