远程监测标准滴定治疗心力衰竭伴射血分数降低,一项开放式临床队列研究。

IF 4.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2025-06-05 eCollection Date: 2025-09-01 DOI:10.1093/ehjdh/ztaf062
Antros Louca, Daniel Thomas, Karin Odefjord, Rami Genead, Charlotte Nordberg Backelin, Charlotta Ljungman, Kristofer Skoglund, Entela Bollano, Araz Rawshani, Helén Sjöland, Niklas Bergh, Tomas Mellberg
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引用次数: 0

摘要

目的:评价远程监护下标准化家庭医疗滴定的可行性、有效性和安全性。心力衰竭伴射血分数降低(HFrEF)的治疗进展迅速,强调指南导向药物治疗(GDMT)的快速启动和滴定以改善预后。在实践中实现这一点仍然是医疗保健的一个重大挑战。本研究提出了一种标准化的家庭滴定过程,包括家庭监测(HBM),以加强GDMT滴定,减少延误,并限制门诊评估访问的需要。方法和结果:60例患者被纳入这项开放队列研究。评估了标准的预先指定的滴定计划与HBM的结合。结果测量包括最佳药物治疗时间(OMT), GDMT在8周和6个月的剂量,以及通过不良事件进行的安全性评估。到OMT的中位时间为48天(IQR 42-60)。所有参与者均在6个月内实现OMT。在8周时,分别有73%、85%和88%的患者达到了β受体阻滞剂、ACE抑制剂和矿物质受体拮抗剂的目标剂量。所有参与者均达到SGLT2i目标剂量。到6个月时,62%、73%、80%和97%的患者使用了这些药物的目标剂量,43%的患者使用了所有四种GDMT药物的目标剂量。滴定过程中未发生严重不良事件。结论:我们提出了一种新的、有希望的方法,可以在HFrEF患者中实现OMT和高剂量GDMT。标准化方案的使用有可能优化GDMT的滴定过程,并且在HBM的支持下,它可以在很少的门诊就诊中完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Telemonitored standardized titration for heart failure with reduced ejection fraction, an open clinical cohort study.

Telemonitored standardized titration for heart failure with reduced ejection fraction, an open clinical cohort study.

Telemonitored standardized titration for heart failure with reduced ejection fraction, an open clinical cohort study.

Telemonitored standardized titration for heart failure with reduced ejection fraction, an open clinical cohort study.

Aims: To evaluate feasibility, efficacy, and safety of standardized medical titration at home using telemonitoring. Treatment for heart failure with reduced ejection fraction (HFrEF) has advanced rapidly, emphasizing swift initiation and titration of guideline-directed medical therapy (GDMT) to improve outcomes. Implementing this in practice remains a significant challenge for healthcare. This study proposes a standardized home-based titration process incorporating home-based monitoring (HBM) to enhance GDMT titration, reduce delays, and limit the need for in-clinic assessment visits.

Methods and results: 60 patients were enrolled in this open cohort study. Standardized pre-specified titration schedules in combination with HBM were evaluated. Outcome measures included the time to optimal medical therapy (OMT), doses of GDMT at 8 weeks and 6 months, and safety evaluation through adverse events. The median time to OMT was 48 days (IQR 42-60). All participants achieved OMT within 6 months. At 8 weeks, 73%, 85%, and 88% had reached target doses for beta-blockers, ACE inhibitors, and mineral receptor antagonists, respectively. All participants reached SGLT2i target dosage. By 6 months, 62%, 73%, 80%, and 97% were on target doses for these medications, and 43% had achieved target doses for all four GDMT drugs. No serious adverse events occurred during titration.

Conclusion: We present a novel and promising approach for achieving OMT and high GDMT doses in patients with HFrEF. The utilization of standardized protocols has the potential to optimize the titration process of GDMT, and with HBM support, it can be accomplished with few in-clinic visits.

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