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PRADOC:一项多中心随机对照试验,旨在评估 PRADO-IC 的有效性,这是一项针对法国心力衰竭住院患者的全国实用过渡护理管理计划。

PRADOC: A Multicenter Randomized Controlled Trial to Assess the Efficiency of PRADO-IC, a Nationwide Pragmatic Transition Care Management Plan for Hospitalized Patients With Heart Failure in France.

机构信息

PhyMedExp Université de Montpellier INSERM CNRS Cardiology Department INI-CRT CHU de Montpellier Montpellier France.

Cardiology Clinique du Pont de Chaume ELSAN Montauban France.

出版信息

J Am Heart Assoc. 2024 Aug 6;13(15):e032931. doi: 10.1161/JAHA.123.032931. Epub 2024 Jul 18.

Abstract

BACKGROUND

The PRADO-IC (Programme de Retour à Domicile après une Insuffisance Cardiaque) is a transition care program designed to improve the coordination of care between hospital and home that was generalized in France in 2014. The PRADO-IC consists of an administrative assistant who visits patients during hospitalization to schedule follow-up visits. The aim of the present study was to evaluate the PRADO-IC program based on the hypotheses provided by health authorities.

METHODS AND RESULTS

The PRADOC study is a multicenter, controlled, randomized, open-label, mixed-method trial of the transition program PRADO-IC versus usual management in patients hospitalized with heart failure (standard of care group; NCT03396081). A total of 404 patients were recruited between April 2018 and May 2021. The mean patient age was 75 years (±12 years) in both groups. The 2 groups were well balanced regarding severity indices. At discharge, patients homogeneously received the recommended drugs. There was no difference between groups regarding hospitalizations for acute heart failure at 1 year, with 24.60% in the standard of care group and 25.40% in the PRADO-IC group during the year following the index hospitalization (hazard ratio, 1.04 [95% CI, 0.69-1.56]; =0.85) or cardiovascular mortality (hazard ratio, 0.67 [95% CI, 0.34-1.31]; =0.24).

CONCLUSIONS

The PRADO-IC has not significantly improved clinical outcomes, though a trend toward reduced cardiovascular mortality is evident. These results will help in understanding how transitional care programs remain to be integrated in pathways of current patients, including telemonitoring, and to better tailor individualized approaches.

REGISTRATION

URL: https://www.clinicaltrials.gov; Unique Identifier: NCT03396081.

摘要

背景

PRADO-IC(心力衰竭后居家康复计划)是一项旨在改善医院和家庭之间护理协调的过渡护理计划,于 2014 年在法国推广。PRADO-IC 由一名行政助理组成,他在住院期间探望患者,安排随访。本研究的目的是根据卫生当局提供的假设评估 PRADO-IC 计划。

方法和结果

PRADOC 研究是一项多中心、对照、随机、开放标签、混合方法试验,比较了过渡计划 PRADO-IC 与心力衰竭住院患者的常规管理(标准护理组;NCT03396081)。2018 年 4 月至 2021 年 5 月期间共招募了 404 名患者。两组患者的平均年龄均为 75 岁(±12 岁)。两组的严重程度指数相当。出院时,两组患者均均匀接受了推荐的药物治疗。两组患者在 1 年内因急性心力衰竭住院的情况无差异,标准护理组为 24.60%,PRADO-IC 组为 25.40%(指数住院后 1 年的危险比为 1.04 [95%置信区间,0.69-1.56];=0.85)或心血管死亡率(危险比,0.67 [95%置信区间,0.34-1.31];=0.24)。

结论

PRADO-IC 并未显著改善临床结局,但心血管死亡率降低的趋势明显。这些结果将有助于了解过渡护理计划如何仍有待整合到当前患者的路径中,包括远程监测,并更好地定制个体化方法。

登记

网址:https://www.clinicaltrials.gov;唯一标识符:NCT03396081。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21d/11964064/bf74e89e5865/JAH3-13-e032931-g003.jpg

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