Digital consults in heart failure care: a randomized controlled trial

被引:2
|
作者
Man, Jelle P. [1 ,2 ,3 ]
Koole, Maarten A. C. [1 ,4 ,5 ]
Meregalli, Paola G. [1 ,3 ]
Handoko, M. Louis [1 ,3 ,6 ]
Stienen, Susan [1 ,3 ]
de Lange, Frederik J. [1 ,3 ]
Winter, Michiel M. [1 ,3 ,4 ]
Schijven, Marlies P. [7 ]
Kok, Wouter E. M. [1 ,3 ]
Kuipers, Dorianne I. [1 ,3 ]
van der Harst, Pim [6 ]
Asselbergs, Folkert W. [1 ,8 ,9 ]
Zwinderman, Aeilko H. [10 ,11 ]
Dijkgraaf, Marcel G. W. [10 ,11 ]
Chamuleau, Steven A. J. [1 ,2 ,3 ]
Schuuring, Mark J. [12 ,13 ,14 ]
机构
[1] Amsterdam UMC, Dept Cardiol, Amsterdam, Netherlands
[2] Netherlands Heart Inst, Utrecht, Netherlands
[3] Univ Amsterdam, Amsterdam Cardiovasc Sci, Amsterdam, Netherlands
[4] Cardiol Ctr Netherlands, Utrecht, Netherlands
[5] Red Cross Hosp, Dept Cardiol, Beverwijk, Netherlands
[6] Univ Med Ctr Utrecht, Dept Cardiol, Utrecht, Netherlands
[7] Amsterdam UMC, Dept Surg, Amsterdam, Netherlands
[8] UCL, Inst Hlth Informat, London, England
[9] UCL, Univ Coll London Hosp, Natl Inst Hlth Res, Biomed Res Ctr, London, England
[10] Amsterdam UMC, Dept Epidemiol & Data Sci, Amsterdam, Netherlands
[11] Amsterdam Publ Hlth, Methodol, Amsterdam, Netherlands
[12] Med Spectrum Twente, Dept Cardiol, Enschede, Netherlands
[13] Univ Twente, Dept Biomed Signals & Syst, Enschede, Netherlands
[14] Univ Twente, Cardiovasc Hlth Res Pillar, Enschede, Netherlands
关键词
MANAGEMENT; HF; TELEMEDICINE;
D O I
10.1038/s41591-024-03238-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Guideline-directed medical therapy (GDMT) has clear benefits on morbidity and mortality in patients with heart failure; however, GDMT use remains low. In the multicenter, open-label, investigator-initiated ADMINISTER trial, patients (n = 150) diagnosed with heart failure and reduced ejection fraction (HFrEF) were randomized (1:1) to receive usual care or a strategy using digital consults (DCs). DCs contained (1) digital data sharing from patient to clinician (pharmacotherapy use, home-measured vital signs and Kansas City Cardiomyopathy Questionnaires); (2) patient education via a text-based e-learning; and (3) guideline recommendations to all treating clinicians. All remotely gathered information was processed into a digital summary that was available to clinicians in the electronic health record before every consult. All patient interactions were standardly conducted remotely. The primary endpoint was change in GDMT score over 12 weeks (Delta GDMT); this GDMT score directly incorporated all non-conditional class 1 indications for HFrEF therapy with equal weights. The ADMINISTER trial met its primary outcome of achieving a higher GDMT in the DC group after a follow-up of 12 weeks (Delta GDMT score in the DC group: median 1.19, interquartile range (0.25, 2.3) arbitrary units versus 0.08 (0.00, 1.00) in usual care; P < 0.001). To our knowledge, this is the first multicenter randomized controlled trial that proves a DC strategy is effective to achieve GDMT optimization. ClinicalTrials.gov registration: NCT05413447.
引用
收藏
页码:2907 / 2913
页数:14
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