Effect of remote monitoring on clinical outcomes in European heart failure patients with an implantable cardioverter-defibrillator: secondary results of the REMOTE-CIED randomized trial

被引:24
作者
Chiu, Cheyenne S. L. [1 ]
Timmermans, Ivy [1 ,2 ]
Versteeg, Henneke [1 ]
Zitron, Edgar [3 ]
Mabo, Philippe [4 ]
Pedersen, Susanne S. [5 ,6 ]
Meine, Mathias [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Cardiol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Tilburg Univ, CoRPS Ctr Res Psychol Somat Dis, Dept Med & Clin, Tilburg, Netherlands
[3] Univ Klinikum Heidelberg, Dept Cardiol, Heidelberg, Germany
[4] CHU, Dept Cardiol, Rennes, France
[5] Univ Southern Denmark, Dept Psychol, Odense, Denmark
[6] Odense Univ Hosp, Dept Cardiol, Odense, Denmark
来源
EUROPACE | 2022年 / 24卷 / 02期
关键词
REMOTE-CIED; Implantable cardioverter-defibrillator; Heart failure; Remote monitoring; Clinical outcomes; ELECTRONIC DEVICES; EXPERT CONSENSUS; THERAPY; METAANALYSIS; GUIDELINES;
D O I
10.1093/europace/euab221
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Remote patient monitoring (RPM) systems offer a promising alternative to conventional In-Clinic check-ups, hereby reducing unnecessary clinic visits. Especially with the rise of the COVID-19 pandemic, this reduction is of paramount importance. Regarding the association between RPM and clinical outcomes, findings of previous studies have been inconsistent. The aim of this study is to elucidate the effect of partly substituting In-Clinic visits by RPM on clinical outcomes in implantable cardioverter-defibrillator (ICD) patients. Methods and results The study included 595 heart failure patients (LVEF <= 35%; NYHA Class II/III) implanted with an ICD compatible with the Boston Scientific LATITUDE (TM) system. Participants were randomized to RPM plus an annual In-Clinic visit or 3-6 months In-Clinic check-ups alone. The investigated endpoints after 2 years of follow-up included a composite of all-cause mortality and cardiac hospitalization, mortality and cardiac hospitalization as independent endpoints and ICD therapy. The incidence of mortality and hospitalization did not differ significantly as independent, nor as composite endpoint between the RPM and In-Clinic group (all Ps <0.05). The results were similar regarding ICD therapy, except for appropriate ICD therapy (odds ratio 0.50; 95% confidence interval 0.26-0.98; P = 0.04). Exploratory subgroup analyses indicated that the effect of RPM differs between patients with specific characteristics, i.e. >= 60 years and permanent atrial fibrillation (all Ps < 0.05). Conclusion RPM is non-inferior to conventional In-Clinic visits regarding clinical outcomes. Routine In-Clinic follow-up may partly be substituted by RPM without jeopardizing safety and efficiency, and thus reducing unnecessary In-Clinic visits. ClinicalTrials.gov identifier NCT01691586.
引用
收藏
页码:256 / 267
页数:12
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