Remote patient monitoring and digital therapeutics in heart failure: lessons from the Continuum pilot study

Abstract

Introduction: The increasing use of digital health solutions to monitor heart failure (HF) outpatients has been driven by the COVID-19 pandemic. An ideal technology should answer the specific needs of a public healthcare system: easy integration and proof of clinical benefit to justify investment in its long-term use. Through a consortium bringing together patients, physicians, industry, and hospital organizations, we developed a digital solution called Continuum, targeting patients with HF and other comorbidities. Hypothesis: A digital health solution combining remote patient monitoring (RPM) and digital therapeutics (DTx) was developed to ensure a better follow-up of patients and to rapidly optimize their medication and subsequently avoid future severe adverse events. Methods: A pilot intervention/control study with a three-month follow-up was conducted. Patients in the intervention group (remote patient monitoring group, RPM+) had a smartphone or tablet and entered in their mobile app their vital signs, weight, and HF symptoms daily. HF patients who either did not have a mobile device or the skills to use the app were enrolled in the control group (RPM-). The HealthCare Professionals (HCPs) used a web-based dashboard to follow the RPM+ patients. They could access the results of a DTx solution to help them optimize the HF treatment according to Canadian guidelines. Results: 52 HF patients were enrolled in this study, 32 in the RPM+: 69+/-9y age, 75% male, ejection fraction 42 +/- 14%. In the RPM- group, more patients had at least one hospitalization (all-cause) compared to the RPM+ group (35% versus 6% respectively; p=0.008). Similarly, the number of patients with at least one HF hospitalization was more significant in the RPM+ group compared to the RPM- (25% versus 6%, p=0.054). Finally, the intervention showed a medium effect on HF treatment optimization (w=0.26) and quality of life for the most compliant patients to the intervention (g=0.48). Conclusion: The results of this pilot study demonstrated the feasibility of an intervention combining RPM and DTx solutions for HF patients. Preliminary results suggest promising impacts on quality of life, hospitalizations, and patients' medication optimization. However, they need to be confirmed in a more extensive study. Keywords: chronic heart failure, telemonitoring, digital therapeutics, software as medical device (SAMD), remote patient management, digital health, mobile health, algorithms

Competing Interest Statement

Conflict of interest. The first author has received speaker fees from Boehringer Ingelheim Canada, and the last author is the President of the Quebec Heart Failure Society (QHFS). 

Clinical Trial

Pilot study #21.403, active RCT following pilot study: NCT05377190

Funding Statement

Research support. This work with the CRCHUM has been supported by a research grant from Medteq+ (QC, Canada) in partnership with Prompt (QC, Canada) and Mitacs (QC, Canada) by Boehringer Ingelheim Canada Ltd, and Greybox Solutions Inc. (Montreal QC, Canada).

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I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee of Hospital of the University of Montreal gave ethical approval for this work

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

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Data Availability

All data produced in the present study are available upon reasonable request to the authors

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