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Standardized assessment of evidence supporting the adoption of mobile health solutions: A Clinical Consensus Statement of the ESC Regulatory Affairs Committee

Caiani, Enrico G; Kemps, Hareld; Hoogendoorn, Petra; Asteggiano, Riccardo; Böhm, Allan; Borregaard, Britt; Boriani, Giuseppe; Brunner La Rocca, Hans-Peter; Casado-Arroyo, Ruben; Castelletti, Silvia; Christodorescu, Ruxandra Maria; Cowie, Martin R; Dendale, Paul; Dunn, Fiona; Fraser, Alan G; Lane, Deirdre A; Locati, Emanuela T; Małaczyńska-Rajpold, Katarzyna; Merșa, Caius O; Neubeck, Lis; Parati, Gianfranco; Plummer, Chris; Rosano, Giuseppe; Scherrenberg, Martijn; Smirthwaite, Amie; Szymanski, Piotr

Authors

Enrico G Caiani

Hareld Kemps

Petra Hoogendoorn

Riccardo Asteggiano

Allan Böhm

Britt Borregaard

Giuseppe Boriani

Hans-Peter Brunner La Rocca

Ruben Casado-Arroyo

Silvia Castelletti

Ruxandra Maria Christodorescu

Martin R Cowie

Paul Dendale

Fiona Dunn

Alan G Fraser

Deirdre A Lane

Emanuela T Locati

Katarzyna Małaczyńska-Rajpold

Caius O Merșa

Gianfranco Parati

Chris Plummer

Giuseppe Rosano

Martijn Scherrenberg

Amie Smirthwaite

Piotr Szymanski



Abstract

Mobile health (mHealth) solutions have the potential to improve self-management and clinical care. For successful integration into routine clinical practice, healthcare professionals (HCPs) need accepted criteria helping the mHealth solutions’ selection, while patients require transparency to trust their use. Information about their evidence, safety and security may be hard to obtain and consensus is lacking on the level of required evidence. The new Medical Device Regulation is more stringent than its predecessor, yet its scope does not span all intended uses and several difficulties remain. The European Society of Cardiology Regulatory Affairs Committee set up a Task Force to explore existing assessment frameworks and clinical and cost-effectiveness evidence. This knowledge was used to propose criteria with which HCPs could evaluate mHealth solutions spanning diagnostic support, therapeutics, remote follow-up and education, specifically for cardiac rhythm management, heart failure and preventive cardiology. While curated national libraries of health apps may be helpful, their requirements and rigour in initial and follow-up assessments may vary significantly. The recently developed CEN-ISO/TS 82304-2 health app quality assessment framework has the potential to address this issue and to become a widely used and efficient tool to help drive decision-making internationally. The Task Force would like to stress the importance of co-development of solutions with relevant stakeholders, and maintenance of health information in apps to ensure these remain evidence-based and consistent with best practice. Several general and domain-specific criteria are advised to assist HCPs in their assessment of clinical evidence to provide informed advice to patients about mHealth utilization.

Citation

Caiani, E. G., Kemps, H., Hoogendoorn, P., Asteggiano, R., Böhm, A., Borregaard, B., Boriani, G., Brunner La Rocca, H.-P., Casado-Arroyo, R., Castelletti, S., Christodorescu, R. M., Cowie, M. R., Dendale, P., Dunn, F., Fraser, A. G., Lane, D. A., Locati, E. T., Małaczyńska-Rajpold, K., Merșa, C. O., Neubeck, L., …Szymanski, P. (2024). Standardized assessment of evidence supporting the adoption of mobile health solutions: A Clinical Consensus Statement of the ESC Regulatory Affairs Committee. European Heart Journal – Digital Health, 5(5), 509-523. https://doi.org/10.1093/ehjdh/ztae042

Journal Article Type Article
Acceptance Date May 14, 2024
Online Publication Date Jun 4, 2024
Publication Date 2024-09
Deposit Date Jun 11, 2024
Publicly Available Date Jun 11, 2024
Journal European Heart Journal - Digital Health
Print ISSN 2634-3916
Electronic ISSN 2634-3916
Publisher Oxford University Press
Peer Reviewed Peer Reviewed
Volume 5
Issue 5
Pages 509-523
DOI https://doi.org/10.1093/ehjdh/ztae042
Keywords mobile health, clinical evidence, requirements, assessment, standardisation

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