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Remote monitoring of cardiac implanted electronic devices: legal requirements and ethical principles - ESC Regulatory Affairs Committee/EHRA joint task force report
- Source :
- Nielsen, J C, Kautzner, J, Casado-Arroyo, R, Burri, H, Callens, S, Cowie, M R, Dickstein, K, Drossart, I, Geneste, G, Erkin, Z, Hyafil, F, Kraus, A, Kutyifa, V, Marin, E, Schulze, C, Slotwiner, D, Stein, K, Zanero, S, Heidbuchel, H & Fraser, A G 2020, ' Remote monitoring of cardiac implanted electronic devices : legal requirements and ethical principles-ESC Regulatory Affairs Committee/EHRA joint task force report ', Europace, vol. 22, no. 11, pp. 1742-1758 . https://doi.org/10.1093/europace/euaa168, Europace
- Publication Year :
- 2020
-
Abstract
- The European Union (EU) General Data Protection Regulation (GDPR) imposes legal responsibilities concerning the collection and processing of personal information from individuals who live in the EU. It has particular implications for the remote monitoring of cardiac implantable electronic devices (CIEDs). This report from a joint Task Force of the European Heart Rhythm Association and the Regulatory Affairs Committee of the European Society of Cardiology (ESC) recommends a common legal interpretation of the GDPR. Manufacturers and hospitals should be designated as joint controllers of the data collected by remote monitoring (depending upon the system architecture) and they should have a mutual contract in place that defines their respective roles; a generic template is proposed. Alternatively, they may be two independent controllers. Self-employed cardiologists also are data controllers. Third-party providers of monitoring platforms may act as data processors. Manufacturers should always collect and process the minimum amount of identifiable data necessary, and wherever feasible have access only to pseudonymized data. Cybersecurity vulnerabilities have been reported concerning the security of transmission of data between a patient's device and the transceiver, so manufacturers should use secure communication protocols. Patients need to be informed how their remotely monitored data will be handled and used, and their informed consent should be sought before their device is implanted. Review of consent forms in current use revealed great variability in length and content, and sometimes very technical language; therefore, a standard information sheet and generic consent form are proposed. Cardiologists who care for patients with CIEDs that are remotely monitored should be aware of these issues. ispartof: EP-Europace vol:22 issue:11 pages:1742-+ ispartof: location:England status: Published online
- Subjects :
- business.industry
Advisory Committees
Cardiology
Computer security
computer.software_genre
Regulatory affairs
Data processing system
Informed consent
Physiology (medical)
General Data Protection Regulation
Medicine
media_common.cataloged_instance
Humans
Human medicine
Pseudonymized
European union
Electronics
Cardiology and Cardiovascular Medicine
business
computer
Register of data controllers
Personally identifiable information
Computer Security
media_common
Monitoring, Physiologic
Subjects
Details
- Language :
- English
- ISSN :
- 10995129
- Database :
- OpenAIRE
- Journal :
- Nielsen, J C, Kautzner, J, Casado-Arroyo, R, Burri, H, Callens, S, Cowie, M R, Dickstein, K, Drossart, I, Geneste, G, Erkin, Z, Hyafil, F, Kraus, A, Kutyifa, V, Marin, E, Schulze, C, Slotwiner, D, Stein, K, Zanero, S, Heidbuchel, H & Fraser, A G 2020, ' Remote monitoring of cardiac implanted electronic devices : legal requirements and ethical principles-ESC Regulatory Affairs Committee/EHRA joint task force report ', Europace, vol. 22, no. 11, pp. 1742-1758 . https://doi.org/10.1093/europace/euaa168, Europace
- Accession number :
- edsair.doi.dedup.....648efacf4eb46e5228a13bcca2273cb2
- Full Text :
- https://doi.org/10.1093/europace/euaa168