TY - JOUR
T1 - Ethical issues in two parallel trials of personalised criteria for implantation of implantable cardioverter defibrillators for primary prevention
T2 - The PROFID project - A position paper
AU - Willems, DIck
AU - Bak, Marieke
AU - Tan, Hanno
AU - Lindinger, Georg
AU - Kocar, Ayca
AU - Seperhi Shamloo, Alireza
AU - Schmidt, Georg
AU - Hindricks, Gerhard
AU - Dagres, Nikolaos
N1 - Publisher Copyright:
© 2021 Massachussetts Medical Society. All rights reserved.
PY - 2021/7/14
Y1 - 2021/7/14
N2 - Aim To discuss ethical issues related to a complex study (PROFID) involving the development of a new, partly artificial intelligence-based, prediction model to enable personalised decision-making about the implantation of an implantable cardioverter defibrillator (ICD) in postmyocardial infarction patients, and a parallel non-inferiority and superiority trial to test decision-making informed by that model. Method The position expressed in this paper is based on an analysis of the PROFID trials using concepts from high-profile publications in the ethical literature. Results We identify ethical issues related to the testing of the model in the treatment setting, and to both the superiority and the non-inferiority trial. We underline the need for ethical-empirical studies about these issues, also among patients, as a parallel to the actual trials. The number of ethics committees involved is an organisational, but also an ethical challenge. Conclusion The PROFID trials, and probably other studies of similar scale and complexity, raise questions that deserve dedicated parallel ethics and social science research, but do not constitute a generic obstacle. A harmonisation procedure, comparable to the Voluntary Harmonization Procedure (VHP) for medication trials, could be needed for this type of trials.
AB - Aim To discuss ethical issues related to a complex study (PROFID) involving the development of a new, partly artificial intelligence-based, prediction model to enable personalised decision-making about the implantation of an implantable cardioverter defibrillator (ICD) in postmyocardial infarction patients, and a parallel non-inferiority and superiority trial to test decision-making informed by that model. Method The position expressed in this paper is based on an analysis of the PROFID trials using concepts from high-profile publications in the ethical literature. Results We identify ethical issues related to the testing of the model in the treatment setting, and to both the superiority and the non-inferiority trial. We underline the need for ethical-empirical studies about these issues, also among patients, as a parallel to the actual trials. The number of ethics committees involved is an organisational, but also an ethical challenge. Conclusion The PROFID trials, and probably other studies of similar scale and complexity, raise questions that deserve dedicated parallel ethics and social science research, but do not constitute a generic obstacle. A harmonisation procedure, comparable to the Voluntary Harmonization Procedure (VHP) for medication trials, could be needed for this type of trials.
KW - ethics
KW - health care
KW - heart arrest
KW - medical
KW - myocardial infarction
KW - outcome assessment
KW - research design
UR - http://www.scopus.com/inward/record.url?scp=85110525076&partnerID=8YFLogxK
U2 - 10.1136/openhrt-2021-001686
DO - 10.1136/openhrt-2021-001686
M3 - Article
AN - SCOPUS:85110525076
SN - 2398-595X
VL - 8
JO - Open Heart
JF - Open Heart
IS - 2
M1 - e001686
ER -