Huge variation in obtaining ethical permission for a non-interventional observational study in Europe | BMC Medical Ethics | Full Text

Huge variation in obtaining ethical permission for a non-interventional observational study in Europe | BMC Medical Ethics | Full Text



BMC Medical Ethics

Huge variation in obtaining ethical permission for a non-interventional observational study in Europe

• Dylan W. de LangeEmail authorView ORCID ID profile,
• Bertrand Guidet,
• Finn H. Andersen,
• Antonio Artigas,
• Guidio Bertolini,
• Rui Moreno,
• Steffen Christensen,
• Maurizio Cecconi,
• Christina Agvald-Ohman,
• Primoz Gradisek,
• Christian Jung,
• Brian J. Marsh,
• Sandra Oeyen,
• Bernardo Bollen Pinto,
• Wojciech Szczeklik,
• Ximena Watson,
• Tilemachos Zafeiridis and
• Hans Flaatten

BMC Medical Ethics201920:39

https://doi.org/10.1186/s12910-019-0373-y

©  The Author(s). 2019

• Received: 28 June 2018
• Accepted: 17 May 2019
• Published: 3 June 2019

Open Peer Review reports

Abstract

Background

Ethical approval (EA) must be obtained before medical research can start. We describe the differences in EA for an pseudonymous, non-interventional, observational European study.

Methods

Sixteen European national coordinators (NCs) of the international study on very old intensive care patients answered an online questionnaire concerning their experience getting EA.

Results

N = 8/16 of the NCs could apply at one single national ethical committee (EC), while the others had to apply to various regional ECs and/or individual hospital institutional research boards (IRBs). The time between applying for EA and the first decision varied between 7 days and 300 days. In 9/16 informed consent from the patient was not deemed necessary; in 7/16 informed consent was required from the patient or relatives. The upload of coded data to a central database required additional information in 14/16. In 4/16 the NCs had to ask separate approval to keep a subject identification code list to de-pseudonymize the patients if questions would occur. Only 2/16 of the NCs agreed that informed consent was necessary for this observational study. Overall, 6/16 of the NCs were satisfied with the entire process and 8/16 were (very) unsatisfied. 11/16 would welcome a European central EC that would judge observational studies for all European countries.

Discussion

Variations in the process and prolonged time needed to get EA for observational studies hampers inclusion of patients in some European countries. This might have a negative influence on the external validity. Further harmonization of ethical approval process across Europe is welcomed for low-risk observational studies.

Conclusion

Getting ethical approval for low-risk, non-interventional, observational studies varies enormously across European countries.