Aubert, Carole E. https://orcid.org/0000-0001-8325-8784
Schnipper, Jeffrey L.
Fankhauser, Niklaus
Marques-Vidal, Pedro
Stirnemann, Jérôme
Auerbach, Andrew D.
Zimlichman, Eyal
Kripalani, Sunil
Vasilevskis, Eduard E.
Robinson, Edmondo
Metlay, Joshua
Fletcher, Grant S.
Limacher, Andreas
Donzé, Jacques
Funding for this research was provided by:
Swiss Society of General Internal Medicine Foundation (N/A)
Clinical Trials Unit from Bern University, Switzerland (N/A)
Article History
Received: 29 September 2018
Accepted: 29 May 2019
First Online: 13 June 2019
Ethics approval and consent to participate
: The ethical committee at each participating site had previously approved the data collection. Because the data were retrospectively collected and fully anonymized, no informed consent was required, according to the Institutional Review Board Committees (IRBs) of all US centers, Swissethics regulations (), and the Sheba Medical Center Helsinki Committee. Because this study falls under a further use of existing fully anonymized data, no further ethical approval was required.The ethical committees were: 1) Brigham and Women’s Hospital/Partners Healthcare IRB, Boston, USA; 2) University of California IRB, San Francisco, USA; 3) University of Washington IRB, Seattle, USA; 4) Vanderbilt University Medical Center IRB, Nashville, USA; 5) Christiana Care Health System IRB, Wilmington, USA; 6) Hospital of the University of Pennsylvania IRB, Philadelphia, USA; 7) Northwestern IRB, Chicago, USA; 8) Cantonal Ethics Committee for research, Bern, Switzerland; 9) Cantonal Ethics Committee for research on human being, Lausanne, Switzerland; 10) Cantonal Ethics Committee for research on human being, Geneva, Switzerland; 11) Sheba Medical Center Helsinki Committee, Tel Hashomer, Israel.
: Not applicable.
: The authors declare that they have no competing interests.