Curtis, Kate http://orcid.org/0000-0002-3746-0348
Dinh, Michael M. http://orcid.org/0000-0002-4034-1059
Shetty, Amith http://orcid.org/0000-0001-7349-1128
Kourouche, Sarah http://orcid.org/0000-0001-6210-6191
Fry, Margaret http://orcid.org/0000-0003-1265-7096
Considine, Julie http://orcid.org/0000-0003-3801-2456
Li, Ling http://orcid.org/0000-0002-1642-142X
Lung, Thomas http://orcid.org/0000-0001-9978-6311
Shaw, Timothy http://orcid.org/0000-0003-0783-1918
Lam, Mary K. http://orcid.org/0000-0001-9451-8203
Murphy, Margaret http://orcid.org/0000-0002-8937-8418
Alkhouri, Hatem http://orcid.org/0000-0002-5569-704X
Aggar, Christina
Russell, Saartje Berendsen http://orcid.org/0000-0002-1380-8469
Seimon, Radhika V. http://orcid.org/0000-0002-3903-4801
Hughes, James A. http://orcid.org/0000-0001-9387-2489
Varndell, Wayne http://orcid.org/0000-0002-4752-9679
Shaban, Ramon Z. http://orcid.org/0000-0002-5203-0557
Funding for this research was provided by:
National Health and Medical Research Council (2017845)
Article History
Received: 7 May 2023
Accepted: 4 June 2023
First Online: 20 June 2023
Declarations
:
: Ethical approval for the research was received from the Sydney Local Health District Research Ethics Committee (Reference Number 2022/ETH01940) on 14 December 2022 (Supplementary material InternalRef removed). The study will be conducted in accordance with the National Statement on Ethical Conduct in Human Research (2007), the CPMP/ICH Note for Guidance on Good Clinical Practice (Link to CPMP/ICH), and consistent with the principles that have their origin in the Declaration of Helsinki [37, 38]. Protocol modifications will go through ethical approval process.A waiver of consent was being sought to retrospectively access the data for emergency patient presentations, and the majority of which is routinely collected data. Participant information statements for clinicians will explicitly state that the decision to participate or not participate is voluntary and confidential with all information shared in surveys being anonymous. Clinicians will indicate their consent in the online survey.For patients and carers, participation will be voluntary and confidential. All participants will be provided with a participant information statement detailing risks and benefits. Participants will sign an electronic consent form.
: Not applicable.
: The authors declare that they have no competing interests.