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Authors
Curtis, Kate https://orcid.org/0000-0002-3746-0348
Dinh, Michael M. https://orcid.org/0000-0002-4034-1059
Shetty, Amith https://orcid.org/0000-0001-7349-1128
Kourouche, Sarah https://orcid.org/0000-0001-6210-6191
Fry, Margaret https://orcid.org/0000-0003-1265-7096
Considine, Julie https://orcid.org/0000-0003-3801-2456
Li, Ling https://orcid.org/0000-0002-1642-142X
Lung, Thomas https://orcid.org/0000-0001-9978-6311
Shaw, Timothy https://orcid.org/0000-0003-0783-1918
Lam, Mary K. https://orcid.org/0000-0001-9451-8203
Murphy, Margaret https://orcid.org/0000-0002-8937-8418
Alkhouri, Hatem https://orcid.org/0000-0002-5569-704X
Aggar, Christina
Russell, Saartje Berendsen https://orcid.org/0000-0002-1380-8469
Seimon, Radhika V. https://orcid.org/0000-0002-3903-4801
Hughes, James A. https://orcid.org/0000-0001-9387-2489
Varndell, Wayne https://orcid.org/0000-0002-4752-9679
Shaban, Ramon Z. https://orcid.org/0000-0002-5203-0557
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Funding
Funding for this research was provided by:
National Health and Medical Research Council (2017845)
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Article History
Received: 7 May 2023
Accepted: 4 June 2023
First Online: 20 June 2023
Declarations
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: 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 ). 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.
