PEACH in Asia: PEriAnesthetic morbidity in CHildren in Asia: A prospective multinational multicenter observational study to investigate epidemiology of severe critical events in pediatric anesthesia in Asia

Abstract

Despite the introduction of better structured programs for pediatric anesthesia training and the development of some recommendations for pediatric anesthesia services, the incidence of severe critical events in children is still unknown in Asia. Considering that the major life threatening complications following general or regional anesthesia are uncommon, it is therefore crucial to consider a large multinational, multicenter trial in order to establish a realistic statistical estimation and identify the risk factors for severe critical events. Thus, this international prospective observational multicenter observational study, Peri anesthetic morbidity in children in Asia (PEACH in Asia) study, is designed to identify the incidence and potential risk factors of severe critical events in children undergoing anesthesia in Asia, which will work as a powerful road map to develop and implement data driven pediatric surgery and anesthesia plans in Asia.

Competing Interest Statement

This study was funded by Kawano Masanori Memorial Public Interest Incorporated Foundation for Promotion of Pediatrics in Japan.

Clinical Protocols

https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000052803

Funding Statement

This study was funded by Kawano Masanori Memorial Public Interest Incorporated Foundation for Promotion of Pediatrics in Japan.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Institutional Review Board at Tokyo Metropolitan Ohtsuka Hospital, Tokyo, Japan gae ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Data Availability

All data produced in the present study in the study protocol will be available upon reasonable request to the authors and the sponsors once the present study will be completed.

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