Outcomes of children with serious traumatic brain injury treated in pediatric vs. adult departments

Abstract

The impact of treatment in a non-pediatric department on mortality and outcomes of children with traumatic brain injury (TBI) is unknown. This study aimed to quantify the impact of the treating department (pediatric (PD) or adult (AD)) on in-hospital case fatality and functional short-term outcomes in children with serious TBI who survived the initial 12 hours after hospital admission. A Nationwide retrospective cohort study was conducted from a dataset that comprises all discharges from German hospitals from 2016 to 2021. Disease and procedural codes were used to retrieve clinical and outcome information. Hierarchical multilevel logistic regression modeling was performed to quantify the effect of the treating department on the outcomes of interest. Eligibility criteria were age < 18 years and hospital admission with serious TBI. The main outcome was in-hospital death and secondary outcomes were pediatric complex chronic conditions category (PCCC) >= 2 in survivors, composite outcome (death or PCCC >= 2), and adjusted mean PCCC in survivors. Of 13,492,528 pediatric cases, 12,275 were included. The adjusted odds ratio (OR) for death was 3.00 (95 % confidence interval 1.93-4.68) for children treated in ADs compared to PDs. The OR for PCCC >= 2 was 0.93 (0.78-1.12) and 1.04 (0.87-1.25) for the composite outcome. Adjusted average PCCC were 0.40 (0.37-0.44) in ADs and 0.44 (0.42-0.46) in PDs. This comprehensive nationwide study found increased odds for in-hospital death but similar functional outcomes at discharge among surviving children with serious TBI who were treated outside of PDs.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by the save-my-brain foundation.

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:

Secondary data were used that do not require ethics approval according to local legislation. All data were checked by the German data protection officer before being approved for publication. The German hospital dataset (GHD) is a nationwide dataset comprising all hospitalizations in public hospitals in the country. As per §21 KHEntgG, it is mandated by law that German hospitals share data on all hospital admissions with the Hospital Remuneration System (InEK). After passing plausibility checks, this data is anonymized and forwarded to the Federal Statistical Office. Detailed information on the structure of the DRG dataset is available at the Federal Statistical Office and further details on the process of data access at https://www.forschungsdatenzentrum.de/en/health/drg.

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).

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

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Data Availability

The data from this study are available at the Federal research data center after written inquiry to the corresponding authorities.

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