# German pediatric intensive care transport registry: study protocol for a prospective multicenter registry

**Authors:** Stefan Winkler, Felix Dittgen, Edmondo Hammond, Nele Börner, Johanna Kossack, Frank Eifinger, Ingeborg Alijda van den Heuvel, Elias Klinghammer, Victoria Lieftüchter, Pia Paul, Alba Perez-Ortiz, Patricia Bimboese, Richard Biedermann, André Jakob, Sarah Irlbeck, Nadine Mand

PMC · DOI: 10.3389/fped.2025.1669094 · Frontiers in Pediatrics · 2025-10-07

## TL;DR

This study aims to create a nationwide registry for transporting critically ill children in Germany to better understand and plan for their medical needs.

## Contribution

The paper introduces a prospective multicenter registry to collect data on pediatric critical care transports in Germany for the first time.

## Key findings

- Currently, there is no structured data on pediatric critical care transports in Germany.
- The registry will collect and analyze transport data to inform future demand planning.
- Participating pediatric centers will submit anonymized data via a secure web-based platform.

## Abstract

In contrast to critical care transport of adults or newborns, transport of pediatric critical care patients in Germany is neither regulated by law nor centrally organized. Due to their different therapeutic needs compared to newborns or adults, critically ill children may receive insufficient treatment during transport. In some regions in Germany, pediatric centers provide specialized pediatric retrieval teams, while others organize each transport individually. Currently, no valid data on pediatric critical care transports in Germany are available, nor are they recorded in a structured manner.

To establish a nationwide registry for pediatric intensive care transports in Germany. The aim is to describe and analyze the need for and current practice of specialized transports. This data may be used for future demand planning.

Transports are documented by pediatric centers admitting pediatric patients via intensive care transports.

All interhospital pediatric intensive care transports of children, aged >27 days and >41 + 0 weeks of corrected gestational, age to <18 years, are eligible for data entry.

The study is designed as a prospective, multicenter registry. Transport data will be collected locally at participating pediatric centers and then submitted digitally and anonymized via a secure, web-based platform.

We anticipate high participation from pediatric intensive care units and expect to present valid data on the need for pediatric intensive care transports in Germany. This data may serve as a foundation for nationwide demand planning for pediatric intensive care transport resources.

## Full-text entities

- **Diseases:** critically ill (MESH:D016638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12537787/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12537787/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12537787/full.md

---
Source: https://tomesphere.com/paper/PMC12537787