# Protocol on establishing a national disease registry–Swiss Pediatric Inflammatory Brain Disease Registry

## TL;DR

This paper describes the establishment of a national registry in Switzerland to study rare pediatric inflammatory brain diseases and improve understanding and treatment.

## Contribution

The paper introduces the Swiss-Ped-IBrainD, a new national registry for pediatric-onset inflammatory brain diseases in Switzerland.

## Key findings

- The registry is multicenter and population-based, collaborating with 11 neuropediatric centers.
- As of May 2023, 275 eligible participants were identified, with 101 having provided informed consent.
- The registry aims to include 300–400 patients and promote research through knowledge exchange and national studies.

## Abstract

Pediatric-onset inflammatory brain diseases are a group of potentially life-threatening central nervous system disorders. Overall, pediatric-onset inflammatory brain diseases are rare and therefore difficult to study. Patient registries are well suited to study the natural history of (rare) diseases and have markedly advanced the knowledge on pediatric-onset inflammatory brain diseases in other countries. Following their example, we established a national pediatric-onset inflammatory brain disease registry in Switzerland (Swiss-Ped-IBrainD).

The Registry aims to describe epidemiology, demographics, diagnostics, management, and treatment, since these areas remain understudied in Switzerland. Additionally, we want to promote research by fostering the knowledge exchange between study centers and setting up studies such as national quality of life surveys. We further aim to facilitate the access to national and international studies for patients with a pediatric-onset inflammatory brain disease living and/or treated in Switzerland.

The Swiss-Ped-IBrainD is a multicentric, population-based, observational cohort study (IRB number: 2019–00377) collaborating with 11 neuropediatric centers in Switzerland. Patient screening, information and recruitment is mainly conducted by the local principal investigators. The data collection is organized centrally by the Executive Office of the registry. The collected data is purely observational. Medical records are the primary data source. All patients who have been diagnosed with a pediatric-onset inflammatory brain disease since 2005 are eligible. We aim to include all pediatric-onset inflammatory brain disease patients living and/or treated in Switzerland who meet the inclusion criteria. Considering existing literature and our single-center experience we anticipate 300–400 eligible patients.

Currently, all 11 neuropediatric centers have been initiated and are recruiting. As of the first of May 2023, we have identified 275 eligible participants and obtained informed consent from 101 patients and/or families. None of the informed patients and/or families have refused participation.