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Published in: Orphanet Journal of Rare Diseases 1/2024

Open Access 01-12-2024 | Research

Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany – a mixed-methods study

Authors: Laura Inhestern, Ramona Otto, Maja Brandt, David Zybarth, Ralf Oheim, Helke Schüler, Thomas S. Mir, Konstantinos Tsiakas, Payam Dibaj, Jana Zschüntzsch, Pamela M. Okun, Ute Hegenbart, Olaf Sommerburg, Christoph Schramm, Christina Weiler-Normann, Martin Härter, Corinna Bergelt

Published in: Orphanet Journal of Rare Diseases | Issue 1/2024

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Abstract

Background

Rare diseases are often complex, chronic and many of them life-shortening. In Germany, healthcare for rare diseases is organized in expert centers for rare diseases. Most patients additionally have regional general practicioners and specialists for basic medical care. Thus, collaboration and information exchange between sectors is highly relevant. Our study focuses on the patient and caregiver perspective on intersectoral and interdisciplinary care between local healthcare professionals (HCPs) and centers for rare diseases in Germany. The aims were (1) to investigate patients’ and caregivers’ general experience of healthcare, (2) to analyse patients’ and caregivers’ perception of collaboration and cooperation between local healthcare professionals and expert centers for rare diseases and (3) to investigate patients’ and caregivers’ satisfaction with healthcare in the expert centers for rare diseases.

Results

In total 299 individuals of whom 176 were patients and 123 were caregivers to pediatric patients participated in a survey using a questionnaire comprising several instruments and constructs. Fifty participants were additionally interviewed using a semistructured guideline. Most patients reported to receive written information about their care, have a contact person for medical issues and experienced interdisciplinary exchange within the centers for rare diseases. Patients and caregivers in our sample were mainly satisfied with the healthcare in the centers for rare diseases. The qualitative interviews showed a rather mixed picture including experiences of uncoordinated care, low engagement and communication difficulties between professionals of different sectors. Patients reported several factors that influenced the organization and quality of healthcare e.g. engagement and health literacy in patients or engagement of HCPs.

Conclusions

Our findings indicate the high relevance of transferring affected patients to specialized care as fast as possible to provide best medical treatment and increase patient satisfaction. Intersectoral collaboration should exceed written information exchange and should unburden patients of being and feeling responsible for communication between sectors and specialists. Results indicate a lack of inclusion of psychosocial aspects in routine care, which suggests opportunities for necessary improvements.
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Metadata
Title
Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany – a mixed-methods study
Authors
Laura Inhestern
Ramona Otto
Maja Brandt
David Zybarth
Ralf Oheim
Helke Schüler
Thomas S. Mir
Konstantinos Tsiakas
Payam Dibaj
Jana Zschüntzsch
Pamela M. Okun
Ute Hegenbart
Olaf Sommerburg
Christoph Schramm
Christina Weiler-Normann
Martin Härter
Corinna Bergelt
Publication date
01-12-2024
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2024
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-024-03207-9

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