Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review

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Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review

Steinkamp Carolin et al · De Gruyter · 2025

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Autor / responsable

Steinkamp Carolin et al

Editorial

De Gruyter

Año

2025

ISSN

2191-0278

ISSN

2191-0278

Idioma

eng

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With over 54,000 people affected, cystic fibrosis is one of the most common rare diseases in Europe. As life expectancy of this disease has steadily increased in recent years, the transition from pediatric to adult care has become a principal issue. This study aimed to identify facilitating and hindering factors in the transitional care of cystic fibrosis patients in order to derive indications for improving care.

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APA 7

al, S. C. E. (2025). Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review. https://doi.org/10.1515/ijamh-2024-0192

MLA

al, Steinkamp Carolin et. "Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review." 2025. https://doi.org/10.1515/ijamh-2024-0192.

Chicago

al, Steinkamp Carolin et. 2025. "Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review.". https://doi.org/10.1515/ijamh-2024-0192.

Harvard

al, S. C. E. 2025, Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review, De Gruyter, available at: https://doi.org/10.1515/ijamh-2024-0192 [Accessed 29 Jun. 2026].

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Título: Barriers and facilitators in the transition from pediatric to adult care in people with cystic fibrosis in Europe – a qualitative systematized review

Autor / colaboradores: Steinkamp Carolin et al

Editorial: De Gruyter

Año de publicación: 2025

ISSN: 2191-0278

ISSN: 2191-0278

Idioma: eng

Materias

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cystic fibrosis; adolescent; transitional care; health services