Adapting to Adulthood: A Review of Transition Strategies for Osteogenesis Imperfecta

Osteogenesis Imperfecta (OI), known as “brittle bone disease,” presents a rare genetic disorder characterized by bone fragility, often accompanied by skeletal deformities and extraskeletal complications. OI is primarily associated with collagen type I defects, responsible for the syndromic nature of...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Calcified tissue international 2024-11
Hauptverfasser: Celli, Luca, Garrelfs, Mark R., Sakkers, Ralph J. B., Elting, Mariet W., Celli, Mauro, Bökenkamp, Arend, Smits, Cas, Goderie, Thadé, Smit, Jan Maerten, Schwarte, Lothar A., Schober, Patrick R., Lubbers, Wouter D., Visser, Marieke C., Kievit, Arthur J., van Royen, Barend J., Gilijamse, Marjolijn, Schreuder, Willem H., Rustemeyer, Thomas, Pramana, Angela, Hendrickx, Jan-Jaap, Dahele, Max R., Saeed, Peerooz, Moll, Annette C., Curro–Tafili, Katie R., Ghyczy, Ebba A. E., Dickhoff, Chris, de Leeuw, Robert A., Bonjer, Jaap H., Nieuwenhuijzen, Jakko A., Konings, Thelma C., Engelsman, Anton F., Eeckhout, Augustinus M., van den Aardweg, Joost G., Thoral, Patrick J., Noske, David P., Dubois, Leander, Teunissen, Berend P., Semler, Oliver, Wekre, Lena Lande, Maasalu, Katre, Märtson, Aare, Sangiorgi, Luca, Versacci, Paolo, Riminucci, Mara, Grammatico, Paola, Zambrano, Anna, Martini, Lorena, Castori, Marco, Botman, Esmee, Westerheim, Ingunn, Zhytnik, Lidiia, Micha, Dimitra, Eekhoff, Elisabeth Marelise W.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Osteogenesis Imperfecta (OI), known as “brittle bone disease,” presents a rare genetic disorder characterized by bone fragility, often accompanied by skeletal deformities and extraskeletal complications. OI is primarily associated with collagen type I defects, responsible for the syndromic nature of the disease affecting a broad range of tissues. As such, its multisystemic complexity necessitates multidisciplinary care approaches in all patient life stages. OI treatment remains largely supportive, commonly including bisphosphonates and orthopedic surgeries, which show promise in children. Although rehabilitation programs for children exist, guidelines for adult care and especially the transition from pediatric to adult care, are lagging behind in OI care and research. The current systematic review summarizes the literature on OI patient pediatric to adult care transition experiences and compares OI transition approaches to other chronic diseases. The review was performed based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Systematic searches were conducted across multiple databases. Search terms encompassed synonyms and closely related phrases relevant to “OI” and “Transition to adult care”. The initial screening involved the evaluation of article titles, followed by a thorough review of abstracts to assess relevance for the purpose of the current review. Programs aimed at easing the transition from pediatric to adult OI care necessitate a multifaceted approach. Collaborative efforts between different medical disciplines including pediatricians, endocrinologists, orthopedics, cardiology, pulmonology, ophthalmology, otolaryngologists, maxillofacial specialists, psychologists and medical genetics, are crucial for addressing the diverse needs of OI patients during this critical life phase. Comprehensive education, readiness assessments, personalized transition plans, and further follow-up are essential components of a structured transition framework. Further research is warranted to evaluate the feasibility and efficacy of sequential stepwise transition systems tailored to individuals with OI.
ISSN:1432-0827
1432-0827
DOI:10.1007/s00223-024-01305-1