Lessons learned from the RE(ACT) Conference on Medical Devices for Rare Diseases.

medtech orphan devices rare disease diagnosis and treatment rare diseases

Journal

European journal of medical genetics
ISSN: 1878-0849
Titre abrégé: Eur J Med Genet
Pays: Netherlands
ID NLM: 101247089

Informations de publication

Date de publication:
05 Oct 2024
Historique:
received: 08 03 2024
revised: 26 07 2024
accepted: 05 10 2024
medline: 8 10 2024
pubmed: 8 10 2024
entrez: 7 10 2024
Statut: aheadofprint

Résumé

The field of rare disease therapeutics has witnessed significant growth in recent years, highlighting the need for diverse therapeutic approaches to cater to the unique needs of individuals with rare diseases. Rare disease therapies encompass a broad spectrum of interventions, including orphan medicinal products, orphan medical devices, rehabilitative therapies, and digital therapeutics, with the lines between these categories blurring. This paper covers the session of the RE(ACT)-IRDiRC Conference 2023 and delves into the landscape of orphan medical device research and development, shedding light on the challenges and opportunities in this burgeoning field. It provides a short overview of the different international legislations in the field. In addition, it highlights several exemplary orphan medical devices. The first example is an exoskeleton for boys with Duchenne Muscular Dystrophy, enabling them to maintain arm functionality and independence. Another example presented was an EEG device linked to an app detecting seizures in rare epilepsy conditions, which alerts caregivers to seizures in real-time but also facilitates objective seizure reporting for clinicians, aiding in diagnosis and treatment optimization. It also showcases the role of gamification and enabling technologies in addressing rare diseases, by showing a game designed for children with cystic fibrosis, and a telemedicine system for rehabilitation therapy. Both solutions aim to improve patients' understanding of their conditions and enhance their self-management. In conclusion, this paper underscores the critical need for patient-centric orphan and pediatric medical devices to provide therapeutic options for individuals with rare diseases. It highlights the impact of existing devices on enhancing the quality of life for rare disease patients and emphasizes the necessity for greater incentives and support for research and development in this field.

Identifiants

pubmed: 39374774
pii: S1769-7212(24)00068-5
doi: 10.1016/j.ejmg.2024.104976
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104976

Informations de copyright

Copyright © 2024. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors A J, M D and JA S do not disclose any conflict of Interest, T B leads his company EpiHunter, P K leads Yumen Bionics and L P leads i-maginary.

Auteurs

Anneliene H Jonker (AH)

University of Twente, Enschede, The Netherlands. Electronic address: a.h.jonker@utwente.nl.

Tim Buckinx (T)

Epihunter, Hasselt, Belgium.

Lucia Pannese (L)

imaginary, Milan, Italy.

Paulien Klap (P)

Yumen Bionics, Amsterdam, The Netherlands.

Jose-Alain Sahel (JA)

Department of Ophthalmology, The University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, US; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France; CHNO des Quinze-Vingts, INSERM-DGOS CIC 1423, Paris, France.

Marc Dooms (M)

University Hospitals, Leuven, Belgium.

Classifications MeSH