TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases.

Genetic counselling Hereditary cardiac diseases Hereditary neuromuscular disorders Telegenetics Telemedicine

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:
Jun 2023
Historique:
received: 11 11 2022
revised: 23 02 2023
accepted: 18 03 2023
medline: 8 5 2023
pubmed: 23 3 2023
entrez: 22 3 2023
Statut: ppublish

Résumé

Telemedicine provides healthcare services remotely and represents a fundamental resource for the management of rare and fragile patients. Tele-health implementation is a main objective of the European Reference Networks (ERNs) mission to accelerate diagnosis for rare diseases. TeleNewCARe is a pilot case-control project which evaluates the efficacy and satisfaction of telegenetics for neuromuscular and cardiac adult patients, compared to face-to-face genetic counselling. The virtual sessions were co-hosted by a medical geneticist and a neurologist/cardiologist. Specific questionnaires (Clinical Genetics Satisfaction Questionnaire (CGS), Telemedicine Satisfaction Questionnaire (TSQ) and a Satisfaction Questionnaire for medical geneticists) were used to assess the effectiveness and fulfilment of telecounselling, both for patients and health care providers. Satisfaction expressed for telegenetics did not significantly differ from face-to-face counselling. The virtually enrolled patients declared they had the possibility to relate confidentially with the specialists, to share information and to be informed in an exhaustive way about their disease. Almost all patients declared themselves willing to reuse the telecounselling in the future. The multidisciplinary care was perceived as a significant added value. No overt technical problems were reported although the need for digital skills and tools can limit patients' compliance. Our experience supports telegenetics as a valid alternative to traditional genetic counselling in cardiac and neuromuscular patients. This innovative approach facilitates multidisciplinary care, grants a periodical follow up, without forcing patients to discomfortable travelling, and allows to maintain expert care. This result meets the ERNs needs to reduce patients' burden to access and monitor their healthcare.

Identifiants

pubmed: 36948289
pii: S1769-7212(23)00055-1
doi: 10.1016/j.ejmg.2023.104749
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104749

Informations de copyright

Copyright © 2023. Published by Elsevier Masson SAS.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflicts of interest to declare.

Auteurs

Marianna Farnè (M)

Medical Genetics Unit, Department of Medical Sciences, University of Ferrara, Ferrara, Italy; Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Fernanda Fortunato (F)

Medical Genetics Unit, Department of Medical Sciences, University of Ferrara, Ferrara, Italy; Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Marcella Neri (M)

Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Matteo Farnè (M)

Department of Statistical Sciences, University of Bologna, Bologna, Italy.

Cristina Balla (C)

Cardiological Center, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Emilio Albamonte (E)

The NEMO Clinical Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, Milan, Italy.

Andrea Barp (A)

The NEMO Clinical Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, Milan, Italy.

Annarita Armaroli (A)

Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Enrica Perugini (E)

Cardiology Unit, Maggiore Hospital, Bologna, Italy.

Valeria Carinci (V)

Cardiology Unit, Maggiore Hospital, Bologna, Italy.

Marco Facchini (M)

Information and Communication Technology Department, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Luca Chiarini (L)

Information and Communication Technology Department, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Valeria A Sansone (VA)

The NEMO Clinical Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, Milan, Italy.

Sofia Straudi (S)

Physical and Rehabilitation Medicine Unit, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Valeria Tugnoli (V)

Neurology Unit, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Elisabetta Sette (E)

Neurology Unit, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Mariachiara Sensi (M)

Neurology Unit, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Matteo Bertini (M)

Cardiological Center, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

Teresinha Evangelista (T)

Functional Unit of Neuromuscular Pathology, Nord/Est/Ile-de-France Neuromuscular Reference Center, Institute of Myology, Pitié-Salpêtrière Hospital, APHP, Sorbonne University, Paris, France.

Alessandra Ferlini (A)

Medical Genetics Unit, Department of Medical Sciences, University of Ferrara, Ferrara, Italy; Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy. Electronic address: fla@unife.it.

Francesca Gualandi (F)

Medical Genetics Unit, Department of Mother and Child, Sant'Anna University Hospital of Ferrara, Ferrara, Italy.

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Classifications MeSH