دورية أكاديمية

Improving Recognition of Treatable Rare Neuromuscular Disorders in Primary Care: A Pilot Feasibility Study

التفاصيل البيبلوغرافية
العنوان: Improving Recognition of Treatable Rare Neuromuscular Disorders in Primary Care: A Pilot Feasibility Study
المؤلفون: Federica S. Ricci, Rossella D’Alessandro, Martina Vacchetti, Anna Salvalaggio, Alessandra Somà, Giorgia Daffunchio, Marco Spada, Renato Turra, Marisa Bobbio, Alessandro Ciuti, Chiara Davico, Benedetto Vitiello, Tiziana E. Mongini
المصدر: Children, Vol 9, Iss 1063, p 1063 (2022)
بيانات النشر: MDPI AG
سنة النشر: 2022
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: neuromuscular disorders, disease modifying treatments, early diagnosis, motor development milestones, primary care pediatricians, screening, Pediatrics, RJ1-570
الوصف: Innovative targeted treatments for neuromuscular disorders (NMDs) can dramatically improve the course of illness. Diagnostic delay, however, is a major impediment. Here, we present a pilot project aimed at assessing the feasibility of a screening program to identify children at high risk for NMDs within the first 30 months of life. The Promoting Early Diagnosis for Neuromuscular Disorders (PEDINE) project implemented a three-step sequential screening in an area of about 300,000 people with (1) an assessment of the motor development milestones to identify “red flags” for NMDs by primary care pediatricians (PCPs) as part of the routine Health Status Check visits; (2) for the children who screened positive, a community neuropsychiatric assessment, with further referral of suspected NMD cases to (3) a hospital-based specialized tertiary care center. In the first-year feasibility study, a total of 10,032 PCP visits were conducted, and twenty children (0.2% of the total Health Status Check visits) screened positive and were referred to the community neuropsychiatrist. Of these, four had elevated creatine kinase (CK) serum levels. This pilot study shows that screening for NMDs in primary care settings is feasible and allows children at high risk for muscular disorder to be promptly identified.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2227-9067
العلاقة: https://www.mdpi.com/2227-9067/9/7/1063Test; https://doaj.org/toc/2227-9067Test; https://doaj.org/article/42f4672ab38f4f8e90f21f42870f3f34Test
DOI: 10.3390/children9071063
الإتاحة: https://doi.org/10.3390/children9071063Test
https://doaj.org/article/42f4672ab38f4f8e90f21f42870f3f34Test
رقم الانضمام: edsbas.E3EEAC4E
قاعدة البيانات: BASE
الوصف
تدمد:22279067
DOI:10.3390/children9071063