دورية أكاديمية
Improving Recognition of Treatable Rare Neuromuscular Disorders in Primary Care: A Pilot Feasibility Study
العنوان: | Improving Recognition of Treatable Rare Neuromuscular Disorders in Primary Care: A Pilot Feasibility Study |
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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 |
تدمد: | 22279067 |
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DOI: | 10.3390/children9071063 |