Knowledge, skills, and attitudinal gaps in fibrodysplasia ossificans progressiva diagnosis and management in the United States.

IF 3 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2026-04-20 eCollection Date: 2026-06-01 DOI:10.1093/jbmrpl/ziag076
Patrice Lazure, Matthew T Drake, Michelle Davis, Corrie J Crowe, Zvi Grunwald, Lu Fan, Suzanne Murray
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引用次数: 0

Abstract

Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and disabling disease. Preventing unnecessary and/or harmful medical procedures to patients requires early and accurate diagnosis, multidisciplinary care, and access to specialists with FOP expertise. This study aims to assess the needs of healthcare providers (HCPs) when providing care to patients with FOP. Knowledge, confidence, and management practices were measured through a short awareness survey, completed by 400 HCPs from different specialties who may encounter patients with FOP. Complementary qualitative data were obtained from a dialogue session about FOP. Quantitative data was analyzed using descriptive and inferential analysis, while qualitative data underwent thematic coding. Results indicate a need for enhanced knowledge and confidence regarding identifying clinical manifestations of FOP, referral to FOP specialists and subsequent patient management. Only 8.8% of HCPs correctly identified FOP from an open-ended question showing malformed great toes, a classical clinical manifestation of FOP, and only 31.8% correctly identified FOP from a multiple-choice question showing heterotopic ossification on a child's back, another classical clinical manifestation of FOP. Structural and system-level issues were also identified as barriers to optimal patient care pathways, with limited access to FOP specialists reported as a prominent concern. These results document a need for improvements in HCP knowledge in addition to local care collaboration and healthcare system optimization to meet the needs of patients with rare diseases. Given that FOP is an ultra-rare disease, educational interventions are recommended to focus on rare disease recognition, with FOP included as one topic. In addition, greater team collaboration and system-level approaches to assist HCPs in overcoming barriers that impede patient access to care and ongoing management, as well as interventions to enhance patients' capacity to have informed communication with their HCPs, are needed.

美国骨化性纤维发育不良进行性诊断和管理的知识、技能和态度差距。
进行性骨化性纤维发育不良(FOP)是一种罕见的致残疾病。预防对患者不必要和/或有害的医疗程序需要早期和准确的诊断、多学科护理以及获得具有FOP专业知识的专家的帮助。本研究旨在评估医疗服务提供者(HCPs)在为FOP患者提供护理时的需求。知识、信心和管理实践是通过一项简短的意识调查来衡量的,该调查由来自不同专业的400名可能遇到FOP患者的HCPs完成。从关于FOP的对话会议中获得了补充的定性数据。定量数据采用描述和推理分析,定性数据采用主题编码。结果表明,需要提高知识和信心,以确定FOP的临床表现,转诊到FOP专家和后续的病人管理。只有8.8%的HCPs正确识别出FOP的开放式问题,表现为畸形的大脚趾,这是FOP的典型临床表现,而只有31.8%的HCPs正确识别出FOP的另一个典型临床表现,儿童背部异位骨化的选择题。结构和系统层面的问题也被确定为最佳患者护理途径的障碍,据报道,获得FOP专家的机会有限是一个突出的问题。这些结果表明,除了本地护理合作和医疗保健系统优化之外,还需要提高HCP知识,以满足罕见病患者的需求。鉴于FOP是一种极为罕见的疾病,建议教育干预以罕见病识别为重点,将FOP纳入一个主题。此外,还需要加强团队协作和系统级方法,以帮助卫生保健提供者克服阻碍患者获得护理和持续管理的障碍,并采取干预措施,提高患者与其卫生保健提供者进行知情沟通的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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