a Department of Rehabilitation Medicine, Graduate School of Medicine , The University of Tokyo , Tokyo , Japan.
b Department of Orthopaedic Surgery , Nagoya University Graduate School of Medicine , Nagoya , Aichi , Japan.
Disabil Rehabil. 2019 Mar;41(6):699-704. doi: 10.1080/09638288.2017.1405083. Epub 2017 Nov 16.
Fibrodysplasia ossificans progressiva is a rare congenital disorder that causes systemic heterotopic ossification, leading to systemic ankyloses and mobility losses. This study aimed to ascertain the natural history of fibrodysplasia ossificans progressiva.
In addition to the medical history questionnaire, patients aged 16 years and older were asked to complete activities of daily living and quality of life surveys using the Barthel Index, MOS 36-Item Short-Form Health Survey, and Health Assessment Questionnaire. The surveys were conducted over a 4-years period.
Of the 15 participating patients, 13 reported swelling during the study period. The Barthel Index and Health Assessment Questionnaire surveys indicated a tendency for questionnaire items related to arm function to reflect early decreases in the activities of daily living. Decreases in activities of daily living functioning were closely related to decreases in the quality of life in physical function domains. Activities of daily living and quality of life were maintained at a similar level to baseline values over the study period (Barthel Index: p = 0.42, MOS 36-Item Short-Form Health Survey: p = 0.43, Health Assessment Questionnaire: p = 0.87).
We obtained longitudinal information relating to natural history on fibrodysplasia ossificans progressiva patients. Implications for rehabilitation Fibrodysplasia ossificans progressiva is a rare congenital disease that causes heterotopic ossification of muscle tissue throughout the body, leading to systemic ankyloses and mobility losses. When the Barthel Index was high and the activities of daily living were relatively stable, the items on the Health Assessment Questionnaire that are related to arm function began to show impairment. Early focus on upper extremity function that includes the use of assistive devices during the period when a patient is still able to perform many activities of daily living is important. Although decreases in activities of daily living functioning were closely related to decreases in the quality of life in the physical function domains, the scores of the domains other than physical function were similar to the national standard score.
进行性骨化性纤维发育不良是一种罕见的先天性疾病,会导致全身异位骨化,从而导致全身僵硬和活动能力丧失。本研究旨在确定进行性骨化性纤维发育不良的自然病史。
除了病史问卷外,年龄在 16 岁及以上的患者还被要求使用巴氏量表、MOS 36 项简短健康调查和健康评估问卷完成日常生活活动和生活质量调查。这些调查在 4 年内进行。
在 15 名参与的患者中,有 13 名在研究期间报告了肿胀。巴氏量表和健康评估问卷调查表明,与手臂功能相关的问卷项目反映了日常生活活动的早期减少。日常生活活动能力的下降与身体功能领域生活质量的下降密切相关。在研究期间,日常生活活动和生活质量保持在与基线值相似的水平(巴氏量表:p=0.42,MOS 36 项简短健康调查:p=0.43,健康评估问卷:p=0.87)。
我们获得了与进行性骨化性纤维发育不良患者自然病史相关的纵向信息。康复的意义 进行性骨化性纤维发育不良是一种罕见的先天性疾病,会导致全身肌肉组织异位骨化,从而导致全身僵硬和活动能力丧失。当巴氏量表得分较高且日常生活活动相对稳定时,健康评估问卷中与手臂功能相关的项目开始出现损伤。在患者仍能进行许多日常生活活动的时期,早期关注包括使用辅助设备在内的上肢功能非常重要。尽管日常生活活动能力的下降与身体功能领域的生活质量下降密切相关,但身体功能以外的领域的分数与国家标准分数相似。