Development and evaluation of RhizoQOL, a quality-of-life caregiver-reported survey for rhizomelic chondrodysplasia punctata, a rare peroxisomal disorder.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Mousumi Bose, Tahra C Anglade, Chelsea I Donlon, Adrian L Kerrihard, Hila F Berger, Ariel S Berkowitz, Shawn A Ritchie, Tara M Smith
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引用次数: 0

Abstract

Background: Rhizomelic chondrodysplasia punctata (RCDP) is a rare genetic disorder characterized by symptoms such as respiratory dysfunction, seizures, orthopedic issues, and neurodevelopmental delay. Potential therapeutics for RCDP warrant the development of clinical outcome assessments to assess the efficacy of treatment and the well-being of patients. Our study aimed to develop a valid quality-of-life (QOL) caregiver-reported survey instrument, RhizoQOL, to be used as a supportive endpoint in RCDP clinical trials.

Methods: Development of the RhizoQOL survey tool included three RCDP caregiver focus groups to elicit concepts to serve as potential domains in a QOL survey instrument for RCDP, pilot survey development and initial testing, cognitive interviewing of revised survey drafts to determine content validity, as well as a three-month longitudinal study for reliability and internal consistency of the survey instrument.

Results: Twenty-eight caregivers participated in the focus groups, reporting that concepts that could be appropriate domains of QOL in RCDP include psychosocial behavior, feeding symptoms, mobility symptoms, respiratory symptoms, seizures and related activity, and impact of treatment. Following pilot survey testing (n = 22) and stakeholder feedback, a revised pilot survey instrument was administered to five caregivers for cognitive interviewing. This resulted in a revised survey instrument with 31 question items, six domains, and a 1-5 Likert scale item response assessing frequency or severity of event in the question item. Longitudinal testing (n = 18) of the revised survey instrument found the average response score was 1.98 ± 0.97 for all question items, and a Cronbach's alpha value of 0.856, suggesting strong intra-survey question reliability. Using individual question item results from reliability testing, linear regression modeling, and testing for required magnitude of significant treatment effects, eight question items were removed from the survey instrument, resulting in a total of 23 question items within 6 discrete domains.

Conclusions: The final RhizoQOL survey instrument, consisting of 23 questions, assesses the symptoms and experiences of RCDP patients as observed by caregivers and serves as a novel clinical outcome assessment for RCDP therapeutic clinical trials to assess the impacts of RCDP and support the overall effectiveness of treatments.

根状软骨发育不良是一种罕见的过氧化物酶体疾病,是一项由护理人员报告的生活质量调查。
背景:点状根状软骨发育不良(RCDP)是一种罕见的遗传性疾病,其症状包括呼吸功能障碍、癫痫发作、骨科问题和神经发育迟缓。RCDP的潜在治疗方法保证了临床结果评估的发展,以评估治疗效果和患者的福祉。本研究旨在开发一种有效的护理人员报告的生活质量(QOL)调查工具,RhizoQOL,作为RCDP临床试验的支持性终点。方法:RhizoQOL调查工具的开发包括三个RCDP护理人员焦点小组,以得出概念,作为RCDP生活质量调查工具的潜在领域,试点调查开发和初步测试,修订调查草案的认知访谈,以确定内容效度,以及为期三个月的纵向研究,以确定调查工具的可靠性和内部一致性。结果:28名护理人员参加了焦点小组,报告了RCDP中可能适合的生活质量领域的概念包括心理社会行为、进食症状、活动症状、呼吸症状、癫痫发作和相关活动,以及治疗的影响。在试点调查测试(n = 22)和利益相关者反馈后,对5名照顾者进行了修订的试点调查工具的认知访谈。这导致了一个修订的调查工具,有31个问题项目,6个领域,1-5李克特量表项目反应评估频率或严重程度的问题项目。对修订后的问卷进行纵向检验(n = 18),所有问题项的平均回答得分为1.98±0.97,Cronbach's alpha值为0.856,表明问卷内问题的信度较强。使用信度检验、线性回归模型和显著治疗效果所需程度检验的单个问题项结果,从调查工具中删除了8个问题项,结果在6个离散域内共有23个问题项。结论:最终的RhizoQOL调查工具由23个问题组成,评估护理人员观察到的RCDP患者的症状和经历,并作为RCDP治疗性临床试验的新型临床结果评估,以评估RCDP的影响并支持治疗的整体有效性。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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