Agreement Between Child Self- and Parent Proxy-Reports of Health-Related Quality of Life in Spinal Muscular Atrophy: Preliminary Insights from a Nationwide Patient Registry in Germany.

IF 1.8 Q3 HEALTH CARE SCIENCES & SERVICES
Patient Related Outcome Measures Pub Date : 2025-06-27 eCollection Date: 2025-01-01 DOI:10.2147/PROM.S517362
Erik Landfeldt, Berenike Leibrock, Justine Hussong, Simone Thiele, Maggie C Walter, Eva Moehler, Michael Zemlin, Ulrich Dillmann, Marina Flotats-Bastardas
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Abstract

Objective: The objective of this pilot study was to examine the agreement between child self- and parent proxy-assessment of health-related quality of life (HRQoL) in spinal muscular atrophy (SMA) in the era of disease-modifying therapy.

Methods: Children with SMA and one of their parents were recruited via the German national TREAT-NMD SMA patient registry. HRQoL was measured using the Pediatric Quality of Life Inventory 3.0 Neuromuscular Module (PedsQL 3.0 NMM), KIDSCREEN-27, and the Health Utilities Index (HUI). Agreement between child self- and parent proxy-ratings of ordinal measures was estimated using Cohen's κ, and for continuous measures using intraclass correlation coefficients (ICCs) from one-way random-effects models.

Results: The final sample comprised 17 children with SMA (mean age: 9.88 years, SD: 4.33 years, range: 5-16 years; 59% female) and one of their parents. All but two patients (88%) were receiving disease-modifying therapy (nusinersen or risdiplam). The ICC for the total PedsQL 3.0 NMM score was estimated at 0.85 (95% CI: 0.64-0.94, p < 0.001) (indicative of excellent agreement). The corresponding estimate for the KIDSCREEN total score was 0.27 (95% CI: 0.00-0.75, p = 0.197) (poor/fair agreement) and the global HUI utility 0.98 (95% CI: 0.93 to 0.9952, p < 0.001) (excellent agreement). The lowest levels of concordance were found for school and family life, as well as mental well-being, as opposed to physical functioning and disability.

Conclusion: We show that the agreement between child self- and parent proxy-reports of HRQoL in SMA varies markedly across HRQoL measures and examined domains, ranging from poor/fair to excellent. Compared with previous research, agreement for the PedsQL 3.0 NMM was markedly higher in our contemporary cohort of patients treated with novel therapies. These preliminary findings will be helpful in informing the design of future research of HRQoL in SMA.

脊髓性肌萎缩患者健康相关生活质量的儿童自我和父母代理报告之间的一致性:来自德国全国患者登记的初步见解
目的:本初步研究的目的是检验在疾病改善治疗时代,儿童自我和父母对脊髓性肌萎缩症(SMA)患者健康相关生活质量(HRQoL)的代理评估之间的一致性。方法:通过德国国家治疗- nmd SMA患者登记处招募SMA儿童及其父母之一。HRQoL采用儿童生活质量量表3.0神经肌肉模块(PedsQL 3.0 NMM)、KIDSCREEN-27和健康实用指数(HUI)进行测量。使用Cohen’s κ估计儿童自我和父母代理评分在顺序测量中的一致性,使用单向随机效应模型中的类内相关系数(ICCs)估计连续测量的一致性。结果:最终样本包括17例SMA患儿(平均年龄:9.88岁,SD: 4.33岁,范围:5-16岁;(59%为女性)和他们的父母之一。除两名患者(88%)外,所有患者均接受了疾病改善治疗(nusinersen或risdiplam)。PedsQL 3.0 NMM总评分的ICC估计为0.85 (95% CI: 0.64-0.94, p < 0.001)(表明非常一致)。KIDSCREEN总分的相应估计值为0.27 (95% CI: 0.00-0.75, p = 0.197)(一致性差/一般),全球HUI效用为0.98 (95% CI: 0.93 - 0.9952, p < 0.001)(一致性极好)。与身体功能和残疾相比,学校和家庭生活以及心理健康的一致性水平最低。结论:我们发现,在不同的HRQoL测量方法和检测领域中,SMA儿童自我报告和父母代理报告的HRQoL之间的一致性存在显著差异,范围从差/一般到优秀。与之前的研究相比,在我们的当代队列患者中,接受新疗法治疗的PedsQL 3.0 NMM的一致性明显更高。这些初步发现将有助于为SMA患者HRQoL的未来研究设计提供参考。
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
Patient Related Outcome Measures
Patient Related Outcome Measures HEALTH CARE SCIENCES & SERVICES-
自引率
4.80%
发文量
27
审稿时长
16 weeks
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