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本文引用的文献

1
Assessment of Health-Related Quality of Life in Adult Spinal Muscular Atrophy Under Nusinersen Treatment-A Pilot Study.在接受诺西那生治疗的成年脊髓性肌萎缩症患者中健康相关生活质量的评估——一项试点研究
Front Neurol. 2022 Jan 24;12:812063. doi: 10.3389/fneur.2021.812063. eCollection 2021.
2
Quality of Life in SMA Patients Under Treatment With Nusinersen.接受诺西那生治疗的脊髓性肌萎缩症患者的生活质量
Front Neurol. 2021 Mar 29;12:626787. doi: 10.3389/fneur.2021.626787. eCollection 2021.
3
Quality of life of children with spinal muscular atrophy and their caregivers from the perspective of caregivers: a Chinese cross-sectional study.从照顾者角度看脊髓性肌萎缩症患儿及其照顾者的生活质量:一项中国横断面研究
Orphanet J Rare Dis. 2021 Jan 6;16(1):7. doi: 10.1186/s13023-020-01638-8.
4
Quality of life in children and adolescents with Spinal Muscular Atrophy.脊髓性肌萎缩症患儿和青少年的生活质量。
Rev Chil Pediatr. 2020 Aug;91(4):512-520. doi: 10.32641/rchped.v91i4.1443. Epub 2020 Sep 11.
5
Nusinersen treatment of spinal muscular atrophy - a systematic review.脊髓性肌萎缩症的 nusinersen 治疗 - 系统评价。
Dan Med J. 2020 Aug 7;67(9):A02200100.
6
The Economic Impact and Health-Related Quality of Life of Spinal Muscular Atrophy. An Analysis across Europe.脊髓性肌萎缩症的经济影响和与健康相关的生活质量。 一项跨越欧洲的分析。
Int J Environ Res Public Health. 2020 Aug 5;17(16):5640. doi: 10.3390/ijerph17165640.
7
Prenusinersen economic and health-related quality of life burden of spinal muscular atrophy.普那司林治疗脊髓性肌萎缩症的经济学和健康相关生活质量负担。
Neurology. 2020 Jul 7;95(1):e1-e10. doi: 10.1212/WNL.0000000000009715. Epub 2020 Jun 8.
8
A Prospective, Crossover Survey Study of Child- and Proxy-Reported Quality of Life According to Spinal Muscular Atrophy Type and Medical Interventions.前瞻性、交叉调查研究根据脊髓性肌萎缩症类型和医疗干预的儿童和代理报告的生活质量。
J Child Neurol. 2020 Apr;35(5):322-330. doi: 10.1177/0883073819900463. Epub 2020 Feb 3.
9
Quality of life of patients with spinal muscular atrophy: A systematic review.脊髓性肌萎缩症患者的生活质量:系统评价。
Eur J Paediatr Neurol. 2019 May;23(3):347-356. doi: 10.1016/j.ejpn.2019.03.004. Epub 2019 Mar 21.
10
Financial, opportunity and psychosocial costs of spinal muscular atrophy: an exploratory qualitative analysis of Australian carer perspectives.脊髓性肌萎缩症的经济、机会和心理社会成本:对澳大利亚照顾者观点的探索性定性分析。
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中国脊髓性肌萎缩症患者健康相关生活质量评估

Assessment of health-related quality of life in patients with spina muscular atrophy in China.

作者信息

Duan Chengaxin, Ai Dandan, Xu Qian, Sui Binyan, Zhao Kun

机构信息

China National Health Development Research Center; National Center for Drug and Technology Assessment, Beijing, China.

Vanke School of Public Health, Tsinghua University; Institute for Healthy China, Tsinghua University, Beijing, China.

出版信息

Intractable Rare Dis Res. 2022 Nov;11(4):189-195. doi: 10.5582/irdr.2022.01094.

DOI:10.5582/irdr.2022.01094
PMID:36457580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9709625/
Abstract

Spinal muscular atrophy (SMA) is a rare disease that has attracted considerable interest in China due to its severity and hefty treatment costs. Few studies have been conducted on Chinese patients. The objective of this study was to assess the quality of life of SMA patients in China and to investigate the real impact of new treatments. We used the Pediatric Quality of Life Inventory (PedsQL) to analyze the Health-related quality of life (HRQoL) of patients with SMA in China. Information on demographics, disease-specific characteristics, and treatment were collected using a child-reported or proxy-reported questionnaire. The mean scores of HRQoL for the Nusinersen treatment group and conventional treatment groups are 55.6 and 48.4, respectively. Patients with SMA type I have the lowest scores, while those with type III have the highest scores. A higher proportion of the medication group showed improvement in the condition in the past six months (56.9% 17.1%). Our results show that the clinical type, motor function and treatment strategy have a significant influence on HRQoL. The findings imply that Nusinersen benefits patients by slowing the progression of the disease and increasing their quality of life in the real world.

摘要

脊髓性肌萎缩症(SMA)是一种罕见疾病,因其严重性和高昂的治疗费用在中国引起了广泛关注。针对中国患者的研究较少。本研究的目的是评估中国SMA患者的生活质量,并调查新治疗方法的实际影响。我们使用儿童生活质量量表(PedsQL)来分析中国SMA患者的健康相关生活质量(HRQoL)。通过儿童自填或家长代填问卷收集人口统计学、疾病特异性特征和治疗相关信息。诺西那生治疗组和传统治疗组的HRQoL平均得分分别为55.6和48.4。I型SMA患者得分最低,而III型患者得分最高。在过去六个月中,用药组病情改善的比例更高(56.9%对17.1%)。我们的结果表明,临床类型、运动功能和治疗策略对HRQoL有显著影响。研究结果表明,在现实世界中,诺西那生通过减缓疾病进展和提高患者生活质量而使患者受益。