AlRuthia Yazed, Almuaythir Ghadah S, H Alrasheed Hala, Alsharif Wejdan R, Temsah Mohamad-Hani, Alsohime Fahad, Sales Ibrahim, Alwhaibi Monira, Bashiri Fahad A
Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Pharmacoeconomics Research Unit, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Patient Prefer Adherence. 2021 Apr 13;15:729-739. doi: 10.2147/PPA.S305849. eCollection 2021.
The recent approval of innovative therapies for spinal muscular atrophy (SMA), such as nusinersen, has brought hope to patients and their families.
The aims of this study were to compare the characteristics and HRQoL of SMA patients treated with nusinersen and those treated with the standard of care.
This was a cross-sectional, interviewer-administered telephone questionnaire, which used a purposive sampling of SMA patients through a social support network. EuroQol five-dimensions-3-level (EQ-5D-3L) and the visual analog scale (VAS) have been used to assess the HRQoL. Different descriptive and inferential tests have been performed to compare the characteristics, EQ-5D responses, and mean scores of EQ-VAS between patients on nusinersen and the standard of care.
Eleven out of 36 SMA patients (30.55%) have been treated with nusinersen. Patients with type I SMA represented 54% of those treated with nusinersen (=0.012). Only 12.5% of SMA patients living in the Mecca region are treated with nusinersen in comparison to 50% of patients living in the Riyadh region (=0.029). No difference was noticed in the proxy-responses for the five domains of the EQ-5D or the mean VAS scores for patients on nusinersen and the standard of care despite controlling for the SMA type and the ability to breathe independently (β= 1.39, 95% CI= - 5.15-7.93, =0.667). However, the mean VAS score for patients who are unable to breathe independently was significantly lower than their counterparts who are able to breathe independently even after controlling for the SMA type and nusinersen treatment (β= -31.61, 95% CI= - 51.59 - -11.63, =0.003).
The results of this study highlight the uncertainty about the impact of nusinersen on SMA patients' HRQoL. Therefore, the impact of nusinersen on HRQoL should be examined using more robust study designs.
脊髓性肌萎缩症(SMA)的创新疗法,如诺西那生钠,最近获得批准,给患者及其家人带来了希望。
本研究旨在比较接受诺西那生钠治疗的SMA患者与接受标准治疗的患者的特征和健康相关生活质量(HRQoL)。
这是一项由访员实施的横断面电话问卷调查,通过社会支持网络对SMA患者进行目的抽样。采用欧洲五维健康量表3级(EQ-5D-3L)和视觉模拟量表(VAS)评估HRQoL。进行了不同的描述性和推断性测试,以比较接受诺西那生钠治疗的患者与接受标准治疗的患者的特征、EQ-5D反应和EQ-VAS平均得分。
36例SMA患者中有11例(30.55%)接受了诺西那生钠治疗。I型SMA患者占接受诺西那生钠治疗患者的54%(P=0.012)。居住在麦加地区的SMA患者中只有12.5%接受诺西那生钠治疗,而利雅得地区的这一比例为50%(P=0.029)。尽管对SMA类型和独立呼吸能力进行了控制,但在EQ-5D的五个领域的代理反应或接受诺西那生钠治疗的患者与接受标准治疗的患者的VAS平均得分方面未发现差异(β=1.39,95%CI=-5.15-7.93,P=0.667)。然而,即使对SMA类型和诺西那生钠治疗进行了控制,无法独立呼吸的患者的VAS平均得分仍显著低于能够独立呼吸的患者(β=-31.61,95%CI=-51.59--11.63,P=0.003)。
本研究结果凸显了诺西那生钠对SMA患者HRQoL影响的不确定性。因此,应使用更稳健的研究设计来研究诺西那生钠对HRQoL的影响。