Efficacy and safety of salbutamol in treatment of children with later-onset spinal muscular atrophy.

Yijie Feng, Jianing Jin, Tingting Chen, Jianhua Wang, Yuan Jiang, Feng Gao, Shanshan Mao
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Abstract

Objectives: To investigate the clinical efficacy and safety of salbutamol in the treatment of children with later-onset spinal muscular atrophy (SMA).

Methods: This study is a prospective single-arm phase Ⅲ clinical study. Pediatric patients with SMA type Ⅱ and Ⅲ who visited Department of Neurology, Children's Hospital, Zhejiang University School of Medicine from December 2020 to June 2022 were enrolled. All patients were evaluated with motor function scales, pulmonary function test and drug safety before study. Patients were treated with salbutamol tablets orally, with an initial dose of 1 mg (tid). If tolerable, the dose was increased to 1.5 mg (tid) in the second week, then increased to 2 mg (tid) from the third week and maintained for 6 months. Patients were followed up at 1, 3 and 6 months of treatment.

Results: Twenty-six patients were enrolled, including 10 boys and 16 girls. There were 16 cases of SMA type Ⅱ and 10 cases of type Ⅲ with age at treatment initiation of 5.67 (3.13, 7.02) years and disease duration of 2.54 (1.31, 4.71) years. The Hammersmith Functional Motor Scale-Expanded (HFMSE) scores were increased from 14.0 (6.5, 43.0) before treatment to 26.0 (15.0, 46.5) after treatment (Z=-4.144, P<0.01) in 25 cases. The Revised Upper Limb Module Scale scores were increased from 33.0 (25.5, 36.0) before treatment to 35.0 (31.0, 36.5) after treatment (Z=-2.214, P<0.05) in 9 cases. In 7 ambulant children with SMA type Ⅲ, the six minutes walking distance was increased by 30 (15, 52) m after a 6-month treatment (Z=-2.366, P<0.05). Compared with the baseline pulmonary functions the patients showed a significant increase in forced vital capacity (FVC), forced expiratory volume in one second (FEV1), and peak expiratory flow (PEF) in 15 cases after treatment (all P<0.05). According to patients and caregivers subjective reporting, there were various degrees of improvement in coughing, sputum production ability and exercise endurance. No serious adverse events were observed during the study.

Conclusions: Short-term oral administration of salbutamol may improve motor and pulmonary functions in later-onset SMA children with good safety.

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沙丁胺醇治疗晚期脊髓性肌萎缩症儿童的疗效和安全性。
目的研究沙丁胺醇治疗晚发型脊髓性肌萎缩症(SMA)患儿的临床疗效和安全性:本研究为前瞻性单臂Ⅲ期临床研究。方法:本研究为前瞻性单臂Ⅲ期临床研究,纳入2020年12月至2022年6月期间在浙江大学医学院附属儿童医院神经内科就诊的SMAⅡ型和Ⅲ型儿童患者。研究前对所有患者进行了运动功能量表、肺功能测试和药物安全性评估。患者口服沙丁胺醇片,初始剂量为1毫克(tid)。如果可以耐受,剂量在第二周增加到 1.5 毫克(tid),然后从第三周开始增加到 2 毫克(tid),并维持 6 个月。患者在治疗 1 个月、3 个月和 6 个月时接受随访:26例患者中包括10名男孩和16名女孩,平均年龄为5.67(3.13,7.02)岁。SMAⅡ型16例,Ⅲ型10例,平均病程2.54(1.31,4.71)年。哈默史密斯功能运动量表扩展版(HFMSE)评分从治疗前的14.0(6.5,43.0)提高到治疗后的26.0(15.0,46.5)(Z=-4.144,PZ=-2.214,PZ=-2.366,P1),治疗后15例患者的呼气流量峰值(PEF)提高(均为PConclusions):短期口服沙丁胺醇可改善晚发型 SMA 儿童的运动和肺功能,且具有安全性。
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CiteScore
3.80
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发文量
67
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