Bentivoglio A R, Di Stasio E, Mulas D, Cerbarano M L, Ialongo T, Laurienzo A, Petracca Martina
Center for Parkinson Disease and Extrapyramidal Disorders, Movement Disorders Unit, Institute of Neurology, Università Cattolica del Sacro Cuore, Largo Agostino Gemelli, 8, 00168, Rome, Italy.
Fondazione Don Carlo Gnocchi, Milan, Italy.
Neurotox Res. 2017 Aug;32(2):291-300. doi: 10.1007/s12640-017-9737-6. Epub 2017 May 6.
Botulinum toxin is considered as first-line therapy for cervical dystonia, but few papers have addressed these issues in the long term. Aim of this study was to investigate the long-term efficacy and safety of abobotulinumtoxin A (A/Abo) in patients with primary cervical dystonia. Consecutive patients who received at least six injections with A/Abo were included. Safety was assessed on patients' self-reports. Efficacy was assessed by recording the total duration of benefit, duration of maximum efficacy, disease severity measured by means of the Tsui score, and pain intensity evaluated by means of the visual analog scale (VAS). Thirty-nine patients with PCD were included. The mean dose injected was 701.5 ± 280.6 U. The mean duration of the clinical improvement was 93.0 ± 30.7 days, while the mean duration of the maximum clinical improvement was 77.1 ± 27.1 days. The mean VAS before and 4 weeks after injection was 4.4 ± 1.8 and 1.8 ± 1.6, respectively. The mean Tsui score before and 4 weeks after treatment was 5.7 ± 1.8 and 3.5 ± 1.5, respectively. Doses of A/Abo and duration of the maximum clinical improvement significantly increased over time, while the Tsui score and VAS displayed a tendency to decrease along time. Side effects occurred in 19.6% of all the treatments but were severe in only four injections. The results of our study confirm the effectiveness and safety profile of A/Abo for the long-term treatment of primary cervical dystonia.
肉毒杆菌毒素被认为是治疗颈部肌张力障碍的一线疗法,但长期探讨这些问题的论文较少。本研究旨在调查阿柏西普(A/Abo)治疗原发性颈部肌张力障碍患者的长期疗效和安全性。纳入连续接受至少6次A/Abo注射的患者。通过患者自我报告评估安全性。通过记录受益总时长、最大疗效持续时间、采用徐氏评分法测量的疾病严重程度以及采用视觉模拟量表(VAS)评估的疼痛强度来评估疗效。纳入39例原发性颈部肌张力障碍患者。平均注射剂量为701.5±280.6单位。临床改善的平均持续时间为93.0±30.7天,而最大临床改善的平均持续时间为77.1±27.1天。注射前和注射后4周的平均VAS分别为4.4±1.8和1.8±1.6。治疗前和治疗后4周的平均徐氏评分分别为5.7±1.8和3.5±1.5。A/Abo剂量和最大临床改善持续时间随时间显著增加,而徐氏评分和VAS随时间呈下降趋势。19.6%的治疗出现副作用,但仅4次注射为严重副作用。我们的研究结果证实了A/Abo长期治疗原发性颈部肌张力障碍的有效性和安全性。