Department of Neurology, Pyhrn-Eisenwurzen Klinikum Steyr, Steyr, Austria.
Department of Neurology, Klinikum Bad Hall and Bad Schallerbach, Bad Schallerbach, Austria.
Brain Behav. 2023 Apr;13(4):e2947. doi: 10.1002/brb3.2947. Epub 2023 Mar 19.
Randomized controlled trials and observational studies of nabiximols oromucosal spray in patients with multiple sclerosis (MS) spasticity have shown improvement in a range of associated symptoms (pain, spasms, fatigue, bladder dysfunction, and sleep disturbances). This study evaluated the effectiveness and tolerability of add-on nabiximols in the routine management of patients with MS spasticity in Austria, with a focus on spasticity-associated symptoms.
This was an open, prospective, multicenter, observational, non-interventional study of patients with MS spasticity receiving add-on treatment with nabiximols oromucosal spray. Main endpoints were patient-reported changes from baseline in the frequency (counts) or severity (mean Numerical Rating Scale [NRS] scores) of spasticity-associated symptoms, and patient-reported changes from baseline in impairment of daily activities due to spasticity, after 1 and 3 months of nabiximols treatment. No analyses were conducted for statistical significance.
There were 55 patients in the effectiveness population, and 62 in the safety population. Patients reported clinically relevant reductions from baseline to month 3 in the average number of spasms/day (-68.2%) and number of urinary incontinence episodes (-69.3%) in the week prior to the clinic visit, and reductions in mean 0-10 NRS scores for sleep impairment (-47.2%), fatigue (-26.4%), pain (40.4%), and spasticity severity (39.0%). There was no change from baseline in daily activity impairment due to spasticity. The majority of patients were at least partly satisfied with add-on nabiximols for spasticity-associated symptoms. There were 31 adverse events (27 treatment related) reported in 19 patients, with no new safety signals.
Add-on nabiximols improved the severity of MS spasticity and a range of spasticity-associated symptoms during real-world use in Austria. Nabiximols is an option for patients with MS spasticity who fail first-line oral antispasticity treatment.
纳比昔单抗口溶膜在多发性硬化症(MS)痉挛患者中的随机对照试验和观察性研究表明,其在一系列相关症状(疼痛、痉挛、疲劳、膀胱功能障碍和睡眠障碍)方面有所改善。本研究评估了纳比昔单抗在奥地利 MS 痉挛患者常规治疗中的有效性和耐受性,重点关注与痉挛相关的症状。
这是一项开放、前瞻性、多中心、观察性、非干预性研究,纳入接受纳比昔单抗口溶膜附加治疗的 MS 痉挛患者。主要终点是患者报告的痉挛相关症状频率(计数)或严重程度(平均数字评定量表[NRS]评分)从基线的变化,以及因痉挛导致日常活动受损的情况从基线的变化,在纳比昔单抗治疗 1 个月和 3 个月后。未进行统计意义的分析。
有效性人群中有 55 例患者,安全性人群中有 62 例患者。与基线相比,在就诊前一周内,患者报告的痉挛平均每日发作次数(减少 68.2%)和尿失禁发作次数(减少 69.3%),以及睡眠障碍(减少 47.2%)、疲劳(减少 26.4%)、疼痛(减少 40.4%)和痉挛严重程度(减少 39.0%)的平均 0-10 NRS 评分均有临床相关的降低。因痉挛导致日常活动受损情况无变化。大多数患者对纳比昔单抗附加治疗痉挛相关症状至少部分满意。19 例患者报告了 31 例不良事件(27 例与治疗相关),无新的安全信号。
在奥地利的真实世界应用中,纳比昔单抗附加治疗改善了 MS 痉挛的严重程度和一系列痉挛相关症状。纳比昔单抗是一线口服抗痉挛治疗失败的 MS 痉挛患者的选择。