McCormick Zachary L, Chu Samuel K, Binler Danielle, Neudorf Daniel, Mathur Sunjay N, Lee Jungwha, Marciniak Christina
Department of Physical Medicine & Rehabilitation (PM&R), Northwestern Feinberg School of Medicine/The Rehabilitation Institute of Chicago, McGaw Medical Center, Northwestern University Feinberg School of Medicine, 345 East Superior Street, Chicago, IL 60605(∗).
Department of Physical Medicine & Rehabilitation (PM&R), Northwestern Feinberg School of Medicine/The Rehabilitation Institute of Chicago, Chicago, IL(†).
PM R. 2016 Jun;8(6):553-62. doi: 10.1016/j.pmrj.2015.10.005. Epub 2015 Oct 20.
Baclofen commonly is used to manage spasticity caused by central nervous system lesions or dysfunction. Although both intrathecal and oral delivery routes are possible, no study has directly compared clinical outcomes associated with these 2 routes of treatment.
To compare spasticity levels, pain, sleep, fatigue, and quality of life between individuals receiving treatment with intrathecal versus oral baclofen.
Cross-sectional matched cohort survey study.
Urban academic rehabilitation outpatient clinics.
Adult patients with spasticity, treated with intrathecal or oral baclofen for at least 1 year, matched 1:1 for age, gender, and diagnosis.
Standardized surveys were administered during clinic appointments or by telephone.
Surveys included the Penn Spasm Frequency Scale, Brief Pain Inventory, Epworth Sleepiness Scale, Fatigue Severity Scale, Life Satisfaction Questionnaire, and Diener Satisfaction with Life Scale.
A total of 62 matched subjects were enrolled. The mean (standard deviation [SD]) age was 46 (11) years with a mean duration of intrathecal baclofen or oral baclofen treatment of 11 (6) and 13 (11) years, respectively. There were 40 (64%) male and 22 (36%) female subjects. Primary diagnoses included spinal cord injury (n = 38), cerebral palsy (n = 10), stroke (n = 10), and multiple sclerosis (n = 4). The mean (SD) dose of intrathecal and oral baclofen at the time of survey were 577 (1429) μg/day and 86 (50) mg/day, respectively. Patients receiving intrathecal compared with oral baclofen experienced significantly fewer (1.44 [0.92] versus 2.37 [1.12]) and less severe (1.44 [0.92] versus 2.16 [0.83]) spasms, respectively as measured by the Penn Spasm Frequency Scale (P < .01; P < .01). There were no significant differences in pain, sleep, fatigue, and quality of life between groups. Subanalysis of patients with SCI mirrored results of the entire study sample, with significant decreases in spasm frequency and severity associated with intrathecal compared to oral baclofen (P < .01; P < .01), but no other between group differences. The mean (SD) percent change in dose of oral (21% [33%]) compared with intrathecal (3% [28%]) baclofen was significantly larger two years prior to the date of survey (P = .02).
Long-term treatment with intrathecal compared with oral baclofen is associated with reduced spasm frequency and severity as well as greater dose stability. These benefits must be weighed against the risks of internal pump and catheter placement in patients considering intrathecal baclofen therapy.
巴氯芬常用于治疗由中枢神经系统病变或功能障碍引起的痉挛。虽然鞘内给药和口服给药途径均可行,但尚无研究直接比较这两种治疗途径的临床疗效。
比较接受鞘内注射与口服巴氯芬治疗的个体之间的痉挛程度、疼痛、睡眠、疲劳及生活质量。
横断面匹配队列调查研究。
城市学术康复门诊。
成年痉挛患者,接受鞘内或口服巴氯芬治疗至少1年,按年龄、性别和诊断1:1匹配。
在门诊预约时或通过电话进行标准化调查。
调查包括宾夕法尼亚痉挛频率量表、简明疼痛量表、爱泼华嗜睡量表、疲劳严重程度量表、生活满意度问卷及迪纳生活满意度量表。
共纳入62例匹配受试者。平均(标准差[SD])年龄为46(11)岁,鞘内注射巴氯芬或口服巴氯芬的平均治疗时间分别为11(6)年和13(11)年。有40例(64%)男性和22例(36%)女性受试者。主要诊断包括脊髓损伤(n = 38)、脑瘫(n = 10)、中风(n = 10)和多发性硬化(n = 4)。调查时鞘内和口服巴氯芬的平均(SD)剂量分别为577(1429)μg/天和86(50)mg/天。根据宾夕法尼亚痉挛频率量表测量,接受鞘内注射巴氯芬的患者与口服巴氯芬的患者相比,痉挛次数明显更少(1.44[0.92]对2.37[1.12])且痉挛程度更轻(1.44[0.92]对2.16[0.83])(P <.01;P <.01)。两组之间在疼痛、睡眠、疲劳和生活质量方面无显著差异。脊髓损伤患者的亚组分析反映了整个研究样本的结果,与口服巴氯芬相比,鞘内注射巴氯芬与痉挛频率和严重程度显著降低相关(P <.01;P <.01),但组间无其他差异。在调查日期前两年,口服巴氯芬(21%[33%])与鞘内注射巴氯芬(3%[28%])剂量的平均(SD)百分比变化显著更大(P =.02)。
与口服巴氯芬相比,鞘内注射巴氯芬长期治疗可降低痉挛频率和严重程度,并提高剂量稳定性。在考虑鞘内注射巴氯芬治疗的患者中,必须权衡这些益处与内置泵和导管置入的风险。