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视神经脊髓炎谱系障碍中的疼痛性强直性痉挛:患病率、临床意义及治疗选择

Painful tonic spasm in neuromyelitis optica spectrum disorders: Prevalence, clinical implications and treatment options.

作者信息

Liu Ju, Zhang Qin, Lian Zhiyun, Chen Hongxi, Shi Ziyan, Feng Huiru, Miao Xiaohui, Du Qin, Zhou Hongyu

机构信息

Department of Neurology, West China Hospital, Sichuan University, Guo Xuexiang #37, Chengdu 610041, China.

Department of Neurology, West China Hospital, Sichuan University, Guo Xuexiang #37, Chengdu 610041, China.

出版信息

Mult Scler Relat Disord. 2017 Oct;17:99-102. doi: 10.1016/j.msard.2017.07.004. Epub 2017 Jul 5.

Abstract

BACKGROUND

Painful tonic spasm (PTS) is a common symptom in patients with neuromyelitis optica spectrum disorders (NMOSD). This study aimed to obtain further insights into the prevalence, characteristics, and treatment of PTS in patients with NMOSD, and to systematically investigate and compare the clinical features and prognosis of NMOSD with and without PTS.

METHODS

We reviewed the medical records and prospectively interviewed patients with NMOSD who attended the West China Hospital of Sichuan University in Chengdu, China between September 2014 and December 2016.

RESULTS

In total, 52 of the 230 patients with NMOSD experienced PTS (22.61%). Patients with NMOSD and PTS were characterized by a higher age at onset (P = 0.017), higher annual relapse rate (ARR) (P = 0.003), higher ARR of myelitis (P = 0.011), and a tendency to experience pruritus (P = 0.025). Sodium channel blocking antiepileptic drugs (carbamazepine or oxcarbazepine) had higher efficacy than gabapentin in the treatment of PTS (P = 0.001). Although the progression index was higher in patients with PTS, this difference did not reach statistical significance (P = 0.05).

CONCLUSIONS

Our study suggested that immunosuppressors for the prevention of relapse should be administered without delay in patients with NMOSD and PTS. Owing to the side effects of carbamazepine, we recommend oxcarbazepine as the first-line of treatment for PTS in patients with NMOSD. Whether PTS is a marker of disease severity in NMOSD remains to be determined, requiring a long-term prospective observational study.

摘要

背景

痛性强直性痉挛(PTS)是视神经脊髓炎谱系障碍(NMOSD)患者的常见症状。本研究旨在进一步了解NMOSD患者中PTS的患病率、特征及治疗情况,并系统调查和比较有PTS和无PTS的NMOSD患者的临床特征及预后。

方法

我们回顾了2014年9月至2016年12月期间在中国成都四川大学华西医院就诊的NMOSD患者的病历,并对其进行了前瞻性访谈。

结果

230例NMOSD患者中,共有52例经历了PTS(22.61%)。伴有PTS的NMOSD患者具有发病年龄较大(P = 0.017)、年复发率(ARR)较高(P = 0.003)、脊髓炎的ARR较高(P = 0.011)以及有瘙痒倾向(P = 0.025)的特点。钠通道阻滞抗癫痫药物(卡马西平或奥卡西平)在治疗PTS方面比加巴喷丁疗效更高(P = 0.001)。尽管有PTS的患者的疾病进展指数较高,但这种差异未达到统计学意义(P = 0.05)。

结论

我们的研究表明,对于患有NMOSD和PTS的患者,应立即给予预防复发的免疫抑制剂。由于卡马西平的副作用,我们推荐奥卡西平作为NMOSD患者PTS的一线治疗药物。PTS是否为NMOSD疾病严重程度的标志物仍有待确定,需要进行长期前瞻性观察研究。

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