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奥卡西平治疗多发性硬化症发作性疼痛症状的一项初步研究。

Oxcarbazepine for treating paroxysmal painful symptoms in multiple sclerosis: a pilot study.

作者信息

Solaro C, Restivo D, Mancardi G L, Tanganelli P

机构信息

Department of Neurology ASL 3 Genovese, Via Oliva 22, I-16123, Genova, Italy.

出版信息

Neurol Sci. 2007 Jun;28(3):156-8. doi: 10.1007/s10072-007-0811-3. Epub 2007 Jun 30.

Abstract

Oxcarbazepine (OXC) is an anitepileptic medication recently approved as monotherapy for partial onset seizure and demonstrated to be useful in the treatment of several neuropathic pain. We performed an open-label pilot study of OXC (dosage 600-1200 mg/day) in 12 multiple sclerosis (MS) patients suffering painful paroxysmal symptoms. Eight subjects were female and 4 male, with a mean age of 43.6 years, mean disease duration of 7.3 years and mean score at the EDSS of 3.2. Ten patients had a relapsing-remitting disease course, 1 had secondary progressive and 1 had primary progressive course. Painful paroxysmal symptoms (PPS) were defined as transient painful symptoms in any area of the body, with abrupt onset, brief duration, from a few seconds to a few minutes, with repetitive and stereotyped features. The subjective level of the PPS was scored using a three-point scale (0-3). The mean dosage of OXC was 1033 mg daily. Nine patients experienced a complete and sustained recovery within 1 month from treatment initiation (T0 vs. T1, p>0.05). Two patients dropped out of the study due to adverse effects: 1 case of nausea and dizziness, 1 case of C. hyponatraemia. The medication was well tolerated in the majority of the subjects. The study results provide a new possibility for treating painful symptoms in MS, but efficacy on PPS must be confirmed in a larger study.

摘要

奥卡西平(OXC)是一种最近被批准用于部分性发作癫痫单药治疗的抗癫痫药物,并且已证明对几种神经性疼痛的治疗有效。我们对12例患有疼痛性阵发性症状的多发性硬化症(MS)患者进行了一项开放标签的奥卡西平(剂量为600 - 1200毫克/天)试验研究。8名受试者为女性,4名男性,平均年龄43.6岁,平均病程7.3年,扩展残疾状态量表(EDSS)平均评分为3.2。10例患者为复发缓解型病程,1例为继发进展型,1例为原发进展型。疼痛性阵发性症状(PPS)被定义为身体任何部位的短暂疼痛症状,起病突然,持续时间短,从几秒到几分钟,具有重复性和刻板性特征。PPS的主观程度使用三点量表(0 - 3)进行评分。奥卡西平的平均剂量为每日1033毫克。9例患者在开始治疗后1个月内实现了完全且持续的恢复(T0与T1相比,p>0.05)。2例患者因不良反应退出研究:1例恶心和头晕,1例低钠血症。大多数受试者对该药物耐受性良好。研究结果为治疗MS中的疼痛症状提供了新的可能性,但PPS的疗效必须在更大规模的研究中得到证实。

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