Brettschneider Johannes, Kurent Jerome, Ludolph Albert
Neurology, University of Ulm, Ulm, Germany.
Cochrane Database Syst Rev. 2013 Jun 5;2013(6):CD005226. doi: 10.1002/14651858.CD005226.pub3.
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is the most common neurodegenerative disorder of the motor system in adults. Pain in ALS is a frequent symptom especially in the later stages of disease and can have a pronounced influence on quality of life and suffering. Treatment of pain therefore should be recognised as an important aspect of palliative care in ALS. This is an update of a review first published in 2008.
To systematically review the evidence for the efficacy of drug therapy in relieving pain in ALS. We also aimed to evaluate possible adverse effects associated with the different drugs and their influence on survival and quality of life.
On 2 July 2012, we searched the following databases: the Cochrane Neuromuscular Disease Group Specialized Register (2 July 2012), CENTRAL (2012, Issue 6 in The Cochrane Library), MEDLINE (January 1966 to June 2012), EMBASE (January 1980 to June 2012), CINAHL (January 1982 to June 2012), AMED (January 1985 to June 2012) and LILACS (January 1982 to June 2012). We checked the bibliographies of trials identified and contacted other disease experts to identify further published and unpublished trials.
We searched for randomised or quasi-randomised controlled trials on drug therapy for pain in amyotrophic lateral sclerosis.
We collected data using a specially designed form and analysed them using the Cochrane Review Manager software.
We found no randomised or quasi-randomised controlled trials on drug therapy for pain in ALS or MND.
AUTHORS' CONCLUSIONS: There is no evidence from randomised controlled trials about the management of pain in ALS. Further research on this important aspect of palliative care in ALS is needed. Randomised controlled trials should be initiated to determine the effectiveness of different analgesics for treatment of pain in ALS.
肌萎缩侧索硬化症(ALS),也称为运动神经元病(MND),是成人运动系统中最常见的神经退行性疾病。ALS患者的疼痛是一种常见症状,尤其是在疾病后期,会对生活质量和痛苦产生显著影响。因此,疼痛治疗应被视为ALS姑息治疗的一个重要方面。这是对2008年首次发表的一篇综述的更新。
系统评价药物治疗缓解ALS疼痛疗效的证据。我们还旨在评估不同药物可能的不良反应及其对生存和生活质量的影响。
2012年7月2日,我们检索了以下数据库:Cochrane神经肌肉疾病组专业注册库(2012年7月2日)、Cochrane系统评价数据库(2012年第6期)、医学索引(1966年1月至2012年6月)、荷兰医学文摘数据库(1980年1月至2012年6月)、护理学与健康领域数据库(1982年1月至2012年6月)、联合和补充医学数据库(1985年1月至2012年6月)以及拉丁美洲和加勒比地区健康科学数据库(1982年1月至2012年6月)。我们检查了已识别试验的参考文献,并联系了其他疾病专家以识别更多已发表和未发表的试验。
我们检索了关于肌萎缩侧索硬化症疼痛药物治疗的随机或半随机对照试验。
我们使用专门设计的表格收集数据,并使用Cochrane系统评价管理软件进行分析。
我们未找到关于ALS或MND疼痛药物治疗的随机或半随机对照试验。
随机对照试验中没有关于ALS疼痛管理的证据。需要对ALS姑息治疗的这一重要方面进行进一步研究。应开展随机对照试验以确定不同镇痛药治疗ALS疼痛的有效性。