Oliveira Marcio M, Conti Cristiane, Saconato Humberto, Fernandes do Prado Gilmar
UNIFESP, Pedro de Toledo st 598, São Paulo, Brazil, 04039001.
Cochrane Database Syst Rev. 2009 Apr 15(2):CD006685. doi: 10.1002/14651858.CD006685.pub2.
Kleine-Levin Syndrome (KLS) is a rare disorder which mainly affects adolescent men. It is characterized by recurrent episodes of hypersomnia, usually accompanied by hyperphagia, cognitive and mood disturbances, abnormal behavior such as hypersexuality, and signs of dysautonomia.In 1990 the diagnostic criteria for Kleine-Levin Syndrome were modified in the International Classification of Sleep Disorders, where it was defined as a syndrome composed of recurring episodes of undue sleepiness lasting some days, which may or may not be associated with hyperphagia and abnormal behavior.The etiology of Kleine-Levin Syndrome remains unknown and several treatment strategies have been used. Some medications have been reported to provide some benefit for the treatment of Kleine-Levin Syndrome patients, but because of the rarity of the condition no long-term follow-up therapies have yet been described.
This review aimed to evaluate:1. whether pharmacological treatment for Kleine-Levin Syndrome is effective and safe; and 2. which drug or category of drugs is effective and safe.
We obtained relevant trials from the following sources: the Cochrane Epilepsy Group Specialized Register (1 December 2007); the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 3, 2007); MEDLINE (1966 to December 2007); EMBASE (1980 to December 2007); LILACS (1982 to December 2007); reference lists of sleep medicine textbooks; review articles and reference lists of articles identified by the search strategies.
All randomized controlled trials (RCTs) and quasi-randomized controlled trials looking at pharmacological interventions for Kleine-Levin Syndrome. We included both parallel group and cross-over studies.
Two review authors (MO and CC) extracted the data reported in the original articles.
No studies met the inclusion criteria for this systematic review.
AUTHORS' CONCLUSIONS: Therapeutic trials of pharmacological treatment for Kleine-Levin Syndrome, with a double-blind, placebo-controlled design are needed.
克莱恩-莱文综合征(KLS)是一种罕见的疾病,主要影响青春期男性。其特征为反复发作的嗜睡,通常伴有贪食、认知和情绪障碍、诸如性欲亢进等异常行为以及自主神经功能紊乱的体征。1990年,克莱恩-莱文综合征的诊断标准在《国际睡眠障碍分类》中进行了修订,被定义为由持续数天的反复过度嗜睡发作组成的综合征,可能伴有或不伴有贪食及异常行为。克莱恩-莱文综合征的病因仍然不明,已经采用了多种治疗策略。据报道,一些药物对治疗克莱恩-莱文综合征患者有一定益处,但由于该病症罕见,尚未有长期随访治疗的描述。
本综述旨在评估:1. 克莱恩-莱文综合征的药物治疗是否有效且安全;2. 哪种药物或药物类别有效且安全。
我们从以下来源获取相关试验:Cochrane癫痫组专业注册库(2007年12月1日);Cochrane对照试验中心注册库(CENTRAL)(《Cochrane图书馆》2007年第3期);医学索引(1966年至2007年12月);荷兰医学文摘数据库(1980年至2007年12月);拉丁美洲和加勒比地区卫生科学数据库(1982年至2007年12月);睡眠医学教科书的参考文献列表;综述文章以及通过检索策略确定的文章的参考文献列表。
所有针对克莱恩-莱文综合征药物干预的随机对照试验(RCT)和半随机对照试验。我们纳入了平行组研究和交叉研究。
两位综述作者(MO和CC)提取了原始文章中报告的数据。
没有研究符合本系统综述的纳入标准。
需要进行具有双盲、安慰剂对照设计的克莱恩-莱文综合征药物治疗试验。