Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/49489
Title: Pharmacological treatment for kleine-levin syndrome
Authors: de Oliveira, Marcio M. [UNIFESP]
Conti, Cristiane [UNIFESP]
Prado, Gilmar F. [UNIFESP]
Keywords: Kleine-Levin Syndrome [drug Therapy]
Rare Diseases [drug Therapy]
HumansLithium
Carbamazepine
Encephalitis
Therapy
Variant
Sleep
Acid
Issue Date: 2016
Publisher: Wiley-blackwell
Citation: Cochrane Database Of Systematic Reviews. Hoboken, n. 5, p. CD006685, 2016.
Abstract: Background This is an updated version of the original Cochrane review, published in 2009, Issue 2. Kleine-Levin syndrome (KLS) is a rare disorder that mainly affects adolescent men. It is characterised by recurrent episodes of hypersomnia, usually accompanied by hyperphagia, cognitive and mood disturbances, abnormal behaviour, 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 KLS was defined as a syndrome comprised of recurring episodes of undue sleepiness lasting some days, which may or may not be associated with hyperphagia and abnormal behaviour. According to the International Classification of Sleepiness Disorders, 3rd version (ICSD-3), revised in 2014, the Kleine-Levin syndrome is a disorder characterized by recurrent episodes of hypersomnia that last from two days to four weeks, with at least annual recurrence, and hyperphagia (rapid consumption of a large amount of food), usually with onset in early adolescence in males but occasionally in later life and in women. A monosymptomatic form of the disorder with hypersomnia only can occur without binge eating or hypersexuality. The cause of Kleine-Levin syndrome remains unknown, and several treatment strategies have been used. Some medications have been reported to provide benefit in the treatment of patients with KLS, but because of the rarity of the condition, no long-term follow-up therapies have yet been described. Objectives This review aimed to evaluate: 1. whether pharmacological treatment for Kleine Levin syndrome was effective and safe. 2. which drug or category of drugs was effective and safe. Search methods For the latest update, we searched the following sources: the Cochrane Epilepsy Group Specialized Register (7 April 2016)
the Cochrane Central Register of Controlled Trials (CENTRAL) via the Cochrane Register of Studies Online CRSO (7 April 2016)
MEDLINE (1946 to April 2016)
LILACS (7 April 2016)
ClinicalTrials.gov (7 April 2016)
WHO International Clinical Trials Registry Platform ICTRP (7 April 2016)
reference lists of sleep medicine textbooks
review articles and reference lists of articles identified by the search strategies. Selection criteria All randomised controlled trials (RCTs) and quasi-randomised controlled trials looking at pharmacological interventions for Kleine-Levin syndrome were eligible. We had planned to include both parallel-group and cross-over studies. Data collection and analysis Two review authors (MMO and CC) had planned to extract the data reported in the original articles. Main results 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.
URI: http://repositorio.unifesp.br/handle/11600/49489
ISSN: 1469-493X
Other Identifiers: http://dx.doi.org/10.1002/14651858.CD006685.pub4
Appears in Collections:Artigo
Artigo

Files in This Item:
File SizeFormat 
WOS000377961800041.pdf195.12 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.