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喹硫平治疗神经性厌食症的开放标签研究。

An open-label study of quetiapine in anorexia nervosa.

作者信息

Bosanac P, Kurlender S, Norman T, Hallam K, Wesnes K, Manktelow T, Burrows G

机构信息

Department of Psychiatry, University of Melbourne, and Austin Hospital, Australia.

出版信息

Hum Psychopharmacol. 2007 Jun;22(4):223-30. doi: 10.1002/hup.845.

Abstract

BACKGROUND

Atypical antipsychotics may be beneficial in treating the core psychopathology of anorexia nervosa (AN).

METHODS

An 8 week open-label study of quetiapine was conducted in eight severely ill DSM-IV AN patients consecutively admitted to a specialist eating disorders unit. Participants were assessed by EDE-12, MADRS, YBOCS, SAPS-delusions and CDR neuropsychological battery at baseline, 4 weeks and 8 weeks, and by weekly body mass index (BMI), CGI and extrapyramidal scores. Quetiapine doses ranged from 50 mg to 800 mg per day, according to efficacy and tolerability.

RESULTS

Seven participants completed 4 weeks and five participants completed 8 weeks. All participants had clinically significant levels of specific eating disorders psychopathology, and mild to moderately severe depressive symptomatology. Apart from initial mild sedation, no subjects experienced any significant adverse events. Over 4 weeks there was no significant difference in BMI, but a significant difference in the EDE-12 restraint score. There were significant differences on BMI and EDE-12 restraint subscale scores over 8 weeks.

CONCLUSIONS

A double-blind placebo controlled study is required to further evaluate the therapeutic utility of quetiapine in severely ill AN patients beyond multidisciplinary specialist intervention.

摘要

背景

非典型抗精神病药物可能对治疗神经性厌食症(AN)的核心精神病理学症状有益。

方法

对连续入住一家专业饮食失调病房的8名重症DSM-IV AN患者进行了一项为期8周的喹硫平开放标签研究。在基线、4周和8周时,通过EDE-12、MADRS、YBOCS、SAPS-妄想量表和CDR神经心理测试组对参与者进行评估,并每周测量体重指数(BMI)、CGI和锥体外系评分。根据疗效和耐受性,喹硫平剂量范围为每天50毫克至800毫克。

结果

7名参与者完成了4周的研究,5名参与者完成了8周的研究。所有参与者都有临床上显著的特定饮食失调精神病理学症状,以及轻度至中度严重的抑郁症状。除了最初的轻度镇静作用外,没有受试者经历任何显著的不良事件。在4周内,BMI没有显著差异,但EDE-12抑制评分有显著差异。在8周内,BMI和EDE-12抑制子量表评分有显著差异。

结论

需要进行一项双盲安慰剂对照研究,以进一步评估喹硫平在重症AN患者中除多学科专业干预之外的治疗效用。

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