Caley C F, Weber S S
Eastern State Hospital, Medical Lake, WA.
Ann Pharmacother. 1993 Oct;27(10):1212-22. doi: 10.1177/106002809302701012.
To review the pharmacology, pharmacokinetics, clinical investigations, adverse effects, and dosing strategies of paroxetine as a treatment of major depression.
Specific paroxetine information was selected from a MEDLINE search using paroxetine as the search term. Other sources included manual searches of pertinent journal article references, meeting abstracts, and the manufacturer.
Clinical investigations with a blind, controlled (placebo and/or active), randomized design were selected. With the exception of treatment-resistant depression, no short-term, open investigations were selected.
Clinical investigations were evaluated for design, sample size, diagnosis, duration, definition of response, and outcome. Data from all investigations were selected by one author and reviewed by both authors.
Paroxetine is a selective serotonin reuptake inhibitor (SSRI) recently approved for the treatment of major depression. It is a potent and selective inhibitor of serotonin reuptake and has weak or no activity on the other monoamines; it is also weakly anticholinergic. Although pharmacokinetic parameters are variable, paroxetine is generally well absorbed, highly protein bound, hepatically cleared, and has no active metabolites. Clinical investigations support paroxetine's effectiveness as an antidepressant in an outpatient population with moderately severe depression. Its effectiveness is superior to that of placebo and is comparable to that of active controls. The majority of investigations have been six weeks in duration. Additional data are required to support paroxetine's promise for longer treatment periods (i.e., > or = 1 y), in the elderly, and for treatment-resistant depression. Adverse effects appear to be similar to those caused by the other SSRIs; some of the most common are nausea, diarrhea, insomnia, dry mouth, and nervousness. Significant drug interactions may occur with the monoamine oxidase inhibitors, phenobarbital, and phenytoin.
Paroxetine is safe and effective for treatment of outpatients with moderately severe depression. Further clinical data and experience are necessary to determine this agent's place in the long-term treatment of major depression.
综述帕罗西汀治疗重度抑郁症的药理学、药代动力学、临床研究、不良反应及给药策略。
以帕罗西汀为检索词,从MEDLINE检索中选取特定的帕罗西汀信息。其他来源包括对相关期刊文章参考文献、会议摘要及生产商的手工检索。
选取采用盲法、对照(安慰剂和/或活性对照)、随机设计的临床研究。除难治性抑郁症外,未选取短期开放性研究。
对临床研究的设计、样本量、诊断、疗程、疗效定义及结果进行评估。所有研究的数据由一位作者选取,并经两位作者审核。
帕罗西汀是一种选择性5-羟色胺再摄取抑制剂(SSRI),最近被批准用于治疗重度抑郁症。它是一种强效且选择性的5-羟色胺再摄取抑制剂,对其他单胺类物质活性较弱或无活性;它也有较弱的抗胆碱能作用。尽管药代动力学参数存在差异,但帕罗西汀一般吸收良好,蛋白结合率高,经肝脏清除,且无活性代谢产物。临床研究支持帕罗西汀对中度重度抑郁症门诊患者作为抗抑郁药的有效性。其有效性优于安慰剂,与活性对照相当。大多数研究疗程为六周。需要更多数据来支持帕罗西汀在更长治疗期(即≥1年)、老年患者及难治性抑郁症治疗中的前景。不良反应似乎与其他SSRI类药物所致相似;一些最常见的不良反应是恶心、腹泻、失眠、口干及紧张。与单胺氧化酶抑制剂、苯巴比妥及苯妥英可能发生显著的药物相互作用。
帕罗西汀治疗中度重度抑郁症门诊患者安全有效。需要更多临床数据和经验来确定该药物在重度抑郁症长期治疗中的地位。