Qaseem Amir, Snow Vincenza, Denberg Thomas D, Forciea Mary Ann, Owens Douglas K
American College of Physicians, Philadelphia, PA 19106, UAS.
Ann Intern Med. 2008 Nov 18;149(10):725-33. doi: 10.7326/0003-4819-149-10-200811180-00007.
The American College of Physicians developed this guideline to present the available evidence on the pharmacologic management of the acute, continuation, and maintenance phases of major depressive disorder; dysthymia; subsyndromal depression; and accompanying symptoms, such as anxiety, insomnia, or neurovegetative symptoms, by using second-generation antidepressants.
Published literature on this topic was identified by using MEDLINE, EMBASE, PsychLit, the Cochrane Central Register of Controlled Trials, and International Pharmaceutical Abstracts from 1980 to April 2007. Searches were limited to English-language studies in adults older than 19 years of age. Keywords for search included terms for depressive disorders and 12 specific second-generation antidepressants-bupropion, citalopram, duloxetine, escitalopram, fluoxetine, fluvoxamine, mirtazapine, nefazodone, paroxetine, sertraline, trazodone, and venlafaxine-and their specific trade names. This guideline grades the evidence and recommendations by using the American College of Physicians clinical practice guidelines grading system. RECOMMENDATION 1: The American College of Physicians recommends that when clinicians choose pharmacologic therapy to treat patients with acute major depression, they select second-generation antidepressants on the basis of adverse effect profiles, cost, and patient preferences (Grade: strong recommendation; moderate-quality evidence). RECOMMENDATION 2: The American College of Physicians recommends that clinicians assess patient status, therapeutic response, and adverse effects of antidepressant therapy on a regular basis beginning within 1 to 2 weeks of initiation of therapy (Grade: strong recommendation; moderate-quality evidence). RECOMMENDATION 3: The American College of Physicians recommends that clinicians modify treatment if the patient does not have an adequate response to pharmacotherapy within 6 to 8 weeks of the initiation of therapy for major depressive disorder (Grade: strong recommendation; moderate-quality evidence). RECOMMENDATION 4: The American College of Physicians recommends that clinicians continue treatment for 4 to 9 months after a satisfactory response in patients with a first episode of major depressive disorder. For patients who have had 2 or more episodes of depression, an even longer duration of therapy may be beneficial (Grade: strong recommendation; moderate-quality evidence).
美国医师协会制定本指南,旨在呈现关于使用第二代抗抑郁药对重度抑郁症、心境恶劣障碍、亚综合征性抑郁及其伴随症状(如焦虑、失眠或神经植物性症状)的急性期、延续期和维持期进行药物治疗的现有证据。
通过使用MEDLINE、EMBASE、PsychLit、Cochrane对照试验中央注册库以及1980年至2007年4月的《国际药学文摘》来识别关于该主题的已发表文献。检索限于19岁以上成年人的英文研究。检索关键词包括抑郁症相关术语以及12种特定的第二代抗抑郁药——安非他酮、西酞普兰、度洛西汀、艾司西酞普兰、氟西汀、氟伏沙明、米氮平、奈法唑酮、帕罗西汀、舍曲林、曲唑酮和文拉法辛——及其特定商品名。本指南采用美国医师协会临床实践指南分级系统对证据和推荐意见进行分级。推荐意见1:美国医师协会建议,临床医生在选择药物治疗急性重度抑郁症患者时,应根据不良反应情况、成本和患者偏好来选择第二代抗抑郁药(分级:强烈推荐;中等质量证据)。推荐意见2:美国医师协会建议,临床医生在开始治疗后的1至2周内开始定期评估患者状态、治疗反应以及抗抑郁治疗的不良反应(分级:强烈推荐;中等质量证据)。推荐意见3:美国医师协会建议,如果患者在重度抑郁症治疗开始后的6至8周内对药物治疗没有充分反应,临床医生应调整治疗方案(分级:强烈推荐;中等质量证据)。推荐意见4:美国医师协会建议,对于首次发作的重度抑郁症患者,在获得满意反应后,临床医生应持续治疗4至9个月。对于有2次或更多次抑郁发作的患者,更长时间的治疗可能有益(分级:强烈推荐;中等质量证据)。