Simon G E, Heiligenstein J H, Grothaus L, Katon W, Revicki D
Center for Health Studies, Group Health Cooperative, Seattle, Wash. 98101-1448, USA.
J Clin Psychiatry. 1998 Feb;59(2):49-55. doi: 10.4088/jcp.v59n0202.
The more sedating antidepressants are often recommended for patients presenting with anxiety or insomnia. We examine whether baseline anxiety or insomnia symptoms (1) show differential response to fluoxetine or imipramine or (2) predict differences between drugs in overall clinical response or likelihood of medication discontinuation.
336 health maintenance organization primary care patients beginning antidepressant treatment for depression were randomly assigned to an initial prescription for fluoxetine or imipramine. All subsequent care (medication dosage, change, or discontinuation) was managed as usual by the primary care physician. The 17-item Hamilton Rating Scale for Depression (HAM-D) and the Hopkins Symptom Checklist (SCL) anxiety and depression subscales were administered prior to randomization and 1 month later.
Rates of improvement in insomnia (HAM-D insomnia items), agitation (HAM-D agitation item), and anxiety (SCL anxiety subscale) were essentially identical in the two treatment groups. Baseline level of insomnia did not predict significant differences between randomization groups in improvement in overall HAM-D score (p = .44) or SCL depression subscale (p = .44). Similarly, baseline level of anxiety did not predict significant differences in improvement in HAM-D (p = .19) or SCL depression subscale (p = .31). Patients assigned to fluoxetine were significantly less likely to change or discontinue antidepressant medication during the first month, but this difference did not vary according to baseline level of insomnia (p = .68) or anxiety (p = .25).
Among patients with moderate depression, baseline levels of insomnia or anxiety should not influence the choice of fluoxetine or imipramine as an initial antidepressant.
对于伴有焦虑或失眠的患者,通常推荐使用镇静作用更强的抗抑郁药。我们研究了基线焦虑或失眠症状是否(1)对氟西汀或丙咪嗪表现出不同的反应,或(2)预测药物在总体临床反应或停药可能性方面的差异。
336名开始接受抗抑郁治疗的健康维护组织初级保健患者被随机分配接受氟西汀或丙咪嗪的初始处方。所有后续治疗(药物剂量、更改或停药)均由初级保健医生按常规管理。在随机分组前和1个月后,使用17项汉密尔顿抑郁评定量表(HAM-D)以及霍普金斯症状清单(SCL)的焦虑和抑郁分量表进行评估。
两个治疗组在失眠(HAM-D失眠项目)、激越(HAM-D激越项目)和焦虑(SCL焦虑分量表)方面的改善率基本相同。失眠的基线水平并未预测随机分组组在总体HAM-D评分改善(p = 0.44)或SCL抑郁分量表(p = 0.44)方面的显著差异。同样,焦虑的基线水平也未预测HAM-D(p = 0.19)或SCL抑郁分量表(p = 0.31)改善方面的显著差异。被分配接受氟西汀治疗的患者在第一个月内更换或停用抗抑郁药物的可能性显著更低,但这种差异并不因失眠(p = 0.68)或焦虑(p = 0.25)的基线水平而有所不同。
在中度抑郁症患者中,失眠或焦虑的基线水平不应影响氟西汀或丙咪嗪作为初始抗抑郁药的选择。