Robinson D S, Cooper T B, Ravaris C L, Ives J O, Nies A, Bartlett D, Lamborn K R
Psychopharmacology (Berl). 1979 Jun 21;63(3):223-31. doi: 10.1007/BF00433554.
In a double-blind phenelzine controlled clinical trial, 49 depressed outpatients were treated with a fixed dose of amitriptyline (AMI) 150 mg/day for 6 weeks. No significant relationships were found between steady-state plasma levels of AMI and its metabolite, nortriptyline, at 4 weeks and therapeutic response at 6 weeks or side effects. In the patient subgroup with more severe endogenous symptoms, there was a general trend for a weak positive association between AMI plasma levels and clinical improvement. Plasma tricyclic determinations appear to have little if any predictive value for antidepressant effect in outpatients treated with AMI.
在一项双盲苯乙肼对照临床试验中,49名门诊抑郁症患者接受固定剂量的阿米替林(AMI)治疗,剂量为150毫克/天,持续6周。在第4周时,未发现AMI及其代谢产物去甲替林的稳态血浆水平与第6周时的治疗反应或副作用之间存在显著关系。在具有更严重内源性症状的患者亚组中,AMI血浆水平与临床改善之间普遍存在弱正相关的趋势。对于接受AMI治疗的门诊患者,血浆三环类药物测定对其抗抑郁效果似乎几乎没有预测价值。