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Plasma Risperidone Concentrations During Combined Treatment with Sertraline.

机译:舍曲林联合治疗期间血浆利培酮浓度。

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The effect of sertraline on the steady-state plasma concentrations of risperidone and its active metabolite 9-hydroxyrisperidone (9-OH-risperidone) was studied in 11 patients with schizophrenia or schizoaffective disorder. To treat concomitant depressive symptoms, additional sertraline, at the dose of 50 mg/d, was administered for 4 weeks to patients stabilized on risperidone (4-6 mg/d). Mean plasma concentrations of risperidone, 9-OH-risperidone, and the active moiety (sum of the concentrations of risperidone and 9-OH-risperidone) did not change significantly during combined treatment with sertraline. At the end of week 4, sertraline dosage was adjusted in some patients on the basis of the individual response and then maintained until the end of week 8. At final evaluation, mean plasma levels of risperidone active moiety were not modified in the 4 patients who were still receiving the initial sertraline dose, but concentrations were slightly but not significantly increased (by a mean 15% over pretreatment) in the subgroup of 5 subjects treated with a final dose of 100 mg/d. In the 2 patients receiving the highest dose of sertraline, 150 mg/d, at week 8 total plasma risperidone concentrations were increased by 36% and 52%, respectively, as compared with baseline values. Sertraline coadministration with risperidone was well tolerated, and no patient developed extrapyramidal symptoms. These findings indicate that sertraline at dosages up to 100 mg/d is not associated with clinically significant changes in plasma risperidone concentrations. However, higher doses of sertraline may elevate plasma risperidone levels, presumably as a result of a dose-dependent inhibitory effect of sertraline on CYP2D6-mediated 9-hydroxylation of risperidone.
机译:在11例精神分裂症或精神分裂症患者中研究了舍曲林对利培酮及其活性代谢物9-羟基利培酮(9-OH-利培酮)稳态血药浓度的影响。为了治疗伴随的抑郁症状,对稳定于利培酮(4-6 mg / d)的患者以50 mg / d的剂量给予另外的舍曲林治疗4周。在舍曲林联合治疗期间,利培酮,9-OH-利培酮和活性部分的平均血浆浓度(利培酮和9-OH-利培酮的浓度之和)没有明显变化。在第4周末,根据个体反应调整某些患者的舍曲林剂量,然后维持至第8周末。在最终评估中,这4例患者的利培酮活性成分平均血浆水平未改变仍接受初始舍曲林剂量,但在最终剂量为100 mg / d的5名受试者的亚组中,其浓度略有但未显着增加(平均比预处理高15%)。与基线值相比,在第8周接受最高剂量舍曲林150 mg / d的2位患者中,总血浆利培酮浓度分别增加了36%和52%。舍曲林与利培酮共同给药的耐受性良好,没有患者出现锥体束外症状。这些发现表明剂量高达100 mg / d的舍曲林与血浆利培酮浓度的临床显着变化无关。然而,较高剂量的舍曲林可能会升高血浆利培酮水平,这可能是舍曲林对CYP2D6介导的利培酮的9-羟基化作用的剂量依赖性抑制作用的结果。

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