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Pharmacokinetic consequences of a citalopram treatment discontinuation.

机译:西酞普兰治疗中止的药代动力学后果。

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In this pilot study, the pharmacokinetics of citalopram (CIT) were examined in five hospitalized depressed patients after an abrupt discontinuation of a treatment with 40 mg/d of this selective serotonin reuptake inhibitor (SSRI). During the 8-day study period, clinical ratings were regularly carried out. Between days 5 and 8, the patients were treated with clomipramine (75 mg/d). The enantiomers of CIT and its metabolites, demethyl-CIT (DCIT) and CIT-propionic acid derivative (CIT-PROP), were measured repeatedly from day 0 to day 8 by a stereoselective high-performance liquid chromatography (HPLC) procedure. The following drug plasma half-lives were measured (means +/- SD): R-CIT: 66+/-11 h; S-CIT: 42+/-13 h; R-DCIT: 228+/-148 h; S-DCIT: 93+/-35 h; R-CIT-PROP: 82+/-31 h; S-CIT-PROP: 186+/-93 h.
机译:在这项前瞻性研究中,在突然中断以40 mg / d的选择性5-羟色胺再摄取抑制剂(SSRI)治疗后,对五名住院的抑郁症患者进行了西酞普兰(CIT)的药代动力学研究。在8天的研究期内,定期进行临床评估。在第5至8天之间,患者接受氯米帕明(75 mg / d)的治疗。通过立体选择性高效液相色谱(HPLC)从第0天到第8天重复测量CIT及其代谢物的对映体,即去甲基CIT(DCIT)和CIT-丙酸衍生物(CIT-PROP)。测量了以下药物血浆半衰期(平均值+/- SD):R-CIT:66 +/- 11 h; S-CIT:42 +/- 13 h; R-DCIT:228 +/- 148小时; S-DCIT:93 +/- 35 h; R-CIT-PROP:82 +/- 31小时; S-CIT-PROP:186 +/- 93小时。

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