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精神分裂症患者帕利哌酮棕榈酸酯治疗的剂量调整和转换的实用指南。

Practical guidance for dosing and switching paliperidone palmitate treatment in patients with schizophrenia.

机构信息

Johnson & Johnson PRD, LLC, 1125 Trenton-Harbourton Rd, Titusville, NJ 08560, USA.

出版信息

Curr Med Res Opin. 2010 Feb;26(2):377-87. doi: 10.1185/03007990903482772.

Abstract

OBJECTIVE

This article overviews the recommended dosing strategies for the treatment of schizophrenia patients using the recently FDA-approved once-monthly long-acting injectable atypical antipsychotic, paliperidone palmitate.

METHODS

Using pharmacokinetic (PK), efficacy and safety data from clinical trials and a comprehensive population PK simulation model, dosing recommendations for paliperidone palmitate have been generated.

RESULTS

The recommended initiation regimen is 150 mg eq. paliperidone palmitate (234 mg) on Day 1 followed by 100 mg eq. paliperidone palmitate (156 mg) on Day 8, each administered into the deltoid muscle, using a 1-inch 23 gauge (G) needle in those <90 kg and a 1.5-inch 22 G needle in those > or =90 kg. No oral supplementation is required. Monthly maintenance doses of paliperidone palmitate range from 25-150 mg eq. (39-234 mg; recommended dose of 75 mg eq. [117 mg]) injected into the deltoid (using weight-adjusted needle) or gluteal (using 1.5 inch 22 G needle) muscle. The Day 8 dose may be administered +/-2 days and monthly doses +/-7 days, without a clinically significant impact on plasma concentrations. In patients with mild renal impairment (creatinine clearance [CrCL]: 50-80 mL/min), dosage should be adjusted. No dose adjustment is required in patients with mild or moderate hepatic impairment; no data currently exist regarding severe hepatic impairment. Elderly patients with normal renal function should receive the same dosage as younger adult patients with normal renal function. In the event of an age-related decline in CrCL, dosage should be adjusted accordingly. Paliperidone palmitate treatment can be initiated the day after discontinuing previous oral antipsychotic treatment. Paliperidone palmitate should be initiated at the next scheduled injection, and monthly thereafter, in patients switching from other long-acting injectable antipsychotics, including long-acting risperidone.

CONCLUSIONS

These data provide practical guidance to clinicians on how to use paliperidone palmitate in adult patients with schizophrenia.

摘要

目的

本文综述了最近经美国食品药品监督管理局(FDA)批准的每月一次长效注射用非典型抗精神病药棕榈酸帕利哌酮的推荐剂量策略,用于治疗精神分裂症患者。

方法

根据临床试验的药代动力学(PK)、疗效和安全性数据以及综合群体 PK 模拟模型,制定了棕榈酸帕利哌酮的推荐剂量方案。

结果

推荐的起始方案为第 1 天给予 150mg 等效剂量的棕榈酸帕利哌酮(234mg),随后第 8 天给予 100mg 等效剂量的棕榈酸帕利哌酮(156mg),均通过 1 英寸 23 号(G)针在 <90kg 体重的患者中、1.5 英寸 22 号针在 >或=90kg 体重的患者中进行三角肌肌内注射。不需要口服补充。棕榈酸帕利哌酮的每月维持剂量为 25-150mg 等效剂量(39-234mg;推荐剂量为 75mg 等效剂量[117mg]),通过三角肌(使用体重调整后的针)或臀肌(使用 1.5 英寸 22 号针)肌肉注射。第 8 天的剂量可在 +/-2 天内给予,每月剂量可在 +/-7 天内给予,不会对血浆浓度产生显著影响。在轻度肾功能不全(肌酐清除率[CrCL]:50-80ml/min)患者中,应调整剂量。在轻度或中度肝功能不全患者中无需调整剂量;目前尚无关于严重肝功能不全患者的相关数据。肾功能正常的老年患者应接受与肾功能正常的年轻成年患者相同的剂量。在 CrCL 与年龄相关下降的情况下,应相应调整剂量。在停止先前的口服抗精神病药物治疗后,可在第二天开始使用棕榈酸帕利哌酮治疗。在切换为其他长效注射用抗精神病药物(包括长效利培酮)的患者中,应在下一次预定注射时开始使用棕榈酸帕利哌酮,并在之后每月使用一次。

结论

这些数据为临床医生提供了如何在成人精神分裂症患者中使用棕榈酸帕利哌酮的实用指导。

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