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Risperidone long acting injection: Findings of a 2-year retrospective follow-up study

机译:利培酮长效注射:为期2年的回顾性随访研究的结果

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Objective. The aim of this retrospective study was to assess the clinical effectiveness of risperidone long acting injection (RLAI) at 2 years within an acute mental health setting. Method. All patients who received RLAI between July 2002 and December 2004 were identified from pharmacy records, and data collected by retrospective case note review. In order to give an indication that their condition was unresponsive to treatment, patients' drug histories were reviewed to determine whether or not they had previously been treated with clozapine or received two or more failed trials of other antipsychotic medication. Results. Eighty-four patients were included in the study and 56 discontinued at 2 years. The most common reason for treatment discontinuation was lack of effectiveness, accounting for 32 patients, whilst eight patients discontinued due to adverse effects. Patients remaining on treatment spent 67% of the time in an outpatient setting. Conclusion. The proportion of patients remaining on RLAI at 2 years was 33%. Limitations of the naturalistic methodology used in this study hindered any precise determination of which patients were likely to continue RLAI. However, it was apparent that a history of previous treatment failure with at least two antipsychotics was associated with RLAI treatment discontinuation.
机译:目的。这项回顾性研究的目的是评估利培酮长效注射液(RLAI)在急性精神健康状况下2年的临床效果。方法。从药房记录中确定所有2002年7月至2004年12月期间接受RLAI的患者,并通过回顾性病例笔记审查收集数据。为了表明他们的病情对治疗无反应,对患者的药物史进行了回顾,以确定他们以前是否曾接受过氯氮平治疗或是否接受过两次或更多次其他抗精神病药物的失败试验。结果。这项研究纳入了84位患者,其中56位在2年后停药。停药最常见的原因是缺乏疗效,占32例,而有8例因不良反应而停药。继续接受治疗的患者在门诊环境中花费了67%的时间。结论。 2年时仍接受RLAI的患者比例为33%。本研究中使用的自然方法学的局限性阻碍了对哪些患者可能继续进行RLAI的任何精确测定。然而,很明显,至少有两种抗精神病药的既往治疗失败史与RLAI治疗中断有关。

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