首页> 外文期刊>The journal of clinical psychiatry >Patient compliance with enteric-coated weekly fluoxetine during continuation treatment of major depressive disorder.
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Patient compliance with enteric-coated weekly fluoxetine during continuation treatment of major depressive disorder.

机译:在持续治疗重度抑郁症期间,患者应每周接受肠溶衣氟西汀治疗。

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BACKGROUND: A once-weekly enteric-coated formulation of fluoxetine represents a new, effective option for the long-term treatment of clinically diagnosed depression. This study assessed compliance with the new once-weekly fluoxetine as compared with once-daily fluoxetine treatment. METHOD: Adult patients from the United Kingdom who had responded to fluoxetine treatment for a current episode of depression (DSM-IV criteria) were monitored for compliance with daily and weekly dose administration of fluoxetine. The study consisted of 2 study phases. Study phase I was a baseline assessment of 20 mg of fluoxetine daily dosing for 4 weeks (N = 117). The second phase of the study consisted of randomly assigning patients to either once-weekly (90 mg/wk) or once-daily (20 mg/day) fluoxetine for 3 months (weekly, N = 56; daily, N = 53). Compliance with the dosing regimen was measured using an electronic Drug Exposure Monitor (eDEM, AARDEX Ltd., Zug, Switzerland). RESULTS: For those patients randomly assigned to weekly fluoxetine, compliance was 85.4% during study period I while on treatment with daily fluoxetine and then 87.5% while on treatment with weekly fluoxetine. This difference was not significant. For once-daily dosing, however, compliance declined from 87.3% during period I to 79.4% during period II (p < .001). After adjusting for compliance during study period I, weekly compliance during study period II was 87.8% and daily compliance was 79.0%, a statistically significant difference (p = .006). CONCLUSION: Compliance with once-weekly fluoxetine was better than that with once-daily fluoxetine. Compliance decreased over time when patients remained on daily dosing; however, when patients switched from daily dosing to weekly dosing, compliance did not decrease. The results of this study allay concerns about inferior compliance with a once-weekly regimen compared with the conventional once-daily regimen.
机译:背景:氟西汀每周一次的肠溶制剂代表了对临床诊断的抑郁症进行长期治疗的一种新的有效选择。这项研究评估了与每周一次氟西汀治疗相比,每周一次新氟西汀的依从性。方法:监测来自英国的对氟西汀治疗引起当前抑郁发作(DSM-IV标准)的成年患者,观察其每日和每周服用氟西汀的依从性。该研究包括两个研究阶段。研究第一阶段是基线评估,每天服用20 mg氟西汀4周(N = 117)。研究的第二阶段包括将患者随机分配至每周一次(90 mg / wk)或每天一次(20 mg /天)氟西汀3个月(每周,N = 56;每天,N = 53)。使用电子药物暴露监测器(eDEM,瑞士祖格市AARDEX Ltd.)测量对给药方案的依从性。结果:对于那些随机分配到每周氟西汀治疗的患者,在研究期I中,每日氟西汀治疗的依从性为85.4%,然后在每周氟西汀治疗的依从性为87.5%。这种差异并不明显。但是,对于每天一次的给药,依从性从第一阶段的87.3%降至第二阶段的79.4%(p <.001)。在对研究阶段I的依从性进行调整后,研究阶段II中的每周依从性为87.8%,每天的依从性为79.0%,具有统计学显着性差异(p = .006)。结论:氟西汀每周一次的依从性优于氟西汀每天一次。当患者每天继续用药时,依从性会随着时间的推移而降低;但是,当患者从每日给药转为每周给药时,依从性并没有降低。这项研究的结果减轻了人们对每周一次的治疗方案与常规每天一次的治疗方案的依从性较差的担忧。

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