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美国食品药品监督管理局的警告对全国样本中抗抑郁药使用情况的影响。

Effects of Food and Drug Administration warnings on antidepressant use in a national sample.

作者信息

Olfson Mark, Marcus Steven C, Druss Benjamin G

机构信息

New York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, 1051 Riverside Dr, New York, NY 10032, USA.

出版信息

Arch Gen Psychiatry. 2008 Jan;65(1):94-101. doi: 10.1001/archgenpsychiatry.2007.5.

Abstract

CONTEXT

In June 2003, the Food and Drug Administration (FDA) recommended that paroxetine hydrochloride not be used to treat young people because of potential increased risk of suicidal behavior, and in October 2004, the FDA issued a black box warning concerning all antidepressants for youth.

OBJECTIVE

To characterize associations between these warnings and antidepressant use.

DESIGN

Interrupted time series analyses of trends in antidepressant use were performed with Medco pharmacy and enrollment data stratified by patient age, sex, antidepressant type, and specialty of the prescribing physician across 3 study periods: prewarning (May 1, 2002 to June 19, 2003), paroxetine warning (June 20, 2003 to October 15, 2004), and black box warning (October 16, 2004 to December 31, 2005).

MAIN OUTCOME MEASURES

The rate of antidepressant use, annualized percentage change in rate of antidepressant use, and difference in trend of antidepressant use between consecutive study periods.

RESULTS

During the prewarning study period, there was a 36.0% per year (P < .001) increase in total youth (aged 6-17 years) antidepressant use, which was followed by decreases of -0.8% per year (P = .85) and -9.6% per year (P = .21) during the paroxetine and black box warning study periods, respectively. The difference in trends between the prewarning and paroxetine warning periods was significant (P < .001). Youth paroxetine use also significantly increased during the prewarning study period (30.0% per year; P < .001) before significantly declining during the paroxetine warning study period (-44.2% per year; P < .001), which was also a significant between-period difference in trends (P < .001). Changes in antidepressant use were less pronounced in adults than in youth. For adults 65 years and older, overall antidepressant use significantly increased (8.1% per year; P < .001) during the black box study period. Changes in the pattern of antidepressant use varied little by patient sex.

CONCLUSIONS

The paroxetine and black box warnings had modest and relatively targeted effects on the intended populations. These changes, which were greatest for youth, were broadly consistent with the FDA warnings and the scientific literature.

摘要

背景

2003年6月,美国食品药品监督管理局(FDA)建议不要使用盐酸帕罗西汀治疗年轻人,因为其有潜在增加自杀行为的风险;2004年10月,FDA发布了关于所有用于青少年的抗抑郁药的黑框警告。

目的

描述这些警告与抗抑郁药使用之间的关联。

设计

利用美可保健公司药房和注册数据进行中断时间序列分析,对抗抑郁药使用趋势进行分析,数据按患者年龄、性别、抗抑郁药类型以及开处方医生的专业在3个研究时间段进行分层:警告前(2002年5月1日至2003年6月19日)、帕罗西汀警告期(2003年6月20日至2004年10月15日)和黑框警告期(2004年10月16日至2005年12月31日)。

主要观察指标

抗抑郁药使用率、抗抑郁药使用率的年化百分比变化以及连续研究时间段之间抗抑郁药使用趋势的差异。

结果

在警告前的研究时间段,青少年(6至17岁)抗抑郁药总使用量每年增加36.0%(P <.001),随后在帕罗西汀警告期和黑框警告期分别下降-0.8%/年(P =.85)和-9.6%/年(P =.21)。警告前和帕罗西汀警告期之间的趋势差异具有统计学意义(P <.001)。在警告前的研究时间段,青少年帕罗西汀使用量也显著增加(每年30.0%;P <.001),在帕罗西汀警告期显著下降(每年-44.2%;P <.001),这也是时间段之间显著的趋势差异(P <.001)。抗抑郁药使用的变化在成年人中不如在青少年中明显。对于65岁及以上的成年人,在黑框警告期,总体抗抑郁药使用量显著增加(每年8.1%;P <.001)。抗抑郁药使用模式的变化在不同性别患者中差异不大。

结论

帕罗西汀和黑框警告对目标人群有适度且相对有针对性的影响。这些变化在青少年中最为显著,与FDA的警告和科学文献大致一致。

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