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美国食品药品监督管理局就青少年自杀风险发布咨询报告前后抗抑郁药处方的全国趋势

National trends in prescribing antidepressants before and after an FDA advisory on suicidality risk in youths.

机构信息

United BioSource Corporation, 430 Bedford St., Lexington, MA 02420, USA.

出版信息

Psychiatr Serv. 2011 Jul;62(7):727-33. doi: 10.1176/ps.62.7.pss6207_0727.

DOI:10.1176/ps.62.7.pss6207_0727
PMID:21724784
Abstract

OBJECTIVE

This study evaluated the national trends in prescribing pharmacologic treatments for pediatric depression before and after a 2003 U.S. Food and Drug Administration advisory linking an increased risk of suicidality with antidepressants among pediatric patients with major depressive disorder.

METHODS

National estimates on outpatient visits between 1998 and 2007 with a diagnosis of depression, a prescription for an antidepressant, or both among children ages 5 to 17 and adults were obtained from the National Ambulatory Medical Care Survey and the National Hospital Ambulatory Medical Care Survey.

RESULTS

Among children, depression visits increased from 1998-1999 to 2002-2003 (3.2 and 4.3 million, respectively) but decreased to 3.2 million in 2006-2007. Antidepressant visits increased from 1998-1999 to 2002-2003 (3.4 and 7.6 million, respectively) but dropped to 6.7 million in 2006-2007. Depression visits with an antidepressant prescribed rose from 1998-1999 to 2002-2003 (1.7 and 2.8 million, respectively) but dropped in 2004-2005 and 2006-2007 (2.4 and 2.1 million, respectively). Nevertheless, the proportion of depression visits with an antidepressant prescribed, having risen from 54% in 1998-1999 to 66% in 2002-2003, remained stable in 2004-2005 (65%) and in 2006-2007 (64%), the result, seemingly, of more prescribing of antidepressants for major depressive disorder and less for other depression. Utilization patterns among adults were not interrupted.

CONCLUSIONS

Children's depression visits and visits with an antidepressant prescribed dropped after the advisory, but children with major depressive disorder appeared no less likely to be prescribed antidepressants.

摘要

目的

本研究评估了美国食品和药物管理局(FDA)于 2003 年发布的一则公告前后,针对儿童重度抑郁症患者,抗抑郁药物可能增加自杀风险这一警示对开具此类药物的国家趋势的影响。

方法

通过国家门诊医疗调查和国家医院门诊医疗调查,我们获得了 1998 年至 2007 年期间,5 至 17 岁儿童和成人的抑郁诊断、抗抑郁药物处方或两者兼有的门诊就诊的全国估计数。

结果

在儿童中,抑郁就诊从 1998-1999 年至 2002-2003 年(分别为 320 万和 430 万)增加,但在 2006-2007 年减少至 320 万。抗抑郁就诊从 1998-1999 年至 2002-2003 年(分别为 340 万和 760 万)增加,但在 2006-2007 年降至 670 万。开抗抑郁药的抑郁就诊从 1998-1999 年至 2002-2003 年(分别为 170 万和 280 万)增加,但在 2004-2005 年和 2006-2007 年(分别为 240 万和 210 万)下降。然而,开抗抑郁药的抑郁就诊比例从 1998-1999 年的 54%上升至 2002-2003 年的 66%,在 2004-2005 年(65%)和 2006-2007 年(64%)保持稳定,这似乎是因为更多地开具抗抑郁药治疗重度抑郁症,而不是其他抑郁症。成年人的使用模式并未中断。

结论

警示发布后,儿童的抑郁就诊和开抗抑郁药的就诊减少,但重度抑郁症患儿似乎更有可能开抗抑郁药。

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