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度洛西汀的给药模式和重度抑郁症患者开具高剂量处方的预测因素:来自美国第三方支付者视角的分析。

Dosing patterns for duloxetine and predictors of high-dose prescriptions in patients with major depressive disorder: analysis from a United States third-party payer perspective.

机构信息

Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.

出版信息

Clin Ther. 2011 Nov;33(11):1726-38. doi: 10.1016/j.clinthera.2011.09.027. Epub 2011 Oct 22.

Abstract

BACKGROUND

Major depressive disorder (MDD) is a common illness that affects ∼7% of adults in the United States each year. Duloxetine is a dual reuptake inhibitor of serotonin and norepinephrine that has demonstrated efficacy and tolerability in the treatment of MDD.

OBJECTIVE

The purpose of our study was to examine dosing patterns and pretreatment predictors of high-dose duloxetine therapy for patients with MDD in the usual clinical setting.

METHODS

Data were from 6132 commercially insured patients with MDD initiated on duloxetine during 2005 and 2006. Patients had no duloxetine use in the previous 6 months and had continuous enrollment in a health plan for the 12 months immediately preceding and following initiation. Dosing patterns and predictors of high-dose therapy with duloxetine were examined.

RESULTS

Initial doses of duloxetine were <60 mg/d, 60 mg/d, 90 mg/d, and ≥120 mg/d for 32.4%, 60.9%, 3.1%, and 3.5% of patients, respectively. Maximum daily doses were <60 mg, 60 mg, 90 mg, and ≥120 mg for 16.3%, 59.3%, 11.0%, and 13.3% of patients, respectively. Patients treated with >60 mg/d for at least 2 months were older, were more likely to have been treated by a psychiatrist, had greater comorbidity, and had used more health care resources and psychotropic and pain medications in the previous year. The following factors were independently associated with doses of >60 mg/d: older age (odds ratio [OR] = 1.33-1.46); comorbid neuropathic pain (OR = 1.88); fibromyalgia (OR = 1.36); dysthymic disorder (OR = 1.24); prior injury/poisoning (OR = 1.19); physician specialty (psychiatrist, OR = 1.55); and prior use of psychostimulants (OR = 1.26), benzodiazepines (OR = 1.19), venlafaxine (OR = 1.35), or atypical antipsychotics (OR = 1.35).

CONCLUSIONS

Most of the commercially insured patients in this dataset were initiated and maintained on a duloxetine dose of 60 mg/d. Although the data are limited in their generalizability, the characteristics associated with higher dose therapy describe a complex group of patients who may require more intensive drug treatment and monitoring.

摘要

背景

重度抑郁症(MDD)是一种常见疾病,每年影响美国约 7%的成年人。度洛西汀是一种 5-羟色胺和去甲肾上腺素的双重再摄取抑制剂,在治疗 MDD 方面已显示出疗效和耐受性。

目的

我们的研究目的是在常规临床环境中检查 MDD 患者接受度洛西汀高剂量治疗的剂量模式和预处理预测因子。

方法

数据来自 2005 年和 2006 年接受度洛西汀治疗的 6132 名商业保险患者。患者在过去 6 个月内没有使用度洛西汀,并且在开始治疗前的 12 个月内连续参加了一项健康计划。检查了度洛西汀高剂量治疗的剂量模式和预测因素。

结果

度洛西汀的初始剂量分别为<60mg/d、60mg/d、90mg/d 和≥120mg/d,占 32.4%、60.9%、3.1%和 3.5%的患者。最大日剂量分别为<60mg、60mg、90mg 和≥120mg,占 16.3%、59.3%、11.0%和 13.3%的患者。至少连续 2 个月接受>60mg/d 治疗的患者年龄较大,更有可能接受精神科医生治疗,合并症更多,并且在过去一年中使用了更多的医疗保健资源和精神药物和止痛药。以下因素与剂量>60mg/d 独立相关:年龄较大(优势比[OR]为 1.33-1.46);伴发神经病理性疼痛(OR=1.88);纤维肌痛(OR=1.36);恶劣心境障碍(OR=1.24);既往损伤/中毒(OR=1.19);医生专科(精神科医生,OR=1.55);以及先前使用精神兴奋剂(OR=1.26)、苯二氮卓类药物(OR=1.19)、文拉法辛(OR=1.35)或非典型抗精神病药(OR=1.35)。

结论

该数据集中的大多数商业保险患者开始并维持度洛西汀 60mg/d 的剂量。尽管数据的普遍性有限,但与更高剂量治疗相关的特征描述了一组可能需要更强化药物治疗和监测的复杂患者。

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