Phuong Tran, Susan dosReis, Eberechukwu Onukwugha, Haeyoung Lee, Julia F Slejko
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引用次数: 0
Abstract
Background: Individuals with depression who do not respond to initial antidepressant may switch to a different antidepressant, add a second antidepressant, or add an atypical antipsychotic. Previous studies comparing these strategies' efficacy and safety reported conflicting results, and the impact of these strategies on subsequent health care utilization is unknown.
Objective: To compare health care utilization between individuals with depression who switched antidepressants, added a second antidepressant (ie, combination), or added an atypical antipsychotic (ie, augmentation) following their initial antidepressant.
Methods: This retrospective cohort study used a 25% random sample of the IQVIA PharMetrics Plus for Academics health plan claims database. The study cohort included individuals aged 10-64 years who newly initiated an antidepressant at any point from January 2016 to December 2020. New use was defined as no evidence of an antidepressant in the 180 days preceding the antidepressant dispensing. Individuals had to have a depression diagnosis and a treatment change in the 180 days following the initial antidepressant. The index date was the date of the first observed antidepressant change, which was defined as a switch, combination, or augmentation. Health care utilization, measured as the number of outpatient visits, any all-cause hospitalization, and any emergency department (ED) visit, was assessed in the 180 days after the index date. Negative binomial regression models evaluated the rate ratio of the number of outpatient visits. Logistic regression models estimated the odds ratio of a hospitalization, and modified Poisson regression estimated the relative risk of an ED visit. Models were adjusted for demographics, clinical characteristics, and previous health care utilization.
Results: Among 3,847 individuals with depression who had the first treatment change following the initial antidepressant, we identified 2,418 (62.9%) who switched, 1,268 (33.0%) who combined, and 161 (4.2%) who augmented their antidepressant. The augmentation group had a significantly higher rate of outpatient visits than the combination group (adjusted rate ratio = 1.14, 95% CI = 1.04-1.25). There was no statistically significant difference in hospitalizations or ED visits between the switch and augmentation vs combination groups.
Conclusions: Augmentation comprised 4% of our antidepressant cohort but had higher outpatient health care utilization than those who combined treatment.
背景:对初始抗抑郁药无反应的抑郁症患者可改用不同的抗抑郁药,加用第二种抗抑郁药,或加用非典型抗精神病药。先前比较这些策略的有效性和安全性的研究报告了相互矛盾的结果,这些策略对随后的医疗保健利用的影响是未知的。目的:比较抑郁症患者在初始抗抑郁药后转换抗抑郁药、添加第二种抗抑郁药(即联合)或添加非典型抗抑郁药(即增强)的医疗保健利用情况。方法:本回顾性队列研究使用IQVIA PharMetrics Plus for Academics健康计划索赔数据库中25%的随机样本。该研究队列包括在2016年1月至2020年12月期间任何时间点新开始服用抗抑郁药的10-64岁个体。新用药被定义为在配发抗抑郁药前180天内没有抗抑郁药的证据。受试者必须在最初服用抗抑郁药后的180天内被诊断出患有抑郁症并改变治疗方法。指标日期是第一次观察到抗抑郁药物变化的日期,其定义为转换、联合或增强。在指标日期后180天内评估医疗保健利用情况,以门诊就诊次数、全因住院次数和急诊就诊次数来衡量。负二项回归模型评估门诊次数的比率。Logistic回归模型估计住院的优势比,修正泊松回归估计急诊科就诊的相对风险。根据人口统计学、临床特征和以前的医疗保健利用情况对模型进行了调整。结果:在3847名抑郁症患者中,我们确定了2418名(62.9%)转换治疗,1268名(33.0%)联合治疗,161名(4.2%)增加抗抑郁药物。增强组门诊就诊率显著高于联合组(调整率比= 1.14,95% CI = 1.04 ~ 1.25)。转换组和增强组与联合组在住院或急诊科就诊方面没有统计学上的显著差异。结论:增强治疗占抗抑郁队列的4%,但门诊保健使用率高于联合治疗组。
期刊介绍:
JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.