Otsuka Pharmaceutical Development and Commercialization Inc, Princeton, NJ, USA.
Lundbeck LLC, Deerfield, IL, USA.
J Med Econ. 2023 Jan-Dec;26(1):316-325. doi: 10.1080/13696998.2023.2178770.
To evaluate the impact of timing of aripiprazole once-monthly (AOM) initiation on healthcare resource utilization (HCRU), risk of hospitalization, and healthcare costs in patients with schizophrenia.
A retrospective cohort study was conducted using data from the Merative MarketScan database (01/01/2013-12/31/2019). Adults aged ≥18 years with a new episode of care for schizophrenia and an AOM claim were included. Patients were classified into two cohorts based on the time between the first schizophrenia diagnosis and the first AOM claim (early cohort: ≤1 year; late cohort: >1 year). All-cause and psychiatric-specific HCRU, risk of hospitalization, and healthcare costs were evaluated over 1-year post-AOM initiation. The relationship between the timing of AOM initiation and HCRU was evaluated using negative binomial regression, and healthcare costs using generalized linear models (log-link with gamma distribution). Logistic regression was used to estimate the likelihood of hospitalization during the follow up period for both all-cause and psychiatric-specific hospitalization.
A total of 945 patients were included (early cohort: = 525; late cohort: = 420). At baseline, the early cohort had lower mean age, a greater proportion of males, and a lower mean Charlson Comorbidity Index score than the late cohort (all < .05). After adjusting for baseline demographic and clinical characteristics, all-cause and psychiatric-specific hospitalization during the 1-year follow-up period were statistically significantly higher for the late cohort versus the early cohort (all-cause: incident rate ratio [IRR] = 1.63, 95% confidence interval [CI]: 1.28-2.07, < .01; psychiatric-specific: IRR = 1.93, 95% CI: 1.46-2.55, < .01). The early cohort had statistically significantly lower adjusted all-cause ($21,686 versus $29,033; = .0002) and psychiatric-specific ($24,414 versus $32,461; = .0002) healthcare costs versus the late cohort.
This study utilized claims data, which are intended for administrative purposes rather than for research.
This analysis extends previous evidence for the benefits of AOM in patients with new episodes of schizophrenia, by demonstrating lower HCRU, risk of hospitalization, and healthcare costs with early AOM initiation compared with later initiation.
评估阿立哌唑一月一次制剂(AOM)起始时间对精神分裂症患者的医疗资源利用(HCRU)、住院风险和医疗成本的影响。
本研究采用 Merative MarketScan 数据库(2013 年 1 月 1 日至 2019 年 12 月 31 日)中的数据进行回顾性队列研究。纳入新诊断为精神分裂症且有 AOM 用药记录的年龄≥18 岁的成年人。根据首次精神分裂症诊断与首次 AOM 用药之间的时间,将患者分为两个队列(早期队列:≤1 年;晚期队列:>1 年)。评估 AOM 起始后 1 年的全因和精神科特定 HCRU、住院风险和医疗成本。使用负二项回归评估 AOM 起始时间与 HCRU 之间的关系,并使用广义线性模型(对数链接,伽马分布)评估医疗成本。使用逻辑回归估计随访期间全因和精神科特定住院的住院可能性。
共纳入 945 例患者(早期队列:n=525;晚期队列:n=420)。基线时,早期队列的平均年龄较低,男性比例较高,Charlson 合并症指数评分较低(均 < .05)。调整基线人口统计学和临床特征后,晚期队列的全因和精神科特定住院在 1 年随访期间均显著高于早期队列(全因:发生率比 [IRR] = 1.63,95%置信区间 [CI]:1.28-2.07, < .01;精神科特定:IRR = 1.93,95% CI:1.46-2.55, < .01)。早期队列的全因($21686 与 $29033; = .0002)和精神科特定($24414 与 $32461; = .0002)医疗成本均显著低于晚期队列。
本研究使用的是旨在用于行政目的而非研究目的的索赔数据。
本分析通过证明与晚期起始相比,早期起始 AOM 可降低新诊断精神分裂症患者的 HCRU、住院风险和医疗成本,扩展了 AOM 对新发作精神分裂症患者有益的证据。