Richards Kristin, Johnsrud Michael, Zacker Christopher, Sasané Rahul
TxCORE (Texas Center for Health Outcomes Research and Education), College of Pharmacy, The University of Texas at Austin, 2409 University Avenue, Mail Stop A1930, Austin, TX, 78712, USA.
Cerevel Therapeutics, LLC, Cambridge, MA, USA.
Community Ment Health J. 2025 Apr;61(3):432-439. doi: 10.1007/s10597-024-01347-7. Epub 2024 Sep 6.
Researchers have used elements of administrative healthcare claims data (e.g., diagnosis codes and medications) to calculate rates of extrapyramidal symptoms (EPS) in patients with schizophrenia who utilize second-generation antipsychotics (SGAs). However, a detailed description of claims-based EPS evidence has not been previously provided, which is the objective of the current study. This descriptive study, using 2016-2020 de-identified multi-state Medicaid administrative claims data, followed patients diagnosed with schizophrenia for 12 months after initiation of SGA therapy to identify and describe the first evidence of EPS. Time to EPS evidence was calculated and continuously-eligible patients were followed for an additional 12 months to examine EPS medication utilization and costs. Following SGA initiation, 13.6% (n = 2,288) of patients had evidence of EPS during the 12-month follow-up period. Mean time to first evidence of EPS after SGA initiation was 103.7 days (sd = 112.2, median = 58). For a majority of patients (n = 1,636, 71.5%), an EPS medication claim was the initial evidence of EPS, rather than an EPS diagnostic claim. Additionally, a quarter of patients (25.3%) in the EPS evidence cohort had a claim for an EPS medication on the same date as SGA initiation, possibly indicating prophylactic prescribing to prevent EPS development. Nearly 93% of those with EPS medication claims were treated with benztropine, while less than 2% received deutetrabenazine or valbenazine (indicated for tardive dyskinesia (TD)). Annual per patient EPS medication expenditures were $804 (sd = 7,080) overall, but only $40 (sd = 104) when excluding the higher-cost TD medications. Nearly 14% of Medicaid patients with schizophrenia who initiated SGA treatment had evidence of EPS based on claims data. The majority of the time, this evidence was derived from a prescription claim for a medication to treat EPS, rather than an EPS diagnostic claim. Prophylactic prescribing for EPS occurred more often than expected and should be explored more fully. While the cost of traditional EPS medications minimally contributes to the overall cost of care in schizophrenia, use of newer TD drugs can substantially increase spending.
研究人员利用行政医疗保健索赔数据中的元素(如诊断代码和药物)来计算使用第二代抗精神病药物(SGA)的精神分裂症患者的锥体外系症状(EPS)发生率。然而,此前尚未对基于索赔的EPS证据进行详细描述,这正是本研究的目的。这项描述性研究使用了2016 - 2020年去识别化的多州医疗补助行政索赔数据,对诊断为精神分裂症的患者在开始SGA治疗后的12个月进行随访,以识别和描述EPS的首个证据。计算出现EPS证据的时间,并对持续符合条件的患者再随访12个月,以检查EPS药物的使用情况和费用。在开始使用SGA后,13.6%(n = 2288)的患者在12个月的随访期内有EPS证据。开始使用SGA后首次出现EPS证据的平均时间为103.7天(标准差 = 112.2,中位数 = 58)。对于大多数患者(n = 1636,71.5%),EPS药物索赔是EPS的初始证据,而非EPS诊断索赔。此外,EPS证据队列中有四分之一的患者(25.3%)在开始使用SGA的同一天有EPS药物索赔,这可能表明为预防EPS发生而进行的预防性处方。在有EPS药物索赔的患者中,近93%接受了苯海索治疗,而接受氘代丁苯那嗪或缬苯那嗪(用于迟发性运动障碍(TD))治疗的患者不到2%。每位患者每年的EPS药物支出总体为804美元(标准差 = 7080),但排除成本较高的TD药物后仅为40美元(标准差 = 104)。根据索赔数据,近14%开始接受SGA治疗的医疗补助精神分裂症患者有EPS证据。大多数情况下,该证据来自治疗EPS药物的处方索赔,而非EPS诊断索赔。EPS的预防性处方比预期更常出现,应进行更充分的探究。虽然传统EPS药物的成本对精神分裂症总体护理成本的贡献极小,但使用新型TD药物会大幅增加支出。