在美国综合卫生服务网络中,经验性治疗失败对女性无并发症尿路感染患者卫生保健资源利用和成本的影响

IF 2.9 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Jeffrey J Ellis, Anushree Iyengar, Hari Bandi, Michiel J M Niesen, Ediz S Calay, Tyler E Wagner, Madison T Preib, Amy G Edgecomb, Meghan E Luck
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引用次数: 0

摘要

背景:无并发症尿路感染(utis)是美国最常见的门诊感染之一。尽管如此,关于口服抗生素治疗失败(TF)对经验性uuti患者的医疗资源利用(HCRU)和成本的影响的数据有限。目的:描述经验性口服抗生素治疗失败(TF队列)和未失败(无TF队列)的女性uuti患者的全因总医疗保健费用。次要目标是描述TF组和非TF组的全因HCRU和尿路相关HCRU以及成本。方法:本研究使用2016年1月至2023年1月期间从美国综合递送网络收集的12岁及以上女性患者的未识别电子健康记录(EHR)数据。入选标准包括uUTI门诊诊断,uUTI指数诊断±5天内的经验性抗生素处方,以及指数前和指数后12个月或更长时间的电子病历活动。TF定义为在指标日期(首次uUTI诊断后5天内首次使用抗生素的日期)后28天内至少出现以下1种情况:第二次口服抗生素处方;静脉注射抗生素;或急诊科(ED)或将尿路感染列为主要诊断的住院患者(指数尿路感染除外)。HCRU和指数后12个月的成本是通过护理设置来获取的,医疗和药房成本估算基于最近可获得的医疗保险和医疗补助服务中心的费用表、报销率和处方成本。倾向得分匹配(1:1)用于控制队列失衡。结果:在28460例诊断为uUTI的患者中,4330例(15.2%)经历了经验性抗生素TF。匹配TF和非TF患者的平均年龄(每个队列3957例)为53岁;白色分别为95%和96%。在指数uUTI发作期间,TF组的平均总全因成本较高(1,369美元vs 482美元)。结论:女性uUTI患者的经经验抗生素TF导致uUTI发作期间及以后的HCRU和成本显著增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of empirical treatment failure on health care resource utilization and costs among female patients with uncomplicated urinary tract infections in a US-based Integrated Health Delivery Network.

Background: Uncomplicated urinary tract infections (uUTIs) are one of the most common outpatient infections in the United States. Despite this, there are limited data on the impact of oral antibiotic treatment failure (TF) on health care resource utilization (HCRU) and costs for patients with empirically treated uUTIs.

Objective: To describe all-cause total health care costs in female patients with uUTIs who fail (TF cohort) and who do not fail (no-TF cohort) initial, empirically prescribed, oral antibiotic treatment. Secondary objectives were to describe all-cause HCRU and UTI-related HCRU and costs in the TF cohort and no-TF cohort.

Methods: This study used deidentified electronic health record (EHR) data for female patients aged 12 years and older collected from a US Integrated Delivery Network between January 2016 and January 2023. Eligibility criteria included a uUTI outpatient diagnosis, empirical antibiotic prescription within ±5 days of index uUTI diagnosis, and 12 months or more of EHR activity pre-index and post-index. TF was defined as at least 1 of the following within 28 days after the index date (date of first antibiotic treatment within 5 days of first uUTI diagnosis): second oral antibiotic prescription; intravenous antibiotic administration; or emergency department (ED) or inpatient stay with UTI listed as the primary diagnosis (index uUTI excluded). HCRU and costs 12 months post-index were captured by setting of care, with medical and pharmacy cost estimates based on the most recent available Centers for Medicare and Medicaid Services fee schedule reimbursement rates and prescription costs. Propensity score matching (1:1) was used to control for cohort imbalances.

Results: Of 28,460 patients with a uUTI diagnosis, 4,330 (15.2%) experienced empirical antibiotic TF. Mean age of matched TF and no-TF patients (3,957 per cohort) was 53 years; 95% and 96%, respectively, were White. During the index uUTI episode, the TF cohort had higher mean total all-cause costs ($1,369 vs $482; P < 0.001) and UTI-related costs ($392 vs $78; P < 0.001) and a higher proportion of the TF cohort compared with the no-TF cohort had all-cause inpatient stays (3.1% vs 0.5%; P < 0.001) and ED visits (19.1% vs 7.6%; P < 0.001). All-cause and UTI-related total costs remained significantly higher in the TF cohort across time intervals during the 12-month post-index period, including the 181 to 365 days interval.

Conclusions: Empirical antibiotic TF in female patients with uUTIs results in significantly increased HCRU and costs during the uUTI episode and beyond.

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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
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.
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