Jesudian Arun, Gagnon-Sanschagrin Patrick, Maitland Jessica, Yokoji Kana, Guérin Annie, Heimanson Zeev, Samson Aaron, Olujohungbe Olamide, Bumpass Brock
Weill Cornell Medicine, 1283 York Avenue, New York, NY, 10065, USA.
Analysis Group, Inc., 1190 Avenue des Canadiens-de-Montréal, Tour Deloitte, Suite 1500, Montréal, QC, H3B 0G7, Canada.
Adv Ther. 2025 Jun;42(6):2739-2753. doi: 10.1007/s12325-025-03145-3. Epub 2025 Apr 7.
Continuous treatment with rifaximin 550 mg (hereafter rifaximin) is associated with lower hospitalization rates in patients with hepatic encephalopathy (HE); however, access barriers may exist. This study assessed gaps in rifaximin access and the impact of treatment gaps, particularly those resulting from claim rejections, on hospitalizations and healthcare costs among patients with HE in the United States.
The IQVIA PharMetrics Plus database linked with Longitudinal Access and Adjudicated Data (2015-2022) were used to identify adults with HE who had ≥ 1 paid rifaximin prescription fill. Rifaximin treatment gaps were assessed during the 12-month period from the first observed attempt at receiving rifaximin (index date). Adjusted number of overt HE (OHE) hospitalizations and healthcare costs were compared over the 6 months following the index date between Cohort 1, who had no gap due to claim rejection and had < 7 days of treatment gap due to other reasons, and Cohort 2, who had ≥ 1 rejection gap or had ≥ 7 days of non-rejection gap.
During the year following the index date, 94.7% of the 1711 patients experienced a treatment gap, including 34.8% with initiation gaps from first attempt at receiving rifaximin to first paid claim (77.7% of initiation gaps due to rejected claims) and 72.0% with gaps in access during active treatment (14.8% of active treatment gaps due to rejected claims). Compared with Cohort 1 (n = 432; mean age 56.3 years), Cohort 2 (n = 679; mean age 54.8 years) had 1.55 times the incidence rate of OHE hospitalizations [adjusted incidence rate ratio: 1.55 (95% confidence interval: 1.10-2.20)] and incurred US$1579 more in healthcare-associated costs per-patient-per-month (all p < 0.05).
Prescription claim rejections frequently led to delays in rifaximin initiation and gaps in access during active treatment. Access barriers to rifaximin were associated with increased hospitalizations and healthcare costs in patients with HE.
连续使用550毫克利福昔明(以下简称利福昔明)治疗可降低肝性脑病(HE)患者的住院率;然而,可能存在获取障碍。本研究评估了利福昔明获取方面的差距以及治疗中断的影响,特别是因理赔被拒导致的治疗中断对美国HE患者住院率和医疗费用的影响。
使用IQVIA PharMetrics Plus数据库与纵向获取和裁决数据(2015 - 2022年)相链接,以识别有≥1次已付费利福昔明处方配药记录的成年HE患者。从首次观察到尝试接受利福昔明(索引日期)开始的12个月期间评估利福昔明治疗中断情况。在索引日期后的6个月内,比较队列1和队列2的显性HE(OHE)住院调整数量和医疗费用,队列1因理赔被拒无治疗中断且因其他原因治疗中断<7天,队列2有≥1次被拒理赔中断或有≥7天非被拒理赔中断。
在索引日期后的一年中,1711例患者中有94.7%经历了治疗中断,包括34.8%从首次尝试接受利福昔明到首次付费理赔存在起始中断(77.7%的起始中断是由于理赔被拒),以及72.0%在积极治疗期间存在获取中断(14.8%的积极治疗中断是由于理赔被拒)。与队列1(n = 432;平均年龄56.3岁)相比,队列2(n = 679;平均年龄54.8岁)的OHE住院发病率是队列1的1.55倍[调整发病率比:1.55(95%置信区间:1.10 - 2.20)],且每位患者每月的医疗相关费用多支出1579美元(所有p<0.05)。
处方理赔被拒经常导致利福昔明起始延迟和积极治疗期间的获取中断。利福昔明的获取障碍与HE患者住院率增加和医疗费用增加相关。