Stanford Children's Inflammatory Bowel Disease Center, Division of Gastroenterology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Division of Colorectal Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Aliment Pharmacol Ther. 2018 Feb;47(3):364-370. doi: 10.1111/apt.14430. Epub 2017 Nov 22.
Real-world data quantifying the costs of increasing use of biologics in inflammatory bowel disease (IBD) are unknown.
To determine the outpatient IBD drug utilization trends, relative market share, and costs in the USA during a 9-year period.
The Truven MarketScan Database was analysed for patients with Crohn's disease (CD) and ulcerative colitis (UC) during 2007-2015. National drug codes were used to identify prescription drugs; Healthcare Common Procedure Coding System J-codes were used to capture biologic out-patient infusions. Proportion of drug usage, relative market share and per-member per-year (PMPY) costs were analysed for biologics, immunomodulators, 5-ASAs and corticosteroids.
In 415 405 patients (188 842 CD; 195 183 UC; 31 380 indeterminate colitis; 54.67% female), utilization trends show a consistent rise in the market share of biologics during the 9-year study period. The proportion of patients using biologics increased from 21.8% to 43.8% for CD and 5.1%-16.2% for UC. This contrasts a small decrease in immunomodulator and 5-ASA use for CD and relative constancy of other classes including corticosteroids-only use as primary IBD medication from 2007 to 2015. The average biologic-taking patient accounted for $25 275 PMPY in 2007 and $36 051 PMPY in 2015. The average paediatric biologic-taking patient accounted for $23 616 PMPY in 2007 and $41 109 PMPY in 2015. In all patients, the share of costs for biologics increased from 72.9% in 2007 to 85.7% in 2015 (81.7% in 2007 to 94.9% in 2015 in paediatrics).
The vast majority of costs allocated to out-patient IBD medications in the USA is attributed to increasing use of biologic therapies despite the relative minority of biologic-taking patients.
目前尚不清楚在炎症性肠病(IBD)中增加使用生物制剂的实际成本的相关数据。
旨在确定美国在 9 年内门诊 IBD 药物利用趋势、相对市场份额和成本。
对 2007 年至 2015 年期间患有克罗恩病(CD)和溃疡性结肠炎(UC)的 Truven MarketScan 数据库进行分析。国家药物代码用于识别处方药;医疗保健通用程序编码系统 J 代码用于捕获生物制剂的门诊输注。分析生物制剂、免疫调节剂、5-ASA 和皮质类固醇的药物使用率、相对市场份额和每患者每年(PMPY)成本。
在 415405 名患者(188842 名 CD;195183 名 UC;31380 名不确定结肠炎;54.67%为女性)中,研究期间市场份额的利用趋势显示生物制剂的份额持续上升。使用生物制剂的患者比例从 CD 的 21.8%增加到 43.8%,UC 从 5.1%增加到 16.2%。相比之下,CD 中免疫调节剂和 5-ASA 的使用略有减少,而包括皮质类固醇仅作为主要 IBD 药物在内的其他类别则保持相对稳定,从 2007 年到 2015 年不变。2007 年平均每位生物制剂患者的 PMPY 费用为 25275 美元,2015 年为 36051 美元。2007 年平均每位儿科生物制剂患者的 PMPY 费用为 23616 美元,2015 年为 41109 美元。在所有患者中,生物制剂的费用份额从 2007 年的 72.9%增加到 2015 年的 85.7%(2007 年为 81.7%,儿科为 2015 年为 94.9%)。
尽管接受生物治疗的患者相对较少,但美国分配给门诊 IBD 药物的绝大多数费用归因于生物治疗使用的增加。