首页> 外文期刊>Journal of managed care pharmacy : >Analysis of drug and administrative costs allowed by U.S. Private and public third-party payers for 3 intravenous biologic agents for rheumatoid arthritis.
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Analysis of drug and administrative costs allowed by U.S. Private and public third-party payers for 3 intravenous biologic agents for rheumatoid arthritis.

机译:分析美国私人和公共第三方付款方允许的3种类风湿关节炎静脉内生物制剂的药物和管理费用。

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BACKGROUND: Rheumatoid arthritis (RA) is a common chronic condition with substantial morbidity that can now be treated with disease-modifying biologic agents that target tumor necrosis factor (TNF) or related mechanisms. The anti-TNF biologic agents are available in either intravenous (IV) or subcutaneous dose forms. The biologic agents with an indication for rheumatoid arthritis and administered only by IV infusion in medical offices include abatacept, infliximab, and rituximab. Although the literature on RA treatments, their outcomes, and aspects of their costs is substantial, the costs of administration by the IV route have not been directly studied. OBJECTIVE: To assess the detailed costs of administering IV biologic agents for the treatment of RA in relation to the total cost of the medication itself in the United States. METHODS: The sample included all patients with at least 1 medical claim with an ICD-9-CM diagnosis code for RA (codes 714.XX) in any claim field and at least 1 claim for infliximab, abatacept, or rituximab (HCPCS codes J1745, J0129, and J9310, respectively) at any time from January 1, 2006, through December 31, 2008, in a database associated with billing and claims administration for 72 U.S. medical clinics. Costs were determined using the payer allowed payment, which is the total contractual amount that the provider should receive, including the patient cost share. Costs were measured as the average cost per IV administration visit and in relation to the dose of medication billed. The authors verified that an RA diagnosis was present on 100% of infusion claims for the study drugs. RESULTS: Over the study period for claims with dates of service from January 1, 2006, through December 31, 2008, 72 medical clinics had claims for a total of 4,248 unique patients with RA and a total of 33,354 clinic visits in which these patients received at least 1 infusion of 1 of 3 biologic agents (26,586 for infliximab, 4,807 for abatacept, and 1,961 for rituximab). Mean (SD) total payment for all drugs and other cost components was Dollars 2,874 (Dollars 1,515) per visit, of which IV administration costs were Dollars 226 (7.9%); the mean cost of the biologic agent itself was Dollars 2,616 (91.0%), and other visit-related services were Dollars 33 (1.1%). For individual agents, the total costs of visits were Dollars 2,828, Dollars 1,827, and Dollars 6,076; and the costs of IV administration were Dollars 224, Dollars 171, and Dollars 390, respectively, for infliximab, abatacept, and rituximab. CONCLUSION: For patients who received an IV biologic agent to treat RA, IV administration costs accounted for 7.9% of the total cost of the visit.
机译:背景:类风湿关节炎(RA)是一种常见的慢性病,​​发病率很高,现在可以用靶向肿瘤坏死因子(TNF)或相关机制的疾病改良生物制剂进行治疗。抗TNF生物制剂可以静脉内(IV)或皮下剂型获得。指示类风湿性关节炎且仅在医疗机构通过静脉输注给药的生物制剂包括阿巴西普,英夫利昔单抗和利妥昔单抗。尽管有关RA治疗,其治疗效果和治疗费用方面的文献很多,但尚未直接研究通过IV途径进行治疗的费用。目的:评估在美国使用IV生物制剂治疗RA的详细费用与药物本身总费用的关系。方法:该样本包括所有在任何索赔领域中具有至少1个医学索赔且具有ICD-9-CM RA诊断代码(代码714.XX)和至少1个英夫利昔单抗,阿巴西普或利妥昔单抗的患者(HCPCS代码J1745 ,J0129和J9310)分别从2006年1月1日到2008年12月31日之间的任何时间存储在与美国72家医疗诊所的帐单和索赔管理相关的数据库中。费用是使用付款人允许的付款确定的,付款人允许的付款是提供者应收到的合同总金额,包括患者的费用份额。费用以每次静脉内就诊的平均费用以及与所开具的药物剂量有关的方式来衡量。作者证实,该研究药物的输注声明中有100%出现了RA诊断。结果:在自2006年1月1日至2008年12月31日期间服务的索赔研究期内,共有72家医疗诊所对4,248例RA的独特患者进行了索赔,并对33,354例患者进行了就诊至少3种生物制剂中的1种进行输注(英夫利昔单抗为26,586,阿巴西普为4,807,利妥昔单抗为1,961)。所有药物和其他费用组成部分的平均(SD)总付款为每次访问2874美元(1515美元),其中静脉注射管理费用为226美元(7.9%);生物制剂本身的平均成本为2,616美元(91.0%),其他与探访相关的服务则为33美元(1.1%)。对于单独的探员,探视的总费用为2828美元,1827美元和6076美元;对于英夫利昔单抗,阿巴西普和利妥昔单抗,静脉给药的费用分别为224美元,171美元和390美元。结论:对于接受静脉内生物制剂治疗RA的患者,静脉内给药费用占到访视总费用的7.9%。

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