Convertino Irma, Lorenzoni Valentina, Gini Rosa, Turchetti Giuseppe, Fini Elisabetta, Giometto Sabrina, Bartolini Claudia, Paoletti Olga, Ferraro Sara, Cappello Emiliano, Valdiserra Giulia, Bonaso Marco, Blandizzi Corrado, Tuccori Marco, Lucenteforte Ersilia
Unit of Pharmacology and Pharmacovigilance, Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Institute of Management, Scuola Superiore Sant'Anna, 56100 Pisa, Italy.
Pharmaceuticals (Basel). 2023 Mar 21;16(3):465. doi: 10.3390/ph16030465.
This study is aimed at describing tofacitinib and baricitinib users by characterizing their prescription and healthcare histories, drug and healthcare utilization patterns, and direct costs from a healthcare system perspective. This retrospective cohort study was performed using Tuscan administrative healthcare databases, which selected two groups of Janus kinase inhibitors (JAKi) incident users (index date) from 1st January 2018 to 31 December 2019 and from 1 January 2018 to 30 June 2019. We included patients ≥18 years old, at least 10 years of data, and six months of follow-up. In the first analysis, we describe mean time, standard deviation (SD), from the first-ever disease-modifying antirheumatic drug (DMARD) to the JAKi, and costs of healthcare facilities and drugs in the 5 years preceding the index date. In the second analysis, we assessed Emergency Department (ED) accesses and hospitalizations for any causes, visits, and costs in the follow-up. In the first analysis, 363 incident JAKi users were included (mean age 61.5, SD 13.6; females 80.7%, baricitinib 78.5%, tofacitinib 21.5%). The time to the first JAKi was 7.2 years (SD 3.3). The mean costs from the fifth to the second year before JAKi increased from 4325 € (0; 24,265) to 5259 € (0; 41,630) per patient/year, driven by hospitalizations. We included 221 incident JAKi users in the second analysis. We observed 109 ED accesses, 39 hospitalizations, and 64 visits. Injury and poisoning (18.3%) and skin (13.8%) caused ED accesses, and cardiovascular (69.2%) and musculoskeletal (64.1%) caused hospitalizations. The mean costs were 4819 € (607.5; 50,493) per patient, mostly due to JAKi. In conclusion, the JAKi introduction in therapy occurred in compliance with RA guidelines and the increase in costs observed could be due to a possible selective prescription.
本研究旨在从医疗保健系统的角度,通过描述托法替布和巴瑞替尼使用者的处方和医疗保健史、药物和医疗保健使用模式以及直接成本,对其进行特征分析。这项回顾性队列研究使用了托斯卡纳行政区医疗保健数据库,从2018年1月1日至2019年12月31日以及从2018年1月1日至2019年6月30日选取了两组 Janus激酶抑制剂(JAKi)初治使用者(索引日期)。我们纳入了年龄≥18岁、至少有10年数据且随访6个月的患者。在首次分析中,我们描述了从首次使用改善病情抗风湿药(DMARD)到使用JAKi的平均时间、标准差(SD),以及索引日期前5年的医疗保健设施和药物成本。在第二次分析中,我们评估了随访期间因任何原因的急诊科(ED)就诊和住院情况、门诊次数及成本。在首次分析中,纳入了363名JAKi初治使用者(平均年龄61.5岁,SD 13.6;女性占80.7%,使用巴瑞替尼的占78.5%,使用托法替布的占21.5%)。首次使用JAKi的时间为7.2年(SD 3.3)。在使用JAKi前从第5年到第2年,每位患者每年的平均成本从4325欧元(0;24,265)增至5259欧元(0;41,630),主要是住院费用导致的。在第二次分析中,我们纳入了221名JAKi初治使用者。我们观察到109次ED就诊、39次住院和64次门诊。损伤和中毒(18.3%)以及皮肤疾病(13.8%)导致了ED就诊,心血管疾病(69.2%)和肌肉骨骼疾病(64.1%)导致了住院。每位患者的平均成本为4819欧元(607.5;50,493),主要是由于使用JAKi。总之,JAKi在治疗中的引入符合类风湿关节炎指南,观察到的成本增加可能是由于可能的选择性处方。