Sylwestrzak Gosia, Liu Jinan, Stephenson Judith J, Ruggieri Alexander P, DeVries Andrea
Research Manager, Payer and Provider Research, HealthCore, Inc.
Senior Research Analyst, Payer and Provider Research, HealthCore, Inc.
Am Health Drug Benefits. 2014 Apr;7(2):71-81.
Anti-tumor necrosis factor (TNF) medications for the treatment of chronic inflammatory conditions represent a large and growing expenditure for health plans. Over the past few years, there has been an increase in options for patients receiving anti-TNFs, including choice of agent, route of administration, and location for receiving the medication.
To examine patient preferences regarding available anti-TNF agents and mode of administration options.
This cross-sectional survey and claims study was based on administrative claims in the HealthCore Integrated Research Database. Patients were identified for this study if they were receiving infliximab (the intravenous [IV] group) or adalimumab, golimumab, etanercept, or certolizumab pegol (the subcutaneous [SC] group) between March 2012 and August 2012 and were diagnosed with conditions for which these agents are indicated by the US Food and Drug Administration. The survey questionnaire was developed specifically for this study. Participants were asked about their use of anti-TNF agents, locations of administration, preferences for IV or SC therapy, interest in anti-TNF home therapy options, and their physician's role in their decision-making process. A validated instrument, the Treatment Satisfaction Questionnaire for Medication (TSQM) version II, was used to assess treatment satisfaction by the patients.
A total of 6000 patients were included in the final list of patients, and the study was stopped when the targeted number of 500 surveys were completed. The IV group consisted of 202 (40%) patients, and the SC group consisted of 298 (60%) patients. Patients in the SC group had a higher preference for the administration route they were using compared with patients in the IV group: 89.9% of the SC group preferred the SC route of administration, whereas 71.8% of the IV group preferred the IV route (P <.001). The global treatment satisfaction scores were similar in both groups (81.9 in the IV group, 80.1 in the SC group; P = .247). The reported likelihood of patients discussing alternative anti-TNF options with their physician was low (45.5% in the IV group vs 49.7% in the SC group; P = .366).
When asked to make a hypothetical choice between IV and SC administration, patients had stronger preferences for SC routes than for IV routes. There was a strong correlation between the route of administration in use and the preference, indicating high level of satisfaction with the current treatment used, which was confirmed with the TSQM version II results. An opportunity for patient education exists, because conversations with physicians about alternative anti-TNF therapies and administration appear to be lacking.
用于治疗慢性炎症性疾病的抗肿瘤坏死因子(TNF)药物给医保计划带来了巨大且不断增长的支出。在过去几年中,接受抗TNF治疗的患者可选择的方案有所增加,包括药物选择、给药途径以及接受治疗的地点。
研究患者对于现有抗TNF药物及给药方式的偏好。
这项横断面调查及索赔研究基于HealthCore综合研究数据库中的管理索赔数据。如果患者在2012年3月至2012年8月期间接受英夫利昔单抗治疗(静脉注射[IV]组)或阿达木单抗、戈利木单抗、依那西普或赛妥珠单抗(皮下注射[SC]组)治疗,且被诊断患有美国食品药品监督管理局批准使用这些药物的疾病,则纳入本研究。调查问卷是专门为该研究设计的。参与者被问及抗TNF药物的使用情况、给药地点、对静脉注射或皮下注射治疗的偏好、对抗TNF家庭治疗方案的兴趣以及医生在其决策过程中的作用。使用经过验证的工具——药物治疗满意度问卷(TSQM)第二版来评估患者的治疗满意度。
最终纳入研究的患者共有6000例,当完成500份调查问卷这一目标数量时,研究停止。静脉注射组有202例(40%)患者,皮下注射组有298例(60%)患者。与静脉注射组患者相比,皮下注射组患者对其正在使用的给药途径有更高的偏好:皮下注射组89.9%的患者更喜欢皮下注射给药途径,而静脉注射组71.8%的患者更喜欢静脉注射途径(P<.001)。两组的总体治疗满意度得分相似(静脉注射组为81.9,皮下注射组为80.1;P = 0.247)。报告显示患者与医生讨论替代抗TNF方案的可能性较低(静脉注射组为45.5%,皮下注射组为49.7%;P = 0.366)。
当被要求在静脉注射和皮下注射给药之间进行假设性选择时,患者对皮下注射途径的偏好强于静脉注射途径。正在使用的给药途径与偏好之间存在很强的相关性,表明对当前使用的治疗高度满意,这一点在TSQM第二版的结果中得到了证实。由于患者与医生之间似乎缺乏关于替代抗TNF疗法及给药方式的讨论,因此存在患者教育的机会。