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患者和医生对生物制剂阿巴西普、英夫利昔单抗和利妥昔单抗输注过程的看法,用于治疗类风湿关节炎。

Patient and physician perception of the infusion process of the biologic agents abatacept, infliximab, and rituximab for the treatment of rheumatoid arthritis.

机构信息

NYU Hospital for Joint Diseases, 246 East 20th Street, Suite 101, New York, NY 10003, USA.

出版信息

Clin Exp Rheumatol. 2009 Nov-Dec;27(6):907-13.

PMID:20149304
Abstract

OBJECTIVES

To assess the process related to each infusible biologic used in rheumatoid arthritis (RA) with regard to patient and physician engagement in the infusion process, ancillary services required, and participant preferences.

METHODS

This was a cross-sectional survey of patients with RA and their physicians. Biologic-naïve patients with RA starting abatacept, infliximab, or rituximab were included. Both patients and physicians completed detailed questionnaires related to the infusion and satisfaction with the process.

RESULTS

A total of 205 patients were enrolled: abatacept (n=102), infliximab (n=74), rituximab (n=29). Patients were primarily female (75%), Caucasian (85%), with a mean age of 58 years. Patients had a mean disease duration of approximately 8 years and had typically failed multiple DMARDs. Rituximab required the most pre-infusion preparation and the longest infusion time. Abatacept was associated with a shorter mean infusion time (42 minutes) than infliximab (131 minutes; p<0.0001) or rituximab (274 minutes; p<0.0001) and required less time away from work/home (p=0.01 and p<0.0001, respectively). Abatacept patients reported significantly less discomfort than rituximab patients (p=0.03), while discomfort was similar between abatacept and infliximab. From the physicians' perspective, compared to infliximab and rituximab abatacept was very easy to administer (57% vs. 27% and 5%, respectively), caused no pain/discomfort (52% vs. 42% and 31%), and had very infrequent infusion reactions (75% vs. 30% and 44%).

CONCLUSION

The process involved in infusion administration, as perceived by both the patient and physician, seems to differ across the three infusible biologic agents and may have an impact on the decision-making process regarding which infusible biologic to use.

摘要

目的

评估类风湿关节炎(RA)中每种可输注生物制剂相关的输注过程,包括患者和医生对输注过程的参与、所需的辅助服务以及患者的偏好。

方法

这是一项针对 RA 患者及其医生的横断面调查。纳入了开始使用阿巴西普、英夫利昔单抗或利妥昔单抗的生物初治 RA 患者。患者和医生均完成了与输注过程及对该过程满意度相关的详细问卷。

结果

共纳入 205 例患者:阿巴西普(n=102)、英夫利昔单抗(n=74)、利妥昔单抗(n=29)。患者主要为女性(75%)、白种人(85%),平均年龄 58 岁。患者的平均病程约为 8 年,通常已接受过多种 DMARDs 治疗。利妥昔单抗需要进行最多的输注前准备,且输注时间最长。阿巴西普的平均输注时间(42 分钟)短于英夫利昔单抗(131 分钟;p<0.0001)和利妥昔单抗(274 分钟;p<0.0001),且需要离开工作/家庭的时间更短(分别为 p=0.01 和 p<0.0001)。与利妥昔单抗相比,阿巴西普患者报告的不适程度显著较低(p=0.03),而阿巴西普和英夫利昔单抗患者的不适程度相似。从医生的角度来看,与英夫利昔单抗和利妥昔单抗相比,阿巴西普非常易于给药(57% vs. 27%和 5%),不会引起疼痛/不适(52% vs. 42%和 31%),且输注反应非常罕见(75% vs. 30%和 44%)。

结论

患者和医生对输注管理过程的看法似乎因三种可输注生物制剂而异,这可能会影响使用哪种可输注生物制剂的决策过程。

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