Identifying physician-perceived barriers to a pragmatic treatment trial in rheumatoid arthritis.

IF 1.3 Q4 RHEUMATOLOGY European journal of rheumatology Pub Date : 2022-07-01 DOI:10.5152/eujrheum.2022.21038
Haiyan Qu, Shamly Austin, Jasvinder A Singh
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Abstract

Objective: The aim of this qualitative research was to identify physician-perceived patient and clinic barriers to patient recruitment in a rheumatoid arthritis (RA) pragmatic trial of anti-tumor necrosis factor (TNF) biologic versus non-TNF biologic/Janus-Kinase inhibitor initiation after an inadequate response to methotrexate.

Methods: Semistructured telephone interviews were conducted with 26 rheumatologists in March 2019. An exploratory thematic analysis approach was used to analyze the interview data.

Results: Physician perceived patient barriers to the implementation of an RA pragmatic trial. This theme covers three subthemes: (1) patients' personal barriers, (2) patients' treatment-related factors, and (3) trial-related factors (eg, patient recruitment, side effects, mode of use, etc). Physicians perceived clinic barriers interfered with the pragmatic trial enrollment from the clinic or the healthcare system perspective. This theme covered four subthemes: (1) clinic-related factors, (2) patient-related factors, (3) research personnel, and (4) facilitators (positive factors of the clinic).

Conclusion: Our results from the inductive thematic analysis will help researchers understand the key patient and clinic/system factors/barriers that may influence pragmatic RA trial implementation. The themes suggest there are factors that can be modified (eg, coordinator effort needed, effective patient recruitment during clinic visits, provider engagement) and challenges to overcome (patient insurance status, busy clinic flow, and space issues including limited number of patient rooms). In summary, these themes provide a basis for our and other research teams to develop clinic-centered and patientcentered strategies to implement a pragmatic RA trial.

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确定医生感知的障碍,以实际治疗类风湿关节炎试验。
目的:本定性研究的目的是确定在对甲氨蝶呤反应不充分后,抗肿瘤坏死因子(TNF)生物制剂与非TNF生物制剂/ janus -激酶抑制剂启动的类风湿性关节炎(RA)实用试验中,医生感知的患者和临床招募患者的障碍。方法:于2019年3月对26名风湿病专家进行半结构化电话访谈。采用探索性专题分析方法对访谈数据进行分析。结果:医生认为患者对实施RA实用试验存在障碍。该主题包括三个子主题:(1)患者的个人障碍;(2)患者的治疗相关因素;(3)试验相关因素(如患者招募、副作用、使用方式等)。从临床或医疗系统的角度来看,医生认为临床障碍干扰了实用的试验登记。该主题包括四个子主题:(1)临床相关因素,(2)患者相关因素,(3)研究人员,(4)促进者(临床积极因素)。结论:我们的归纳专题分析结果将有助于研究人员了解可能影响实际RA试验实施的关键患者和临床/系统因素/障碍。这些主题表明,有一些因素可以修改(例如,需要协调员的努力,在诊所就诊期间有效的患者招募,提供者的参与)和需要克服的挑战(患者保险状况,繁忙的诊所流量和空间问题,包括有限的病房数量)。总之,这些主题为我们和其他研究团队制定以临床为中心和以患者为中心的策略来实施实用的RA试验提供了基础。
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审稿时长
7 weeks
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