The perspective of Polish patients with rheumatoid arthritis - treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study).

IF 1.4 Q3 RHEUMATOLOGY
Reumatologia Pub Date : 2023-01-01 Epub Date: 2023-10-06 DOI:10.5114/reum/171625
Marcin Stajszczyk, Grażyna Świerkowska, Katarzyna Smolik, Izabela Domysławska, Karol Charkiewicz, Włodzimierz Samborski
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引用次数: 0

Abstract

Introduction: A widely accepted treat-to-target strategy for rheumatoid arthritis (RA) requires the patient's perspective in making treatment decisions. However, data on treatment preferences and expectations of Polish patients with RA are scarce. The aim of the study was to determine the satisfaction with treatment and the nature of therapeutic preferences and expectations of Polish patients with moderate to severe RA.

Material and methods: Fifty-two adult Polish patients with moderately to highly active RA were asked to complete patient-reported outcomes and patient-provided information questionnaires. Additionally, patient sociodemographic and clinical data and information on patient current and planned treatment strategies were collected.

Results: The mean global assessment of patient satisfaction with treatment was 64.1 ±24.6, below the level of indicating satisfaction. Rheumatoid arthritis negatively impacted patients' lives, resulting in a 37.8% impairment of work efficiency and 45% impairment of total activity. Primary treatment expectations for patients were lasting relief of RA symptoms, reduced pain and swelling in joints, increased flexibility of joints, and general improvement of arthritis. The most acceptable potential side effect was weight gain and the least acceptable were increases in the risk of cardiovascular disease, infection, and malignancies. The rapid onset of the drug effect (up to 1 week) was a preference of 48.1% of patients. Access to internet health resources was important for 44.2% of patients, but the median total eHealth literacy score in the study population was 24.0 (interquartile range: 20.5-28.0, range 8-37), which means low digital health literacy (DHL).

Conclusions: Understanding these treatment preferences and expectations of patients with RA is essential for clinical practitioners to facilitate shared treatment decision-making. Digital health literacy data suggest the need of further improvement.

波兰类风湿关节炎患者的视角——治疗预期、患者报告的结果和数字素养(SENSE研究)。
导读:一种被广泛接受的治疗类风湿性关节炎(RA)的靶向策略需要患者的观点来做出治疗决定。然而,关于波兰类风湿性关节炎患者的治疗偏好和期望的数据很少。该研究的目的是确定波兰中重度类风湿性关节炎患者对治疗的满意度、治疗偏好的性质和期望。材料和方法:52名波兰成人中度至高度活动性RA患者被要求完成患者报告的结果和患者提供的信息问卷。此外,还收集了患者的社会人口学和临床数据以及患者当前和计划治疗策略的信息。结果:患者对治疗的总体满意度平均为64.1±24.6,低于指示满意水平。类风湿关节炎对患者的生活产生负面影响,导致37.8%的工作效率受损,45%的总活动受损。患者的主要治疗期望是持久缓解类风湿性关节炎症状,减轻关节疼痛和肿胀,增加关节柔韧性,以及关节炎的总体改善。最可接受的潜在副作用是体重增加,最不可接受的是心血管疾病、感染和恶性肿瘤的风险增加。48.1%的患者偏好快速起效(最多1周)。对44.2%的患者来说,获得互联网健康资源很重要,但研究人群的电子健康素养总分中位数为24.0(四分位数范围:20.5-28.0,范围8-37),这意味着数字健康素养(DHL)较低。结论:了解RA患者的这些治疗偏好和期望对临床医生促进共同治疗决策至关重要。数字卫生素养数据表明需要进一步改进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reumatologia
Reumatologia Medicine-Rheumatology
CiteScore
2.70
自引率
0.00%
发文量
44
审稿时长
10 weeks
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