Knowledge and Attitudes of Patients with Rheumatoid Diseases towards Biosimilars.

Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2024-12-31 eCollection Date: 2024-12-01 DOI:10.31138/mjr.140323.kaa
Athanasios Chantzaras, John Yfantopoulos, Katerina Koutsogianni
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引用次数: 0

Abstract

Objective: To assess patients' understanding and attitudes towards biosimilars in rheumatoid diseases in Greece.

Methods: A convenience sample of patients with rheumatoid diseases who were members of the largest rheumatoid patient association (RHEUMAZIN) in Greece was selected for this survey. Data on patients' knowledge and attitudes towards biosimilars were collected with a web-based questionnaire.

Results: Among the 309 patients, 60.2% were being treated with bio-originator products, 11% with biosimilars and another 28.8% did not know the type of their biologic therapy. Only 43.7% of the respondents reported they had adequate information about biologic treatments. About 47.9% knew what biosimilars are exactly and 81.2% stated that they need more information about them. The most influential patient information sources about biologics were rheumatologists (88.3%), the Internet (45%), and patient associations (40.5%). Only about 55-60% of the participants thought that biosimilars are comparable to their reference products in terms of safety, effectiveness, quality and regulatory requirements. Patients with adequate knowledge about biosimilars were significantly less concerned about switching from their reference products. A higher education level, previous biosimilar treatment experience, having rheumatologists, patient associations, regulatory bodies and the internet as main information sources, being better informed about the disease, biologic therapies and biosimilars, working and having adequate information about biosimilars were univariately associated with a significantly higher likelihood of having a positive attitude towards biosimilars.

Conclusions: There is an urgent need for patient education about biosimilars in rheumatic diseases in Greece to enhance patient knowledge and ensure informed decisions on biosimilar use.

目的:评估希腊类风湿病患者对生物仿制药的理解和态度:评估希腊类风湿病患者对生物仿制药的理解和态度:本次调查选取了希腊最大的类风湿患者协会(RHEUMAZIN)成员中的类风湿患者作为样本。通过网络问卷收集了患者对生物仿制药的认识和态度:在309名患者中,60.2%的患者正在接受生物原研产品治疗,11%的患者正在接受生物仿制药治疗,另有28.8%的患者不知道自己的生物治疗类型。只有 43.7% 的受访者表示他们对生物制剂治疗有足够的了解。约 47.9% 的受访者知道什么是生物仿制药,81.2% 的受访者表示他们需要更多有关生物仿制药的信息。最有影响力的患者生物制剂信息来源是风湿免疫科医生(88.3%)、互联网(45%)和患者协会(40.5%)。只有约 55-60% 的参与者认为生物仿制药在安全性、有效性、质量和监管要求方面与其参照产品相当。对生物仿制药有充分了解的患者对更换参照产品的担忧程度要低得多。教育程度较高、有过生物仿制药治疗经验、有风湿病医生、患者协会、监管机构和互联网作为主要信息来源、对疾病、生物疗法和生物仿制药有更多了解、有工作以及对生物仿制药有充分了解,这些因素都与患者对生物仿制药持积极态度的可能性显著增加有关:在希腊,急需开展有关风湿病生物仿制药的患者教育,以提高患者对生物仿制药的认识,确保患者在知情的情况下做出使用生物仿制药的决定。
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
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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