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如何在患有合并症的类风湿关节炎患者中使用生物制剂。

How to use biologic agents in patients with rheumatoid arthritis who have comorbid disease.

机构信息

Veterans Affairs Medical Center, Washington DC 20422, USA Georgetown University, Washington, DC, USA

Howard University, Washington, DC, USA.

出版信息

BMJ. 2015 Aug 17;351:h3658. doi: 10.1136/bmj.h3658.

Abstract

Although biologic disease modifying anti-rheumatic drugs (bDMARDs) have improved the quality of life of patients with rheumatoid arthritis, side effects remain a problem, especially for patients with pre-existing comorbidities. Randomized controlled trials of such drugs in rheumatoid arthritis typically exclude patients with comorbidities and are of short duration, so they do not provide data on adverse events in these people. Other data sources such as national bDMARD registries are limited by the preselection of patients for both conventional synthetic chemical compound disease modifying anti-rheumatic drugs (csDMARDs) and bDMARDs, and although these databases document comorbidity, they rarely report its severity. This too limits definitive statements on the progression or resolution of pre-existing disease. Although bDMARDs may not be contraindicated in patients with rheumatoid arthritis and certain comorbid diseases, additional assessments or precautions are recommended. This review summarizes current data on the use of bDMARDs in people with rheumatoid arthritis and common comorbid diseases. It provides an evidence base for doctors and their patients when discussing and selecting the appropriate bDMARDs.

摘要

虽然生物制剂类改善病情抗风湿药(bDMARDs)提高了类风湿关节炎患者的生活质量,但副作用仍然是一个问题,尤其是对于有合并症的患者。此类药物治疗类风湿关节炎的随机对照试验通常排除了合并症患者,且试验持续时间较短,因此无法提供这些患者不良事件的数据。其他数据来源,如国家生物制剂注册处,受到对常规合成的化学药物改善病情抗风湿药(csDMARDs)和 bDMARDs 进行患者选择的限制,而且尽管这些数据库记录了合并症,但很少报告其严重程度。这也限制了对预先存在的疾病的进展或缓解做出明确的结论。尽管 bDMARDs 对于类风湿关节炎和某些合并症患者可能并非禁忌,但建议进行额外的评估或预防措施。本综述总结了目前关于 bDMARDs 在类风湿关节炎和常见合并症患者中的使用数据。在讨论和选择合适的 bDMARDs 时,它为医生及其患者提供了证据基础。

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