生物药物治疗强直性脊柱炎的疗效评价:队列研究,米纳斯吉拉斯州,2018-2023。

IF 2
Bárbara Rodrigues Alvernaz Dos Santos, Gerusa Araújo de Oliveira, Grazielle Dias Silva, Jessica Barreto Ribeiro Dos Santos, Marina Morgado Garcia, Augusto Afonso Guerra Junior, Francisco de Assis Acurcio, Juliana Alvares-Teodoro
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引用次数: 0

摘要

目的:评估巴西统一卫生系统治疗的强直性脊柱炎患者生物药物的持续时间和停药时间,并调查与之相关的因素。方法:从2018年至2023年的开放历史队列中收集数据,了解巴西米纳斯吉拉斯州药品援助专业部门申请药品所需的行政流程。收集社会人口学、临床资料及治疗史。对变量进行描述性分析。Cox比例风险模型用于确定与首个生物药物停药时间相关的因素。采用logistic回归模型评估治疗12个月和24个月时与持续性相关的因素。结果:共纳入530名参与者,平均年龄46岁,其中50.0%为男性。阿达木单抗和戈利木单抗是处方最多的药物。平均随访26.4个月,中位停药时间34个月。12个月和24个月的持续率分别为82.0%和63.0%。生物药物间无明显差异。结论:两种药物的持续时间和停药时间分析显示,两种药物在方案的一线治疗中维持治疗是合理的。与使用者临床资料相关的因素可能与有效性差异有关,但鉴于在流行病学研究中使用行政数据的局限性,需要进行更深入的研究来证实这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of the performance of biological drugs in the treatment of ankylosing spondylitis: cohort study, Minas Gerais, 2018-2023.

Evaluation of the performance of biological drugs in the treatment of ankylosing spondylitis: cohort study, Minas Gerais, 2018-2023.

Evaluation of the performance of biological drugs in the treatment of ankylosing spondylitis: cohort study, Minas Gerais, 2018-2023.

Objectives: To assess the persistence and time until discontinuation of biological drugs used by people with ankylosing spondylitis treated in the Brazilian Unified Health System and to investigate the factors associated with them.

Methods: Data were collected from an open historical cohort between 2018 and 2023 on the administrative processes required for requesting medicines from the specialized component of pharmaceutical assistance in Minas Gerais, Brazil. Sociodemographic and clinical data and treatment history were collected. A descriptive analysis of the variables was performed. The Cox proportional hazards model was used to identify factors associated with time to discontinuation of the first biological drug. The logistic regression model was used to evaluate the factors associated with persistence at 12 and 24 months of treatment.

Results: A total of 530 participants were included, with an average age of 46 years, of which 50.0% were male. Adalimumab and golimumab were the most prescribed drugs. The mean follow-up time was 26.4 months, and the median time to discontinuation was 34 months. Persistence at 12 and 24 months was 82.0% and 63.0%. No significant differences were observed between biological drugs.

Conclusion: The analysis of persistence and time to discontinuation showed no differences between the drugs, which justified their maintenance in the first line of treatment of the protocol. Factors associated with the clinical profile of users may be related to differences in effectiveness, but more in-depth studies are needed to confirm these results, given the limitations of using administrative data in epidemiological research.

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