降低预期:类风湿性关节炎退伍军人的糖皮质激素减量在稳定的生物治疗中实现低疾病活性。

ACR Open Rheumatology Pub Date : 2023-09-01 Epub Date: 2023-07-25 DOI:10.1002/acr2.11584
Beth I Wallace, Bryant R England, Joshua F Baker, Jorge Rojas, Brian C Sauer, Punyasha Roul, Gary A Kunkel, Tawnie J Braaten, Alison Petro, Ted R Mikuls, Grant W Cannon
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引用次数: 0

摘要

目的:在类风湿性关节炎(SEMIRA)的类固醇清除试验中,65%的低疾病活动性类风湿性关节病(RA)患者在稳定的生物治疗中成功地减少了糖皮质激素。我们的目的是评估退伍军人事务部类风湿性关节炎登记中类似患者的糖皮质激素减量率。方法:在一个多中心、前瞻性RA队列中,我们使用2003年至2021年的注册数据和相关药房声明来确定在启动一种新的生物或靶向合成疾病修饰抗风湿药物(b/tsDMARD)后达到LDA的慢性泼尼松使用者。我们将索引日期定义为出现在60到180之间的第一个LDA b/tsDMARD启动后几天。LDA后第180天评估的成功减量的主要结果要求30天的泼尼松平均剂量小于或等于5mg/天,并且比指标日期至少低50%。次要结果是停药,定义为第180至210天泼尼松剂量为0 mg/天。我们使用单变量统计来比较主要结果的实现情况下的患者特征。结果:我们评估了95例患者的100个b/tsDMARD疗程。五十四门课程成功地缩减了规模;33例导致停药。类风湿因子阳性,红细胞沉降率更高,背景DMARD更多,从b/tsDMARD开始到LDA的时间更短,糖皮质激素剂量更高30 LDA前几天与更大的成功减量可能性相关。结论:在一个由LDA中的慢性糖皮质激素使用者组成的真实RA队列中,在启动一种新的b/tsDMARD后6个月内,一半的患者成功地减量化,三分之一的患者停用了泼尼松。基于声明的糖皮质激素减量和停用算法可能有助于评估管理数据集中减量的预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lowering Expectations: Glucocorticoid Tapering Among Veterans With Rheumatoid Arthritis Achieving Low Disease Activity on Stable Biologic Therapy.

Lowering Expectations: Glucocorticoid Tapering Among Veterans With Rheumatoid Arthritis Achieving Low Disease Activity on Stable Biologic Therapy.

Objective: In the Steroid EliMination In Rheumatoid Arthritis (SEMIRA) trial, 65% of patients with rheumatoid arthritis (RA) in low disease activity (LDA) on stable biologic therapy successfully tapered glucocorticoids. We aimed to evaluate real-world rates of glucocorticoid tapering among similar patients in the Veterans Affairs Rheumatoid Arthritis registry.

Methods: Within a multicenter, prospective RA cohort, we used registry data and linked pharmacy claims from 2003 to 2021 to identify chronic prednisone users achieving LDA after initiating a new biologic or targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD). We defined the index date as first LDA occurring 60 to 180 days after b/tsDMARD initiation. The primary outcome of successful tapering, assessed at day 180 after LDA, required a 30-day averaged prednisone dose both less than or equal to 5mg/day and at least 50% lower than at the index date. The secondary outcome was discontinuation, defined as a prednisone dose of 0 mg/day at days 180 through 210. We used univariate statistics to compare patient characteristics by fulfillment of the primary outcome.

Results: We evaluated 100 b/tsDMARD courses among 95 patients. Fifty-four courses resulted in successful tapering; 33 resulted in discontinuation. Positive rheumatoid factor, higher erythrocyte sedimentation rate, more background DMARDs, shorter time from b/tsDMARD initiation to LDA, and higher glucocorticoid dose 30 days before LDA were associated with greater likelihood of successful tapering.

Conclusion: In a real-world RA cohort of chronic glucocorticoid users in LDA, half successfully tapered and a third discontinued prednisone within 6 months of initiating a new b/tsDMARD. Claims-based algorithms of glucocorticoid tapering and discontinuation may be useful to evaluate predictors of tapering in administrative data sets.

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