Division of Immunology, Boston Children's Hospital, Boston, MA, United States; Division of Rheumatology, Inflammation, and Immunity, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, United States.
Division of Rheumatology, Inflammation, and Immunity, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, United States.
Semin Arthritis Rheum. 2023 Feb;58:152122. doi: 10.1016/j.semarthrit.2022.152122. Epub 2022 Oct 25.
Glucocorticoids ("steroids") are frequently used in systemic lupus erythematosus (SLE). Prolonged use may contribute to racial/ethnic disparities in avoidable adverse outcomes. We examined racial/ethnic differences in longitudinal patterns of steroid use and dose.
We identified Medicaid beneficiaries 18-65 years with incident SLE who received steroids for 12 months following the index date. Group-based trajectory modeling was used to identify patterns of daily prednisone-equivalent steroid doses. We examined demographic, clinical and healthcare utilization factors during the baseline period and used multinomial logistic regression to estimate the odds of belonging to the higher vs. lowest steroid dose trajectories over time.
We identified 6314 individuals with SLE with ≥1 dispensed steroid prescription. The mean (SD) prednisone-equivalent dose was 7 (23) mg/day for Black, 7 (26) for Hispanic, 7 (13) for Asian, and 4 (10) for White individuals. Adjusted multinomial models demonstrated higher odds of belonging to the highest vs. lowest steroid trajectory for Black (OR 2.07, 95% CI 1.65-2.61), Hispanic (OR 1.81, 95% CI 1.38-2.39), and Asian (OR 2.42, 95% CI 1.53-3.83) vs. White individuals. Having >5 outpatient visits during the baseline period was associated with lower odds of being in the persistently high-dose steroid trajectory (OR 0.77; 95% CI 0.60-0.98).
Black, Hispanic, and Asian (vs. White) individuals had higher odds of persistently high-dose steroid use. Sustained access to outpatient care and the development of standardized steroid-tapering regimens from clinical trials with diverse populations may be targets for intervention to mitigate disparities in steroid-related adverse outcomes.
糖皮质激素(“类固醇”)在系统性红斑狼疮(SLE)中经常使用。长期使用可能导致可避免不良结局的种族/民族差异。我们研究了类固醇使用和剂量的纵向模式中的种族/民族差异。
我们确定了 Medicaid 受益人为 18-65 岁的新发病例 SLE 患者,他们在索引日期后接受了 12 个月的类固醇治疗。基于群组的轨迹建模用于确定每日泼尼松等效类固醇剂量的模式。我们在基线期间检查了人口统计学,临床和医疗保健使用因素,并使用多项逻辑回归来估计随着时间的推移属于较高与最低类固醇剂量轨迹的几率。
我们确定了 6314 名有≥1 种类固醇处方的 SLE 患者。黑人的平均(SD)泼尼松等效剂量为 7(23)mg/天,西班牙裔为 7(26),亚洲人为 7(13),白人为 4(10)。调整后的多项逻辑回归模型表明,与白人相比,黑人(OR 2.07,95%CI 1.65-2.61),西班牙裔(OR 1.81,95%CI 1.38-2.39)和亚洲人(OR 2.42,95%CI 1.53-3.83)属于最高与最低类固醇轨迹的几率更高。在基线期间有> 5 次门诊就诊与处于持续高剂量类固醇轨迹的几率较低相关(OR 0.77;95%CI 0.60-0.98)。
黑人,西班牙裔和亚洲人(与白人相比)持续使用高剂量类固醇的可能性更高。从具有不同人群的临床试验中获得持续的门诊护理和制定标准化的类固醇减量方案可能是干预以减轻类固醇相关不良结局差异的目标。