四分位间距
医学
内科学
风湿性多肌痛
危险系数
血脂异常
单变量分析
胃肠病学
置信区间
中止
比例危险模型
入射(几何)
多元分析
巨细胞动脉炎
疾病
血管炎
光学
物理
作者
Juan Pablo Vinicki,Oscar Gut,María del Rosario Maliandi,José Luis Velasco Zamora,Miguel Linarez,Maria Alejandra Cusa,Julio Got,María Andrea Spinetto,Adrián Estévez,Alejandro Brigante,Ana Carolina Curti,Ana Carolina Costi,Javier A. Cavallasca
标识
DOI:10.1097/rhu.0000000000001969
摘要
Background In polymyalgia rheumatica (PMR) relapses and long-term GC dependency are common. We assessed risk factors for higher relapse rate and/or prolonged glucocorticoid therapy in PMR patients. Methods A multicenter and observational study (chart review) of PMR patients seen between 2006 and 2021 who had at least a 3-month follow-up period after starting GCs was performed. Results were expressed as median and interquartile range 25th–75th or mean ± standard deviation for numerical variables and percentage for categorical ones. Relapse versus nonrelapse groups were compared using Cox proportional analysis. Hazards ratios (HRs) with 95% confidence intervals (CIs) are reported. In all cases, a p value <0.05 was considered to indicate statistical significance. Results We included 185 patients (69.1% female). The median follow-up time was 17.1 months (interquartile range, 6.8–34.7). Incidence of relapses was 1.2 per 100 persons/month. In univariate analysis, PMR patients with a previous history of dyslipidemia had a lower risk of relapse (HR, 0.55; 95% CI, 0.33–0.94; p = 0.03); high-dose GC (HR, 2.35; 95% CI, 1.42–3.87; p = 0.001) and faster GC dose reduction had higher risk of relapse (HR, 3.04; 95% CI, 1.77–5.21; p = 0.001). In multivariate analysis, a previous history of dyslipidemia had a lower risk of relapse (HR, 0.54; 95% CI, 0.32–0.92; p = 0.023), and high dose of GC (HR, 2.46; 95% CI, 1.49–4.08; p = 0.001) remained the only risk factors for relapse. Conclusions Lower doses of corticosteroids and a slow rate of reduction are critical to avoid relapse in PMR. Risk factors for higher relapse rate rely on therapy more than clinical characteristics of the patients at the time of diagnosis of PMR.
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