系统性红斑狼疮相关免疫血小板减少症显著复发的风险因素和适当的维持治疗策略。

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Chronic Disease Pub Date : 2023-03-21 eCollection Date: 2023-01-01 DOI:10.1177/20406223231160688
He-Jun Li, Yi-Qing Zheng, Ling Chen, Shun-Ping Lin, Xiang-Xiong Zheng
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引用次数: 0

摘要

背景:系统性红斑狼疮相关免疫性血小板减少症(SLE-ITP)的特点是复发。复发的风险因素和适当的维持治疗策略值得进一步探讨:确定首次完全应答后明显的系统性红斑狼疮-ITP 患者(血小板计数 ⩽30 × 109/l)复发的风险因素和适当的维持治疗:设计:回顾性队列研究,使用2012年12月至2021年3月期间福建医科大学附属协和医院确诊为重大系统性红斑狼疮-ITP的105例患者的病历。方法:利用 2012 年 12 月至 2021 年 3 月期间在福建医科大学附属协和医院确诊为重大系统性红斑狼疮-ITP 的 105 例患者的病历资料进行回顾性队列研究:分析数据包括人口统计学、初始临床特征、诱导和维持治疗以及随访结束时的结果。采用多变量逻辑回归模型分析了显著复发的风险因素。估计了明显复发的累积危险度和反应持续时间,并使用 Cox 回归分析比较了不同组间的结果差异:结果:共有 65 名明显复发的 SLE-ITP 患者符合最终分析条件。随访时间中位数[四分位数间距(IQR)]和应答时间中位数[IQR]分别为 62.2 [41.0-79.6] 个月和 43.4 [20.3-68.7] 个月。首次完全缓解后,有 19/65 例(29.2%)患者出现明显复发。与持续临床缓解(SCR)+持续应答(SR)组相比,明显复发组的停药患者比例更高(47.4% 对 8.7%,P = 0.001)。在 13 名停药患者中,明显复发组患者的维持治疗时间明显短于 SCR + SR 组患者(月数,中位数 [IQR], 43.1 [32.0-62.4] 对 12.0 [5.1-22.0], p = 0.009)。多变量逻辑回归分析显示,停药是导致严重复发的独立风险因素[几率比(OR)= 10.4,置信区间(CI)95% 2.2-47.8,P = 0.003]。糖皮质激素(GCs)+羟氯喹(HCQ)组与GCs+HCQ+免疫抑制剂(ISAs)组在明显复发率上无明显差异(26.7% 对 22.2%,P > 0.05)。通过 Cox 回归分析,GCs + HCQ 组和 GCs + HCQ + ISA 组的两条 SR 曲线基本吻合,显示出可比的长期疗效(P > 0.05):结论:停药,尤其是突然停药且维持治疗时间不足,是系统性红斑狼疮-ITP明显复发的独立危险因素。HCQ联合GCs有望成为系统性红斑狼疮-ITP患者维持治疗的首选。
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Risk factors of significant relapse and appropriate maintenance therapy strategy in SLE-associated immune thrombocytopenia.

Background: Systemic lupus erythematosus-associated immune thrombocytopenia (SLE-ITP) is characterized by relapse. The risk factors of relapse and appropriate maintenance therapy strategy deserve further exploration.

Objectives: To determine the risk factors for relapse and appropriate maintenance therapy in significant SLE-ITP patients (a platelet count ⩽30 × 109/l) after the first complete response.

Design: Retrospective cohort study using the medical records of 105 patients diagnosed as significant SLE-ITP in Fujian Medical University Union Hospital during December 2012 to March 2021. Patients were followed through a call for observations in January 2022.

Methods: Data including demographics, initial clinical feature, induction and maintenance therapy, and outcome at the end of follow-up were analyzed. Risk factors for significant relapse were analyzed using multivariate logistic regression models. The cumulative hazard of significant relapse and the duration of response were estimated, and the differences in outcome between groups were compared using the Cox regression analysis.

Results: A total of 65 significant SLE-ITP patients were eligible for the final analysis. Median [interquartile range (IQR)] follow-up duration and median [IQR] duration of response were 62.2 [41.0-79.6] months and 43.4 [20.3-68.7] months, respectively. After the first complete response, 19/65 (29.2%) had a significant relapse. Compared with sustained clinical remission (SCR) + sustained response (SR) group, significant relapse group had a higher proportion of discontinued patients (47.4% versus 8.7%, p = 0.001). Among the 13 discontinued patients, the duration of maintenance therapy of the patients in significant relapse group was significantly shorter than that of the patients in SCR + SR group (months, median [IQR], 43.1 [32.0-62.4] versus 12.0 [5.1-22.0], p = 0.009). Multivariate logistic regression analysis showed that drug withdrawal was an independent risk factor for significant relapse [odds ratio (OR) = 10.4, confidence interval (CI) 95% 2.2-47.8, p = 0.003]. There was no significant difference between glucocorticoids (GCs) + hydroxychloroquine (HCQ) group and GCs + HCQ + immunosuppressive agents (ISAs) group in significant relapse rate (26.7% versus 22.2%, p > 0.05). The two SR curves of GCs + HCQ and GCs + HCQ+ ISA group basically coincided by the Cox regression analysis, demonstrating comparable long-term outcomes (p > 0.05).

Conclusion: Drug withdrawal, especially abrupt withdrawal with insufficient duration of maintenance therapy, is an independent risk factor for significant relapse of SLE-ITP. HCQ combined with GCs is expected to be the first choice of the maintenance therapy for SLE-ITP patients.

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来源期刊
Therapeutic Advances in Chronic Disease
Therapeutic Advances in Chronic Disease Medicine-Medicine (miscellaneous)
CiteScore
6.20
自引率
0.00%
发文量
108
审稿时长
12 weeks
期刊介绍: Therapeutic Advances in Chronic Disease publishes the highest quality peer-reviewed research, reviews and scholarly comment in the drug treatment of all chronic diseases. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers involved in the medical treatment of chronic disease, providing a forum in print and online for publishing the highest quality articles in this area.
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