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血小板减少症对突尼斯系统性红斑狼疮患者的临床意义和预后意义。

Clinical implications and prognostic significance of thrombocytopenia in Tunisian patients with systemic lupus erythematosus.

机构信息

Department of Internal Medicine, Hedi Chaker University Hospital, Sfax, Tunisia.

出版信息

Lupus. 2012 May;21(6):682-7. doi: 10.1177/0961203312438630. Epub 2012 Feb 21.

DOI:10.1177/0961203312438630
PMID:22354537
Abstract

OBJECTIVE

The objective of this study was to determine the role of thrombocytopenia in terms of disease manifestations, disease activity and prognostic impact in a cohort of Tunisian systemic lupus erythematosus (SLE) patients.

METHODS

The charts of 182 SLE patients diagnosed between 1996 and 2009 were retrospectively reviewed. The clinical manifestations, immunological profiles, disease activity, SLE relapses and survival rate at the time of follow-up were recorded.

RESULTS

Thrombocytopenia (<100,000/mm(3)) and severe thrombocytopenia (<20,000/mm(3)) was observed in 19.2% and 4.4%, respectively. Hemorrhagic manifestations were observed in 11 patients (31.4%). Thrombocytopenia was significantly associated with splenomegaly, renal disorders, neurologic manifestations, arterial thrombosis, leucopenia, low C3 level at SLE diagnosis, SLE relapses and infectious complications. Using multivariate logistic regression, thrombocytopenia was independently associated with splenomegaly (odds ratio [OR] = 9.36, p = 0.001), neurologic manifestations (OR = 4.6, p = 0.006) and renal disease (OR = 4.15, p = 0.02). By multivariable Cox proportional hazard regression analyses, thrombocytopenia was associated with the occurrence of mortality after adjusting for variables known to influence it (hazard ratio [HR] = 1.79, p = 0.045). The cause of death was unrelated to hemorrhagic complications in all patients.

CONCLUSION

Our results, concerning North-African SLE patients, confirm the findings of previous studies which suggest that thrombocytopenia correlates with more severe disease and has a negative impact on the survival of lupus patients.

摘要

目的

本研究旨在确定血小板减少症在突尼斯系统性红斑狼疮(SLE)患者队列中的疾病表现、疾病活动度和预后影响中的作用。

方法

回顾性分析了 1996 年至 2009 年间诊断的 182 例 SLE 患者的病历。记录了临床表现、免疫特征、疾病活动度、SLE 复发和随访时的生存率。

结果

血小板减少症(<100,000/mm³)和严重血小板减少症(<20,000/mm³)分别占 19.2%和 4.4%。11 例(31.4%)出现出血表现。血小板减少症与脾肿大、肾脏疾病、神经系统表现、动脉血栓形成、白细胞减少、SLE 诊断时 C3 水平低、SLE 复发和感染性并发症显著相关。使用多变量逻辑回归分析,血小板减少症与脾肿大(比值比 [OR] = 9.36,p = 0.001)、神经系统表现(OR = 4.6,p = 0.006)和肾脏疾病(OR = 4.15,p = 0.02)独立相关。通过多变量 Cox 比例风险回归分析,在调整已知影响其的变量后,血小板减少症与死亡率的发生相关(风险比 [HR] = 1.79,p = 0.045)。所有患者的死亡原因与出血并发症无关。

结论

我们的结果,针对北非的 SLE 患者,证实了先前研究的发现,即血小板减少症与更严重的疾病相关,对狼疮患者的生存有负面影响。

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