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首页> 外文期刊>International journal of clinical rheumatology. >Systemic lupus erythematosus-associated pulmonary hypertension: Clinical variables and survival outcome
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Systemic lupus erythematosus-associated pulmonary hypertension: Clinical variables and survival outcome

机译:系统性红斑狼疮相关性肺动脉高压:临床变量和生存结果

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摘要

Aim: Compare systemic lupus erythematosus (SLE) patients with pulmonary hypertension (PH) versus SLE without PH, to study the variables associated with PH. Methods: Case-control cross-sectional study of SLE patients from 2006 to 2011. PH was diagnosed by echocardiogram or cardiac catheterization. Controls were randomly selected from SLE patients with no PH. PH cases: controls ratio was 39:69, matching for age and gender. Clinical, serologic profiles and outcome were analyzed. Results: We identified 39 PH patients. Anti-ribonucleoprotein was positively associated with PH; malar rash was negatively associated. The 3-year survival of SLE-PH patients was 87.2%. Conclusion: The differences associated with SLE-PH may aid early recognition and treatment. We suggest a lower threshold for screening or even routine screening of PH in patients with anti-ribonucleoprotein positivity and negative malar rash.
机译:目的:比较患有肺动脉高压(PH)的系统性红斑狼疮(SLE)患者与没有PH的SLE患者,以研究与PH相关的变量。方法:2006年至2011年SLE患者的病例对照横断面研究。通过超声心动图或心脏导管检查诊断PH。从没有PH的SLE患者中随机选择对照组。 PH病例:对照比率为39:69,符合年龄和性别。临床,血清学特征和结果进行了分析。结果:我们确定了39名PH患者。抗核糖核蛋白与PH呈正相关。黄斑皮疹呈负相关。 SLE-PH患者的3年生存率为87.2%。结论:与SLE-PH相关的差异可能有助于早期识别和治疗。对于具有抗核糖核蛋白阳性和黄斑皮疹阴性的患者,我们建议降低筛查甚至常规筛查PH的阈值。

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