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伴有胸膜肺受累、发热和 C 反应蛋白升高的急性心包炎:一种系统性自身炎症性疾病?一项队列研究。

Acute pericarditis with pleuropulmonary involvement, fever and elevated C-reactive protein: A systemic autoinflammatory disease? A cohort study.

机构信息

Department of Internal Medicine, ASST Fatebenefratelli-Sacco, Milan, Italy.

Department of Internal Medicine, ASST Fatebenefratelli-Sacco, Milan, Italy.

出版信息

Eur J Intern Med. 2023 Jul;113:45-48. doi: 10.1016/j.ejim.2023.03.034. Epub 2023 Apr 15.

Abstract

OBJECTIVES

This cohort study describes a systemic phenotype of pericarditis, comparing this phenotype with other forms of pericarditis.

PATIENTS AND METHODS

Patients in our center were enrolled in a prospectively maintained registry from 2019 to 2022. 412 patients with idiopathic recurrent pericarditis were analyzed. "Systemic inflammatory" subset was defined as the presence of all the following criteria: fever ≥38C°, CRP ≥2 times normal values, pleural effusion detected with any imaging techniques. The absence of any of the 3 criteria was defined as "isolated" subset.

RESULTS

We found that 211 (51.2%) of 412 patients (188 female) presented the systemic subset and the variables significantly associated with this subset in univariate analysis (p<0.001) were: higher mean age: 45.5 (±SD 17.2) vs 39.9 (±SD 16.4) years, higher mean CRP values: 128.8 vs 49.9 mg/L, higher proportion of pericardiocentesis: 19% vs 1.5%, higher mean leukocyte count: 13,143.3 vs 9910.3/mm, higher mean neutrophils number: 10,402.5 vs 6779.8 /mm and lower mean lymphocyte count: 1693.9 vs 2079.3 /mm. As results the neutrophil-to-lymphocyte ratio was higher in systemic inflammatory phenotype: 6.6 vs 3.4 (p< 0.001). Anti-IL1 therapy was started more frequently in the systemic subgroup (26%) than in the isolated subset (7.5%) (p < 0.001). On multivariate analysis neutrophil count and lymphopenia were statistically associated with the systemic subset (p < 0.001).

CONCLUSION

This results demonstrate the relevance of the systemic inflammatory phenotype, characterized by pleural effusions, confirming its analogy with autoinflammatory diseases, thus possibly requiring an eventual escalation of therapy to IL-1 inhibitors.

摘要

目的

本队列研究描述了心包炎的全身表型,并将其与其他形式的心包炎进行了比较。

方法

我们中心的患者于 2019 年至 2022 年期间纳入前瞻性维护的登记处。分析了 412 例特发性复发性心包炎患者。“全身炎症”亚组定义为存在以下所有标准:体温≥38°C,C 反应蛋白(CRP)≥正常值的 2 倍,胸腔积液可通过任何影像学技术检测到。不存在这 3 个标准中的任何一个被定义为“孤立”亚组。

结果

我们发现,412 例患者中有 211 例(51.2%)表现出全身亚组,在单变量分析中与该亚组显著相关的变量(p<0.001)为:更高的平均年龄:45.5(±17.2)岁 vs 39.9(±16.4)岁,更高的平均 CRP 值:128.8 与 49.9mg/L,更高的心包穿刺比例:19%与 1.5%,更高的平均白细胞计数:13143.3 与 9910.3/mm,更高的平均中性粒细胞数:10402.5 与 6779.8/mm,更低的平均淋巴细胞计数:1693.9 与 2079.3/mm。结果,中性粒细胞与淋巴细胞比值在全身炎症表型中更高:6.6 与 3.4(p<0.001)。在全身亚组中更频繁地开始抗 IL-1 治疗(26%)比在孤立亚组(7.5%)中更频繁(p<0.001)。多变量分析显示,中性粒细胞计数和淋巴细胞减少与全身亚组有统计学关联(p<0.001)。

结论

这些结果表明全身炎症表型的重要性,其特征为胸腔积液,证实其与自身炎症性疾病类似,因此可能需要将治疗升级为白细胞介素-1 抑制剂。

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