Wang Jinxia, Lei Kai, Li Jinxia, Zhang Yanan, Chi Shuhong, Zhang Zhengping, Huang Lingyan, Yang Xia
Ningxia Medical University, Yinchuan, China.
Department of Respiratory and Critical Care Medicine, General Hospital of Ningxia Medical University, Yinchuan, China.
Medicine (Baltimore). 2024 May 3;103(18):e37992. doi: 10.1097/MD.0000000000037992.
Multiple takayasu arteritis (TA) is a chronic nonspecific large to medium vasculitis disease that mainly accumulates the aorta and its branches. Pulmonary vascular disease is often seen as stenosis and occlusion, and patients may show no moderate to severe pulmonary hypertension (PH). This study aims to summarize the clinical characteristics and analysis of prognostic factors in patients with PH caused by TA.
Patients diagnosed with aortitis involving the pulmonary artery by pulmonary arteriography or pulmonary artery and total aortic computed tomography arteriography (CTA). All patients underwent detailed clinical assessment, laboratory data collection, and analysis of imaging data. Patients were followed up and factors affecting the prognosis of the pulmonary arteries were analyzed.
Most of the patients' complaints were chest tightness, shortness of breath, decreased activity tolerance, hemoptysis and chest pain. 56.90% of the patients were in at the time of admission. Echocardiographic estimation of pulmonary artery systolic pressure was 90.39 ± 22.87 mm Hg. In terms of laboratory tests, 39.66%% of the patients had elevated C-reactive protein and erythrocyte sedimentation rate, and amino-terminal natriuretic peptide precursor on admission. In terms of imaging, all patients had pulmonary artery involvement, which was combined with aortic involvement in 31.03%. Nuclide lung perfusion/ventilation imaging of the patients revealed multiple perfusion defects/absences in the segmental and subsegmental distribution of the lungs. Univariate Cox regression model analysis suggested that patients' WHO functional class at admission, age ≧ 51 years at the time of consultation, and amino-terminal natriuretic peptide precursor ≧ 3500 pg/mL were factors affecting the prognosis. Further multifactorial Cox regression model analysis suggested amino-terminal natriuretic peptide precursor ≧ 3500 pg/mL was an independent predictor of poor prognosis with a hazard ratio (HR) value of 5.248.
Electrocardiogram and echocardiogram may suggest an increased right heart load; some patients have elevated serum inflammatory indexes. Characteristic imaging manifestations include widening of the main pulmonary artery, multiple pulmonary segmental and subsegmental stenoses.
多发性大动脉炎(TA)是一种慢性非特异性大中血管炎疾病,主要累及主动脉及其分支。肺血管病变常表现为狭窄和闭塞,患者可能无中度至重度肺动脉高压(PH)。本研究旨在总结TA所致PH患者的临床特征并分析预后因素。
通过肺动脉造影或肺动脉及全主动脉计算机断层血管造影(CTA)诊断为累及肺动脉的主动脉炎患者。所有患者均接受详细的临床评估、实验室数据收集及影像资料分析。对患者进行随访并分析影响肺动脉预后的因素。
大多数患者的主诉为胸闷、气短、活动耐力下降、咯血和胸痛。56.90%的患者入院时处于[此处原文缺失具体状态描述]。超声心动图估算肺动脉收缩压为90.39±22.87 mmHg。实验室检查方面,39.66%的患者入院时C反应蛋白、红细胞沉降率及氨基末端脑钠肽前体升高。影像学方面,所有患者均有肺动脉受累,其中31.03%合并主动脉受累。患者的核素肺灌注/通气显像显示肺部节段性和亚节段性分布存在多处灌注缺损/缺失。单因素Cox回归模型分析提示,患者入院时的世界卫生组织功能分级、就诊时年龄≥51岁以及氨基末端脑钠肽前体≥3500 pg/mL是影响预后的因素。进一步多因素Cox回归模型分析提示,氨基末端脑钠肽前体≥3500 pg/mL是预后不良的独立预测因素,风险比(HR)值为5.248。
心电图和超声心动图可能提示右心负荷增加;部分患者血清炎症指标升高。特征性影像表现包括主肺动脉增宽、多处肺段和亚段狭窄。