医学
内科学
纤维化
肺纤维化
风险因素
特发性肺纤维化
胃肠病学
肺
作者
L-Y. Zhai,H-H. Gong,WC Yu
出处
期刊:International Journal of Tuberculosis and Lung Disease
[International Union Against Tuberculosis and Lung Disease]
日期:2023-05-01
卷期号:27 (5): 395-400
被引量:1
标识
DOI:10.5588/ijtld.22.0604
摘要
OBJECTIVE: To determine whether mediastinal lymph node enlargement (MLNE) predicts progressive pulmonary fibrosis (PPF). METHODS: A total of 800 patients hospitalised for interstitial lung diseases (ILDs) were included in our study. The clinical presentations, radiographic features and laboratory findings of the patients were reviewed. RESULTS: MLNE was present in 313 (39.1%) ILD patients and were associated with higher total fibrosis score and risk of death than ILD patients without MLNE. The risk factors for PPF were age (OR 1.044, 95% CI 1.020–1.069; P < 0.001), the total extent of fibrosis (OR 1.396, 95% CI 1.116–1.746; P = 0.003) and MLNE (OR 2.130, 95% CI 1.362–3.332; P = 0.001) compared to non-PPF. Multivariable analysis showed that age, the lactate dehydrogenase level, MLNE, the total fibrosis score and pulmonary arterial systolic pressure were risk/prognostic factors for ILD patients. The model was robust in patients with idiopathic pulmonary fibrosis. However, the only risk/prognostic factor common to other ILD subgroups was the total fibrosis score. CONCLUSIONS: MLNE is associated with higher total fibrosis score and worse prognosis in ILD patients and could predict the occurrence of PPF. The only risk/prognostic factor applicable to all subgroups of ILDs is the total pulmonary fibrosis score.
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