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DOI 10.21037/jtd-2025-638

Медицинская библиотека · Journal of thoracic disease · 2025

Computed tomography characteristics of chronic bronchitis and its association with disease severity and clinical outcomes in viral pneumonia: a retrospective cohort study.

Wang Xiaofei, Zhou Zhentao, Peng Yuting, Tang Yinying, Dai Qi, Zheng Jianjun, Zhang Jingfeng

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Аннотация

BACKGROUND

Chronic bronchitis (CB) patients' excessive mucus and airway changes may worsen viral pneumonia severity, but there is a lack of objective clinical/imaging assessment criteria. This study used quantitative computed tomography (CT) to link CB pathology with pneumonia severity/prognosis, guiding early interventions for high-risk groups.

METHODS

This retrospective cohort study included 42 patients with CB diagnosed with viral pneumonia and 208 non-CB viral pneumonia controls. Baseline demographic, clinical, and laboratory parameters were collected alongside thoracic CT-derived metrics, including mucus plugging score (a bronchopulmonary segment-based scoring system quantifying mucus obstruction severity), CT severity score (range, 0-25 per lobe), and emphysema quantification. Follow-up CT imaging was performed at 3 months post-diagnosis to assess pulmonary structural remodeling, with longitudinal documentation of CT severity scores. Participants were stratified into two cohorts by mucus plugging score: high mucus burden (≥4, group 1) and low mucus burden (<4, group 2). Intergroup comparisons utilized Fisher's exact test for categorical variables, with continuous variables analyzed via independent t-tests (normally distributed) or Mann-Whitney U tests (non-parametric distributions). Multivariate logistic regression modeling identified independent predictors of disease progression.

RESULTS

This study enrolled 260 patients who were categorized into group 1 (n=42; CB prevalence: 35.70%) and group 2 (n=218; CB prevalence:19.70%). Comparative analysis demonstrated that CB patients in group 2 were significantly older [70, interquartile range (IQR) (62, 77) vs. 79, IQR (74.5, 86.5) years; P<0.001] and exhibited a higher female predominance (74.4% vs. 25.6%; P=0.03), alongside lower red blood cell count (RBC) [3.73, IQR (3.39, 4.29)×1012/L vs. 4.05, IQR (3.81, 4.53)×1012/L; P=0.02] and hemoglobin levels [119, IQR (105.5, 131) vs. 124, IQR (115.5, 136) g/L; P=0.04] compared to non-CB counterparts. Imaging analysis revealed that non-CB patients had greater thoracic reticular patterns [6.02, IQR (1.42, 10.08) vs. 2.50, IQR (0.57, 6.19) cm3; P=0.02] and emphysema severity [0.21, IQR (0.04, 0.73) vs. 0.05, IQR (0.01, 0.19) cm3; P<0.001], whereas CB patients across both groups showed marked bronchial wall thickening [group 1: 21.60, IQR (10.30, 37.69) vs. 6.28, IQR (1.54, 15.71) cm3, P=0.03; group 2: 35.08, IQR (13.38, 51.59) vs. 18.90, IQR (3.43, 45.53) cm3, P=0.01]. Notably, CB patients in group 2 displayed larger bronchial lumen volumes [13.63, IQR (5.19, 25.29) vs. 5.00, IQR (0.67, 13.46) cm3; P<0.001]. Multivariate analysis of the low mucus burden group identified female sex [odds ratio (OR) =3.39], age (OR =1.06), and emphysema (OR =1.56) as independent risk factors for disease progression (all P<0.05). Longitudinal CT follow-up indicated stable severity scores in non-CB patients, whereas high mucus-secreting CB patients (group 1) demonstrated significant reductions in mucus plugging scores over time.

CONCLUSIONS

CB features-mucus hypersecretion, emphysema, and airway thickening-worsen viral pneumonia severity and prognosis. Key predictors include advanced age (OR =1.06), female sex (OR =3.39), and emphysema (OR =1.56). High-risk CB patients, especially with emphysema, need enhanced CT monitoring and therapies improving mucociliary clearance and airway repair.

Для цитирования: Wang Xiaofei, Zhou Zhentao, Peng Yuting, Tang Yinying, Dai Qi, Zheng Jianjun, Zhang Jingfeng. Computed tomography characteristics of chronic bronchitis and its association with disease severity and clinical outcomes in viral pneumonia: a retrospective cohort study.. Journal of thoracic disease. 2025. DOI: 10.21037/jtd-2025-638.
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