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Published on: August 25, 2017
Construction and validation of a nomogram for predicting chronic obstructive pulmonary disease with bronchiectasis
Zhipeng Feng1, Chuanxiang Li2, Si Fang2
1Department of Respiratory and Critical Care Medicine, Wuhan Third Hospital, School of Medicine, Wuhan University of Science and Technology, Wuhan, China.
This study identified key risk factors for chronic obstructive pulmonary disease (COPD) with bronchiectasis (BE), developing a nomogram to predict COPD-BE. The model aids early identification and targeted management, potentially improving outcomes for COPD patients.
Area of Science:
- Pulmonology and Respiratory Medicine
- Clinical Prediction Modeling
- Epidemiology of Respiratory Diseases
Background:
- Chronic obstructive pulmonary disease (COPD) coexisting with bronchiectasis (BE) significantly worsens patient prognosis, increasing symptom severity and mortality.
- Accurate identification of COPD-BE is crucial for implementing targeted management strategies and improving clinical outcomes.
- Existing diagnostic approaches may not sufficiently identify BE in COPD patients early.
Purpose of the Study:
- To identify independent risk factors (RFs) associated with the presence of bronchiectasis (BE) in patients with chronic obstructive pulmonary disease (COPD).
- To develop and validate a nomogram-based clinical prediction model for early identification of COPD-BE.
- To provide clinicians with a tool for timely diagnosis and tailored management of COPD-BE patients.
Main Methods:
- Retrospective analysis of 382 COPD patients, randomly divided into training (268) and validation (114) cohorts.
- Logistic regression (univariate, LASSO, and multivariable) employed to identify independent RFs for COPD-BE.
- A predictive nomogram was constructed using identified RFs and validated using ROC analysis, calibration, and decision curve analysis (DCA).
Main Results:
- Independent risk factors for COPD-BE included female sex, hemoptysis, history of pulmonary tuberculosis, Pseudomonas aeruginosa infection, globulin levels, and mechanical ventilation duration.
- The developed nomogram showed good discriminative ability with an AUC of 0.840 in the training set and 0.829 in the validation set.
- Calibration analyses confirmed good agreement between predicted and actual outcomes, and DCA suggested potential clinical utility.
Conclusions:
- Female sex, hemoptysis, pulmonary tuberculosis history, Pseudomonas aeruginosa infection, globulin level, and mechanical ventilation duration are significant independent RFs for COPD-BE.
- The nomogram demonstrates robust predictive performance for identifying COPD-BE, validated through internal testing.
- This nomogram shows promise as a valuable clinical tool for early COPD-BE detection, pending external validation.
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