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Published on: June 28, 2018
Diagnostic Utility of HBP, PCT, and CRP in Identifying Bacterial Complications in Severe COVID-19
Ying Cai1, Yi-Feng Sun2, Qi-Hui Zhang1
1Department of Critical Care Medicine, Hongqi Hospital affiliated to Mudanjiang Medical University, Mudanjiang City, Heilongjiang Province 157011, China.
Insights
Combined procalcitonin (PCT), C-reactive protein (CRP), and heparin-binding protein (HBP) levels accurately identify bacterial infections in critically ill COVID-19 patients. This aids in optimizing antibiotic therapy timing for better patient outcomes.
Area of Science:
- Biomarkers
- Infectious Disease Diagnostics
- Critical Care Medicine
Background:
- Delayed diagnosis of bacterial infections complicates critical COVID-19 care.
- Need for reliable biomarkers to guide antibiotic therapy in severe COVID-19 patients.
Purpose of the Study:
- Evaluate serum procalcitonin (PCT), C-reactive protein (CRP), and heparin-binding protein (HBP) performance.
- Assess bronchoalveolar lavage fluid HBP as a biomarker.
- Differentiate bacterial infections from COVID-19 in critically ill patients.
Main Methods:
- Enrolled severe/critical COVID-19 patients and healthy controls.
- Measured serum PCT, CRP, and HBP levels.
- Stratified COVID-19 patients by bacterial culture results for statistical analysis.
Main Results:
- Serum PCT and HBP were significantly elevated in bacterial infections versus COVID-19 and controls.
- Combined PCT, CRP, and HBP showed high diagnostic performance (AUC 0.978, sensitivity 0.966, specificity 0.933).
- CRP alone had limited ability to distinguish bacterial infections from COVID-19.
Conclusions:
- Combined PCT, CRP, and HBP detection improves classification of co-occurring bacterial infections in COVID-19.
- Biomarker panel informs optimal timing for initiating antibiotic treatment.
Background:
To address the challenge of delayed bacterial infection diagnosis in critically ill COVID-19 patients, we evaluated the performance of serum procalcitonin (PCT), C-reactive protein (CRP), and heparin-binding protein (HBP), and bronchoalveolar lavage fluid HBP as potential biomarkers for guiding antibiotic therapy.
Methods:
Patients meeting the inclusion criteria for severe and critical COVID-19 were enrolled as the case group, while age- and gender-matched healthy individuals were selected as the control group. Levels of PCT, CRP, and HBP were measured. The case group was further stratified based on bacterial culture results, and differences in serum, sputum, or bronchoalveolar lavage fluid markers were subjected to statistical analysis.
Results:
Plasma levels of PCT and HBP were significantly higher in patients with bacterial infection compared to both the COVID-19 group and the healthy control group, while CRP was only significant in distinguishing cases from the healthy control group. The AUC for PCT in differentiating COVID-19 patients from those with bacterial infection was 0.937 with a sensitivity of 0.828 and specificity of 0.933, while the AUC for CRP was 0.564 with a sensitivity of 0.828 and specificity of 0.400. The AUC for HBP was 0.775 with a sensitivity of 0.690 and specificity of 0.967. The combined detection of PCT+CRP+HBP exhibited the highest diagnostic performance, with an AUC of 0.978, a sensitivity of 0.966, and a specificity of 0.933.
Conclusions:
The combined detection of PCT, CRP, and HBP can enable more precise classification of COVID-19 patients with concurrent bacterial infections and inform the optimal timing of antibiotic initiation.
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