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Independent risk factors for refractory mycoplasma pneumoniae pneumonia in children: a multivariate analysis
Qi Guo1, Hui Guo2, Jie-Jie Chen3
1Department of Pediatrics, Anhui Provincial Second People's Hospital, No. 1868, North Second Ring Road, Hefei City, Anhui Province, 230041, China. q4i_gg816uo@163.com.
Objective:
To investigate the risk factors for refractory Mycoplasma pneumoniae pneumonia (RMPP) in children.
Methods:
Children with Mycoplasma pneumoniae pneumonia who were treated in our hospital from January 1, 2024 to June 1, 2025 were retrospectively collected and divided into the refractory Mycoplasma pneumoniae pneumonia group with 144 cases and the general Mycoplasma pneumoniae pneumonia (GMPP) group with 161 cases according to the occurrence of RMPP. The clinical data and serological indicators of the two groups were compared using the t-test, χ²-test and Logistic regression analysis.
Result:
Leukocyte count (8.62 ± 4.48 vs. 9.84 ± 1.01, P = 0.002), C-reactive protein (21.64 ± 14.76 vs. 26.61 ± 6.71, P < 0.001), D-dimer (0.72 ± 0.10 vs. 1.08 ± 0.60, P < 0.001), lactate dehydrogenase (281.05 ± 80.22 vs. 326.02 ± 43.92, P < 0.001) and neutrophil-to-lymphocyte ratio (NLR, 3.11 ± 2.11 vs. 4.84 ± 0.95, P < 0.001) in the RMPP group were significantly higher than those in the GMPP group. The Clinical Pulmonary Infection Score (CPIS, OR = 2.617, 95%CI:1.603-4.273), D-dimer (OR = 9.891, 95%CI:3.848-25.426), NLR (OR = 1.865, 95%CI:1.490-2.336), presence of pulmonary rales (OR = 5.265, 95%CI:2.305-12.026), abnormal chest imaging findings (P = 0.005), complicated infections (P < 0.001) and positive drug-resistant gene loci (OR = 14.023, 95%CI:5.712-34.426) were identified as independent influencing factors for RMPP infection. NLR yielded the highest area under the curve (AUC) for predicting RMPP infection with an AUC of 0.836 (95%CI:0.788-0.885), followed by the CPIS with an AUC of 0.700 (95%CI:0.640-0.759) and D-dimer with an AUC of 0.691 (95%CI:0.620-0.762).
Conclusion:
The CPIS, D-dimer, NLR, presence of pulmonary rales, abnormal chest imaging findings, complicated infections and positive drug-resistant gene loci are independent influencing factors for RMPP infection, and vigilance for the development of RMPP is warranted in the presence of these factors.
Insights
Refractory Mycoplasma pneumoniae pneumonia (RMPP) in children is associated with higher leukocyte counts and specific inflammatory markers. Factors like elevated neutrophil-to-lymphocyte ratio (NLR) and Clinical Pulmonary Infection Score (CPIS) predict RMPP development.
Area of Science:
- Pediatric Infectious Diseases
- Respiratory Medicine
- Clinical Microbiology
Background:
- Mycoplasma pneumoniae pneumonia (MPP) is a common childhood respiratory infection.
- Refractory MPP (RMPP) presents a significant clinical challenge due to persistent symptoms and potential complications.
- Identifying risk factors for RMPP is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To investigate the independent risk factors associated with the development of refractory Mycoplasma pneumoniae pneumonia (RMPP) in pediatric patients.
- To compare clinical and serological indicators between children with RMPP and those with general MPP (GMPP).
Main Methods:
- A retrospective study involving 144 RMPP cases and 161 GMPP cases treated between January 1, 2024, and June 1, 2025.
- Comparison of clinical data and serological indicators using t-tests, chi-squared tests, and Logistic regression analysis.
- Evaluation of predictive values for key indicators using Area Under the Curve (AUC).
Main Results:
- Children with RMPP exhibited significantly higher leukocyte counts, C-reactive protein, D-dimer, lactate dehydrogenase, and neutrophil-to-lymphocyte ratio (NLR) compared to GMPP.
- Independent risk factors for RMPP included Clinical Pulmonary Infection Score (CPIS), D-dimer, NLR, pulmonary rales, abnormal chest imaging, complicated infections, and positive drug-resistant gene loci.
- NLR demonstrated the highest predictive value (AUC=0.836) for RMPP, followed by CPIS (AUC=0.700) and D-dimer (AUC=0.691).
Conclusions:
- CPIS, D-dimer, NLR, pulmonary rales, abnormal chest imaging, complicated infections, and positive drug-resistant gene loci are significant independent risk factors for RMPP in children.
- Vigilance for RMPP is recommended when these factors are present.
- NLR is a highly valuable biomarker for predicting RMPP development.
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