<p>This study aims to identify independent risk factors for severe Human Bocavirus 1(HBoV1) pneumonia in children across different age groups and to develop reliable age-stratified nomogram models based on early admission data for the rapid prediction of disease progression and severity. A total of 370 children with HBoV1 pneumonia hospitalized at Tianjin Children’s Hospital from September 2022 to August 2024 were retrospectively analyzed. Patients were divided into three age groups for analysis: Group 1 (&lt; 24&#xa0;months), Group 2 (24–47&#xa0;months), and Group 3 (≥ 48&#xa0;months). Multivariate logistic regression was used to identify independent risk factors. Of 370 HBoV1 pneumonia cases, severe pneumonia occurred in 145 (39.2%), with the highest incidence in Group 3 (50.6%, 42/83) versus 37.7% (43/114) and 34.7% (60/173) in other groups. For Group 1, the prediction model included BMI, maximum temperature before admission, pleural thickening, CK, CKMB, and IL-6. For Group 2, the key predictors were history of eczema, pleural thickening, and N%. For Group 3, the model incorporated L%, ALB, CK, C3, and Absolute CD3 Cell Count. The areas under the ROC curve for the three age-specific models were 0.819 (95% CI: 0.7405–0.8978), 0.729 (95% CI: 0.652–0.8064), and 0.801 (95% CI: 0.7064–0.8952), respectively. The decision curve analysis curve demonstrated outstanding net benefit. The C-index values in each group were respectively 0.791, 0.727, and 0.768. <i>Conclusion</i>: This study develops age-stratified prediction models for severe human bocavirus 1 pneumonia in children based on early admission data. Nomograms for all three age groups exhibited good calibration performance and demonstrated clinical applicability.<Table Float="No" ID="Taba"> <tgroup align="left" cols="2"> <colspec align="left" colname="c1" colnum="1" /> <colspec align="left" colname="c2" colnum="2" /> <tbody> <row> <entry nameend="c2" namest="c1"> <p><b>What is Known:</b></p> <p>• <i>Human Bocavirus 1 (HBoV1) is a significant respiratory pathogen in children, capable of causing pneumonia with varying severity,&#xa0;from mild to life-threatening.</i></p> <p>• <i>Age is a key predictor of severe pneumonia in children.</i></p> </entry> </row> <row> <entry nameend="c2" namest="c1"> <p><b>What is New:</b></p> <p>• <i>The clinical manifestations and laboratory findings in children with Human Bocavirus 1 pneumonia exhibit age-specific&#xa0;characteristics.</i></p> <p>• <i>Based on early admission data, this study developed age-stratified prediction models for severe Human Bocavirus 1 pneumonia in&#xa0;children, which demonstrated good performance.</i></p> </entry> </row> </tbody> </tgroup> </Table></p>

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Early and rapid prediction of severe Human Bocavirus 1 pneumonia in children: an age-stratified Nomogram Model based on admission data

  • Zixuan Wang,
  • Xinxin Chen,
  • Diwei Wei,
  • Zhen Xu,
  • Wen Yu,
  • Yuerong Wang,
  • Yongsheng Xu,
  • Tongqiang Zhang,
  • Wei Guo

摘要

This study aims to identify independent risk factors for severe Human Bocavirus 1(HBoV1) pneumonia in children across different age groups and to develop reliable age-stratified nomogram models based on early admission data for the rapid prediction of disease progression and severity. A total of 370 children with HBoV1 pneumonia hospitalized at Tianjin Children’s Hospital from September 2022 to August 2024 were retrospectively analyzed. Patients were divided into three age groups for analysis: Group 1 (< 24 months), Group 2 (24–47 months), and Group 3 (≥ 48 months). Multivariate logistic regression was used to identify independent risk factors. Of 370 HBoV1 pneumonia cases, severe pneumonia occurred in 145 (39.2%), with the highest incidence in Group 3 (50.6%, 42/83) versus 37.7% (43/114) and 34.7% (60/173) in other groups. For Group 1, the prediction model included BMI, maximum temperature before admission, pleural thickening, CK, CKMB, and IL-6. For Group 2, the key predictors were history of eczema, pleural thickening, and N%. For Group 3, the model incorporated L%, ALB, CK, C3, and Absolute CD3 Cell Count. The areas under the ROC curve for the three age-specific models were 0.819 (95% CI: 0.7405–0.8978), 0.729 (95% CI: 0.652–0.8064), and 0.801 (95% CI: 0.7064–0.8952), respectively. The decision curve analysis curve demonstrated outstanding net benefit. The C-index values in each group were respectively 0.791, 0.727, and 0.768. Conclusion: This study develops age-stratified prediction models for severe human bocavirus 1 pneumonia in children based on early admission data. Nomograms for all three age groups exhibited good calibration performance and demonstrated clinical applicability.

What is Known:

Human Bocavirus 1 (HBoV1) is a significant respiratory pathogen in children, capable of causing pneumonia with varying severity, from mild to life-threatening.

Age is a key predictor of severe pneumonia in children.

What is New:

The clinical manifestations and laboratory findings in children with Human Bocavirus 1 pneumonia exhibit age-specific characteristics.

Based on early admission data, this study developed age-stratified prediction models for severe Human Bocavirus 1 pneumonia in children, which demonstrated good performance.