Evidence map›Paper›PMID 41484962›Full record

ArticleBMC infectious diseases2026

Clinical analysis of Mycoplasma pneumoniae necrotizing pneumonia in children.

Yuhui Zhang, Lina Xie, Te Feng, Yanjun Guo

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Clinical Diagnosis and Treatment of 31 Children withInternational journal of general medicine · 2026
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yuhui ZhangDepartment of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, 450018, China.
Lina XieDepartment of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, 450018, China.
Te FengDepartment of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, 450018, China.
Yanjun GuoDepartment of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, 450018, China. 15838106076@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the clinical features and risk factors of Mycoplasma pneumoniae necrotizing pneumonia (MPNP) in children, providing a scientific basis for early diagnosis, effective treatment, and preventive strategies.

methodsA retrospective analysis of 138 children diagnosed with Mycoplasma pneumoniae pneumonia (MPP) admitted to the Children’s Hospital Affiliated to Zhengzhou University from August 2023 to December of the same year was performed. The patient population was divided into the MPNP group (41 cases) and the N-NP (N-Necrotizing pneumonia) group (97 cases) based on the presence or absence of comorbid MPNP. Baseline data, laboratory results, and imaging characteristics were compared. Logistic regression was used to identify risk factors for MPNP, and receiver operating characteristic (ROC) curve analysis was applied to evaluate diagnostic efficacy.

resultsCompared with the N-NP group, children in the MPNP group showed older age, longer hospitalization days, higher fever peak and fever days, and higher rates of chest pain, dyspnea, shortness of breath and combined extrapulmonary complications (all P < 0.05). Laboratory findings showed elevated white blood cells (WBC), neutrophil-to-lymphocyte ratio (NLR), C-reactive protein (CRP), interleukin−6 (IL−6), serum amyloid A (SAA), serum ferritin (SF), D-dimer (D-D), alanine aminotransferase (ALT), aspartate aminotransferase (AST), immunoglobulin A (IgA), immunoglobulin M (IgM), and lactate dehydrogenase (LDH). While total protein (TP), Albumin (ALB), complement component 4 (C4) levels were significantly lower (P < 0.05). The proportion of children with combined pleural effusion and the percentage of those who underwent fiberoptic bron-choscopic alveolar lavage (FBAL) with alveolar lavage were higher in the MPNP group than in the N-NP group (P < 0.05). Multivariate logistic regression identified age, fever days, D-D, LDH and pleural effusion as independent risk factors for MPNP. ROC curve analysis indicated that children with MPP who were aged > 5.45 years, fever days > 7.5 days, D-D > 0.73 mg/L, LDH > 399 U/L and concurrent pleural effusion predicted MPNP with a sensitivity of 0.878, specificity of 0.876, and area under the curve (AUC) of 0.940 (95%CI: 0.900−0.979).

conclusionAge, fever days, D-D, LDH, and pleural effusion are independent risk factors for MPNP in children. These factors should be closely examined in clinical practice in children with MPP to alert them to the potential risk of NP. Early identification of changes in these risk factors and implementation of timely and effective interventions hold significant clinical value for preventing and controlling the risk of MPP children developing MPNP.

Indexed as

Mycoplasma pneumoniaePneumonia, MycoplasmaPneumonia, NecrotizingChildChild, PreschoolChinaC-Reactive ProteinFemaleHumansInfantMaleRetrospective StudiesRisk FactorsROC CurveC-Reactive ProteinChildrenMycoplasma pneumoniaeNecrotizing pneumoniaRisk factor

Identifiers

PMID41484962
PMCPMC12866016

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.