Evidence map›Paper›PMID 39017999›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2024

Clinical characteristics and logistic regression analysis of macrolide-resistant Mycoplasma pneumoniae pneumonia in children.

Mengzhen Yan, Ran Tao, Shigang Li, Jinwen Xiong, Jinbo Xiang

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Clinical features and risk factors for severe macrolide-resistant mycoplasma pneumoniae pneumonia induced by 23 S rRNA A2063G mutation: a retrospective observational study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Observational
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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

5 authors.

Mengzhen YanAffiliated Renhe Hospital of China Three Gorges University, Neonatology Wujiagang District, Yichang City, Hubei Province, China.ORCID http://orcid.org/0009-0008-8418-7429
Ran TaoAffiliated Renhe Hospital of China Three Gorges University, Neonatology Wujiagang District, Yichang City, Hubei Province, China.
Shigang LiAffiliated Renhe Hospital of China Three Gorges University, Neonatology Wujiagang District, Yichang City, Hubei Province, China.
Jinwen XiongAffiliated Renhe Hospital of China Three Gorges University, Neonatology Wujiagang District, Yichang City, Hubei Province, China.
Jinbo XiangAffiliated Renhe Hospital of China Three Gorges University, Neonatology Wujiagang District, Yichang City, Hubei Province, China. 594669464@qq.com.

Funding

Affiliated Renhe Hospital of China Three Gorges University RHKFBL2022-03China Young Talent Programme Q20211203
6 · The paper itself

Abstract

purposeTo investigate macrolide-resistant Mycobacterium pneumoniae (MRMP) pneumonia in children and construct a logistic regression model for mutations in the Mycoplasma pneumoniae drug-resistant gene.

methodsClinical data of 281 children were analyzed. Sequencing confirmed a mutation at the A2063G locus of the 23 S rRNA gene in 227 children (A2063G group); 54 children showed no mutations (non-MRMP [NMRMP] group). We compared clinical features, laboratory tests, imaging, and bronchoscopy results and constructed a multifactorial logistic regression model to analyze risk and protective factors.

resultsThe A2063G group had longer durations of fever and hospitalization before admission, a higher proportion of treatment with sodium methylprednisolone succinate (MPS)/dexamethasone, longer time to discontinue hormones, and higher probability of combined infections. Monocyte percentage was significantly higher in the A2063G group. Imaging suggested a higher incidence of infections in the right lung compared to both lungs. Univariate analysis revealed fever duration before admission, hormone dose and duration, monocyte percentage, and mixed infections as risk factors for Mycoplasma pneumoniae infection with the A2063G mutation. The logistic regression model showed that mixed infections were an independent risk factor for the A2063G locus mutation, whereas hormone dose was a protective factor.

conclusionA prevalence of macrolide resistance of 80.8% among children was observed in the region. Logistic regression analysis revealed that co-infection with other respiratory pathogens is an independent risk factor for the development of resistance genes, while the use of hormone dosage acts as a protective factor.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialMacrolidesMycoplasma pneumoniaePneumonia, MycoplasmaRNA, Ribosomal, 23SChildChild, PreschoolFemaleHumansInfantLogistic ModelsMaleMutationRetrospective StudiesRisk FactorsAnti-Bacterial AgentsMacrolidesRNA, Ribosomal, 23SGlucocorticoidLogistic regression analysisMacrolide resistanceMycoplasma pneumoniae

Identifiers

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Registered trials

None linked

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 Socratic graph.