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大环内酯类抗生素对23S rRNA基因携带大环内酯类耐药突变的小儿支原体肺炎的临床疗效

Clinical efficacy of macrolide antibiotics in mycoplasma pneumoniae pneumonia carrying a macrolide-resistant mutation in the 23 S rRNA gene in pediatric patients.

作者信息

He Mengyuan, Xie Junfeng, Rui Pu, Li Xiaoyu, Lai Min, Xue Hongman, Chen Chun

机构信息

Pediatric Hematology Laboratory, Division of Hematology/Oncology, Department of Pediatrics, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, China.

出版信息

BMC Infect Dis. 2024 Jul 31;24(1):758. doi: 10.1186/s12879-024-09612-6.

Abstract

BACKGROUND

The global prospective surveillance data showed the re-emergence of mycoplasma pneumoniae pneumonia (MPP) in Europe and Asia after the coronavirus disease 2019 pandemic. We sought to observe the effect of macrolide antibiotics in the treatment of MPP carrying a macrolide-resistant mutation gene and the potential of targeted next-generation sequencing (tNGS) as a front-line diagnostic in MPP patients.

METHODS

The baseline characteristics of 91 children with MPP hospitalized from January to October 2023 were retrospectively analyzed. They were divided into two groups according to whether carrying the macrolide-resistant mutation or not. The logistic and linear regression analyses were used to determine whether the mutation was a standalone predictive predictor of the duration of fever and hospital length of stay.

RESULTS

First, no patients had a fever for ≥ 7 days after macrolide treatment. But length of stay and hormone concentration were significantly different between the two groups (P < 0.05). There were also no statistical association between the mutation and the duration of fever and hospital length of stay.

CONCLUSION

Macrolides can be administered to MPP children carrying a macrolide-resistant mutation. tNGS can be seen as a front-line diagnostic in MPP.

摘要

背景

全球前瞻性监测数据显示,2019冠状病毒病大流行后,支原体肺炎(MPP)在欧洲和亚洲再度出现。我们试图观察大环内酯类抗生素对携带大环内酯耐药突变基因的MPP的治疗效果,以及靶向二代测序(tNGS)作为MPP患者一线诊断方法的潜力。

方法

回顾性分析2023年1月至10月住院的91例MPP患儿的基线特征。根据是否携带大环内酯耐药突变将他们分为两组。采用逻辑回归和线性回归分析来确定该突变是否是发热持续时间和住院时间的独立预测指标。

结果

首先,大环内酯治疗后没有患者发热≥7天。但两组之间的住院时间和激素浓度有显著差异(P<0.05)。该突变与发热持续时间和住院时间之间也没有统计学关联。

结论

可以对携带大环内酯耐药突变的MPP患儿使用大环内酯类药物。tNGS可被视为MPP的一线诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/528e/11292884/45895d637709/12879_2024_9612_Fig1_HTML.jpg

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