23s rRNA A2063G突变致重症大环内酯耐药肺炎支原体肺炎临床特征及危险因素的回顾性观察研究

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Wenrui Ding, Yan Guo, Houyu Chen, Houxi Bai, Xiaotao Yang, Yanchun Wang, Yonghan Luo
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引用次数: 0

摘要

目的:探讨23s rRNA A2063G突变诱导的重症大环内酯耐药肺炎支原体肺炎(MRMP)的临床特点及危险因素。方法:收集昆明儿童医院诊断为肺炎支原体肺炎(MPP)的526例患儿的临床资料,为2023年10月至2024年2月进行的单中心队列研究。其中483例(91.83%)检测出23s rRNA A2063G突变阳性。根据临床严重程度将患者分为重症组(n = 192)和一般组(n = 291)。进行单因素和多因素logistic回归分析,以确定严重MRMP的危险因素。结果:单因素分析显示,与普通组相比,重症组年龄更小,病程更长,高烧高峰温度更高,发烧持续时间更长。重度组的喘息、呼吸困难和呼吸音减少的发生率明显更高。放射学结果显示,严重组肺实变、肺不张、胸腔积液和多肺受累的发生率较高。实验室检查显示,重症组中性粒细胞、血小板、肝酶、乳酸脱氢酶(LDH)、d -二聚体和红细胞沉降率升高,同时白蛋白、血尿素氮和肌酐水平降低。在治疗方面,多西环素是MRMP的主要替代方案,但在重症组中更频繁地使用氟喹诺酮类药物,同时糖皮质激素的使用也明显增加。此外,重症组更常需要氧气治疗,2%的患者需要机械通气或进入儿科重症监护病房。结论:发热时间延长、多肺叶实变、LDH升高、d -二聚体水平升高是严重MRMP的关键预测指标。虽然严重的MRMP与临床病程延长和治疗复杂相关,但及时调整抗生素方案和支持性护理可有效改善预后。临床试验号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical features and risk factors for severe macrolide-resistant mycoplasma pneumoniae pneumonia induced by 23 S rRNA A2063G mutation: a retrospective observational study.

Objectives: This study aimed to investigate the clinical characteristics and risk factors of severe macrolide-resistant Mycoplasma pneumoniae pneumonia (MRMP) induced by the 23 S rRNA A2063G mutation.

Methods: Clinical data were collected from 526 pediatric patients diagnosed with Mycoplasma pneumoniae pneumonia (MPP) at Kunming Children's Hospital, representing a single-center cohort study conducted between October 2023 and February 2024. Among them, 483 cases (91.83%) tested positive for the 23 S rRNA A2063G mutation. Patients were categorized into severe (n = 192) and general (n = 291) groups based on clinical severity. Univariate and multivariate logistic regression analyses were performed to identify risk factors for severe MRMP.

Results: Univariate analysis revealed that the severe group had younger age, longer disease duration, higher peak fever temperatures, and prolonged fever duration compared to the general group. The incidence of wheezing, dyspnea, and decreased breath sounds was significantly higher in the severe group. Radiological findings indicated a higher prevalence of pulmonary consolidation, atelectasis, pleural effusion, and multi-lobar involvement in the severe group. Laboratory tests showed elevated levels of neutrophils, platelets, liver enzymes, lactate dehydrogenase (LDH), D-dimer, and erythrocyte sedimentation rate, alongside reduced levels of albumin, blood urea nitrogen, and creatinine in the severe group. Regarding treatment, doxycycline was the primary alternative for MRMP, but fluoroquinolones were more frequently administered in the severe group, along with a significantly higher usage of glucocorticoids. Additionally, oxygen therapy was more commonly required in the severe group, with 2% of patients necessitating mechanical ventilation or admission to the pediatric intensive care unit. Compared to the general group, the severe group had significantly longer hospital stays (P < 0.01), prolonged lung rales, slower decline in inflammatory markers, and delayed radiological improvement. However, no fatalities were recorded in this cohort. Multivariate logistic regression analysis identified prolonged fever duration, multi-lobar consolidation, elevated LDH, and increased D-dimer levels as independent risk factors for severe MRMP. Receiver Operating Characteristic (ROC) curve analysis demonstrated that the combination of fever duration, multi-lobar consolidation, LDH, and D-dimer had high sensitivity and specificity for diagnosing severe MRMP, with an area under the curve (AUC) of 0.90.

Conclusion: Prolonged fever duration, multi-lobar consolidation, elevated LDH, and increased D-dimer levels are key predictive indicators for severe MRMP. Although severe MRMP is associated with a prolonged clinical course and complex treatment, timely adjustment of antibiotic regimens and supportive care can effectively improve outcomes.

Clinical trial number: Not applicable.

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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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