Cheng Jie, Liu Ya, Zhang Guangli, Tan Liping, Luo Zhengxiu
Department of Emergency, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Big Data Engineering Center, Children's Hospital of Chongqing Medical University, Chongqing, 400014, People's Republic of China.
Department of Pediatrics, Chongqing Youyoubaobei Women and Children's Hospital, Chongqing, 401147, People's Republic of China.
Infect Drug Resist. 2024 Jul 11;17:2933-2942. doi: 10.2147/IDR.S466994. eCollection 2024.
(MP) is highly resistant to macrolides in China. However, macrolides still exhibit clinical effectiveness in some macrolide-resistant patients. We tend to explore azithromycin effectiveness in pneumonia (MPP) children with A2063/2064G mutation.
This retrospective observational cohort study was conducted at the Children's Hospital of the Chongqing Medical University. Children with macrolide-resistant mutations (A2063/2064G) diagnosed as MPP were retrospectively enrolled. Receiver operating characteristic (ROC) curves and logistic regression analysis were used to evaluate and identify independent risk factors for treatment failure (progress to refractory pneumonia [RMPP]) in macrolide-unresponsive pneumonia (MUMPP) children with the A2063/2064G mutation.
One hundred fifty-five children were retrospectively enrolled. More than 20% (36/155, 23.23%) of patients experienced defervescence within 3 days of azithromycin treatment. RMPP was diagnosed in 54 patients (54/155, 34.84%) and the incidence of RMPP during hospitalization was 22.72 per 1000 person-days. Logistic regression analysis showed that lactate dehydrogenase (LDH) ≥ 399 (U/L) was an independent risk factor for RMPP (odds ratio [OR] 4.66, 95% confidence interval [CI] 1.31-17.10, P=0.017). During the year followed, RMPP patients had a significantly higher incidence of bronchiolitis obliterans and bronchiectasis than non-RMPP patients (16.67% vs 1.98%, P=0.001; 9.26% vs 0.00%, P=0.005, respectively).
Azithromycin was effective in children with MPP with the A2063/2064G mutation. For MUMPP children with A2063/2064G mutation, children with LDH ≥ 399 (U/L) had significant higher risk for progression to RMPP, and should consider to be treated with alternative antibiotics (eg tetracyclines, and fluoroquinolones).
在中国,肺炎支原体(MP)对大环内酯类药物高度耐药。然而,大环内酯类药物在一些耐药患者中仍显示出临床疗效。我们旨在探讨阿奇霉素对携带A2063/2064G突变的肺炎支原体肺炎(MPP)患儿的疗效。
本回顾性观察队列研究在重庆医科大学附属儿童医院开展。回顾性纳入诊断为MPP且携带大环内酯类耐药突变(A2063/2064G)的患儿。采用受试者工作特征(ROC)曲线和逻辑回归分析,评估并确定携带A2063/2064G突变的大环内酯类无反应性肺炎(MUMPP)患儿治疗失败(进展为难治性肺炎[RMPP])的独立危险因素。
回顾性纳入155例患儿。超过20%(36/155,23.23%)的患者在阿奇霉素治疗3天内退热。54例患者(54/155,34.84%)被诊断为RMPP,住院期间RMPP的发病率为每1000人日22.72例。逻辑回归分析显示,乳酸脱氢酶(LDH)≥399(U/L)是RMPP的独立危险因素(比值比[OR]4.66,95%置信区间[CI]1.31 - 17.10,P = 0.017)。在随后的一年中,RMPP患者闭塞性细支气管炎和支气管扩张的发病率显著高于非RMPP患者(分别为16.67%对1.98%,P = 0.001;9.26%对0.00%,P = 0.005)。
阿奇霉素对携带A2063/2064G突变的MPP患儿有效。对于携带A2063/2064G突变的MUMPP患儿,LDH≥399(U/L)的患儿进展为RMPP的风险显著更高,应考虑换用其他抗生素(如四环素类和氟喹诺酮类)治疗。