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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Therapeutic efficacy of macrolides, minocycline, and tosufloxacin against macrolide-resistant Mycoplasma pneumoniae pneumonia in pediatric patients
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Therapeutic efficacy of macrolides, minocycline, and tosufloxacin against macrolide-resistant Mycoplasma pneumoniae pneumonia in pediatric patients

机译:大环内酯类,米诺环素和托沙沙星对小儿环内酯类耐药性肺炎支原体肺炎的治疗作用

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The importance of macrolide-resistant (MR) Mycoplasma pneumoniae has become much more apparent in the past decade. We investigated differences in the therapeutic efficacies of macrolides, minocycline, and tosufloxacin against MRM. pneumoniae. A total of 188 children withM. pneumoniae pneumonia confirmed by culture and PCR were analyzed. Of these, 150 patients had a strain with an MR gene and 134 had one with an A-to-G mutation at position 2063 ofM. pneumoniae 23S rRNA domain V. Azithromycin (n=27), clarithromycin (n=23), tosufloxacin (n=62), or minocycline (n=38) was used for definitive treatment of patients with MRM. pneumoniae. Defervescence within 48 h after the initiation of antibiotic therapy was observed in 41% of the patients in the azithromycin group, 48% of those in the clarithromycin group, 69% of those in the tosufloxacin group, and 87% of those in the minocycline group. The average number of days of fever after the administration of antibiotic treatment was lower in the minocycline and tosufloxacin groups than in the macrolide groups. The decrease in theM. pneumoniae burden, as estimated by the number of DNA copies, after 48 to 96 h of treatment was more rapid in patients receiving minocycline (P- 0.016) than in those receiving tosufloxacin (P=0.049), azithromycin (P=0.273), or clarithromycin (P=0.107). We found that the clinical and bacteriological efficacies of macrolides against MRM. pneumoniae pneumonia was low. Our results indicated that minocycline rather than tosufloxacin can be considered the first-choice drug for the treatment ofM. pneumoniae pneumonia in children aged>8 years.
机译:在过去的十年中,大环内酯耐药(MR)肺炎支原体的重要性变得更加明显。我们调查了大环内酯类,米诺环素和托沙沙星对MRM的疗效差异。肺炎共有188名儿童患有M。肺炎肺炎经培养和PCR确诊后进行分析。其中150例患者的MR基因菌株,134例患者的M位2063发生A-to-G突变。肺炎23S rRNA结构域V.阿奇霉素(n = 27),克拉霉素(n = 23),托沙沙星(n = 62)或米诺环素(n = 38)用于MRM患者的明确治疗。肺炎在开始抗生素治疗后的48小时内,阿奇霉素组,克拉霉素组的48%,托苏沙星组的69%和米诺环素组的47%的患者出现了神经萎缩。与大环内酯组相比,米诺环素和托沙沙星组在给予抗生素治疗后平均发烧天数较低。 M的下降。根据DNA拷贝数估算,接受米诺环素治疗的患者在治疗48至96小时后的肺炎负担(P-0.016)要比接受托氟沙星(P = 0.049),阿奇霉素(P = 0.273)或克拉霉素(P = 0.107)。我们发现大环内酯类药物对MRM的临床和细菌学疗效。肺炎肺炎低。我们的结果表明,米诺环素而不是托氟沙星可以被视为治疗M的首选药物。肺炎> 8岁儿童的肺炎。

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