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本文引用的文献

1
Emergence of macrolide-resistant Mycoplasma pneumoniae with a 23S rRNA gene mutation.具有23S rRNA基因突变的大环内酯类耐药肺炎支原体的出现。
Antimicrob Agents Chemother. 2005 Jun;49(6):2302-6. doi: 10.1128/AAC.49.6.2302-2306.2005.
2
Characterization and molecular analysis of macrolide-resistant Mycoplasma pneumoniae clinical isolates obtained in Japan.对在日本获得的大环内酯类耐药肺炎支原体临床分离株的特性鉴定及分子分析
Antimicrob Agents Chemother. 2004 Dec;48(12):4624-30. doi: 10.1128/AAC.48.12.4624-4630.2004.
3
Update of practice guidelines for the management of community-acquired pneumonia in immunocompetent adults.免疫功能正常的成年人社区获得性肺炎管理实践指南的更新
Clin Infect Dis. 2003 Dec 1;37(11):1405-33. doi: 10.1086/380488. Epub 2003 Nov 3.
4
Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial.阿奇霉素用于长期感染铜绿假单胞菌的囊性纤维化患者:一项随机对照试验。
JAMA. 2003 Oct 1;290(13):1749-56. doi: 10.1001/jama.290.13.1749.
5
Eaton agent pneumonia.伊顿因子肺炎
JAMA. 1961 Apr 15;176:118-23. doi: 10.1001/jama.1961.03040150034009.
6
Characteristics of macrolide-resistant Mycoplasma pneumoniae strains isolated from patients and induced with erythromycin in vitro.从患者分离并在体外经红霉素诱导的耐大环内酯类肺炎支原体菌株的特征
Microbiol Immunol. 2001;45(8):617-20. doi: 10.1111/j.1348-0421.2001.tb01293.x.
7
Clarithromycin inhibits NF-kappaB activation in human peripheral blood mononuclear cells and pulmonary epithelial cells.克拉霉素可抑制人外周血单核细胞和肺上皮细胞中的核因子-κB激活。
Antimicrob Agents Chemother. 2001 Jan;45(1):44-7. doi: 10.1128/AAC.45.1.44-47.2001.
8
Re-annotating the Mycoplasma pneumoniae genome sequence: adding value, function and reading frames.重新注释肺炎支原体基因组序列:增添价值、功能和阅读框。
Nucleic Acids Res. 2000 Sep 1;28(17):3278-88. doi: 10.1093/nar/28.17.3278.
9
Interleukin-8 gene repression by clarithromycin is mediated by the activator protein-1 binding site in human bronchial epithelial cells.克拉霉素对白细胞介素-8基因的抑制作用是通过人支气管上皮细胞中的激活蛋白-1结合位点介导的。
Am J Respir Cell Mol Biol. 2000 Jan;22(1):51-60. doi: 10.1165/ajrcmb.22.1.3400.
10
Fourteen-member macrolides inhibit interleukin-8 release by human eosinophils from atopic donors.十四元大环内酯类药物可抑制特应性供体来源的人嗜酸性粒细胞释放白细胞介素-8。
Antimicrob Agents Chemother. 1999 Apr;43(4):907-11. doi: 10.1128/AAC.43.4.907.

大环内酯类耐药肺炎支原体的临床评估

Clinical evaluation of macrolide-resistant Mycoplasma pneumoniae.

作者信息

Suzuki Satowa, Yamazaki Tsutomu, Narita Mitsuo, Okazaki Norio, Suzuki Isao, Andoh Tomoaki, Matsuoka Mayumi, Kenri Tsuyoshi, Arakawa Yoshichika, Sasaki Tsuguo

机构信息

Department of Bacterial Pathogenesis and Infection Control, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Antimicrob Agents Chemother. 2006 Feb;50(2):709-12. doi: 10.1128/AAC.50.2.709-712.2006.

DOI:10.1128/AAC.50.2.709-712.2006
PMID:16436730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1366908/
Abstract

Macrolide-resistant Mycoplasma pneumoniae (MR M. pneumoniae) has been isolated from clinical specimens in Japan since 2000. A comparative study was carried out to determine whether or not macrolides are effective in treating patients infected with MR M. pneumoniae. The clinical courses of 11 patients with MR M. pneumoniae infection (MR patients) treated with macrolides were compared with those of 26 patients with macrolide-susceptible M. pneumoniae infection (MS patients). The total febrile days and the number of febrile days during macrolide administration were longer in the MR patients than in the MS patients (median of 8 days versus median of 5 days [P = 0.019] and 3 days versus 1 day [P = 0.002], respectively). In addition, the MR patients were more likely than the MS patients to have had a change of the initially prescribed macrolide to another antimicrobial agent (63.6% versus 3.8%; odds ratio, 43.8; P < 0.001), which might reflect the pediatrician's judgment that the initially prescribed macrolide was not sufficiently effective in these patients. Despite the fact that the febrile period was prolonged in MR patients given macrolides, the fever resolved even when the initial prescription was not changed. These results show that macrolides are certainly less effective in MR patients.

摘要

自2000年以来,日本已从临床标本中分离出耐大环内酯类肺炎支原体(MR肺炎支原体)。开展了一项比较研究,以确定大环内酯类药物对治疗MR肺炎支原体感染患者是否有效。将11例接受大环内酯类药物治疗的MR肺炎支原体感染患者(MR患者)的临床病程与26例大环内酯类敏感肺炎支原体感染患者(MS患者)的临床病程进行了比较。MR患者的总发热天数和大环内酯类药物给药期间的发热天数均长于MS患者(中位数分别为8天对5天[P = 0.019]和3天对1天[P = 0.002])。此外,MR患者比MS患者更有可能将最初开具的大环内酯类药物更换为另一种抗菌药物(63.6%对3.8%;比值比,43.8;P < 0.001),这可能反映了儿科医生的判断,即最初开具的大环内酯类药物对这些患者的疗效不足。尽管给予大环内酯类药物的MR患者发热期延长,但即使不改变初始处方,发热也会消退。这些结果表明,大环内酯类药物对MR患者的疗效肯定较差。