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囊性纤维化患者病情加重期间的耐抗生素专性厌氧菌

Antibiotic-resistant obligate anaerobes during exacerbations of cystic fibrosis patients.

作者信息

Worlitzsch D, Rintelen C, Böhm K, Wollschläger B, Merkel N, Borneff-Lipp M, Döring G

机构信息

Institute of Hygiene, University of Halle, Halle, Germany.

出版信息

Clin Microbiol Infect. 2009 May;15(5):454-60. doi: 10.1111/j.1469-0691.2008.02659.x. Epub 2009 Jan 22.

Abstract

Pseudomonas aeruginosa and Staphylococcus aureus are thought to cause the majority of lung infections in patients with cystic fibrosis (CF). However, other bacterial pathogens may contribute to the pathophysiology of lung disease. Here, obligate anaerobes were identified in a cross-sectional study, and cell numbers and antibiotic susceptibilities of facultative and obligate anaerobes from 114 sputum samples from nine children and 36 adults with CF were determined. Furthermore, in 12 CF patients, we investigated whether conventional intravenous antibiotic therapy, administered during acute exacerbations, would affect the numbers of obligate anaerobes. Fifteen genera of obligate anaerobes were identified in 91% of the CF patients. Cell numbers (mean: 2.2 x 10(7) +/- standard deviation 6.9 x 10(7) CFU/mL of sputum sample) were comparable to those of P. aeruginosa and S. aureus. Staphylococcus saccharolyticus and Peptostreptococcus prevotii were most prevalent. Infection with P. aeruginosa did not increase the likelihood that obligate anaerobes are present in sputum specimens. Single obligate anaerobic species persisted for up to 11 months in sputum plugs in vivo. Patients with and without obligate anaerobes in sputum specimens did not differ in lung function. Intravenous therapy directed against P. aeruginosa during acute exacerbations increased lung function, but did not reduce the numbers of obligate anaerobes. Obligate anaerobic species differed widely in their patterns of resistance against meropenem, piperacillin-tazobactam, clindamycin, metronidazole and ceftazidime. In 58% of patients with acute exacerbations, obligate anaerobes were detected that were resistant to the antibiotics used for treatment. Antibiotic therapy, optimized to target anaerobes in addition to P. aeruginosa, may improve the management of CF lung disease.

摘要

铜绿假单胞菌和金黄色葡萄球菌被认为是导致囊性纤维化(CF)患者肺部感染的主要原因。然而,其他细菌病原体可能也参与了肺部疾病的病理生理过程。在此,通过一项横断面研究鉴定出了专性厌氧菌,并测定了来自9名儿童和36名成年CF患者的114份痰液样本中兼性厌氧菌和专性厌氧菌的细胞数量及抗生素敏感性。此外,在12名CF患者中,我们研究了急性加重期给予的常规静脉抗生素治疗是否会影响专性厌氧菌的数量。在91%的CF患者中鉴定出了15个专性厌氧菌属。细胞数量(平均值:2.2×10⁷±标准差6.9×10⁷CFU/毫升痰液样本)与铜绿假单胞菌和金黄色葡萄球菌的细胞数量相当。解糖葡萄球菌和普氏消化链球菌最为常见。铜绿假单胞菌感染并未增加痰液标本中存在专性厌氧菌的可能性。单一专性厌氧菌种在体内痰液栓子中可持续存在长达11个月。痰液标本中有和没有专性厌氧菌的患者在肺功能方面并无差异。急性加重期针对铜绿假单胞菌的静脉治疗可改善肺功能,但并未减少专性厌氧菌的数量。专性厌氧菌种对美罗培南、哌拉西林 - 他唑巴坦、克林霉素、甲硝唑和头孢他啶的耐药模式差异很大。在58%的急性加重期患者中,检测到了对所用治疗抗生素耐药的专性厌氧菌。除了针对铜绿假单胞菌外,优化靶向厌氧菌的抗生素治疗可能会改善CF肺部疾病的管理。

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