非哺乳期肉芽肿性乳腺炎病原菌分布及药敏分析。

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
Hongye Ma, Yifei Zeng, Di Qu, Xiaoxia Huang, Xuanyu Wang, Xiang Gao, Honglin Guo
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引用次数: 0

摘要

背景:综合探讨非哺乳期肉芽肿性乳腺炎患者乳腺穿刺液病原菌分布及药敏情况,优化治疗方案。方法:收集首都医科大学北京中医医院乳腺科2023年3月至2023年10月非哺乳期肉芽肿性乳腺炎患者乳腺穿刺液中分离的15株致病菌。采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)和16S rRNA测序进行细菌鉴定。采用e检验法测定各菌株的最低抑菌浓度(MIC),采用EUCAST标准进行药敏解释。采用1% Tween-80血板进行对照亲脂实验。结果:15例非哺乳期肉芽肿性乳腺炎患者的平均年龄为32.73±3.37岁,其中14例(93.3%)有妊娠史,平均产后乳腺炎为6.38±9.65个月。MALDL-TOF MS结果与纳米孔16S rRNA测序结果一致。在分离出的苛养菌中,有15株克氏棒状杆菌(CK)。这些菌株对利福平和头孢曲松的敏感性分别为93.3%和80%。青霉素耐药率高达80%。环丙沙星耐药率为46.7%,中间耐药率为53.3%。莫西沙星的敏感性为53.3%。未发现万古霉素耐药和利奈唑胺耐药菌株。结论:CK在非哺乳期肉芽肿性乳腺炎的发生发展中起重要作用。根据临床抗生素用药规范及药敏结果分析,亲脂性利福平和利奈唑胺可能是ck相关性非哺乳期肉芽肿性乳腺炎患者的首选经验性药物。同时,临床实验室应努力优化培养条件,利用MALDL-TOF MS进行准确鉴定,提高培养物的检出率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of Pathogenic Bacteria and Analysis of Antimicrobial Susceptibility in Non-Lactation Granulomatous Mastitis Patients.

Background: The aim was to comprehensively explore the distribution of pathogenic bacteria and antimicrobial susceptibility in the breast puncture fluid of the patients with non-lactation granulomatous mastitis to optimize treatment programs.

Methods: Fifteen strains of pathogenic bacteria isolated from the breast puncture fluid of the patients with non-lactation granulomatous mastitis were collected in the breast department, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University from March 2023 to October 2023. Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) and 16S rRNA sequencing were used to bacterial identi-fication. The E-test method was used to determine the minimum inhibitory concentration (MIC) for each isolate, and the EUCAST standard was used for conducting the antimicrobial susceptibility interpretation. The control lipophilic experiment was performed by adopting the 1% Tween-80 blood plate.

Results: The mean age of 15 patients with non-lactation granulomatous mastitis was 32.73 ± 3.37 years old, of which 14 (93.3%) had a history of pregnancy, and the mean postpartum mastitis was 6.38 ± 9.65 months. MALDL-TOF MS results were consistent with 16S rRNA sequencing by nanopore. Among the isolated fastidious bacteria, there were 15 strains of Corynebacterium kroppenstedtii (CK). These strains showed a high susceptibility rate to rifampicin and ceftriaxone (respectively, 93.3% and 80%). The resistance rate of penicillin was as high as 80%. The resistance rate of ciprofloxacin was 46.7%, and the intermediate rate was 53.3%. The sensitivity rate of moxifloxacin was 53.3%. There were no vancomycin-resistant or linezolid-resistant strains found.

Conclusions: CK plays an important role in the occurrence and development of non-lactation granulomatous mastitis. According to the analysis of clinical antibiotic medication norms and drug sensitivity results, lipophilic rifampicin and linezolid may be the preferred empirical drugs for CK-related non-lactation granulomatous mastitis patients. Meanwhile, the clinical laboratory should endeavor to optimize the culture conditions and use MALDL-TOF MS for accurate identification to improve the detection rate of culture.

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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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