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从埃塞俄比亚西北部贡德尔的 Gene X-pert 结核阴性成年患者中分离出的病原菌。

Pathogenic bacteria recovered from Gene X-pert tuberculosis-negative adult patients in Gondar, Northwest Ethiopia.

机构信息

Department of Immunology and Molecular biology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.

Department of Medical Microbiology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.

出版信息

BMC Pulm Med. 2023 Jun 6;23(1):197. doi: 10.1186/s12890-023-02500-w.

Abstract

INTRODUCTION

Lower respiratory tract infections (LRTIs) caused by drug-resistant pathogenic bacteria is a major problem in developing countries including Ethiopia. Therefore, this study aimed to determine the pathogenic bacteria and their antimicrobial susceptibility patterns among Gene X-pert tuberculosis-negative adult patients with clinically suspected LRTIs at the University of Gondar Comprehensive Specialized Referral Hospital, Gondar, Northwest Ethiopia.

METHODS

This institutional-based cross-sectional study was conducted from February 01 to March 15, 2020. Socio-demographic data were collected by using a structured questionnaire. A total of 254 sputum specimens were collected from Gene X-pert tuberculosis-negative patients. Bacterial recovery was performed using blood, chocolate, and MacConkey agar plates. Bacterial isolates were identified based on Gram staining, colony characteristics, and biochemical reactions. Antimicrobial susceptibility testing was performed using the Kirby-Bauer disk diffusion method. Methicillin resistance of S. aureus was confirmed using cefoxitin (30 µg). Descriptive statistics were calculated for each variable and results are shown in tables and figures.

RESULTS

In this study, the overall sputum culture positivity rate was 145/254 (57.1%). Gram-negative bacteria 111 (64.9%) were predominant compared to Gram-positive bacteria 60 (35.1%). Of the 145 culture-positive cases, 26 (14.8%) had poly-bacterial infections. S. aureus 40 (66.7%) was the predominant Gram-positive bacterium whereas K. pneumoniae 33 (29.7%), was the most isolated Gram-negative bacterium. Bacterial species, such as S. aureus were sensitive to ciprofloxacin 38/40 (95.0%), gentamicin 37/40 (92.5%), cefoxitin 36/40 (90.0%), and clindamycin 34/40 (85.0%). The proportion of Methicillin-resistant S. aureus was low, 4(10.0%). S. pneumoniae was sensitive to chloramphenicol 8/9 (88.9%) and resistant to ciprofloxacin 6/9 (66.7%). K pneumoniae, P. aeruginosa, E. coli, Serratia species, and H. influenzae also demonstrated high levels of resistance to ampicillin at rates of 21/33 (63.6%), 8/8 (100.0%), 15/17 (88.2%), 7/10 (70.0%), and 6/6 (100.0%), respectively.

CONCLUSION

This study revealed a higher burden of Gram-negative and Gram-positive pathogenic bacterial agents, which is responsible for LRTs. Therefore, routine sputum culture identification and antibiotic susceptibility testing should be performed in Gene X-pert tuberculosis-negative patients.

摘要

简介

在包括埃塞俄比亚在内的发展中国家,由耐药病原菌引起的下呼吸道感染(LRTIs)是一个主要问题。因此,本研究旨在确定在埃塞俄比亚贡德尔大学综合专科医院,经 Gene X-pert 结核检测为阴性但临床疑似患有 LRTIs 的成年患者中,导致 LRTIs 的病原菌及其对抗菌药物的敏感性模式。

方法

本研究为 2020 年 2 月 1 日至 3 月 15 日进行的基于机构的横断面研究。采用结构化问卷收集社会人口统计学数据。共从 Gene X-pert 结核检测为阴性的患者中采集了 254 份痰液标本。采用血液、巧克力和麦康凯琼脂平板进行细菌回收。根据革兰氏染色、菌落特征和生化反应对细菌分离株进行鉴定。采用 Kirby-Bauer 纸片扩散法进行抗菌药物敏感性试验。使用头孢西丁(30µg)确认金黄色葡萄球菌的耐甲氧西林情况。用表格和图表展示了每个变量的描述性统计数据。

结果

在这项研究中,总体痰培养阳性率为 145/254(57.1%)。与革兰氏阳性菌 60 株(35.1%)相比,革兰氏阴性菌 111 株(64.9%)更为常见。在 145 例培养阳性的病例中,26 例(14.8%)为混合细菌感染。40 株(66.7%)金黄色葡萄球菌是主要的革兰氏阳性菌,而 33 株(29.7%)肺炎克雷伯菌是最主要的革兰氏阴性菌。金黄色葡萄球菌等细菌对环丙沙星 38/40(95.0%)、庆大霉素 37/40(92.5%)、头孢西丁 36/40(90.0%)和克林霉素 34/40(85.0%)敏感。耐甲氧西林金黄色葡萄球菌的比例较低,为 4(10.0%)。肺炎链球菌对氯霉素 8/9(88.9%)敏感,对环丙沙星 6/9(66.7%)耐药。肺炎克雷伯菌、铜绿假单胞菌、大肠杆菌、沙雷氏菌和流感嗜血杆菌对氨苄西林的耐药率分别为 21/33(63.6%)、8/8(100.0%)、15/17(88.2%)、7/10(70.0%)和 6/6(100.0%)。

结论

本研究表明,导致 LRTIs 的病原菌以革兰氏阴性菌和革兰氏阳性菌为主。因此,Gene X-pert 结核检测为阴性的患者应进行常规痰培养鉴定和抗菌药物敏感性试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a465/10246094/cd15415396b0/12890_2023_2500_Fig1_HTML.jpg

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