ISSN 2097-5724 CN 61-1535/R 主管·主办:陕西省疾病预防控制中心
疾 疾病预防与控制 Disease Prevention and Control 医学学术期刊 月刊
2026-07-012 预防医学研究 2026, 2(07): 45-48

临床病原微生物药敏试验结果分析及质量控制实践探讨

遵义医科大学第五附属(珠海)医院

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摘要

目的 回顾性分析2025年2月至2026年2月临床病原微生物分布、药敏试验结果,探讨药敏试验质量控制要点及效果,为临床合理用药、防控多重耐药菌株提供依据。方法 选取同期临床送检标本31 350份,筛选合格标本31 343份,分离病原微生物后采用纸片扩散法和微量肉汤稀释法进行药敏试验,建立全流程质控体系,选用标准质控菌株每周校准。结果 共分离病原微生物4 776株,革兰氏阴性菌3 342株(70.0%),以大肠埃希菌(来源于741例患者)为主,其次为解脲脲原体阳性529例、肺炎克雷伯菌来源于390例患者。主要病原微生物对碳青霉烯类、万古霉素等敏感率较高,对头孢类、喹诺酮类耐药率较高,多重耐药菌株468株(11.0%)。结论 同期临床病原微生物中以革兰氏阴性菌为主,大肠埃希菌为全院最常见病原微生物且占主导地位,耐药性形势严峻。全流程质量控制有效降低试验的误差,提高结果准确性,对临床精准用药、防控多重耐药菌株具有重要价值。

Abstract

Objective To analyze the distribution of clinical pathogens and susceptibility test results from February 2025 to February 2026, explore key quality control points and their effectiveness, and provide a basis for rational drug use and the prevention of multidrug-resistant strains in clinical practice. Methods A total of 31,350 clinical specimens were selected during the same period, with 31,343 qualified specimens screened. Pathogens were isolated, and susceptibility tests were conducted using the disk diffusion method and micro broth dilution method. A full-process quality control system was established, with standard control strains calibrated weekly. Results A total of 4,776 pathogenic bacteria were isolated. Among them, 3,342 were Gram-negative bacteria(70.0%), mainly Escherichia coli(with 741 samples submitted for testing), followed by positive Ureaplasma urealyticum(529 samples) and Klebsiella pneumoniae(390 samples). The predominant pathogenic bacteria exhibited high susceptibility to carbapenems and vancomycin, but high resistance to cephalosporins and quinolones. There were 468 multi-drug resistant strains(11.0%). Conclusion Gram-negative bacteria dominated the clinical pathogens during the same period, with Escherichia coli being the most common and prevalent pathogen in the hospital. The antimicrobial resistance situation is severe. Full-process quality control effectively reduces test errors and improves result accuracy, holding significant value for precise clinical drug use and the prevention of multidrug-resistant strains.

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[1]赖伯灵,王国乐.临床病原微生物药敏试验结果分析及质量控制实践探讨[J].疾病预防与控制,2026,2(07):45-48.