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Clinical Relevance of Antibiotic Susceptibility Profiles for Screening Gram-negative Microorganisms Resistant to Beta-Lactam Antibiotics

机译:抗生素敏感性曲线对抗β-内酰胺抗生素抗生素抗生素微生物的临床相关性

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摘要

The increasing resistance to antibiotics is compromising the empirical treatment of infections caused by resistant bacteria. Rapid, efficient, and clinically applicable phenotypic methods are needed for their detection. This study examines the phenotypic behavior of β-lactam-resistant Gram-negative bacteria grown on ChromID ESBL medium with ertapenem, cefoxitin, and cefepime disks, reports on the coloration of colonies, and establishes a halo diameter breakpoint for the detection of carbapenemase-producing bacteria. We studied 186 β-lactam-resistant Gram-negative microorganisms (77 with extended spectrum beta lactamase (ESBL), 97 with carbapenemases, and 12 with AmpC β-lactamases (AmpC)). Susceptibility profiles of Gram-negative bacteria that produced ESBL, AmpC, and carbapenemases were similar to the expected profiles, with some differences in the response to cefepime of ESBL-producing microorganisms. Coloration values did not differ from those described by the manufacturer of ChromID ESBL medium. In the screening of carbapenemase production, inhibition halo diameter breakpoints for antibiotic resistance were 18 mm for Enterobacterales and ertapenem, 18 mm for Pseudomonas and cefepime, and 16 mm for Acinetobacter baumannii and cefepime. This innovative phenotypic approach is highly relevant to clinical laboratories, combining susceptibility profiles with detection by coloration of high-priority resistant microorganisms such as carbapenemase-producing A. baumannii, carbapenemase-producing Pseudomonas spp., and ESBL and/or carbapenemase-producing Enterobacterales.
机译:对抗生素的抗性越来越大损害了由抗性细菌引起的感染的经验治疗。检测需要快速,高效,临床适用的表型方法。本研究检测β-内酰胺植物革兰阴性细菌的表型行为,在铬酸盐培养基上生长的含有ErtapeNem,Cefoxitin和头孢隙盘,报道菌落着色,并建立了用于检测碳结构酶的卤素直径断点细菌。我们研究了186个β-内酰胺克革兰阴性微生物(77,其中延长光谱β内酰胺酶(ESBL),97,带有碳基淀粉酶,12个用AMPCβ-内酰胺酶(AMPC))。产生ESBL,AMPC和碳结构酶的革兰氏阴性细菌的敏感性谱与预期的曲线相似,对ESBL制剂微生物的活性的反应有一些差异。着色值与ChromIt ESBL介质制造商描述的那些没有不同。在碳碱酶生产的筛查中,抗生素抗性的抑制卤素直径断裂点为肠杆菌和抗生素,18 mm的抗生素和头孢塞和头孢酮,16毫米,用于肺杆菌Baumannii和头孢者。这种创新的表型方法与临床实验室高度相关,与高优先级微生物的着色相结合的敏感性曲线,如碳碱酶促酶A. Baumannii,碳碱酶促酶Pseudomonas SPP。和/或碳结构酶产生的肠杆菌。

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