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Impact of Delays between Clinical and Laboratory Standards Institute and Food and Drug Administration Revisions of Interpretive Criteria for Carbapenem-Resistant Enterobacteriaceae

机译:临床和实验室标准协会之间的延误以及食品和药物管理局对耐碳青霉烯的肠杆菌科细菌解释标准的修订的影响

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摘要

Delays often occur between CLSI and FDA revisions of antimicrobial interpretive criteria. Using our Regional Healthcare Ecosystem Analyst (RHEA) simulation model, we found that the 32-month delay in changing carbapenem-resistant Enterobacteriaceae (CRE) breakpoints might have resulted in 1,821 additional carriers in Orange County, CA, an outcome that could have been avoided by identifying CRE and initiating contact precautions. Policy makers should aim to minimize the delay in the adoption of new breakpoints for antimicrobials against emerging pathogens when containment of spread is paramount; delays of <1.5 years are ideal.
机译:在CLSI和FDA修订抗菌解释标准之间经常会出现延迟。使用我们的地区医疗保健生态系统分析师(RHEA)模拟模型,我们发现更改耐碳青霉烯类肠杆菌科(CRE)断裂点的时间延迟了32个月,这可能导致在加利福尼亚的奥兰治县增加了1,821例携带者,这一结果可以避免通过识别CRE并启动联系预防措施。决策者应着眼于在控制蔓延至为关键的情况下,尽量减少采用新的针对新兴病原体的抗菌剂的断点的延迟; <1.5年的延迟是理想的。

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