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Clinical and Financial Benefits of Rapid Bacterial Identification and Antimicrobial Susceptibility Testing

机译:快速细菌鉴定和药敏试验的临床和财务效益

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摘要

To assess the expected clinical and financial benefits of rapid reporting of microbiology results, we compared patients whose cultured samples were processed in the normal manner to patients whose samples were processed more rapidly due to a minor change in work flow. For the samples tested in the rapid-reporting time period, the vast majority of bacterial identification and antimicrobial susceptibility testing (AST) results were verified with the Vitek system on the same day that they were available. This time period was called rapid AST (RAST). For RAST, a technologist on the evening shift verified the data that became available during that shift. For the control time period, cultures were processed in the normal manner (normal AST [NAST]), which did not include evening-shift verification. For NAST, the results for approximately half of the cultures were verified on the first day that the result was available. The average turnaround time for the reporting of AST results was 39.2 h for RAST and 44.4 h for NAST (5.2 h faster for RAST [P = 0.001]). Subsequently, physicians were able to initiate appropriate antimicrobial therapy sooner for patients whose samples were tested as part of RAST (P = 0.006). The mortality rates were 7.9 and 9.6% for patients whose samples were tested as part of RAST and NAST, respectively (P = 0.45). The average length of stay was 10.7 days per patient for RAST and 12.6 days for NAST, a difference of 2.0 days less for RAST (P = 0.006). The average variable cost was $4,927 per patient for RAST and $6,677 for NAST, a difference of $1,750 less per patient for RAST (P = 0.001). This results in over $4 million in savings in variable costs per year in our hospital.
机译:为了评估快速报告微生物学结果的预期临床和财务收益,我们将以正常方式处理培养样品的患者与由于工作流程的微小变化而以更快的速度处理样品的患者进行了比较。对于在快速报告期内测试的样品,在可用的同一天,就通过Vitek系统验证了绝大多数细菌鉴定和抗菌药敏试验(AST)结果。该时间段称为快速AST(RAST)。对于RAST,一位在晚上轮班的技术人员验证了该轮班期间可用的数据。在控制时间段内,以正常方式(正常AST [NAST])处理培养,其中不包括夜班验证。对于NAST,在可获得结果的第一天就验证了大约一半培养物的结果。报告AST结果的平均周转时间对于RAST是39.2 h,对于NAST是44.4 h(对于RAST快5.2 h [P = 0.001])。随后,对于能够将样品作为RAST一部分进行测试的患者,医生能够更快地开始适当的抗菌治疗(P = 0.006)。将样本作为RAST和NAST的一部分进行测试的患者的死亡率分别为7.9和9.6%(P = 0.45)。 RAST的平均住院时间为每位患者10.7天,NAST的平均住院时间为12.6天,RAST的差异为2.0天(P = 0.006)。 RAST的平均可变成本为每位患者$ 4,927,NAST的平均可变成本为$ 6,677,RAST的每位患者平均差额为$ 1,750(P = 0.001)。这样,我们医院每年可节省的可变成本超过400万美元。

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