这样的重复值得吗?优化综合征组病原体检测方案。

Filipe M Cerqueira, Linh Do, Janet Enderle, Ping Ren
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引用次数: 0

摘要

研究目的本研究旨在比较重复检测 BioFire FilmArray 胃肠道(GI)和呼吸道(RP)检测小组中 3 个和 4 个病原体目标阳性结果的成本和临床影响:我们分析了 12,027 份胃肠道和呼吸道样本,对我们的重测政策进行了评估,与制造商的 4 种病原体(4 种病原体方案)建议相比,我们的重测政策是对检测到 3 种或更多病原体的样本进行重测(3 种病原体方案)。我们比较了重新检测的结果,计算了成本影响,并回顾了对抗生素处方和患者疗效的临床影响:根据我们的 3 种病原体方案进行的复检显示,81%(39/48)的消化道样本和 76%(26/34)的生殖道样本复检结果相同,而 19%(9/48)的消化道样本和 24%(8/34)的生殖道样本复检结果不一致。与制造商的方案相比,我们的方案产生的额外费用为 9820.32 美元。没有证据表明我们更严格的政策会影响抗生素处方或临床结果:结论:与生产商的 4 种病原体方案相比,我们更严格的 3 种病原体复检方案并没有改善患者管理,反而产生了不必要的成本,并增加了在供应短缺时耗尽检测试剂盒的风险。因此,我们采纳了生产商的建议,强调实验室检测方案需要在临床严谨性和成本效益之间取得平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is the repeat worth it? Optimizing syndromic panel pathogen detection protocols.

Objective: The aim of the study was to compare the cost and clinical impact of repeating BioFire FilmArray gastrointestinal (GI) and respiratory (RP) panel assays with 3 vs 4 pathogen targets positive.

Method: We analyzed 12,027 GI and RP panels to evaluate our retesting policy, which retested panels with 3 or more detected pathogens (3-pathogen protocol) compared with the manufacturer's 4-pathogen (4-pathogen protocol) recommendation. We compared the retesting results, calculated the cost implications, and reviewed the clinical impact on antibiotic prescriptions and patient outcomes.

Results: Retesting with our 3-pathogen protocol revealed that 81% (39/48) of GI and 76% (26/34) of RP panels had identical results, whereas 19% (9/48) of GI and 24% (8/34) of RP panels showed discrepancies on retesting. The additional cost incurred by our protocol compared with the manufacturer's protocol was $9820.32. There was no evidence that our more stringent policy affected antibiotic prescription or clinical outcomes.

Conclusion: Our more stringent 3-pathogen protocol for retesting panels did not improve patient management compared with the manufacturer's 4-pathogen protocol but resulted in unnecessary costs and increased the risk of depleting testing kits during supply shortages. Consequently, we adopted the manufacturer's suggestions, highlighting the need to balance clinical rigor with cost-effectiveness in laboratory testing protocols.

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