Balance of Risk in COVID-19 Reveals the Extreme Cost of False Positives

James Lyons-Weiler
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引用次数: 1

Abstract

COVID-19 public health responses, including lockdowns and diagnostic testing strategies, have had consequences. Economic costs (see the CHD paper in this issue) could reach $16 trillion dollars, 90% of the US annual GDP. While harm to small businesses, unemployment, worsening poverty, death from cancer, increased suicides, social isolation, and restriction of freedom all increase the perceived need for drastic responses from the top, flawed measures are costly. A diagnostic assay[1] of tests for COVID-19 depends for its validity on its sensitivity and specificity assessed in terms of the true positive rate (TPR), false positive rate (FPR), true negative rate (TNR), and false negative rate (FNR) of the assays. In this pandemic, Real Time — Polymerase Chain Reaction (RT-PCR) testing has been relied on for drastic top-down responses (as in shutting down the economy of whole nations or the entire world). Here I focus on false positive results where RT-PCR testing suggests many infections by SARS-CoV-2 where there are none. I show by mathematical modeling how reporting positive results of RT-PCR testing, ones known to be false in a measurable percentage of instances, is at least 40 times more impactful (in a detrimental way) than increasing or decreasing the number of tests conducted. To balance the risks of errors in diagnosis, false positive results must be minimized by validating nucleotide sequences and estimates of viremia to avoid flagging individuals as contagious when they are not.
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2019冠状病毒病的风险平衡揭示了假阳性的极端代价
COVID-19公共卫生应对措施,包括封锁和诊断检测策略,已经产生了后果。经济成本可能达到16万亿美元,相当于美国年GDP的90%。虽然对小企业的伤害、失业、贫困加剧、癌症死亡、自杀率上升、社会孤立和自由限制都增加了人们对高层采取激烈应对措施的需求,但有缺陷的措施代价高昂。新冠肺炎诊断检测方法[1]的有效性取决于检测方法的真阳性率(TPR)、假阳性率(FPR)、真阴性率(TNR)和假阴性率(FNR)评估的敏感性和特异性。在这次大流行中,实时聚合酶链反应(RT-PCR)检测一直依赖于激烈的自上而下的应对措施(如关闭整个国家或整个世界的经济)。这里我关注的是假阳性结果,即RT-PCR检测显示许多SARS-CoV-2感染,而实际上没有感染。我通过数学模型表明,报告RT-PCR检测的阳性结果(在可测量的百分比中已知是错误的结果)的影响(以有害的方式)至少是增加或减少进行的检测数量的40倍。为了平衡诊断错误的风险,必须通过验证核苷酸序列和病毒血症估计来最大限度地减少假阳性结果,以避免在没有传染性的情况下将个体标记为传染性。
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