Jørgensen Lone G M, Brandslund Ivan, Hyltoft Petersen Per
Department of Clinical Biochemistry, Vejle County Hospital, Vejle, Denmark.
Clin Chem Lab Med. 2004;42(7):747-51. doi: 10.1515/CCLM.2004.126.
The reference interval is probably the most widely used decision-making tool in clinical practice, with a modern use aiming at identifying wellness during health check and screening. Its use as a diagnostic tool is much less recognised and may be obsolete. The present study investigates the consequences of the new practice for the interpretation of prospective value, negative vs. positive, the probability of confirming wellness, and number of false results based on selected strategy for reference interval establishment. Calculations assumed normalised Gaussian-distributed reference intervals with analytical variation set to zero and absolute accuracy. Also assumed is the independency of tests. Probability for no values outside reference intervals in healthy subjects was calculated from the formula p(no) outside=(1 - p(single)) and according to the formula for repeated testing: p(one) outside =n x p(single) (1 - p(single))n-1 etc. Here n is the number of tests performed and p(single) is the probability of one result outside reference limits with the general formula p(i) outside n-i=k x p(single)i (1- p(single))n-i, with k being the binominal coefficient and i the number outside the reference intervals. Use of the 99.9 centile for health checks will increase the probability for no false from 60% to 99% for 10 tests, and from 46% to 98% for 15 tests. The probability for one false-positive result in 10 tests in a panel can be reduced from 32% to 1% if the 99.9% centile is substituted for the 95% centile. For two in 10 tests, the probability can be reduced from 8% to below 0.1%. In both cases, selection of the 99.9% centile improves the diagnostic accuracy. Reference intervals are needed as a "true" negative reference for absence of disease, and should cover the 99.9% centile of the reference distribution of an analyte to avoid false positives. For this new use, it is critical that reference persons are absolutely normal without clinical, genetic and biochemical signs of the condition being investigated. However, reference intervals cannot substitute clinical decision limits for diagnosis and medical intervention.
参考区间可能是临床实践中使用最广泛的决策工具,现代用途旨在在健康检查和筛查中识别健康状况。其作为诊断工具的用途鲜为人知,可能已过时。本研究基于选定的参考区间建立策略,调查了新实践对前瞻性价值解释(阴性与阳性)、确认健康的概率以及假结果数量的影响。计算假设参考区间为正态高斯分布,分析变异设为零且具有绝对准确性。还假设测试是独立的。健康受试者中无值超出参考区间的概率根据公式p(无)超出=(1 - p(单个))计算,并根据重复测试公式:p(一个)超出 =n×p(单个)(1 - p(单个))n - 1等。这里n是进行的测试次数,p(单个)是一个结果超出参考限值的概率,通用公式为p(i)超出n - i = k×p(单个)i(1 - p(单个))n - i,其中k是二项式系数,i是超出参考区间的值的数量。在健康检查中使用第99.9百分位数,对于10次测试,无假阳性的概率将从60%提高到99%,对于15次测试,从46%提高到98%。如果用第99.9百分位数代替第95百分位数,一组中10次测试出现一个假阳性结果的概率可从32%降至1%。对于10次测试中有两个假阳性结果的情况,概率可从8%降至0.1%以下。在这两种情况下,选择第99.9百分位数都可提高诊断准确性。参考区间需要作为无疾病的“真正”阴性参考,应涵盖分析物参考分布的第99.9百分位数以避免假阳性。对于这种新用途,至关重要的是参考人群绝对正常,没有所研究疾病的临床、遗传和生化迹象。然而,参考区间不能替代用于诊断和医疗干预的临床决策界限。