Diehr P, Cain K, Ye Z, Abdul-Salam F
Department of Biostatistics, University of Washington, Seattle 98195.
Med Care. 1993 May;31(5 Suppl):YS45-53.
In small-area variation analysis, the variation of health care utilization rates, e.g., admission rates, among small areas is calculated. Frequently, the variation of one diagnosis, diagnosis-related group (DRG), or procedure is compared with the variation of another. Unfortunately, the methods generally used to make these comparisons are not consistent. They differ on whether they 1) adjust for the prevalence of the DRGs, 2) distinguish between variation among areas and variation within areas, 3) weight all areas equally, and 4) adjust for multiple admissions per person. None has an associated confidence interval. These discrepancies occur in part because there is no statistical model of small area variation. Without such a model, it is not known how to measure variation, and thus, it is not known how to compare different DRGs. Here, the authors use data on 473 DRGs from 28 counties in Washington state to study the nature of variability. The variation was higher for the more prevalent DRGs, suggesting that adjusting for prevalence may be reasonable. The true coefficient of variation appears to be a "natural" measure of variation, but the usual small area variation statistics do not provide good estimates of the true coefficient of variation. A new estimate is proposed that can be used to compare and test the variability of several DRGs.
在小区域差异分析中,计算小区域间医疗保健利用率(如住院率)的差异。通常会将一种诊断、诊断相关分组(DRG)或医疗程序的差异与另一种进行比较。遗憾的是,用于进行这些比较的方法并不一致。它们在以下方面存在差异:1)是否对DRG的患病率进行调整;2)是否区分区域间差异和区域内差异;3)是否平等对待所有区域;4)是否对每人多次住院进行调整。而且都没有相关的置信区间。出现这些差异部分是因为没有小区域差异的统计模型。没有这样一个模型,就不知道如何衡量差异,因此也就不知道如何比较不同的DRG。在此,作者使用华盛顿州28个县473个DRG的数据来研究差异的本质。患病率较高的DRG差异更大,这表明对患病率进行调整可能是合理的。真正的变异系数似乎是差异的“自然”度量,但通常的小区域差异统计数据并不能很好地估计真正的变异系数。本文提出了一种新的估计方法,可用于比较和检验多个DRG的差异。