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使用微型计算机诊断人类畸形模式:两种不同算法的评估

Diagnosing human malformation patterns with a microcomputer: evaluation of two different algorithms.

作者信息

Schorderet D F

机构信息

Department of Genetics, University of Washington, Seattle 98195.

出版信息

Am J Med Genet. 1987 Oct;28(2):337-44. doi: 10.1002/ajmg.1320280211.

Abstract

SYNDROC, a microcomputer-aided differential diagnostic approach to human malformation patterns, is based on a pseudo-Bayesian algorithm. This means that, for each sign, the frequency of this sign in the general population, its frequency in a particular syndrome, and the frequency of that particular syndrome have to be determined. These parameters are easy to find in common syndromes but tend to be difficult for rare or isolated cases. Thus, we implemented a new algorithm called the "descriptive algorithm," which defines a diagnosis by a set of anomalies all having the same weight. To test this algorithm, we analyzed 100 cases representing 100 different syndromes out of the register of the Division of Medical Genetics, Children's Hospital and Medical Center, University of Washington. The descriptive algorithm was allowed to give 3 sets of diagnoses. In 91% of the cases, this algorithm proposed the correct diagnosis (54% in the first window, 28% in the second window, and 9% in the third window). The number of diagnoses proposed was 18.78 +/- 16.57. The same cases were analyzed with the pseudo-Bayesian algorithm. The concordant diagnosis was proposed in 92% of the cases (55% at the top place, 11% at the second place, and 26% at the third place or beyond). The number of diagnoses submitted was 13.5 +/- 11.04. The combined algorithm gave the correct diagnosis in 96% of the cases. This study shows that the descriptive algorithm is as accurate as the pseudo-Bayesian algorithm in diagnosing malformation patterns, but this level is accompanied by an increased number of proposed diagnoses.

摘要

SYNDROC是一种用于人类畸形模式的微机辅助鉴别诊断方法,它基于一种伪贝叶斯算法。这意味着,对于每个体征,必须确定该体征在一般人群中的频率、在特定综合征中的频率以及该特定综合征的频率。这些参数在常见综合征中很容易找到,但对于罕见或孤立病例往往很难确定。因此,我们实施了一种名为“描述性算法”的新算法,该算法通过一组权重相同的异常来定义诊断。为了测试该算法,我们从华盛顿大学儿童医院和医疗中心医学遗传学部门的登记册中分析了代表100种不同综合征的100个病例。描述性算法被允许给出3组诊断。在91%的病例中,该算法提出了正确的诊断(第一个窗口中为54%,第二个窗口中为28%,第三个窗口中为9%)。提出的诊断数量为18.78±16.57。使用伪贝叶斯算法对相同的病例进行了分析。在92%的病例中提出了一致的诊断(第一名占55%,第二名占11%,第三名或更靠后占26%)。提交的诊断数量为13.5±11.04。联合算法在96%的病例中给出了正确的诊断。这项研究表明,描述性算法在诊断畸形模式方面与伪贝叶斯算法一样准确,但这种准确性伴随着提出的诊断数量的增加。

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