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R Gasko

Publications and source records attributed to R Gasko.

5 recordsLinked to original sources

Statistical hypothesis testing--how exact are exact p-values?

OBJECTIVES AND BACKGROUND: When testing a hypothesis statistically, a principle is generally accepted that exact p values shall be stated in the treatise. Researchers have the choice of many statistical computer programmes with implemented hypothesis tests. Are exact p values calculated in the same statistical tests by diverse statistical programmes identical? METHODS: The respective zero hypothesis were tested in 5 artificially created data sets by the parametric unpaired t-test, non-parametric Mann-Whitney test, two-tailed F-test. The calculations were carried out by the following programmes: Statistix, version 7.1 (source www.statistix.com), Analyse-it, version 1.62 (source www.analyse-it.com), MedCalc, version 6.14 (source www.medcalc.be). The p values in the same tests were mutually compared. RESULTS: All three programmes calculated identical exact p values for the t-test. In the remaining two tests in case of 26 out of 44 calculations (59.1 per cent; 95 per cent confidence interval 43-73 per cent) different p values were calculated. The greatest difference was 18.35 per cent. In two cases the values oscillated about 0.05 and this fact caused essentially different interpretation of results. CONCLUSIONS: Using the significance test in the biomedical research has been subject to criticism for a longer period of time. The testing of the zero hypothesis on the arbitrary significance level of 0.05 should be substituted by other methods. Our discoveries should undermine the ungrounded belief of the users of statistical tests--physicians in ununderminable accuracy of mathematical procedures. The use of confidence intervals deems much more suitable although there are objections against them as well. (Tab. 4, Fig. 1, Ref. 19.).

Confidence Intervals↗

[Differentiation of malignant and non-malignant origin of ascites by determination of levels of cholesterol and lactate dehydrogenase in ascitic fluid is not absolute].

The authors Castaldo et al. (Clin. Chem., 1994, 30: 478-83) state, that the ascitic lactate dehydrogenase and ascitic cholesterol association correctly identified 100% of malignant ascites from ascites associated with cirrhosis and/or hepatocellular carcinoma, with help of stepwise multiple linear discriminant analysis. The free software Capsules--Ascites is via internet available (http:¿www.leeds.ac.uk/acb), which use the mathematical formula from this article. As we argue, Castaldo's state is not correct. Three independent multidimensional statistical methods--bivariate reference regions (program EVAL-KIT), cluster analysis (program BioAnalyst), geometrical distance classification (program GEODICLA) applicated on Castaldo's original data showed that lactate dehydrogenase and cholesterol have not satisfactory absolute discriminative power between malignant from nonmalignant ascites in general, but the probability to determinate the right diagnosis is about 91-93%. Research conducted in correctly selected probands should provide information which is valid not only for the selected sample but for the entire population, to achieve more generally valid conclusions, useful for practical decisions. In addition, in the compiled table show we sensitivity and specificity of different laboratory parameters publicated in 11 original articles in the nineties, all with diagnostic efficiency less 100%.

Ascites↗

[Diagnostic validity of tests--binary tables or multidimensional statistical methods?].

The authors criticize the use of concepts of sensitivity and specificity calculated by means of a binary table in differential diagnostic reflections pertaining to more than one disease or several, i.e. more than one diagnostic test. On examples they present possibilities of different ways for calculating these concepts with different not correlating results. They indicate the justification of using multidimensional statistical methods in those instances and their better diagnostic yield.

Diagnosis↗