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In clinical practice, post-test probabilities are often just estimated or even guessed. This is usually acceptable in the finding of a pathognomonic sign or symptom, in which case it is almost certain that the target condition is present; or in the absence of finding a sine qua non sign or symptom, in which case it is almost certain that the target condition is absent.
Pre-test probability: For example, if about 2 out of every 5 patients with abdominal distension have ascites, then the pretest probability is 40%. Likelihood Ratio: An example "test" is that the physical exam finding of bulging flanks has a positive likelihood ratio of 2.0 for ascites.
The first two groups receive the evaluation test before and after the study, as in a normal two-group trial. The second groups receive the evaluation only after the study. [citation needed] The effectiveness of the treatment can be evaluated by comparisons between groups 1 and 3 and between groups 2 and 4. [citation needed]. In addition, the ...
The positive predictive value (PPV), or precision, is defined as = + = where a "true positive" is the event that the test makes a positive prediction, and the subject has a positive result under the gold standard, and a "false positive" is the event that the test makes a positive prediction, and the subject has a negative result under the gold standard.
In statistics, econometrics, political science, epidemiology, and related disciplines, a regression discontinuity design (RDD) is a quasi-experimental pretest–posttest design that aims to determine the causal effects of interventions by assigning a cutoff or threshold above or below which an intervention is assigned.
The example discussed by Duncan in his 1955 paper is of a comparison of many means (i.e. 100), when one is interested only in two-mean and three-mean comparisons, and general p-mean comparisons (deciding whether there is some difference between p-means) are of no special interest (if p is 15 or more for example). Duncan's multiple range test is ...
Matching is a statistical technique that evaluates the effect of a treatment by comparing the treated and the non-treated units in an observational study or quasi-experiment (i.e. when the treatment is not randomly assigned).
In a scientific study, post hoc analysis (from Latin post hoc, "after this") consists of statistical analyses that were specified after the data were seen. [ 1 ] [ 2 ] They are usually used to uncover specific differences between three or more group means when an analysis of variance (ANOVA) test is significant. [ 3 ]