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Report in English with a Dutch summary (KCE reports 45A)

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<strong>KCE</strong> <strong>reports</strong> vol.45 Screen<strong>in</strong>g for Colorectal Cancer 13<br />

Prevalence<br />

Primary care<br />

Prognosis<br />

Prognostic factor<br />

person <strong>with</strong> a negative test truly does not have the disease. The<br />

predictive value of a screen<strong>in</strong>g test is determ<strong>in</strong>ed by the sensitivity and<br />

specificity of the test, and by the prevalence of the condition for which<br />

the test is used.<br />

The number of events <strong>in</strong> a given population at a designated time (po<strong>in</strong>t<br />

prevalence) or dur<strong>in</strong>g a specified period (period prevalence).<br />

First contact, cont<strong>in</strong>uous, comprehensive and coord<strong>in</strong>ated care<br />

provided to <strong>in</strong>dividuals and populations undifferentiated by age, gender,<br />

disease or organ system.<br />

the possible outcomes of a disease or condition and the likelihood that<br />

each one will occur.<br />

Demographic, disease-specific, or co-morbid characteristics associated<br />

strongly enough <strong>with</strong> a condition's outcomes to predict accurately the<br />

eventual development of those outcomes. Compare <strong>with</strong> risk factors.<br />

Neither prognostic nor risk factors necessarily imply a cause and effect<br />

relationship.<br />

Study design where one or more groups (cohorts) of <strong>in</strong>dividuals who<br />

Prospective study have not yet had the outcome event <strong>in</strong> question are monitored for the<br />

number of such events which occur over time.<br />

Providers Organisations and health professionals provid<strong>in</strong>g health services.<br />

A sample that is arrived at by select<strong>in</strong>g sample units <strong>in</strong> such way that<br />

Random sample<br />

Randomised<br />

controlled trial<br />

Recall bias<br />

Reference<br />

standard<br />

Referral filter bias<br />

Relative risk<br />

Relative risk<br />

reduction<br />

Reliability<br />

Repeatability<br />

Reproducibility<br />

each possible unit has a fixed and determ<strong>in</strong>ate probability of selection.<br />

An epidemiologic experiment <strong>in</strong> which subjects <strong>in</strong> a population are<br />

randomly allocated <strong>in</strong>to groups - rather than by conscious decisions of<br />

cl<strong>in</strong>icians or patients - to receive or not receive an experimental<br />

preventive or therapeutic procedure, manoeuvre, or <strong>in</strong>tervention.<br />

Randomised controlled trials are generally regarded as the most<br />

scientifically rigorous method of hypothesis test<strong>in</strong>g available <strong>in</strong><br />

epidemiology. If the sample size is large enough, this study design<br />

avoids problems of bias and confound<strong>in</strong>g variables by assur<strong>in</strong>g that both<br />

known and unknown determ<strong>in</strong>ants of outcome are evenly distributed<br />

between treatment and control groups.<br />

Systematic error due to the differences <strong>in</strong> accuracy or completeness of<br />

recall to memory of past events or experiences.<br />

An <strong>in</strong>dependently applied test that is compared to a screen<strong>in</strong>g or<br />

diagnostic test be<strong>in</strong>g evaluated <strong>in</strong> order to verify the latter s accuracy.<br />

A reference standard, therefore, provides an accurate or truth<br />

diagnosis for verification of positive and negative diagnoses. It is<br />

sometimes described as provid<strong>in</strong>g f<strong>in</strong>al truth determ<strong>in</strong>ation .<br />

The sequence of referrals that may lead patients from primary to<br />

tertiary centres raises the proportion of more severe or unusual cases,<br />

thus <strong>in</strong>creas<strong>in</strong>g the likelihood of adverse or unfavorable outcomes.<br />

The ratio of the risk of disease or death of those exposed to the risk<br />

compared to the risk among those unexposed, <strong>in</strong> a specified period of<br />

time. It is a measure of the strength or degree of association applicable<br />

to cohort studies and RCTs.<br />

The proportional reduction <strong>in</strong> rates of events between experimental<br />

and control participants <strong>in</strong> a trial. If there was an <strong>in</strong>crease <strong>in</strong> the rate of<br />

events <strong>in</strong> the experimental group, the term would then be relative risk<br />

<strong>in</strong>crease.<br />

The results of a test or measure are identical or closely similar each<br />

time it is conducted.<br />

Repeat screen<strong>in</strong>g Rescreen<strong>in</strong>g offers made only to persons complet<strong>in</strong>g a prior test or

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