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