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Public Health Sciences   PUBLIC HEALTH SCIENCES—Epidemiology and Biostatistics SECTION II 263

Precision vs accuracy
Precision (reliability) The consistency and reproducibility of a test. Random error  precision in a test.
The absence of random variation in a test.  precision Ž  standard deviation.
 precision Ž  statistical power (1 − β).
Accuracy (validity) The closeness of test results to the true values. Systematic error  accuracy in a test.
The absence of systematic error or bias in a test.

Accuracy Accuracy
High Low High Low

High High Low Low


Precision Precision

Incidence vs # of new cases Incidence looks at new cases (incidents).


Incidence = (per unit of time)
prevalence # of people at risk
# of existing cases (at a point in Prevalence looks at all current cases.
Recurrence Prevalence =
Total # of people    time)
Incidence
in a population
Prevalence Prevalence
= Incidence rate × average duration
1 – prevalence of disease
Mortality Cure
Prevalence ≈ incidence for short duration disease Prevalence ∼ pretest probability.
(eg, common cold).  prevalence Ž  PPV and  NPV.
Prevalence > incidence for chronic diseases, due to
large # of existing cases (eg, diabetes).
SITUATION INCIDENCE PREVALENCE

 survival time — 
 mortality — 
Faster recovery time — 
Extensive vaccine administration  
 risk factors  
 diagnostic sensitivity  
New effective treatment started — 
 contact between patients with and — —
without noninfectious disease
 contact between infected and  
noninfected patients with airborne
infectious disease

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264 SECTION II Public Health Sciences   PUBLIC HEALTH SCIENCES—Epidemiology and Biostatistics

Bias and study errors


TYPE DEFINITION EXAMPLES STRATEGIES TO REDUCE BIAS
Recruiting participants
Selection bias Nonrandom sampling Berkson bias—cases and/ Randomization (creates groups
or treatment allocation or controls selected from with similar distributions
of subjects such that hospitals (bedside bias) are of known and unknown
study population is not less healthy and have different variables)
representative of target exposures Ensure the choice of the right
population Attrition bias—participants lost comparison/reference group
Most commonly a sampling to follow up have a different
bias prognosis than those who
complete the study
Performing study
Recall bias Awareness of disorder alters Patients with disease recall Decrease time from exposure
recall by subjects; common in exposure after learning of to follow-up; use medical
retrospective studies similar cases records as sources
Measurement bias Information is gathered in a Using a faulty automatic Use objective, standardized,
systemically distorted manner sphygmomanometer and previously tested methods
Hawthorne effect—participants of data collection that are
change behavior upon planned ahead of time
awareness of being observed Use placebo group
Procedure bias Subjects in different groups are Patients in treatment group Blinding (masking) and
not treated the same spend more time in highly use of placebo reduce
specialized hospital units influence of participants and
Observer-expectancy Researcher’s belief in the An observer expecting researchers on procedures and
bias efficacy of a treatment changes treatment group to show signs interpretation of outcomes
the outcome of that treatment of recovery is more likely to as neither are aware of group
(also called Pygmalion effect) document positive outcomes assignments
Interpreting results
Confounding bias Factor related to both exposure An uncontrolled study shows Multiple/repeated studies
and outcome (but not on an association between Crossover studies (subjects act
causal path) distorts effect drinking coffee and lung as their own controls)
of exposure on outcome (vs cancer; however, people who Matching (patients with
effect modification, in which drink coffee may smoke more, similar characteristics in both
the exposure leads to different which could account for the treatment and control groups)
outcomes in subgroups association Effect modification—
stratified by the factor) association is shown
differently in individual
subgroups due to stratification
by given factor even when
there is association between
exposure and outcome
Lead-time bias Early detection interpreted as Breast cancer diagnosed early Measure “back-end” survival
 survival, but the disease by mammography may (adjust survival according to
course has not changed appear to exaggerate survival the severity of disease at the
time because patients are time of diagnosis)
known to have the cancer for
longer

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