lecture 1 Flashcards
progression of disease
Preclinical phase (disease onset, symptom onset)
Clinical phase (clinical diagnosis, death)
- disease persists along a continum
levels of prevention
primordial: maintain health, avoid risk
primary: reduce and eliminate risk, avoid clinical disease events
secondary: minimize severity, reduce likelihood of repeat events
tertiary: minimize impact of chronic clinical disease
syndemic factors
when 2 or more concurrent factors exacerbate prognosis or burden of a disease (social, mental, environmental factors that promote and worsen disease)
comprehensive approach to disease understanding and management
symptoms
patient complaints, descriptions
signs
what you can detect with senses
pathogenesis
natural history, how a disease develops
etiology
cause of disease
diagnosis
determination of nature and cause of illness
(clinical history, physical examination, differential diagnosis)
prognosis
eventual outcome of disease
treatment
directed at underlying cause
symptomatic treatment
alleviates symptoms but doesn’t influence course of disease
clinical history (5 components)
- history of current illness
- medical history
- family history
- social history (syndemic factors)
- review of symptoms (symptoms other than disclosed in history of present illness, suggesting other parts of body affected by disease)
differential diagnosis
- consideration of other diseases or symptoms explaining signs and symptoms of patient
- diagnostic possibilities narrowed by lab tests/ other diagnostic procedures
- opinion of medical consultant?
physical exam
systematic exam of patient with emphasis on parts of body affected by illness
- ex. vitals, resp exam, cardiac exam, abdominal exam, neuro exam, psych exam, ocular exam, abnormalities noted (see notes for details of each exam)
- after this, revisit differential diagnosis
general diagnostic test considerations (6 things)
-cost
-speed/timing/ availability
- invasive vs noninvasive
- false positive/ false negative ratio (specificity/ sensitivity)
- target/ evidence based (vast and growing number/ types of testing available)
- inform treatment
sensitivity and specificity
-highly sensitive = few false neg
-highly specific = few false pos
a perfect test does not exist, most have a crossover of sensitivity and specificity
- move cutoff left: less false neg, more false pos, more sensitive, less specific
- move cutoff right: less false pos, more false neg, more specific, less sensitive
sensitivity
how well a test picks up disease (truly pos)
measures threshold of detection
%sensitivity = TP/(TP + FN)
- poor sensitivity = more false neg (not picking people up as positive)
specificity
how well a test identifies one who doesn’t have disease (truly neg)
ability to not get an incorrect result from cross reaction
%specificity = TN/(TN+FP)
- poor spec = more false pos
screening tests for disease
- detect EARLY ASYMPTOMATIC diseases amenable to treatment to prevent or minimize late-stage organ damage/ cancer
- routine for pts (physicals, cholesterol, skin, BP)
- Ontario/ Province wide programs (breast, cervical, lung, colon)
- specific risks/ occasions (infectious disease, prenatal/ newborn)
screening for genetic diseases/ susceptibility
- screen for CARRIERS of genetic diseases transmitted from parent to child as a dominant or recessive trait
- ex. recessive gene for sickle cell anemia
- identifying carriers lets them decide if they want to have kids
requirements for affective screening
- groups suitable for screening (significant number of people at risk in screening group)
- suitable screening test (appropriate, inexpensive, non-invasive, low # of false neg and false pos, actionable results/ benefit, are weaknesses warrented?)
- benefits of screening (benefit outweighs risks)
- invasive vs non-invasive