8 Mortality + Morbidity Stats. Flashcards

1
Q

Why do classifications of disease change over time

A
  • Recognition of new diseases
  • Changes in classification
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2
Q

leading cause of death male vs. female

A
  • Coronary heart disease (male)
  • Dementia (female)
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3
Q

CRUDE death rates

A

BASED on actual number of events
* often not useful

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4
Q

Crude Annual Death Rate

A

Total number of deaths in a 12-month period

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5
Q

Why do we need to use specific death rates as opposed to crude?

A

Need to look at specififc death rates and population composition SEPERATLEY

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6
Q

Specific Death Rates

A

Measure mortality for a specific group in a population
* usually consider 1 factor (e.g. age)

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7
Q

Confounding Factors

A

distortion of a measure of the effect of an exposure on an outcome due to the association of the exposure with other factors influencing the outcome

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8
Q

Age Adjustment or Standardisation

A

Adjusting rates for differences in population age structure
* Attempt to remove age as a confounding factor
* Create ‘dummy‘ age composition
* Re-calculate overall rates

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9
Q

Why are Adjusted (standardised) Rates
more efficient.

A

Remove the need for comparison of each stratum (of characteristic) within pop. at one time

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10
Q

What is used to standardise rates?

A

A fictitious pop. or rate matrix
* Get age specific death rate from each age group > multiply by number for overall pop.

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11
Q

Direct Standardisation

A
  • Age-specific rate in YOUR population(s)
  • Age-distribution in “standard” population
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12
Q

Indirect Standardisation

A
  • Age distribution in YOUR population
  • Age-specific rate in “standard” population
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13
Q

Sources of morbidity stats.

A
  1. Insurance companies
  2. Gov.
  3. Armed Forces
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14
Q
A
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15
Q

Types of Data Collected
(Morb. Stats.)

A
  1. Screening (high vol, low qual.)
  2. Hospital Records
  3. Long-term reg. (low vol, high qual).
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16
Q

Screening

A

Tests on “well” people
* reduce morb. > prevent progression
* need confirmatory tests

17
Q

Interview Data

A

Greatest problem is under-reporting
* Worse if hearsay

18
Q

Permanent Long-Term Registration

A

Best data
* Costly
* Compliance?
* e.g. cancer registry

19
Q

Cancer Incidence by Sex

A

Prostate 1# for males
Breast 1# for females

20
Q

Migration and cancer incidence

A

Rates of certain cancers in migrated populations would increase and match local rates
* enviro factors in each place

21
Q

How to assess validity of a test

A
  1. SENSITIVITY of the test (True Pos/All with disease)
  2. SPECIFICITY of test (True Neg/All with disease)
22
Q

Continuous Variable (biomarker): IDEAL Case

A

There would be minimal cross over between healthy and diseased based on serum levels

23
Q

Continuous Variable (biomarker): REALITY

A

There is some cross over
* False neg + pos
* need to choose a lower threshold of serum > fewer false neg

24
Q

SENSITIVITY

A

a/(a + b) = True POS rate

refer to table in doc

25
SPECIFICITY
**d**(**c** + **d**) = True ***NEG rate*** ## Footnote refer to table in doc
26
Receiver Operating Characteristic Curves (ROC curves)
Plotting **sensitivity** against **1 - Specificity** * Area under ROC determines ***quality*** of **biomarker** * ***BEST*** possible **threshold** is the ***upper leftmost*** data point
27
incidence
no. of ***new*** cases occurred during given **time** interval ***divided*** by **pop. at risk** at *beginning* of time interval
28
What does a change in incidence indicate?
A change it ***etiological*** factors
29
prevalence | p
no. of individuals with ***given disease*** at ***given moment*** in time **divided** by **pop. at risk** at that moment in time
30
What does a chnage in prevalence mean?
Change in: * ***incidence*** * **outcome** (cure) * **duration** * **diagnosis** * **pop**. (migration
31
Incidence density
no. of **new cases** over a given period ***divided*** by total ***"person-time" observation***