| |
Biostatistics |
|
|
|
|
| 1. |
Sensitivity
and specificity: |
|
|
|
Disease
present |
Disease
absent |
|
Positive screening |
A
(90) |
B (20) |
| Negative
screening |
C
(10) |
D (80) |
|
|
|
Sensitivity
=A / A + C = 90 / 100 = 90% |
|
|
Specificity = D/ B + D = 80 / 1OO = 80% |
|
|
Positive
predictive value = A / A + B = 90 / 110 = 81% |
|
|
Negative
predictive value D / C +D = 80 / 90 = 88% |
|
|
|
|
|
Sensitivity
Persons with the disease and positive screening test divided by number of
persons tested with disease (100). i.e sensitivity of test means it gives
a positive finding when the person has the disease. |
|
|
Specificity
= Persons without the disease and negative screening test is divided by
number of persons tested without diseases (100), i.e.specificity of a test
means it gives a negative result when the person does not have disease. |
|
|
Positive
predictive value = Persons with the disease and positive screening test
divided by the total number of positive screening test. |
|
|
Negative
predictive value Persons without the disease and negative screening tests
divided by the total number of negative screening test. In syphilis, RPR
and VDRL have high sensitivity, so the test can give high false positive
and few false negative results, but FTA-ABS has high specificity which gives
correct diagnosis. |
|
|
Overall
accuracy A + D / A + B +C + D = 170 / 200 = 85% |
|
|
A =
True positive, D True negative.
|
|
|
B False
positive, C = False negative. |
|
|
|
|
| 2. |
Incidence
of the exposed and non exposed group: |
|
|
|
Disease
present |
Disease
absent |
|
Exposure present |
A
(80) |
B (20) |
| Exposure
absent |
C
(30) |
D (70) |
|
|
|
Incidence
rate of exposed group = A / A + B = 80 / 80+ 20 = 80% |
|
|
Incidence
rate of non exposed group = C / C + D 30 / 30 + 70 = 30% |
|
|
incidence
rate = Only new disease cases over a period of time is divided by population
at risk, so incidence means new cases. |
|
|
Prevalence
rate Total number of cases at a given time is divided by total populations,
so prevalence means all eases. |
|
|
|
|
| 3 |
Case control
studies. |
|
|
|
Lung
failure |
Normal
Lung |
|
Smoker |
A
(70) |
B (20) |
| Non-Smoker |
C
(30) |
D (80) |
|
|
|
Cases =
A / A + C = 70 / 100 = 70% |
|
|
Controls
= B / B + D = 20 / 100 = 20% |
|
|
Incidence
of exposed group = A / A + B = 70 / 90 = 77% |
|
|
Incidence
of non-exposed group = C / C + D = 30 / 110 = 27% |
|
|
|
|
| 4. |
Mean Sum
of the numbers associated with the observations is divided by the number
of observations. |
|
|
Median
= Middle number. |
|
|
Mode Most
frequently occuring number. |
|
|
|
|
| 5. |
Relative
risk Incidence rate among exposed group is divided by incidence rate among
non-exposed group 77% / 27% = 2.9% (calculated from Lung failure and Smoking
abuse). |
|
|
The odds
ratio: In case control studies or when the proportion of disease is small
in cohort studies, odds ratio is used to estimate the relative risk, which
cannot be calculated directly. |
|
|
(A x D)
/ (B x C) = (70 x 80) / (20 x 30) = 9.33 |
|
|
Attributal
risk Incidence rate among exposed group minus incidence rate among non-
exposed group = 77% - 27% = 50% (calculated from Lung failure and smoking
abuse). Absolute risk Same as incidence. |
|
|
A / A +
B = 70 / 90 = 77% (calculated from Lung failure and smoking abuse from item
3 in case control study). |
|
|
|
|
| 6. |
Probability
of a disease condition. |
|
|
Probability
= Total number of times disease occurs is divided by total number of times
disease can occur (e.g., total number of AIDS patients = 60, total number
of pneumocystis pneumonia = 20, so probability = 20 / 60 = 33%). |
|
|
|
|
| 7. |
Chi-square
test: This test is most commonly used for differences between proportions,
i.e., comparing effects of two different drugs used in two different groups. |
|
|
|
|
| 8. |
Null hypothesis:
When we compare two groups in a study and notice some differences between
them, the null hypothesis may suggest that the observed differences are
due to random variation in the data. If you accept null hypothesis, you
think that observed differences are due to such random variations, but if
you reject the null hypothesis, you think that observed differences are
not due to random variations. Null hypothesis may he true or false. |
|
|
Type I
(alpha) error means null hypothesis is true, but rejected. |
|
|
Type II
(beta) error means null hypothesis is false, but accepted. |
|
|
No error
means either null hypothesis is true and accepted or is false and rejected. |
|
| 9. |
The P value:
P value < 0.01 means the result is statistically significant because the
probability of random variation alone is very small. |
|
| |
|
|
| |
|
|
| |
©
2002 Windsor University School of Medicine. All rights reserved.
|
|