Statistics for AKT

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Statistics for AKT

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Statistics for AKT. Discriptive Statistics. Mean: true average Median: middle number once ranked Mode: most repetitive Range : difference between largest and smallest. Find out the Mean, Median, Mode and Range for following. 8, 9, 9, 10, 11, 11, 11, 11, 12, 13 - PowerPoint PPT Presentation

Transcript of Statistics for AKT

Page 1: Statistics for AKT

Statistics for AKT

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Mean: true average Median: middle number once ranked Mode: most repetitive Range : difference between largest and smallest.

Discriptive Statistics

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Find out the Mean, Median, Mode and Range for following.  8, 9, 9, 10, 11, 11, 11, 11, 12, 13

The mean is the usual average: (8 + 9 + 9 + 10 + 11 + 11 + 11 + 11 + 12 + 13) ÷ 10 = 105 ÷ 10 = 10.5

The median is the middle value. In a list of ten values, that will be the (10 + 1) ÷ 2 = 5.5th value which will be 11.

The mode is the number repeated most often. 11

The largest value is 13 and the smallest is 8, so the range is 13 – 8 = 5.

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Normal Distribution: Mean=Median=Mode Positive Skewed: Mean>Median>Mode Negative Skewed: Mean<Median<Mode

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Skewed Data

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Test Result Disease Present Disease Absent

Positive TP FP

Negative FN TN

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Sensitivity: How good is the test at detecting those with the condition

TRUE POSITIVESACTUAL NUMBER OF CASES

Specificity: How good is the test at excluding those without the condition

TRUE NEGATIVESACTUAL NUMBER OF PEOPLE WITHOUT CONDITION

Sensitivity and Specificity

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Positive Predictive Value: How likely is a person who tests +ve to actually have the condition

TRUE POSITIVESNUMBER OF PEOPLE TESTING POSITIVE

Negative Predictive Value: How likely is a person who tests –ve to not have the condition

TRUE NEGATIVESNUMBER OF PEOPLE TESTING NEGATIVE

Predictive Values

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Incorporates both sensitivity and specificity

Quantifies the increased odds of having the disease if you get a positive test result, or not having the disease if you get a negative test result.

Positive Likelihood ratio:Sensitivity

(1 – Specificity)

Negative Likelihood ratio:(1-Sensitivity)

Specificity

Likelihood Ratios

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Odds are a ratio of the number of people who incur a

particular outcome to the number of people who do not incur the outcome.

NUMBER OF EVENTS NUMBER OF NON-EVENTS

Odds: what are the chances

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Odds ratio:

The odds ratio may be defined as the ratio of the odds of a particular outcome with experimental treatment and that of control.

Odds ratios are the usual reported measure in case-controlstudies.

It approximates to relative risk if the outcome of interest israre.

ODDS IN TREATMENT GROUPODDS IN CONTROL GROUP

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For example, if we look at a trial comparing the use of paracetamol for dysmenorrhoea compared to placebo we may get the following results

Total no of Patients

Pain relief achieved

Paracetamol 60 40

Placebo 90 30

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The odds of achieving significant pain relief with paracetamol = 40 / 20 = 2

The odds of achieving significant pain relief with placebo = 30 / 60 = 0.5

Therefore the odds ratio = 2 / 0.5 = 4

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Prevalence: rate of a disorder in a specified population

Incidence: Number of new cases of a disorder developing over a given time (normally 1 year)

Incidence and Prevalence

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Questions

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Relative risk (RR) is the ratio of risk in the experimental group (experimental event rate, EER) to risk in the control group (control event rate, CER).

Relative risk is a measure of how much a particular risk factor (say cigarette smoking) influences the risk of a specified outcome such as lung cancer, relative to the risk in the population as a whole.

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Absolute risk: Risk of developing a condition

Relative risk: Risk of developing a condition as compared to another group

EVENTS IN CONTROL GROUP – EVENTS IN TREATMENTGROUP EVENTS IN CONTROL GROUP

X 100- My lifetime risk of dying in a car accident is 5% - If I always wear a seatbelt, my risk is 2.5%

- The absolute risk reduction is 2.5%- The relative risk reduction is 50%

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For example, if we look at a trial comparing the use of paracetamol for dysmenorrhoea compared to placebo we may get the following results

Total no of Patients

Pain relief achieved

Paracetamol 100 60

Placebo 80 20

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Experimental event rate, EER = 60 / 100 = 0.6

Control event rate, CER = 20 / 80 = 0.25

Therefore the relative risk = EER / CER = 0.6 / 0.25 = 2.4

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Relative risk reduction (RRR) or relative risk increase (RRI) is calculated by dividing the absolute risk change by the control event rate Using the above data,

RRI = (EER - CER) / CER (0.6 - 0.25) / 0.25 = 1.4 = 140%

Relative Risk Reduction

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Numbers needed to treat (NNT) is a measure that indicates how many patients would require an intervention to reduce the expected number of outcomes by one

It is calculated by 1/(Absolute risk reduction)

Absolute risk reduction = (Experimental event rate) - (Control event rate)

Numbers needed to treat and absolute risk reduction

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A study looks at the benefits of adding a new anti platelet drug to aspirin following a myocardial infarction. The following results are obtained:

Percentage of patients having further MI within 3 months Aspirin 4% Aspirin + new drug 3%

What is the number needed to treat to prevent one patient having a further myocardial infarction within 3 months?

NNT = 1 / (control event rate - experimental event rate) 1 / (0.04-0.03) 1 / (0.01) = 100

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Remember that risk and odds are different.

If 20 patients die out of every 100 who have a myocardial infarction then the risk of dying is 20 / 100 = 0.2 whereas the odds are 20 / 80 = 0.25.

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The null hypothesis is that there are no differences between two groups.

The alternative hypothesis is that there is a difference.

Null Hypothesis

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Type 1 error:- Wrongly rejecting the null hypothesis- False +ve

Type II error:- Wrongly accepting the null hypothesis- False -ve

Study Error

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Probability of establishing the expected difference between the treatments as being statistically significant- Power = 1 – Type II error (rate of false –ve’s)

Adequate power usually set at 0.8 / 80%

Is increased with- increased sample size- increased difference between treatments

Power of the study

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A result is called statistically significant if it is unlikely to have occurred by chance

P values

- Usually taken as <0.05

- Study finding has a 95% chance of being true

- Probability of result happening by chance is 5%

Significance

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Statistical Tests

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1. Parametric / Non-parametricParametric if: - Normal distribution

- Data can be measured

2. Paired / Un-pairedPaired if data from a single subject group (eg before and after intervention)

3. Binomial – ie only 2 possible outcomes

Types of Tests

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Student’s T-test- compares means- paired / unpaired

Analysis of variance (ANOVA)- use to compare more than 2 groups

Pearsons correlation coefficient- Linear correlation between 2 variables

Parametric Tests

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Mann Whitney- unpaired data

Kruskal-Wallis analysis of ranks / Median test

Wilcoxon matched pairs- paired data

Friedman's two-way analysis of variance / Cochran Q

Spearman or Kendall correlation- linear correlation between 2 variables

Non Parametric Data

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Compares proportions

Chi squared ± Yates correlation (2x2)

Fisher’s exact test- for larger samples

Binominal Data (non-parametric)

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The standard deviation (SD) represents the average difference each observation in a sample lies from the sample mean

SD = square root (variance)

Standard Deviation

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In statistics the 68-95-99.7 rule, or three-sigma rule, or empirical rule, states that for a normal distribution nearly all values lie within 3 standard deviations of the mean

About 68.27% of the values lie within 1 standard deviation of the mean.

Similarly, about 95.45% of the values lie within 2 standard deviations of the mean.

Nearly all (99.73%) of the values lie within 3 standard deviations of the mean.

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Normal Distribution

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Thank you for all your patience!!!!