Beruflich Dokumente
Kultur Dokumente
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Retrospective = looking back to determine factors leading to current disease Cross sectional = a one short survey measuring variables at one point in time Prospective = begin in the present and follow subjects in time Studies Cross sectional study First stage Looks for potential relationships Eg. Visited dental professionals by disadvantage Case control study (Outcome Exposure) Eg. People who have MS and exposure to amalgam Retrospective Advantages Disadvantages Cheap, easy, quick Case & Control selection difficult Multiple exposures can be studied Subject to bias Rare disease / Long latency disease can be Direct incidence estimation impossible studied Suitable when randomisation is unethical Temporal relationship not clear Multiple outcome cannot be studied Hard to estimate attributable fraction (reduction in disease when risk factor is removed) Temporal relationship not clear Cohort study (Exposure Outcome) Eg. Does exposed to day care result in asthma?
Prospective Advantages Can establish population based incidence Accurate relative risk (risk of an event after exposure) Can examine rare exposures Time to event analysis possible Where randomization not possible Magnitude of risk factors quantifiable Less bias Multiple outcomes can be studied Disadvantages Lengthy & expensive May need large samples Not suitable for rare disease Not suitable for long latency diseases Unexpected environmental changes influence association
High blood pressure (eligible patients) given random treatment, checked for outcome
Expressed in = percent, number of cases per 10 000, number of cases per 100 000 Use = Overall impact of disease in a community, need for health care resources Incidence of disease
o Cumulative incidence = No. of new cases over a period of time Population at risk at start of the period
Expressed in = percent, number of cases per 10 000 population at risk per year, number of cases per 100 person years of observation o Used = Identify factors associated with disease, measuring strength of association between a factor and a disease Uncertainty principle o Physicians who know which treatment is best for patient cannot enter patient into a RCT Variables o Independent o Dependent o Control o
Types of data Quantitative data Discrete (in steps) Continuous (may take any value) o Grouping causes loss in information and use of arbitrary values Qualitative data (recorded in numbers only for convenience) Categorical (can tae a number of levels that have no intrinsic numerical meaning) Binary (two levels only) Ordinal (have a natural order to their outcomes) Measures of centrality Mean = average (best when have a symmetric distribution with thin tails) Median = middle (if skewed use median) Mode = set of values occurring most frequently (not good measurement of centrality) Measures of dispersion Range = diff between max and min values Variance = quantifies the amount of variability or spread around the mean, the average of the squared deviations Standard deviation = square root of variance Normal distribution Symmetric Two parameters, mean and mode Highest point is at the mean, median and mode 68.26% within 1sd 95.44% within 2sd 99.72% within 3sd
Safe storage of data HREC (Human research ethics committee) o Committee made of 7+ members: A chairperson 2 lay members M/F knowledgable in research domains knowledgeable in health care religion lawyer o Role is to consider protocols, record decisions, monitor research, handle complaints, report to AHEC
Advantages
Disadvantages
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Quick results High refusal rate Can use large samples No way of verifying ID or respondent Economical Excludes other collection ways (eg. observation) More open communication Restricted sample to those with phones Reduces bias as interview unseen Offers greater anonymity Interview Postal survey Formulate + format questions Use focus groups / in-depth interviews Consultation with stakeholders (those involved) Critical review of literature and reports Focus on objectives of study Closed questions = easier to analyse, lack additional info Open questions = harder to analyse, yield the less predicted data and additional info Choice b/n open and closed depends on purpose of survey, respondent characteristics, access to skilled coders, time to develop and code the questionnaires Check design Concise and clear Introduce what you are doing Clear instructions Natural sections Instructions on how to return form Check wording Language simple? Shorter questions possible? Question double-barrelled? Question leading? Question negative? Can respondent answer question/have necessary knowledge? Words have same interpretation for everyone? Pre-testing and piloting questions Test questionnaire (eg. Colleagues) Also pilot (guide) the subjects as similar to the actual study sample Estimate cost, duration and develop protocols Drawing the sample Be clear about sample Type (convenience, strata, cluster) Execute and monitor survey Improve response rate by: Being concise Pre-survey info sheets Incentives Reply paid envelopes Follow up call Preparing, planning, implementing data analysis Data into Excel, Stata, SAS or SPSS Coding sheet: variable name (eg. Sex), codes used (eg. 1=M,2=F) , explanation variable (eg. Sex recorded by parent) Writing + disseminating research report
Know data Frequency distributions o Symmetrical o Skewed Positive hump to the left, (L R)mode, median, mean Negative hump to the right, (L R)mean, median, mode o Normal distribution (1sd = 68.26%, 2sd = 95.44%, 3sd = 99.72%) Inferential statistics o p-values o Confidence intervals Hypothesis testing 1. Set up null hypothesis (H0) The null hypothesis is a theory which says that there is no association between the variables It basically means that the results of the study are all due to chance, not due to an actual relationship Eg. Trialling a new drug, H0 could be that there is no difference between the new drug and old drug 2. Set up alternative 3. Choose alpha 4. Take a sample and calculate 5. Look up table for p-value P-value is the probability that the result is due to chance rather than a true relationship between the variables If the P-value is less than 0.05 we reject the null hypothesis (i.e. reject the idea that there is no relationship and say that there is a statistically significant relationship) 6. Compare p to alpha 7. Decide whether to reject H0 Example Data Analysis Effect of Alcohol on performance time Errors 1. State the null hypothesis and alternative H0 is True H0 is False a. H0: There is no decrease in time b. Alternative: There is a decrease in time Reject Type 1 error ok 2. Verify data conditions + analyse data with stats Accept ok Type 2 error a. No outliers, skewness with a boxplot o Type 1 Error ( = false +ve) = the null hypothesis is true b. Mean, SD, p-value, t-value etc. 3. Find p-value (i.e. that there is NO relationship between A and B) but a. p-value = 0.013 you rejected it saying that there IS a relationship 4. Decide whether it is statistically significant or not between A and B a. Using a=0.05, p=0.013<0.05 thus reject H0 o Type 2 Error ( = false ve) = the null hypothesis is false b. Alcohol has a statistically significant effect and decreases performance time (i.e. that there IS a statistically significant relationship between A and B) but you accepted it saying that there is a NO relationship between A and B when there really was! You wrongly concluded there to be no association between A and B. You Type II error idiot. Power o P (rejecting null when false) = 1 P() o Want to have as much power! (Usually about 80%) o Eg. H0 stated that there was no relationship between A and B, you rejected it saying there was a relationship. You were correct, there was a relationship. i.e. the right thing to do Controlling Type 1 and Type 2 errors o = constant, n o n = constant, n o n o There is an inverse relationship between the two errors Confidence intervals o CI is the expected range in which population statistic will be found at a given level of confidence o Eg. CI 95% means we are 95% certain that the true mean will be found within this range Non-parametric statistics Advantages Disadvantages Can be used for non-normal data Loose information Ordinal scale data can be used Some non-parametric tests are labour intensive for large samples Some protection against outliers Can be used if we know little of sample population
Lecture 9 Epidemiology
Definition o The study of the distribution and determinants of health related states and events in populations and the application of study to control of health problems Assumptions o Diseases does not occur by chance o Diseases are not randomly distributed Error Types Components 1. Random Error (noise) o Frequency o Individual variation o Distribution o Sampling error o Measurement error o Determinants 2. Systematic Error (bias) Uses o Selection bias o Establish a cause o Measurement bias o Study natural history of a disease o Assess health status o Evaluate the impact of intervention Qualitative vs Quantitative Qualitative Quantitative Understanding Prediction Interview/Observation Surveys/Questionnaires Discovering frameworks Existing frameworks Textual (words) Numerical Theory generating Theory testing Quality > Sample size Sample size core to reliability Subjective Objective Embedded knowledge Public Models of analysis: Fidelity to text Model of analysis: Parametric, non-parametric Causation o Strength o Consistency o Specificity o Temporality o Biologic gradient o Plausibility o Coherence o Experimental evidence o Analogy Strength of association Relative Risk Odds Ratio Strength of Association 0.83 1.00 1.0 1.2 None 0.67 0.83 1.2 1.5 Weak 0.33 0.67 2.5 3.0 Moderate 0.10 0.33 3.0 10.0 Strong <0.01 >10.0 Approaching infinity Prevalence vs Incidence Prevalence Incidence Prob (already having disease) Prob (getting disease in given time period) Numerator = all cases of disease Requires follow up Depends on duration of disease Does not depend on duration of disease Estimates burden of disease Used when studying causes of disease Relative risk o For cohort
Disease Not Diseased b d
o -
Relative Risk =
a/(a+b) c/(c+d)
a c
Odds ratio =
a/b c/d
a c
Lecture 10 Epidemiology 2
Case-control Advantages Appropriate for rare diseases Usually quick Does not require large samples Allows exploration of multiple exposures Disadvantages Recall bias Selection bias (controls as similar to cases as possible) Representive bias (typical cases) May not get all risk factors Time-sequence may not be determined Cannot calculate incidence Survival bias
Randomised Controlled (Clinical) Trial o Strongest design for clinical study because of randomisation minimises bias by patients in each group are as similar as possible Advantages Disadvantages Respected approach Not suitable of many research questions Quality data produced Loss of data due to lack of follow up Random allocation Time consuming and expensive Strength if double blind Often ethical problems Can study multiple outcomes Difficult to ensure compliance + avoid contamination Incidence can be measured Excellent data on baseline measures Systematic review o Comprehensive survey of a topic in which all of the primary studies of highest level evidence have been systematically identified, appraised and then summarised according to an explicit and reproducible methodology Meta-analysis o Survey in which all the studies are similar enough statistically that the results are combined and analysed as one study
Dude. *epic pause* Exams are over. 2 year is freaking over. Sweeeet. Have fun studying. UCS is a great unit.
My Arse.
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If you actually read this, you really are a loser. =P Its in small font for a reason. Sooo, what, youre like on a billion percent zoom? Oh [rant] If you had the freaking FCD 08 paper, you should have posted it. Selfish *bad word* Heard of sharing before? >:-( Not cool, not the right attitude. Take Foos example. [/rant] This box is actually a waste of time. This unit is actually a waste of time. I bet Bayan is hunching up trying to read this. Glad this is all going to end up looking like a line when you print it. Hey this actually counts to the word count.
You guys are pretty awesome. 2 year wasnt. Im kidding. It was actually pretty cool. But you guys were what made it cool. -Hsern Ern, 8:20pm 11 Nov 2009
PS. Stuff studying the other boxes. This is the box to study. :P
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