Epidemiology in Practice Flashcards

FOCP

You may prefer our related Brainscape-certified flashcards:
1
Q

Define ‘population excess fraction’

A

The proportion of the cases observed in the study population attributable to the exposure of interest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

When is the perinatal period?

A

The period immediately before and after birth - typically a few weeks in either direction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Define incidence

A

The number of new cases in a given time interval

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Define prevalence

A

The frequency of a disease in a population at a point in time.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are proximal factors?

A

Factors measured in clinic, such as blood pressure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are distal factors?

A

Factors measured upstream, such as socioeconomics, poverty and inequality.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Define epidemiological transition

A

Decline in total mortality
Significant reduction in infectious and deficiency diseases
Increase in chronic, non-communicable diseases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How many cancers have an inherited component?

A

1% –> 99% are sporadic.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is specificity?

A

Ability to correctly identify those without the disease (true negative).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is sensitivity?

A

Ability to correctly identify those with the disease (true positive).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Give the hierarchy of study designs.

A

1a: systematic review of RCTs, meta-analysis
1b: single RCT with narrow confidence interval
1c: All or none case series (all patients died before a new therapy introduced - all now survive)
2a: systematic review of cohort studies
2b: individual cohort study or RCT with <80% follow-up
2c: outcomes research
3a: systematic review of case-control studies
3b: case control study
4: case report/series
5: expert opinion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the standardised mortality rate?

A

The rate ratio adjusted for age. An SMR for bladder cancer of 1.70 in the exposed group would mean that there is 70% more cases of death due to bladder cancer in the cohort than in the reference population.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the relationship between probability and odds?

A

Odds = probability / (1-probability)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Define attributable risk.

A

Incidence in exposed - incidence in unexposed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is primary prevention?

A

Prevention of disease of injury before it occurs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is secondary prevention?

A

Reducing the impact of a disease or injury which has already occurred (detecting as soon as possible).

17
Q

What is tertiary prevention?

A

The aim of softening the impact of an ongoing disease or illness which has lasting effects.

18
Q

What is a cross sectional study?

A

An observational study which analyses data from a population at a particular point in time.

19
Q

What is the healthy worker effect / healthy user bias?

A

Sampling bias: those who voluntarily enrol in a clinical trial and follow the advice are not representative of the whole population and can be expected to be, on average, healthier.

20
Q

What is the difference between a cohort study and a case-control study?

A

Cohort study has no control group and is PROSPECTIVE.

Case-control study compares cases to controls and is RETROSPECTIVE.

21
Q

What is primordial prevention?

A

Prevention of factors promoting the emergence of lifestyles, behaviours, exposure patterns which contribute to increased risk of disease.

22
Q

What does NTD stand for and give some examples.

A

Neglected tropical diseases.
Intestinal worms
Schistosomiasis
Leprosy

23
Q

What are the strategies used to treat NTDs?

A

Diagnosis and treatment: leprosy and sleeping sickness

4 drugs used to provide annual mass treatment for the rest.

24
Q

What is the difference between a meta analysis and a systematic review?

A

A meta-analysis is a statistical procedure for combining numerical data from multiple separate studies.
A systematic review is a detailed, systematic and transparent means of gathering, appraising and synthesising evidence to answer a well-defined question.

25
Q

What does a symmetrical funnel plot suggest?

A

There is no publication bias.

26
Q

What four factors are used to evaluate association?

A

Chance, confounding, causality, bias.

TEMPORAL RELATIONSHIP used to assess causality.

27
Q

How can confounding variables be controlled for at the analysis stage of discussion?

A

By REGRESSION.

28
Q

What is the difference between sensitivity and PPV?

A
Sensitivity = ability (of the screening test)
PPV = likelihood
29
Q

What could cause incidence and prevalence to increase respectively?

A

Incidence could increase by better diagnosis and treatment

Prevalence could increase by sufferers living longer.

30
Q

What are the four drugs used for the mass treatment of NTDs?

A

Mectizan, Albendazole, Zithromax, Prazuquantel

31
Q

What is lead time bias?

A

The time between detection and normal presentation. If you pick something up earlier from screening they might not actually live longer than if they’d waited until it was noticeable but it seems as though the time from detection to death is longer.

32
Q

Match the drugs to their NTDs

A

Praziquantel: schistomiasis
Albendazol - helminths and LF
Mectizan; onchoceriasis and LF
Zithromax - blinding trachoma

33
Q

Match the NTDs to their animal vectors.

A

Schistomiasis - snails
Lymphatic filiaris - mosquito
Onchoceriasis - blackfly