38. Epidemiology and Population Health (HT) Flashcards

1
Q

What is epidemiology?

A

The study of health and disease in populations (epi = on; demos = population).

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2
Q

Define prevalence.

A
  • How commonly a disease or condition occurs at a given time.
  • Prevalence = Number of diseased persons / Population size
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3
Q

Define risk.

A
  • The probability of an event in a specified interval of time.
  • Risk = Number of people who become diseased in a given period of time / Number of people in the beginning
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4
Q

What is the limitation of risk as a concept?

A
  • It only works in ‘closed’ populations, so it does not account for births or deaths.
  • Incidence is better.
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5
Q

Define incidence.

A
  • Probability of developing a disease in a very small time interval.
  • Incidence = Number of people who become diseased while observed / Sum of observation times of all people

This is better than risk because it does not assume a closed population.

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6
Q

Give an example of prevalence, risk and incidence.

A
  • Prevalence -> 5,875 cases of diabetes in a population of 45,193 = 0.13 (13%)
  • Risk -> 226 new cases of diabetes in one year in a town with a population of 45,193, equivalent to a risk of 0.005
  • Incidence -> 5.2 per 1000 per year cases of diabetes
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7
Q

How are incidence and prevalence related?

A
  • Incidence is positively correlated with prevalence
  • e.g. An incidence of 5.2 per 1000 per year cases of diabetes with an average disease length of 25 years results in a prevalence of 13% (0.52 x 25).
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8
Q

What are the different types of study done in epidemiology?

A

Observational:

  • Case report
  • Case series
  • Cross-sectional (or prevalence)
  • Case-control (or retrospective) [IMPORTANT]
  • Cohort (or prospective) [IMPORTANT]

Eexperimental (interventional):

  • Randomised controlled trials (RCTs) [IMPORTANT]
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9
Q

What is a case report?

A

Study of one individual with a disease, timely or rare information. This is often done if the disease is rare.

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10
Q

What is a case series?

A
  • A study of several patients with similar symptoms. May lead to general hypothesis. No controls.
  • It is essentially a set of case reports.
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11
Q

What is a cross-sectional (a.k.a. prevalence) study?

A
  • A study that measures exposure and disease in study group at one time point (“snapshot”).
  • Frequently takes the form of survey, e.g. questions about diagnosed coronary heart disease, family history, diet.
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12
Q

What is the purpose of cohort and case-control studies?

A

They aim to explore what causes a disease.

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13
Q

How do case control studies work?

A
  • They are a form of observational study where a group of cases (i.e. people with the disease) are compared with controls (i.e. people without the disease)
  • They try to find relationships between risk factors and the likelihood of developing the disease
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14
Q

Describe the different steps in a case-control study.

A
  • Choose a well-recorded population containing some people who now have or who did have a precisely defined disease
  • Define Cases (those with the disease)
  • Hypothesise (“guess”) what may have caused illness (morbidity) or death (mortality)
  • Select matched population who might have developed pathology but didn’t (i.e. Controls, who stayed healthy)
  • Obtain data about the guessed cause (put same questions
  • Determine incidence of supposed causative factor
  • Compare the results from the two groups
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15
Q

Give some examples of classic observational studies in epidemiology and the researchers who carried them out.

[EXTRA]

A
  • Ignaz Semmelweis -> Child bed fever in Vienna’s maternity wards
  • John Snow -> Cholera outbreak in London
  • Joseph Goldberger -> Pellagra
  • Alice Stewart -> Childhood Leukaemia
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16
Q

Describe Ignaz Semmelweis’ study about child bed fever. What type of study was this?

[EXTRA]

A
  • Child bed fever (puerperal fever) is a bacterial infection frequently developed after childbirth. It can result in septicaemia.
  • Semmelweis’ noticed that incidence of child bed fever was much higher in a Vienna hospital ward 1 than 2.
  • He noted that ward 1 was attended by doctors who also performed autopsies, while ward 2 was attended by midwives who did not perform autopsies
  • He hypothesised that this had something to do with the matter
  • This was sort of a CASE-CONTROL (retrospective) study
  • Semmelweis then initiated a controlled trial using chloride of lime solution (bleach) for hand-washing.
  • Mortality rate fell to 2% in the First Maternity Ward (same as Second).
  • However, his ideas were not accepted by the medical community since there was no evidence of germ theory yet.
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17
Q

Describe John Snow’s study about cholera in London. What type of study was this?

[EXTRA]

A
  • John Snow lived when there was a high incidence of cholera in London
  • He noticed that there were two companies supplying water from different sources (one cleaner than the other)
  • He used this as an opportunity for a COHORT (prospective) study
  • He compared the cholera death rates of people supplied by the two water supplies, finding that one water supply lead to much higher incidence of cholera, suggesting that this water was contaminated
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18
Q

Describe Joseph Goldberger’s study about pellagra.

[EXTRA]

A
  • Pellagra is a disease characterised by the 4 D’s (diarrhea, dermatitis, dementia and death)
  • It is caused by chronic lack of niacin (vitamin B3) in the diet
  • It was throught that pellagra was an infectious disease.
  • But in the first three weeks of studying Pellagra in the Southern parts of the US, Goldberger noticed that Pellagra was:
    • a) Present almost exclusively in rural areas
    • b) Associated with poverty
    • c) Associated with the relative cheap and filling diet consisting of meat, meal (corn meal) and molasses (3 Ms)
    • d) Not acquired by nurses, attendants or employees of hospitals or orphanages whose inmates had the disease
  • He therefore hypothesised that pellagra is not an infectious disease and showed this by (1) inducing pellagra in prisoners by giving them mostly corn-based diets and (2) by giving “filth” from pellagra patients to healthy volunteers
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19
Q

In case-control studies, what are odds?

A

Odds are the probability of an event occurring, divided by the probability of the event not occurring.

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20
Q

What is odds ratio?

A

A statistic that quantifies the strength of the association between two events, A and B.

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21
Q

Calculate the odds ratio for this data.

A

Odds ratio = Odds that child with leukaemia had been X-rayed / Odds that child without leukaemia had been X-rayed

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22
Q

What are the strengths and weaknesses of case-control studies?

A

Strengths:

  • Good for rare disease
  • Relatively fast
  • Relatively inexpensive
  • Can look at the association between the disease of interest and many kinds of exposures

Weaknesses:

  • Susceptible to bias
  • May be hard to find suitable controls
  • Time relations may not be clear
  • Associations that are revealed may not be causal
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23
Q

Describe Richard Doll’s study about smoking and lung cancer.

A
  • Richard Doll carried out a COHORT (prospective) study about smoking and whether it elads to cancer
  • He sent out a survey to thousands of British doctors, asking about their smoking habits
  • There was then follow-up about various causes of death in the doctors over the following years
  • The study showed that smoking increased the risk of developing lung cancer
24
Q

What is the general principle of a randomised control trial?

A

The subjects are randomly allocated into two groups and then one group is given an experimental treatment. Outcomes are then assessed.

25
Q

What is the advantage of a RCT being double blind?

A

Prevents preconceived views of doctors or patients systematically biasing the outcome.

26
Q

Why is randomisation necessary in RCTs?

A
  • To allow clear conclusions to be drawn
  • But may lead to ethical problems (exposing patients to potentially inferior treatments or withholding potentially effective treatment may be considered unethical).
27
Q

What is relative risk?

A

Ratio of the risk of developing a disease in the group exposed to a factor divided by the risk in the unexposed group.

For example, the risk of developing CVD in a statins group divided by the risk in the control group.

28
Q

What do these relative risk values signify:

  • RR = 1
  • RR < 1
  • RR > 1
A
  • If RR = 1, there is no association between the factor under consideration and the disease.
  • If RR < 1 there is a decreased risk of developing the disease if one is exposed to the factor under consideration.
  • If RR > 1 there is an increased risk of developing the disease if one is exposed to the factor under consideration.
29
Q

Compare relative risk and odds ratio, including when each is used.

A
  • Relative risk is used in RCTs, while odds ratio is used in case-control studies
  • Note that odds are calculated differently than risk
30
Q

What are some important aspects of RCTs?

A
31
Q

What are the main phases of clinical trials?

[IMPORTANT - need to know 3 phases]

A
  • Phase 0: Small number of participants and low dose of drug. Confirmation that drug behaves as expected from laboratory research.
  • Phase 1: Small trials, cohorts are treated with increasing doses of drug (dose escalation study). Safe dose? Side effects? Effect on the disease?
  • Phase 2: More patients involved. Best dose? How to manage side effects?
  • Phase 3: New treatment is compared to standard treatment. May involve thousands of patients because differences between treatments may be quite small.
  • Phase 4: Carried out after the drug has been licensed. Used to find out more about long term risks and benefits.
32
Q

What is the purpose of phase 0 clinical trials?

A
  • Involve a small number of participants and low dose of drug.
  • Used to confirm that a drug behaves as expected from laboratory research (e.g. animal studies).
33
Q

What is the purpose of phase 1 clinical trials?

A
  • Small trials where the cohorts are treated with increasing doses of drug (dose escalation study).
  • Used to establish a safe dose, side effects and the effect on the disease.
34
Q

What is the purpose of phase 2 clinical trials?

A
  • Studies where more patients are involved than phase 1.
  • Used to establish the best dose and how to manage side effects.
35
Q

What is the purpose of phase 3 clinical trials?

A
  • Involve thousands of patients because differences between treatments may be quite small.
  • Used to compare new treatment to standard treatment.
36
Q

What is the purpose of phase 4 clinical trials?

A
  • Large scale studies.
  • Carried out after the drug has been licensed.
  • Used to find out more about long term risks and benefits.
37
Q

What does an infection cycle need?

A
  • An infectious source
  • Receptive susceptible host(s)
  • Spread to further hosts
38
Q

What are the two main types of spread of infections?

A
  • Direct
  • Indirect (“reservoir” or “vector” -> e.g. mosquitos in the case of malaria)
39
Q

What is incubation period?

A
  • The time between catching an infection and symptoms appearing.
  • Varies between different diseases, e.g. rubella 14-21 days; diphtheria 2-5 days
40
Q

What is latent period?

A

Time between catching an infection and diagnostic signs of an infection (immune response) but still asymptomatic.

41
Q

Compare the incubation period and latent period.

A
  • Latent period = The time between catching an infection and CLINICAL SIGNS (i.e. immune response) appearing.
  • Incubation period = The time between catching an infection and SYMPTOMS appearing.
42
Q

What is the infectious period?

A

The time period during which an infected person is able to transmit the disease to a susceptible host or vector. Not necessarily associated with symptoms.

43
Q

What is R0?

A

Basic reproduction rate, which is the average number of persons infected by one disease source.

44
Q

What does it mean if R0 is greater than or less than 1?

A
  • If R0 < 1, the disease will eventually disappear
  • If R0 > 1, the disease will continue to spread
45
Q

Give an equation for R0.

A
46
Q

What are some infection control tactics?

A
  • Reduce symptoms that spread infection
  • Reduce bacterial/microbial loads through treatment
  • Interrupt transmission through the environment (face masks & social distancing for Covid-19, condoms for HIV)
  • Shorten infective period by treatment
  • Shorten infective period by isolation
  • Reduce the number of susceptibles by vaccination
  • Reduce the number of susceptibles by prophylaxis”
47
Q

Compare difference in transmission and infection with enveloped and non-enveloped viruses.

A

Non-enveloped viruses (e.g. Polio):

    1. The outermost covering is the capsid made up of proteins
    1. Non enveloped viruses are more virulent and causes host cell lysis
    1. These viruses are resistant to heat, acids, and drying
    1. It can survive inside gastrointestinal tract
    1. It can retain its infectivity even after drying
    1. It will induce antibody production in the host
    1. Mode of transmission is through fecal or oral matter and dust

Enveloped viruses (e.g. Covid-19):

    1. The outermost envelope is made up of phospholipids, proteins or glycoprotein which surround the capsid
    1. Enveloped viruses are less virulent often released by budding and rarely cause host cell lysis
    1. Are sensitive to heat, acids, and drying
    1. Generally cannot survive inside gastrointestinal tract
    1. Lose infectivity on drying
    1. Will induce both cell mediated and antibody mediated immune response in the host
    1. Mode of transmission is through blood or organ transplants or through secretions
48
Q

What is the purpose of vacination?

A
  • Protection of the individual
  • Herd immunity
49
Q

Where is a population said to have herd immunity?

A

A population shows herd immunity if the frequency of immune, non-susceptible people is high enough to break the chain of transmission.

50
Q

What are some side effects of vaccines?

A
51
Q

Give an equation for the critical level of immunisation need to eradicate a disease.

A
  • pc = Critical rate of immunisation
  • The equation shows that if there is a very infectious, quickly spreading virus, high levels of immunisation are required for eradication
52
Q

State some of the main routine vaccinations in children in the UK.

A

Also: Meningitis B, Rotavirus

53
Q

What are the main arguments against a chickenpox vaccine?

A
  • Immunising children against chickenpox may lead to more cases of shingles (a re-activation of the Varicella virus) in the elderly, since chickenpox-infected children are believed to provide a natural booster for Varicella-carrying adults (thus preventing reactivation of the virus).
  • However, no evidence of increased shingles in countries that do immunise children against chickenpox.
  • The other main argument against chickenpox vaccine is cost
54
Q

Summarise measles, mumps and rubella infection symptoms.

A
55
Q

Summarise the main ways of controlling transmission of infectious diseases.

A
  • Physical isolation
    • Quarantine, to give enough time for an infection in a host to manifest itself without being allowed to infect others
    • Barriers • e.g. during sex, against Sexually Transmitted Diseases (STDs)
  • Control of vectors and reservoirs (e.g. Malaria)
  • Prophylactic immunisation - vaccination
  • Clean air, water, food
  • Education