PBL 4 Flashcards

1
Q

Why is the case control better than cohort

A

Quicker to do usually – the outcome follow up in some cohort studies will be long.

More practical if is rare – (cohort would need many more patients)

Usually cheaper – fewer patients and quicker.

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2
Q

Why is the case control worse than cohort

A

May suffer from recall bias.

Cannot calculate absolute risks.

Different sorts of people may be more likely to take part, depending on whether they are a case or a control, not true of a cohort where patients are usually all well at the start

Can only study one outcome (cohort studies can look at several outcomes)

May suffer from bias in selecting patients for cases and controls.

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3
Q

Why are case control and cohort similar

A

Both can suffer from confounding – hence less accurate than randomised controlled trials – although matching deals with some confounding in case control studies

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4
Q

Why is a clinical trial not used

A

It is unethical to test something that may be potentially harmful, let alone the ethics of giving people recreational drugs!

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5
Q

Which study should have been used

A

Case control because it is more useful and practical

- outcome is rare and some of the exposures are reasonably common

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6
Q

What are the pros and cons for screening medical students for this type of cancer? Would you recommend all medical students get screened for this? Why or why not?

A

Students will be expected to talk about tailoring of information to person’s needs. Because this cancer is so rare, it may not be a good idea to screen all medical students and put them at risk for false positives.

Pros

  • cancer screening may give you an indication of cancer before any symptoms develop
  • cancer screening may find cancer at an early stage when treatment is more likely to be curative
  • if cancer is diagnosed at an earlier stage treatment is more likely to be successful

Cons

  • cancer screening can miss a number of cancers and provide false reaurrance as no cancer screening test is 100% accurate
  • cancer screening can lead to unnecessary worry and investigations when there is no cancer present
  • positive screening result may cause anxiety by diagnosing a slow growing tumour that may never value any harm or symptoms
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7
Q

How could you adapt your screening process to accommodate people who identify as nonbinary?

A

Depends on how person is registered with GP whether they are registered as the gender they were assigned with/to or not.

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8
Q

What potential discrimination and stigma could Shahid be worried about? What social determinants are intersecting and compounding here?

A
  • Stereotyping and stigma occur in relation to some external feature such as skin colour, race, visible disease, gender or disability.

Race, gender and sexuality are the main intersecting or clustering of social influences.

We do not know if poverty is an issue although we might assume that most medical students are poor.

Likewise, we do not know if violence or abuse is an issue, if we look at this from a syndemic suffering framework perspective.

Students are asked to consider whether social determinants be seen as potential confounders.

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9
Q

How do you determine whether the results is causal

A

Bradford Hill criteria

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10
Q

What do you have to do before checking the bradford hill criteria

A

you have to know that the association is statistically significant, otherwise there could be no relationship

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11
Q

name the factors that make up the Bradford hills criteria

A
  • strength of the assocaition
  • dose reposnes
  • reversibility
  • temporality (does the exposure occur a reasonable time before the disease)
  • consistency
  • biological plausibility
  • Coherence of evidence
  • specificity
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12
Q

describe the parts of the Bradford hill criteria in the study

A

Strength of the association

  • This is measured by OR or - RR, If OR >10 or <1/10 then it is strong.
  • OR for Marijuana use is 2.42 for Nonseminoma / Miexed GCT so it is not that strong

Dose response

  • Table 3: Frequency <1 vs ≥1 per week amongst current and former users does not show dose response. However the confidence intervals are wide so it does not preclude a dose- response effect
  • Similarly <10 years vs ≥10 years doesn’t show dose response in current users, but is in right direction for former users. However the confidence intervals are wide so it does not preclude a dose- response effect

Reversibility

  • If you stop the exposure does the risk change revert to 1.
  • Table 3 does give current users and former users, with the risk for former users not reverting back to 1. However it might be that you need to have stopped for more than, say, 5 years for the risk to revert to 1. So this study does not have the power to detect reversibility.

Temporality
- An increased risk for current users is irrelevant as clearly there must be a time lag for the disease to develop.
- The OR is increased for > 10 years though it isn’t significant due to power of study (median age is 27 so unlikely for half of them to have 10 years exposure). Some evidence for causality

Consistency [B10]
- Has the result been repeated by different people in different places and in different circumstances and times? Yes the authors refer to two other published case-control studies

Biological Plausibility
- It helps if we think the result is biologically plausible.
The authors have given details as to why it is biologically plausible.

Coherence of Evidence
- the results should be consistent with other sorts of studies such as cohort and cross-sectional as well as perhaps animal models.
- The authors state that both TGCT and marijuana rates have been increasing in recent decades. There are no other cohort studies referred to.

Specificity
- Is the relationship with the exposure limited to specific diseases.
- Table 3 demonstrates that Marijuana use is linked to Nonseminoma rather than Seminoma tumours.

Conclusions: Causal, but not strong evidence. Other reason for the association would be confounding by other unidentified risk factors

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13
Q

How is the strength of association measured by in the Bradford hill criteria

A
  • Strength of association is measured by either the odds ratio or the relative risk
  • if the odds ratio is greter than 10 or less than 1/10 then it is a strong assocation
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14
Q

what is a casual relationship

A

A causal relationship is one where the cause directly affects the outcome of interest.
(There can be many causes and a causal relationship does not necessarily mean that all those with the cause will get the outcome).

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15
Q

What are the controls that are used in the study

A

The controls reflect the population from which cases have arisen and are matched for age, race, ethnicity and neighbourhood, i.e. important confounders. The study demonstrates how hard it is to find matched controls.

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16
Q

what happens if the controls are not representative of the population

A
  • if the controls are not representative of the population from which the cases have arisen this can lead to bias results and the odds ratio could be wrong
17
Q

what biases might the study have and not have

A
  • probably would not have recall bias as risk factors asked about just one year previously
  • large number of risk factors were asked about for a reference period 1 year before diagnosis therefore there is little potential for trained interviewers to bias response to drug questions
  • no evidence that data collected prospectively it would be collected any better
  • 80% participation rate in both cases and controls therefore participation bias is unlikely
18
Q

What is an odds ratio

A

An odds ratio is the ratio of the odds of the cases (those with the disease) being exposed compared with the odds of the controls (those without the disease) being exposed

19
Q

When is the odds ratio equal to the relative risk

A

For rare diseases (i.e. diseases with an incidence or prevalence less than around 1%) the odds ratio is equivalent to the relative risk and can be interpreted as the ratio of the risk of developing the disease amongst an exposed person compared to an unexposed person.

20
Q

describe how you would work out the odds ratio in this case

A

Odds Marijuana use in cases = 113/26 = 4.35

Odds Marijuana use in controls = 222/70 = 3.17

Odds ratio Marijuana use in cases compared with controls = 4.35/3.17 = 1.37

A value of 1.32 is given in the paper as it says they have analysed the data taking account of the matching for age, race and neighbourhood [NOT strictly crude!]. The adjusted OR differs

21
Q

describe the adjusted odds ratio

A

Adjusted OR = 1.94 can be interpreted as meaning that men that used Marijuana in this study had a 94% increased risk of developing testicular germ cell tumours after taking into account their other risk factors.

22
Q

describe the 95% confidence interval

A

The 95% confidence interval of 1.02 to 3.68 can be interpreted as meaning that we are 95% confident that the true increased risk of developing testicular germ cell tumours after taking into account their other risk factors lies between a 2% risk and a greater than 3 fold risk . OR If we repeated the same study 100 times we would obtain an estimate of the increased risk of developing testicular germ cell tumours after taking into account their other risk factors between a 2% risk and a greater than 3 fold risk. Hence we are 95% confident that using Marijuana does increase the risk of developing testicular germ cell tumours.

23
Q

What is a crude result

A

Crude (also called univariate or unadjusted) results, tell us the relationship between one risk factor and the outcome for everyone in the study.

24
Q

what is the crudeodds ratio in the study

A

For example in Table 2 the crude odds ratio for Marijuana use of 1.32 (95% CI: 0.79 – 2.22) tells us that the men who used Marijuana had a 30% increased risk of testicular germ cell tumours compared to those who do not

25
Q

What is the crude odds ratio useful for

A

The crude odds ratios are useful for identifying high risk groups of individuals.

26
Q

What does in adjusted odds ratio result tell us

A

Adjusted (also called multivariate) results tell us the effect we would get if we changed that factor if all the adjusting factors remain the same. It is closer to the effect you would get if you persuaded someone to stop taking Marijuana, while all their other risk factors stayed the same

27
Q

when is the adjusted odds ratio used

A

The adjusted Odds Ratios are more useful for investigating causality and for deciding on what advice to give a patient or a group of patients.

28
Q

What are cofounders

A

Confounders are factors that are associated with both the exposure of interest and the outcome. In the example of alcohol consumption and lung cancer, smoking is a confounder as it is associated with both lung cancer and people who drink heavily tend to smoke also

29
Q

what is not a confounder in the study

A

In this study there does not appear to be any association between cigarette smoking and testicular germ cell tumours and therefore cigarette smoking is NOT a confounder and hence the results do not need to be adjusted for it.