MODULE 3 Flashcards

1
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Temporality

A

From the exposure to outcome. Essential to establish a casual relation E -> O

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2
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Strength of Association

A

The stronger an association, the more likely to be causal in absence of known biases (selection, information, and confounding) e.g RR RD P Values CI

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3
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Consistency of Association

A

Replication of the findings by different investigators, at different times, in different places, with different methods

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4
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Biological plausibility

A

If the association makes sense biologically

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5
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Biological gradient (dose-response)

A

Increasing change in disease rates in conjunction with corresponding changes in exposure

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6
Q

The Bradford Hill criteria is a framework used to describe causality. Explain Specificity of Association

A

A cause leads to a single effect. However, a single cause often leads to multiple effects

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7
Q

In a causal pie, explain a Sufficient cause

A

a factor that will inevitably produce the specific die-ease

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8
Q

In a causal pie, explain a Component cause

A

a factor that contributes towards dis-ease causation, but is not sufficient to cause dis-ease on it’s own

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9
Q

In a causal pie, explain a Necessary cause

A

a factor (or component) that must be present if a specific disease is to occur

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10
Q

What are the factors that determine prioritisation

A
TOGSS
Treatment options
Opportunity cost
Group affect
Size
Severity
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11
Q

In regards to priroritisation explain the factor: Treatment options

A

Are they available, cost effective, do we understand cause, is treatment efficacious

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12
Q

In regards to prioritisation explain the factor: Treatment options

A

Are they available, cost effective, do we understand cause, is treatment efficacious

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13
Q

In regards to prioritisation explain the factor: Opportunity cost

A

Compared to number 2 on the priority list, is it more worth it? How much more will you be spending?

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14
Q

In regards to prioritisation explain the factor: Group affects

A

How large/significant is the group (age, gender)

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15
Q

In regards to prioritisation explain the factor: Size

A

How common is the disease?

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16
Q

In regards to prioritisation explain the factor: Severity

A

How sever is the illness? -Duration

  • impact on QoL
  • Morbidity
  • Implications on prevalence/incidence
  • Infectivity
  • DALYS
  • Relapse
  • Time till death
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17
Q

Why do we prioritise?

A
HOEC
Health resources are limited
Opportunity cost
Evidence may not be sufficient
Competing interests
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18
Q

How does epidemiology play an important role in prevention of dis-eases?

A

Unravel causal pathways
Direct action
Evaluate

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19
Q

Explain the Primordial level of prevention

A

Preventing disease from occurring by reducing their chance of exposure to the risk

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20
Q

Explain the Primary level of prevention

A

Preventing the disease from occurring by reducing risk factors they are already exposed to

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21
Q

Explain the Secondary level of prevention

A

Preventing the disease from getting worse

22
Q

Explain the Tertiary level of prevention

A

Preventing very serious complications (They’re going to die anyway so focus on promoting QoL)

23
Q

Explain High-risk strategies

A

Aimed at high-risk populations (clinician - patient)

24
Q

Explain the benefits of High risk strategies

A
  • high benefit
  • individually appropriate
  • personal motivation
25
Explain the disadvantages of high risk strategies
- Need to identify high risk individual - Behaviorally inappropriate ( is it socially or ethically approp?) - Small, temporary affect
26
Explain Population strategy
Looking at populations as a whole
27
Explain the benefits of Population strategies
- Overall benefit - Behaviorally appropriate - Don't need to identify high risk groups - Focus on underlying causes/wider determinants
28
Explain the disadvantages of Population strategies
- Individual inappropriate - Low personal motivation (Clinician - patient POV) - High consequence of potential failure - Low individual benefit
29
Explain Promotion
``` DAW Determinants Autonomy Whole population Focus on health and wellbeing Advocate healthy lifestyle Empower people ```
30
Name the two frameworks used in Health promotion
- Alma Ata | - Ottowa charter
31
What is the Alma Ata framework
``` Are the pre requisites of good health SIPEEFS Shelter Income and economic support Peace + Safety Education stable Ecosystem + sustainable resources Social justice Food ```
32
What does the Ottawa Charter focus on?
``` DSCBR Develop personal skills Strengthen community action Create appropriate environments Build healthy public health policies Re orientate Health services towards primary ```
33
Explain protection
``` MOAR Monitoring population Occupation hazards + risks Assesing Communicating what the risks are ```
34
What are the factors significant to Maori Health
``` A-DRIM it effects All New Zealanders exposed to more negative Determinants of Health they have a Right to health Inequalities/inequities exist Mainstream promotion does not work ```
35
Problems with conventional health promotion in regards to Maori Health
Based on western models, universal formula and doesn't consider the differing values and beliefs of Maori people
36
What is the Maori model of health promotion
Te Pae Mahutonga
37
What are the 4 tasks of Te Pae Mahutonga
Mauriora Waiora Toiroa Te Oronga
38
What does Mauriora focus on
Cultural identity
39
What does Waiora focus on
Environmental protection
40
Toiora
Healthy lifestyle
41
Te Oronga
Participation in society
42
What are the two prerequisites of Te Pae Mahutonga
Nga Manukura | Te Mana Whakahaere
43
What is Nga Manukura
Health professional and community leadership
44
What is Te Mana Whakahaere
Autonomy
45
Why primary screening?
to prevent risk factors
46
Why secondary screening
to prevent complications once disease is already present
47
What is High risk screening
Works with specific high risk groups
48
What is population screening
A more broad approach
49
How to determine which diseases to screen for?
Suitable disease Suitable test Suitable programme Suitable treatment
50
How to determine whether it is a suitable disease to screen for
If it is beneficial to catch early on Is it treatable Is there a significant lead time Relatively common
51
How to determine whether it is a suitable test when screening
Acceptable? Affordable? Accurate/reliable? (sensitivity/specificity)
52
How to determine whether it is the suitable screening programme
Benefits must outweigh harm | RCT evidence that screening will result in reduced mortality/morbidity and increase survival