Prevention Flashcards

1
Q

what has improved life expectancy in the last 100 years?

A

largely better infrastructure and sanitation. improved healthcare has also had a significant impact.

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2
Q

what is Geoffrey Rose’s Single Population theory?

A

a way of looking at interventions and how effective they are based on the impact they have on a population

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3
Q

what is a high risk approach to an intervention? example?

A

identify and treat the “top end” of the population distribution. large individual benefits but small population ones.

case finding/ screening in general practice

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4
Q

what is a population approach to an intervention? example?

A

shift the mean of the entire distribution to the left. large population benefits but small individual ones.

increase exercise; reduce salt in diet; reduce obesity

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5
Q

what is primary/secondary/tertiary intervention?

A
  • Primary prevention – preventing onset (behaviour/environment)
  • Secondary prevention – catch disease before it is fully fledged (early diagnosis/screening)
  • Tertiary prevention – limit disability (rehabilitation)
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6
Q

what were the Wanless findings?

A
  • Numerous policy statements and initiatives in the field of public health have not resulted on a rebalancing of policy away from health care (a “national sickness service”) to health (a “national health service”).
  • There must be a realignment of incentives in the system to focus on reducing the burden of disease and tackling the key lifestyle and environmental risks.
  • Recognising the NHS is only one contributor to delivering the public health agenda ……..

BASICALLY THAT WE SHOULD FOCUS ON PREVENTION MORE INSTEAD OF TREATMENT ALONE.

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7
Q

what type of intervention is screening?

A

secondary

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8
Q

what is the definition of screening?

A

Screening is a public health service in which members of a defined population, who do not necessarily perceive they are at risk of, or are already affected by a disease or its complications, are asked a question or offered a test, to identify those individuals who are more likely to be helped than harmed by further tests or treatment to reduce the risk of a disease or its complications.

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9
Q

what is specificity?

A

• Specificity is the proportion of people without the disease who are correctly re-assured by a negative test result

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10
Q

what is sensitivity?

A

• Sensitivity is the proportion of people with the disease who are identified as having it by a positive test result

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11
Q

what is the Positive Predictive Value

A

• The Positive Predictive Value is the probability that a person with a positive test result actually has the disease

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12
Q

what is the Negative Predictive Value

A

• The Negative Predictive Value is the probability that a person with a negative test result does not actually have the disease.

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13
Q

what does a test with high sensitivity provide?

A

– Maximised identification of diseased people in the screened population
– Relatively few false negatives
– But unnecessary investigations or treatments for others
– Lots of false positives

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14
Q

what does a test with high specificity provide?

A

– detection of only people with the disease
– Relatively few false positives
– But will also miss some people who have or at risk of the disease
– Lots of false negatives

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15
Q

when is high sensitivity desirable?

A

– Adverse consequences of missed diagnosis for the individual e.g. late treatment might be significantly worse than early
– Adverse consequences of missed diagnosis for society e.g. serious communicable disease
– Diagnosis is to be confirmed by other tests so period of anxiety is short, or correct diagnosis is given before treatment is started

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16
Q

when is high specificity desirable?

A

– The diagnosis is associated with anxiety or stigma
– Further investigations are time-consuming, painful or expensive
– Cases are likely to be detected by other means before it is ‘too late’ for effective treatment
– Treatment, especially if painful or expensive, is to be offered without further investigations

17
Q

what is lead time bias?

A

Early diagnosis falsely appears to prolong survival

(prognosis is the time between diagnosis and death. As those caught by screening are diagnosed earlier, they have a longer prognosis even if they received no beneficial treatment.)

18
Q

what is length time bias?

A

Screening over-represents less aggressive disease.

(screening is much more likely to catch a less aggressive form of a disease as these less aggressive diseases have longer windows between onset and the time symptoms develop)

19
Q

what is the ethical distinction between screening and normal practice?

A

Screening has important ethical differences from clinical practice as the health service is targeting apparently healthy people

20
Q

what is an example of a “bad” screening program

A

Prostate cancer screening/.

21
Q

why is prostate cancer screening limited?

A

About two thirds of men with an elevated PSA do NOT have prostate cancer detectable at biopsy.

Up to 20% of all men with clinically significant prostate cancer will have a normal PSA

22
Q

what are Wilson and Jungner’s principles and practice of screening for disease

A
  • The condition sought should be an important problem
  • There should be an acceptable treatment for patients with recognised disease
  • Facilities for diagnosis and treatment should be available
  • There should be a recognised latent or early symptomatic stage
  • The natural history of the condition, including its development from latent to declared disease, should be adequately understood
  • There should be a suitable test or examination
  • The test or examination should be acceptable to the population
  • There should be agreed policy on whom to treat as patients
  • The cost of case-finding (including diagnosis and subsequent treatment of patients) should be economically balanced in relation to the possible expenditure as a whole
  • Case finding should be a continuous process and not a ‘once and for all’ project.