Screening Flashcards

1
Q

Giving a example, why is screening not always a good thing?

A

Neuroblastoma (childhood cancer of nerve) has a better prognosis if caught early so Japan started screening detecting lots of cases with a good survival rate HOWEVER, death rate remain unchanged as no. presenting above 1 year didn’t change so incidence increased so there was no benefit of screening and 3 deaths as a result of treatment complications for unnecessary treatment in cases that probably would have resolved themselves

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

What is overdiagnosis and overtreatment?

A

Overdiagnosis = correct diagnosis of a disease (TP) but the diagnosis is irrelevant because disease will never cause symptoms within the patients life time (found across Medicine but an ethical issue in screening) associated with…

Overtreatment = unnecessary treatment which does not improve health

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

What is the problem with breast cancer screening?

A

Unnecessary and potentially harmful cancer treatment i.e. surgery/radiotherapy in some cases

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

What is the problem with prostate cancer screening?

A

Most men get it at some point not causing any problems and they will most likely die from other causes so we wouldn’t want to know in screening if this was the case as it would provide unnecessary worry meaning over-treatment would occur and result can also be unclear causing worry (disease reservoir) -> SO its not screened for but they can ask for PSA test if doctor warns of risks/benefits

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

What is the popularity paradox?

A

If people get screened, a disease is detected, they are treated and are healthy after they will be happy and promote the screening which will increase over-diagnosis and over-treatment which is why you should be cautious before beginning screening

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

What is a disease reservoir?

A

When a person has detectable levels of a disease e.g. prostate, thyroid or breast cancer but it is likely to not cause them any problems in their life so they are at high risk of overdiagnosis/overtreatment if screening occurs

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

What indicates overdiagnosis and overtreatment is occurring?

A

If diagnosis has increased of a disease BUT deaths have not changed

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

What are incidental findings?

A

Pathologies that are found when carrying out other tests e.g. chest CT that may or may not cause a problem

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

What does the Wilson and Jungner criteria state for screening to be introduced?

A
  1. Condition should be an important health problem (severity rather than commonality)
  2. Accurate and acceptable test/examination to diagnose condition
  3. Treatment should be available
  4. There should be a latent stage of disease and early treatment should be clearly more beneficial than later treatment
  5. Natural history of disease should be adequately understand
  6. Agreed policy on who to treat
  7. Total cost of finding a case should be economically balanced in relation to medical expenditure as a whole
  8. Case-finding should be a continuous process, not just a “once and for all” project
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What screening tests are borderline acceptable to the population?

A

Cervical: intra-vaginal exam

Colorectal: faeces collection and if a +ve result is found a colonoscopy

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

What considerations must be taking into account when applying the Wilson and Jungner criteria to screening decisions as stated by UK National Screening Committee (part of PHE)?

A
How do we define population?
How frequently to test?
Which test to use?
Which results to use?
How to gain informed uptake?
External pressures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What conditions does the UK screen for in antenatal and newborns?

A
Downs syndrome
Fetal anomaly US
Infectious disease in pregnancy
Antenatal sickle cell and thalassaemia
Newborn and infant physical exam
Newborn blood spot
Newborn hearing screen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What conditions does the UK screen for in young persons and adults?

A
AAA
Diabetic retinopathy
Breast cancer
Cervical cancer
Bowel cancer
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the different types of test results that can come back?

A

TP
FP
TN
FN

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

What is sensitivity?

A

Proportion of people who have the disease that the test correctly detects i.e. it doesn’t miss many (FNs)

TP/TP + FN

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

What is specificity?

A

Proportion of people who do not have the disease that the test correctly identifies as not having the disease i.e. not many FPs

TN/TN + FP

17
Q

What do you want to be very high in screening programme tests? Why?

A

Specificity as a high no. of FPs will come back meaning there is not tests which cost a lot of money however, we can deal with a lower sensitivity ~50-75% as a FN is just the same as not being screened at all

18
Q

What does sensitivity and specificity measure?

A

The TEST performance so they are independent of disease prevalence therefore, if you have the disease, sensitivity tells you the probability the test will pick it up and if you dont have disease, specificity tells you probably that test will pick this up too but if you test positive or negative, neither can tell you the probability you have the disease or not as this depends in prevalence (PPV/NPV)

19
Q

What is positive predictive value (PPV)?

A

Probability that a person has the disease given that they have had a positive test result

TP/TP + FP

20
Q

What is negative predictive value (NPV)?

A

The probability a person does not have the disease given they have a negative test result

TN/TN + FN

21
Q

What are the common types of bias?

A

Healthy screenee
Length time effect
Lead time effect
Overdiagnosis

22
Q

What is healthy screenee bias?

A

People who attend screening when invited live longer than those that do not even is the screening is useless because these people are more proactive in taking care of their health in day-to-day life and people who do not attend are more likely to smoke, drink, have a low income, poor diet and existing medical conditions

23
Q

What study design would show healthy screenee bias?

A

Comparisons between self-selected screened and unscreened groups

24
Q

What is lead time bias?

A

Useless screening can appear to increase survival time by simply detecting the disease earlier but not actually resulting in longer life

25
Q

What is length-time bias?

A

Screening is better at detecting disease that develops more slowly (as screening usually occurs every few years for e.g.) rather than a fast aggressive progressing condition, and in more slowly developing diseases, people tend to live longer anyway so have a better prognosis so useless screening can appear to increase survival time by detecting disease that develops more slowly but not resulting in longer life - overdiagnosis/overtreatment is an extension of this as it may not have ever been symptomatic due to the mildness

26
Q

What study design should be used to look at screening effectiveness?

A

RCTs comparing offer of screen with no offer of screen with an intention-to-treat analysis looking at mortality after a long length of follow-up (expensive)