Question

In: Statistics and Probability

3. You are designing an antenatal screening programme for a rare but serious disease in the...

3. You are designing an antenatal screening programme for a rare but serious disease in the foetus and you have two tests available. Test A, which is based on a blood sample has 95% sensitivity and 95% specificity, whereas test B, which is an invasive inter-uterus test , has 99% sensitivity and 99% specificity. Which test will:

a) minimize false positives?

b) minimize false negatives?

c) assume that you wish to use both screening tests–discuss the pros and cons of doing test A then B or test B then A? Remember that when using screening tests in sequence only those that are positive in the first study are then screened by the second test.

d) Work out the Net Sensitivity and Net Specificity the 2 stage sequential testing programme (A then B) assuming that the tests are applied to 100,000 pregnant women of whom 2% have a foetus with a major abnormality. Show the various stages in your calculations with appropriate tables.

Solutions

Expert Solution

test sensitivity is the ability of a test to correctly identify those with the disease (true positive rate), whereas test specificity is the ability of the test to correctly identify those without the disease (true negative rate)

1.

for false postives to be minimum specificity should be maximum : which is for test B

2.

for false negatives to be minimum specificity should be maximum : which is for test B

3.

This is serial testing [serial : studies are performed sequentially, with the second study dependent on the results of the first]

sensitivity = (A)sen x (B)sen = 0.95*0.99=94.05%

as we can see from the formula in serial testing for sensitivity the order doesn't make any difference

sensitivityA then B = sensitivity B then A = 94.05%

specificity:

A then B : (A)spec + [1 - (A)spec] x (B)spec = 0.95 + (1-0.95)*(0.99) = 0.9995 = 99.95%

B then A : (B)spec + [1 - (B)spec] x (A)spec = 0.99 + (0.01)*0.95 = 99.95%

A then B and B then A are same

d.

A then B :

sensitivityA then B = 94.05%

net sensitivity = (sensitivityA then B)*(P(have disease))*n

= 0.9405*0.02*100,000 = 1881

specificityA then B = 99.95%

net specificity = (specificityA then B)*(P(don't have disease))*n

= 0.9995*0.98*100,000 = 97951

P.S. (please upvote if you find the answer satisfactory)


Related Solutions

Following a pilot programme in Waitemata, a national screening programme to detect bowel cancer early is...
Following a pilot programme in Waitemata, a national screening programme to detect bowel cancer early is being introduced in New Zealand. People aged 60-74 years will be invited to take part in the bowel screening programme, starting from 2017. (a) An anticipated benefit of the screening programme is a reduction in deaths from bowel cancer among people who take part in the screening programme. This benefit is more likely to occur if the programme is of high quality. Discuss how...
1. A general insurance company is debating introducing a new screening programme to reduce the claim...
1. A general insurance company is debating introducing a new screening programme to reduce the claim amounts that it needs to pay out. The programme consists of a much more detailed application form that takes longer for the new client department to process. The screening is applied to a test group of clients as a trial whilst other clients continue to fill in the old application form. It can be assumed that claim payments follow a normal distribution. The claim...
Huntington disease is a rare neurodegenerative human disease determined by an autosomal dominant allele. (Because it...
Huntington disease is a rare neurodegenerative human disease determined by an autosomal dominant allele. (Because it is a rare disease, homozygous individuals are also rare.) The disorder is typically a late onset disease with symptoms appearing after the age of 30. A young man has learned that his father has developed the disease. What is the probability that the young man will also develop the disease? What is the probability that a child of the young man develops the disease?
Carbohydrate intolerance is a rare but very serious hereditary disorder. Cases due to lack of digestive...
Carbohydrate intolerance is a rare but very serious hereditary disorder. Cases due to lack of digestive enzyme and to impaired hexose transport have been reported. It is estimated that glucose-galactose malabsorption accounts for 2% of the patients with protracted diarrhea of infancy. In two reported cases of glucose-galactose malabsorption, the infants developed diarrhea soon after birth. Their stools contained reducing sugars and had an acidic pH. Analysis of tissue obtained by biopsy of the small intestine showed normal villi with...
A family is affected by a rare genetic disease with a Mendelian pattern of inheritance. The...
A family is affected by a rare genetic disease with a Mendelian pattern of inheritance. The father is affected, and the mother is unaffected by this disease. They have three children: an affected son and daughter and an unaffected son. If they have a fourth child, what is the probability that this child will be affected by the disease? 100% 50% 33% 25% 0%
Identify some non-communicable diseases. Why is screening tests necessary? How Can Screening for Disease Address the...
Identify some non-communicable diseases. Why is screening tests necessary? How Can Screening for Disease Address the Burden of Non-communicable Disease? – pg. 130-137-Public Health 101.
It is claimed that a new treatment of a very serious disease will substantially reduce the...
It is claimed that a new treatment of a very serious disease will substantially reduce the mortality of that disease from its present rate of 25%.We observe an SRS of 100 patients who have submitted to the new treatment and note that only 10 of them die from this disease. Does the new treatment seem to make a significant improvement?
In a large population of people, some individuals are infected with a rare disease and some...
In a large population of people, some individuals are infected with a rare disease and some are not. Let POS represent the event that an individual is infected, and let NEG represent the event that an individual is not infected.   A blood test can be administered to try to find out whether an individual is infected. Let represent the event that the test result is positive [i.e., the test indicates that the individual is infected] and let represent the event...
In a large population of people, some individuals are infected with a rare disease and some...
In a large population of people, some individuals are infected with a rare disease and some are not. Let POS represent the event that an individual is infected, and let NEG represent the event that an individual is not infected.   A blood test can be administered to try to find out whether an individual is infected. Let represent the event that the test result is positive [i.e., the test indicates that the individual is infected] and let represent the event...
Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by...
Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by a build-up of mucus in the lungs and difficulty breathing. A woman whose maternal uncle had the disease is trying to determine the probability she and her husband could have an affected child. Her husband's sister died of the disease. Assuming the uncle and the sister are the only family members who had the disease, what is the chance that the couple's first child...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT