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Screening PHIL THIRKELL

Screening

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Screening. Phil Thirkell. What is screening?. A process of identifying apparently healthy people who may be at risk of a disease or condition Identify Apparently healthy Increased risk of a disease/condition. Give 4 screening programmes undertaken in the UK. Antenatal screening - PowerPoint PPT Presentation

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Page 1: Screening

ScreeningPHIL THIRKELL

Page 2: Screening

What is screening?

A process of identifying apparently healthy people who may be at risk of a disease or condition

Identify Apparently healthy Increased risk of a disease/condition

Page 3: Screening

Give 4 screening programmes undertaken in the UK.

Antenatal screening Postnatal screening – hearing, heel prick, neuroblastoma Cervical smear Mammography Chlamydia screening Bowel Cancer – FOBT Prostate cancer Abdominal Aortic Aneurysm Depression – PHQ-9 questionnaire etc.

Page 4: Screening

Criteria for a Screening Programme Wilson + Jungner criteria

1. Important health problem2. Treatment available3. Facilities available for diagnosis and treatment4. Latent stage of the condition5. Test available to detect the condition6. Test is acceptable to the population7. Natural history of the disease is known8. Policy of who gets treatment has been made9. Financially viable

10. Case-finding is a continual process, not just a one off

Page 5: Screening

Neonatal screening

Which conditions are screened for with blood spot testing? Phenylketonuria Sickle cell disease Cystic fibrosis Congenital hypothyroidism Medium-chain acyl-CoA dehydrogenase deficiency

Page 6: Screening

Antenatal Screening

What is a pregnant woman screened for? Pre-eclampsia Rhesus antigen status / blood group Anaemia Diabetes Syphilis Hepatitis B/C HIV

Page 7: Screening

Anomaly Scan – USS between 18-21 weeks

What is an anomaly scan used for? Spina bifida Down’s syndrome Hydrocephalus Cleft lip/palate

Date the pregnancy Sex of the baby Multiple pregnancy Organ development

Abdominal wall

Page 8: Screening

Test Outcomes

Diseased Non-Diseased

Test positive True Positive False Positive

Test negative False Negative True Negative

Page 9: Screening

Sensitivity

The number of people who have the disease who get a positive test result True positive / (True positive + False Negative)

e.g. 50 people with known Rheumatoid Arthritis. RhF blood test is positive in 42 of the patients. Sensitivity is 84%

Page 10: Screening

Specificity

The number of people who don’t have a disease who are correctly told they don’t have it True negatives / (True negatives + False positives)

E.g. 30 patients with no evidence of rheumatoid arthritis have a blood test for RhF. 2 patients have a positive result. Specificity = 93%

Page 11: Screening

Positive Predictive Value

The number of people who have a positive test result who actually do have the disease True positives / (True positives/False positives)

e.g. 2500 PSA blood tests performed on men >65yr. 800 are raised above normal levels. Biopsy reveals that 95 of these have prostate cancer. PPV = 95/(95+800) = 11%

Page 12: Screening

Negative Predictive Value

The number of people who have a negative test result who definitely don’t have the disease True negatives / (true negatives + false negatives)

e.g. 2500 PSA blood tests on men >65yrs. 1700 have normal PSA results. 20 of these turn out to currently have prostate cancer despite a normal PSA. 1680/ (20 + 1680) = 98.8%

Page 13: Screening

Diseased Non-Diseased

Test positive True Positive False Positive

Positive Predictive Value

TP / (TP + FP)

Test negative False Negative True Negative

Negative Predictive Value

TN / (TN + FN)

Sensitivity

TP / (TP + FN)

Specificity

TN / (TN + FP)

Page 14: Screening

Screening Bias

Healthy screenee Length time Lead time Overdiagosis

Page 15: Screening

Healthy screenee

Proactive patients who turn up to screening opportunities take better care of themselves are less likely to have a positive result Less likely to smoke, drink too much, have low income More likely to exercise, eat healthily, attend healthcare at other times

Internal locus of control

Page 16: Screening

Length time

Screening appears to improve prognosis because slow-forming conditions are detected and treated earlier than they would compared to waiting for symptoms to start

e.g. 500 slow forming and 500 fast forming cancers happen each year Slow forming – no symptoms and better prognosis Fast forming – obvious symptoms and poor prognosis

Screening can detect lots of slow forming, but not many fast cancers

Because slow has better prognosis, it appears that screening helps outcome, but actually just selects a high proportion of slow cancers

Page 17: Screening

Lead time

A screening test diagnoses something earlier but has no impact on outcome Appears to increase survival time, but doesn’t

Screening detects a disease

Symptoms start

Death

Screened patients

Non-screened patients

Lead time

Page 18: Screening

Overdiagnosis

Patients are diagnosed with a condition which isn’t going to affect their life expectance e.g. prostate cancer diagnosis in old men Get a PSA blood test done, high result but managing with symptoms ok Now told they have cancer – anxiety, health insurance etc.

Page 19: Screening

A new blood test is developed for rheumatoid arthritis. What is the sensitivity, specificity, PPV and NPV?

Diseased Non-Diseased

New test positive 250 26

New test negative 3 150

Sensitivity = 250 / (250+3) = 98.8 % Specificity = 150 / (150+26) = 85.2 %

PPV = 250 / (250+26) = 90.5 %NPV =150 / (150 + 3) = 98 %