Screening Programmes Flashcards

1
Q

What is a screening programme?

A
  • A test offered to an asymptomatic person to detect those who have a high probability of having a disease.
  • It is not a diagnostic procedure and those with a positive test need further investigation.
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2
Q

What are the different epithelias in the cervix?

A
  • Ectocervix; sqamous epithelium, only bottom layer should contain dividing cells
  • Endocervix; single layer of cuboidal cells containing mucin, no visible cell division.
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3
Q

What does microabrasion or epithelial trauma to the cervix do?

A

IT exposes part of the basement membrane, allowing virus entry.

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4
Q

What is the 1st to 3rd requirement for a screening programme?

A
  1. Condition should be an important problem for the individual and for the community.
  2. There should be an accepted treatment for patients with the disease.
  3. Facilities for diagnosis and treatment should be available.
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5
Q

What are the 4th to 6th requirement for a screening programme?

A
  1. There should be a recognisable latent or early stage.
  2. There should be a suitable test or examination.
  3. The test should be acceptable to the population.
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6
Q

What are the 7th to 10th requirements for a screening programme?

A
  1. The natural history of the condition, including development from latent to declared disease, should be adequately understood.
  2. There should be an agreed policy on who to treat as patients.
  3. The cost of the case finding programme should be economically balanced in relation to expenditure on medical care as a whole.
  4. Case finding should be a continous process
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7
Q

What are some more requirements of screening programmes?

A
  • These should be q quality assurance, with mechanisms to minimise potential risks of screening.
  • Programme should ensure informed choice, confidentiality and respect for autonomy.
  • Programme should promote equity and access to screening for the entire target population
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8
Q

Describe the pathophysiology of cervical cancer?

A
  • Majority of cervical cancers have a high risk subtype of human papilloma virus (HrHPV) as an underlying cause.
  • Persistant infection with HrHPV can cause changes in cells which in some people progresses to cancer.
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9
Q

What are some more risk factors of cervical cancer?

A
  • Smoking
  • Poor immune function
  • Multiple sexual partners
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10
Q

What is HPV, who does it usually infect and what tends to be the outcome?

A
  • HPV are a group of DNA viruses, which are grouped into high and low risk.
  • 80% of sexually active people will become infected at some point during their lifetime.
  • Most clear it with no intervention
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11
Q

Where does the virus enter the cervix and how does it mature?

A
  • Virus enters cervical epithelia at the transformation zone

- HPV replicates in maturing squamous cells producing koilocytes

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12
Q

What happens in the high risk subtypes of HPV?

A
  • Patients who have persisting infection with a high risk oncogenic subtype of HPV are at risk of developing pre cancerous changes and cervical cancer.
  • High risk HPV subtypes incorporate their DNA into that of the host cell.
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13
Q

What happens in low risk HPV subtypes?

A

Low risk HPV subtypes tend to result in free viral DNA within the cell.
-They are responsible for viral warts (eg. subtypes 6, 11, 42, 44)

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14
Q

What are high risk HPV subtypes E6 and E7 responsible for?

A

They reactivate the cell cycle in cells which are not normally proliferating.

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15
Q

What is the result of persistant infection disruption of the cell cycle by high risk HPV subtypes?

A

Results in proliferation of the epithelial cells without an external stimulus - precursor lesions for cervical cancer. These are termed CIN and CGIN.

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16
Q

What is CIN?

A
  • Cervical intraepithelial neoplasia

- Divided into CIN 1, 2, 3.

17
Q

What are the outcomes of CIN 1, 2 and 3?

A
  • In most patients CIN 1 resolves without treatment, so patients are monitored.
  • CIN 3 is the precursor lesion for squamous cell carcinoma (usually takes more than 2 years to develop into invasive carcinoma).
  • Main purpose of cervical screening programme is to detect and treat CIN 2 and CIN 3.
18
Q

What is CGIN?

A
  • Cervical glandular intraepithelial neoplasia.

- Much less common and is precursor lesion for adenocarcinoma

19
Q

Who is invited for cervical screenings?

A

Women aged 25-65 invited every 5 years

Women with abnormal tests called more frequently

20
Q

What are samples tested for in cervical screening?

A
  • All samples get HPV testing

- 15% get cytology testing: samoles with positive HPV test, samples from patients on follow up pathways

21
Q

Describe HPV testing?

A
  • Runs automated test for 14 high risk HPV subtypes
  • Specific type found is not reported
  • Negative: recall in 5 years
  • Positive: tested for cytology
22
Q

Describe cervical cytology testing?

A

-Cells from transformation zone are spread out
-Abnormal cells have enlarged, irregularly shaped nuclei
This is called dyskaryosis and is graded as mild, moderate or severe depending on the size of the nucleus.
-These roughly equate to CIN 1, 2, 3 on histology specimens, biopsy needed to confirm degree of abnormality.
-Patients who have cell changes referred to colposcopy for investigation.
-Patients with positive HPV but no cell changes are called back in 1 year for repeat HPV test.

23
Q

Describe colposcopy?

A
  • Uses specialist microscope, acetic acid applied to highlight any abnormalities
  • Patients can have biopsies taken and treatments for abnormalities detected.
24
Q

Who is invited for breast screening?

A

-Women aged 50-70 are invited every 3 years for a mammogram, with the aim of detecting disease early.

25
Q

What is the process of breast screening?

A

-30 min appointment and 2 x X-rays are taken of each breast.

Images are interpretated an the results sent to the GP an patient.

26
Q

What is the process for those with abnormal breast screens?

A

-Those with abnormal or unsatisfactory results are seen at a specialist clinic for triple assessment: -clinical exam, radiology (repeat mammogram or ultrasound if needed), biopsy.

27
Q

What is normal breast tissue like compared to cancerous version?

A
Normal = ductile tissue, lobular tissue, adipose tissue, fibrous tissue
Cancer = fatty tissue has cells infiltrating between fat cells, no structure, ductules or lobules, variation in nuclei subtle
28
Q

What is the aim of bowel screening?

A

-Aim to detect precancerous changes (often polyps) and early cancers which are treatable and have better prognosis.

29
Q

Who is invited for bowel screening?

A

-Men and women aged 50-74 are invited to participate every 2 years

30
Q

What is the process of bowel screening?

A

-A faecal immunochemical test (FIT) is sent in post for completing at home.
-One sample of stool is collected and returned in a pre paid envelope.
This is tested for haemoglobin, results sent back within 2 weeks.
-If the level of haemoglobin is above 80ugHb/g faeces, patients are referred to colonoscopy.

31
Q

What is a polyp?

A

Are things that grow into lumen of tube and can be removed. They have disordered architecture.

32
Q

What is the histology of the bowel?

A

-Have tube like glandular cells lined by cells that make musin to lube stool.

33
Q

What is dysplasia histology?

A

Appears bluer, larger nuclei, glands close and arranged haphazardly.

34
Q

Describe the test for cervical screening?

A
  • A cervical smear test:
  • carried out at GP surgery/sexual health clinic
  • brush used to remove cells from cervix
  • these are transferred to a pot of preservative
  • are tested for HPV +/- cytology