Screening Programmes Flashcards

1
Q

what is a screening?

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, those who have a positive test will need further investigation.

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2
Q

what is the purpose of the cervical screening programme?

A

uses early detection the earlier it it found the less urgent medical attention needed.

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3
Q

what are the 10 stages for early disease detection?

A

-condition should be an important problem for the individual and the community
-there should be an accepted treatment for the patient with the disease
-facilities for diagnosis and treatment should be available
-there should be a recognisable latent or early stage
-there should be a suitable test or examination
-the test should be acceptable to the population
-the natural history of the condition including development from latent to declared disease, should be understood adequately
-there should be an agreed policy on whom to treat as patients
-the cost of the case finding programme should be economically balanced in relation to expenditure on medical care as a whole
-case finding should be a continuing process

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3
Q

what are the later additions of screening programmes?

A

-option to opt out
-minimise risks
-promote equity for entire population
-benfits should outweigh harm

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4
Q

what is an underlying cause of cervical cancer?

A

Human papilloma virus

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5
Q

how does HPV progress to cervical cancer?

A

-persistent infection can cause changes in cells which for some people will progress to cancer

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6
Q

what are some other risk factors for cervical cancer?

A

-smoking
-poor immune function
-multiple sexual partners

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7
Q

what is HPV

A

-a group of DNA viruses
-over 200 types
-80% of people infect it but most clear it
-patients who have persisting infection with a high risk oncogenic
subtype of HPV are at risk of developing pre cancerous changes and cervical cancer

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8
Q

how does the virus enter the cervix?

A

it is thought that microabrasions in the basement membrane allow it to get into replicating cells. it can enter the cervical epithelia at the transformation zone

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8
Q

where does HPV replicate?

A

in maturing squamous cells which then turn into koilocytes (mature squamous cells which have noticable cytoplasmic alterations)

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9
Q

what does low risk HPV tend to result in?

A

free viral DNA within the cell
-responsible for viral warts

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10
Q

how does high risk HPV result in neoplasia?

A

-they incorporate their DNA into the host cell
-viral E6 and E7 proteins are responsible for reactivating the cell cycle in cells which are not normally proliferating

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11
Q

what does persistent infection and disruption of the cell cycle result in?

A

proliferation of the epithelial cells without an external stimulus. precursor lesions for cervical cancer. these are termed CIN (Cervical intraepithelial neoplasia) and CGIN (cellular glandular intraepithelial neoplasia)

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12
Q

what are precursor regions?

A

cervical inreaepithelial neoplasia, divided into CIN1, CIN2, CIN3

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12
Q

what are the high risk subtypes for HPV?

A

16, 18, 31, 45

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13
Q

what occurs in CIN1?

A

resolves without treatment, patients are monitored

14
Q

what happens in CIN3?

A

the precursor lesion for squamous cell carcinoma, usually takes more than 2 years to develop into invasive carcinoma

15
Q

what is CGIN?

A

cervical glandular intraepithelial neoplasia, MUSCH LESS COMMON AND IS THE PRECUROSOR LESION FOR ADENOCARCINOMA

16
Q

what precursor region is the cervcial screening trying to detect?

A

CIN2 CIN3

17
Q

what is cervical cytology?

A

the cells from the transformation zone are spread out
-abnormal cells are enlarged, irregularly shaped nuclei
-this is called dyskaryosis, graded as mild, moderate or severe depending on size of nucleus.
-roughly correlate to CIN1, CIN2 AND CIN3
-biposy needed to confirm after

18
Q

what are some characteristics of high grade dyskaryosis?

A

-irregular nuclear outline
-darker nuclei
-much bigger
-take up more room

19
Q

what is applied during colposcopy to highlight any abnormalities?

A

acetic acid

20
Q

who is treated as a patient?

A

any patient who has any cell changes are referred to colposcopy immediately.

21
Q

how many women in Scotland will develop breast cancer?

A

1 in 8

22
Q

how can the bad cells be removed?

A

cold coagulation
loop of hot wire is used to remove the area of conern

23
Q

how is a breast screening offered?

A

woman aged 50-70 are invited every 3 years

24
Q

why does a histological sample appear more blue?

A

larger nucleus taking up more of the cell

25
Q

what is the prevalence of bowel cancer?

A

-third most common cancer in Scotland
-4000 new cases a year mostly in over 50’s
-5 year survival is 60%

26
Q

what is the aim of bowel screenings?

A

detect pre cancerous changes (often polyps) and early cancers which are treatable and have better prognosis

27
Q

what does the bowel screening programme consist of?

A

-men and women aged 50-74 invited to participate every 2 years
-faecal immunochemical test sent for completing at home
-tested for haemoglobin

28
Q

what is done after a bowel screening?

A

-if haemoglobin levels above 80ugHb/g faeces patient referred for colonoscopy
-1 in 50 patients referred
-of those around 5 will have cancer

29
Q

what happens to the cells of the bowel when cancer is present?

A

have less mucin