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CYT 2113 Cytology I Lesson 7: Introduction to Pap Smear Test

7.Pap smear

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  • CYT 2113 Cytology I

    Lesson 7:

    Introduction to Pap Smear Test

  • Pap Smear

    An examination under the microscope of cells

    scraped from the tip of the cervix

    (Cervix the lower part of the uterus that

    opens at the top of vagina)opens at the top of vagina)

    Done as part of a gynecological exam

  • How Pap Smear Test is Performed

    The patient will lie and position pelvis for

    examination

    The health care provider will insert speculum

    into vagina and open it slightly to see inside

    the vaginal canalthe vaginal canal

  • A cotton swab is sometimes used to clear away

    mucus that might interfere with an optimal

    sample

    A sample of cells is taken from the outside and

    just inside the opening of the cervix (cervical

    canal) by gently scrapping the outside of the

    cervix with a wooden or plastic spatula, then cervix with a wooden or plastic spatula, then

    inserting a small brush into the canal

  • The cells are placed on a glass slide, or put in a

    bottle containing a preservative and then sent

    to the lab for examination

    The cells are examined under a microscope in

    order to look for pre-malignant or malignant order to look for pre-malignant or malignant

    changes

  • Pap Smear

  • Pap Smears

    Conventional smears are often obtained using

    the combination of a spatula and brush

    The spatula is used first

    Although a wooden or plastic spatula is Although a wooden or plastic spatula is

    acceptable, the plastic spatula is

    recommended because wooden fibers trap

    diagnostic material

    The spatula is rotated 360 degrees

  • The sample can be smeared on one half of a

    slide and spray fixed (the other half should be

    covered to avoid coating it with fixative before

    the endocervical sample is applied)the endocervical sample is applied)

    Alternatively, one may set aside the spatula

    sample momentarily while the endocervical

    brush sample is obtained

  • After the brush is inserted in the endocervical

    canal, some bristles should still be visible

    If inserted too far, there may be inadvertent

    sampling of the lower uterine segment (LUS), sampling of the lower uterine segment (LUS),

    which causes diagnostic difficulties because its

    epithelium resembles a high-grade squamous

    intraepithelial lesion (HSIL) and

    adenocarcinoma in situ (AIS)

  • The brush should be rotated gently only one

    quarter turn

    A larger rotation is unnecessary because the

    circumferential bristles are in contact with the

    entire surface the moment the brush is

    insertedinserted

    The spatula sample, if not already applied and

    fixed, should be applied to the slide, then the

    brush sample rolled over the slide, followed

    by immediate fixation

  • The two samples can be placed in quick

    succession on two separate halves of the slide,

    or the endocervical sample can be rolled

    directly over the spatula sample, both directly over the spatula sample, both

    covering the entire slide

    Immediate fixation (within seconds) is critical

    to prevent air-drying artifact, which distorts

    the cells and hinders interpretation

  • The broomlike brush (broom) has a flat

    array of plastic strips contoured to conform to

    the cervix, with longer strips in the middle

    This design allows simultaneous sampling of This design allows simultaneous sampling of

    the endocervix and ectocervix

    The long middle strips are inserted into the os

    until the shorter outer strips bend against the

    ectocervix

  • The broomlike brush

  • The broom is rotated three to five times

    To transfer the material, each side of the

    broom is stroked once across the slide in a

    painting motionpainting motion

    The cotton swab moistened with saline is no

    longer recommended because its fiber trap

    cells, reducing the efficiency of cell transfer

    onto slides

  • Cervex brush Cytobrush

    Spatula

  • There are two options for smear fixation

    Coating fixatives contain alcohol and

    polyethylene glycol and applied by pump

    sprays, by droppers from dropper bottles, or sprays, by droppers from dropper bottles, or

    by pouring from an individual envelope

    included as part of a slide preparation kit

    Alternatively, the smear can be immersed

    directly into a container filled with 95%

    ethanol

  • Samples for liquid-based cytology (LBC) are

    obtained as described except that, instead of

    smearing the cells on a slide, the collection

    device is rinsed in a vial containing liquid device is rinsed in a vial containing liquid

    fixative

  • How to Prepare for the Test

    Tell the health care provider if you:

    Are taking any medications or birth control pills

    Have had an abnormal Pap smear

    Might be pregnant

    Within 24 hours of the test, avoid:

    Douching

    Having intercourse

    Taking a tub bath

    Using tampons

  • Avoid scheduling Pap smear while

    menstruating because blood and cells from

    the uterus may affect the accuracy of the Pap

    smearsmear

    Empty the bladder just before the test

  • Pap Smear

    A simple, quick and relatively painless screening

    test

    Specificity (its ability to avoid classifying a normal

    smear as abnormal) is very good but not perfectsmear as abnormal) is very good but not perfect

    Sensitivity (its ability to detect every single

    abnormality) is good but also not perfect

    Some false negative results (in which

    abnormalities are present but not detected by

    the test) will occur

  • Thus, a few women develop cervical cancer

    despite having regular Pap screening

    In the vast majority of cases, a Pap test does

    identify minor cellular abnormalities before they identify minor cellular abnormalities before they

    have had a chance to become malignant and at a

    point when the condition is most easily treatable

    The Pap smear is not intended to detect other

    forms of cancer such as those of the ovary, vagina

    or uterus

  • Cancer of these organs may be discovered

    during the course of the gynecologic (pelvic)

    exam, which usually is done at the same time

    as the Pap smearas the Pap smear

  • Why the Test is Performed

    The Pap smear can detect cancerous or

    precancerous conditions of the cervix

    Most invasive cancers of the cervix can be

    detected early if women have Pap tests and detected early if women have Pap tests and

    pelvic examinations

    Screening should start within 3 years after first

    having vaginal intercourse or by age 21

  • After the first test:

    Woman should have a Pap smear every 2

    years to check for cervical cancer

    If the woman is over age 30 or the Pap smears

    have been negative for 3 times in a row, the

    doctor may recommend Pap smear to be done doctor may recommend Pap smear to be done

    every 3 years

    If the woman or her sexual partner have other

    new partners, then she should have a Pap

    smear every 2 years

  • After age 65-70, most women can stop having

    Pap smears as long as they have had three

    negative tests within the past 10 years

    If the woman has a new sexual partner after If the woman has a new sexual partner after

    age 65, she should begin having Pap smear

    screening

  • Who Should Have a Pap Smear

    Women who have had a total hysterectomy

    (uterus and cervix removed) and have not had

    any previous history of cervical dysplasia

    (abnormal cells), cervical cancer or any other kind (abnormal cells), cervical cancer or any other kind

    of pelvic cancer, may not need to have Pap

    smears

    Pregnancy does not prevent a woman from

    having a Pap smear

    Pap smears can be safely done during pregnancy

  • The screening guidelines of American Cancer Society 2004:

    When to start Pap smear testing 3 years after vaginal intercourse, no later than age 21

    Frequency of Pap smear testing yearly with exceptions: every 2 years if liquid-based kit; every 2-3 years if three normal tests in a row in women 2-3 years if three normal tests in a row in women 30 years old

    Age to stop having Pap smears total hysterectomy of benign disease 70 years old with at least three normal Pap smear results in the last 10 years

  • The screening guidelines of United States

    Preventative Services Task Force 2003:

    When to start Pap smear testing within 3

    years of onset of sexual activity or age 21,

    whichever comes firstwhichever comes first

    Frequency of Pap smear testing at least

    every 3 years (no evidence that every year is

    better than every 3 years)

  • Age to stop having Pap smears

    -recommend against doing Pap smears in

    women older than 65 years of age, if adequate

    screening with normal resultsscreening with normal results

    - recommend against doing Pap smears in

    women who have had a total hysterectomy for

    benign disease

  • The screening guidelines of American College of Obstetrics and Gynecology:

    When to start Pap smear testing 3 years after first sexual intercourse or age 21, whichever comes first

    Frequency of Pap smear testing yearly until age 30 years. Beginning at age 30, if three normal annual Pap results, can do a Pap alone every 2-3 annual Pap results, can do a Pap alone every 2-3 years

    Age to stop having Pap smears difficult to set an upper age limit- postmenopausal women screened within the prior 2-3 years have a very low risk of developing abnormal Pap smears

  • It has been seen that women who do not

    participate in screening programs, and women

    whose interval between smears is more than 3

    years, are at highest risk for developing cervical

    carcinoma

    In Malaysia, all women who are, or who have

    been sexually active, between the ages of 20 and been sexually active, between the ages of 20 and

    65 years, are recommended to undergo Pap

    smear testing

    If the first two consecutive Pap results are

    negative, screening every three years is

    recommended.

  • Women with a history of cervical cancer, in

    utero diethylstilbestrol (DES) exposure, and

    who are immunocompromised (organ

    transplantation, chemotherapy, chronic transplantation, chemotherapy, chronic

    corticosteroid treatment, or positive for

    human immunodeficiency virus) may benefit

    from more frequent screening

  • Normal results

    A normal value is negative, meaning there are no abnormal cells present

    Abnormal results

    Atypical cells of uncertain significance (ASCUS) these changes may be due to infection with HPV but may also mean there are precancerous but may also mean there are precancerous changes present

    Low-grade dysplasia or high-grade dysplasia: this means precancer changes are likely to be present; the risk of cancer is greater if the result is high-grade dysplasia

  • Carcinoma in situ (CIS) this usually means the abnormal changes are likely to progress to cancer

    Atypical squamous cells (ASC-H) this means Atypical squamous cells (ASC-H) this means abnormal changes have been found and may be high-grade squamous intraepithelial lesion

    Atypical glandular cells (AGC) cell changes are seen that suggest precancer of the upper part of the cervical canal or inside the uterus

  • When a Pap smear shows abnormalities, further testing or follow-up is needed

    The next step depends on the results of the Pap smear, previous history of Pap smears and risk factors for cervical cancer

    This may include

    - colposcopy-directed biopsy- colposcopy-directed biopsy

    - An HPV test to check for the presence of the HPV virus types most likely to cause cancer

    For minor cell changes, doctors usually recommend having a repeat Pap smear in 3-6 months

  • (colposcopy a procedure to closely examine

    cervix, vagina and vulva for signs of disease)

  • Which women are at increased risk for having an

    abnormal Pap smear?

    A number of risk factors have been identified for

    the development of cervical cancer and

    precancerous changes in the cervix.

    HPV: The principal risk factor is infection with the HPV: The principal risk factor is infection with the

    human papillomavirus (HPV), although most

    women with HPV infection do not get cervical

    cancer

  • Smoking: Smoking increased the risk of cervical

    cancer about two to four fold.

    Weakened immune system: Women whose

    immune systems are weakened by medications (for

    example, those taken after an organ transplant)

    also have a higher risk of precancerous changes in

    the cervix. the cervix.

    Medications: Women whose mothers took the

    drug diethylstilbestrol (DES) during pregnancy also

    are at increased risk.

    Other risk factors: having multiple sexual partners

    and becoming sexually active at a young age.

  • Strengths of Cytology Screening

    The decades of experience in its use

    High specificity

    Its adaptability to computer-assisted reading

    The lesions identified are easy to treat The lesions identified are easy to treat

    Relatively low cost

  • Limitations of Cytology Screening

    The test is difficult to comprehend in many

    cultures

    Invasive and potentially embarrassing

    Trained personnel are required Trained personnel are required

    Smear adequacy is not intrinsically obvious

    It is necessary to recall women for further

    tests if the results are not clearly negative

    The test has only moderate sensitivity

  • Unable to distinguish progressive disease from

    that destined to regress

    It is impossible by screening to eliminate all

    cervical cancer mortalitycervical cancer mortality

  • Essential Elements for a Successful

    Cytology Screening Programme

    Training of the relevant health care professionals,

    including smear takers, smear readers

    (cytotechnologists), cytopathologists,

    colposcopists and programme managerscolposcopists and programme managers

    An agreed decision on the priority age group to

    be screened

    Adequately taken and fixed smears

    Efficient and high quality laboratory services, that

    should preferably be centralized, quality control

    of cytology reading

  • A means to rapidly transport smears to the

    laboratory

    A mechanism to inform the women screened

    of the results of the test in an understandable of the results of the test in an understandable

    form

    A mechanism to ensure that women with an

    abnormal test result attend for management

    and treatment

  • An accepted definition of an abnormality to

    be treated, i.e. high grade lesions

    A mechanism to follow up treated women

    A decision on the frequency of subsequent A decision on the frequency of subsequent

    screens

    A mechanism to invite women with negative

    smears for subsequent smears

  • Elements that Interfere with the

    development of Successful Cervical

    Screening Programmes

    Over-reliance on maternal and child health

    services for screening, especially for defining

    the target groupthe target group

    Opportunistic (spontaneous) screening, often

    focusing on frequent screening of low risk

    women

  • Low compliance with screening of the target

    group (evaluation by counting smears, rather

    than counting women screened)

    Setting too low a threshold for referral for Setting too low a threshold for referral for

    colposcopy (over-treating non-progressive

    disease)