Gynae1 Flashcards
(54 cards)
What is the relationship between HPV and Cervical cancer?
Persistent infection with oncogenic subtypes (10-15 years) can lead to cervical cancer
The oncogenic subtypes - 16 and 18 have increased risk of invasion and squamous intraepithelial lesions (SIL) (cervical and anal ca)
What are the important HPV subtypes and what do they cause?
16 and 18 are oncogenic - they can cause cervical ca (And anal ca)
THey can cause invasion OR squamous intraepithelial lesions
6 and 11 - cause warts
What are the risk factors for cervical cancer
- No screening
- DES exposure in utero
- 5 years on OCP
- Early pregnancy
- More than 3 pregnancy
- Smoking
- Age 35 or higher
- Immunocompromise
What is the difference in regression of Low grade and High grade SIL (LSil and HSil)
low grade squamous intraepithelial lesions are faster to regress
high grade SIL is slower to regress
Must sample trasnformation zone during HPV testing.
When does CST testing begin in Australia?
At the age of 25 or 2 years after first intercourse - whichever is LATER
If had Pap smear - then can have CST 2 years after last pap
eg pap at 28 can have CST at 30
For women UNDER 25 who had a Pap which was normal then can have their CST 2 years after OR at 25 which ever one is Later
HOWEVER
patient with symptoms - pain or bleeding can have a CST at any age
What are the two components to the CST?
- HPV testing
- Liquid based cytology
What are the risk factors for endometrial cancer
you are overweight or obese
you are over 50 years and have gone through menopause
your endometrium grows too thick (known as endometrial hyperplasia)
one or more people in your family has had endometrial, bowel, breast or ovarian cancer, or Lynch syndrome (known as hereditary non-polyposis colorectal cancer – HNPCC)
you take an oestrogen hormone replacement that does not have progesterone
you are taking the drug tamoxifen (which is used to treat breast cancer)
you have high blood pressure (known as hypertension) and diabetes
you have never had children -nulliparity
you have had pelvic radiation in the past to treat another cancer
you have a tumour in one of your ovaries - ovarian ca
you have polycystic ovary syndrome (PCOS).
What is the difference between primary and secondary amenorrhea?
PRIMARY - no secondary sexual characteristics by 14. (year 9)
No menstruation by 16. (year 11)
Secondary - No menstruation for six months after a period of menstruation in the absence of pregnancy.
Causes of Primary Amenorrhea
Imperforate hymen
Transverse vaginal septum
Mellerian agenesis (Female - has ovaries, but no uterus or vagina on u/s)
Androgen insensitivity (XY - genotypically male, grows up phenotypically female, external female sexual characteristics due to oestrogens in utero and b/down of testost - should have gonads removed as potentially carcinogenic)
Excessive exercise
Severe weight loss (anorexia nervosa)
Pitutaty adenoma - secreting prolactin
Turners Syndrome
What are causes of secondary amenorrhea?
- Prolactinoma is the commonest after pregnancy
- PCOS
- cervical stenosis
- Asherman syndrome
- Premature ovarian failure
- Excessive exercise, severe weight loss, stress, anorexia nervosa - affects HPO axis
- Hypopituitarism from destruction of pituitary eg craniopharygnioma, TB, sarcoidosis
- Hypo and hyperthyroid
- Sheehans syndrome (hypopituitarism caused by ischaemic necrosis of pituitary - blood loss during delivery or post partum/hypovolaemia
- Use of illicit drugs eg cocaine
- Medications - antipsychotics, antidepressants, antihypertensives
What is the process for collecting a HPV molecular test with LBC?
- Collect by inserting the central bristles of the collecting brush gently into the endocervical canal. (If lubricant is used for the speculum, use sparingly on the exterior surface and avoid applying lubricant to the tip of the speculum)
- Gently Rotate 3-5 times to collect sample.
- Rinse the bristles in the solution within the vial and tap the bristles against the base (Approximately 10 times) forcing bristles apart. Then discard the collecting device.
- Document patients details on the vial and send to lab.
- If for asymptomatic screening - write Cervical screening test on the form.
If Symptomatic - write Co-test (HPV and LBC)

Once CST is done what are the possible outcome?
- RETURN for CST screening in 5 years - IF NO HPV IS FOUND.
- REPEAT in 12 months - IF HPV is found (but not oncogenic) and Reflex LBC is either negative or shows pLSIL or LSIL. On the pathology form you would write FOLLOW UP HPV.
- REFER TO COLPOSCOPY - if any oncogenic HPV is found (regardless of LBC result) OR if non oncogenic HPV but the reflex LBC demonstrates pHSIL or HSIL. (The colposcopy will determine whether biopsy etc is needed)
- IF an UNSATISFACTORY SAMPLE was collected - the sample must be recollected within 6-12 weeks
What are symptoms which are suggestive of cervical cancer?
- Abnormal bleeding (post coital, intermenstrual, post menopausal)
- Unusual vaginal discharge
- Pain during sexual intercourse
How would you investigate a patient who has symptoms which might suggest cervical carcinoma?
CO-TEST - HPV and LBC
this means that regardless of the HPV result, they will also perform a liquid based cytology.
Write CO-test on the form and describe the symptoms eg abnormal bleeding.
When is a co-test for cervical cancer required?
- Symptomatic patients
- Patients exposed to DES and if requested, their daugthers
- Patients undergoing TEST OF CURE surveillance
- Patients who have been treated for glandular abnormalities
How do you perform a TEST OF CURE after a patient has been treated for high grade abnormalities?
These patients need a YEARLY CO-test
Until at least 2 consecutive negative co-test results
Then they can go back to 5 yearly screening
A pregnant patient wants CST screening? What is important in regards to the procedure?
Can happen at any time provided that The correct equipment must be used. Certain brushes like the cytobrush can cause bleeding and so are not recommended. THe pathology provider can give information about appropriate device to use in this case.
Self collected Vaginal sample tests for HPV - who is eligible and whats the process?
- MUST BE OVER 30 and declined clinician based collection AND
- OVERDUE for cervical screening by 2 years or longer
OR
- Have never screened
On the form write HPV ONLY (cos its a vaginal sample they cant do LBC)
NOT SUTIABLE IF - under 30, symptomatic, exposed to DES in utero, or had a total hysterectomy with hx of previous HSIL
What’s the process after a self collected vaginal HPV test?
If HPV is detected (not oncogenic) - Encourage the patient to have a clinician collected cervical sample for LBC. If they REFUSE - then encourage a repeat HPV test - preferably by a healthcare provider in 12 months time.
If oncogenic HPV is detected - REfer to gynaecologist for colposcopy and they will collect a cervical sample for LBC at that visit.
Would you offer CST to a woman who has had a total hysterectomy? A subtotal one (cervix not removed)
- Total hysterectomy and prior screening has been documented as NORMAL - then no further screening is required.
- IF total hysterectomy and previous High SIL was documented - then yearly CO- Test (Sample from the vaginal vault - write this on the form) taken yearly until 2 consecutive negative results. Then can stop screening.
- IF Subtotal - cervix still in tact - then they continue 5 yearly screening as normal.
What are the effectiveness rates of male condoms and female condoms? Correct use vs typical use
98Male —> 82 typical
95Female —> 79 typical
A woman presents seeking emergency contraception
a) within 4 days of sex
b) within 5 days of sex
a) WITHIN FOUR DAYS
ORAL LEVENORGESTROL 1.5mg STAT
b) within FIVE DAYS
Copper IUD (Copper intra uterine device)
or Ulipristal 30mg orally stat
What is the quick start method of contraception?
All contraception should be commenced within the first 5 days of the cycle.
If LATER than that when commencing contraception.
1) Use condoms for first 7 days
2) Repeat Pregnancy test in 4 weeks
3) Advice patient that there is a possibility of pregnancy in the current cycle
What are the options for contraception in an adolescent female
IUCD
Implanon
Depo Progestogen injection