Regular & Emergency Contraception Flashcards
in motivational interviewing for contraception what are the risks of treatment?
- CVS (hormones & DVT),
- neoplastic,
- emotional,
- infection,
- allergic (copper, rubber)
- Iatrogenic:
- harm caused by medical treatment
in motivational interviewing for contraception what are the benefits of treatment?
Benefits:
- non-contraceptive (cancer risk, painful periods),
- psychosexual, choice,
- sexual health,
- cost savings,
- female quality
in motivational interviewing for contraception what are the benefits of no-treatment?
- non-interference,
- population growth,
- control of women
in terms of motivational interviewing for contraception what are the risks of no treatmnet?
- childbirth related
- abortion related,
- social & ecomonic costs
What is “MEC catergory”?
MEC = medical eligibility criteria for contraceptive use
WHO categories for the safety of each contraception in certain medical situations
1 = condition where there is no restriction for use of contraceptive method –> 4- condition representing unacceptable health risk if the contraceptive method is used
2 = advantages of method generally outweigh theoretical/proven risks
3 = theoretical risks outweigh advantages of using this method - needs specialist referral to decide
What drug interactions are of concern for hormonal contraception?
What should you do about this?
enzyme inducers: if pts needs these and they are on COCP/POP consider switch to TUD, IM progesterons (depo-provera), mirena
- anticonvulsants,
- (Carbamazepine, Esclicarbazepine , Oxcarbazepine Phenobarbitol, Phenytoin, Primidone , Topirimate)
- antifungals,
- grisofulvin
- antiretrovirals
- NNRTIs
- and abx
- rifampicin, rifabutin
+ St Johns wort
A woman wants the most efficient contraceptive method possible, she doesnt care about anything else. What methods have what woman years failure rate?
the best for lowest woman years (WY’s) is:
- Male Sterilisation - 1/2,000 WY’s (after 2 -ve sperm analysis @8 & 12 weeks)
- Female sterilisation (1/200 WY’s failure rate and > ectopic risk, male sterilisation is quicker, safer and less morbidity than female)
- IUD and IUS (hormonal) implant and injection = all <1/100 WY’s
- COCP <1/100 WY’s - as long as taken properly
- POP = 1/100 WY’s
- male condoms 2/100 WY’s
- Female condoms 5/100 WY’s
- diaphragm/caps ~6/100 WY;s
A female patient is worried about fertility on stopping contraception. Which methods can you recommend?
- male / female condoms / diaphragm / caps will have fertility return if you dont use them
- Implant & IUS/IUS fertility return immediately after removal [NB: implant takes serum levels 1 week to return though]
- COCP = within 10 D
- injectable/depo-provera is only hormonal method that may delay returning of fertility (6-9 months / 1 yr) but NO permanent impairment
How does this contraception work?
- Microgynon®
- – 30µg ethinylestradiol,&150µg levonorgestrel (progesterone).
thhe combined oral contraceptive pill
- E2 (supra-physiological): -ve feedback on hypothal, pituitary, ovary & endometrium – no LH surge, no ovulation
- sudden rise in oestrogen/switch to +ve feedback changes amplitude and frequency of hypothalamus pulses –> pituitary LH surge
- P: -ve feedback, on endometrium (thin, non-proliferative), stop cilia working, thickens cervical mucus
What are “phasic” COCP?
COCP with varying amount of E2 and P across cycle
- Femulen® – etynodiol diacetate 500µg.
- •Norgeston® – levonorgestrel 30µg.
- •Noriday® – norethisterone 350µg.
- •Micronor® – norethisterone 350µg.
- •Cerazette® – desogestrel 75µg.
How do these contraceptions work?
they are progesterone only pills - POP
Prevent ovulation (99% in high dose, 50% in low dose);
- Endometrial thinning;
- Reduced tubal cilia action;
- block passage of sperm - thickens cervical mucus
A patient is taking femulen - a POP. She has missed a pill and had unprotected sexual intercourse 0-2 days after? What should be done?
- unprotected sexual intercourse 1-2 days after missed POP ==> emergency contraception
- need condoms for 2 days after a missed POP as mucous is less hostile
[some POP have 12hr window, some have 3hr window]
For POP
If missed pill –
UPSI before missed POP = no action e.g. asking what time they normally take it…
USPI 0-2d after missed POP –> Emergency Contraception
Need condoms for 2d after missed POP as mucous is less hostile
What is the window period pts have to take their POP in?
- Some have 12hrs window (preferred for young people)
- some have 3hr window
A patient is on microgynon - a COCP. She has missed a pill, what should she do next?
if 1x missed pill - take the next as planned, no need for EC
A patient is on microgynon - a COCP. She has missed 2 pills, what should she do next?
if 2 or > pills missed use condoms for 7d AND
- if pill missed in week 1 take EC = as worst time to miss mill
- week 2 = no EC; but use condoms
- wk 3 = miss mill free interval
A patient has decided that she would like to start taking the COCP. How does she need to take it?
- Start the 1st packet on 1st day of period
- (as you would know that shes not pregnant, as having period)
- take 21 D of pills e.g. 3w –> 7D withdrawal bleed
- Start the new packet on the 8th day –> the same weekday as started
- Don’t start the new packet late (e.g. after 8D - as the next cycle kicks in)
if >2 pills are missed use &d condom, Wk1 take EC if wk2 = no EC, if wk 3 = miss pill free intverval and keep taking)
With barrier contraception what is
- the MOA?
- how to use?
- side effects/risks?
- health benefits?
- Block passage of sperm
- incorrect use means failure rates more like ~24% - esp w/female condoms (2/100 vs 5/100, & caps/diaphragms 4-8/100)
- latex allergy, psycho-social difficulties, oily preparations not rubber, dependent on male erection, otherwise no serious health risks
- beneficial for STI protection, easily available & free
A patient has heard the COCP increases risk of cancer and other bad things, she is now scared and wants to come off it. What are the side effects and risks of COCP e.g. microgynon?
- some pts (~15%) have Intermenstural Bleeding (IMB)
- VTE (inc. migraine) (risk biggest in 1st year –> unmasking of thrombophilias)
- Arterial thrombosis
- Increased risk breast, liver, cervical cancer; risk drops again after stopping
But overall 12%↓ risk any cancer;
- Reduced insulin metabolism,
- Crohn’s
- Gallstones
- Derm
- Chloasma (large brown patches form on the skin), acne, erythema multiforme
- Psych:
- Mood swings, depression, libido
- Headaches, breast changes
A patient on the COCP is due for surgery (from VTE risk?) when should the COCP be stopped befoer surgery and restarted?
stop COCP 4wks before surgery and restart 2w after
A patient on the COCP e.g. Microgynon is worried about the cancer risk but you have explained to her about
Risks/SE’s:
- IMB (~15%)
- VTE (inc. migraine) (risk biggest in 1st year –> unmasking of thrombophilias)
- Arterial thrombosis
- Increased risk breast, liver, cervical cancer NB: risk reduced back down on stopping
- But overall 12%↓ risk any cancer (risk ovarian/endo/CRC)
- Reduced insulin metabolism, Crohn’s
- Gallstones
- Chloasma, acne, erythema multiforme
- Mood swings, depression, libido
- Headaches, breast changes
WHAT ARE THE HEALTH BENEFITS OF COCP?
Beneficial for
- irregular/ heavy/ painful menses,
- endometriosis,
- fibroids,
- PMS,
- hirsutism,
- acne,
- risk ovarian / endometrial / colorectal cancer
The CI’s and interactions for COCP are MEC 4. What does that mean?
4 = a condition that represents an unacceptable health risk if the contraceptive method is used
MEC = medical eligibiltiy for contraception criteria
(1 being no restriciton , 2 = pros of using outweigh risks, 3 = risks outweigh pro’s unless under specialist’s care when they an be watched)
What are the MEC criteria for contraceptive use 4 CI’s for the COCP?
MEC 4 –
- Migraines with aura
- >35yrs + smoker
- Multiple serious RFs for CVD (migraine with aura)
- those with migraine w/aura is linked to 50% incrase stroke, CVD & MI!
- HTN ≥160/96mmHg or with vascular disease
- BMI ≥35 kg/m2
- VTE, MI, CVA (current or past)
- Thrombogenic mutations (factor V Leiden)
- Current breast cancer or 1o liver tumours
- as COCP = increased breast, liver and cervical cancer
-
Breastfeeding & <6wks postpartum
- (as oestrogen switches off HPG axis–> affects PRL/milk)
A patient is deciding to start on femulen (a POP), what are the side effects?
- Irregular bleeding (4/10)
- or amenorrhoea (2/10)
- Headaches, breast tenderness, skin changes, unexplained mood swings and loss of libido
- Risk simple ovarian cysts (3/10)
- Small increased risk of breast cancer
A patient is wanting to go onto femulen (a pop), what are CI for the POP that should be checked for with the patients/notes?
- Breast cancer (current or past)
- due to small increased risk of breast cancer
- liver cirrhosis or tumours
- CVA or CHD (current or past)
- if >70kg… POP has lower efficacy
(e.g. like in cocp looking for cvs stuff and liver too even if cocp is the one that increases liver cancer and gallstones etc)
What is POP beneficial for?
endometrial cancer –
if the COCP is CI’d
e.g. >35yrs + smoker & migranes with aura (breastfeeding etc)
NB: it is bad for increased risk of breast cancer (while COCP is liver, cervix and breast; but good for enometrial, CRC and ovarian)
What are the methods of action of female and male sterilisation?
prevents egg and sperm meeting
NB: male sterilisation is generally quicker, safer and less morbidity than female. males can be done in GP surgery ??? while female has to be done hysteroscopic or laparoscopic.
A woman has undergone sterilisation
- laparoscopically
- hysteroscopically
they have stopped taking contraception, as they said they are sterile now. Is this correct in cases (1) or (2)?
no!
contraception is required!
- in laparoscopic –> until the menstural period after (1 month)
- hysteroscopic –> 3 months following procedure
A female patient is considering female sterilisation, what are the risks associated with the procedure?
- irreversible
- risk trauma to internal structures
- no STI protection
- increased relative risk of ectopic
- & risks of GA (laparoscopic surgery)
How does the IUS (hormonal) & IUD (copper) work?
They both prevent IMPLANTATION
IUS (hormonal) - levongestrel 52mg LNG-IUS (mirena); or 13.5mg LNG-IUS (jaydes) also means NO ENDOMETRIAL PROLIFERATION
IUD (copper) - prevent implantation, causes inflammatory reaction (macrophages, leukocytes, PG & enzymes in uterus & tubal fluid) –> toxic to sperm, egg & interfere w/sperm transport
How does the implant
(3-year 68mg rod of 3-keto-desogeatrel: intially ~65ul/day falls to ~25 by 3 years)
and injection
(depo-provera)
work?
(1) PREVENT OVULATION & (2) BLOCK passage of sperm (mucus)
depo also thins the endometrium