Progestogen-only Injectable Contraception FSRH Mar 2015 Flashcards
“progestogen-only injectable contraception”
When administered at the recommended dosing interval the failure rate in the first year of use & with typical use ?
- approximately 0.2% in the first year of use.
- With typical use the failure rate is approximately 6%
DMPA use benefits
- may reduce pain endometriosis.
- may reduce the severity of sickle crisis pain.
Use of DMPA & cancer risk
- not associated with an increased risk of ovarian or endometrial cancer and may offer some protection.
- possibly a weak association between current use of DMPA and breast cancer. Any increased risk is likely to be small and reduce with time after stopping.
- weak association between cervical cancer and use of DMPA for 5 years or longer. Any increased risk reduce with time after stopping and could be due to confounding factors.
Use of DMPA
age
- advised to switch to another method at age 50 years. If not to continue, providing the benefits and risks have been assessed and informed of potential risks.
- under 18 , can be used after consideration of alternative methods. (weight gain, particularly under 18 years BMI ≥30 kg/m2)
The efficacy of DMPA affected by?
- not reduced withenzyme inducing drugs.
- UPA reduce efficacy of hormonal, additional precautions are advised for 14 days after UPA for EC (outside product licence).
- No increased risk of pregnancy users with higher body weight, although data limited in BMI ≥40 kg/m2.
DMPA timing
- every 13 weeks IM or SC, DMPA (outside the product licence for IM DMPA).
- up to 7 days late (up to 14 weeks after last injection) without need for additional contraceptive precautions (outside the product licence for IM DMPA).
- If necessary, an early repeat injection of DMPA can be administered from 10 weeks and from 6 weeks for NET-EN (outside product licence).
DMPA & unscheduled bleeding
- who are medically eligible can be offered a combined COC for 3 months. (cyclic manner or continuously without HFIl (outside product licence).
- Longer-term use of the injectable and COC is a matter of clinical judgement.
- offere 500 mg mefenamic acid up to TID for 5 days.
DMPA & STI
- consistent and correct use of condoms (male/ female) reduce risk of STI transmission and should be recommended
- A causal relationship between POIC and HIV
transmission/acquisition not been established but cannot be completely excluded.
DMPA & return of fertility
- can be a delay of up to 1 year in the return of
fertility after discontinuation of IM or SC DMPA.
DMPA discontinue
Still wants contraception
to start another contraceptive method before or at the
time of their next scheduled injection even if amenorrhoeic.
DMPA site of injection
- gluteal muscle preferred site for IM DMPA
- can be deltoid muscle
. If deep adipose tissue in gluteal area, standard-length needles may not reach muscle layer and SC DMPA or deltoid for IM DMPA should be considered. - SC DMPA should be injected into the abdomen or anterior thigh.
DMPA
Injection site reactions
- more common with SC than IM
DMPA
weight gain,
- associated with weight gain, particularly in women under 18 years of age with a body mass index (BMI) ≥30 kg/m2.
- Women who gain more than 5% of their baseline body weight in first 6 months of DMPA use are likely to experience continued weight gain.
DMPA & CERVICAL CANCER
- weak association b/w cervical cancer and DMPA for 5 years or longer.
- Any increased risk appears to reduce with time after stopping and could be due to confounding factors.
- up-to-date with cervical cytology screening and, if relevant, have completed HPV vaccination.
- inform: link between HPV and cervical cancer, and
- advise: reduce risk, as condom, smoking cessation,
regular cervical screening and, where appropriate, vaccination against HPV.
DMPA & thromboembolism
- causal association with VTE not demonstrated in small number of studies.
- From the limited evidence available it is not possible to confirm or exclude an association between POIC use and myocardial infarction or stroke.