Progestogen-only Injectable Contraception FSRH Mar 2015 Flashcards

1
Q

“progestogen-only injectable contraception”

When administered at the recommended dosing interval the failure rate in the first year of use & with typical use ?

A
  • approximately 0.2% in the first year of use.

- With typical use the failure rate is approximately 6%

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2
Q

DMPA use benefits

A
  • may reduce pain endometriosis.

- may reduce the severity of sickle crisis pain.

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3
Q

Use of DMPA & cancer risk

A
  • 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.
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4
Q

Use of DMPA

age

A
  • 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)
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5
Q

The efficacy of DMPA affected by?

A
  • 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.
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6
Q

DMPA timing

A
  • 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).
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7
Q

DMPA & unscheduled bleeding

A
  • 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.
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8
Q

DMPA & STI

A
  • 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.
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9
Q

DMPA & return of fertility

A
  • can be a delay of up to 1 year in the return of

fertility after discontinuation of IM or SC DMPA.

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10
Q

DMPA discontinue

Still wants contraception

A

to start another contraceptive method before or at the

time of their next scheduled injection even if amenorrhoeic.

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11
Q

DMPA site of injection

A
  • 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.
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12
Q

DMPA

Injection site reactions

A
  • more common with SC than IM
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13
Q

DMPA

weight gain,

A
  • 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.
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14
Q

DMPA & CERVICAL CANCER

A
  • 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.
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15
Q

DMPA & thromboembolism

A
  • 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.
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16
Q

Women using DMPA who wish to continue use should be reviewed How frequently?

A

every 2 years to assess individual situations, and to discuss benefits and potential risks.

17
Q

POIC & BMD

A
  • associated with a small loss, which is usually recovered after discontinuation.
18
Q

Whilst there is little evidence available to demonstrate causation, BUT have been reported with use of DMPA

A
acne, 
decreased libido, 
mood swings, 
headache, 
hot flushes and 
vaginitis .