Contraception Flashcards

1
Q

How are contraceptives broadly categorised?

Preferred method is life table failure probabilities.

Some methods have no difference between typical and perfect use failure rates and those that have large differences. There are also different likelihoods of discontinuation for different methods.

A

Long Acting Reversible Contraception (LARC): all require administration <1 per cycle: injectable, subdermal implant, copper IUD, progestogen-only intrauterine system (IUS).

Reversible: require action around time of sex: abstinence, male and female condoms, diaphragms, caps, sponges

Require regular action: POPs, COCPs, combined transdermal patch, combined vaginal ring, fertility awareness. NB: withdrawal and spermicide alone are not deemed effective methods of contraception in the UK.

Permanent: vasectomy (reversal can be attempted), tubal occlusion with clips/rings (usually via laproscopy); reversal can be attempted. Tubal occlusion via hysteroscope, reversal cannot be attempted.

Barrier methods: condoms, caps and diaphragms work by acting as a mechanical barrier to sperm (men – condoms, women – condoms diaphragms and caps). Condoms do not require additional spermicide. Generally recommended that spermicide is used with diaphragms and caps.

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2
Q

How does combined hormonal contraception act?

A
  • Ovarian suppression: decreased GnRH pulsatility in hypothalamus > decreased pituitary responsiveness to GnRH stimulation > suppression of LH + FSH production > inhibition of mid-cycle LH surge
  • Thickening the cervical mucus to prevent sperm entry into upper genital tract
  • Endometrial effect also doubtless occurs but contribution to the contraceptive effect has never been substantiated.
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3
Q

How does progestogen only contraception act?

A
  • Thickening of cervical mucus and a decrease in its amount (increased visoscity)
  • Ovulation suppression: prevention of LH surge - FSH + oestrogen remain in normal range
  • Endometrial alterations which may inhibit implantation (decrease in thickness)

Injectables suppress ovulation in all women (main mechanism of action). The POP may or may not suppress ovulation so main mode of action is on mucus (but the desogestrel POP suppresses ovulation in about 97% of cycles). The implant suppresses ovulation, but this is not absolute, especially towards the end of the 3 years.

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4
Q

How does progestogen only EMERGENCY contraception act?

A

Levonelle contains Levonorgestrel (3 days) or EllaOne contains UPA (5 days)

Follicular development arrested / delayed > LH surge blocked / delayed / blunted. No effect on sperm migration or tubal transport has been demonstrated.

There is no discernible effect on endometrial development. This means that progestogen-only emergency contraception in the luteal phase of the cycle may be less effective.

The progesterone receptor modulator (PRM) ulipristal acetate is now also available as emergency contraception (EllaOne). PRMs block receptors in the ovary, inhibit the LH surge and have a powerful endometrial inhibitory effect. The endometrial effect is probably not a significant mechanism of action at the low dose of ulipristal acetate used for emergency contraception.

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5
Q

How does the IUS act?

A

Profound effect on the endometrium and cervical mucus. The foreign body effect is much less important than with the IUD.

Endometrial proliferation is inhibited; the endometrium becomes thin + atrophic which makes it impossible for implantation. Cervical mucus becomes thickened and impenetrable to sperm. Although ovulation not usually inhibited, follicular diameter is reduced + the normal increased secretion of progesterone from the corpus luteum in the luteal phase (second half) of the menstrual cycle is reduced in some individuals.

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6
Q

How does the IUD act?

A

Foreign body reaction with increased prostaglandin production and leucocyte infiltration within the endometrium. The copper also affects endometrial enzymes, glycogen metabolism + oestrogen uptake. Copper has a direct toxic effect on sperm & ova.

Effect on endometrium as is apparent as sperm phagocytosis + interference with sperm transfer and implantation.

Prevention of fertilisation is considered to be the primary mode of action of IUDs when used as regular contraception. Prevention of implantation is a back-up mechanism in use a regular method of contraception, but is likely to be a more important mechanism in use as emergency contraception.

Primary effect through copper ions: direct effect on sperm and ova, decreased sperm motility and survival. Secondary effect on endometrium: sperm phagocytosis and impeded implantation.

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7
Q

Summarise how the IUD and IUS act differently?

A

IUD prevents fertilisation, IUS does not

IUS suppresses endometrium and thickens mucus, IUD does not.

BOTH will create a foreign body response and prevent implantation.

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8
Q

Outline whether the following primarily act on ovulation, cervix or endometrium

COCP
POP
Injection
Subdermal implant
IUS
A
COCP - ovulation
POP - cervix
Injection - ovulation
Subdermal implant - ovulation
IUS - endometrium
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9
Q

Efficacy vs effectiveness?

A

Efficacy: how well a method works in phase 3 trials. Subjects in the trials are not representative of the general population + daily calendar recording, which is mandatory in trials + enhances adherence.

Effectiveness: how well a method works in real life, effectiveness is dependent on using the method according to the instructions and not abandoning the method.

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10
Q

What is UKMEC?

A

Assessment of Risk & Medical Eligibility for Contraceptives - not to be substituted for clinical judgement + does not provide guidance on multiple comorbidities

UKMEC 1: condition with no restriction for use of method

UKMEC2: advantages of method outweigh theoretical or proven risk

UKMEC3: theoretical or proven risks usually outweigh advantages – can be used but may require expert clinical judgement and/or referral to specialist contraceptive provider, since use of method not usually recommended unless other methods not available or acceptable.

UKMEC4: condition which represents an unacceptable health risk if the method were to be used.

In general 2 or more category 2s does not necessarily make a 3, but two or more category 3s is likely to make a 4.

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11
Q

What might cause the UKMEC category to vary for a certain condition?

A

For a particular method, category may differ depending on:

  • Whether woman is starting a method of contraception when she already has a specific medical condition (initiation)
  • Whether she is continuing to use a method and develops a condition (continuation)

For example, if a woman has an MI while taking the POP (continuation) this is regarded as UKMEC3. If woman has had MI in past (initiation) wishes to start POP – UKMEC2.

Duration of use particularly relevant when assessing safe continuation. e.g. if POP is used for many years and symptoms are of recent onset, continuation is unlikely to be a problem, whilst recent initiation and recent symptom onset may make continuation less safe.

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12
Q

History taking before deciding on contraceptive method? / exams?

A
  • Vascular: headache especially migraine, veins: varicose, phlebitis, thrombosis, heart disease: ischaemic, valvular, congenital, stroke, hyperlipidaemia, venous thromboembolism: especially if on anticoagulants
  • Medical conditions: epilepsy, liver/gall bladder disease, autoimmune diseases, bowel disorders, diabetes, cancer (especially breast, ovarian, endometrial)
  • Lifestyle: smoking status, partner(s) in <12 months, sexual activity, contraceptive history: previous use and experience of methods
  • Other medical history: mental health, especially depression, medication, allergies, including latex, immobility, STIs / HIV / PID, FHx: MI, CV incident, VTE and breast/ovarian cancer in 1st degree relatives, last menstrual period, unexplained vaginal bleeding, obstetric history (deliveries, caesareans, miscarriages, abortions, ectopics), postpartum (breast feeding or not), post-abortion, gynae problems: severe dysmenorrhoea, endometriosis (fibroids, toxic shock syndrome), GTD, CIN

BP management only relevant for oestrogen containing products.

Weight & height relevant for oestrogen and a baseline for those initiating hormonal products who may gain weight or perceive weight gain / bloating.

Pelvic examination must only be performed when strictly necessary. IUD/IUS/female barrier/combined vaginal ring: pelvic examination. General principle is that exams must be relevant to method – lab investigations rarely needed (waste resources). Over-medicalisation of contraceptive consultation can be off-putting for women (especially young)- can become barrier to access.

Combined hormonal: BP at 3 month review, BMI at baseline, annual check BP and BMI.

Urine, blood testing and breast exam are not indicated / not evidence based.

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13
Q

Migraine with aura - UK MEC?

A

COCP UKMEC4 – risk of ischaemic stroke in pill takers without aura has no increased risk or 3x increased risk.

Migraine with aura risk ranges from 2x increase to 9x increase in different studies.

Progestogen only method is UKMEC2.

Combined vaginal ring and combined transdermal patch are UKMEC4 (oestrogen).

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14
Q

How to differentiate migraine with aura from other headaches?

A

Positive response to recent unilateral headaches associated with nausea photophobia and malaise in otherwise well person suggests migraine

Headache in migraine typically throbbing, whereas tension headache usually described as pressure or muscle tightness

Migraine: premonitory phase (craving / tiredness / heightened perception / fluid retention) may or may not be followed by aura. Aura lasts <1 hour then headache starts.

Migraine with aura is less common than migraine without aura. Most auras = bright homonymous scotoma which gradually enlarges from a small spot into a C-shape. Sensory symptoms are less common than visual symptoms in aura - generally consists of pins and needles spreading up the arm and into face. Speech disturbance is rare

V important to distinguish aura symptoms from not aura - generalised flashing lights or blurred vision and photophobia are not part of aura

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15
Q

BMI UKMEC?

A

Obesity is risk factor for combined hormonal contraception (CHC). Care must be taken when making clinical judgements about BMI – pregnancy has higher risk of VTE than taking CHC!

30-34 = UKMEC2
35 = UKMEC3
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16
Q

3 types of COCP?

A
  • Monophasic COCP (most widely used): 21 identical daily tablets, followed by 7 pill free days (withdrawal bleed)
  • Phasic COCP : diff hormone strengths taken in order mimicking hormonal fluctuations of a normal cycle – withdrawal bleed usually occurs in pill free interval (PFI)
  • Every day COCP: placebo pills taken instead of PFI
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17
Q

Non-contraceptive benefits of the COCP?

A
  • Regulate menstruation and decrease blood loss
  • Reduce risk of benign ovarian cysts and functional ovarian tumours (related to duration of use)
  • Raises sex hormone binding globulin (SHBG) levels and suppresses ovarian androgen production – may lead to reduction in hirsutism, acne and seborrhoea with maximum benefit after 3-6 months.
  • Reduction in risk: ovarian cancer 50% cumulative over 15 years, endometrial cancer 0.5 RR, colorectal cancer 0.82 RR
  • Endometriosis: drug of choice for symptoms of endometriosis – safe and economical alternative to surgery
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18
Q

COCP and VTE?

A

Increases risk

But pregnancy is higher risk

Increased by smoking, obesity and postpartum

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19
Q

COCP and ischaemic heart disease?

A

May be very small increased risk, this risk increases with smoking and hypertension

UKMEC3 - adequately controlled HTN, BP 140-159/90-99, smoking <15/day and age >35, stopped smoking <1 year and age >35

UKMEC4 - >160 / 100, vascular disease, smokes >15/day and age >35

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20
Q

COCP and breast cancer?

A

Advise women that if there is an increased risk of breast cancer it is likely to be very small and to return to background risk ten years after stopping

UKMEC3 - remission and no recurrence last 5 years, carrier of mutation associated with breast cancer e.g. BRCA1, past history of breast cancer

UKMEC 4 - current breast cancer

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21
Q

UKMEC3 for COCP?

A

Gall bladder disease - symptomatic, medically treated or current

Past CHC related cholestasis

Multiple risk factors for CV disease

Diabetes with nephropathy / retinopathy / neuropathy and other vascular disease

Acute viral hepatitis or flare at initiation

Complicated organ transplant

History of bariatric surgery with BMI >35

Breast cancer - remission and no recurrence last 5 years, carrier of mutation associated with breast cancer e.g. BRCA1, past history of breast cancer

Adequately controlled HTN, BP 140-159/90-99, smoking <15/day and age >35, stopped smoking <1 year and age >35

22
Q

UKMEC4 for COCP?

A
Severe decompensated cirrhosis
Stroke
Current or history of IHD
Vascular disease
Complicated valvular and congenital heart disease
Cardiomyopathy with impaired cardiac function
Atrial fibrillation
Hepatocellular carcinoma and adenoma
23
Q

COCP and cervical cancer?

A

Associated with increased risk of squamous carcinoma of cervix (starting 5 years after use). The risk returns to baseline after 10 years cessation of COC. Therefore after 10 years of use, risk of cervical cancer may double, even among women who are HPV negative, but there is no acceleration of the disease and the combined pill is not causative.

Women taking the CHC do not require extra cervical screening and should have cervical screens as indicated by the National Cervical Screening Programme.

24
Q

Side effects of combined hormonal contraception?

A

Hormone-related side effects:

  • Breast tenderness/enlargement
  • Bloating
  • Nausea
  • Increased non-infective vaginal discharge
  • Headache
  • Chloasma (skin pigmentation – may persist for a long time after method is stopped)
  • Acne
  • Greasy skin / hair
  • Depression
  • Hirsutism
  • Loss of libido
  • Vaginal dryness

Breakthrough bleeding common when CHC method commenced and may also occur if used incorrectly. Try and exclude other causes: disease, drug interactions (inducers), miscarriage, diarrhoea/vomiting, disturbance of absorption, dose, duration of use (more common in first few months)

Specific to CTP: skin reaction to adhesive / patch material, skin discolouration around patch

Specific to CVR: vaginitis, awareness of CVR during intercourse, foreign body sensation, ring expulsion

25
Q

Describe combined hormonal contraception (not including the pill)

A

Combined transdermal patch

  • Three layer matrix patch contains hormones between 2 polyester films
  • 28 day patch cycle – applied weekly on same day for 3 weeks, followed by one patch free week

Combined vaginal ring

  • Soft ring releases 15mcg ethinyl estradiol and 120mcg etonogestrol daily. Stored in pharmaceutical fridge – only 4 months active life following dispensing. Most clinics prescribe 3 months at a time.
  • CVR cycle: single cycle contraceptive, which is inserted into the vagina and after 3 weeks of continuous vaginal use it is removed and discarded. A seven day ring free interval follows, during which a withdrawal bleed usually occurs.
26
Q

What is the SDI? How does it work?

A

Subdermal implant

Primarily through inhibition of ovulation by prevention of LH.

Increased viscosity of mucus inhibits sperm penetration. Possibly prevents implantation by thinning the endometrium.

One day after insertion, levels of ENG are sufficient to inhibit ovulation. Within a week after removal ENG drops to an undetectable level. >90% of women ovulate in the first 30 days after removal.

27
Q

Pros of the SDI?

A
  • Highly effective
  • Long action (3 years)
  • Independent of intercourse
  • Quickly reversible
  • No user-failure
  • Estrogen-free
  • No relevant effects on metabolism (lipids, clotting, blood pressure and therefore no increased risk of thrombotic events or decrease in BMD)
  • Relief of dysmenorrhoea and ovulatory pain
  • Very few contraindications
28
Q

Side effects of the SDI?

A

Bleeding pattern changes, acne worsening or improvement, localised atrophy possible over area of implant

Infrequent bleeding is the most common change seen after insertion of SDI, occurring in 1/3 of women. Amenorrhoea occurs in 20% of women, however, about ¼ have prolonged or frequent bleeding which is the most common reason for dissatisfaction with the method and requests for removal. Preparation by counselling important.

30% removed within 2 years – 80% of those cases due to bleeding problems. Eligible women may be offered COC cyclically or continuously for 3 months (outside product licence) after exclusion of other causes.

Can be used on women up to 55 years. If stopped earlier, FSH level tests 1-2 months apart. If both levels above 30, ovarian failure likely. Continue implant for 2 years if under 50, continue for 1 year if over 50.

Efficacy may be reduced by enzyme inducing medication – additional cover for 28 days after stopping them. They do not affect breast feeding.

29
Q

SDI UKMEC categories?

A

No evidence of change to weight/mood/libido and no evidence for causal association with headache, but women who have migraine with aura, or who develop migraine +/-aura are put in UKMEC2.

UKMEC 3 - current IHD (continuation), stroke (continuation), unexplained vaginal bleeding (suspicious for serious underlying condition), past history of breast cancer, cirrhosis (severe decompensated), liver tumours (benign hepatocellular adenoma or malignant)

UKMEC 4 - current breast cancer

30
Q

Male sterilisation

A

Spermatozoa are manufactured in the testes and stored there + in the epididymis. They travel up the vas deferens passing the seminal vesicles and the prostate gland. Sperm then travel through the penis and are released by ejaculation. The purpose of male sterilisation to block passage of sperm > azoospermic and infertile.

After procedure, sperm continue to be made but due to the blockage of the vas deferens, unable to move proximally to be released. The sperm then gradually age + deteriorate and are removed by the body’s immune system. The ejaculate is unchanged in quantity but may appear initially blood-stained (haematospermia – normal immediately after a vasectomy) and then later slightly less cloudy. The vasectomy does not cause impotence or lower the libido.

31
Q

How to rank effectiveness of family planning methods

A

% = number in every 100 women who experience unintended pregnancy within first year of typical use

Implant - 0.05%
IUD - 0.2% LNG, 0.8% copper T
Female sterilisation - 0.5%
Male sterilisation - 0.15%
Injectable - 6%
Pill - 9%
Patch - 9%
Ring - 9%
Diaphragm - 12%
Male condom - 18%
Female condom - 21%
Withdrawal - 22%
Sponge - 12% nulliparous women 24% parous women
Spermicide - 28%
32
Q

What may affect absorption / metabolism of hormonal contraception?

A

Oral EE and progestogens absorbed in mall intestine, may be affected by vomiting, diarrhoea, chelating drugs and those altering gastric pH / gut transit. PPIs, antacids and H2 antagonists increase gastric PH and may reduce absorption / efficacy of ulipristal acetate (UPA).

If CYP450 INDUCED - increases metabolism and decreases contraceptive efficacy (antiepileptics, rifabutuin / rifampicin, antiretrovirals, st joh’s wart, modafanil etc)

If CYP450 INHIBITED - lowers metabolism and increases contraceptive efficacy (erythromycin, fluconazole, itraconazole, ketoconazole, ataanavir, tacrolimus, etoricoxib, atorvastatin, sitaxetan sodium)

lamotrigine and griseofulvin not enzyme inducing but thought to reduce contraceptive efficacy. unclear whether acitretin, etretinate and isotretinoin (retinoids) affect the reliability of oral POPs but not considered reliable enough for use with these teratogens. COCPs not affected.

33
Q

Smoking guidelines for combined hormonal contraception?

A

If age >35

<15/day - UKMEC 3
> = 15/day - UKMEC 4
Stopped <1 year - UKMEC 3
Stopped > = 1 year - UKMEC 2

BMI + BP documented for all women prior to first CHC prescription.

34
Q

CHC - what to do if missed pill?

A

Missed pill = >24 hours late (48 hours from last pill) but <48 hours late. Should take missed pill as soon as remembered and remaining pills continued at usual time.

If 2 pills missed (more than 48 hours late); take most recent as soon as possible, remaining continued at usual time. Condoms should be avoided or sex avoided until 7 consecutive active pills have been taken.

If pills are missed in first week (pills 1-7) consider EC if sex occurred in pill-free interval or in first week of pill taking

If missed in second week (pills 8-14) no indication for EC if preceding week taken consistently and correctly - assuming pills thereafter taken correctly and additional precautions are taken

If missed in 3rd week (15-21) - OMIT pill free interval by finishing pills in current pack (or discarding placebos) and start a new pack next day.

35
Q

What to do if missed transdermal patch?

A

If patch delayed or detached <48 hours, apply new one with no additional precautions.

If patch delayed or detached >48hrs, new patch with additional protection for 7 days and consider EC if unprotected sex in patch free interval.

Change new patch day accordingly.

36
Q

What to do if missed combined vaginal ring?

A

New inserted and retained for 3 weeks – does not need to be positioned precisely. Removal is followed by 7 day ring free interval after which new CVR is inserted.

Delayed insertion <48 hours – change ring with no additional cover.

If >48 hours, change ring and additional cover for 7 days.

Consider EC if unprotected sex in ring free interval. If extended use <4 weeks, ring free interval can be taken with no additional cover. If >4 weeks, change ring and additional cover required for 7 days. However, if >4 but less than 5 weeks, efficacy could be maintained by immediately starting new ring without ring free interval.

37
Q

What are different types of POP?

A

Traditional = norethisterone (Micronor, Noriday) or levonorgestrel (Norgeston). Work primarily by thickening cervical mucus. Must be taken within 3h of same time each day.

With traditional POPs, frequent and irregular bleeding is common while prolonged bleeding and amenorrhoea are less likely.

Desogestrel (DSG) containing POPs - primarily by supressing ovulation. May be more effective and less likely to be associated with follicular cysts / ectopic pregnancy. May be more suitable for younger women or those with Hx of symptomatic simple ovarian cysts. Must be taken within 12h of same time each day.

With DSG-containing POPs:

  • 5 in 10 amenorrhoea or infrequent bleeding
  • 4 in 10 regular bleeding
  • 1 in 10 frequent bleeding.

Efficacy is altered by liver inducing enzymes.

38
Q

How to injectable progestogens work?

Are they likely to fail?

A

DMPA IM or SC. Given every 13 weeks. Women will self-administer first dose following training under supervision of professional. Both can be given late: up to 14 weeks without the loss of contraceptive cover or the need for extra contraceptive precautions.

Work primarily by inhibiting ovulation and changing cervical mucus to limit sperm penetration.

Like all LARCs they have very low typical user failure rate – 6% in real life and 0.2% in first year of perfect use. Failure could occur if:
• DMPA (IM and SC) later than 14 weeks since last injection
• NET-EN later than 10 weeks since last injection
• Woman was already pregnant when last injection was given

39
Q

How safe are injectable progestogens?

A

Safe for more women. UKMEC3: multiple risk factors CVD, vascular disease, stroke, current and history of IHD, past history breast cancer, cirrhosis (severe decompensated), malignant liver tumour or hepatocellular adenoma, unexplained vaginal bleeding. UKMEC4: current breast cancer.

40
Q

Compare the POP to COC

A

POP - causes irregular bleeding patterns, suitable for all ages, suitable regardless of BMI, suitable for migraine with aura, taken every day with no pill free interval

COC - risk of VTE increases with use, regulates bleeding patterns, not suitable for women >50, not recommended if BMI >35, not recommended for migraine with aura

41
Q

Non-contraceptive benefits of injectable progestogens?

A
  • Reduction in menorrhagia and dysmenorrhoea
  • Improvement in symptoms of endometriosis
  • Possible reduction in risk of endometriosis and ovarian cancer
  • Up to 70% of DMPA users are amenorrhoeic at one year of use, which may help with anaemia
  • May reduce the severity of sickle crisis pain in women with sickle cell disease
42
Q

Side effects of injectable progestogens?

A
Altered bleeding pattern, amenorrhoea/infrequent bleeding/spotting/prolonged bleeding. 
Weight gain (but not restricted in obesity). 
Injection site reactions (induration, scarring, atrophy). 
No evidence for headache/mood change/vaginitis/loss of libido. Acne reported but not commonly caused by injectables. Breast tenderness rare but galactorrhoea recognised side effect and serum prolactin should be checked if it occurs. 

Bone mineral density drop: caution in women >45 and <18 (UKMEC2). Women generally advised to switch to another method at age 50, if not then consider continuing with benefits and risk assessment – no upper limit for duration of use.

Possible 1 year delay in return of fertility but no reduction long term

May be weak association with breast cancer. Prolonged (>5 year) use has weak association with the occurrence of cervical cancer which may reduce with time after cessation.

Limited evidence for association with MI/stroke. Small number of studies failed to show association with VTE.

Ideally start on days 1-5 of cycle (no additional contraceptive required). Can start at any time if certain not pregnant but additional cover needed for 7 days. Postpartum can start with immediate effect but if after day 21 postpartum need 7 day cover. If still breastfeeding delay until atleast 6 weeks post natal (UKMEC2).

If initiated first 5 days following miscarriage/abortion – immediate action. If later than day 5 need additional cover for 7 days. Following emergency contraception or where pregnancy cannot be excluded – immediate use but additional cover for 7 days – should pregnancy occur NICE advises no harm to fetus.

Changes in bleeding patterns are associated with dissatisfaction amongst some users and women should be advised about changes that will occur

No with liver enzyme inducing drugs but may reduce efficacy of UPA (emergency contraceptive).

43
Q

Diaphragms and caps?

A

Both require spermicide. Only cover cervix (don’t prevent exposure to vaginal mucosa / cervico-vaginal secretions).

3 caps: arcing spring, coiled spring and polymer spring.

  • arcing spring easier to insert correctly and good if high vaginal tone
  • coil spring may be more comfortable
  • silicone polymer designed to fit 80% of women (one size) does not require fitting by professional

One type of cap available in 3 sizes. If in situ for >3 hours need additional spermicide cream and must be left in situ >6 hours after last SI. Diaphragms max 30 hours, and caps max 48 hours.

Diaphragms and caps may be unsuitable if: woman is at risk of HIV, woman has history of TSS, vaginal muscles cannot hold diaphragm, cervix unusual shape or malpositioned, sensitivity to spermicide or latex or silicone materials, woman is uncomfortable about vaginal self-examination.

Cystitis due to bladder base irritation if diaphragm too large – changing to smaller or softer rimmed (coil spring) diaphragm or cervical cap may help with symptoms of recurrent cystitis.

Health professional must: advise about use, perform vaginal exam to identify appropriate size, select most appropriate device, ensure cervix is covered by method chosen.

Emergency contraception: if dislodged or removed within 6 hours, if left in longer than three hours before sex and no additional spermicide applied. Condom splittage/breaking/slippage.

Not advised if high risk of HIV (spermicide use can cause genital lesions which increases transmission risk).

Avoid use during menstruation and in people with TSS history. Unsuitable if less than six weeks postpartum.

44
Q

Advantages of copper IUD?

A
Immediately effective
Long lasting (5-10 year license)
No systemic side effects
Not reliant on user's memory
Do not interact with other drugs
Independent of SI
Easily reversible
No effect on lactation
Inexpensive
Does not affect return to fertility
Can be used for EC within 120 hours of first UPSI in a cycle or up to 5 days after estimated day of ovulation
May be associated with reduced risk of endometrial and cervical cancer
45
Q

Disadvantages of copper IUD?

A
Periods may be longer, more painful and up to 50% heavier
Infection
Expulsion
Perforation
Ectopic pregnancy
46
Q

Non-contraceptive uses of hormonal IUD?

A

Mirena

First-line for heavy bleeding, reduction in menstrual loss of up to 90% by one year is usual, many amenorrhoeic by 3-6 months

Licensed for 4 years of endometrial protection in women using oestrogen replacement therapy, although the FSRH advise it may be used for 5 years

Effective first line Tx for dysmenorrhoea in absence of heavy bleeding (unlicensed)

May be used as Tx for endometriosis (unlicensed) - symptoms improve presumably due to hormonal effect on patches of endometrial tissue

Not officially advisable in women with fibroids but evidence suggests can reduce symptoms and cause the fibroids to shrink

Insufficient evidence that Mirena alone effective in Tx of prementrual symptoms

Levosert - similar to Mirena however not licensed for endometrial protection in women using oestrogen replacement therapy

47
Q

Advantages of hormonal IUD

A
Effective
Long lasting - 3 (Jaydess), 4 (Levosert) or 5 (MIrena / Kyleena) years for contraception
Reversible
Not reliant on memory
May reduce dysmenorrhoea
No effect on lactation
Does not react with other drugs
Does not affect return to fertility
Menstrual loss reduced by up to 90% (Mirena / Levosert) - kyleena and jaydess also reduce loss but to lesser extent
Independent of SI
Little or no increased risk of VTE or MI

NOTE: LNG-IUS not effective or licensed for EC use

48
Q

Side effects of hormonal IUD?

A

Breast tenderness, acne, bloating, mood change, headaches may occur but not significantly different from hormonal symptoms experienced in CU-IUD users
Increased incideince of benign functional ovarain cysts with 52mg LNG-IUS use, however, majority asymptomatic and resolve spontaneously

Irregular bleeding and spotting common in first 6 months after insertion

Despite lower levels of LNG with Kyleena and Jaydess, current evidence does not suggest any clinically significant advantage in terms of side effect profile

49
Q

Complications of both the Cu-IUD and LNG-IUS?

A
  • Expulsion (1 in 20, most common in first year of use especially 3 months, small increase risk post abortion)
  • Infection: first 20 days, BV associated with Cu-IUD.
  • Perforation (rare), 6x higher if breastfeeding
  • Ectopic: 18-50% risk ectopic if pregnancy does occur, but risk is lower than no contraception. Previous ectopic not a contraindication (UKMEC1).
  • Ovarian cysts; with LNG-IUS most asymptomatic and resolve spontaneously.
50
Q

Timing of insertion for Cu-IUD?

A

Any time if no risk of pregnancy (abstinent that cycle or using hormonal or barrier method consistently and correctly), from 4 weeks after vaginal delivery or C-section, immediately after 1st or 2nd trimester abortion

For EC up to 5 days after earliest expected day of ovulation or can be inserted on any menstrual cycle day if all episodes of unprotected SI occurred within the previous 120 hours.

51
Q

Timing of insertion for LNG-IUS?

A

Safely inserted as late as day 7 with no risk of pregnancy from UPSI earlier in the cycle or after insertion

Any time if no risk of prengnacy (abstinent or contraception), extra precautions needed for 7 days if fitted later than day 77, from 4 weeks after delivery or CS, immediately after 1st or 2nd trimester abortion

Not suitable for EC use.

52
Q

Timing of follow up visits for an IUD?

A

advisable to see women 3 weeks after insertion of Cu-UID for EC, exclude preg and expulsion of device and to ascertain future need.

Routine can be advised after first period following insertion or 3-6 weeks later.