Oral contraceptives: selecting a pill

Oral contraceptive pills are a safe and effective contraceptive method widely used in New Zealand. For patients using a combined ethinylestradiol/progestogen pill, omitting the monthly withdrawal bleed may improve contraceptive efficacy and reduce associated symptoms such as pain, bloating or headache. Progestogen-only contraceptives are a suitable alternative for patients with contraindications to oestrogen use, such as those at high risk of venous thromboembolism.

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Key practice points:

  • Combined and progestogen-only oral contraceptives are equally effective for preventing pregnancy; the estimated rate of pregnancy is 2–3 per 1000 during the first year if used correctly and consistently, however, with typical use, the rate of pregnancy is 90 per 1000
  • A reasonable choice for a first-time combined oral contraceptive (COC)-user is a formulation containing ≤ 30 micrograms ethinylestradiol with either levonogestrel or norethisterone
  • Avoid use of COCs in patients with risk factors for venous thromboembolism, myocardial infarction or ischaemic stroke, such as those aged over 35 years who smoke, have migraine with aura or are likely to be immobile for a prolonged period, e.g. undergoing major surgery
  • Progestogen-only oral contraceptives, commonly referred to as progestogen-only pills (POPs), can be used if oestrogen is contraindicated
  • COCs can be initiated from six weeks post-partum in patients who are breastfeeding; previous guidance recommended waiting until six months post-partum

Oral contraceptives are available in two formulations, a combined ethinylestradiol/ progestogen pill and a progestogen-only pill (POP). Combined oral contraceptives (COCs) are generally the first-line choice for those who wish to use an oral contraceptive, unless oestrogen use is contraindicated. This is because COCs require less strict adherence to regular dosing times than POPs and provide additional non-contraceptive benefits. When COCs and POPs are taken correctly, the estimated rate of pregnancy is 2–3 per 1000 during the first year of use.1

COCs prevent ovulation, thicken cervical mucus to inhibit sperm penetration of the upper reproductive tract and alter the endometrial lining to make implantation less likely. They are taken as one pill, daily, at approximately the same time of day.

All COCs in New Zealand contain the same oestrogen (ethinylestradiol) in varying doses along with differing progestogens (Table 1). The progestogens vary in their androgenic properties; noresthisterone and levonorgestrel are more androgenic than desogestrel; drospirenone and cyproterone are anti-androgenic and therefore most effective for treating acne.2

Which COCs are available in New Zealand?

A range of fully or partly subsidised* COCs are available in New Zealand. Other unsubsidised oral formulations are also available. Formulations with lower doses of ethinylestradiol are just as effective for preventing pregnancy as those with a higher dose.3, 4

* For partly subsidised COCs, higher subsidy is available with Special Authority approval for patients with a low income if at least one fully subsidised option has been trialled and not tolerated, see: www.pharmac.govt.nz/2019/02/01/SA0500.pdf


Table 1: COC formulations available in New Zealand 5

Oestrogen (ethinylestradiol) dose Progestogen dose Brand names
20 micrograms Levonorgestrel 100 micrograms Microgynon 20
    Loette
Desogestrel 150 micrograms Mercilon
Drospirenone 3 mg     Yaz
30 micrograms

Levonorgestrel 150 micrograms

Levlen ED
    Ava 30
Microgynon 30
    Microgynon 30 (ED formulation)
    Monofeme
Desogestrel 150 micrograms Marvelon
Drospirenone 3 mg     Yasmin
35 micrograms

Norethisterone 500 micrograms

Brevinor * †
Norimin
Norethisterone 1 mg Brevinor-1 21 Day * †
Brevinor-1 28 Day ED
Cyproterone 2 mg     Estelle-35
    Estelle-35 ED
Ginet
    Diane-35 ED
50 micrograms Levonorgestrel 125 micrograms Microgynon 50 ED

Fully subsidised      Partly subsidised

ED = every day formulation – this is a COC regimen that includes placebo pills to be taken during the hormone-free interval. NB. Not all brand names include “ED” even though they are an ED regimen.

COC formulations that do not contain placebo pills
* Brevinor will be delisted from 01 July, 2019 and Brevinor-1 21 Day will be delisted from 1 Jan, 2020

Venous thromboembolism (VTE) risk

COC use is associated with a three to 3.5-fold increase in the relative risk of VTE.1 However, if there are no additional risk factors, the absolute risk of VTE associated with COC use is very small, particularly when compared to the risk during pregnancy and post-partum (Table 2).1 The risk of VTE is highest in the first few months after initiating a COC and reduces over the first year of use.1

If the patient has existing risk factors for VTE, the absolute risk is higher and COCs should not be used.

For information on non-oestrogen-containing contraceptive options appropriate for patients at high risk of VTE, see: “Contraception: which option for which patient”.

Risk factors for VTE that are contraindications to COC use include:1, 5, 6

  • Current or past VTE
  • Thrombogenic mutations, e.g. factor V Leiden,* prothrombin mutation, Protein S, Protein C, antithrombin deficiencies
  • Major elective surgery, any surgery to the legs or surgery resulting in prolonged immobility, i.e. more than one week
  • Age ≥ 35 years and smoke ≥ 15 cigarettes per day

* If homozygous for factor V Leiden or heterozygous with a history of VTE, COCs should be avoided. If heterozygous but no history of VTE and no alternative contraceptive is suitable, COCs may be used but avoid formulations with a higher VTE risk (Table 5).7

The COC should be stopped four weeks prior to surgery and can be restarted from two weeks after mobilisation.8 These recommendations do not apply to minor surgical procedures, e.g. a tooth extraction, or those requiring a short duration of general anaesthesia (< 30 minutes).8

Increasing age and smoking are independent risk factors for VTE, however, when these factors are in combination, the additive risks are considered to outweigh the benefits of COCs.1

Risk factors for VTE where COC use is strongly cautioned, include:1

  • Family history of VTE in a first-degree relative aged < 45 years
  • Immobile for a prolonged period due to illness or disability, i.e. without the added risk of VTE associated with surgery
  • Aged ≥ 35 years and smoke < 15 cigarettes per day or stopped smoking less than one year ago
  • Obesity (body mass index [BMI] ≥ 35 kg/m2)

Table 2: Risk of VTE for different patient groups9, 10

Group Risk of VTE per 10,000 females per year
Childbearing age, non-COC users 2–4
COC users 7–10
Pregnant and post-partum 20–30 *

* The risk of VTE two days before and after delivery is estimated to be 300–400 per 10,000 females per year and for the first 12 weeks post-partum is 40–65 per 10,000 females per year

Best practice tip: Remind patients who use COCs and are going to be travelling to maintain mobility on long-haul flights (> 3 hours). Compression stockings are not essential unless other risk factors for VTE are present.1 If the patient is going to spend more than one week at an altitude > 4500 metres they should consider switching to a non-oestrogen-containing contraceptive, particularly if they have other risk factors for VTE.1

Other cardiovascular disease (CVD) risk

COC use is associated with a 1.6-fold and 1.7-fold increase in the relative risk of myocardial infarction and ischaemic stroke, respectively.11* However, the absolute risk of each of these outcomes is small unless additional risk factors for arterial disease are present.1 It is estimated that among 10,000 females the use of COCs for one year would result in:1

  • Two additional cases of thrombotic stroke
  • One additional case of myocardial infarction

* The duration of COC use was not reported in this meta-analysis

COCs should not be used if there are additional risk factors for myocardial infarction or stroke, including:1

  • Hypertension (systolic ≥ 140 mmHg or diastolic ≥ 90 mmHg) or use of antihypertensive medicines, even if hypertension is well controlled
  • Multiple risk factors for CVD, e.g. increasing age, smoking, hypertension, obesity, dyslipidaemia, diabetes
  • Current or past ischaemic heart disease, stroke, complicated valvular or congenital heart disease, e.g. pulmonary hypertension, and other vascular disease
  • Impaired cardiac function or atrial fibrillation
  • Migraine with aura or migraine without aura that is new onset during use of COC *

* Could consider initiating a COC with caution if history of migraine without aura, provided no other CVD risk factors

Current breast cancer

COCs should not be used in patients with current breast cancer and use is strongly cautioned against in those with a history of breast cancer or who are known carriers of gene mutations associated with breast cancer, e.g. BRCA1 or BRCA2.1

N.B. COCs may be protective against ovarian cancer associated with these mutations; discussion with an oncologist is recommended.

Post-partum

COCs can be started from six weeks post-partum if breastfeeding, provided breastfeeding is well established and there are no concerns with the infant’s growth.1, 12

COCs can be started from three weeks post-partum if not breastfeeding, provided there are no other risk factors for VTE;* those with additional risk factors should wait six weeks to begin the COC.1

* Other risk factors for VTE post-partum include immobility, transfusion at delivery, BMI ≥ 30 kg/m2, caesarean section delivery, haemorrhage, pre-eclampsia, smoking

For further information on suitable contraceptive options post-partum, see: ”Contraception: which option for which patient?”.

Age ≥ 50 years

The use of COCs is not recommended in those aged ≥ 50 years due to the risks outweighing the benefits.13

For further information on suitable contraceptive methods for older patients, see: ”Contraception: which option for which patient”.

For further information on medical conditions where COC use is contraindicated or cautioned, e.g. systemic lupus erythematosus, refer to the New Zealand Formulary: www.nzf.org.nz/nzf_4178 and the United Kingdom Medical Eligibility Criteria: www.fsrh.org/standards-and-guidance/external/ukmec-2016-digital-version/

A reasonable option for a first-time COC user is 30 micrograms ethinylestradiol with either 150 micrograms levonorgestrel or 500 micrograms norethisterone. A lower dose of ethinylestradiol is recommended for older patients, e.g. > 40 years.13

The choice of oral contraceptive may also be influenced by whether the patient seeks non-contraceptive benefits from the medicine, e.g. a formulation containing cyproterone may be appropriate for a patient with acne or polycystic ovary syndrome, however the benefits should be weighed against the higher VTE risk.

If a patient experiences adverse effects with one COC, another formulation may be trialled (see: “Adverse effects depend on dosing and formulation” and Table 3).

COCs can be initiated on any day of the menstrual cycle, however, if starting six or more days after the onset of menses, condoms should be used for the first seven days of hormone pills.


Table 3: Managing adverse effects associated with COCs1, 2, 4, 5

Adverse effect Suggested actions
Acne Increase oestrogen; and/or
Decrease progestogen or select a less androgenic or anti-androgenic progestogen, i.e. desogestrel, drospirenone* or cyproterone
Bloating/fluid retention Decrease oestrogen; and/or
Change to a progestogen with a mild diuretic effect, i.e. drospirenone*
Breakthrough bleeding Increase oestrogen; and/or
Change the type of progestogen, e.g. levonorgestrel or desogestrel
Breast tenderness Decrease oestrogen and/or progestogen; and/or
Change progestogen, e.g. levonorgestel
Headache Decrease oestrogen; and/or
Change progestogen, e.g. levonorgestrel
If headaches occur in the hormone-free interval, consider an extended or continuous regimen
Abdominal cramping or heavy bleeding during the hormone-free interval Extended or continuous regimen
Nausea Decrease oestrogen and/or take the pill at night
Change to a POP

* Drospirenone may increase potassium levels. If there are risk factors for hyperkalaemia such as renal insufficiency, liver dysfunction or adrenal gland insufficiency a COC containing this progestogen should not be used. COC formulations containing drospirenone are currently not subsidised in New Zealand.

Tailored regimens can be offered to omit the pill-free week

COCs are typically taken in a regimen of 21 “active” hormone pills followed by a hormone-free interval of seven days, during which withdrawal bleeding occurs. However, there is no evidence to support any health benefits from having a monthly withdrawal bleed.1 Lengthening the hormone-free interval by missing pills at the beginning or end of a cycle may increase the risk of pregnancy by allowing follicular development and ovulation in some patients.1

Omitting the hormone-free interval may improve contraceptive effectiveness, reduce heavy bleeding and improve symptoms associated with the withdrawal bleed, such as bloating/fluid retention, headache and altered mood.1, 6 Data directly comparing the risk of cardiovascular events and cancer between standard and extended regimens are not yet available, however indirect evidence suggests no difference in cardiovascular risk.1 There is also no evidence of endometrial thickening or histological abnormalities with extended or continuous regimens.1 There is an increased risk of breakthrough bleeding when pills are taken continuously, but this declines with time.14

If breakthrough bleeding persists for three to four days when taking pills continuously, the pills should be stopped for four days and then resumed.1

If patients do not wish to omit the hormone-free interval completely, another option is to shorten this period from seven to four days. This reduces the chance of return to ovarian activity and therefore may decrease the risk of contraceptive failure, e.g. if pills are missed.1

A tailored regimen can be recommended to patients who are starting or already using a COC (Table 4). There is an additional cost associated with requiring more pill packs per year, i.e. if used continuously, a six-month prescription will last 18 weeks instead of 24 weeks. However, this cost may be offset by savings made from not having to purchase sanitary products.


Table 4: Examples of different regimens for COC use1

Regimen Duration of hormone pills (days) Hormone-free interval (days)
Standard 21 7
Shortened hormone-free interval 21 4
Extended 63 or 84, i.e. 3 or 4 packets of pills 4–7 (every 3–4 packets of pills)
Continuous use Continuous use of active pills None

Ensure that patients understand how to follow the tailored regimen correctly

Tailoring a COC regimen requires deviation from the instructions on the COC packaging which may lead to medicine errors. Discuss the regimen options with the patient and ensure that they understand how to omit the hormone-free interval, i.e. by discarding the unused placebo pills and starting on the next pack of active pills.

For further information on initiating an oral contraceptive, including changing from another method of contraception, refer to the New Zealand Formulary: www.nzf.org.nz/nzf_4163

Patient information on how to take a pill continuously can be found here: www.familyplanning.org.nz/advice/contraception/combined-oral-contraceptive-pill

Cancer

COCs are associated with a reduced risk of several cancers including endometrial, ovarian and colorectal cancers, but an increased risk of breast and cervical cancers.1

A longitudinal study conducted in the United Kingdom which followed females* for up to 44 years estimated that COC use resulted in the prevention of:17

  • 19% of colorectal cancers
  • 34% of endometrial cancers
  • 34% of ovarian cancers

COC use was associated with an estimated:

  • 25% of cervical cancers
  • 3% of breast cancers

The increased risk of breast and cervical cancer was only present in current and recent users; the risk was no longer present in this study five years after stopping the COC.17

* Average age at recruitment was approximately 28 years; 82% had at least one child at the time of recruitment

Human papillomavirus (HPV) infection is necessary for the development of cervical cancer. It is not certain whether the COC itself increases the risk of cervical cancer, or whether its use is associated with an increase in HPV infection rates due to sexual activity without a condom. COC use for more than five years is associated with a small increase in the risk of cervical cancer, but the risk reduces over time.1

Mood changes

Evidence of an association between COC use and changes in mood is variable. In one study of over 600 females, 16% reported a deterioration in mood while 12% reported an improvement in mood with use of COCs.18 COCs should be used with caution if there is a history of depression and all patients should be monitored for abnormal changes in mood.5

Weight gain due to use of COCs is unlikely

A 2014 Cochrane review covering 49 studies concluded there was no convincing evidence that use of COCs affects body weight or composition, and if any effect exists it is likely to be small.19

Progestogen-only formulations are a suitable alternative for those who wish to use an oral contraceptive but have contraindications to oestrogen use or prefer not to use a COC.

POPs thicken cervical mucus to inhibit sperm penetration and may also prevent ovulation (50% of cycles).20 The desogestrel-only formulation consistently inhibits ovulation (97% of cycles), but is not subsidised in New Zealand (Table 6).20

POPs can be initiated on any day of the menstrual cycle, however, if starting six or more days after the onset of menses, condoms should be used for the first two days (48 hours) of hormone pills.

Which POPs are available in New Zealand?

There is currently one fully subsidised POP available in New Zealand (Table 6). Although robust head-to-head studies are not available, evidence suggests that when used correctly the different formulations of POPs available in New Zealand are equally effective in preventing pregnancy.20


Table 6: POP formulations available in New Zealand 5

Progestogen type and dose Brand name
Desogestrel 75 micrograms Cerazette
Levonorgestrel 30 micrograms Microlut
Norethisterone 350 micrograms Noriday

Fully subsidised

Cautions and contraindications to POP use

POPs should not be used in patients with current breast cancer. They may be considered with caution, i.e. only if there are no other suitable options, if cancer has been in remission for more than five years.21 POPs, as with COCs, should be used with caution in patients with systemic lupus erythematosus who are positive for antiphospholipid antibodies, and in those with some liver diseases, e.g. decompensated cirrhosis.21

Correct and consistent use is essential for POPs to provide effective contraception

POPs are taken continuously, i.e. an active pill each day. Advise patients considering a POP that regular adherence is essential for these medicines to be maximally effective. Norethisterone and levonorgestrel-only pills must be taken within three hours of the regular dosing time each day. Desogestrel-only pills have a wider window for error and must be taken within 12 hours of the regular dosing time.

POPs offer the same level of contraceptive effectiveness as COCs and can be used in clinical situations where COCs are not recommended.20

POPs may be used when breastfeeding and can be initiated at any time post-partum, unlike COCs which should not be used in the first six weeks if breastfeeding (see: “Cautions and contraindications: when to avoid COCs”).1

Bleeding patterns may be unpredictable, due to the variable inhibition of ovulation; it is estimated that 50% of patients using a POP will continue to have a normal menstrual cycle, 40% an irregular menstrual cycle and 10% no menstrual cycle.22 Up to 70% of patients using POPs report breakthrough bleeding and 10% report frequent bleeding, i.e. more than five episodes in 90 days.20, 23

Problematic bleeding does not always settle over time. Changing to a different POP, e.g. a desogestrel-only pill, may improve bleeding regularity in some patients.20 An alternative method of contraception may be required in some cases.

N.B. There is no convincing evidence that POPs cause weight gain.24

The effectiveness of COCs and POPs can be reduced by interactions with medicines that induce hepatic metabolism by the CYP3A4 enzyme, e.g. rifampicin, rifabutin, carbamazepine, oxcarbazepine, nevirapine, phenytoin, phenobarbital, primidone, ritonavir, St John’s wort and topiramate.25 COC or POP absorption may be reduced by concurrent use of laxatives if they cause diarrhoea or are used excessively or inappropriately.

Interactions between oral contraceptives and other medicines can be checked here: www.nzf.org.nz/nzf_1

Managing patients taking enzyme-inducing medicines 25

Patients who are taking an oral contraceptive and an enzyme-inducing medicine short-term, i.e. less than two months, should be advised to use condoms for the duration of treatment with the enzyme-inducing medicine and for a further four weeks after stopping.*

* Using a high-dose COC, e.g. 50 micrograms of ethinylestradiol, has been suggested to counteract the change in hepatic metabolism, however there is no data on the contraceptive effectiveness of this approach.26

If the enzyme-inducing medicine is required long-term, recommend an alternative contraceptive, e.g. medroxyprogesterone injection or an intrauterine device.

For further information on the use of antiepileptic medicines in females, see: www.bpac.org.nz/2018/antiepileptic.aspx

Most broad-spectrum antibiotics do not interact with oral contraceptives

Most antibiotics, aside from rifampicin and rifabutin, do not have a clinically relevant interaction with oral contraceptives and patients do not need to take extra precautions as long as they are taking their contraceptive consistently and correctly.1 However, if the antibiotic or the illness it is treating causes vomiting or diarrhoea, additional contraceptive precautions might be required (see: “Recommendations for missed COCs or POPs”).

Acknowledgement:

Thank you to Dr Beth Messenger, National Medical Advisor, Family Planning New Zealand for expert review of this article

N.B. Expert reviewers are not responsible for the final content of the article.


Published: 7 March 2019 | Updated:

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