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Progestogen-only Contraceptive Pill

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Synonyms: POP, mini-pill

Mode of action1,2
  • Ovulation is inhibited in about 60% of cycles1 although it does not occur in 100% of cycles without hormonal contraception. With desogestrel ovulation is inhibited in 97% of cycles.3
  • Transport of the ovum is delayed.
  • The cervical mucus becomes more viscous and impenetrable to sperm.
  • The endometrium is unsuitable for implantation.
Advantages of a POP compared with a combined oral contraceptive (COC)2
  • It is an effective and safe form of contraception and is often used when combined pill contraindicated - e.g. venous thromboembolism or past history or tendency to venous thromboembolism.
  • It contains an even lower dose of progestogen than low-dose combined contraceptives and no oestrogen.
  • It is a suitable alternative for those over 35 who need to be changed from a COC, heavy smokers, those with hypertension, valvular heart disease, diabetes mellitus, migraine.There is however very little data on cardiovascular risk and the POP.
  • It can be used during breast feeding.
  • It is suitable for women with valvular heart disease and those about to undergo major surgery or surgery on their legs.
  • It is suitable for those who want a minimal dose of hormone as it gives a very low dose.
  • It can be used by those who must not take oestrogens for various reasons like a history of deep vein thrombosis or migraine with aura.
  • It is no less effective in women weighing over 70kg.
Disadvantages of a POP compared with a COC4
  • It has to be taken meticulously at the same time each day. The error for forgotten pills is just 3 hours late for POPs with the exception of Cerazette® that has a licence for 12 hours.
  • It is just as susceptible to substances that cause enzyme induction like rifampicin, many anticonvulsants and St John's wort. It is not affected by broad spectrum antibiotics.
  • It does not give the regulation of menstruation of the COC, including its tendency to alleviate symptoms of PMT, dysmenorrhoea and making menstruation lighter. It may produce irregular menstruation or amenorrhoea. This may be trouble enough for some to lead to cessation of the method. If oestrogen levels fall and cause amenorrhoea there may be concern that there is a risk of osteoporosis. This has been considered in relation to depot and implant contraception. An overview of the relationship between use of progestogen-only contraceptives and bone mineral density found little evidence about this in users of the POP, but the study involved only a small number of lactating women.5 A larger study suggested that there may be a skeletal effect.6
  • There is an increased risk of ovarian cysts, perhaps up to 30%. They are usually reversible and do not require operation.7
  • The data on the risk of breast cancer is unreliable because of small numbers but it may be that the risk is small but finite as with the COC. After stopping the method the risk disappears after 10 years.8
Contraindications4
  • The POP must not be used in the presence of breast cancer as this is a hormone dependent tumour. It may be considered if there has been no evidence of disease for 5 years if other methods do not seem acceptable.
  • The risk of thromboembolism is much less than with the COC but in the presence of deep vein thrombosis or pulmonary embolism it should be avoided.
  • There is concern about reduction in the levels of HDL, although this may be less marked with the newer progestogens. Hence they are better avoided in established CHD or stroke.
  • As with any other form of hormonal contraception it should be avoided in liver disease.
Instructions for use4
  • It is usually started on the first day of menstruation and then no additional contraceptive is required.
  • After childbirth it can be started on day 21, irrespective of whether the woman is breastfeeding. There is no need for contraception before then. There is a theoretical risk of intermenstrual bleeding if started earlier but the guidelines suggest that if the woman requests earlier contraception, this can be offered.9
  • It can be started immediately after termination of pregnancy in any trimester and it is immediately effective.
  • If changing from a COC to a POP, start at the end of a COC pack, moving straight on from the last COC pill to the POP the following day. If the COC is an ED (every day) pack then start after the last active pill.
  • Pills must be taken about the same time each day. It is regarded as late if it is taken more than 3 hours after the usual time or 12 hours with Cerazette®. The missed pill should be taken as soon as possible. The subsequent pills should be taken as usual but additional contraception should be used until pills have been taken correctly for 2 days.
  • Vomiting or severe diarrhoea may impair absorption of the hormone. Additional contraception should be used during this phase and for 7 days after.
  • Irregular menstrual pattern may settle with time or a change to a different formulation.
Desogestrel

Desogestrel is a newer progestogen that is converted in the body to the active form of etonogestrel. The only contraceptive pill containing desogestrel currently licensed in the UK is Cerazette®.10 Desogestrel tends to be metabolically "cleaner" than the older progestogens and appears very promising. Amenorrhoea is more likely to occur, being present in 50% of desogestrel users compared with 10% of those taking levonorgestrel in one study.11 Failure rate was also lower with desogestrel but the numbers were so small that confidence intervals were very wide and there was considerable overlap. The feature of this formulation that is likely to have the greatest impact is the 12 hours window for "forgetfulness" rather than just 3 hours.12


Document references
  1. No authors listed; A double-blind study comparing the contraceptive efficacy, acceptability and safety of two progestogen-only pills containing desogestrel 75 micrograms/day or levonorgestrel 30 micrograms/day. Collaborative Study Group on the Desogestrel-containing Progestogen-only Pill. Eur J Contracept Reprod Health Care. 1998 Dec;3(4):169-78. [abstract]
  2. Contraception - current issues: MeReC - 17 Number 2 (2006)
  3. Trussell, J. (2004) Contraceptive efficacy. In: Hatcher, R.A., Trussell, J., Stewart, F., et al, (Eds.) Contraceptive technology. 18th edn. New York: Ardent Media
  4. Contraception, Clinical Knowledge Summaries (2007)
  5. Banks E, Berrington A, Casabonne D; Overview of the relationship between use of progestogen-only contraceptives and bone mineral density.; BJOG. 2001 Dec;108(12):1214-21. [abstract]
  6. Hartard M, Kleinmond C, Luppa P, et al; Comparison of the skeletal effects of the progestogens desogestrel and levonorgestrel in oral contraceptive preparations in young women: controlled, open, partly randomized investigation over 13 cycles. Contraception. 2006 Nov;74(5):367-75. Epub 2006 Aug 17. [abstract]
  7. Tayob Y, Guillebaud J, Adams J, et al; Studies on ovarian function in users of the progestagen only contraceptive pill. J Obstet Gynaecol (Lahore). 1986 Apr;6 Suppl 2:S91-5.
  8. No authors listed; Breast cancer and hormonal contraceptives: collaborative reanalysis of individual data on 53 297 women with breast cancer and 100 239 women without breast cancer from 54 epidemiological studies. Collaborative Group on Hormonal Factors in Breast Cancer.; Lancet. 1996 Jun 22;347(9017):1713-27. [abstract]
  9. Contraceptive choices for breastfeeding women; National Guideline Clearing House 2008.
  10. Cerazette Guidance, Faculty of Family Planning and Reproductive Health Care (2003)
  11. No authors listed; Oral contraceptives and cardiovascular risk. Drug Ther Bull. 2000 Jan;38(1):1-5. [abstract]
  12. Summary of Product Characteristics - Cerazette® 75 microgram film-coated tablet (desogestrel); Organon Laboratories Limited, Updated May 2004; electronic Medicines Compendium.

Internet and further reading Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2008.
DocID: 471
Document Version: 3
DocRef: bgp146
Last Updated: 12 Oct 2008
Review Date: 12 Oct 2010

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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