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CMAJ : Canadian Medical Association Journal logoLink to CMAJ : Canadian Medical Association Journal
. 2014 Jan 7;186(1):13–14. doi: 10.1503/cmaj.131320

Medical abortion in Canada: behind the times

Sheila Dunn 1,, Rebecca Cook 1
PMCID: PMC3883814  PMID: 24277708

An estimated 1 in 3 Canadian women will have an abortion during her lifetime, most commonly performed in the first trimester of pregnancy.1 However, Canadian women lack access to a safe, effective and often preferred method of early abortion that is available in many other countries. The internationally recognized “gold standard” for medical (i.e., nonsurgical) abortion, mifepristone (followed by misoprostol), is not available in Canada. Although registered in 57 countries, mifepristone has yet to be approved and distributed in this country (Figure 1). Mifepristone became available in France and China in 1988, in the United Kingdom in 1991 and in most European countries by 1999. It was approved in the United States in 2000 and in Australia in 2012. Mifepristone is included in the WHO Model List of Essential Medicines,2 and yet Canadian women do not have access to it.

Figure 1:

Figure 1:

Approval of mifepristone between 1988 and 2013. Reproduced with permission. ©2013 Gynuity Health Projects.

There is now some hope that the situation may change. In 2012, a pharmaceutical company that supplies mifepristone in many countries, including France, Australia and Sweden, brought forward the first known new drug submission for mifepristone to Health Canada. The results of the submission are pending. It is important that this submission not be allowed to fail.

Medical abortion uses drugs rather than surgery to induce an early abortion. Mifepristone, developed in the 1980s for medical abortion, is an orally administered antiprogestin that blocks the action of progesterone, causing degeneration of the endometrial lining, softening of the cervix and sensitization to prostaglandins. Administration of a prostaglandin, typically the widely available misoprostol, at home 1–2 days after administration of mifepristone causes expulsion of the destabilized products of conception in a process similar to early miscarriage.2

Millions of women worldwide have used mifepristone safely and effectively. A recent systematic review of 45 000 abortions with mifepristone found that ongoing pregnancy occurred in only 1.1% of patients, less than 5% received a surgical procedure to complete the abortion and serious complications occurred in only 0.4%.3 Abortion with mifepristone is increasingly common and now accounts for more than 60% of abortions in some European countries and about 20% of abortions in the US.3,4

Unfortunately, Canadian women who want a medical abortion (assuming they can find a provider) must resort to a more cumbersome method that uses the cytotoxic drug methotrexate, followed 5–7 days later by misoprostol. Although the methotrexate–misoprostol approach provides a nonsurgical option, it is the second-best method. If allowed to take its course, the regimen is as effective as mifepristone and misoprostol for abortions at up to 7 weeks’ gestation, but its time course is longer and less predictable, with some abortions delayed several weeks after administration of methotrexate.5 Because methotrexate is teratogenic, the World Health Organization does not recommend it for abortion because of its association with serious deformities in the infant if the abortion fails and the pregnancy continues.2

In a randomized trial comparing the 2 methods, women found mifepristone to be more acceptable than methotrexate overall (88% v. 83%, p < 0.03), but more so for pain (86% v. 78%, p < 0.001) and wait time (92% v. 80%, p < 0.001).5 Abortions with methotrexate are also labour-intensive for practitioners, who must be willing to obtain the drug, administer it intramuscularly and follow women over weeks to ensure the abortion is complete. Therefore, it is not surprising that medical abortion is not widely used in Canada. A recent study from British Columbia, where most medical abortions in Canada are thought to be performed by a few large-volume providers, showed that 15% of abortions are done medically.6 Rates are thought to be much lower elsewhere in Canada.1

In fact, access to any type of abortion remains limited in many areas across Canada. A recent study that mapped women’s travel to abortion clinics showed that women from Atlantic Canada and those from rural and northern communities often travel long distances and face long wait times to obtain services.7 Better access to mifepristone abortion provided by primary care providers, including family physicians, nurse practitioners and midwives, could reduce these gaps in service delivery and free up operating room time. Availability of mifepristone in other countries has been associated with abortions occurring earlier in gestation, when they are safer, and in reduced wait times for surgical abortions.4

In 2009, The Society of Obstetricians and Gynaecologists of Canada urged Health Canada “to work with professional organizations and industry to make this product (mifepristone) available to women living in Canada.”8 So why is mifepristone still not available in Canada? One factor may be that pharmaceutical companies are deterred from bringing forward submissions because the Canadian market is relatively small, and obtaining regulatory approval can be costly. Some have also argued that Health Canada is biased against reproductive health medications, with more onerous requirements for regulatory approval compared with Europe and the US.9,10 Drug approval generally takes longer in Canada than in the US, but the lag time difference is longer for contraceptives.10

Is the Canadian government shirking its responsibility to facilitate availability of mifepristone, as some have suggested?9 Health Canada is accountable under the Canadian Charter of Rights and Freedoms to not unreasonably obstruct or delay women’s exercise of their rights to security, liberty and equality. Failure to provide essential drugs that only women need, including mifepristone, is a form of discrimination that Canada is obligated to remedy. Moreover, Canada, as a party to the International Covenant on Economic, Social and Cultural Rights, has a responsibility to undertake legislative, administrative and budgetary measures to ensure women’s right to health through access to essential reproductive health medicines.9

It is time that Canadian women had the ability to choose the best regimen for medical abortion. Availability of mifepristone, with the attendant probability of reduced demand and therefore shortened wait lists for surgical abortions, could improve the capacity of the health care system to provide abortions earlier, when they are safest. Moreover, the distribution of mifepristone would enhance access to abortion, particularly among underserved populations. Ultimately, the availability of mifepristone in Canada would provide an important therapy that would help to optimize the health of Canadian women.

Key Points

  • Canadian women lack access to the internationally recognized “gold standard” for medical abortion, mifepristone (combined with misoprostol).

  • Currently, Canadian women who want a medical abortion must resort to the second-best method, the cytotoxic drug methotrexate, followed 5–7 days later by misoprostol, a method that is not recommended by the World Health Organization.

  • Availability of mifepristone could improve access to abortion and improve the capacity of the health care system to provide medical abortions earlier, when they are safest.

Footnotes

Competing interests: Sheila Dunn is on the board of the National Abortion Federation, a nonprofit agency that promotes access to quality abortion care in the United States, Canada and Latin America. No competing interests were declared by Rebecca Cook.

This article was solicited and has not been peer reviewed.

Contributors: Both authors developed the idea for the commentary. Sheila Dunn wrote the medical content, Rebecca Cook wrote the legal content and both authors contributed to the policy component. Both authors approved the final version submitted for publication.

References

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