A more accurate approach to define abortion cohorts using linked administrative data: an application to Ontario, Canada
Main Article Content
The shifting landscape of abortion care from a hospital-only to a distributed service including primary care has implications for how to identify abortion cohorts for research and surveillance. The objectives of this study were to 1) create an improved approach to define abortion cohorts using linked administrative data sets and 2) evaluate the performance of this approach for abortion surveillance compared with standard approaches.
We applied four principles to identify induced abortion cohorts when some services are delivered beyond hospital settings; 1) exclude early pregnancy losses and postpartum procedures; 2) use multiple data sources; 3) define episodes of care; 4) apply a hierarchical algorithm to determine abortion date to a population-based cohort of all abortion events in Ontario (Canada) from January 1, 2018-March 15, 2020. We calculated risk differences (RD, with 95% confidence intervals) comparing the proportion of medication vs. surgical, first vs. second trimester, and complication incidence applying these principles vs. standard approaches.
Hospital-only data (versus multiple data sources) underestimated the frequency of medication abortion (16.1% vs. 31.4%; RD -15.3% [-14.3, -16.3]) and first-trimester abortion (82.1% vs. 94.5%; RD -12.8 [-11.4, 13.4]) and overestimated incidence of abortion complication (2.9% vs. 0.69%; RD 2.2% [1.8, 2.7]). An unlinked (versus linked) approach underestimated the frequency of abortion complications (0.19% vs 0.69%, -RD 0.50% [-0.44 - -0.56]). Including (versus excluding) abortions following early pregnancy loss or delivery events increased the estimated incidence of abortion complications (1.29% vs. 0.69%, RD 0.60% [0.51-0.69].
New methods are required to accurately identify abortion cohorts for surveillance or research. When legal or regulatory approaches to medication abortion evolve to enable abortion in primary care or office-based settings, hospital-based surveillance systems will become incomplete and biased; to continue valid and complete abortion surveillance, methods must be adjusted to ensure complete capture of procedures across all settings.
Accurate health service utilization and safety surveillance data are essential for health policy and for decision-makers to plan, evaluate, and improve health service delivery, access, and health outcomes. Abortion frequency, access, and outcomes are key indicators of a jurisdiction’s reproductive population health, necessary for understanding access to family planning services and women’s health [1, 2]. Monitoring the incidence of pregnancy, abortion, and birth is important to understand population trends in fertility and the ability for individuals and families to achieve their reproductive goals [2, 3]. Accurate tracking of abortion frequency enables surveillance of abortion safety, a key component of reproductive population health .
The centrality of sexual and reproductive health service access for reproductive population health and gender equity is demonstrated by its inclusion as target 5.6 in the United Nation’s Sustainable Development Goal 5 “Achieve gender equality and empower all women and girls” . Abortion, however, is unlike other reproductive health outcomes (e.g., births and infant deaths , severe maternal morbidity ) in that it is illegal in some settings and stigmatized in others. This often impacts the quality of abortion surveillance data .
Over the past four decades, abortion practice has changed substantially across the globe with the advent of mifepristone, a highly effective medication abortion drug. First synthesized in 1980, mifepristone was approved for use for induced abortion in 1988 in France, 1991 in Great Britain, 1992 in Sweden, 2000 in the United States and 2015 in Canada [7, 8]. Before mifepristone availability, the vast majority (>95%) of abortions in the first trimester (i.e., less than 14 weeks of gestational age) were provided as surgical procedures, via vacuum or suction aspiration . Although the rate of mifepristone uptake following regulatory approval has varied substantially by country [7, 10]; in 2018, mifepristone medication abortion accounted for more than a quarter of abortions in Canada  and nearly 40% of abortions in the United States . In 2020, nearly 75% of abortions in England and Wales , and over 80% of abortions in Sweden  were provided using mifepristone. In most settings, regulatory restrictions on mifepristone provision, such as observed dosing, only-by-physician dispensing, or restrictions on the location where an abortion may be performed, have resulted in mifepristone medication abortion delivery in purpose-specific abortion clinics, most usually those that also provide surgical abortion services. However, in some settings (e.g., Canada)  mifepristone is now regulated as a normal prescription medication (without medication-specific regulatory limits), and as a result medication abortion provision frequently occurs in distributed, generalist office-based and primary care settings .
In some countries, induced abortion surveillance historically relied on single data sources . This approach supports valid surveillance if the single source captures all abortions. For example, in Canada, abortion care was restricted to hospital-based provision from decriminalization in 1969 until a Supreme Court decision removed the hospital-based abortion service requirement, which facilitated abortion provision outside hospital settings, in 1988 [15, 18]. Thus, hospital-based abortion surveillance data provided accurate measures of abortion frequency, characteristics, and complications until 1988, after which multiple data sources were required for accurate surveillance [15, 17, 19]. In the United States, induced abortion surveillance is conducted by the Centres for Disease Control and Prevention based on voluntary state-level reporting (33 of 50 states report) with limited detail or follow-up and no individual-level data available . In contrast, in many countries, such as Finland, England, Scotland, and Wales, physicians providing abortion services must report each abortion directly to a national registry of induced abortions using a standardized form . Creating abortion cohorts using multiple data sources requires careful consideration of situations in which a single abortion event may generate multiple encounters in various data sets. For example, an uncomplicated medication abortion would generate both a practitioner billing and pharmacist dispensation records, while an abortion resulting in a complication may also follow-up encounters in office-based or hospital settings.
The shifting landscape of abortion care provision has implications for how we capture and analyze these services. In settings where abortion care has expanded from exclusively hospital-based provision of surgical abortion to distributed provision of both surgical and medication abortion in a range of community healthcare and office settings, surveillance using hospital-only data will no longer capture all abortion events. In these settings, abortion surveillance is more complex, potentially requiring linkages across multiple data sources to achieve complete capture of the number of abortions, abortion characteristics, and abortion complications (which may not be tracked using the same data sources). Thus, abortion surveillance and abortion cohorts used for research and evaluation must consider the local health services and systems context to ensure complete capture of abortion events and outcomes. This is particularly important to understand trends over time and evaluate the impact of how changes in health system and service provision models may impact access, outcomes, and safety.
The objectives of this study were to 1) create a rigorous approach to define abortion cohorts using linked administrative data sets and 2) evaluate the performance of these methods for abortion surveillance compared with a simpler approach.
Our interdisciplinary team of clinicians, health services researchers, epidemiologists, and linked health administrative data experts conducted this study. We identified and applied four principles to develop a rigorous approach for defining induced abortion cohorts when surgical and medication abortion services are distributed across multiple practice settings and when a single abortion may generate several health service encounters:
- Principle 1: Exclude early pregnancy losses and postpartum treatment. This differentiates between the need for uterine evacuation for reasons other than abortion, such as can occur with early pregnancy loss or postpartum procedures (e.g., managing postpartum hemorrhage). In a single pregnancy, an abortion cannot co-occur with an early pregnancy loss or a delivery. Because reimbursement structures may incentivize billing for abortion when providing care for early pregnancy loss or performing postpartum procedures, any abortion events co-occurring with codes for early pregnancy loss or postpartum management should be excluded from abortion cohorts.
- Principle 2: Use multiple linked data sources to capture comprehensively all relevant encounters: practitioner billing/claims records coded using fee and diagnostic codes; inpatient and ambulatory care hospital records (using intervention and diagnostic codes); and prescription records for mifepristone. These databases must be linkable at the record-level.
- Principle 3: Define episodes of care and identify all records within an episode that are considered part of a single abortion episode. This prevents double-counting for abortions that require multiple encounters. There is uncertainty in optimal episode length, with some suggesting a follow-up period as short as one to three weeks , with four  or six [24, 25] weeks used most often by researchers.
- Principle 4: Apply a hierarchical algorithm to determine the abortion date when multiple records occur during an abortion episode. This type of algorithm requires clinical expertise. It should identify any abortion-related service occurring before or after the index abortion event but during the (6 week) abortion episode as a follow-up to the index event. It must be able to distinguish routine or complication-related follow-up care from a subsequent abortion event.
We applied these principles to construct an abortion cohort using Ontario’s linked, population-based administrative health data from January 1, 2018 – March 15, 2020. We chose this study period to exclude the first year of mifepristone medical abortion availability in Canada due to the rapid and multiple changes to medication abortion regulatory restrictions at that time  and to exclude abortions occurring after the declaration of the COVID-19 pandemic .
Our data included all records from practitioner encounters from the Ontario Health Insurance Program (OHIP billing/reimbursement records), hospitalization records from the Discharge Abstract Database (inpatient) and the National Ambulatory Care Reporting System (outpatient ambulatory clinics, subdivided as emergency department visits or ambulatory care visits), and outpatient mifepristone prescription dispensations from the Ontario Drug Benefit database (ODB). We accessed these data through Ontario’s health administrative data warehouse (ICES). These data sets are created through the provision of health care through Ontario’s provincial single-payer health insurance program which covers all Ontario residents, excluding newcomers to Ontario that have not yet achieved residency status (3-month waiting period) or for non-residents accessing health care in Ontario. We linked across databases using the “ICES key number”, an encoded version of the Ontario Health Insurance Program number assigned to individuals covered by provincial health insurance, created by ICES. Linkage using this key number is routine in analyses using Ontario’s health administrative data. As this number is directly derived from individual identifiers, duplicates or false positive linkages are not a concern. Billing/reimbursement records include fee codes for each encounter coupled with a diagnostic code from the International Classification of Disease Version 9 (ICD-9) coding system. Hospitalization records include intervention codes from the Canadian Classification of Interventions coding system and diagnostic codes from the International Classification of Disease Version 10-CA (ICD-10-CA) coding system.
We applied the four principles to these data sets to create a cohort of abortions as follows: After identifying all records with an abortion billing, diagnostic, or prescription code from these databases, we excluded records with simultaneous codes for clinical events with similar treatment or cascades of care (Principle 1). At the record level, we linked across datasets using the individual identifier to create unique abortion identifiers (Principle 2). We defined episodes of care such that any event within 6 weeks of the first event was considered part of the same abortion episode with the first event starting the episode (Principle 3). Finally, for those records with multiple abortion events, we identified which event was the most likely abortion date using a hierarchical approach to start the abortion episode (e.g., first encounter vs. prescription dispensation vs. post-abortion management) through consultation with clinician partners (Principle 4).
To evaluate the impact of applying these methods, we identified the resulting number of abortions with and without each principle in place and compared the frequency of abortion characteristics with and without each principle using x2 tests and risk differences (RD, with 95% confidence intervals). We examined incidences of the following abortion characteristics: percent medication vs. surgical, percent first (<14 completed weeks of gestational age) vs. second or third trimester (≥14 weeks), and the incidence of abortion complications (including infection, hemorrhage, embolism, shock, metabolic disorders, renal failure, damage to pelvic organs, other venous complications, and other), all estimated with 95% confidence intervals.
Applying each of these principles to a population-based cohort of all abortions in Ontario, Canada from January 1, 2018 – March 15, 2020 using linked data from multiple sources yielded a cohort of 84,032 abortions (see complete cohort derivation in Figure 1).
Of these, 26,414 (31.4%, 95% CI 31.1–31.8) were medication abortions, 57,581 (68.5%, 68.2–68.8) were surgical abortions, and 39 (0.1%, 0.0-0.1) were unclassified/unknown method. Nearly all (n = 79,385, 94.5% [94.3–94.6]) were first trimester abortions, while 5.1% (5.0–5.3) occurred in the second or third trimester, and 0.4% (0.4–0.5) had unknown/missing gestational age. The incidence of abortion complications was 0.69% (0.63–0.74; n = 578).
We found that including records with codes for abortion that also had codes for early pregnancy loss or postpartum events (versus excluding these, Principle 1) yielded a larger abortion cohort (91,174 vs. 84,032) and overestimated medication abortion frequency (32.6% vs. 31.4%, RD 1.2%[0.76–1.6], p < 0.001). In addition, including records with early pregnancy loss or postpartum treatment codes underestimated first trimester abortion frequency (93.9% vs. 94.5%, RD -0.60[-0.82–0.38], p < 0.001) and overestimated the incidence of abortion complications (1.29% vs. 0.69%, RD 0.60%[0.51–0.69], p < 0.001), as shown in Table 1.
|Excluding all early pregnancy loss and postpartum events (novel approach)||Including early pregnancy loss and postpartum events|
|Number of abortions||84,032||91,174|
|% (95% CI)||% (95% CI)||difference (95% CI)||p-value|
|Medication abortion||31.4% (31.1, 31.8)||32.6% (32.3, 32.9)||1.2% (0.76, 1.6)||<0.001|
|First trimester abortion||94.5% (94.3, 94.6)||93.9% (93.7, 94.0)||-0.60% (-0.38, 0.82)||<0.001|
|Abortion complications||0.69% (0.63, 0.74)||1.29% (1.21, 1.36)||0.60% (-0.51, 0.69)||<0.001|
Table 2 compares the abortion cohort identified using multiple data sources (linked inpatient and ambulatory hospital records, practitioner billing records, outpatient prescription dispensation records) with cohorts identified using a single source (only inpatient/outpatient hospital records or only billing/claims records). We found that multiple data sources identified 77,994 more abortions than hospital-only records and 3,751 more than practitioner billing records only. Hospital-only data underestimated the frequency of medication abortion (16.1% vs. 31.4%; risk difference (RD) -15.3% [-14.3, -16.3], p < 0.001) and first-trimester abortion (82.1% vs. 94.5%; RD -12.8 [-11.4, -13.4], p < 0.001) and overestimated the incidence of abortion complications (2.9% vs. 0.69%; RD 2.2% [1.8, 2.7] p < 0.001). The cohort identified using billing data underestimated medication abortion frequency (26.2% vs 31.4%, RD -5.2% [-10.4%, 0.0], p < 0.001), underestimated abortion complication frequency (0.61% vs 0.69%, RD -0.08 [0.0, -0.16], p < 0.001) and yielded similar first trimester abortion frequency (94.9% vs 94.5%, RD 0.4% [0.18, 0.62], p = 0.933) compared with the multiple linked data source approach.
|Multiple linked data sources (novel approach)||Hospital data only (inpatient and outpatient)||Billing data only|
|Number of abortions||84,032||6,038||80,281|
|(95% CI)||(95% CI)||(95% CI)||(95% CI)||(95% CI)|
|Medication abortion||31.4%||16.1%||-15.3%||p < 0.001||26.2%||-5.2%||p < 0.001|
|(31.1–31.8)||(15.2, 17.1)||(-14.3, -16.3)||(25.9, 26.5)||(0.0, -10.4%)|
|First trimester abortion||94.5%||82.1%||-12.4%||p < 0.001||94.9%||0.4%||p = 0.933|
|(94.3–94.6)||(81.1, 83.0)||(-11.4, -13.4)||(94.8, 95.1)||(0.18, 0.62)|
|Abortion complications||0.69%||2.9%||2.2%||p < 0.001||0.61%||-0.08%||p < 0.001|
|(0.63–0.74)||(2.5, 3.3)||(1.8, 2.7)||(0.56, 0.67)||(-0.0, -0.16)|
In our comparison of an episodic approach versus an unlinked approach considering each abortion event as a separate abortion (Principle 3, Table 3), we found that the unlinked approach overestimated the number of abortions (99,965 vs. 84,032) and overestimated the frequency of medication abortion (37.2% vs. 31.4%, RD 5.8%[5.4–6.2], p < 0.001). The unlinked (versus episodic) approach accurately estimated the frequency of first trimester abortion (94.5% vs. 94.4%, p = 0.351), but underestimated the frequency of abortion complications (0.19% vs 0.69%, -RD 0.50%[-0.44–-0.56], p < 0.001).
|Episodic (novel) approach||Standard unlinked approach|
|Number of abortions||84,032||99,965|
|% (95% CI)||% (95% CI)||difference (95% CI)||p-value|
|Medication abortion||31.4% (31.1–31.8)||37.2% (36.9, 37.5)||5.8% (5.4, 6.2)||p < 0.001|
|First trimester abortion||94.5% (94.3–94.6)||94.4% (94.3, 94.6)||-0.1% (-0.11, 0.31)||p = 0.351|
|Abortion complications||0.69% (0.63–0.74)||0.19% (0.16, 0.21)||-0.50% (-0.44, -0.56)||p < 0.001|
In Table 4, we show the impact of using a hierarchical approach to define the abortion date (based on line-level clinical information) with a simpler ‘first event is abortion’ approach. These approaches yielded nearly identical abortion cohorts (84,328 vs. 84,032 abortions) and similar estimates of medication abortion frequency (31.7% vs. 31.4%, p = 0.185), first trimester abortion frequency (94.5% vs. 94.5%, p = 1.0), and abortion complications (0.66% vs 0.69%, p = 0.452).
|Hierarchical approach (novel approach)||First event is abortion approach|
|Number of abortions||84,032||84,328|
|% (95% CI)||% (95% CI)||difference (95% CI)||p-value|
|Medication abortion||31.4% (31.1, 31.8)||31.7% (31.4, 32.0)||0.3% (-0.14, 0.74)||p = 0.185|
|First trimester abortion||94.5% (94.3, 94.6)||94.5% (94.34, 94.65)||0.0% (-0.22, 0.22)||p = 1.0|
|Abortion complications||0.69% (0.63, 0.74)||0.66% (0.61, 0.72)||-0.03% (-0.05, 0.11)||p = 0.452|
In this study, we compared the number of abortions identified and key abortion characteristics (abortion method, trimester, and complication incidence) using standard methods with refined methods that applied four key principles to define abortion cohorts. This analysis proposes a conceptual framework to guide abortion surveillance and abortion cohort creation across jurisdictions when medication abortion becomes more frequent and/or when abortion services move from single or uniform service delivery settings to distributed practice models.
We found that the number of abortions identified, abortion type, and trimester of care were most impacted by number and type of data sources used, while abortion complication incidence was differentially impacted by number and type of data sources used, linkage across events for the same abortion, and inclusion of procedures following delivery or early pregnancy loss as an abortion procedure.
In particular, using hospital-only data dramatically underestimated the number of abortions identified, while using billing-only data only slightly underestimated the number of abortions. On the other hand, using an unlinked (vs episodic) approach and failing to exclude procedures following a recent delivery or early pregnancy loss both somewhat overestimated the number of abortions. Abortion type was most frequently misclassified (underestimating the proportion of medication abortions) with hospital-only data; similarly, the proportion that were medication abortions was slightly underestimated with billing-only data, and slightly overestimated when postpartum and pregnancy loss management procedures were not excluded. Using a hierarchical approach to determine the abortion event date (compared with using the first abortion event as the anchor date in every instance) had little impact on number of abortions identified or abortion characteristics.
Each methodological approach differentially impacted estimates of abortion complication incidence. Using hospital-only data and retaining abortion procedures following delivery or early pregnancy loss both overestimated the frequency of complications more than two-fold, while complication frequency with an unlinked approach was less than a third of that found using our proposed linked approach.
When local legal and practice regulations evolve to allow medication abortion provision outside hospital settings, selection or continuation of hospital-based surveillance will underestimate the number of abortions, overestimate the proportion of surgical abortions, and will systematically capture more complex abortion cases occurring at later gestational ages. This type of selection process has previously been demonstrated to induce selection bias [27, 28]; hospital-only abortion surveillance will overestimate the frequency of second trimester and surgical abortion (relative to first trimester medication abortion) and will overestimate the risk of abortion complications [29–37].
This change in methods to define induced abortion cohorts using administrative data mirrors other clinical practice contexts in which a treatment moved from a single service delivery model within a single setting to multiple delivery models provided in distributed settings [38–41]. Unlike these clinical areas, induced abortion practice, surveillance, and research are challenged with a historical context of legal and regulatory restrictions which have impeded access to the appropriate range of World Health Organization supported reproductive healthcare options [42–45].
This analysis demonstrates that these four principles are robust and will improve the accuracy of abortion surveillance across a range of health systems that support medication abortion in distributed practice settings [1–3]. Adopting this improved approach for abortion surveillance and creation of abortion cohorts for research purposes will become more important as health policy makers, systems, and service decision makers, and advocates struggle to understand the equitable distribution and safety of abortion services under a growing range of models of care [37, 46–49]. For example, as medication abortion becomes more frequent, hospital-only surveillance systems will draw qualitatively incorrect conclusions about the impact of this practice change on abortion safety.
The application and implementation of these principles must be adapted to local conditions and contexts; however, these underlying principles are generalizable to contexts in which induced abortion practice is distributed across systems and settings. The importance of excluding abortion events that co-occur with early pregnancy losses or postpartum treatment is important for creating valid abortion cohorts in all countries or jurisdictions, and particularly for reporting the incidence of abortion complications or adverse events. We expect that the approach we outlined to create valid abortion cohorts using multiple data sets is generalizable to any context where abortions occur in distributed practice settings (i.e., not restricted to hospital settings or to a defined number of purpose-specific abortion clinics). Our analysis may not be replicable in jurisdictions that do not enable linkages of health data across health care settings or where mifepristone is available online; in these jurisdictions it may not be possible to create valid abortion cohorts. Our findings indicate that universal health system payment, service, and outpatient prescription records are needed to accurately monitor abortion frequency, characteristics, and outcomes. When this is not feasible, any abortion surveillance or research activities should be transparent regarding the impact of these data set limitations on abortion frequency, characteristics, and complication incidence. Our results may be useful to estimate the potential direction and magnitude of bias induced by these data set limitations.
In settings where legal or regulatory approaches to medication abortion evolve to enable abortion provision in primary care or office-based settings, surveillance systems that rely on standard reporting by institutions will become incomplete and biased. For valid and complete abortion surveillance to continue when abortion practice disseminates to wider settings, methods must be overhauled to ensure complete capture of procedures across all settings. In this paper, we provide a conceptual framework to guide this process across jurisdictions.
This study was supported by ICES, which is funded by an annual grant from the Ontario Ministry of Health (MOH) and the Ministry of Long-Term Care (MLTC). This study also received funding from: the Canadian Institutes for Health Research (Project Grants PJT-168964, and 202010P15-461003) and a Catalyst Grant from the Women’s Health Research Institute of the Provincial Health Services Authority, British Columbia. Parts of this material are based on data and information compiled and provided by CIHI, MOHLTC, and IQVIA Solutions Canada Inc. The analyses, conclusions, opinions, and statements expressed herein are solely those of the authors and do not reflect those of the funding or data sources; no endorsement is intended or should be inferred. We thank IQVIA Solutions Canada Inc. for use of their Drug Information File.
Laura Schummers holds a Canadian Institutes of Health Research Fellowship: Patient-Oriented Research Award – Transition to Leadership Stream Fellowship (#TLS-170676) with early project support from a Michael Smith Foundation for Health research Trainee award (#17934) and a Health System Impact Fellowship jointly funded by the British Columbia Ministry of Health (#18183) and the Canadian Institutes of Health Research (HI7-160383).
Elizabeth K Darling holds an Early Career Investigator award from the Canadian Institutes of Health Research (#167971).
Sheila Dunn holds a Clinician Investigator Award from the Department of Family and Community Medicine, University of Toronto and a Scientist Award from the Women’s College Research Institute.
Janusz Kaczorowski holds the Docteur Sadok Besrour Chair in Family Medicine, the GSK Chair in Optimal Management of Chronic Disease, and the Canadian Institutes for Health Research-Heart & Stroke-Hypertension Canada Chair in Prevention and Control of Hypertension.
Wendy V Norman held a Scholar Award from the Michael Smith Foundation for Health Research (2012-2020 5139 HSR) and holds the Canadian Institutes for Health Research-Public Health Agency of Canada Applied Public Health Chair in Family Planning Research CPP-329455-107837 2014-2024). The authors are part of the “The CART Mife-Outcomes study: Relating Canada’s unique mifepristone regulations to health system events, costs and access to abortion, using linked health administrative data”, and the “CART PREG-Epi” study teams within Canada’s Contraception and Abortion Research Team (CART, www.cart-grac.ubc.ca) and are grateful to our partner organizations and colleagues who have contributed to planning, guiding and interpreting this work.
Ethics approval for this study was granted by the University of British Columbia research ethics board (H18-03739). The use of data in this project was authorized under section 45 of Ontario’s Personal Health Information Protection Act, which does not require review by a Research Ethics Board.
Conflicts of interest
The authors have no conflicts of interest to declare.
Sedgh G, Singh S, Shah IH, Ahman E, Henshaw SK, Bankole A. Induced abortion: incidence and trends worldwide from 1995 to 2008. Lancet. 2012;379(9816):625–32. 10.1016/S0140-6736(11)61786-8https://doi.org/10.1016/S0140-6736(11)61786-8
Popinchalk A, Beavin C, Bearak JM. The state of global abortion data: an overview and call to action. BMJ Sexual & Reproductive Health. 2021;Epub ahead of print(Jul 20, 2021). 10.1136/bmjsrh-2021-201109https://doi.org/10.1136/bmjsrh-2021-201109
Bearak JM, Popinchalk A, Sedgh G, Ganatra B, Moller AB, Tuncalp O, Alkema L. Pregnancies, abortions, and pregnancy intentions: a protocol for modeling and reporting global, regional and country estimates. Reproductive health. 2019;16(1):36. 10.1186/s12978-019-0682-0https://doi.org/10.1186/s12978-019-0682-0
New York, NY: United Nations: Transforming Our World: The 2030 Agenda for Sustainable Development; 2015.
Martin JA, Hamilton BE, Osterman MJK. Births in the United States, 2019. NCHS Data Brief. 2020;387:1–8.
Journal of Obstetrics and Gynaecology Canada; 2019.
Jones RK, Henshaw SK. Mifepristone for early medical abortion: experiences in France, Great Britain and Sweden. Perspectives on sexual and reproductive health. 2002;34(3):154–61.
Regulatory decision summary: MIFEGYMISO Ottawa, Canada: Government of Canada; 2015.
Norman WV, Guilbert ER, Okpaleke C, Hayden AS, Steven Lichtenberg E, Paul M, White KO, Jones HE. Abortion health services in Canada: Results of a 2012 national survey. Canadian family physician Medecin de famille canadien. 2016;62(4):e209–e17.
Berard V, Fiala C, Cameron S, Bombas T, Parachini M, Gemzell-Danielsson K. Instability of misoprostol tablets stored outside the blister: a potential serious concern for clinical outcome in medical abortion. PloS one. 2014;9(12):e112401. 10.1371/journal.pone.0112401https://doi.org/10.1371/journal.pone.0112401
Yalahow A, Doctoroff J, Mark A, Foster AM. Trends in medication abortion provision before and after the introduction of mifepristone: A study of the National Abortion Federation’s Canadian member services. Contraception. 2020;102(2):119–21. 10.1016/j.contraception.2020.04.012https://doi.org/10.1016/j.contraception.2020.04.012
New York: Guttmacher Institute; 2019.
England and Wales: Abortion Statistics; 2019.
Induced abortions. Statistics – Health and Medical Care; 2010.
Shaw D, Norman WV. When there are no abortion laws: A case study of Canada. Best practice & research Clinical obstetrics & gynaecology. 2020;62:49–62. 10.1016/j.bpobgyn.2019.05.010https://doi.org/10.1016/j.bpobgyn.2019.05.010
Munro S, Guilbert E, Wagner M-S, Wilcox ES, Devane C, Dunn S, Brooks M, Soon JA, Mills M, Leduc-Robert G, Wahl K, Zannier E, Norman WV. Perspectives Among Canadian Physicians on Factors Influencing Implementation of Mifepristone Medical Abortion: A National Qualitative Study. Annals of family medicine. 2020;18(5):413–21. 10.1370/afm.2562https://doi.org/10.1370/afm.2562
Government of Canada: Data Quality in the Therapeutic Abortion Survey 2006; 2009.
Supreme Court Judgments. Supreme Court Judgments; 1988.
Government of Canada: Induced Abortions Reported in Canada in 2018 Ottawa, Canada; 2020.
Ahrens KA, Hutcheon JA. Time for Better Access to High-Quality Abortion Data in the United States. American journal of epidemiology. 2020;197(7):640–7. 10.1093/aje/kwaa048https://doi.org/10.1093/aje/kwaa048
Niinimaki M, Suhonen S, Mentula M, Hemminki E, Heikinheimo O, Gissler M. Comparison of rates of adverse events in adolescent and adult women undergoing medical abortion: population register based study. BMJ. 2011;342(apr19 2):d2111–d. 10.1136/bmj.d2111https://doi.org/10.1136/bmj.d2111
Fiala C, Cameron S, Bombas T, Parachini M, Agostini A, Lertxundi R, Lubusky M, Saya L, Gemzell Danielsson K. Outcome of first trimester medical termination of pregnancy: definitions and management. The European journal of contraception & reproductive health care : the official journal of the European Society of Contraception. 2018;23(6):451–7. 10.1080/13625187.2018.1535058https://doi.org/10.1080/13625187.2018.1535058
Taylor D, Upadhyay UD, Fjerstad M, Battistelli MF, Weitz TA, Paul ME. Standardizing the classification of abortion incidents: the Procedural Abortion Incident Reporting and Surveillance (PAIRS) Framework. Contraception. 2017;96(1):1–13. 10.1016/j.contraception.2017.05.004https://doi.org/10.1016/j.contraception.2017.05.004
Upadhyay UD, Desai S, Zlidar V, Weitz TA, Grossman D, Anderson P, Taylor D. Incidence of emergency department visits and complications after abortion. Obstetrics and gynecology. 2015;125(1):175–83. 10.1097/AOG.0000000000000603https://doi.org/10.1097/AOG.0000000000000603
Roberts SCM, Upadhyay UD, Liu G, Kerns JL, Ba D, Beam N, Leslie DL. Association of Facility Type With Procedural-Related Morbidities and Adverse Events Among Patients Undergoing Induced Abortions. Jama. 2018;319(24):2497–506. 10.1001/jama.2018.7675https://doi.org/10.1001/jama.2018.7675
Geneva, Switzerland: United Nations; 2020.
Neupane B, Walter SD, Krueger P, Loeb M. Community controls were preferred to hospital controls in a case -control study where the cases are derived from the hospital. Journal of clinical epidemiology. 2010;63(8):926–31. 10.1016/j.jclinepi.2009.11.006https://doi.org/10.1016/j.jclinepi.2009.11.006
Dantas O, Ximenes RA, De Albuquerque MDFP, Montarroyos UR, De Souza WV, Varejão P, Rodrigues LC. Selection bias: neighbourhood controls and controls selected from those presenting to a Health Unit in a case control study of efficacy of BCG revaccination. BMC Medical Research Methodology. 2007;7(1):11. 10.1186/1471-2288-7-11https://doi.org/10.1186/1471-2288-7-11
Grimes DA, Schulz KF. Morbidity and mortality from second-trimester abortions. J Reprod Med. 1985;30(7):505–14.
Lawson HW, Frye A, Atrash HK, Smith JC, Shulman HB, Ramick M. Abortion mortality, United States, 1972 through 1987. American journal of obstetrics and gynecology. 1994;171(5):1365–72. 10.1016/0002-9378(94)90162-7https://doi.org/10.1016/0002-9378(94)90162-7
Ferris LE, McMain-Klein M, Colodny N, Fellows GF, Lamont J. Factors associated with immediate abortion complications. CMAJ : Canadian Medical Association journal = journal de l’Association medicale canadienne. 1996;154(11):1677–85.
Ostbye T, Wenghofer EF, Woodward CA, Gold G, Craighead J. Health services utilization after induced abortions in Ontario: a comparison between community clinics and hospitals. Am J Med Qual. 2001;16(3):99–106. 10.1177/106286060101600305https://doi.org/10.1177/106286060101600305
Bartlett LA, Berg CJ, Shulman HB, Zane SB, Green CA, Whitehead S, Atrash HK. Risk factors for legal induced abortion-related mortality in the United States. Obstetrics and gynecology. 2004;103(4):729–37. 10.1097/01.AOG.0000116260.81570.60https://doi.org/10.1097/01.AOG.0000116260.81570.60
Costescu D, Guilbert E. No. 360-Induced Abortion: Surgical Abortion and Second Trimester Medical Methods. Journal of obstetrics and gynaecology Canada : JOGC = Journal d’obstetrique et gynecologie du Canada : JOGC. 2018;40(6):750–83. 10.1016/j.jogc.2017.12.010https://doi.org/10.1016/j.jogc.2017.12.010
White K, Carroll E, Grossman D. Complications from first-trimester aspiration abortion: a systematic review of the literature. Contraception. 2015;92(5):422–38. 10.1016/j.contraception.2015.07.013https://doi.org/10.1016/j.contraception.2015.07.013
Schmidt-Hansen M, Lohr PA, Cameron S, Hasler E. Surgical or medical abortion of pregnancies between 13w0d and 23w6d gestation? A systematic review and new NICE national guidelines. BMJ Sexual & Reproductive Health. 2020;in press:bmjsrh-2019-200460. 10.1136/bmjsrh-2019-200460https://doi.org/10.1136/bmjsrh-2019-200460
Costescu D, Guilbert E, Bernardin J, Black A, Dunn S, Fitzsimmons B, Norman WV, Pymar H, Soon J, Trouton K, Wagner MS, Wiebe E, Gold K, Murray ME, Winikoff B, Reeves M, Society of Obstetricians and Gynecologists of Canada. Medical Abortion. Journal of obstetrics and gynaecology Canada : JOGC = Journal d’obstetrique et gynecologie du Canada : JOGC. 2016;38(4):366–89. 10.1016/j.jogc.2016.01.002https://doi.org/10.1016/j.jogc.2016.01.002
Burger D, Travis S. Conventional Medical Management of Inflammatory Bowel Disease. Gastroenterology. 2011;140(6):1827–37.e2. 10.1053/j.gastro.2011.02.045https://doi.org/10.1053/j.gastro.2011.02.045
Waters EA, Cronin KA, Graubard BI, Han PK, Freedman AN. Prevalence of Tamoxifen Use for Breast Cancer Chemoprevention Among U.S. Women: Table 1. Cancer Epidemiology Biomarkers & Prevention. 2010;19(2):443–6. 10.1158/1055-9965.epi-09-0930https://doi.org/10.1158/1055-9965.epi-09-0930
Kahan NR, Waitman D-A, Blackmon S, Vardy DA. Drug Use Evaluation of Tamoxifen Focusing on Off-Label Use in a Managed Care Population in Israel. Journal of Managed Care Pharmacy. 2010;16(5):355–9. 10.18553/jmcp.2010.16.5.355https://doi.org/10.18553/jmcp.2010.16.5.355
Lanas A, Chan FKL. Peptic ulcer disease. The Lancet. 2017;390(10094):613–24. 10.1016/S0140-6736(16)32404-7https://doi.org/10.1016/S0140-6736(16)32404-7
World Health Organization. Safe Abortion: Technical and Policy Guidelines for Health Systems. WHO Technical and Policy Guidelines. 2012;2012(Second Edition).
World Health Organization & UNDP/UNFPA/ UNICEF/WHO/World Bank Special Programme of Research Development and Research Training in Human Reproduction. Sexual health and its linkages to reproductive health: an operational approach. World Health Organization. 2017.
World Health Organization DoRHaR. Monitoring reproductive health: selecting a short list of national and global indicators. 1997.
Hoggart L, Berer M. Making the case for supported self-managed medical abortion as an option for the future. BMJ Sexual & Reproductive Health. 2021:2021–201181. 10.1136/bmjsrh-2021-201181https://doi.org/10.1136/bmjsrh-2021-201181
Raymond EG, Blanchard K, Blumenthal PD, Cleland K, Foster AM, Gold M, Grossman D, Pendergast MK, Westhoff CL, Winikoff B, Mifeprex REMS Study Group. Sixteen Years of Overregulation: Time to Unburden Mifeprex. The New England journal of medicine. 2017;376(8):790–4. 10.1056/NEJMsb1612526https://doi.org/10.1056/NEJMsb1612526
Raymond EG, Grossman D, Mark A, Upadhyay UD, Dean G, Creinin MD, Coplon L, Perritt J, Atrio JM, Taylor D, Gold M. No-Test Medication Abortion: A Sample Protocol for Increasing Access During a Pandemic and Beyond. Contraception. 2020;101(6):361–6. 10.1016/j.contraception.2020.04.005https://doi.org/10.1016/j.contraception.2020.04.005
Society of Obstetricians and Gynaecologists of Canada; 2020.
This work is licensed under a Creative Commons Attribution 4.0 International License.