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Contraceptive risk events among family planning specialists: a cross sectional study
Reproductive Health volume 21, Article number: 133 (2024)
Abstract
Background
Proponents of abortion restriction cite advancements in contraceptive technology as a reason against the need for abortion care today, most recently through oral arguments in the Supreme Court of the United States case, Dobbs v. Jackson Women’s Health. However, consistent and correct use of contraception requires reproductive health literacy. Our objectives were to quantify contraceptive risk events and assess contraceptive history and preferences among a population well-equipped to evade contraceptive risks, family planning specialists following initiation of their medical training. “Risk events” are defined as reported episodes of contraceptive failure, emergency contraception use and/or unprotected or underprotected intercourse.
Methods
This was a cross-sectional study among current members of a professional organization of family planning specialists. Inclusion criteria included: status as a current or retired clinician, consensual penile-vaginal intercourse and personal or partner capacity to become pregnant since the start of medical training. Descriptive statistics were performed. This study was IRB exempt.
Results
Among 229 respondents, 157 (69%) reported experiencing a contraceptive risk event since training. Twenty-nine (13%) respondents reported an occurrence within the last year. By category, 47% (108/229; 3 reported unknown) reported under- or unprotected intercourse, 35% (81/229) reported emergency contraception use, and 52% of participants (117/227; 2 unknown) reported known or suspected contraceptive failure. The mean number of contraceptive methods used was 3.7 (SD 1.7) out of the 13 methods listed. Almost all (97%) participants reported at least one method was not an acceptable option, with a mean of 5.6 (SD 2.7) of the 13 listed methods.
Conclusions
The majority of family planning specialists have experienced contraceptive risk events during times of active pregnancy prevention since their medical training. Contraceptive method change is common and most respondents were limited in the number of methods that were personally acceptable to them. Dialogue idealizing the role of contraception in minimizing or eliminating abortion need is simplistic and inaccurately represents the lived realities of pregnancy-capable individuals and their partners, including among those with exceptional contraceptive literacy and access.
Abstract
Antecedentes
Los que apoyan la restricción del aborto citan los avances en la tecnología anticonceptiva como una razón en contra de la necesidad de la atención del aborto hoy en día, más recientemente a través de los argumentos orales en el caso de la Corte Suprema de los Estados Unidos, Dobbs v. Jackson Women's Health. Sin embargo, el uso sistemático y indicado de los anticonceptivos requiere unos conocimientos sobre salud reproductive. Nuestros objetivos eran cuantificar los eventos de riesgo anticonceptivo y evaluar los antecedentes y las preferencias entre una población bien equipada para eludir los riesgos anticonceptivos, los especialistas en planificación familiar tras el inicio de su formación médica. Los "eventos de riesgo" se definen como episodios reportados de fallo anticonceptivo, uso de anticoncepción de emergencia y/o relaciones sexuales sin protección o con protección insuficiente.
Métodos
Este fue un estudio transversal entre miembros actuales de una organización profesional de especialistas en planificación familiar. Los criterios de inclusión incluyeron: condición de clínico/a en activo/a o jubilado/a, relaciones sexuales consentidas pene-vagina desde el inicio de la formación médica y capacidad personal o de la pareja para quedarse embarazada. Se realizaron estadísticas descriptivas. Este estudio estaba exento de IRB.
Resultados
De las 229 encuestadas, 157 (69%) declararon haber sufrido un evento de riesgo anticonceptivo desde la formación. Veintinueve (13%) encuestadas declararon haberlo sufrido un incidente en el último año. Por categoría, el 47% (108/229; 3 informaron de forma desconocida) informaron de relaciones sexuales sin protección o con poca protección, el 35% (81/229) informaron del uso de anticonceptivos de emergencia y el 52% de los participantes (117/227; 2 informaron de forma desconocida) informaron de un fallo anticonceptivo conocido o sospechado. El promedio de métodos anticonceptivos utilizados fue 3,7 (DE 1,7) de los 13 métodos enumerados. Casi todas las participantes (97%) informaron de que al menos un método no era una opción aceptable, con un promedio de 5,6 (DE 2,7) de los 13 métodos enumerados.
Conclusiones
La mayoría de los especialistas en planificación familiar han experimentado eventos de riesgo anticonceptivo en momentos de prevención activa del embarazo desde su formación médica. El cambio de método anticonceptivo es frecuente y la mayoría de los encuestados tenían un número limitado de métodos que les resultaban personalmente aceptables. El diálogo que idealiza el papel de la planificación familiar a la hora de minimizar o eliminar la necesidad de abortar es simplista y representa de forma inexacta las realidades vividas por las personas con capacidad de embarazo y sus parejas, incluso entre aquellas con conocimientos y acceso excepcionales a la anticoncepción.
Plain English Summary
Since Dobbs v. Jackson, the landmark Supreme Court of the United States case overturning the right to abortion, it is very important to better understand current birth control use and the risk of unintended pregnancy. While birth control helps people to avoid unintended pregnancy, current methods are not perfect. This study examined the limitations of current birth control, even when used by expert clinicians with special knowledge and access. We provided an online survey to doctors and advanced practice clinicians who specialize in birth control. We measured risk of unintended pregnancy by asking about experiences with birth control failure, emergency contraceptive use (such as plan B), and unprotected sex since the start of medical training. We also asked about reasons for changing or avoiding certain birth control methods. Among 229 expert clinicians, we found that nearly 70% had experienced a risk of unintended pregnancy since beginning their medical training. Birth control method change was common, and many reported that several options were unacceptable. Participants shared that they found methods difficult, unreliable, unpleasant, or had health conditions that limited the number of safe options available. Our findings suggest that, even among experts, everyone remains at risk of unintended pregnancy. The study highlights the need for improved birth control options as well as access to safe and legal abortion.
Background
Major advancements in contraceptive technology since the 1960s have been cited as a reason against the need for abortion care today, recently in the pivotal Supreme Court case, Dobbs v. Jackson Women’s Health [1]. Specifically, oral arguments in the Dobbs case contended that “contraception is more accessible and affordable and available than it was at the time of Roe or Casey. It serves the same goal of allowing women to decide if, when, and how many children to have.”[2] Justice Barrett also remarked that safe-haven laws further mitigate concerns regarding unwanted parenthood. Thus, authoritative sources have made a simplified conclusion that between contraception and adoption placement, the role of abortion is not as relevant as it was at the time of Roe’s passage.
Consistent and correct use of contraception requires access, health literacy, tolerance of side effects, and for some methods, a willing partner. Even among recent medical school graduates, however, contraceptive knowledge is low [3]. Further, despite rigorous medical training, physicians report high rates of unprotected intercourse when not seeking conception and when partner sexually transmitted infection status is unknown [4]. It follows that abortion is not uncommon (11.5%) among physicians measured over the life course [5]. Thus, even among trained healthcare experts, let alone the general public, contraception does not eliminate the possibility of unintended pregnancy.
There are few populations more knowledgeable about contraceptive use and fertility than clinicians specializing in family planning. The purpose of this study was to assess the contracepting behaviors among this highly specialized group of individuals during their professional practice to assess whether their expertise was sufficient to nullify the risk of unintended pregnancy. Whether the lived experience of contemporary contraception use fully delivers on the point of deciding if, when, and how a pregnancy occurs, must be measured, starting with a population well-equipped to evade contraceptive risks.
Methods
This was a cross-sectional study exploring contraceptive practices and risk of unintended pregnancy among reproductive health experts during their professional careers. Participants were members of the Society of Family Planning, a professional reproductive health organization, including physicians, physician assistants, certified midwives, and nurse practitioners. Individuals were invited to participate through an email communication in the Society of Family Planning email listserv and a posting on an online research message board, available exclusively to members of the Society of Family Planning. There were two reminders to participate. Recruitment occurred between June 2022 to December 2022. Surveys were self-administered with data collection and management using REDCap electronic data capture tools hosted by Mass General Brigham Research Computing, Enterprise Research Infrastructure & Services (ERIS) group. REDCap (Research Electronic Data Capture) is a secure, web-based application designed to support data capture for research studies [6]. The first page of the survey included a consent fact sheet; consent was implied by survey continuation. Inclusion criteria were (1) report of penile-vaginal intercourse since starting medical training; (2) personal or partner capacity to become pregnant since starting medical training; and (3) status as a current or retired clinician. This study consulted the CHERRIES (The Checklist for Reporting Results of Internet E-Surveys) reporting guidelines [7].
Our primary outcome measured contraceptive risk events: times when participants or their partners were at potential risk of pregnancy when not seeking conception. We defined this measure through three questions: (1) How many different times have you or a sexual partner used emergency contraception, including oral medications and IUDs? (2) Have you had consensual penile-vaginal intercourse without using contraception (other than emergency contraception) or partial penile-vaginal intercourse (partial meaning starting intercourse without a condom or other contraceptive method, but using one before ejaculation, using the pullout method, etc.) when you or a sexual partner wanted to prevent pregnancy? and (3) Have you had consensual penile-vaginal intercourse and thought the contraception may have failed? We defined underprotected and unprotected intercourse using adapted items from Aiken and Trussell [4]. Specifically, we measured underprotected intercourse to document the common practice of beginning intercourse without a form of contraception, given the risk of sperm exposure in pre-ejaculatory fluid, while also including withdrawal as a method of contraception. Participants were prompted to respond with events that occurred since the start of participants medical training.
We also included survey questions about participants’ contraceptive history. Participants reported all methods (n = 13) used personally or by their partner since the start of medical training and their reasons for discontinuing each method not currently being used. Participants were also asked about any method they would not want to use and their reasons for avoidance. The survey included write-in options for participants who indicated “other” as a reason for contraceptive method discontinuation and avoidance. These items were developed as adaptations from the National Survey for Family Growth, The Henry J. Kaiser Family Foundation, and Nelson et al.[8,9,10] The survey concluded with demographic items using items adapted from Kaplowitz and Laroche [11]. Item display order was not randomized or alternated; however, conditional display was utilized to supply additional questions only to participants who answered affirmatively to contraceptive risk events (to determine recency of event), method discontinuation items and method avoidance items (to identify reasons for discontinuation or avoidance for only and each method selected). No survey items required a response beyond the three initial screening items. Survey items were pilot testing among five medical professionals. At the end of the web-based survey, participants were invited to enter a drawing for a gift card via a separate survey link to preserve anonymity. Data storage was protected behind an institutional firewall.
We conducted descriptive statistical analyses to illustrate the prevalence of contraceptive risk events, method use, and reasons for method discontinuation or avoidance. This was a convenience sample; the sampling frame was determined by active registration as clinician with the Society of Family Planning. Qualitative responses to the write-in questions were thematically coded and compiled. All data analyses were conducted in STATA (StatCorp, 2019, College Station, TX). The study was reviewed by the Mass General Brigham Institutional Review Board and deemed exempt (2022P001454).
Results
Of 711 currently registered clinicians, 253 (36% click rate) opened the survey invitation, and 229 (91% completion; 32% total sample frame) completed all three screening questions, met the inclusion criteria, and answered at least one of the three primary outcome items (Fig. 1). Participants trained across 35 states and Washington, D.C. The majority of respondents identified as women (95%), and the majority of respondents reported completing an MD degree (85%). Nearly half of participants (49%) responded that it had been one to two decades since they completed their training. A full summary of demographic data is included in Table 1.
Overall, 69% (n = 157) of respondents reported at least one contraceptive risk event during a time when pregnancy was undesired. Four individuals reported they did not know if a risk event had occurred. Thirteen percent (29/229) of all participants reported that the risk event occurred within the past year; all but one of these individuals reported being more than six years into their career. By risk event, 47% (108/229; 3 reported unknown) reported under- or unprotected intercourse, 35% (81/229) reported emergency contraception use, and 52% of participants (117/227; 2 reported unknown) reported known or suspected contraceptive failure since their training. Among emergency contraception users, seventeen individuals reported using emergency contraception more than three times, with some individuals (3/81) reporting use more than ten times.
The most common contraceptive methods participants reported using since beginning their medical training were hormonal IUDs, condoms and oral contraception; for each method, more than 70% of respondents reported personal or partner use since the start of their medical training. Contraceptive injection, spermicide, arm implant, contraceptive patch, and diaphragm were uncommon methods among family planning clinicians, with less than 10% of respondents reporting prior use per method (Fig. 2).
The mean number of contraceptive methods used since medical training was 3.7 (SD 1.7), including emergency contraception. Almost all (215/222, 97%) participants reported they would personally avoid at least one type of contraceptive method. On average, participants reported that 5.6 (SD 2.7) of the 13 methods available would be unacceptable to them for personal use. Figures 3 and 4 show reasons participants reported deciding to discontinue or avoid various methods. [Additional file 1] displays write-in “other” reasons respondents chose to discontinue or avoid particular methods.
Discussion
Approximately 7 in 10 family planning specialists reported a contraceptive risk event during their professional careers when pregnancy prevention was desired. While most participants were over a decade into their careers, 29 (13%) reported a risk event within the past year. These data show that even in the context of significant knowledge and high uptake of the most effective methods, risk of unintended pregnancy persists, underscoring the need for robust abortion access.
Our findings parallel metrics of similar contraceptive risks events in the general public. In an analysis of a national population of reproductive-aged women in 2015, 23% reported prior emergency contraception use, less than in our sample (35%) [12], which may be explained by improved access to, knowledge of, and comfort with reporting use of this contraceptive method among family planning specialists. This reported higher use among our study population may also be impacted by the measure of ever use since training (including older individuals, not just reproductiveaged) and ongoing increases in use since 2015 facilitated by lower costs and easier acquisition of emergency contraception. Participants’ report of under- or unprotected intercourse was similar to findings from a survey administered in 2014 to family planning specialists using the same definition: 76% lifetime risk and 7% past-year risk. Our ever-risk is likely lower because our query was limited to time since training commenced; our past-year risk of 13% may be accounted for by omission of withdrawal from the comparative study’s figure [4]. Regardless, among the family planning clinician population, contraceptive risks have been, and continue to be, part of the lived experience after the initiation of medical training. We measured perceived failure rather than pregnancy incidence. In a population of users highly trained to identify failure like incorrect or inconsistent use or device expulsion, capturing the potential for pregnancy may better address our research question than the overestimated performance deduced from clinically recognizable pregnancy used to calculate Pearl indices. Consequently, we refrain from situating our final metric of contraceptive failure in the context of the general typical use effectiveness measuring pregnancy incidence.
The most common methods used among both participants and the US population include oral contraception, external condoms, and intrauterine devices (IUDs), with a higher rate of IUD use among our participants compared to the general US population [13]. The hormonal IUD was the most common method still being used with the highest rate of discontinuation for planned conception. Individuals remain at risk of pregnancy, unsurprisingly, even with perfect use of contraception; multiple participants described experiences of IUD failures. However, it is unrealistic and unforgiving to expect that anyone—including reproductive health experts—will have perfect contraceptive use at each sexual encounter for a multitude of reasons, including the shortcomings of currently available contraceptive methods. Problems with access and adverse effects were infrequently reported reasons for discontinuation of a method in this cohort. Similarly, in the general population, side effects among oral contraception users have been reported as absent or mild, with minimal method discontinuation attributable to side effects [14]. However, side effects were a common reason for method avoidance in our study, particularly for the injection, nonhormonal IUD and implant. Prior study has found that among first time contraceptive users, nearly half were worried about side effects before starting contraception [9]; however, the degree to which these concerns have contributed to method avoidance among the general public is not clear. Given the unique expertise of family planning clinicians, extensive knowledge around potential side effects across methods likely contributed to informed decision-making and method avoidance. Participants’ report of side effects had overlap with other studies including bleeding and interference with sexual pleasure; although, based on write-in responses, weight and mood concerns were underrepresented in this population [9].
Participants also reported development of contraindications. In other studies, up to one third of individuals using combined oral contraceptives reported a relative or absolute contraindication to use, due to medical comorbidities [15, 16]. The high prevalence of these comorbidities may limit the number of contraceptive options safely available to many pregnancy-capable individuals. Notably, participants echoed the sentiments of many other contraceptive users in emphasizing the importance of control over the method – rather than reliance on a partner for use or a clinician for initiation or discontinuation [17,18,19]. As is the case in all populations, there are a diverse set of factors contributing to the (un)desirability of a contraceptive method, again highlighting that effectiveness is not the only metric influencing contraceptive decision-making. This is consistent with other work demonstrating that the contraceptive decision-making process is often a dynamic and nuanced process that changes over the course of decades [20]. Contraceptive decision-making changes with changing bodies, belief systems, environments and relationships [21].
In examining a population with a unique knowledge base and likely excellent access to contraception, including long-acting reversible methods, contraceptive risk events are common over the course of individuals’ professional lives, as is method discontinuation (for reasons other than conception) and method avoidance. These findings normalize contraceptive risk behaviors, emphasize that “typical use” describes use among all contraceptive users, and highlights the narrow range of contraceptive choice when accounting for method contraindications, performance features, and evolving user preferences. These findings work to dismantle the idea of an ideal contraceptive method or contraceptive user in an era characterized by intolerance of undesired pregnancy and loss of abortion access. Such considerations factor into clinical care, by, for example, reducing “otherization” in contraceptive counseling, building empathy for contraceptive dissatisfaction, and expanding the image of potential abortion beneficiaries to everyone. More tangibly, this translates to provision of universal guidance and access to emergency contraception, counseling on the reality of contraceptive switching and discontinuation for many users, and consideration of the inclusion of abortion counseling with contraceptive counseling [22].
These data have implications for the contemporary social and environmental factors affecting sexual and reproductive health by highlighting contraceptive shortcomings and events representing potential abortion need. Further exploration of contraceptive dissatisfaction may facilitate public understanding of the limitations of contraceptive technology and the demands put on pregnancy-capable people in navigating method use. These findings also emphasize the need for expansion of contraceptive options with critical research focused on development of novel agents and delivery systems, including male hormonal contraceptive methods [23].
The strengths of this study include its unique insight into contraceptive risk behavior and contraceptive choices among family planning specialists using quantitative input. These are salient data for generating a response to current questions around the role of contraception, particularly as it pertains to abortion need. Our study is limited by a design that did not allow for a comparison between contraceptive risk event and method at the time of event. However, the focus of this study was on the prevalence of risk in a population with access to and knowledge about all contraceptive options; the relevance of method data was intentionally focused on exploring imperfections of current technology. Our survey did not fully explore the adverse impacts of each individual method. Finally, our response rate, while consistent with or better than most online surveys, may be subject to non-response bias, including the possibility of preferential response among those with a specific interest in sharing their contraceptive risk histories [24]. While demographics of the Society of Family Planning membership are not publicly available data, the geographic diversity of this sample is similar to those in the member directory providing support of generalizability along one dimension.
Conclusions
Family planning specialists report contraceptive risk events while actively avoiding pregnancy; thus, optimization of the role of contraception with education and access does not generate immunity to abortion need. Advances in contraceptive method diversity and technology should be celebrated, as should contraceptive uptake that meets the needs of its user. However, dialogue focusing on the role of contraception in minimizing or eliminating abortion need perpetuates stigma around abortion and does not accurately represent individuals’ lived experiences, including those with significant educational and social privilege like family planning specialists [25]. Further, like all contraceptive users, those with specialized knowledge of contraception also use individualized algebra to determine method goodness of fit, not limited to considerations of efficacy. Contraceptive preferences and method avoidance are driven by practical and important concerns, like side effects and ease of use, that greatly reduces the menu of options available to the contemporary contraceptive user. Contraception has not and never will eliminate the need for abortion, even among individuals with considerable personal interest and professional training in contraception. In the wake of significant losses in abortion protection, the expansion of contraception options and abortion access, together, should be celebrated in the effort to support reproductive liberty.
Availability of data and materials
The datasets generated during the current study are available from the corresponding author on reasonable request.
Abbreviations
- IRB:
-
Institutional review board
- REDCap:
-
Research electronic data capture
- ERIS:
-
Enterprise research infrastructure & services
- CHERRIES:
-
The checklist for reporting results of internet E-surveys
- IUD:
-
Intrauterine device
- SD:
-
Standard deviation
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Acknowledgements
We would like to thank Alexandra Gero, MPH, University of Utah School of Medicine, who greatly improved the survey through her review and editing of the survey items. We would also like to thank Maddy Mullholand, MPA, University of Utah School of Medicine, who masterfully envisioned data presentation and figure production.
Funding
KF receives support from the Eunice Kennedy Shriver National Institute of Child Health & Human Development (K12HD103096). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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TW was responsible for data analysis, interpretation of results, draft manuscript preparation and final manuscript preparation. JB and RS were responsible for study design, interpretation of results, and manuscript revision. KF was responsible for study conception and design, data collection, analysis and interpretation of results, and draft manuscript preparation. All authors read and approved the final manuscript.
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The study was reviewed by the Mass General Brigham Institutional Review Board and deemed exempt (2022P001454). The first page of our online survey contained a consent fact sheet, and consent was implied by completing the survey.
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KF is a consultant for Medicines360.
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Weckstein, T.N., Simmons, R.G., Baayd, J. et al. Contraceptive risk events among family planning specialists: a cross sectional study. Reprod Health 21, 133 (2024). https://doi.org/10.1186/s12978-024-01870-6
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DOI: https://doi.org/10.1186/s12978-024-01870-6