Abstract
Background:
Gender-based stigma (GBS) is widely recognized as a barrier to health care-related outcomes globally, including in North America. Although GBS permeates health care institutions, little research has examined the individual-level experiences of GBS in health care, how these may intersect with other marginalized social positions, or how GBS shapes health care outcomes.
Materials and Methods:
Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews guidelines, this scoping review synthesized the peer-reviewed English scientific literature, through April 2023, on GBS related to health care for cisgender persons. Articles were included if they were from North America and quantitatively or qualitatively investigated either (1) experiences of GBS in health care settings or (2) the relationship between GBS and health care outcomes (e.g., health care access, health care engagement, and treatment adherence).
Results:
Of the 25 studies included, the quantitative articles (n = 13) demonstrated mixed findings regarding both the prevalence of experiences of GBS in health care (8 − 53%) and the impact of GBS on health care outcomes. However, all (n = 14) of the qualitative articles demonstrated that GBS negatively shapes health care experiences, particularly for those occupying intersectional social positions, and is influenced by societal gender norms. Furthermore, gendered experiences of violence and abuse negatively shape care outcomes, both inside and outside of health care contexts.
Conclusions:
The quantitative literature lacks consensus regarding the influence of GBS in health care, but the qualitative literature more clearly demonstrates GBS’s deleterious effect on health care, especially for women. The use of validated GBS measures and intersectional approaches is needed to fully understand the role of GBS in health care.
Introduction
Sexism in health care
Gender-based stigma (GBS) has fundamentally shaped the conceptualization of the diagnosis and treatment of illnesses in Western medicine since its inception, profoundly shaping health along gender lines. 1 GBS (also termed sexism, gender-based discrimination, and gender bias), broadly, has been conceptualized as a multilevel social process whereby individuals are labeled, devalued, and rejected based on one’s gender. 2 Although GBS can be perpetuated at multiple levels (i.e., structural, interpersonal, and individual levels), much of the existing literature has focused on the structural (i.e., how members of specific gender groups are disadvantaged by policies, laws, and institutions) and interpersonal levels (i.e., the perspectives of individuals perpetuating GBS).3–7 At the structural level, GBS permeates North American health care institutions, with research on women-specific diseases being underfunded and with women being underrepresented in the medical literature.4,8 Additionally, structural-level GBS is linked to greater barriers to accessing care and poorer health outcomes for women. 5 At the interpersonal level, sexism among health care professionals may result in the underdiagnosis of certain disorders and the bullying, coercion, and nonconsensual treatment (e.g., obstetric violence) of women.7,9,10
Despite the emerging field of structural sexism research 11 and what is known about interpersonal-level GBS, little is known about women’s experiences with individual-level GBS (i.e., the perspective of persons experiencing GBS) 3 in health care and how those experiences may impact health care outcomes. This limited knowledge on individual-level GBS necessitates a synthesis of the literature to better understand the state of the research, both in terms of the quantity and focus of research on this topic. This review focuses on GBS in health care in North America, where rapidly changing laws, policies, and social norms related to reproductive and other health care-related rights are profoundly impacting women’s health care experiences and outcomes. Concomitantly, there is growing investment in advancing women’s health research, 12 and a greater understanding of the state of the literature can guide future work on GBS in health care in North America at this historically significant timepoint.
Intersectional stigma
Intersectional stigma is a framework combining intersectionality (i.e., an acknowledgment of interlocking systems of oppression) and stigma.13–16 One’s experiences of gender are inextricably linked with one’s experiences occupying other social positions (e.g., race, HIV status) and necessitate an acknowledgment that individual-level stigma occurs within larger power structures (e.g., health care policies and institutions). Given other reviews demonstrating that GBS intertwines with other forms of stigma, 17 and that leading intersectionality scholars argue that examining stigmatized social positions in isolation can conceal complex experiences of stigma and their impacts on health disparities,14,18 we employed an intersectional lens in the design and conduct of the current review.
The current study
Considering the existence of sexism within health care, the limited research employing intersectional, individual-level approaches to investigations of GBS, and the potential negative ramifications of GBS on women’s health care, this scoping review synthesized the North American scientific literature on (1) individual-level experiences of GBS within health care from the perspective of cisgender persons and (2) how experiences of GBS impact health care-related outcomes.
Methods
Search strategy
All review procedures adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews guidelines, 19 and a review protocol may be accessed through the corresponding author. Search terms were developed and piloted to capture published articles that examined (1) gender (i.e., gender-based, sex-based, sexist, sexism, or misogyny), (2) stigma (i.e., social stigma, discrimination, bias, mistreatment, shame, perceived stigma, anticipated stigma, internalized stigma, or enacted stigma), and (3) health care (i.e., healthcare, health care, health services, health care access, or health care engagement) in PubMed and PsycINFO (Supplemental Document 1). Given that initial piloting of the search terms across multiple databases revealed considerable overlap in search results and that research indicates searching as few as two databases can achieve sufficient coverage, 20 the PubMed and PsycINFO databases were used for the current review. The initial search was conducted on August 18th, 2021, yielding an initial sample of 983 articles, and was updated on April 20th, 2023, yielding a final sample of 1157 articles.
Title and abstract screening and full-text review
After excluding 87 duplicate entries, the titles and abstracts of 1070 unique articles were screened to identify articles that potentially contained topics related to stigma, gender, and health care and warranted a full-text review. A total of 125 articles were excluded that lacked one or more of the requisite topics in the title or abstract.
Next, trained coders (S.A.M.P., J.M., and I.Y.) reviewed the text of the remaining 945 articles. Articles were excluded if they (1) were not in English (n = 26), (2) were not an original, peer-reviewed research article (n = 377), (3) did not measure GBS for cisgender individuals (n = 250), (4) did not measure stigma from the individual perspective (n = 93), (5) did not measure a health care-related outcome (n = 123), or (6) if the research was conducted outside of North America (n = 51). This review focused on research within North America, given that both stigma and health care are fundamentally shaped by structural and sociocultural environments that vary across geographical contexts. We chose to synthesize the literature from Canada, the United States, and Mexico together given the economic, political, and historic linking of (e.g., the North American Free Trade Agreement), and frequent border crossings and coordination of health care research and services across, these countries.21–26 We also focused on the experiences of cisgender persons as the experiences of transgender and gender diverse persons with transphobia and gender identity stigma may differ markedly from the experiences of cisgender persons who experience GBS.27,28 Following the full-text review, 920 articles were excluded for not meeting inclusion criteria, resulting in the retention of 25 articles for this review. All articles were double-coded by two independent raters, and coding decisions were reviewed at weekly team meetings. Code-by-code comparisons were reviewed, and any coding discrepancies were discussed by coders until they came to consensus and determined a final code category. Article screening and coding were conducted in Covidence. 29
Study quality ratings
We employed the 14-item Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies to evaluate the quality of the included quantitative studies. 30 Quality scores ranged from 0 to 14, and items assessed whether the measures were clearly defined, valid, reliable, and implemented consistently across all study participants and whether key potential confounding variables were measured and adjusted for statistically.
The quality of qualitative studies was evaluated using the 10-item Critical Appraisal Skills Program checklist, with scores ranging from 0 to 10.17,31,32 Sample criteria included whether the research design was appropriate to address the research aims and whether data analyses were sufficiently rigorous. For both checklists, higher scores represent higher study quality. Quality ratings were conducted individually (S.A.M.P. and J.M.), and any scoring discrepancies were resolved in weekly consensus meetings.
Analysis of data
The primary quantitative outcomes of interest were health care-related variables (e.g., health care engagement and treatment adherence), and the secondary quantitative outcomes were GBS/discrimination-related variables. Data related to the study characteristics (i.e., sample size, population, location, and design), 32 GBS measure used, the health care outcome(s) measured, and the main findings related to GBS (including intersectional stigma) and health care were extracted and organized into tables for synthesis.
Qualitative data were analyzed via thematic synthesis, 33 which involves the development of descriptive and analytical themes through the coding of original studies.17,32,33 After reviewing the qualitative articles, two coders (S.A.M.P. and J.M.) iteratively developed a coding framework to guide the synthesis of study themes related to GBS, the intersection of GBS and other stigmas, and health care. Our approach emphasized the constructs identified by study authors to prevent potential biases that may result from the reinterpretation of primary data, given our limited understanding of the original study context and the potential for misinterpreting isolated data fragments.17,32,33 The coding framework and process facilitated the “reciprocal translation” of findings,17,32,33 which allowed the synthesis of concepts across studies. The study team discussed and achieved consensus on the coding and analysis process, the translation of concepts from different studies, the comparison of codes within code categories, and the grouping of codes into categories.
Results
Study selection and characteristics
Twenty-five articles met inclusion criteria and were retained for analysis (Fig. 1), of which 11 (44%) were quantitative, 10 (40%) were qualitative, and 4 (16%) were mixed methods. Mixed-methods articles were analyzed as quantitative (n = 2) and/or qualitative (n = 4) based on which portion(s) of the studies pertained to the current review. Most studies were conducted in the United States (n = 16; 64%), with 20% (n = 5) in Canada, 8% in Mexico (n = 2), and 8% being continent-wide (n = 2).

A flow chart of the scoping review process for the current study investigating the gender-based stigma related to health care according to PRISMA-ScR guidelines. PRISMA-ScR, Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews.
Methodological quality assessment
Of the 13 quantitative articles included, all were observational. Most investigated GBS related to health care cross-sectionally (n = 10; 76.9%). The mean quality score was 8.5 (range: 6–12; interquartile range [IQR]: 8–9), with nearly all adjusting for confounding variables (n = 11; 84.6%) and providing sample size justifications, power, or variance and effect estimates (n = 11; 84.6%). Given that most studies were cross sectional, only one (7.7%) measured the exposure of interest prior to the outcome(s), and none measured their exposure variable more than once over time.
Of the 14 included qualitative articles, the mean quality score was 9.1 (range: 8–10; IQR: 9–9.8), with all articles providing sufficient details on participant recruitment and most providing adequate details of the analysis process (n = 13; 92.9%). Ten (71.4%) of the articles, however, did not adequately describe whether the relationship between the research team and participants had been considered.
Quantitative synthesis
For the 13 quantitative articles, 4 (30.8%) investigated individuals’ experiences of GBS within health care settings, 7 (53.8%) investigated GBS and a health care-related outcome, and 2 (15.4%) investigated both (Table 1).
A Scoping Review of Studies Investigating Gender-Based Stigma Related to Health Care Within North American Settings (n = 25)
Quantitative synthesis of GBS in health care
The five quantitative articles that assessed GBS within health care contexts investigated this phenomenon among general samples of women,34,35 women receiving mammography services, 36 women veterans, 37 and women living with HIV (WLHIV). 38 The percentage of participants reporting experiencing GBS within a health care setting included 7.8% from women receiving mammography services [1; see Table 1 for article numbers referenced in brackets], 18%–24% from women [8, 12], 33.7% from women veterans [10], and 53% from WLHIV [3].
Quantitative synthesis of GBS and health care outcomes
Within the nine quantitative articles that assessed the relationship between GBS and health care outcomes, this phenomenon was investigated among WLHIV,39–45 women veterans, 37 and women receiving mammography services. 36 Three articles (33.3%; [4, 6, 11]) measured both GBS and health care outcomes but did not test the association between them. Three articles, however, found that greater levels of GBS were associated with poorer health care outcomes (i.e., barriers to HIV care, lower HIV medication adherence, and missed HIV care appointments; [5, 7, 9]). For example, study findings from longitudinal multivariable analyses found that WLHIV (n = 1578) who reported GBS had a greater prevalence of missing an HIV care appointment in the past 6 months (United States; [9]). In contrast, three articles did not find a significant, direct association between GBS and health care outcomes (i.e., mammography screening, HIV viral load, and HIV medication adherence; [1, 2, 13]).
GBS is intersectional and complex
The quantitative articles also indicate that GBS is intersectional and warrants complex analytical approaches. For example, three studies either employed an intersectional measure of stigma (i.e., gendered racial microaggressions scale; [5, 13]) or created a latent class of stigma [7] to explore the co-formation of gender-, race-, and/or HIV-related discrimination and how that intersection relates to HIV care outcomes, although these studies produced disparate results (see section “Quantitative synthesis of GBS and health care outcomes”). Other studies found marginalized social positions significantly impacted experiences of GBS in health care settings [3, 8, 10] or that GBS was a significant factor within moderation or path analyses [1, 2, 6, 9]. Specifically, these studies indicated that income [1], HIV serostatus [3], race/ethnicity [8, 9], and a history of medical or mental illness and/or military sexual trauma [10] either exacerbated experiences of GBS in health care settings or impacted the relationship between GBS and health care outcome(s). Additionally, complex mediation and path analyses identified that critical consciousness (i.e., an awareness of social oppression that promotes uniting with others to advance social change) [2], depression [6], and women-centered care [6] were important factors in understanding the relationship between GBS and health care outcomes.
Quantitative stigma measurement
There was large variability in the measures employed to assess GBS; six (46.2%) studies used three different pre-existing measures of GBS [4, 5, 6, 7, 9, 13], three (23.1%) studies developed GBS items [3, 8, 12], and four studies (30.8%) adapted an existing stigma measure to assess GBS [1, 2, 10, 11]. Nearly half (46.2%) reported or provided a reference for the reliability and validity of the measure employed, a quarter of the studies (23.1%) provided information regarding just the reliability, and nearly a third of the studies (30.8%) did not provide any information on the reliability or validity of the GBS measure(s) used.
Qualitative thematic synthesis
The 14 included qualitative articles examined GBS in health care among women who were eligible for and/or received sexual and reproductive health care,35,46–49 WLHIV,38,50,51 women veterans,52,53 child sexual abuse survivors, 54 persons with schizophrenia, 55 Black women self-care experts, 56 and Black breast cancer survivors. 57 The overarching analytical theme for this synthesis explored how GBS negatively impacts health care for women and men and four descriptive themes were identified: (1) GBS is intersectional, (2) differential treatment due to societal gender norms, (3) gendered loss of autonomy and human rights violations, and (4) gender-based violence (GBV; Fig. 2). While these themes capture unique facets of GBS in health care, they were not mutually exclusive, and there were instances in which they overlapped (Table 2; Supplementary Table S2).

The analytical themes, descriptive themes, and codes developed for a synthesis of the qualitative studies exploring gender-based stigma related to health care (n = 14). *Numbers in parentheses indicate the number of articles that contained these codes.
Examples of the Qualitative Excerpts Featuring Gender-Based Stigma Related to Health Care, with the Corresponding Descriptive Themes and Code Categories Derived from the Thematic Synthesis
GBS is intersectional
Similar to the quantitative literature, most articles (n = 12; 85.7%) contained themes related to individuals’ experiences with GBS as it intersected with other marginalized social positions, namely HIV status [3, 15, 16], mental health [16, 18, 21], race [22, 23, 24, 25], sexual orientation [19], sex work [15], immigration status [24], socioeconomic status [17, 23], and substance use [12]. These studies described how stigma within health care can be amplified for those who occupy intersecting marginalized social positions, leading to negative health ramifications:
Women veterans with PTSD seemed to be particularly vulnerable to perceiving dismissal and devaluation from providers, causing an additive negative effect related to gender and mental health on their reproductive health and family planning interactions. One veteran explained of her experience with counseling at VA, “they kind of blow me off with, ‘you have PTSD and you’re a woman, so it must be in your head, it’s not something real’.” (Callegari, 2019, United States, p. 3, [18])
Differential treatment due to gendered social norms
Several articles explored how societal expectations surrounding womanhood and motherhood perpetuated and shaped experiences of GBS [12, 14, 15, 17, 18, 21, 22, 23, 24, 25]. These studies described how GBS within health care can result from societal standards surrounding cleanliness and purity for women, as well as the moral-based ideals for what makes a “good” mother. Study themes demonstrated that women experienced GBS from health care providers when they were viewed as violating any of these expectations, which, in turn, negatively impacted the care they received. The following excerpt depicts how HIV serostatus can be viewed as a violation of the societal norms surrounding womanhood and motherhood within health care:
Women who wanted to have children were often constructed as wanting to transmit the virus… This construction of women living with HIV as wanting to transmit the virus through childbirth resulted in some respondents unwillingly choosing not to have children: “When I found out I was HIV positive, my doctor at Planned Parenthood told me I could never have children. That I might infect them and I would be [a] ‘horrible woman’ to do so. I didn’t have children but I have regretted that decision every day of my life since.” (Orza, 2015, North America, p. 6, [16])
Limited accounts also suggest that societal expectations surrounding masculinity and manhood may also diminish men’s ability to ask for, and receive good quality, health care [14, 21]. Further, other studies demonstrated how these gender norms have resulted in a distinct lack of gender-responsive health care options, particularly for women [15, 25].
Gendered loss of autonomy and human rights violations
Several articles detailed a gendered loss of autonomy and the commission of human rights violations in health care contexts, ranging from feelings of disempowerment, patronization, and dismissal, to being uninformed or misinformed about available treatment options, to being forced or coerced into procedures. Specifically, study themes highlighted gendered disempowerment within health care settings, where women recounted feeling powerless and unable to advocate for themselves in health care settings [12, 19, 24], as well as instances where health care workers neglected to share, or provided inaccurate/incomplete health-related information [3, 12, 16]. Further, over half of the articles highlighted themes related to the patronization and/or dismissal of women in health care contexts [12, 14, 18, 19, 20, 21, 23, 24]. These studies, exemplified below, illustrate how women are often perceived as not being the experts of their own bodies and that the stereotypes of the hysterical and hormonal woman persist:
Many women interviewed for this study had been told by doctors that their health concerns or conditions were directly attributable to their hormonal states, or that they were overreacting to their subjective experiences of pain and discomfort. One female combat veteran described her experiences as following: “I was told by my VA doctor that though I was a woman in combat, I should be over it by now. That, you know, my female hormones are in overdrive and that’s my problem.” (Mattocks, United States, 2020, p. 116, [20])
In extreme examples of lost autonomy, studies discussed gendered human rights violations, most often in the form of coercion into long-acting birth control methods or forced tubal ligation (sterilization) [3, 16, 24].
GBV and health care
Many articles demonstrated that extreme forms of GBS (i.e., gender-based abuse) limited women’s engagement with health care and exists within health care environments [3, 12, 15, 17, 19, 24]. Study findings highlighted how past experiences of GBV outside of health care contexts adversely impacted women’s access to, and engagement with, health care services [3, 15, 19]. Furthermore, article themes underscored accounts in which women depicted experiences of verbal abuse and/or neglect [12, 17] and physical violence [12, 17, and 24] within health care contexts. Importantly, all instances of abuse were within the context of women accessing reproductive health services (i.e., pelvic examinations/pap-smears, childbirth, and/or postpartum care), illuminating a potentially precarious point of care for women. The following excerpt demonstrates the vulnerability that can accompany these services:
The physical abuse reported by the women was characterized by the following actions: having their legs manipulated roughly, being slapped, pinched and strapped to the bed. Physical abuse also translated into poorly practiced routine clinical procedures, for example, … performing medical procedures, such as an episiotomy, without anesthesia, and repeating pelvic examinations carelessly and without providing an explanation. (Santiago, 2018, Mexico, p. 6, [17])
Discussion
Summary of the evidence
This scoping review synthesized the North American scientific literature to provide critically needed information on intersectional and individual-level experiences of GBS within health care settings, and how those experiences of GBS impact health care-related outcomes. Findings across 13 quantitative studies provided mixed evidence for both the prevalence of experiences of GBS in health care (ranging from 7.8% to 53%) and whether GBS is associated with health care-related outcomes. Importantly, few articles tested the association between GBS and health care-related outcomes, indicating a critical gap in our understanding of this phenomenon. The quantitative studies did, however, provide preliminary evidence demonstrating GBS is likely intersectional, with HIV serostatus, race/ethnicity, and medical or mental illness and/or military sexual trauma, being identified as potentially important factors in experiences of GBS within health care, and that critical consciousness and depression may be potential intervenable targets within GBS processes. This quantitative synthesis, however, highlights that further study is warranted for fully understanding the intersectional and complex relationship between GBS and health care.
Among 14 qualitative studies, there was agreement that GBS negatively impacts health care experiences and outcomes. Specifically, findings from this synthesis demonstrated that GBS is rooted in societal expectations surrounding both womanhood and manhood and that stigma is amplified for those occupying intersecting marginalized social positions (e.g., race/ethnicity, HIV serostatus, and mental health). Interestingly, despite our aim of exploring individual-level experiences of GBS, these results further underscore the need for intersectional approaches by highlighting how individual-level experiences of GBS are inextricably linked to the structures, systems, and interpersonal environments (e.g., societal norms and expectations) in which individuals are situated.13,14,18,58 The qualitative literature also demonstrates that GBS can take many forms, ranging from a loss of agency (e.g., disempowerment, misinformation, and patronization/dismissal) to forced/coerced procedures and GBV. These accounts illustrate a dearth of gender-responsive (i.e., women-centered) services and a need for gender bias training among providers, both of which may improve care for women. It is recommended that gender-responsive care models, such as the Woman-Centered HIV Care Model, 59 be employed to improve health care-related outcomes.
The varied findings observed across the quantitative studies suggest that current approaches may not adequately capture GBS related to health care, particularly for women occupying intersecting social positions. This could be due, in part, to the large variability in GBS measures employed across studies. This variability in GBS measurement mirrors the variability noted in other stigma research,17,60 and further emphasizes the need for scientific coordination regarding the operationalization, standardization, and validation of GBS measures. Consequently, future research should draw from the existing published qualitative literature and intersectional measures of stigma to better develop measures of GBS. Accurately capturing GBS, and the intersectional nature of stigma, could lay the foundation for the development and evaluation of tailored interventions targeting GBS and associated health care-related harms.
Limitations
This scoping review was limited in a few important ways. First, only articles published in English were included due to language limitations among the study team. Twenty-six non-English articles were excluded, including articles in Spanish (n = 9) and French (n = 5); two official languages spoken in North America that could have potentially biased our findings. However, English is still the most widely spoken language in North America, and the inclusion of articles from three North American countries allowed us to avoid overgeneralizing our findings given that experiences of gender, stigma, and health care vary across sociogeographical contexts. Furthermore, although the heterogeneity of the GBS measures employed limits the robustness of the current review’s findings, 61 we exposed existing gaps in the scientific literature. To protect against bias, inclusion and exclusion criteria were determined prior to analysis, independent raters screened for inclusion, applied codes, and assessed study quality, 62 and themes and codes were developed iteratively and agreed upon by scientists with qualitative research experience.
Implications
To the best of our knowledge, this is the first scoping review of intersectional and individual-level GBS in North America as it relates to health care. The results of current synthesis contribute valuable insights into the experiences of women, and in some contexts men, with the gendered social norms that produce heightened levels of stigma, reduced agency, and abuse within health care contexts. Importantly, this synthesis identified that experiences with GBS negatively impact participants’ engagement with, or experiences within, health care, and that critical consciousness, depression, and women-centered care may be potentially critical areas for intervention and future research on this phenomenon. This review also identifies potential methodological weaknesses in the existing quantitative measurement of GBS as it relates to health care. Current approaches to assessing GBS are not only lacking consistent operationalization and well-validated measures but also have not been designed to capture the unique experiences of GBS in health care settings, or as it intersects with other marginalized social positions. As such, the lack of consensus in the conclusions across the quantitative studies highlights the need for nuanced and intersectional approaches to GBS- and health care-related research. This information could be crucial for developing gender-responsive treatments and interventions to reduce stigma within health care, thereby promoting greater safety, health, and well-being for women, a group disproportionately impacted by stigma- and health-related harms.
Footnotes
Acknowledgments
The authors wish to thank the participants and investigators whose work collectively informed this review. Additionally, the authors wish to thank Josef Kim Salazar and Lindsay Atkins whose work informed the current scoping review.
Funding Statement
S.A.M.P. was supported through NIDA grants
Author Contributions
S.A.M.P.: Conceptualization, data collection, analysis, and writing—original draft preparation. J.M.: Data collection, analysis, and writing—original draft preparation. K.J.H.: Resources, supervision, and writing—reviewing and editing. I.Y.: Data collection, analysis, and writing—reviewing and editing. C.H.L.: Conceptualization and writing—reviewing and editing. C.R.: Conceptualization and writing—reviewing and editing. V.A.E.: Conceptualization, supervision, and writing—reviewing and editing.
Conflict of Interest
The authors declare that they have no conflicts of interest.
Abbreviation Used
References
Supplementary Material
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