Exploring Gender Bias in Cardiovascular Medical Education Through Clinical Simulation

Abstract

While it has been proven that women suffer disproportionately from cardiovascular disease-related deaths, the origins of this differential gender-based outcome remain unidentified. One possible cause is gender bias and associated discrepancies in how physicians assess the need for interventions in male versus female patients. This study aimed to identify early gender biases in cardiovascular care by assessing medical students' management of a ruptured abdominal aortic aneurysm case presentation in male and female simulated patients. Clerkship students (n = 187) were randomly assigned to either a male or female patient with identical case presentations, simulated using high-fidelity mannequins. Minutes passed until point-of-care ultrasound (POCUS) usage served as a surrogate for diagnostic reasoning, while minutes passed until surgery consultation call served as a surrogate for successful intervention. Two-way ANCOVA of time to surgery call and POCUS use showed no significant interaction between student and patient gender (p=0.819). Likewise, neither patient gender (p=0.210) nor student gender (p=0.653) had an impact on ultimate correct diagnosis. However, there appeared to be an association (p=0.010) between patient and student gender in the factorial ANOVA of POCUS use, F(1,183) = 6.862 effect size 0.36. While slight in-group bias was identified within the context of imaging, students predominantly called for the correct intervention regardless of their own or their patient's gender. It is thus unlikely that medical students develop gender biases serious enough to impact clinical outcomes during clerkship- instead, these heuristics may be formed later in training.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

n/a

Funding Statement

No funding was received from a third party for any aspect of the submitted work.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Augusta University IRB number: 1468291-13

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

The datasets generated and analyzed during the study are not publicly available but may be available from the corresponding author on reasonable request.

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