Publications by authors named "Sean Phelan"

Efforts to improve diversity, equity, and inclusion (DEI) in healthcare have increased, targeting healthcare worker biases with the goal of increasing inclusion of employees from racial and ethnic minoritized groups and improving care for patients from these groups. Virtual reality (VR) remains an underutilized mechanism for effecting behavior and attitude change. VR educational interventions work through two primary pathways, behavior rehearsal and embodiment.

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Nurse leaders are foundational to the success of creating an inclusive culture and climate and responding to situations of discrimination, racism, microaggressions, and bias in healthcare settings. This article describes a leadership education initiative using virtual reality to provide diversity, equity, and inclusion training for nurse leaders. Immersion in a lived experience provides a safe and effective learning environment to promote, improve, and exemplify diversity, equity, and inclusion principles and should be explored for other educational applications.

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Article Synopsis
  • Multi-gene hereditary cancer screenings can enhance prevention and treatment for patients and their families, but require integration into various cancer care settings to ensure diverse communities benefit.
  • A survey of 230 diverse cancer patients revealed a strong intent to share genetic results with family, but this intent varied; patients were more likely to disclose to sisters than brothers, and many were uncertain about sharing with at-risk relatives.
  • Recognizing the factors influencing sharing decisions among patients can help clinicians improve genetic screening support and address disparities in cancer care.
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Objectives: How to best care for larger-bodied patients is a complicated issue in modern medicine. The present study seeks to inform current medical practices to ensure the delivery of high-quality and evidence-based care through the examination of higher-weight patients' experiences with weight-related care.

Methods: Higher-weight patients (N = 34) completed semi-structured interviews about their experiences and recommendations for weight-related care.

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Racism shapes the distribution of the social determinants of health (SDoH) along racial lines. Racism determines the environments in which people live, the quality of housing, and access to healthcare. Extensive research shows racism in its various forms negatively impacts health status, yet few studies and interventions seriously interrogate the role of racism in impacting health.

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Background: Assessing perceptions of the COVID-19 vaccines is essential for understanding vaccine hesitancy and for improving uptake during public health emergencies. In the complicated landscape of COVID-19 vaccine mandates and rampant misinformation, many individuals faced challenges during vaccination decision-making. The purpose of our mixed methods study is to elucidate factors affecting vaccine decision-making and to highlight the discourse surrounding the COVID-19 vaccines in diverse and underserved communities.

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Objectives: Racial disparities are pervasive in access to pediatric surgery. The goal of this study was to test the hypotheses that, compared with White children, non-White and Hispanic children: (1) were less likely to attend evaluations by otolaryngologists after a diagnosis of otitis media (OM) eligible for surgical referral, and (2) these children were less likely to receive tympanostomy tube (TT) after surgical consultation.

Methods: The OptumLabs Data Warehouse is a de-identified claims database of privately insured enrollees.

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Objective: This qualitative study applies a community-based participatory research approach to elicit formative data on pediatric patient experiences of racism in the health care setting and to explore clinic-based opportunities for supporting pediatric patients experiencing racism.

Methods: The study is situated within the outpatient practice of a large tertiary academic medical center in a midsize Midwestern city. Community partners were involved in all aspects of the research, including research protocol design, recruitment, data analysis, community dissemination, and manuscript preparation.

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Background: Patients with high body weight are persistently stigmatized in medical settings, with studies demonstrating that providers endorse negative stereotypes of, and have lower regard for, higher-weight patients. Very little is known about how this weight bias varies across specialties.

Objective: The purpose of this study is to examine how explicit weight bias varies between resident providers among sixteen of the largest residency specialties in the USA.

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Aim: To evaluate a modular didactic training intervention called Keep My Teeth designed by special care dentists, for a range of healthcare students to provide oral homecare for people with intellectual developmental disorders (PwIDD).

Methods: To evaluate the intervention a one-group pre-test post-test pre-experimental research design was utilized. The intervention was delivered by virtual platforms or face-to-face, with a sub-sample of participants also receiving practical training.

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Evidence-based treatments have been developed for a range of pediatric mental health conditions. These interventions have proven efficacy but require trained pediatric behavioral health specialists for their administration. Unfortunately, the widespread shortage of behavioral health specialists leaves few referral options for primary care providers.

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Objective: To examine the experience of interracial anxiety among health professionals and how it may affect the quality of their interactions with patients from racially marginalized populations. We explored the influence of prior interracial exposure-specifically through childhood neighborhoods, college student bodies, and friend groups-on interracial anxiety among medical students and residents. We also examined whether levels of interracial anxiety change from medical school through residency.

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Research Question: What is the patient experience of women with high body mass index (BMI) with BMI restrictions that limit fertility care?

Design: Qualitative study using in-depth, semi-structured interview methodology. Interview transcripts were analysed for iterative themes in accordance with principles of grounded theory.

Results: Forty women with a BMI of 35 kg/m or higher with scheduled or completed appointment at the Reproductive Endocrinology and Infertility (REI) clinic completed an interview.

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Article Synopsis
  • Current guidelines for treating eating disorders (EDs) often reinforce weight stigma, negatively impacting individuals of higher weight across various aspects of life and leading to harmful health outcomes.
  • The focus on weight in ED treatment can worsen internalized weight bias, shame, and stigma among patients and providers, contributing to ineffective treatment responses.
  • The authors advocate for a shift towards weight-inclusive care that promotes health behavior change instead of focusing on weight, aiming to combat weight stigma and address social injustices in the treatment of eating disorders.
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  • Telehealth gained popularity during the COVID-19 pandemic, offering convenience but also facing access and quality barriers for both patients and clinicians.
  • This study aimed to understand diverse and underserved community experiences with telehealth, involving mixed methods and focus groups in various U.S. regions from January to November 2021.
  • Data was collected from 47 focus groups, contributing to insights on telehealth perceptions, with a total of 3,447 English and 146 Spanish responses from community outreach efforts.
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Purpose: We undertook a study to evaluate the current state of pedagogy on antiracism, including barriers to implementation and strengths of existing curricula, in undergraduate medical education (UME) and graduate medical education (GME) programs in US academic health centers.

Methods: We conducted a cross-sectional study with an exploratory qualitative approach using semistructured interviews. Participants were leaders of UME and GME programs at 5 institutions participating in the Academic Units for Primary Care Training and Enhancement program and 6 affiliated sites from November 2021 to April 2022.

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  • The study investigates how stigma surrounding mental health acts as a barrier to utilizing integrated behavioral health (IBH) services within primary care.
  • Through interviews with 16 patients and 15 healthcare professionals, the research identifies common themes related to barriers (like external stigma from others and self-stigma) and facilitators (such as normalizing discussions about mental health).
  • Recommendations include using empathetic and patient-centered communication, promoting professional self-disclosure, and tailoring discussions to align with patients' understanding in order to reduce stigma and encourage engagement with IBH services.
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  • - Obesity carries significant stigma, affecting individuals who undergo bariatric surgery not only for their weight but also for the surgery itself, leading to feelings of shame and social isolation.
  • - Many patients struggle with dietary adherence post-surgery and often avoid follow-up appointments due to fears of weight regain, complicating the ability to track long-term outcomes.
  • - The chapter explores how weight bias, internalization of weight stigma, and negative perceptions surrounding the surgery contribute to disordered eating, lower motivation for physical activity, and ultimately hinder successful weight maintenance.
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Patient satisfaction (PS) surveying has become a commonly used measure of physician performance, but little is known about the impact on pediatricians. To investigate our hypothesis that PS surveys negatively impact pediatricians, we conducted a survey at an academic children's medical center. Of 155 eligible physicians, 115 responded (response rate 74%).

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Background: The COVID-19 pandemic has exacerbated existing income inequality and health disparities in the United States (US). The objective of this study was to conduct timely, community-engaged research to understand the disproportionate impact of the COVID-19 pandemic on historically under-resourced communities with the goal of improving health equity. The initiative focused on priorities identified by Community Health Needs Assessments (CHNA) conducted every 3 years per Federal funding requirements.

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Introduction: The COVID-19 pandemic has disproportionally affected historically marginalized populations and their access to resources and healthcare. In times of crisis, authentic community engagement is more important than ever. This study was Phase 1 of a larger 3-phase study to conduct timely community-engaged research with community members to understand the disproportionate impact of COVID-19 on historically underserved communities.

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Background: Health systems are increasingly recognizing the importance of collecting social determinants of health (SDoH) data. However, gaps remain in our understanding of facilitators or barriers to collection. To address these gaps, we evaluated a real-world implementation of a SDoH screening tool.

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Background: For people with a psychotic disorder lack of insight can be detrimental on their condition and recovery. For this reason, insight has been considered as a target for therapy. We conducted a systematic review of the literature on pharmacological, psychological and other treatments to test the hypothesis that these interventions could improve insight.

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