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2023 Accepted Projects

Evaluation of Medical Student Knowledge of the Holocaust & its Impact on Medical Ethics Adina Greene
Poster

In September 2020, the results of the U.S. Millennial Holocaust Knowledge and Awareness Survey revealed a significant lack of Holocaust-related knowledge among young Americans. This deficit in awareness comes as fewer Holocaust survivors are alive to share their experiences. Holocaust remembrance may be of particular importance among medical professionals, as this group played an essential role in the rationale and implementation of Nazi ideologies. The Doctors’ Trials led to the indictment of physicians for cruel and unethical practices, as well as the establishment of the Nuremberg Code, which is the foundation for medical research ethics today. Despite the establishment of the Nuremberg Code, there remain instances of human rights violations in medicine and research settings. Current and future generations will continue to deal with racism, hatred and political turmoil. This climate necessitates continued education, discussion and reflection of the atrocities of the Holocaust. Through awareness of these events, medical trainees and providers may better comprehend the important role of physicians in the preservation of human dignity. We conducted a series of 34 interviews containing both open-ended and factual questions regarding these topics with medical students. Our analysis revealed that 85% of students rated their knowledge of the Holocaust and its impacts on medicine as less than good and 100% of these students showed interest in additional Holocaust education in the medical school curriculum. This preliminary study demonstrates significant deficits in medical student knowledge of Holocaust events and thus its impact on medical ethics and informed consent. A JAMA-published survey revealed that only 16% of medical schools in the United States and Canada have any required curricular elements on the roles of physicians in the Holocaust. Our preliminary research indicates that there is both a need and an interest in the inclusion of Holocaust education in medical school curricula.

Hebrew Prayer Books

Comparison of Short Chain Fatty Acids (SCFAs) in Lean and Obese Children with Type 1 Diabetes Mayowa Awosika
Poster

Recent studies have shown that an increase in Short Chain Fatty Acids (SCFAs) produced by the gut microbiota is associated with reducing inflammation in the gut and lowering appetite. Here, we hypothesized that the stool SCFAs concentration will be higher in lean children (BMI ≥5%≤84%) versus obese children (BMI≥ 95%). In this study, the fecal SCFA concentration (mainly acetic, propionic, and butyric acid) of 44 children with Type 1 Diabetes (T1D) comprising 23 lean and 21 obese were compared and analyzed. Average age was 15.4 with a mean diabetes duration of 62.2 months and glycemic control levels greater than 130 mg/dL. A significant difference was observed between the stool SCFA levels in lean and obese individuals, with higher levels seen in the obese group (p

Diabetes Self Management Program

Self-Determination Theory: An Effective Strategy to Increase Genetic Testing in the NICU Keeley Higley
Presentation

In this proposal, I explain how I will develop a patient decision aid informed by neonatal intensive care unit (NICU) communication research and self-determination theory to increase consent to genetic testing in the NICU. Genetic testing is an essential but often misunderstood diagnostic tool in the NICU. Earlier diagnosis of genetic conditions can shorten infants’ length of stay, change their plans of care, and save time and lives. However, many barriers prevent guardians from consenting to genetic testing. Barriers include feeling overwhelmed and uncertain, having low health literacy levels, and being confused about incidental findings and pricing. One strategy to address these barriers is the effective use of communication, best guided by the creation of a patient decision aid. Patient decision aids guide guardians through the different genetic testing options, results, and other essential information regarding tests. However, the strongest patient decision aids are guided by a behavior change theory. In the case of NICU genetic testing, self-determination theory may be the answer. Self-determination theory posits that addressing the need for autonomy, competence, and relatedness creates an environment for better decision-making. I propose iterative focus groups with NICU guardians to review and enhance a patient decision aid informed by self-determination theory.

Newborn Baby

Poetry in Neurosurgery: A Brief Scoping Review Nikhil Dholaria
Poster

Just as neurosurgery is regarded to be an art in medicine, poetry is regarded to be a form of art in the humanities discipline. The utilization of poetry in neurosurgery bridges the divide between physician and patient. For the surgeon, poetry allows self-awareness and the acceptance of ambiguity in patient care. For the patient, poetry provides a means to escape from diagnosis and be whole. Taken together, poetry creates a common ground, uniting both the neurosurgeon and the patient to the experience of living through illness. The purpose of this scoping review is to highlight current uses of poetry in neurosurgery and define the necessity of continued implementation.

Image by Álvaro Serrano

A girl feeling sad

Survey of Neurological Causes of Death from a Medical Humanities Perspective from the Indiana Central State Hospital from 1899 – 1947 Vivian Valadares
Presentation 

The goal of this study was to review, quantify, and analyze the cause of neurological deaths from patients of the Central State Hospital (CSH) from 1899-1947. We focused on deaths resulting from psychosis, dementia praecox, paresis, paralysis, mania, and melancholia as these were representative of the most common diseases of that time.​ Families of CSH patient’s granted permission for doctors in the pathology department at CSH to perform autopsies where specimens of brain and spinal cord were commonly collected for further research and examination. It was from records of these autopsies that we acquired our data. IRB approval was granted and the records were examined at the Indiana State Archives in Indianapolis, IN​. The study included 1444 cases from 1898-1947. There were 309 cases for psychosis, 229 cases for dementia praecox, 162 cases of paresis, 154 cases of paralysis, 133 cases of mania, and 96 cases of melancholia. In 234 of the cases, syphilis was a contributing factor to the mental decline and death. In the time period we studied, psychosis and dementia praecox were commonly used as a blanket diagnosis for patients with rapid cognitive deterioration in their early adult life. The wide use of these terms were a factor in generalizing and stigmatizing mental health in the early 1900s. Diagnosis and treatments at this time were not largely evidence based, but instead anecdotal and based on many societal notions. These factors tended to affect women on a larger scale. A small number of patients in this study also had various diseases such as tuberculosis, rheumatic brain disease, cancer, and heart disease. However, these diseases were not highly evaluated here as it was based on neurological diseases in this time period.

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Comparison of 10% Neutral Buffered Formalin to 70% Ethanol for Long-Term Storage in Approximately 50-year-old Gross Pathology Museum Specimens Bryce Selman
Presentation

The Indiana University Department of Pathology displays collections of various formalin-fixed human tissue specimens. Over time, this formalin breaks down into formic acid and evaporates as a gas if the jar is not completely sealed. This breakdown causes tissue degradation and discoloration. Because they may be used for morphological, ecological, and educational purposes, these rare and valuable specimens required maintenance every few years to be kept in a presentable state. Many of these specimens have had their formalin replaced with ethanol because of safety reasons. The recent restoration in the summer of 2021 went from 10% NBF to 70% ethanol. Most jars were restored in the summer of 2022 to replace other formalin jars with ethanol and previously ethanolized jars with fresh ethanol. To determine long-term efficacy of ethanol preservation, restoration rates comparing formalin longevity versus ethanol longevity were compared to identify which preservative better prevents tissue breakdown. Approximately 41% of specimens in ethanol required re-ethanolization after 1 year with nearly 75% of jars requiring re-ethanolization within two years. Conversely, 61% of specimens in formalin required maintenance after 5-7 years, with the remaining percentage lasting for years later, showing that specimens in ethanol require significantly more frequent preservative maintenance compared to specimens in formalin. It is necessary to assess the quality of preservatives to ensure specimen longevity to teach future generations about past illnesses, medical history, and medical ethics.

Brown Containers

The Lessons Taken from the Patient Perspective Supriya Chittajallu
Flash Presentation

Critical limb threatening ischemia (CLTI) is the most severe form of peripheral arterial disease (PAD) and is caused by atherosclerotic occlusion of blood vessels to lower extremities. It is highly associated with excruciating pain as well as the development of skin ulcers or gangrene for those affected. However, there are currently no accepted non-surgical therapies that improve circulation to extremities for people with CLTI. The current standard of care for CLTI is to improve blood flow to the leg with either a surgical bypass or angioplasty with stents to open existing blockages. Unfortunately, about 30 percent of patients with CLTI will not be candidates for a surgical bypass or angioplasty and amputation is the only treatment available to remove a painful or infected leg. It presents an even more significant risk for lower limb amputation in diabetic patients with poor options for revascularization. A survey of this population was conducted to assess patient quality of life and additional factors revealed that all the participants had been in pain for months to years because of downstream effects of their disease like toe or foot ulcers. Most patients have stated that they were motivated to amputate their limb due to the amount of pain they experience because of infection or ulcers. The decision that these patients have come to, has come after years of suffering and a shared story of pain that they could no longer fathom bearing. The PAD/CLTI experience is also marked by disparities by sex, race, and socioeconomic status resulting in lower outcomes for women, black patients, and those of a lower socioeconomic status. This project aims to address this patient narrative through disease development and treatment with the compounding factors that contribute to their vulnerability and the experiences that unify them.

Podiatrist

Minimizing Subjectivity in Mental Health (Neuro Psycho Immunology) Alecsander Zareb
Presentation

The stress we experience day to day causes biological consequences and over time these consequences change the way we think and act. The more technical aspects involve how our immune system and its proteins respond to this stress and cause damage. I want to also touch upon how those more likely to live under this chronic stress, the disadvantaged and discriminated, have a higher risk of experiencing worse health as a result. Psychiatry as we know it today can be a very subjective practice. This subjectivity in diagnosis and treatment can cost lives and result in prolonged suffering. As our understanding of the human body and its physiology progresses, new questions may be raised about the relationship between seemingly unrelated biological processes. My paper is a meta-analysis that discusses the immune connection to mental illness. Major depressive disorder and suicidality are the focus, but during my research other illnesses such as PTSD, CTE, and Alzheimer's are implicated as well. Minimizing the subjectivity in psychiatry has the potential to save lives, validate suffering, destigmatize mental illness, and unlock new models of care. For this presentation, I will discuss the aforementioned subjectivity and its consequences, the immune connection, and the future implications of a more accurate and humanistic practice.

Mindfulness

March for Mahsa Amini Arya Tavakoulnia and Kiara Timmerman
Video & Presentation

On September 16th 2022, a 22-year-old woman named Mahsa Amini was arrested in Iran for wearing her hijab incorrectly. While in official custody, she was beaten and sustained life ending injuries. In a matter of hours following her death, the people of Iran sparked a revolutionary movement for women all over the world by engaging in peaceful protests in an effort to finally obtain the freedom that was taken from them many decades ago. In Iran, there is a tradition known as “Chehelom” where family members and friends gather on the 40th day after a loved one’s death to honor their life. On October 26th 2022, exactly 40 days following the death of Mahsa Amini, medical students from the Central Michigan University College of Medicine and its Student Diversity Committee recognized this tradition by organizing a march in Mt. Pleasant, Michigan to honor Mahsa Amini’s life as well as the lives of all the women in Iran. More than 150 students and faculty members across the undergraduate, graduate, and medical campuses of Central Michigan University came together to participate in this march with a sea of white coats leading the way. This march not only achieved its goal of honoring Mahsa Amini and raising awareness for the movement that her death sparked, but it has also spread a message to future physicians regarding the influential power that their white coat carries with them. As future physicians, we must understand that there is more to saving lives than the medical knowledge that we gain from medical school. We must master a skill that cannot be taught within the four walls of any medical school. We must learn to use our powerful voices in instances like these to bring people together, and to save lives in ways that traditional medicine cannot.

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"Body of Politic" Investigating the Resurgence of Institutionalization in New York Hospitals Jess Gallagher and Rosemary O'Mahony
Poster

This past November, New York City Mayor, Eric Adams, announced a new plan to “remove people with severe, untreated mental illness from the city’s streets and subways,” and instead commit them to psychiatric hospitals. This announcement was met with understandable backlash, but Adams’ proposal has destructive implications that go beyond the current moment. New York City is not innocent in America’s long history of eugenicist, disablist policies that have defined mental health care for vulnerable populations. This decision will not only overwhelm our hospital systems that have already been pushed beyond their limits, but it is a direct violation of the least restrictive option approach that has been critical to MHL and progress in the Disability Rights movement. As an interdisciplinary team of Columbia University graduate students studying Human Rights and Narrative Medicine, our collaborative, multi-modal poster presentation will explore the destructive implications of Mayor Adams’ decision through the lens of Disability Justice. We will approach this analysis via an Oral History interview. Historically, institutionalization, medical experimentation, and abuse of individuals with intellectual, developmental, and mental disabilities have been a common occurrence across hospitals and ‘training schools’ in the state of NY. In investigating these historical contexts alongside current litigation that protects the rights of persons with disabilities, we aim to uncover how Adams’ proposal violates the rights of people with mental disabilities and encourages regressive policies to manifest.

Skyscrapers

“It is a Violation of Trust”: The Ethics of Drug Testing Black Mothers and Newborns Trey Saunders
Presentation

While the birth of a child is often one of the most joyous moments in a mother’s life, some mothers are unable to celebrate this occasion due to drug testing, often, taken without informed consent during labor. Additionally, this drug testing is documented to disproportionately impact Black mothers, as they and their newborns are 1.5 times more likely to be tested for illicit drugs compared to non-Black women, despite similar positivity rates (Kunins et al. 2007). Once a positive drug test is reported by the medical provider, familial separation and criminalization often occurs and these mothers must fight to regain custody of their child from the child welfare system in addition to fighting criminal charges. This paper examines the ethics of drug testing Black mothers and their newborns through an intersectional lens, by arguing how illicit drug testing disproportionately impacts women at the intersections of gender, race, and class. First, I define intersectionality and explain how intersectionality assists in better understanding the ways mother and infant drug testing is racialized, gendered, and classed. Next, I discuss how this unethical practice has a disproportionate impact on Black women and leads to unnecessary familial separations involving the child welfare system. Finally, I argue for appropriate, immediate steps that should be taken to reduce the separation of newborns from their mothers and why these matters should be removed from the criminal-legal system. Even though Black mothers are regularly drug tested at the hands of our healthcare system, the impact it has on these families remains largely under-studied. This paper shines light on this seldom studied issue by advocating for much needed change. Mothers should not worry about having their child removed from their care because of drug tests often ordered without their informed consent.

Baby's Grasp

Saturday Morning Physician: Anthropomorphizing Emotion in Animated Media Daniel Martin
Flash Presentation

 

Anthropomorphism is a common cognitive sense-making approach in which human characteristics are attributed to non-human entities. It has frequently been considered unfit for serious scientific inquiry. Despite this status, anthropomorphism is commonly used in narrative frameworks, such as in popular animated media that anthropomorphize human emotional states such as Anger from Pixar’s Inside Out, and Logic Rock from Netflix’s Human Resources. This emergence as a framework to explain emotions may have some benefit for those in the medical profession as they serve to translate complex medical concepts and have difficult emotional conversations with patients. The project presented here, which is in its early stages, will serve to analyze some of the afore mentioned animated media from a medical humanities lens. Building on these popular examples, it will argue for the increased and enhanced use of anthropomorphism in medical education, specifically in the professional development of medical students as they develop their emotional intelligence and identity as physicians. The use of popular media provides greater access for students to engage with their emotional state and to understand the emotions of their patients. It will address potential reasons why we naturally tend to anthropomorphize, how these anthropomorphisms may serve to educate patients, and how we may understand our emotions more effectively through anthropomorphism.

Talking Heads

Analyzing the Design and Implementation of Social Justice and Bioethics Curricula in U.S. Medical Schools Shivam Bhargava
Presentation

Social Determinants of Health influence patient care outcomes and are important for healthcare professionals to recognize as they treat patients of all backgrounds, especially marginalized communities. Poverty, illiteracy, discrimination, and many other structural factors have been proven to have negative health consequences on minority groups across the country. With health disparities rising at an alarming rate in our country, it is essential that future health care professionals are trained to recognize and treat patients of all backgrounds in order to alleviate these disparities. Implementing bioethics and medical humanities education in higher education helps students become socially aware and enables them to holistically deliver healthcare to individuals within a community. Despite growing awareness surrounding health disparities in the United States, there remains significant barriers to successful inclusion of social justice in medical education curricula across the country. While there are medical schools across the country that are actively working towards implementing social justice in their curriculum, research remains scarce when it comes to the design and implementation of a social justice curriculum. Synthesizing the existing research that goes into detail about the successes of a social justice curriculum in medical education will contextualize the methodologies necessary for other medical schools to address social justice and bioethics in medical education. The synthesis of this research will illuminate the challenges involved with including social justice and bioethics in medical education curricula and the steps still needed to be taken by educators to push for health disparities to be addressed in a medical student’s 4 year education. This research, conducted through the UNC School of Education, will highlight how a number of medical schools in the United States that have successfully implemented topics of bioethics and humanities into their curriculum and what the positive outcomes of this are on students and surrounding communities.

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Taking A Closer Look at “Franken-science” Omayma Jabara 
Presentation

The specialization of Medical Humanities has been around since the mid-20th century. Many concepts utilized in the discipline of Medical Humanities can be identified in multiple literary classics. Specifically, the principles of Biomedical Ethics are pertinent in Mary Shelley’s Frankenstein. The idea of assembling a creature out of old body parts and strange chemicals was originally pursued by Victor Frankenstein. Frankenstein’s “mad science” has the new name of xenotransplantation, which is a solution to the global organ shortage through the use of animal organs in human bodies. However, this process entails extensive risks to animals and humans. Specifically, through the use of pig organs, there is ethical questioning that can be raised for the sake of animals and humans. These pigs are subjected to a harsh lifestyle where they suffer from confinement and unusual procedures in order to reduce diseases and defects in their bodies. While the benefits for humans are considerable, there are many risks that need to be taken into account. For example, new diseases that only existed in animals can transmit to humans from these surgeries, and can possibly become transmissible between people. This paper presentation views Frankenstein as a reference that can stimulate ethical discourse on xenotransplantation.

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Improving Human Trafficking Interventions in the Emergency Department through Protocol Implementation and Education Bernadine Guimary 
Flash Presentation

Human trafficking (HT) is the exploitation of individuals to perform sex or labor, which affects about 25 million people worldwide. Trafficking victims rarely get medical treatment. When they do, it is often to treat conditions threatening their ability to work. This can include pregnancy or visible beatings on the victims’ faces that make them look less marketable for sex trafficking or injuries that inhibit labor trafficking victims from farming. Most victims’ main interaction with the healthcare system is through the emergency department (ED) as they are federally mandated to provide patient care despite the individual's medical insurance coverage or condition. Many trafficking victims have difficulty receiving healthcare elsewhere due to a lack of health insurance, legal status in the country, or inability to access other forms of medical care. Unfortunately, ED staff have historically received insufficient HT training and care education despite being on the front lines of identifying and caring for trafficking victims. There has also been a lack of a streamlined approach for helping victims once identified during their hospital stay and after leaving. Through the analysis of various studies and articles regarding HT, the implementation of HT protocols in EDs, and current protocol toolkits, it has been found that policies and procedures can be enforced in the hospital to improve how HT victims are cared for from an individual to an institutional level. This includes the implementation of a multidisciplinary HT protocol committee that constructs an HT protocol with a patient screening tool, plans for helping HT victims after they leave the hospital, and education plans for ED staff members on HT prevention and care.

Shadow

History of Migraine Treatment Malina Montgomery & Jessica Mac
Website

We will present a website that Is set up like an online pharmacy. You can "shop online" for migraine relief medications from throughout time. There are descriptions of the time period the treatments were popular, the school of thought/thoery it was born from, and other fun facts. Scan the QR Code to explore the website on your own device. These various relief methods represents for the larger scope of migraine and its suffers. The purpose will be to push against migraine stigma and instead show migraine as a real, often disstabilizing disease that has been affecting people for centuries. It will became appearnt that migrane has a long history with a variety of treatments. Throughout history, migrane treatment is influcenced by the social and political climate. Our website is inspired by the book: Migraine: A History, by Medical Historian Katherine Foxhall

Herbal Medicine

Night Terrors Faith Chadwick
Poetry reading

“I think about you in my sleep./ Dreaming, of the lives you stifle breath out of, the lives you freely take.” So begins my poem, a pathography of my experience during my mother’s two-time battle with breast cancer. The title “Night Terrors” references the medical condition, as the narrator’s experience is framed through her sleep. Addressed to cancer itself, the narrator chronicles the frailty of seeing a loved one suffer while feeling powerless and undeserving of grief. This poem also highlights the agony of healthcare workers who must watch the same disease that afflicts their patients follow them home. As the poem progresses, the narrator’s relationship with the disease evolves as she finds her inner agency amidst the turmoil, emerging triumphant. This piece is an intimate glimpse into the thoughts of those who have defined themselves through the illness of another.

Image by Greta Bartolini

Medical Ageism Faced by Young Adults and Children: How Young-Onset Rheumatoid Arthritis is Overlooked as a Potential Diagnosis in Youth Deirdre Welch
Flash Presentation

It is well-known that ageism amplifies healthcare disparities in geriatric contexts, but systemic ageism against children/young adults is largely denied. Popular institutional definitions of ageism describe the term as discrimination strictly against mature parties. However, younger people are not immune to this form of inequity. “Youth” is, socially and professionally, synonymous with the idea of “health” and wellbeing. This bias inevitably bleeds into the healthcare system and has the effect of leading healthcare providers to dismiss complaints from younger patients. Throughout this study, I will perform a qualitative analysis of interviews which will explore the experiences of chronically ill young adults aged 18-25 diagnosed with young-onset rheumatoid arthritis in their childhood (under 18). The number of young adults ages 18-34 diagnosed with rheumatoid arthritis (RA) is about .008%, while there are no known statistics on the number of minors diagnosed. While rare, it is not impossible for a child or young adult to be diagnosed with RA; the unwritten expectation that younger people cannot have RA leads to postponed diagnosis and treatment. I will argue that ageism against young adults/children is prominent in the American healthcare system and significantly impacts the resources available to younger people with health conditions, specifically RA. The reduced quality of care and deferred diagnosis experienced by young adults with RA results in prolonged physical suffering and discomfort.

Teenagers

The Consideration of Physician-Assisted Suicide: A Case Against Extending the Suffering of the Terminally Ill Deirdre Welch
Presentation

Though it is a claim of success that modern medicine has extended the average lifespan across all demographics and increased the survival rate of most ailments, this also entails another implication that necessarily goes in hand with these developments: the prolongation of the lifetime of patients suffering from various debilitating and distressing symptoms, and, by extension, the continuation of their discomfort. Because of the established and colloquially assumed role of a healthcare professional to “do no harm,” withholding harm is generally thought to be synonymous with extending care and supporting life, even into the most excruciating stages of physical affliction. It is from the standpoint that allowing a patient the privilege to have the guidance and support of their medical professional during their end of life provides significant physical and mental relief that I will argue that the act of physician-assisted suicide should be legally and morally acceptable and considered in medical scenarios only where the prognosis for the patient is unrelenting suffering and decline in quality of life. I also present that there should be an additional caveat that removes the stipulation that a patient's death must result from only passive methods, but holds that physician-assisted death only be done upon the direct request of the patient or the patient’s designated surrogate in a case where the patient is incapable of communicating his/her desires.

Hospital
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