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Identifying Info in Medical Treatment May Encourage Racial Bias

June 17th, 2021 News & Politics 3 minute read
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Identifying Info in Medical Treatment May Encourage Racial Bias

 The personal identifying factors listed along with the patient’s presenting concerns may perpetuate racism within medical communities.  The verbiage continues to be used despite racial bias and disparities within the system that have been made more evident amid the Covid-19 pandemic.For example, identifying information may read something like, “A 30-year-old African American male presented in the e emergency department with heart palpitations,” and many providers believe race is a vital factor in the clinical decision-making process.  However, sometimes this information can reinforce racial biases and prevent patients from receiving standard medical treatments.  It’s also important to note that physicians generally place label on the patient rather than asking a patient to self-identify.On the other hand, patients are usually asked to self-identify in clinical trials.  And this has shown that many patients do not self-identify in the same ways as the labels given to them by researchers.  A person’s phenotype may not hold important information about their genotype.  In fact, a landmark study in the journal Science found that “two people of European descent may be more genetically similar to an Asian person than they are to each other.”

Identifying Info in Medical Treatment May Encourage Racial BiasPhoto by Klaus Nielsen from Pexels

Many people look to the medical community to operate objectively.  By using this outdated practice, physicians may be reinforcing the incorrect idea that race differentiation holds scientific value.  Estimated glomerular filtration rate (eGFR), for example, and vaginal birth after Cesarean section (VBAC), are both processes that factor race into decision-making.  Plugging in a Black or nonwhite/Hispanic into the calculations could prevent them from receiving a kidney transplant or being offered a vaginal birth.Another example is the prescribing methods of clozapine, an antipsychotic that is under-prescribed to Black Americans.  This is due to physician fear of benign ethnic neutropenia (BEN).  BEN is a diagnosis that was created some sixty years ago when African Americans were found to have lower neutrophil counts compared to white Americans.  Now, Black American patients who would benefit from receiving clozapine are oftentimes either not offered it or decide against it themselves because they’ve been forewarned that they will need blood draws and frequent monitoring.  BEN has also affected breast cancer treatment in African American patients by creating bias.The authors of a recent study published in JAMA Online contend, “Race may well be a surrogate, albeit imperfect, for sociologic constructs. However, the most important sociologic variables (eg, social determinants of health) and, in particular, differential opportunities (eg, good access to and quality of care) fail to associate with sufficient precision when race is used as the placeholder.”Some organizations and research publications have already made a move to eliminate race as an identifying factor.  In Canada, neither the Canadian Medical Association Journal nor the Canadian Journal of Surgery reports race in their case reports.  The National Kidney Foundation recently announced that it would no longer be using race as part of its eGFR calculation for kidney transplant necessity.A viable alternative?  Genetic mapping can be used to treat high-risk patients – although, it is a more costly option than phenotyping.   However, as civil rights activist Audre Lorde wrote, “The master’s tools will never dismantle the master’s house.” If medical practitioners continue to use tools developed by predominantly white pioneers in the medical profession without questioning them, racial bias and health disparities will likely persist.

Sources:

A Tool Doctors Use Every Day Can Perpetuate Medical RacismRecalibrating the Use of Race in Medical Research
Sara E. Teller

About Sara E. Teller

Sara is a credited freelance writer, editor, contributor, and essayist, as well as a novelist and poet with nearly twenty years of experience. A seasoned publishing professional, she's worked for newspapers, magazines and book publishers in content digitization, editorial, acquisitions and intellectual property. Sara has been an invited speaker at a Careers in Publishing & Authorship event at Michigan State University and a Reading and Writing Instructor at Sylvan Learning Center. She has an MBA degree with a concentration in Marketing and an MA in Clinical Mental Health Counseling, graduating with a 4.2/4.0 GPA. She is also a member of Chi Sigma Iota and a 2020 recipient of the Donald D. Davis scholarship recognizing social responsibility. Sara is certified in children's book writing, HTML coding and social media marketing. Her fifth book, PTSD: Healing from the Inside Out, was released in September 2019 and is available on Amazon. You can find her others books there, too, including Narcissistic Abuse: A Survival Guide, released in December 2017.

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