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Frankly, what we know about the healthcare provided to people of color with type 1 diabetes (T1D) is heartbreaking and infuriating.
Today, we celebrate Juneteenth — the commemoration of the end of slavery in the United States — but this day should also look at life today and in the future for Black people. While equality has come a long way, our research reminds us how much further we need to go.
In diabetes, we know that Black people are not receiving the same healthcare as non-Black patients. In fact, we can give you the nitty gritty details that paint this picture quite clearly thanks to research from the T1D Exchange Health Equity Advancement Lab (HEAL) program.
Our research says people of color with diabetes are:
- Less likely to be prescribed a continuous glucose monitor (CGM)
- Less likely to be prescribed an insulin pump
- Less likely to receive education regarding newer diabetes technology
- Less likely to have access to CGM and insulin pump technology
- Less likely to be prescribed newer types of insulin and glucagon medications
- More likely to develop complications including neuropathy, retinopathy, and nephropathy
- More likely to be frequently hospitalized for severe hypoglycemia
- More likely to be frequently hospitalized for diabetic ketoacidosis (DKA)
Is your race preventing your doctor from prescribing a CGM?
Unfortunately, the answer is yes. Your skin. Your name. Your clothing. Your voice. These beautiful details that makeup who you are can trigger a conscious or unconscious prejudice in your healthcare provider, changing the way they manage your diabetes care.
Our research finds that many healthcare providers have an “implicit bias” towards patients of a certain race or ethnicity that they are likely not even aware of — and it’s preventing that provider from prescribing things like continuous glucose monitors and insulin pumps.
Research led by Dr. Nestoras Mathioudakis, an endocrinologist and Associate Professor of Medicine at Johns Hopkins University School of Medicine determined the following difference in technology use based on race and ethnicity.
In a study with about 1,200 participants:
- Only 7.9% of Black patients use a CGM
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- vs. 30.3% of non-Black patients use a CGM
- Only 18.7% of Black patients use an insulin pump
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- vs. 49.6% of non-Black patients use an insulin pump
Mathioudakis also points out that a large majority of hospitalized patients with diabetes don’t have this critical technology — highlighting the impact it has on your daily safety managing T1D.
We are working to change this
This won’t change overnight, but we believe we can make a difference — and we work daily on this endeavor. We’ve developed a custom “bias training” program to help providers identify, prevent, and change prejudice in healthcare provided to people of color with diabetes. The results are clear:
More than 200 healthcare providers received our custom “bias training”.
The impact on 880 patients of those providers:
- 21%increase in CGM prescriptions for all races/ethnicities
- 32% increase in prescriptions for Black people
How YOU can help change healthcare for Black people with diabetes
We need your voice. We need your participation. We need people of color to participate in impactful diabetes research by joining the T1D Exchange Registry. When you join the Registry, you’re simply creating your own personalized portal that invites you to participate in a huge variety of research throughout the year — mostly from the comfort of your own couch!
We value your voice. We need your voice. We want to make a difference and we need your help.
Ginger Vieira
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Juneteenth: A Critical Reminder that Black People with Diabetes Deserve Better Healthcare Cancel reply
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Doing a diabetes support group at an adult rehab center in San Diego the disparity in care was very evident. Each class day, students were picked up from different areas. The students from the South Bay were sicker, had more complications, almost never had seen an endocrinologist ever, and were undertreated by the HCPs they did manage to see. Culturely competent care was rare. The students from central San Diego were usually in the same condition with incompetent care also. This reality was starkly contrasted by the state of the students from the East County where almost everyone was white. In years that most of the other day’s students had nephropathy, I remember only one East County dialysis patient. None of any days students had adequate care, only a handful of long duration T1Ds had ever seen an endocrinologist; the first “diabetes specialist” these students saw was a nephrologist.
I tried to help one time, but unfortunately, in an ineffective way. One care group that I belonged to at the time had a policy that no surgeries would be performed on diabetics with an A1c over 7.2 or 7.5 (sorry, I can’t remember the actual number because it was awhile ago). Because of data I’d seen on the A1cs of POC and the data on A1cs not being all that and a bag of chips, I tried to get them to change their policy to include other criteria that might more closely reflect the health of the patient. And, I was concerned that the 7.2 (or 7.5) criteria was based on an incomplete patient data set.
I was ignored.
It felt like they just wanted one point to dismiss some patients’ concerns. It was beyond disheartening, but I think I just needed to readdress how I approached the group. They were not great for listening to any patient, so that was also a problem.
I came across this quote which is appropriate here:
“Of all the forms of inequality, injustice in health is the most shocking and the most inhuman.” – Martin Luther King, Jr.