"We won't be content until this is indeed performed in 98% of babies," Stephen Kingsmore, MD, DSc, explains.
One of the goals of the BeginNGS newborn genomic sequencing program is equitable access, according to Stephen Kingsmore, MD, DSc, president and CEO, Rady Children's Institute for Genomic Medicine. He discusses the types of disparities seen in genetic testing as the phase 2 clinical trial is underway.
Transcript
What's the plan to ensure equitable access to genome sequencing screening for newborns across different health care systems?
This is a difficult question—equitable access—it speaks to 2 or 3 different things. First of all, genomic medicine, the backdrop here, is the idea that the genome informs medical care and results in better outcomes. So far, it has actually exacerbated disparity.
There are 3 different types of disparity that we see. Number 1, ethnic and racial minorities tend to not get it relative to White folks. Second of all, poor people tend not to get it, whereas rich people do. And third, one that people overlook, is what we call geographic disparity, which means if you're close to a regional center of excellence—we're at Rady Children's Hospital—you get genomic medicine, and if you're in the boonies, you don't.
So, how do we overcome that? We follow in the wake of newborn screening. Ninety-eight percent of babies today get a newborn screening heel prick test. So we want to emulate that. Now, it's not as easy, because one of the reasons why newborn screening hits 98% of babies is nobody asks mom's permission. It's done generally without mom knowing about it, or dad, because it's federally mandated. You can opt out, but you have to consciously say, “Don't do that to my baby,” whereas a genome needs consent.
We need to think through how to solve for those 3 types of disparities. How are we realistically going to do that? Now, we can pick our populations. So for example, we're enrolling babies at Rady Children's Hospital, and we have a Hispanic Latino majority. We're going to be enrolling in Memphis, Tennessee, where we have a Black majority. So, we can do things like that. The geographic inequity, much tougher. The socioeconomic, much tougher. We just need to keep focused on it honestly and understand that we can do what we can do today. But we won't be content until this is indeed performed in 98% of babies.
New Study Finds Risk Groups, Outpatient Care Barriers in Chronic Liver Disease
November 20th 2024Patients with chronic liver disease who were unable to establish care were 85% more likely to require recurrent hospitalizations. This group included a disproportionate number of women and individuals with physical limitations affecting their health.
Read More
Exploring Racial, Ethnic Disparities in Cancer Care Prior Authorization Decisions
October 24th 2024On this episode of Managed Care Cast, we're talking with the author of a study published in the October 2024 issue of The American Journal of Managed Care® that explored prior authorization decisions in cancer care by race and ethnicity for commercially insured patients.
Listen