A Different Kind of Crisis: More Doctors Needed for Adults with Sickle Cell Disease

In the United States, pediatric patients younger than age 18 with Sickle Cell Disease (SCD) have more options than adults for ongoing health management through pediatricians, family medicine doctors, and hematology specialists.  When patients turn 18 and need to transition their care, a critical shortage of adult healthcare providers leaves this population in a vulnerable position. On November 9th, 2018 Dr. Wanda Whiten-Shurney, CEO and Medical Director of the Sickle Cell Disease Association of America – Michigan Chapter (SCDAA-MI), discussed this topic and others as well as a way she is working to address it at the 2018 Management of Sickle Cell Disease Conference in Chicago, IL.

One way that Dr. Whitten-Shurney is attempting to address the lack of access to care is through the support of the HRSA Treatment Demonstration Project.  As a participant in the HRSA Treatment Demonstration Project grant, the SCDAA-MI receives federal funding to:

  • Increase the number of providers treating persons for sickle cell disease or sickle cell related issues;
  • Increase the number of providers prescribing disease-modifying therapies, such as hydroxyurea, and L-glutamine
  • Increase the number of patients receiving regular care from providers knowledgeable about treating sickle cell disease.

Partnerships include sickle cell treatment centers, Federally Qualified Health Centers (FQHCs), community-based organizations, parents and patients. Dr. Whitten-Shurney, along with a team of community health workers, helps educate and connect adult patients to primary care. Through education, these families learn how to manage the disease on the “home front” through lifestyle changes, nutrition, and they learn when to seek medical help.  Additionally, the SCDAA-MI team has started a project to work on facilitating adult care by reaching out to FQHCs and others.

Dr. Shurney also discussed that there are many ongoing clinical studies in sickle cell.  She is part of the National Institutes of Health (NIH) Cure Sickle Cell Initiative and is optimistic that we should see results of this effort in 5 years.  As part of her commitment to patients, she has partnered with the Sickle Cell Community Consortium (SCCC) to develop a patient empowerment toolkit.  This toolkit includes a nutrition guide, the NHLBI publication, “Evidence-based Management of Sickle Cell Disease”, information on where to find helpful apps as well as the personalized passport to health which helps patients keep all their information in one place.

Awareness is simply the first step. We must act now to improve the quality of care for the people living with sickle cell disease. Without doctors, nurses, and allied medical professionals who proactively seek training in evidence-based care, existing and future treatments for this condition will not reach the patients. Collectively, we can change the narrative of sickle cell disease in the US.

 

Disclaimer: As of this writing, Micromattie Consulting Inc. is not affiliated with the Sickle Cell Disease Association of America.

 

This blog article was sponsored by Global Blood Therapeutics Inc. GBT Logo Small, the views expressed by the author are her own

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s