Our pediatric diabetes quality improvement program has the ultimate goal of improving health outcomes and quality of life for our patients and families. We maintain a clinic registry and are using the data to identify needs and develop interventions for improving care. We are also one of ten centers participating in the T1D Exchange Collaborative Improvement Network, a learning community focused on improving patient and family outcomes. See below for a description of the major initiatives we are currently working on.
Patient-Centered Clinic Design
The U-M Pediatric Diabetes Clinic is committed to creating a positive, patient- and family-focused experience. We are using different methods to engage with our patients and families to better understand how we can help lessen the burden of diabetes. This includes gathering input from patients and families, such as conducting surveys to address coverage issues, working closely with our lead patient/family advisor, and developing virtual communications tools like the updated UMPedsDiabetes.com website and email newsletter to improve communication and dissemination of resources.
Patient Portal Enrollment
In an effort to improve communication between our patients/caregivers and the U-M Pediatric Diabetes Team, we have been working to increase enrollment in the Patient Portal (MyUofMHealth.org). Using the Patient Portal, patients and caregivers can easily upload blood sugar logs, send secure messages to the U-M Pediatric Diabetes Team, view lab results, request prescription refills, view and pay bills online, and review other health records. We recognize that the sign-up process can be confusing so we developed a process to help enroll patients/caregivers while they were in clinic. We also created a set of step-by-step sign-up instructions that patients/caregivers can follow at home. To date, nearly 50% of our patients/families have joined the Patient Portal.
Our team is currently working on developing a process to integrate depression screening for teens seen in our clinic. We are starting with a small pilot trial, but eventually all teens with T1D aged 13-17 will be asked to complete a brief survey during their clinic visit to screen for depression. Just like routine eye and foot screening, the information from the questionnaire will be used as part of your child’s diabetes treatment plan.
Quality Improvement Staff
Director of Quality Improvement
Joyce Lee, MD, MPH
Associate Director of Quality Improvement
Ashley Garrity, MPH
Pediatric Endocrinology Division Director
Ram Menon, MD
Pediatric Diabetes Clinical Director
Michael Wood, MD