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Transitioning Care of Young Adults Complications: DKA and Neuropathy

Transitioning Care of Young Adults Complications: DKA and Neuropathy. Anne Peters, MD, CDE Professor, USC Keck School of Medicine Director, USC Clinical Diabetes Programs. DKA Rates in Adolescents in DCCT.

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Transitioning Care of Young Adults Complications: DKA and Neuropathy

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  1. Transitioning Care of Young AdultsComplications: DKA and Neuropathy Anne Peters, MD, CDE Professor, USC Keck School of Medicine Director, USC Clinical Diabetes Programs

  2. DKA Rates in Adolescents in DCCT • In DCCT, DKA rates = 4.7/100 patient years (control), 2.8/100 patient years (intensive group). NS between 2 groups. J Pediatrics 125:177, 2004

  3. Rates of DKA at Diagnosis Fall with Increasing Age • The prevalence of DKA at diagnosis was 25.5%. The prevalence was 37.3% in children aged 0 – 4 years and fell to 14.7% in those 15 – 19 years. Presence of Diabetic Ketoacidosis at Diagnosis of Diabetes Mellitus in Youth: The Search for Diabetes in Youth Study. Pediatrics 2008;121;e1258-e1266

  4. Basic Information Diabetes Care 27 (Suppl 1):S94, 2004

  5. Age Separation for Treatment Guidelines • Adult patients defined as >20 years of age; pediatric <20 years. • Main difference in treatment of DKA are in terms of fluid resuscitation—concern over cerebral edema in those <20 years old.

  6. Age Distribution of Cerebral Edema and DKA 15-16 17 J Ped 141:793, 2002

  7. DKA Treatment: Kids

  8. DKA Treatment: Adults

  9. Precipitating Factors for DKA—ETOH?

  10. HNKS in Young Adults

  11. HNKS in Young Adults

  12. Transition Care Program Reduces DKA Admission Rates by 30%

  13. Measurable Neuropathy Present in Children and Adolescents with DM

  14. Rates of Neuropathy in Australian Adolescents Over 10 Years: Cross-sectional Analysis related to height/BMI increases N=250-300, age ~14.6 1990-94 1995-2002 Thermal/vibration Heart Rate/BP variation Diabetes Care 28:1974–1980, 2005

  15. DCCT: Benefit of Tight Control on Neuropathy in Adolescents (13-17 yrs) N = 195, clinical sxs neuropathy 6 cont/3 int J Pediatrics 125:177, 1994

  16. Eating Disorders and Painful Neuropathy

  17. What Parents Say Changes in Parental Involvement with DM Care for High School Age Children “Before I used to be more careful and tell her and be on her case about diabetes…so her doctor advised me not to be that way and that it would be better to leave her more independent…now I am not as focused on what her food is…” “Yes it has changed. When he was younger, he was more conscientious and more responsible. Now that he’s older he’s become more irresponsible. I told him he was going backwards like the crabs.”

  18. What Parents Say Issues with Providers “My daughter when we go to the nutrition class she will carb count for the first few days then she forgets because she comes home and she’s so hungry and she wants to eat everything…The doctor told me that she could eat anything she wants as long as she gives herself the right amount of insulin. Then the nutritionist says eat small portions so it can be confusing.” “My daughter was embarrassed of having a ball of fat right here and she hid it with her hair. It’s her fault she didn’t mention it to the doctor. Visit after after she didn’t mention it. So I asked her when are you going to take responsibility…finally I asked for her…she has to take responsibility and learn how to ask.”

  19. What Parents Say Leaving Pediatric Care “They are going to finish pediatrics. That’s not the problem. The problem is that they are going to continue to study and will not be working so how are they going to afford their medical costs? To me this topic is very important…” “That the transition will be from your part so that they won’t stop going to school so that they can work to pay for the medications. That is my biggest fear. And then they will not have a future.”

  20. What Providers Say • Participants • Phone survey • Seventeen providers from 6 academic centers in LA County (LAC+USC, CHLA, White Memorial, Harbor UCLA, Miller Long Beach Children’s Hospital, Mattel Children’s UCLA Hospital) • 41% MD’s, 35% RN’s, remainder SW, NP, PA, LVN. • Data • Age at which transition discussion starts: 15-17 • When does change occur? 18-21

  21. What Providers Say • Challenges • Greatest challenge is insurance coverage • Next is lack of adult endocrine providers • Resources • 82% reported discussing fears/concerns with patients before transfer • 65% provide patient education and support tools • 29% completed formal consultation and discharge letter to adult provider

  22. What Providers Say • What Would Help • Develop and maintain an updated list of adult providers • A tool to assess readiness to change/knowledge level • Group meetings/peer education and mentoring programs • “Young adult” clinic • Guidelines for transition—a checklist to follow to be sure patient makes the transition safely • Letter from adult providers for pts—what to bring/what to expect from first visit

  23. Thank You

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