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A Lifetime
Lindsay O’Hara
Dr. Sokola
October 4, 2018
RUNNING HEAD: Transitional Care for Young Diabetics 2
Adolescence and young adulthood are filled with lots exciting and new events such
attending prom, graduating high school and learning to drive. There are also new responsibilities
these young adults face as they leave the comfort of their parents’ home. Becoming responsible
for themselves is a bigger task than most young adults realize. Managing a chronic lifetime
disease such as diabetes, only makes this time in a young adult’s life that much harder. More
and more, health care is seeing young adults being hospitalized with diabetic complications such
emerging adults with T1D are at risk for adverse health outcomes, including: acute diabetes
complications, such as nephropathy and retinopathy; and early mortality” (Garvey, et al., 2014).
Health care professional have insisted on putting into place better transitional care for these
emerging adults in order to prevent these complications, and keep compliance. The transition
process has many obstacles, but with fine tuning, can result in lowered glycemic values and
lowered hospital occurrences. It is important to help this vulnerable population manage their
lifelong disease, and establish a well-balanced medical routine early, in order to avoid multiple
Statement of Problem
The increased risk of diabetic complications may experience from non-compliance and
lack of medical care, this vulnerable population needs help and guidance when transitioning from
pediatric care into the adult care system. They must assume responsibility for blood glucose
monitoring, medication administration, and making appointments for follow ups. Without proper
transition, the adverse outcomes begin to add up. With the proper transition tools and guidance,
is it possible that it will lead to less hospitalizations for young adults with diabetes? More and
more, I see young adults hospitalized with diabetic ketoacidosis. These patients are non-
compliant and often are not able to tell me when the last check their blood sugar or what are
normal blood sugar should be. Upon admission, my facility screens for diabetes. I ask several
questions related to diabetes such as “Do you know what a normal blood sugar level is?” and
“Do you know what do you if your blood sugar is too high/low?” 8 out 10 young patients are not
able to answers these questions. I feel like as nurses it is our job to help educate our patients and
give them the resources to successfully manage their disease once they are discharged. If these
young adults are unable to manage their chronic disease, we will see an increase in
Literature Review
Transition Clinic
A recurring theme in my research showed that health care providers have relied on that
has shown improvement in glycemic levels is a pediatric to adult care transition clinic in order to
facilitate a smooth transition. The clinics are established in order to prevent any gaps in medical
coverage and to introduce young adults to new providers. During one study at the University of
Pennsylvania, hemoglobin A1C levels decreased from 9.7 to 9.0 after 6 months of attendance at
a clinic. One of the main concerns is the gap in coverage that this population seems to
experience. The same study from above showed that about a quarter of the referred participants
were unreachable. “Of the 122 referrals, 30 participants (24.6%) did not complete the transfer
and were not able to be contacted by either the adult or pediatric teams after referral was made”
(Agarwal, et al., 2016). These clinics have been proven to bridge the gap and improve the health
of the young adults willing to attend. It has been proven that structured transition using a clinic
produces better results in attendance and reduction in A1C level than unstructured transition. “At
3 years: ↑ clinic attendance in IG compared with CG (P < 0.05)” (O’Hara, et al., 2016). The
Diabetic ketoacidosis admissions (P < 0.05) and ↓ diabetic ketoacidosis re‐admission length of
Coordination of Care
Another theme that was seen throughout most of my research was the need for
coordination of care between the pediatric and adult settings. It is important to have care
coordination between the pediatric care and the proposed adult care. “Transition programs that
participants” (Agarwal, et al., 2016). During a qualitative study that gave participants a chance to
express how they felt about the transition from pediatric to adult care. “In addition, various ideas
for overlapping visits with the pediatric team and a specific adult diabetes provider were
proposed. Seamless information-sharing was one commonly noted purpose for coordination
between pediatric and adult providers” (Hilliard et al., 2013). Coordination between the two
providers would help ensure accurate patient history, medication reconciliation and current
regimens.
Psychosocial Monitoring
substance abuse and eating disorders. It is important that patient have access to professionals,
peer and support groups to help manage these ailments. A qualitative study was performed using
open ended questions surveying endocrinologists, and they were asked how they felt about
transitional care, and about 30% of the sample expressed concern about psychosocial monitoring.
“Similarly, for the mental health scenarios, 30% of endocrinologists endorsed lack of expertise
as a barrier for substance and eating disorder cases (both 30%), followed by developmental
disability (24%) and depression (15%), in contrast to minimal expertise barriers (1–3%) for
recurrent ketoacidosis, obesity, and continuous glucose monitoring (Garvey et al., 2015). Many
young adults also expressed the need for peer support at the time of transition in order feel
RUNNING HEAD: Transitional Care for Young Diabetics 6
comradery. “Finally, patients felt that peer mentoring from other emerging adults who had
navigated the health care transition would be an invaluable source of support: I would have liked
to have had some kind of support system when I entered into adult care. I remember asking my
doctor, ‘are there any other college students that are doing this as well?’ [female, age 24]”
(Garvey et al., 2014). It’s paramount that these young adults feel like they have the support and
Analysis
There were mixed methods used in all the research that I found. Mostly, qualitative
research was used because it’s important for researcher to understand the perception and
concerns of everyone involved in transitional care for diabetic patients, none more important
than the patient themselves. In order to improve upon the process, researchers need to hear from
the patients and use their suggestions to improve the process. Quantitative research was used in
order to evaluate if the transition process is helping by a reduction in hemoglobin A1C levels and
clinic attendance. I feel like the gaps in the research were minimal at best. One gap I did find
were qualitative responses from subjects that were post transition. After reading the studies, most
of the qualitative studies concluded it was hard to get hold of subjects after transition. Part of this
is due to the crazy schedule that a young adult has. All in all, the research I found all
recommended structured transition care with the use of a clinic was acceptable way to help
facilitate the needs of the population. The most important factor being the coordination of care
Recommendation
the needs of young adults with Type I diabetes. I would suggest the clinic have care coordinator
on staff in order to help the patients with finding outside resources such as a peer support group.
Perhaps some research into the use of text messaging in order to report glucose values to clinic
staff would be more convenient to this population, who already seem to have erratic schedules to
begin with. The more resources that are available to these young adults, I feel like we may be
References
Argawal, S., Raymond, J., Schutta, M., Cardillo, S., Miller, V., and Long, J. (2017). An
Adult Health Care–Based Pediatric to Adult Transition Program for Emerging Adults
https://doi.org/10.1177/014572171667709
Garvey, K.C., Beste, M., Luff, D., Atakov-Castillo, A., Wolpert, H., and Ritholz, M. (2014).
Experiences of health care transition voiced by young adults with type 1 diabetes: a
https://doi.org/10.2147/AHMT.S67943
Garvey, K.C., Telo, G., Needleman, J., Forbes, P., Finkelstein, J., and Laffel, L. (2016) Health
https://doi.org/10.2337/dc15-1775
Hilliard, M. E., Perlus, J. G., Clark, L. M., Haynie, D. L., Plotnick, L. P., Guttmann-Bauman, I.,
& Iannotti, R. J. (2014). Perspectives From Before and After the Pediatric to Adult Care
https://doi:10.2337/dc13-1346
RUNNING HEAD: Transitional Care for Young Diabetics 9
O’Hara, M.C., Hynes, L., O’Donnell, M., Nery, N., Byrne, M., Heller, S.R., and Dinneen, S.F.
(2016) A systematic review of interventions to improve outcomes for young adults with
https://doi.org/10.1111/dme.13276