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Transition Readiness in Teens and Young Adults with Congenital Heart Disease: Can We Make a Difference? - 20/05/20

Doi : 10.1016/j.jpeds.2020.02.040 
Karen Uzark, PhD, CPNP 1, 2, , Sunkyung Yu, MS 1, Ray Lowery, BA 1, Katherine Afton, BS 1, Anji T. Yetman, MD 3, Jonathan Cramer, MD 3, Nancy Rudd, MS, CPNP 4, Scott Cohen, MD 4, 5, Russell Gongwer, MPH 6, Michelle Gurvitz, MD 6
1 Department of Pediatrics, University of Michigan Mott Children's Hospital, Ann Arbor, MI 
2 Department of Cardiac Surgery, University of Michigan Mott Children's Hospital, Ann Arbor, MI 
3 Department of Pediatrics, Children's Hospital and Medical Center, Omaha, NE 
4 Department of Pediatrics, Children's Hospital of Wisconsin, Milwaukee, WI 
5 Department of Internal Medicine, Children's Hospital of Wisconsin, Milwaukee, WI 
6 Department of Cardiology, Boston Children's Hospital, Boston, MA 

Reprint requests: Karen Uzark, PhD, CPNP, University of Michigan Mott Children's Hospital, L2110 Women's, SPC 5202, 1500 E Medical Center Dr, Ann Arbor, MI 48109-5202.University of Michigan Mott Children's HospitalL2110 Women'sSPC 52021500 E Medical Center DrAnn ArborMI48109-5202

Abstract

Objectives

To examine changes in transition readiness (knowledge, self-efficacy, self-management) over time and explore factors associated with transition readiness, including psychosocial quality of life (QOL) and health service utilization in teens/young adults with congenital heart disease.

Study design

In a multicenter prospective cohort study, 356 patients, age 14-27 years, completed transition readiness and QOL assessments at routine cardiology visits at baseline and 1-year follow-up.

Results

Median patient age was 19.8 years at 1.03 years (IQR 0.98-1.24) following baseline transition readiness assessment. Average knowledge deficit scores decreased at follow-up (P < .0001) and self-efficacy scores increased (P < .0001). Self-management scores increased (P < .0001), but remained low (mean 57.7, 100-point scale). Information was requested by 73% of patients at baseline and was associated with greater increase in knowledge at follow-up (P = .005). Increased knowledge (P = .003) and perceived self-efficacy (P = .01) were associated with improved psychosocial QOL, but not health service utilization at follow-up. Patients who preferred face-to-face information from healthcare providers (47%) vs other information sources were more likely to request information (P < .0001). In patients <18 years old, greater agreement between teen and parental perception of teen's knowledge was associated with greater increase in patient knowledge (P = .02) and self-efficacy (P = .003).

Conclusion

Transition readiness assessment demonstrated improved knowledge, self-efficacy, and self-management at 1-year follow-up in teens/young adults with congenital heart disease. Improved knowledge and self-efficacy were associated with improved psychosocial QOL. Self-management remained low. Supplemental media for conveying information and greater involvement of parents may be needed to optimize transition readiness.

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Keywords : adult congenital heart disease, patient education, self-management, healthcare transition, quality of life

Abbreviations : QOL, CHD, PedsQL


Plan


 Funded in part by the University of Michigan Congenital Heart Center, Departments of Cardiac Surgery and Pediatrics, Charles Woodson Research fund, C.S. Mott Children’s Hospital, Save A Heart, and CHAMPS for Mott. The authors declare no conflicts of interest.


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Vol 221

P. 201 - juin 2020 Retour au numéro
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