Literature DB >> 19229973

Transition of patients with sickle cell disease from pediatric to adult care: Assessing patient readiness.

Marianne McPherson1, Lisa Thaniel, Caterina P Minniti.   

Abstract

BACKGROUND: Transfer of care from pediatric to adult-oriented providers is challenging for adolescents with sickle cell disease (SCD). The need for transition programs is known, however many SCD patients leave pediatric care without adequate preparation. This study has two aims: to assess adolescent SCD patients' preparation for transition and to identify variables that predict patient readiness. PROCEDURE: Adolescent patients receiving care at a pediatric SCD center received a survey regarding essential steps of the transition process. Patients' level of prior thought, interest, anticipated difficulty, and perceived importance of transition were graded on a scale of 0 to 3. Knowledge of individual transition plans was scaled 0 to 4. Responses were analyzed according to age, sex, and disease severity.
RESULTS: Seventy patients ages 14 to 20 years (median 16.7 years) were assessed. Mean readiness scores were low, with greatest deficiencies in prior thought (mean 0.88 [0.66-1.09]), knowledge (mean 0.85 [0.61-1.09]), anticipated difficulty (mean 1.42 [1.23-1.61]), and interest (mean 1.71 [1.47-1.95]). Perceived importance of transition received the highest score (mean 2.71 [2.58-2.84]). Younger age (<or=16 years) was associated with less knowledge (P = 0.003) and interest (P = 0.023); disease severity (>or=3 crises/year) was associated with lower interest (P = 0.043) but greater anticipated difficulty (P = 0.001). Anticipated difficulty trended higher among females (P = 0.028).
CONCLUSIONS: Adolescents with SCD acknowledge the importance but demonstrate poor preparation for transition to adult-oriented care. Readiness improves with age but remains insufficient. This analysis highlights the need for improvements in anticipatory guidance for transition during adolescence. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19229973     DOI: 10.1002/pbc.21974

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  33 in total

1.  Applicability of the SMART Model of Transition Readiness for Sickle-Cell Disease.

Authors:  Siddika S Mulchan; Jessica M Valenzuela; Lori E Crosby; Claudia Diaz Pow Sang
Journal:  J Pediatr Psychol       Date:  2015-12-30

Review 2.  Childhood to adult transition and long-term follow-up after blood and marrow transplantation.

Authors:  M C Cupit; C Duncan; B N Savani; S K Hashmi
Journal:  Bone Marrow Transplant       Date:  2015-12-07       Impact factor: 5.483

3.  Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina.

Authors:  Joshua R Mann; Julie A Royer; Suzanne Mcdermott; James W Hardin; Orgul Ozturk; Natalie Street
Journal:  Muscle Nerve       Date:  2015-08-14       Impact factor: 3.217

4.  Assessing readiness for transition from paediatric to adult health care: Revision and psychometric evaluation of the Am I ON TRAC for Adult Care questionnaire.

Authors:  Melissa Moynihan; Elizabeth Saewyc; Sandra Whitehouse; Mary Paone; Gladys McPherson
Journal:  J Adv Nurs       Date:  2015-01-23       Impact factor: 3.187

5.  A Systematic Review of Transition Readiness in Youth with Chronic Disease.

Authors:  Maureen Varty; Lori L Popejoy
Journal:  West J Nurs Res       Date:  2019-09-18       Impact factor: 1.967

Review 6.  Pediatric sickle cell disease: past successes and future challenges.

Authors:  Emily Riehm Meier; Angeli Rampersad
Journal:  Pediatr Res       Date:  2016-10-05       Impact factor: 3.756

7.  Concentration of hospital care for acute sickle cell disease-related visits.

Authors:  J A Panepinto; P L Owens; A L Mosso; C A Steiner; D C Brousseau
Journal:  Pediatr Blood Cancer       Date:  2011-12-16       Impact factor: 3.167

8.  Transfer from paediatric rheumatology to the adult rheumatology setting: experiences and expectations of young adults with juvenile idiopathic arthritis.

Authors:  Deborah Hilderson; Leen Eyckmans; Kristien Van der Elst; Rene Westhovens; Carine Wouters; Philip Moons
Journal:  Clin Rheumatol       Date:  2012-12-14       Impact factor: 2.980

Review 9.  Improving outcomes in children with sickle cell disease: treatment considerations and strategies.

Authors:  Ali Amid; Isaac Odame
Journal:  Paediatr Drugs       Date:  2014-08       Impact factor: 3.022

10.  The medical home concept and congenital adrenal hyperplasia: a comfortable habitat!

Authors:  Selma Feldman Witchel
Journal:  Int J Pediatr Endocrinol       Date:  2010-06-08
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