Literature DB >> 21796763

Young adults with SCD in US children's hospitals: are they different from adolescents?

Amanda K Dickerson1, Jennifer Klima, Melissa M Rhodes, Sarah H O'Brien.   

Abstract

BACKGROUND: The period of transition from pediatric to adult care is a vulnerable time for patients with sickle cell disease (SCD). The optimal time for transition is unknown and there is no standard of care regarding this timing in the United States. PROCEDURES: We collected administrative data from the Pediatric Health Information System for all SCD admissions from 2000 to 2009. We compared reasons for hospitalization and resulting charges in adolescents (13-17 years) and young adults (18-21 years).
RESULTS: We identified 25,371 admissions of adolescents (n = 18,299) and young adults (n = 7,072) with SCD. Median admissions per patient per year was higher in young adults (0.6) compared to adolescents (0.2, P < 0.001), but reasons for hospitalization were similar between the two age groups. Complications of adult SCD such as nephropathy and pulmonary hypertension were rare (<2.5% of discharges) but more frequent in older patients (P = 0.001). Although length of stay was similar between the two groups (median = 4 days), young adults tended to incur higher charges (median +$1,314, P < 0.001) and were less likely to utilize private insurance (P < 0.001). Deaths (0.2% of admissions) were rare and similar across age groups (P = 0.7).
CONCLUSION: In a national sample of US children's hospitals, adolescents (13-17 years) and young adults (18-21 years) with SCD had similar reasons for hospitalization and low mortality. Further studies are needed to investigate whether extending the age of transition to ≥ 21 years as a national standard may decrease morbidity and mortality, improve health-related quality of life, or increase readiness for transition in patients with SCD.
Copyright © 2011 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2011        PMID: 21796763     DOI: 10.1002/pbc.23262

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


  11 in total

1.  Exploring Adult Care Experiences and Barriers to Transition in Adult Patients with Sickle Cell Disease.

Authors:  C J Bemrich-Stolz; J H Halanych; T H Howard; L M Hilliard; J D Lebensburger
Journal:  Int J Hematol Ther       Date:  2015-09-06

2.  Predictors of health-related quality of life over time among adolescents and young adults with sickle cell disease.

Authors:  Jamie L Jackson; Kathleen L Lemanek; Emily Clough-Paabo; Melissa Rhodes
Journal:  J Clin Psychol Med Settings       Date:  2014-12

3.  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

4.  Sickle cell disease is not so benign.

Authors:  M M Hsieh
Journal:  Bone Marrow Transplant       Date:  2015-04-20       Impact factor: 5.483

5.  Decision-Making Involvement, Self-Efficacy, and Transition Readiness in Youth With Sickle Cell Disease.

Authors:  Maureen Varty; Barbara Speller-Brown; Bonnie J Wakefield; Russell D Ravert; Katherine Patterson Kelly; Lori L Popejoy
Journal:  Nurs Res       Date:  2022 Jan-Feb 01       Impact factor: 2.381

6.  Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.

Authors:  Natalie B Stollon; Christine W Paine; Matthew S Lucas; Lauren D Brumley; Erika S Poole; Tamara Peyton; Anne W Grant; Sophia Jan; Symme Trachtenberg; Miriam Zander; Christopher P Bonafide; Lisa A Schwartz
Journal:  J Pediatr Hematol Oncol       Date:  2015-11       Impact factor: 1.289

7.  Barriers in transition from pediatrics to adult medicine in sickle cell anemia.

Authors:  Jeffrey D Lebensburger; Christina J Bemrich-Stolz; Thomas H Howard
Journal:  J Blood Med       Date:  2012-09-19

8.  Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project.

Authors:  Donna K McClish; Wally R Smith; James L Levenson; Imoigele P Aisiku; John D Roberts; Susan D Roseff; Viktor E Bovbjerg
Journal:  Biomed Res Int       Date:  2017-03-28       Impact factor: 3.411

Review 9.  Methods for Measuring the Time of Transfer from Pediatric to Adult Care for Chronic Conditions Using Administrative Data: A Scoping Review.

Authors:  Rayzel Shulman; Eyal Cohen; Eric I Benchimol; Meranda Nakhla
Journal:  Clin Epidemiol       Date:  2020-06-30       Impact factor: 4.790

10.  Estimated Life Expectancy and Income of Patients With Sickle Cell Disease Compared With Those Without Sickle Cell Disease.

Authors:  Deborah Lubeck; Irene Agodoa; Nickhill Bhakta; Mark Danese; Kartik Pappu; Robin Howard; Michelle Gleeson; Marc Halperin; Sophie Lanzkron
Journal:  JAMA Netw Open       Date:  2019-11-01
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