Literature DB >> 25188623

Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?

Sarah Mennito1, Paul Hletko1, Myla Ebeling1, Lee Ann Amann1, James Roberts1.   

Abstract

OBJECTIVES: Most patients with sickle cell disease (SCD) survive to adulthood; however, young adults with SCD have high rates of morbidity and mortality and may struggle in the transition to a healthy adulthood. The purpose of this study was to determine the readiness of a rural SCD population for the transition to adulthood and adult medical care.
METHODS: Adolescents and young adults who were current/former patients of a rural pediatric practice were surveyed. Assessments included difficulty dealing with daily care issues and perceived/encountered barriers to transition. Adolescents were asked if a doctor had discussed transition to adult care. Young adults also were asked about satisfaction with their transition experience and about the utility and composition of a transition program.
RESULTS: Surveys were completed by 13 adolescents and 5 young adults. Adolescents reported difficulty leaving their pediatrician (62%) and knowing how SCD differs from other types of anemia (54%). They had concerns about finding an adult doctor (54%), arranging transportation (54%), preparing to use an adult hospital (46%), and handling financial issues (46%). Two-thirds had not discussed or did not know whether their doctor had discussed transitions. Young adults described difficulty leaving their pediatrician (100%), finding an adult doctor (80%), keeping a job (60%), knowing what to expect (40%), and knowing how to pay for medical care (40%). Two-thirds were not satisfied with their transition and all believed a transition program would be helpful. Services suggested for a transition program to provide included information about adult providers/adult healthcare services, ways to take control of one's own care, and helping adult providers understand more about SCD.
CONCLUSIONS: Adolescents with SCD in a rural community identify potential barriers in the transition to adult health care. Several barriers mirror what young adults report encountering. A rural SCD transition clinic can provide individualized preparation to promote a successful transition to adulthood.

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Year:  2014        PMID: 25188623     DOI: 10.14423/SMJ.0000000000000162

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  4 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.  High Healthcare Utilization in Adolescents with Sickle Cell Disease Prior to Transition to Adult Care: A Retrospective Study.

Authors:  Julie Kanter; Menaka Bhor; Xin Li; Frank Yunfeng Li; Jincy Paulose
Journal:  J Health Econ Outcomes Res       Date:  2019-10-09

3.  Transition of patients with mucopolysaccharidosis from paediatric to adult care.

Authors:  C Lampe; B McNelly; A K Gevorkian; C J Hendriksz; T V Lobzhanidze; J Pérez-López; K M Stepien; N D Vashakmadze; M Del Toro
Journal:  Mol Genet Metab Rep       Date:  2019-10-21

4.  Pre-Transition Readiness in Adolescents and Young Adults with Four Chronic Medical Conditions in South East Nigeria - An African Perspective to Adolescent Transition.

Authors:  Adaeze C Ayuk; Vivian O Onukwuli; Ijeoma N Obumneme-Anyim; Joy N Eze; Uzoamaka C Akubuilo; Ngozi R Mbanefo; Kenechukwu K Iloh; Osita U Ezenwosu; Israel O Odetunde; Henrietta U Okafor; Ifeoma J Emodi; Tagbo Oguonu
Journal:  Adolesc Health Med Ther       Date:  2020-03-11
  4 in total

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