Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.

Literature DB >> 21594889

Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.

Amy Sobota¹, Ellis J Neufeld, Philippa Sprinz, Matthew M Heeney.

Abstract

Entities: Disease Species

Mesh：

Year: 2011 PMID： 21594889 PMCID： PMC5804481 DOI： 10.1002/ajh.22016

Source DB: PubMed Journal: Am J Hematol ISSN： 0361-8609 Impact factor: 10.047

× No keyword cloud information.

23 in total

1. Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease.

Authors: Joseph Telfair; Akhlaque Haque; Marc Etienne; Shenghui Tang; Sheryl Strasser
Journal: Public Health Rep Date: 2003 Jan-Feb Impact factor: 2.792

2. Providers' perspectives and beliefs regarding transition to adult care for adolescents with sickle cell disease.

Authors: Joseph Telfair; Leah R Alexander; Penny S Loosier; Patty L Alleman-Velez; Julie Simmons
Journal: J Health Care Poor Underserved Date: 2004-08

3. Improving transition from pediatric to adult cystic fibrosis care: lessons from a national survey of current practices.

Authors: Suzanne Elizabeth McLaughlin; Marie Diener-West; Alka Indurkhya; Haya Rubin; Rebekah Heckmann; Michael Patrick Boyle
Journal: Pediatrics Date: 2008-05 Impact factor: 7.124

4. The number of people with sickle-cell disease in the United States: national and state estimates.

Authors: David C Brousseau; Julie A Panepinto; Mark Nimmer; Raymond G Hoffmann
Journal: Am J Hematol Date: 2010-01 Impact factor: 10.047

5. Transition from child-centered to adult health-care systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine.

Authors: R W Blum; D Garell; C H Hodgman; T W Jorissen; N A Okinow; D P Orr; G B Slap
Journal: J Adolesc Health Date: 1993-11 Impact factor: 5.012

6. Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.

Authors: Marsha Treadwell; Joseph Telfair; Robert W Gibson; Shirley Johnson; Ifeyinwa Osunkwo
Journal: Am J Hematol Date: 2011-01 Impact factor: 10.047

7. A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services.

Authors: Elizabeth A Wojciechowski; Anita Hurtig; Louise Dorn
Journal: J Pediatr Nurs Date: 2002-02 Impact factor: 2.145

8. Health care transition: youth, family, and provider perspectives.

Authors: John G Reiss; Robert W Gibson; Leslie R Walker
Journal: Pediatrics Date: 2005-01 Impact factor: 7.124

9. Transition to adult care for youths with diabetes mellitus: findings from a Universal Health Care System.

Authors: Meranda Nakhla; Denis Daneman; Teresa To; Gilles Paradis; Astrid Guttmann
Journal: Pediatrics Date: 2009-11-23 Impact factor: 7.124

10. Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.

Authors: J Telfair; J Myers; S Drezner
Journal: J Adolesc Health Date: 1994-11 Impact factor: 5.012

16 in total

10. Effectiveness of Clinical Decision Support Based Intervention in the Improvement of Care for Adult Sickle Cell Disease Patients in Primary Care.

Authors: Arch G Mainous; Peter J Carek; Kim Lynch; Rebecca J Tanner; Mary M Hulihan; Jacquelyn Baskin; Thomas D Coates
Journal: J Am Board Fam Med Date: 2018 Sep-Oct Impact factor: 2.657

Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.

1. Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease.

2. Providers' perspectives and beliefs regarding transition to adult care for adolescents with sickle cell disease.

3. Improving transition from pediatric to adult cystic fibrosis care: lessons from a national survey of current practices.

4. The number of people with sickle-cell disease in the United States: national and state estimates.

5. Transition from child-centered to adult health-care systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine.

6. Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.

7. A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services.

8. Health care transition: youth, family, and provider perspectives.

9. Transition to adult care for youths with diabetes mellitus: findings from a Universal Health Care System.

10. Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.

1. Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.

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

3. Pediatric to Adult Care Transition: Perspectives of Young Adults With Sickle Cell Disease.

4. Evaluation of spina bifida transitional care practices in the United States.

5. Understanding sickle cell disease: impact of surveillance and gaps in knowledge.

Review 6. Reducing Health Care Disparities in Sickle Cell Disease: A Review.

7. Perceptions of young adults with sickle cell disease concerning their disease experience.

8. Role of self-care in sickle cell disease.

9. Self-reported transition readiness among young adults with sickle cell disease.

10. Effectiveness of Clinical Decision Support Based Intervention in the Improvement of Care for Adult Sickle Cell Disease Patients in Primary Care.