Literature DB >> 21434965

The relation between health-related quality of life, treatment adherence and disease severity in a paediatric sickle cell disease sample.

B Fisak1, M H Belkin, A C von Lehe, M M Bansal.   

Abstract

BACKGROUND: The purpose of this study was to provide a comprehensive examination of the potential factors associated with health-related quality of life (HRQOL) in a paediatric sickle cell disease sample.
METHODS: Caregivers of 78 paediatric sickle cell disease patients completed surveys, which included measures of HRQOL, treatment adherence and barriers to treatment adherence. Medical chart reviews were also conducted to assess disease severity.
RESULTS: Barriers to treatment adherence and pain crisis frequency were found to be the most robust factors associated with HRQOL.
CONCLUSIONS: This study provides insight into the factors related to paediatric sickle cell disease and informs both clinicians and researchers interested in understanding and improving HRQOL in this population. In particular, the reduction of pain crises frequency and barriers to adherence may be particularly effective strategies to improve HRQOL.
© 2011 Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2011        PMID: 21434965     DOI: 10.1111/j.1365-2214.2011.01223.x

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  9 in total

1.  Barriers to care and quality of primary care services in children with sickle cell disease.

Authors:  Eufemia Jacob; Courtney Childress; Joana Duran Nathanson
Journal:  J Adv Nurs       Date:  2015-09-15       Impact factor: 3.187

2.  Quality of Life of Latino and Non-Latino Youth With Sickle Cell Disease as Reported by Parents and Youth.

Authors:  Jennel C Osborne; Nancy S Green; Arlene M Smaldone
Journal:  Hisp Health Care Int       Date:  2020-03-03

Review 3.  Systematic and Meta-Analytic Review: Medication Adherence Among Pediatric Patients With Sickle Cell Disease.

Authors:  Kristin Loiselle; Jennifer L Lee; Lauren Szulczewski; Sarah Drake; Lori E Crosby; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-09-18

4.  Parental problem-solving abilities and the association of sickle cell disease complications with health-related quality of life for school-age children.

Authors:  Lamia P Barakat; Lauren C Daniel; Kelsey Smith; M Renée Robinson; Chavis A Patterson
Journal:  J Clin Psychol Med Settings       Date:  2014-03

5.  NECROSIS OF THE FEMORAL HEAD AND HEALTH-RELATED QUALITY OF LIFE OF CHILDREN AND ADOLESCENTS.

Authors:  Marcos Almeida Matos; Luanne Lisle Dos Santos Silva; Giordano Bruno Alves; Walter Silva de Alcântara; Davi Veiga
Journal:  Acta Ortop Bras       Date:  2018       Impact factor: 0.513

6.  Health-Related Quality of Life Assessments by Children and Adolescents with Sickle Cell Disease and Their Parents in Portugal.

Authors:  Clara Abadesso; Susana Pacheco; Maria Céu Machado; G Allen Finley
Journal:  Children (Basel)       Date:  2022-02-18

7.  The Correlation Between Surgical Procedures and Quality of Life Among Sickle Cell Disease Patients: A Perspective Saudi Study.

Authors:  Ali J Al Saad; Rayan A Buhalim; Faisal A Al Jabr; Abdulaziz M Al Dehailan; Abdulaziz A Albahrani
Journal:  Cureus       Date:  2022-01-18

Review 8.  Health-Related Quality of Life and Adherence to Hydroxyurea and Other Disease-Modifying Therapies among Individuals with Sickle Cell Disease: A Systematic Review.

Authors:  Mira Yang; Lena Elmuti; Sherif M Badawy
Journal:  Biomed Res Int       Date:  2022-07-18       Impact factor: 3.246

9.  Saudi SCD patients' symptoms and quality of life relative to the number of ED visits.

Authors:  Anwar E Ahmed; Ahmed S Alaskar; Donna K McClish; Yosra Z Ali; Mohammed H Aldughither; Ahmad M Al-Suliman; Hafiz M Malhan
Journal:  BMC Emerg Med       Date:  2016-08-20
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.