Literature DB >> 20331954

Health status and healthcare use in a national sample of children with sickle cell disease.

Sheree L Boulet1, Emad A Yanni, Melissa S Creary, Richard S Olney.   

Abstract

BACKGROUND: There is a paucity of population-based data describing health status and use of health services among children with sickle cell disease (SCD).
PURPOSE: This study provides estimates of co-occurring conditions, health impact and utilization, and barriers to care for a national sample of children with SCD.
METHODS: Data were derived from the 1997-2005 National Health Interview Survey Child Sample Core. The study included 192 children aged 0-17 years with SCD whose race was reported as black or African-American, and 19,335 children without SCD of the same age and race. Parents or other knowledgeable adults reported on medical and developmental conditions, health status, and healthcare use and access.
RESULTS: After adjusting for demographic characteristics, black children with SCD had higher odds of frequent severe headaches or migraines, intellectual disabilities, regular use of prescription medication, and fair or poor health status compared with black children without SCD. While healthcare and special education services use were generally higher for black children with SCD than for black children in the general population, those with SCD also had higher odds of reporting delays in accessing health care.
CONCLUSIONS: The health burden for children with SCD and their families is profound and may be exacerbated by barriers to accessing comprehensive medical care. Additional study of the extent of unmet needs for U.S. children with SCD is warranted. Published by Elsevier Inc.

Entities:  

Mesh:

Year:  2010        PMID: 20331954     DOI: 10.1016/j.amepre.2010.01.003

Source DB:  PubMed          Journal:  Am J Prev Med        ISSN: 0749-3797            Impact factor:   5.043


  23 in total

1.  Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.

Authors:  Lori E Crosby; Naomi E Joffe; Nina Reynolds; James L Peugh; Ellen Manegold; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-08-13

2.  Evaluation and Treatment of Sickle Cell Pain in the Emergency Department: Paths to a Better Future.

Authors:  William T Zempsky
Journal:  Clin Pediatr Emerg Med       Date:  2010-12-01

3.  Care Coordination for Children With Sickle Cell Disease: A Longitudinal Study of Parent Perspectives and Acute Care Utilization.

Authors:  Tiffany L Rattler; Annette M Walder; Hua Feng; Jean L Raphael
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

4.  Newborn Screening Programs and Sickle Cell Disease: A Public Health Services and Systems Approach.

Authors:  Cynthia S Minkovitz; Holly Grason; Marjory Ruderman; James F Casella
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

5.  Risk Factors for Attention and Behavioral Issues in Pediatric Sickle Cell Disease.

Authors:  Eboni I Lance; Anne M Comi; Michael V Johnston; James F Casella; Bruce K Shapiro
Journal:  Clin Pediatr (Phila)       Date:  2015-07-06       Impact factor: 1.168

6.  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

7.  Silent cerebral infarction, income, and grade retention among students with sickle cell anemia.

Authors:  Allison A King; Mark J Rodeghier; Julie Ann Panepinto; John J Strouse; James F Casella; Charles T Quinn; Michael M Dowling; Sharada A Sarnaik; Alexis A Thompson; Gerald M Woods; Caterina P Minniti; Rupa C Redding-Lallinger; Melanie Kirby-Allen; Fenella J Kirkham; Robert McKinstry; Michael J Noetzel; Desiree A White; Janet K Kwiatkowski; Thomas H Howard; Karen A Kalinyak; Baba Inusa; Melissa M Rhodes; Mark E Heiny; Ben Fuh; Jason M Fixler; Mae O Gordon; Michael R DeBaun
Journal:  Am J Hematol       Date:  2014-08-04       Impact factor: 10.047

8.  Performance of ICD-10-CM diagnosis codes for identifying children with Sickle Cell Anemia.

Authors:  Sarah L Reeves; Brian Madden; Meng Wu; Lauren S Miller; David Anders; Michele Caggana; Lindsay W Cogan; Mary Kleyn; Isabel Hurden; Gary L Freed; Kevin J Dombkowski
Journal:  Health Serv Res       Date:  2020-01-09       Impact factor: 3.402

9.  Association of care in a medical home and health care utilization among children with sickle cell disease.

Authors:  Jean L Raphael; Tiffany L Rattler; Marc A Kowalkowski; David C Brousseau; Brigitta U Mueller; Thomas P Giordano
Journal:  J Natl Med Assoc       Date:  2013       Impact factor: 1.798

10.  Adverse neurological outcomes in Nigerian children with sickle cell disease.

Authors:  I A Lagunju; B J Brown
Journal:  Int J Hematol       Date:  2012-11-06       Impact factor: 2.490

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