Literature DB >> 30561880

Racial disparities in clinic follow-up early in life among survivors of congenital heart disease.

Jamie L Jackson1, Jennifer Morack2, Millie Harris2, Jennifer DeSalvo3, Curt J Daniels4, Deena J Chisolm2.   

Abstract

OBJECTIVE: The current study aims to identify the rates of lapses in care and loss to follow-up before age one through age five for white and nonwhite congenital heart disease (CHD) survivors. Nonwhite CHD survivors were hypothesized to experience an earlier lapse in care and be lost to follow-up than whites.
DESIGN: Patients were from a large pediatric hospital and had (1) at least one outpatient cardiology clinic visit or cardiac surgery visit before the age of one and (2) a diagnosis of moderate or complex structural CHD. Cardiology outpatient utilization rates were tracked from before age one through age five. Lapse in follow-up was defined as not having at least one outpatient cardiology visit per year, and loss to follow-up was not returning after a lapse in care by age five. Race was categorized as white and nonwhite. Covariates included sex, insurance type, noncardiology inpatient and outpatient hospital utilization, and CHD severity.
RESULTS: The sample included 1034 patients. Overall, 75.7% experienced a lapse in care with only 41.6% of those returning by age five. Nonwhites experienced lapses in care at younger ages than whites. Nonwhites had a 53% increased risk of lapse in care. Medicaid patients and those with moderate CHD diagnoses also had an increased risk for lapse in care.
CONCLUSIONS: Lapse in care appears prevalent among CHD survivors by age five, with nonwhites demonstrating elevated risk. Future multisite prospective studies should include the assessment of parental knowledge, barriers to accessing care, and satisfaction with care.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  children; clinic follow-up; congenital heart disease; racial disparities

Mesh:

Year:  2018        PMID: 30561880     DOI: 10.1111/chd.12732

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  5 in total

1.  Prevention and awareness of birth defects across the lifespan using examples from congenital heart defects and spina bifida.

Authors:  Sherry L Farr; Catharine Riley; Alissa R Van Zutphen; Timothy J Brei; Vinita Oberoi Leedom; Russell S Kirby; Laura J Pabst
Journal:  Birth Defects Res       Date:  2021-12-18       Impact factor: 2.661

2.  Disparities in surgical outcomes of neonates with congenital heart disease across regions, centers, and populations.

Authors:  Flora Nuñez Gallegos; Joyce L Woo; Brett R Anderson; Keila N Lopez
Journal:  Semin Perinatol       Date:  2022-03-13       Impact factor: 3.311

3.  Social determinants of health and outcomes for children and adults with congenital heart disease: a systematic review.

Authors:  Brooke Davey; Raina Sinha; Ji Hyun Lee; Marissa Gauthier; Glenn Flores
Journal:  Pediatr Res       Date:  2020-10-17       Impact factor: 3.756

4.  A Randomized Clinical Trial Demonstrating Feasibility and Preliminary Efficacy of a Videoconference-Delivered Physical Activity Lifestyle Intervention Among Adolescents With a Congenital Heart Defect.

Authors:  Jamie L Jackson; Kristen R Fox; Joseph R Rausch; Taylor N Swenski; Steven P Neville; Noelle C Marousis; Christina X Korth; Clifford L Cua; Vidu Garg; Kathryn Vannatta
Journal:  Ann Behav Med       Date:  2022-07-12

Review 5.  Advances in Managing Transition to Adulthood for Adolescents With Congenital Heart Disease: A Practical Approach to Transition Program Design: A Scientific Statement From the American Heart Association.

Authors:  Anitha S John; Jamie L Jackson; Philip Moons; Karen Uzark; Andrew S Mackie; Susan Timmins; Keila N Lopez; Adrienne H Kovacs; Michelle Gurvitz
Journal:  J Am Heart Assoc       Date:  2022-03-17       Impact factor: 6.106

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.