Literature DB >> 25910824

Age-Related Emergency Department Reliance in Patients with Sickle Cell Disease.

Morey A Blinder1, Mei Sheng Duh2, Medha Sasane3, Alex Trahey2, Carole Paley3, Francis Vekeman4.   

Abstract

BACKGROUND: Emergency Department Reliance (EDR: total emergency department [ED] visits/total ambulatory [outpatient + ED] visits) differentiates acute episodic ED users from those who may not have adequate access to outpatient care.
OBJECTIVE: This study's aim was to investigate age-related patterns of EDR and associated health-care costs in pediatric patients with sickle cell disease (SCD) and those transitioning from pediatric to adult care.
METHODS: State Medicaid data were used for this study. Patients with two or more SCD diagnoses and one or more blood transfusion were included. Quarterly rates of ED visits, EDR, SCD complications associated with ED visits, and ED visits resulting in hospitalization were evaluated. Risk factors associated with high EDR and the association between high EDR and health-care costs were explored through regression analyses.
RESULTS: A total of 3208 patients were included. The most common SCD complications associated with ED visits were pain, infection, and pneumonia. Beginning at the age of 15 years, EDR rose from 0.17 to 0.29 visits per quarter at age 22 years, and remained high throughout adulthood. Regression analyses indicated that patients were most likely to have high EDR during the post-transition period and when experiencing an SCD complication. Patients with high EDR incurred statistically significantly higher inpatient and ED costs, resulting in significantly higher total health-care costs.
CONCLUSIONS: Compared to children, patients transitioning to adulthood relied more on the ED for their care. In addition, patients with high EDR incurred more days in the hospital and significantly higher health-care costs, highlighting the need to improve transition-related support, including better access to primary care and increased engagement with patients with SCD.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  access to care; acute care; emergency department; emergency department reliance; health-care costs; sickle cell disease; transfusion

Mesh:

Year:  2015        PMID: 25910824     DOI: 10.1016/j.jemermed.2014.12.080

Source DB:  PubMed          Journal:  J Emerg Med        ISSN: 0736-4679            Impact factor:   1.484


  19 in total

1.  Emergency department utilization by Californians with sickle cell disease, 2005-2014.

Authors:  Susan T Paulukonis; Lisa B Feuchtbaum; Thomas D Coates; Lynne D Neumayr; Marsha J Treadwell; Elliott P Vichinsky; Mary M Hulihan
Journal:  Pediatr Blood Cancer       Date:  2016-12-21       Impact factor: 3.167

2.  Decision-Making Involvement, Self-Efficacy, and Transition Readiness in Youth With Sickle Cell Disease.

Authors:  Maureen Varty; Barbara Speller-Brown; Bonnie J Wakefield; Russell D Ravert; Katherine Patterson Kelly; Lori L Popejoy
Journal:  Nurs Res       Date:  2022 Jan-Feb 01       Impact factor: 2.381

3.  Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemia.

Authors:  Grace Champlin; Scott N Hwang; Andrew Heitzer; Juan Ding; Lisa Jacola; Jeremie H Estepp; Winfred Wang; Kenneth I Ataga; Curtis L Owens; Justin Newman; Allison A King; Robert Davis; Guolian Kang; Jane S Hankins
Journal:  Exp Biol Med (Maywood)       Date:  2021-08-18

4.  Preliminary evaluation of the clinical implementation of cognitive-behavioral therapy for chronic pain management in pediatric sickle cell disease.

Authors:  Soumitri Sil; Kristina Lai; Jennifer L Lee; Jordan Gilleland Marchak; Beth Thompson; Lindsey Cohen; Peter Lane; Carlton Dampier
Journal:  Complement Ther Med       Date:  2020-02-15       Impact factor: 2.446

5.  Characteristics of Children Enrolled in Medicaid With High-Frequency Emergency Department Use.

Authors:  Alon Peltz; Margaret E Samuels-Kalow; Jonathan Rodean; Matthew Hall; Elizabeth R Alpern; Paul L Aronson; Jay G Berry; Kathy N Shaw; Rustin B Morse; Stephen B Freedman; Eyal Cohen; Harold K Simon; Samir S Shah; Yiannis Katsogridakis; Mark I Neuman
Journal:  Pediatrics       Date:  2017-08-01       Impact factor: 7.124

6.  Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use.

Authors:  Nancy Crego; Christian Douglas; Emily Bonnabeau; Marian Earls; Kern Eason; Elizabeth Merwin; Gary Rains; Paula Tanabe; Nirmish Shah
Journal:  J Am Board Fam Med       Date:  2020 Jan-Feb       Impact factor: 2.657

7.  Variation in hospital admission of sickle cell patients from the emergency department using the Pediatric Health Information System.

Authors:  Seethal A Jacob; Emily L Mueller; Anneli R Cochrane; Aaron E Carroll; William E Bennett
Journal:  Pediatr Blood Cancer       Date:  2019-11-14       Impact factor: 3.167

8.  Youths' Experiences of Transition from Pediatric to Adult Care: An Updated Qualitative Metasynthesis.

Authors:  Maureen Varty; Barbara Speller-Brown; Leslie Phillips; Katherine Patterson Kelly
Journal:  J Pediatr Nurs       Date:  2020-09-20       Impact factor: 2.145

9.  Transition care continuity promotes long-term retention in adult care among young adults with sickle cell disease.

Authors:  Kristen E Howell; Anjelica C Saulsberry-Abate; Joacy G Mathias; Jerlym S Porter; Jason R Hodges; Kenneth I Ataga; Sheila Anderson; Vikki Nolan; Jane S Hankins
Journal:  Pediatr Blood Cancer       Date:  2021-07-19       Impact factor: 3.838

10.  Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project.

Authors:  Donna K McClish; Wally R Smith; James L Levenson; Imoigele P Aisiku; John D Roberts; Susan D Roseff; Viktor E Bovbjerg
Journal:  Biomed Res Int       Date:  2017-03-28       Impact factor: 3.411

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