Literature DB >> 28527641

Identifying Social-Behavioral Health Needs of Adults with Sickle Cell Disease in the Emergency Department.

Sophia K Smith1, Julia Johnston1, Carlton Rutherford1, Rachel Hollowell1, Paula Tanabe2.   

Abstract

INTRODUCTION: Sickle cell disease (SCD) is a complex illness with many social-behavioral co-morbidities. The aim of this project was to describe unmet social-behavioral health needs for adults with SCD who presented to the emergency department for treatment of vaso-occlusive episodes (VOEs).
METHODS: A descriptive study using 1:1 interviews during an ED visit for a VOE was conducted; a brief social behavioral health screening interview guide was used. A convenience sample of adults with SCD treated in the emergency department for a VOE were eligible for inclusion.
RESULTS: We conducted 147 interviews over 14 months. Patients reported transportation and/or scheduling difficulties with clinic appointments in one third of the interviews. Four major themes emerged: clinic appointment barriers, medication barriers, other care barriers, and social-behavioral issues. A majority of patients (53%) reported being brought to the emergency department by a family member at their current visit. Patients cited having insurance coverage issues in more than one quarter (27%) of the interviews. Difficulties in obtaining prescriptions were cited as a result of a financial copay (17%), transportation (11%), and pharmacy (9%) issues. Almost one third of patients (29%) reported feeling depressed, and 20% reported feeling anxious. DISCUSSION: Many patients with SCD who are treated in the emergency department have social or behavioral health risk factors. Emergency departments have an opportunity to screen and refer patients for follow-up. Future research should investigate referral outcomes and their effect on ED and hospital use.
Copyright © 2017 Emergency Nurses Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Emergency department; Sickle cell disease; Social behavioral health

Mesh:

Year:  2017        PMID: 28527641     DOI: 10.1016/j.jen.2017.04.009

Source DB:  PubMed          Journal:  J Emerg Nurs        ISSN: 0099-1767            Impact factor:   1.836


  3 in total

1.  CE: Understanding the Complications of Sickle Cell Disease.

Authors:  Paula Tanabe; Regena Spratling; Dana Smith; Peyton Grissom; Mary Hulihan
Journal:  Am J Nurs       Date:  2019-06       Impact factor: 2.220

2.  Barriers to Care for Persons With Sickle Cell Disease: The Case Manager's Opportunity to Improve Patient Outcomes.

Authors:  Jill Brennan-Cook; Emily Bonnabeau; Ravenne Aponte; Christina Augustin; Paula Tanabe
Journal:  Prof Case Manag       Date:  2018 Jul/Aug

3.  Patient Perspectives of Sickle Cell Management in the Emergency Department.

Authors:  Nancy Crego; Rita Masese; Emily Bonnabeau; Christian Douglas; Gary Rains; Nirmish Shah; Paula Tanabe
Journal:  Crit Care Nurs Q       Date:  2021 Apr-Jun 01
  3 in total

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