Literature DB >> 25047808

Self-efficacy, transition, and patient outcomes in the sickle cell disease population.

Brittany L Molter1, Kathleen Abrahamson2.   

Abstract

Severe pain is a common symptom of sickle cell disease (SCD). Transitions between adult and pediatric care are a point of particular vulnerability for patients, increasing the risk for poor pain management. The purpose of this literature review was to investigate the relationships among self-efficacy, transition, and SCD health outcomes. A systematic literature search was performed within CINAHL, Academic Search Premier, MEDLINE, and PubMed on published papers between 2003 and 2013. After applying exclusion criteria, 20 articles were used in the final review. Few studies were identified that directly tested the relationship between self-efficacy and SCD outcomes. Although there are few studies on this topic, most demonstrated positive correlations between self-efficacy during transition and positive patient outcomes in the SCD population. Additional studies are needed to support causation. Studies were commonly limited by small sample sizes and attrition. Furthermore, there is a large gap in the literature regarding how self-efficacy can be increased in these patients. Interventions that promote self-efficacy have the potential to improve SCD pain outcomes, but more research is needed to develop interventions to increase these adolescents' self-efficacy. If providers can identify individuals in this population with low self-efficacy, they may be able to intervene early to improve patient outcomes. Most identified studies point to the positive correlation between self-efficacy and positive health outcomes in adolescents with SCD. Self-efficacy has the potential to guide self-care interventions and further research with the SCD population.
Copyright © 2015 American Society for Pain Management Nursing. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 25047808     DOI: 10.1016/j.pmn.2014.06.001

Source DB:  PubMed          Journal:  Pain Manag Nurs        ISSN: 1524-9042            Impact factor:   1.929


  11 in total

1.  Increased Patient Activation Is Associated with Fewer Emergency Room Visits and Hospitalizations for Pain in Adults with Sickle Cell Disease.

Authors:  Robert M Cronin; Tim Lucas Dorner; Amol Utrankar; Whitney Allen; Mark Rodeghier; Adetola A Kassim; Gretchen Purcell Jackson; Michael R DeBaun
Journal:  Pain Med       Date:  2019-08-01       Impact factor: 3.750

2.  Development and evaluation of iManage: A self-management app co-designed by adolescents with sickle cell disease.

Authors:  Lori E Crosby; Russell E Ware; Alana Goldstein; Ashley Walton; Naomi E Joffe; Craig Vogel; Maria T Britto
Journal:  Pediatr Blood Cancer       Date:  2016-08-30       Impact factor: 3.167

3.  Improving self-management in adolescents with sickle cell disease.

Authors:  Lori E Crosby; Anna Hood; Katherine Kidwell; Cara Nwankwo; James Peugh; Heather Strong; Charles Quinn; Maria T Britto
Journal:  Pediatr Blood Cancer       Date:  2020-07-22       Impact factor: 3.167

4.  Disease Self-Efficacy and Health-Related Quality of Life in Adolescents With Sickle Cell Disease.

Authors:  Alana Goldstein-Leever; James L Peugh; Charles T Quinn; Lori E Crosby
Journal:  J Pediatr Hematol Oncol       Date:  2020-03       Impact factor: 1.170

5.  Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers.

Authors:  Robert Michael Cronin; Tilicia L Mayo-Gamble; Sarah-Jo Stimpson; Sherif M Badawy; Lori E Crosby; Jeannie Byrd; Emmanuel J Volanakis; Adetola A Kassim; Jean L Raphael; Velma M Murry; Michael R DeBaun
Journal:  BMC Hematol       Date:  2018-06-08

6.  Barriers experienced in self-care practice by young people with sickle cell disease.

Authors:  Sumaya Giarola Cecilio; Sônia Aparecida Dos Santos Pereira; Valquíria Dos Santos Pinto; Heloísa de Carvalho Torres
Journal:  Hematol Transfus Cell Ther       Date:  2018-02-17

7.  Exploring self-management in adult sickle cell disease patients' at a Teaching Hospital in Ghana.

Authors:  Ninon P Amertil; Elikem Keli Ayitey; Doris Grace Kpongboe; Priscilla Y A Attafuah
Journal:  Nurs Open       Date:  2020-12-27

8.  Factors Influencing Motivation and Engagement in Mobile Health Among Patients With Sickle Cell Disease in Low-Prevalence, High-Income Countries: Qualitative Exploration of Patient Requirements.

Authors:  David-Zacharie Issom; André Henriksen; Ashenafi Zebene Woldaregay; Jessica Rochat; Christian Lovis; Gunnar Hartvigsen
Journal:  JMIR Hum Factors       Date:  2020-03-24

9.  Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care.

Authors:  Julie Kanter; Robert Gibson; Raymona H Lawrence; Matthew P Smeltzer; Norma L Pugh; Jeffrey Glassberg; Rita V Masese; Allison A King; Cecelia Calhoun; Jane S Hankins; Marsha Treadwell
Journal:  JAMA Netw Open       Date:  2020-05-01

10.  Web-Based Technology to Improve Disease Knowledge Among Adolescents With Sickle Cell Disease: Pilot Study.

Authors:  Anjelica C Saulsberry; Jason R Hodges; Audrey Cole; Jerlym S Porter; Jane Hankins
Journal:  JMIR Pediatr Parent       Date:  2020-01-07
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