Literature DB >> 18247376

Testing the Theory of Self-care Management for sickle cell disease.

Coretta M Jenerette1, Carolyn Murdaugh.   

Abstract

Factors predicting health outcomes in persons with sickle cell disease (SCD) were investigated within the framework of the theory of self-care management for SCD, which proposes that vulnerability factors negatively affect health care outcomes and self-care management resources and positively mediate the relationship between vulnerability factors and health care outcomes. A cross-sectional descriptive design was used to test the model with a sample of 232 African American adults with SCD. Results supported the negative effect of vulnerability factors on health outcomes. The overall model was supported, however, self-care management resources did not mediate the relationship between vulnerability and health care outcomes. The findings provide support for interventions to increase self-care management resources to improve health care outcomes. 2008 Wiley Periodicals, Inc

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Year:  2008        PMID: 18247376     DOI: 10.1002/nur.20261

Source DB:  PubMed          Journal:  Res Nurs Health        ISSN: 0160-6891            Impact factor:   2.228


  15 in total

1.  Applicability of the SMART Model of Transition Readiness for Sickle-Cell Disease.

Authors:  Siddika S Mulchan; Jessica M Valenzuela; Lori E Crosby; Claudia Diaz Pow Sang
Journal:  J Pediatr Psychol       Date:  2015-12-30

2.  Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  J Sick Cell Dis Hemoglobinopathies       Date:  2017-05

3.  Stigma of Sickle Cell Disease: A Systematic Review.

Authors:  Dominique Bulgin; Paula Tanabe; Coretta Jenerette
Journal:  Issues Ment Health Nurs       Date:  2018-04-13       Impact factor: 1.835

4.  Successful Aging with Sickle Cell Disease: Using Qualitative Methods to Inform Theory.

Authors:  Coretta M Jenerette; Gloria Lauderdale
Journal:  J Theory Constr Test       Date:  2008-04-01

5.  A Qualitative Study of Chronic Pain and Self-Management in Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Diana Ross; Cynthia Sinha; Kirshma Khemani; Nitya Bakshi; Lakshmanan Krishnamurti
Journal:  J Natl Med Assoc       Date:  2018-09-26       Impact factor: 1.798

6.  Role of self-care in sickle cell disease.

Authors:  Nadine Matthie; Coretta Jenerette; Susan McMillan
Journal:  Pain Manag Nurs       Date:  2014-10-31       Impact factor: 1.929

7.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

8.  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

9.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

10.  Psychosocial risk and health care utilization in pediatric sickle cell disease.

Authors:  Kerri E Woodward; Yelena L Johnson; Lindsey L Cohen; Carlton Dampier; Soumitri Sil
Journal:  Pediatr Blood Cancer       Date:  2021-05-24       Impact factor: 3.167

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