Literature DB >> 19838320

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

Coretta M Jenerette1, Gloria Lauderdale.   

Abstract

Little is known about the lives of adults with sickle cell disease (SCD). This article reports findings from a qualitative pilot study, which used life review as a method to explore influences on health outcomes among middle-aged and older adults with SCD, Six females with SCD, recruited from two urban sickle cell clinics in the U.S., engaged in semi-structured, in-depth life review interviews. MaxQDA2 software was used for qualitative data coding and analysis. Three major themes were identified: vulnerability factors, self-care management resources, and health outcomes. These themes are consistent with the Theory of Self-Care Management for Sickle Cell Disease. Identifying vulnerability factors, self-care management resources, and health outcomes in adults with SCD may aid in developing theory-based interventions to meet health care needs of younger individuals with SCD. The life review process is a useful means to gain insight into successful aging with SCD and other chronic illnesses.

Entities:  

Year:  2008        PMID: 19838320      PMCID: PMC2762231     

Source DB:  PubMed          Journal:  J Theory Constr Test        ISSN: 1086-4431


  57 in total

Review 1.  Managing sickle cell disease.

Authors:  Susan Claster; Elliott P Vichinsky
Journal:  BMJ       Date:  2003-11-15

Review 2.  Sickle cell disease related pain: crisis and conflict.

Authors:  Knox H Todd; Carmen Green; Vence L Bonham; Carlton Haywood; Evera Ivy
Journal:  J Pain       Date:  2006-07       Impact factor: 5.820

3.  Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis.

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Journal:  Clin Sci (Lond)       Date:  1998-02       Impact factor: 6.124

Review 4.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

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Journal:  Int J Behav Med       Date:  2005

5.  Spirituality in African-American mothers coping with a seriously ill infant.

Authors:  S M Wilson; M S Miles
Journal:  J Soc Pediatr Nurs       Date:  2001 Jul-Sep

6.  Symptoms, quality of life, and health service contact among young adults with mild asthma.

Authors:  L M Osman; C Calder; R Robertson; J A Friend; J S Legge; J G Douglas
Journal:  Am J Respir Crit Care Med       Date:  2000-02       Impact factor: 21.405

7.  Adult sickle cell patients' perceptions of nurses' caring behaviors.

Authors:  C Dorsey; K D Phillips; C Williams
Journal:  ABNF J       Date:  2001 Sep-Oct

8.  The use of life review to enhance quality of life of people living with AIDS: a feasibility study.

Authors:  J A Erlen; M P Mellors; S M Sereika; C Cook
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

9.  A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services.

Authors:  Elizabeth A Wojciechowski; Anita Hurtig; Louise Dorn
Journal:  J Pediatr Nurs       Date:  2002-02       Impact factor: 2.145

10.  Genetic counseling in sickle cell anemia: experiences with couples at risk.

Authors:  F Neal-Cooper; R B Scott
Journal:  Public Health Rep       Date:  1988 Mar-Apr       Impact factor: 2.792

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  8 in total

1.  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

2.  Perceptions of young adults with sickle cell disease concerning their disease experience.

Authors:  Nadine Matthie; Jill Hamilton; Diana Wells; Coretta Jenerette
Journal:  J Adv Nurs       Date:  2015-09-09       Impact factor: 3.187

3.  A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.

Authors:  Lou Ella V Taylor; Nancy A Stotts; Janice Humphreys; Marsha J Treadwell; Christine Miaskowski
Journal:  Pain Manag Nurs       Date:  2011-12-14       Impact factor: 1.929

4.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

5.  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

6.  Self-management recommendations for sickle cell disease: A Ghanaian health professionals' perspective.

Authors:  Andrews Druye; Brian Robinson; Katherine Nelson
Journal:  Health Sci Rep       Date:  2018-09-05

7.  Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease.

Authors:  Nadine Matthie; Coretta Jenerette; Ashley Gibson; Sudeshna Paul; Melinda Higgins; Lakshmanan Krishnamurti
Journal:  Health Psychol Open       Date:  2020-04-28

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
  8 in total

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