Literature DB >> 21141294

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

Coretta M Jenerette1, Cheryl Brewer.   

Abstract

Health-related stigma is increasingly becoming a major public health issue that is receiving more attention. Young adults with sickle cell disease (SCD) are at risk for health-related stigmatization due to the many challenges of the disease. SCD includes the lifelong challenges of managing the chronic illness while accessing and navigating the health care system. The burdens of the disease can affect all aspects of the lives of individuals with SCD to include physiological, psychological, and social well-being. Although others may be involved in the process of stigmatization, the purpose of this paper was to support the need to develop patient-oriented interventions to prevent and treat health-related stigma in young adults with SCD, as these individuals may face health-related stigma throughout their lives, but especially immediately after transitioning from pediatric to adult care. Additionally, the Revised Theory of Self-Care Management for Sickle Cell Disease is offered as a framework from which theory-based interventions can be derived.

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Year:  2010        PMID: 21141294      PMCID: PMC3119340          DOI: 10.1016/s0027-9684(15)30732-x

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  68 in total

Review 1.  Adjustment difficulties of adolescents with sickle cell disease.

Authors:  Rosie B Pinckney; Gail W Stuart
Journal:  J Child Adolesc Psychiatr Nurs       Date:  2004 Jan-Mar

2.  Pre-emptive analgesia.

Authors:  H J McQuay
Journal:  Br J Anaesth       Date:  1992-07       Impact factor: 9.166

Review 3.  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

4.  Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study.

Authors:  Kenneth Epstein; Elaine Yuen; Jeff M Riggio; Samir K Ballas; Stephanie M Moleski
Journal:  J Natl Med Assoc       Date:  2006-07       Impact factor: 1.798

Review 5.  A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease.

Authors:  Christopher L Edwards; Mischca T Scales; Charles Loughlin; Gary G Bennett; Shani Harris-Peterson; Laura M De Castro; Elaine Whitworth; Mary Abrams; Miriam Feliu; Stephanie Johnson; Mary Wood; Ojinga Harrison; Alvin Killough
Journal:  Int J Behav Med       Date:  2005

6.  Are there phases to the vaso-occlusive painful episode in sickle cell disease?

Authors:  Eufemia Jacob; Judith E Beyer; Christine Miaskowski; Marilyn Savedra; Marsha Treadwell; Lori Styles
Journal:  J Pain Symptom Manage       Date:  2005-04       Impact factor: 3.612

7.  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

8.  Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions.

Authors:  F D Armstrong; C H Pegelow; J C Gonzalez; A Martinez
Journal:  J Pediatr Psychol       Date:  1992-10

9.  Impact of an emergency department pain management protocol on the pattern of visits by patients with sickle cell disease.

Authors:  Melissa Givens; Cynthia Rutherford; Girish Joshi; Kathleen Delaney
Journal:  J Emerg Med       Date:  2007-02-07       Impact factor: 1.484

10.  Mothers raising children with sickle cell disease at the intersection of race, gender, and illness stigma.

Authors:  David P R Burnes; Beverley J Antle; Charmaine C Williams; Lisa Cook
Journal:  Health Soc Work       Date:  2008-08
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  33 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.  Use of the Spiritual Development Framework in Conducting Spirituality and Health Research with Adolescents.

Authors:  Dora Clayton-Jones; Kristin A Haglund; Jame Schaefer; Harold G Koenig; Safiya George Dalmida
Journal:  J Relig Health       Date:  2019-08

4.  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

5.  Perspectives and Practices of Athletic Trainers and Team Physicians Implementing the 2010 NCAA Sickle Cell Trait Screening Policy.

Authors:  Mary Anne McDonald; Melissa S Creary; Jill Powell; Lori-Ann Daley; Charlotte Baker; Charmaine Dm Royal
Journal:  J Genet Couns       Date:  2017-06-03       Impact factor: 2.537

6.  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

7.  Sexuality and sickle cell disease.

Authors:  Maria Stella Figueiredo
Journal:  Rev Bras Hematol Hemoter       Date:  2013

8.  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

9.  Nurses' attitudes toward patients with sickle cell disease: a worksite comparison.

Authors:  Coretta M Jenerette; Bosny J Pierre-Louis; Nadine Matthie; Yasmeen Girardeau
Journal:  Pain Manag Nurs       Date:  2015-06       Impact factor: 1.929

10.  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

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