Literature DB >> 16894227

Managing a medically and socially complex life: women living with lupus.

Cindy Mendelson1.   

Abstract

Systemic lupus erythematosus is a systemic autoimmune illness that affects women more frequently than men and disproportionately affects women of color. Because so little is known about living with lupus, the author undertook a qualitative study to identify salient aspects of affected women's daily experiences. Seven women with lupus participated in three interviews, each separated by 1 month, and they also maintained a daily symptom journal. In addition, 23 women recruited from the Internet submitted narrative accounts of their experiences of living with lupus. Analysis of the findings suggests that living with lupus involves managing a medically and socially complex life. The complexity of life with lupus is dimensionalized by the overlapping themes, identified as a life of uncertainty, a shifting sense of identity, and managing the financial burden of illness.

Entities:  

Mesh:

Year:  2006        PMID: 16894227     DOI: 10.1177/1049732306290132

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  9 in total

1.  Development of an informational web site for recruiting research participants: process, implementation, and evaluation.

Authors:  Patricia E Hershberger; Karen Kavanaugh; Rebekah Hamilton; Susan C Klock; Lisa Merry; Ellen Olshansky; Penny F Pierce
Journal:  Comput Inform Nurs       Date:  2011-10       Impact factor: 1.985

2.  Socioeconomic Predictors of Incident Depression in Systemic Lupus Erythematosus.

Authors:  Natalie Mccormick; Laura Trupin; Edward H Yelin; Patricia P Katz
Journal:  Arthritis Care Res (Hoboken)       Date:  2017-12-08       Impact factor: 4.794

Review 3.  Effective Self-Management Interventions for Patients With Lupus: Potential Impact of Peer Mentoring.

Authors:  Edith M Williams; Leonard Egede; Trevor Faith; James Oates
Journal:  Am J Med Sci       Date:  2017-02-03       Impact factor: 2.378

4.  Psychosocial dimensions of SLE: implications for the health care team.

Authors:  Nancy L Beckerman; Charles Auerbach; Irene Blanco
Journal:  J Multidiscip Healthc       Date:  2011-04-05

5.  Patient Uncertainty Questionnaire-Rheumatology (PUQ-R): development and validation of a new patient-reported outcome instrument for systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) in a mixed methods study.

Authors:  Sophie Cleanthous; David Alan Isenberg; Stanton Peter Newman; Stefan John Cano
Journal:  Health Qual Life Outcomes       Date:  2016-03-01       Impact factor: 3.186

6.  How do patients with systemic autoimmune rheumatic disease perceive the use of their medications: a systematic review and thematic synthesis of qualitative research.

Authors:  Hans Haag; Tim Liang; J Antonio Avina-Zubieta; Mary A De Vera
Journal:  BMC Rheumatol       Date:  2018-04-02

7.  Patients' experiences of living with and receiving treatment for fibromyalgia syndrome: a qualitative study.

Authors:  Heidi K Lempp; Stephani L Hatch; Serene F Carville; Ernest H Choy
Journal:  BMC Musculoskelet Disord       Date:  2009-10-07       Impact factor: 2.362

8.  Treating Systemic Lupus Erythematosus (SLE): The Impact of Historical Environmental Context on Healthcare Perceptions and Decision-Making in Charleston, South Carolina.

Authors:  Wendy Rodgers; Edith M Williams; Brittany L Smalls; Tyler Singleton; Ashley Tennessee; Diane Kamen; Gary Gilkeson
Journal:  Int J Environ Res Public Health       Date:  2020-03-28       Impact factor: 3.390

9.  Cognitive impairment in systemic lupus erythematosus is negatively related to social role participation and quality of life: A systematic review.

Authors:  Sierra Mendelsohn; Lina Khoja; Sofia Alfred; Jennifer He; Melanie Anderson; Denise DuBois; Zahi Touma; Lisa Engel
Journal:  Lupus       Date:  2021-07-15       Impact factor: 2.911

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.