Literature DB >> 30656611

"I Try Not to Even Think About My Health Going Bad": a Qualitative Study of Chronic Kidney Disease Knowledge and Coping Among a Group of Urban African-American Patients with CKD.

Lydia Lissanu1, Fanny Lopez1, Akilah King2, Eric Robinson3, Erik Almazan1, Gabrielle Metoyer1, Michael Quinn1, Monica E Peek1, Milda R Saunders4.   

Abstract

CONTEXT: African-Americans with chronic kidney disease (CKD) are more likely to progress to end-stage renal disease (ESRD). However, African-Americans are less likely to receive care to delay progression of their CKD and to prepare for ESRD treatment.
OBJECTIVE: The objectives of the study are to understand knowledge among urban, African-American patients diagnosed with CKD and to discover ways they managed their illness and prepared for kidney disease progression.
DESIGN: A qualitative study was conducted using structured interviews. Thematic analysis was used for data interpretation. All 23 participants identified as African-American and had CKD but had not yet reached ESRD requiring renal replacement therapy (RRT). Over half of the participants were women (57%), and the mean age was 53 years old.
RESULTS: Three themes emerged from the data. African-Americans often did not know the severity of their CKD. They struggled to complete all of the diet, exercise, and medication tasks recommended to manage their health conditions, including CKD. Finally, participants, even those with stage 5 CKD, viewed progression to RRT in the next 12 months as unlikely.
CONCLUSION: African-Americans face many barriers to CKD self-care and preparation for ESRD. Improving outcomes requires clinicians to help patients understand the severity of their CKD, to make informed choices about their care, all the while motivating patients to take actions to prevent CKD progression.

Entities:  

Keywords:  African-American; Chronic kidney disease; Qualitative research

Mesh:

Year:  2019        PMID: 30656611      PMCID: PMC6530586          DOI: 10.1007/s40615-019-00561-4

Source DB:  PubMed          Journal:  J Racial Ethn Health Disparities        ISSN: 2196-8837


  23 in total

1.  Qualitative research in CKD: an overview of methods and applications.

Authors:  Allison Tong; Wolfgang C Winkelmayer; Jonathan C Craig
Journal:  Am J Kidney Dis       Date:  2014-04-24       Impact factor: 8.860

Review 2.  Hemodialysis Disparities in African Americans: The Deeply Integrated Concept of Race in the Social Fabric of Our Society.

Authors:  Keith C Norris; Sandra F Williams; Connie M Rhee; Susanne B Nicholas; Csaba P Kovesdy; Kamyar Kalantar-Zadeh; L Ebony Boulware
Journal:  Semin Dial       Date:  2017-03-09       Impact factor: 3.455

3.  Accelerated Health Declines among African Americans in the USA.

Authors:  Roland J Thorpe; Ruth G Fesahazion; Lauren Parker; Tanganiyka Wilder; Ronica N Rooks; Janice V Bowie; Caryn N Bell; Sarah L Szanton; Thomas A LaVeist
Journal:  J Urban Health       Date:  2016-10       Impact factor: 3.671

4.  African American patient knowledge of kidney disease: A qualitative study of those with advanced chronic kidney disease.

Authors:  Abby S Kazley; Emily Johnson; Kit Simpson; Kenneth Chavin; Prabhakar Baliga
Journal:  Chronic Illn       Date:  2014-10-21

5.  Influence of a pre-dialysis education programme (PDEP) on the mode of renal replacement therapy.

Authors:  Tony Goovaerts; Michel Jadoul; Eric Goffin
Journal:  Nephrol Dial Transplant       Date:  2005-05-26       Impact factor: 5.992

6.  Knowledge deficit of patients with stage 1-4 CKD: a focus group study.

Authors:  Pamela A Lopez-Vargas; Allison Tong; Richard K S Phoon; Steven J Chadban; Yvonne Shen; Jonathan C Craig
Journal:  Nephrology (Carlton)       Date:  2014-04       Impact factor: 2.506

7.  The context of context: Examining the associations between healthy and unhealthy measures of neighborhood food, physical activity, and social environments.

Authors:  Candice A Myers; Kara D Denstel; Stephanie T Broyles
Journal:  Prev Med       Date:  2016-09-06       Impact factor: 4.018

Review 8.  Social environmental stressors, psychological factors, and kidney disease.

Authors:  Marino A Bruce; Bettina M Beech; Mario Sims; Tony N Brown; Sharon B Wyatt; Herman A Taylor; David R Williams; Errol Crook
Journal:  J Investig Med       Date:  2009-04       Impact factor: 2.895

9.  Psychosocial Interventions for Depressive and Anxiety Symptoms in Individuals with Chronic Kidney Disease: Systematic Review and Meta-Analysis.

Authors:  Michaela C Pascoe; David R Thompson; David J Castle; Samantha M McEvedy; Chantal F Ski
Journal:  Front Psychol       Date:  2017-06-13

10.  Patient Perspectives on the Choice of Dialysis Modality: Results From the Empowering Patients on Choices for Renal Replacement Therapy (EPOCH-RRT) Study.

Authors:  Claudia Dahlerus; Martha Quinn; Emily Messersmith; Laurie Lachance; Lalita Subramanian; Erica Perry; Jill Cole; Junhui Zhao; Celeste Lee; Margie McCall; Leslie Paulson; Francesca Tentori
Journal:  Am J Kidney Dis       Date:  2016-06-21       Impact factor: 8.860

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  5 in total

1.  Renal Replacement Knowledge and Preferences for African Americans With Chronic Kidney Disease.

Authors:  Akilah King; Fanny Y Lopez; Lydia Lissanu; Eric Robinson; Erik Almazan; Gabrielle Metoyer; Jacob Tanumihardjo; Michael Quinn; Monica Peek; Milda Saunders
Journal:  J Ren Care       Date:  2020-01-09

Review 2.  The psychosocial needs of patients who have chronic kidney disease without kidney replacement therapy: a thematic synthesis of seven qualitative studies.

Authors:  Christina Seery; Sarah Buchanan
Journal:  J Nephrol       Date:  2022-09-01       Impact factor: 4.393

3.  The Knowledge Assessment of Renal Transplantation (KART) 2.0: Development and Validation of CKD and Transplant Knowledge Scales.

Authors:  Amy D Waterman; Devika Nair; Intan Purnajo; Kerri L Cavanaugh; Brian S Mittman; John Devin Peipert
Journal:  Clin J Am Soc Nephrol       Date:  2022-03-24       Impact factor: 8.237

4.  Patient perspectives on chronic kidney disease and decision-making about treatment. Discourse of participants in the French CKD-REIN cohort study.

Authors:  Lucile Montalescot; Géraldine Dorard; Elodie Speyer; Karine Legrand; Carole Ayav; Christian Combe; Bénédicte Stengel; Aurélie Untas
Journal:  J Nephrol       Date:  2022-06-13       Impact factor: 4.393

5.  Improving CKD Patient Knowledge and Patient-Physician Communication: A Pilot Study of a CKD Report Card.

Authors:  Jasmine Tzeggai; Keyira Jones; Tipu Puri; Milda Saunders
Journal:  Kidney Med       Date:  2020-04-18
  5 in total

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