Literature DB >> 18336519

Information topics important to chronic kidney disease patients: a systematic review.

Paula Ormandy1.   

Abstract

It is essential to identify the information topics that are important to chronic kidney disease (CKD) patients to provide 'appropriate' information that will improve their knowledge, promote independence and encourage them to self-manage their illness. This paper, through a systematic review, explores the existing body of evidence on the information needs of CKD patients to identify information topic areas important to these patients and highlight factors that influence a patient's information needs.

Entities:  

Mesh：

Year:  2008        PMID： 18336519     DOI： 10.1111/j.1755-6686.2008.00006.x

Source DB:  PubMed          Journal:  J Ren Care        ISSN： 1755-6678


  13 in total

1.  Development and results of a kidney disease knowledge survey given to patients with CKD.

Authors:  Julie A Wright; Kenneth A Wallston; Tom A Elasy; T Alp Ikizler; Kerri L Cavanaugh
Journal:  Am J Kidney Dis       Date:  2010-12-18       Impact factor: 8.860

2.  Patient satisfaction with in-centre haemodialysis care: an international survey.

Authors:  Suetonia C Palmer; Giorgia de Berardis; Jonathan C Craig; Allison Tong; Marcello Tonelli; Fabio Pellegrini; Marinella Ruospo; Jörgen Hegbrant; Charlotta Wollheim; Eduardo Celia; Ruben Gelfman; Juan Nin Ferrari; Marietta Törok; Marco Murgo; Miguel Leal; Anna Bednarek-Skublewska; Jan Dulawa; Giovanni F M Strippoli
Journal:  BMJ Open       Date:  2014-05-19       Impact factor: 2.692

3.  Views of Canadian patients on or nearing dialysis and their caregivers: a thematic analysis.

Authors:  Lianne Barnieh; Kathryn King-Shier; Brenda Hemmelgarn; Andreas Laupacis; Liam Manns; Braden Manns
Journal:  Can J Kidney Health Dis       Date:  2014-04-07

4.  How does pre-dialysis education need to change? Findings from a qualitative study with staff and patients.

Authors:  Gill Combes; Kim Sein; Kerry Allen
Journal:  BMC Nephrol       Date:  2017-11-23       Impact factor: 2.388

5.  Person-centred care in chronic kidney disease: a cross-sectional study of patients' desires for self-management support.

Authors:  Kathryn Havas; Clint Douglas; Ann Bonner
Journal:  BMC Nephrol       Date:  2017-01-13       Impact factor: 2.388

6.  A Digital Modality Decision Program for Patients With Advanced Chronic Kidney Disease.

Authors:  Ruth Dubin; Anna Rubinsky
Journal:  JMIR Form Res       Date:  2019-02-06

7.  Development of a decision aid to inform patients' and families' renal replacement therapy selection decisions.

Authors:  Jessica M Ameling; Priscilla Auguste; Patti L Ephraim; LaPricia Lewis-Boyer; Nicole DePasquale; Raquel C Greer; Deidra C Crews; Neil R Powe; Hamid Rabb; L Ebony Boulware
Journal:  BMC Med Inform Decis Mak       Date:  2012-12-01       Impact factor: 2.796

8.  Selecting renal replacement therapies: what do African American and non-African American patients and their families think others should know? A mixed methods study.

Authors:  Nicole DePasquale; Patti L Ephraim; Jessica Ameling; Lapricia Lewis-Boyér; Deidra C Crews; Raquel C Greer; Hamid Rabb; Neil R Powe; Bernard G Jaar; Luis Gimenez; Priscilla Auguste; Mollie Jenckes; L Ebony Boulware
Journal:  BMC Nephrol       Date:  2013-01-14       Impact factor: 2.388

9.  Types of vicarious learning experienced by pre-dialysis patients.

Authors:  Kate McCarthy; Jackie Sturt; Ann Adams
Journal:  SAGE Open Med       Date:  2015-04-10

10.  What are the information needs and concerns of individuals with Polycystic Kidney Disease? Results of an online survey using Facebook and social listening analysis.

Authors:  Tiffany Ma; Kelly Lambert
Journal:  BMC Nephrol       Date:  2021-07-14       Impact factor: 2.388
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