Literature DB >> 18658178

Support interventions for caregivers of people with chronic kidney disease: a systematic review.

Allison Tong1, Peter Sainsbury, Jonathan C Craig.   

Abstract

BACKGROUND: A growing number of patients with chronic kidney disease (CKD) rely on non-professional healthcare providers, such as family and friends, to manage their long-term condition throughout the trajectory of CKD. These informal caregivers can experience stress, depression, lack of confidence and poor quality of life. Yet, the needs of caregivers are often neglected and under-prioritized. The objective of this review is to evaluate the effectiveness of interventions aimed at providing support to caregivers of people with CKD.
METHODS: We conducted a systematic review of studies that evaluated any intervention for informal caregivers of CKD patients. We searched five electronic databases (up to January Week 5, 2008) including Medline, EMBASE, PsychINFO, CINAHL, Cochrane Central Register and reference lists of relevant articles.
RESULTS: Three studies were identified that evaluated an intervention for caregivers of CKD patients. All three only assessed the effect of educational material on caregivers' knowledge. Two evaluated information provided to caregivers of dialysis patients using a pre- and post-test study design. The other study used participatory action research methods to develop and evaluate an information handbook for transplant patients and their caregivers. Studies consistently found that the provision of information improved caregivers' knowledge. No other outcomes were reported.
CONCLUSIONS: Despite the growing recognition of the burden and adverse effects of CKD on caregivers, no high-quality evidence is available about the effect of information or support interventions on the physical or psychosocial well-being of informal caregivers and the patients. More attention towards the development and evaluation of services that respond to the support and informational needs of caregivers is needed, and this may also lead to improved outcomes for patients.

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Year:  2008        PMID: 18658178     DOI: 10.1093/ndt/gfn415

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  31 in total

1.  The other side of the coin in renal replacement therapies: the burden on caregivers.

Authors:  Simge Bardak; Serap Demir; Eda Aslan; Kenan Turgutalp; Havva Didem Celikcan; Murside Esra Dolarslan; Cennet Kılıcarslan; Filiz Karasu; Ayse Jini Gunes; Cemal Kurt; Ahmet Kıykım
Journal:  Int Urol Nephrol       Date:  2018-12-04       Impact factor: 2.370

2.  Patient and Caregiver Priorities for Outcomes in Peritoneal Dialysis: Multinational Nominal Group Technique Study.

Authors:  Karine E Manera; David W Johnson; Jonathan C Craig; Jenny I Shen; Lorena Ruiz; Angela Yee-Moon Wang; Terence Yip; Samuel K S Fung; Matthew Tong; Achilles Lee; Yeoungjee Cho; Andrea K Viecelli; Benedicte Sautenet; Armando Teixeira-Pinto; Edwina Anne Brown; Gillian Brunier; Jie Dong; Tony Dunning; Rajnish Mehrotra; Saraladevi Naicker; Roberto Pecoits-Filho; Jeffrey Perl; Martin Wilkie; Allison Tong
Journal:  Clin J Am Soc Nephrol       Date:  2018-12-20       Impact factor: 8.237

3.  Burden on caregivers as perceived by hemodialysis patients in the Frequent Hemodialysis Network (FHN) trials.

Authors:  Rita S Suri; Brett Larive; Amit X Garg; Yoshio N Hall; Andreas Pierratos; Glenn M Chertow; Irina Gorodetskeya; Alan S Kliger
Journal:  Nephrol Dial Transplant       Date:  2011-03-18       Impact factor: 5.992

4.  The multi-dimensional burden of cirrhosis and hepatic encephalopathy on patients and caregivers.

Authors:  Jasmohan S Bajaj; James B Wade; Douglas P Gibson; Douglas M Heuman; Leroy R Thacker; Richard K Sterling; R Todd Stravitz; Velimir Luketic; Michael Fuchs; Melanie B White; Debulon E Bell; HoChong Gilles; Katherine Morton; Nicole Noble; Puneet Puri; Arun J Sanyal
Journal:  Am J Gastroenterol       Date:  2011-05-10       Impact factor: 10.864

5.  Care of the pediatric patient on chronic peritoneal dialysis.

Authors:  Annabelle N Chua; Reeti Kumar; Bradley A Warady
Journal:  Pediatr Nephrol       Date:  2022-05-19       Impact factor: 3.651

6.  Assessing burden and its determinants in caregivers of chronic kidney disease patients undergoing haemodialysis.

Authors:  Shijo John Joseph; Samrat Singh Bhandari; Sanjiba Dutta; Dheeraj Khatri; Apoorva Upadhyay
Journal:  Open J Psychiatry Allied Sci       Date:  2022-04-11

7.  Experiences of patients undergoing dialysis who are from ethnic and racial minorities.

Authors:  Neha Nagpal; Carla Boutin-Foster; Jennifer Melendez; Patryk Kubiszeswki; Kamalani Uehara; Emanuela Offidani; Zenobia Faussett; Richie Chen; Cathy Redel; Clarence Waltrous; Barry Smith
Journal:  J Ren Care       Date:  2016-12-15

8.  Quality of Life in Caregivers of Patients Randomized to Standard- Versus Extended-Hours Hemodialysis.

Authors:  Melissa Nataatmadja; Rathika Krishnasamy; Li Zuo; Daqing Hong; Brendan Smyth; Min Jun; Janak R de Zoysa; Kirsten Howard; Jing Wang; Chunlai Lu; Zhangsuo Liu; Christopher T Chan; Alan Cass; Vlado Perkovic; Meg Jardine; Nicholas A Gray
Journal:  Kidney Int Rep       Date:  2021-02-01

9.  The beliefs and expectations of patients and caregivers about home haemodialysis: an interview study.

Authors:  Allison Tong; Suetonia Palmer; Braden Manns; Jonathan C Craig; Marinella Ruospo; Letizia Gargano; David W Johnson; Jörgen Hegbrant; Måns Olsson; Steven Fishbane; Giovanni F M Strippoli
Journal:  BMJ Open       Date:  2013-01-24       Impact factor: 2.692

10.  Effect of Psycho Education on Depression and Anxiety Symptoms in Patients on Hemodialysis.

Authors:  Fatemeh Espahbodi; Hamzeh Hosseini; Mohamad Mehdi Mirzade; Arefeh Beygom Shafaat
Journal:  Iran J Psychiatry Behav Sci       Date:  2015-01-10
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