Problems experienced by haemodialysis patients in Greece

Kaba, Evridiki; Bellou, Panagiota; Ιορδάνου, Παναγιώτα Σ.; Andrea, Stavroula; Kyritsi, Eleni Magdalini; Gerogianni, Georgia; Zetta, Stella; Swigart, Valerie

doi:10.12968/bjon.2007.16.14.24325

Cited by 42 publications

(65 citation statements)

References 15 publications

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“…It has been also reported that the world of a dialysis patient can be isolated and social activities are greatly reduced (Faber et al, 2003). Furthermore, several studies have shown that, in comparison to the general population, patients with ESRD commonly report reduced physical functioning and overall physical activities (Covic et al, 2004;Molsted et al, 2004;Kaba et al, 2007;Seica et al, 2009;Kring and Crane, 2009;Santos et al, 2009). The World Health…”

Section: Impact Of End-stage Renal Diseasementioning

confidence: 99%

Quality of life and well‐being of people receiving haemodialysis treatment in Scotland: A cross‐sectional survey

Alshraifeen

McCreaddie

Evans

2013

Int J of Nursing Practice

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End-stage renal disease is a complex, progressive and debilitating illness that affects patients' quality of life, physical and mental health, well-being, social functioning and emotional health. A cross-sectional survey was carried out in renal dialysis centres in Scotland to assess patients' health status and the impact of haemodialysis treatment on quality of life and well-being. A sample of 72 participants was recruited. Participants scored considerably lower than the UK general population in all domains of health-related quality of life, although mental health components were nearer to general population norms than physical health components. However, 34 (47%) participants achieved a score on a general well-being questionnaire that was indicative of stress and anxiety. Increasing age was associated with better overall mental health, but worse physical functioning. Increasing levels of hope and support were associated with improved general well-being

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Section: Impact Of End-stage Renal Diseasementioning

confidence: 99%

Quality of life and well‐being of people receiving haemodialysis treatment in Scotland: A cross‐sectional survey

Alshraifeen

McCreaddie

Evans

2013

Int J of Nursing Practice

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“…When commencing hemodialysis, some participants struggled with feelings of vulnerability and their dependency on both dialysis treatment and caregivers (24,26,(28)(29)(30)(31)(32)(35)(36)(37)(38)(39)(40). The "assembly line" (26) nature of dialysis and lack of interest shown by staff could result in a loss of personal identity (24,26,28,35). Interference with earlier roles in society and social networks could also affect identity.…”

Section: Synthesismentioning

confidence: 99%

“…Interference with earlier roles in society and social networks could also affect identity. Those required to give up employment reported this affected their sense of self as reliable and able to provide for their families (29,35,40). Additionally, dialysis affected the physical self through the creation of vascular access and other changes in appearance (25,29,36,37,39).…”

Section: Synthesismentioning

confidence: 99%

A Thematic Synthesis of the Experiences of Adults Living with Hemodialysis

Reid

Seymour

Jones

2016

CJASN

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Background and objectives Patients on in-center dialysis spend significant amounts of time in the dialysis unit; additionally, managing ESRD affects many aspects of life outside the dialysis unit. To improve the care provided to patients requiring hemodialysis, their experiences and beliefs regarding treatment must be understood. This systematic review aimed to synthesize the experiences of patients receiving in-center hemodialysis.Design, setting, participants, & measurements We searched Embase, MEDLINE, CINAHL, PsychINFO, Google Scholar, and reference lists for primary qualitative studies published from 1995 to 2015 that explored the experiences of adult patients receiving treatment with in-center hemodialysis. A thematic synthesis was conducted.Results Seventeen studies involving 576 patients were included in the synthesis. Four analytic themes were developed. The first theme (a new dialysis-dependent self) describes the changes in identity and perceptions of self that could result from dialysis dependence. The second theme (a restricted life) describes the physical and emotional constraints that patients described as a consequence of their dependence. Some patients reported strategies that allowed them to regain a sense of optimism and influence over the future, and these contributed to the third theme (regaining control). The first three themes describe a potential for change through acceptance, adaption, and regaining a sense of control. The final theme (relationships with health professionals) describes the importance of these relationships for in-center patients and their influence on perceptions of power and support. These relationships are seen to influence the other three themes through information sharing, continuity, and personalized support.Conclusions Our synthesis has resulted in a framework that can be used to consider interventions to improve patients' experiences of in-center hemodialysis care. Focusing on interventions that are incorporated into the established relationships that patients have with their health care professionals may enable patients to progress toward a sense of control and improve satisfaction with care.

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“…Hemodialysis causes changes in individuals' lifestyle, health status and roles. These patients face with multiple physical, mental and social stressors (3). Patients treated with hemodialysis experience restrictions on lifestyle, diet and fluids (4).…”

Section: Introductionmentioning

confidence: 99%

The outcomes of stress exposure in hemodialysis patients

Naderifar¹,

Tafreshi²,

Ilkhani³

et al. 2017

J Renal Inj Prev

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Nurses and policy makers should have special attention to consequences of stress in patients undergoing hemodialysis. It plays an important role to provide a framework for appropriate supportive measures and gives the opportunity for nurses to manage the problems facing these patients. Please cite this paper as: Introduction:Chronic renal failure (CRF) is a common problem in today's world. Patients with hemodialysis are subjected to stress even more severe than others. Objectives: This study aimed to explain patients' perception with hemodialysis about stress exposure and its consequences. Patients and Methods:This study is a qualitative approach based on directed content analysis. The data were collected using semi-structured in-depth interviews with patients treated with hemodialysis. Participants were selected using purposive sampling method and data saturation was reached by conducting 11 interviews so that, the new finding was not added. Data analysis was simultaneously conducted based on Grant's model of the consequence of exposure to stress. The validity and reliability of the data was confirmed using peer review method and results were also confirmed by participants. Results: Four themes, including support, psychological outcomes, adherence to treatment and physical trouble, 12 categories and 33 sub-categories were obtained during data analysis process. According to the results, "support" was added. Conclusion:The results showed that patients, with the help of available supportive resources, confront with the difficulties that lie ahead and reduce the hemodialysis-related stress in themselves. Support resources including; family, medical personnel, similar patients, friends and community resources.

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Problems experienced by haemodialysis patients in Greece

Cited by 42 publications

References 15 publications

Quality of life and well‐being of people receiving haemodialysis treatment in Scotland: A cross‐sectional survey

Quality of life and well‐being of people receiving haemodialysis treatment in Scotland: A cross‐sectional survey

A Thematic Synthesis of the Experiences of Adults Living with Hemodialysis

The outcomes of stress exposure in hemodialysis patients

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