Literature DB >> 14520621

ESRD patient quality of life: symptoms, spiritual beliefs, psychosocial factors, and ethnicity.

Paul L Kimmel1, Seth L Emont, John M Newmann, Helen Danko, Alvin H Moss.   

Abstract

BACKGROUND: Recent research suggests that patients' perceptions may be more important than objective clinical assessments in determining quality of life (QOL) for patients with end-stage renal disease (ESRD).
METHODS: We interviewed 165 hemodialysis patients from 3 sites using a QOL questionnaire that included the Satisfaction With Life Scale (SWLS) and the McGill QOL (MQOL) scale, which includes a single-item global measure of QOL (Single-Item QOL Scale [SIS]). The MQOL scale asks patients to report their most troublesome symptoms. We also initiated the use of a Support Network Scale and a Spiritual Beliefs Scale.
RESULTS: Mean patient age was 60.9 years, 52% were men, 63% were white, and 33% were African American. Patients had a mean treatment time for ESRD of 44 months, mean hemoglobin level of 11.8 g/dL (118 g/L), mean albumin level of 3.7 g/dL (37 g/L), and mean Kt/V of 1.6. Forty-five percent of patients reported symptoms. Pain was the most common symptom (21% of patients). There was an inverse relationship between reported number of symptoms and SWLS (P < 0.01), MQOL scale score (P < 0.001), and SIS (P < 0.001). The Spiritual Beliefs Scale correlated with the MQOL scale score, SWLS (both P < 0.01), and SIS (P < 0.05). The Support Network Scale score correlated with the MQOL Existential (P = 0.01) and MQOL Support (P < 0.01) subscales. No clinical parameter correlated with any measure of QOL, spiritual beliefs, or social support.
CONCLUSION: Symptoms, especially pain, along with psychosocial and spiritual factors, are important determinants of QOL of patients with ESRD. Additional studies, particularly a longitudinal trial, are needed to determine the reproducibility and utility of these QOL measures in assessing patient long-term outcome and their association with other QOL indices in larger and more diverse patient populations.

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Mesh:

Year:  2003        PMID: 14520621     DOI: 10.1016/s0272-6386(03)00907-7

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  76 in total

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2.  Religiosity and social support: implications for the health-related quality of life of African American hemodialysis patients.

Authors:  Claudie J Thomas; Thomas Alex Washington
Journal:  J Relig Health       Date:  2012-12

Review 3.  A Thematic Synthesis of the Experiences of Adults Living with Hemodialysis.

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4.  Association of social support with outcomes in incident dialysis patients.

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5.  Psychosocial intervention improves depression, quality of life, and fluid adherence in hemodialysis.

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Review 6.  Palliative and end-of-life care issues in chronic kidney disease.

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Review 8.  Assessing and improving the health-related quality of life of patients with ESRD.

Authors:  Fredric O Finkelstein; Kelli L Arsenault; Ana Taveras; Kwabena Awuah; Susan H Finkelstein
Journal:  Nat Rev Nephrol       Date:  2012-10-23       Impact factor: 28.314

9.  Religiosity and Health-Related Quality of Life: A Cross-Sectional Study on Filipino Christian Hemodialysis Patients.

Authors:  Jonas Preposi Cruz; Paolo C Colet; Hikmet Qubeilat; Jazi Al-Otaibi; Erwin I Coronel; Roderick C Suminta
Journal:  J Relig Health       Date:  2016-06

10.  Survival of patients from South Asian and Black populations starting renal replacement therapy in England and Wales.

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Journal:  Nephrol Dial Transplant       Date:  2009-07-21       Impact factor: 5.992

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