Quality of Life, Social Support, Fatigue and Satisfaction from Nursing Care in Dialysis Patients: The Impact of Sociodemographic and Clinical Profile

Research Article

Ann Nurs Res Pract. 2023; 8(1): 1052.

Quality of Life, Social Support, Fatigue and Satisfaction from Nursing Care in Dialysis Patients: The Impact of Sociodemographic and Clinical Profile

Paraskevi Theofilou¹*, Christina Vassilopoulou¹ and Foteini Tzavella²

1Hellenic Open University, School of Social Sciences, Patra, Greece

2University of Peloponnese, School of Health Sciences, Department of Nursing, Tripoli, Greece

*Corresponding author: Paraskevi Theofilou Hellenic Open University, School of Social Sciences,Patra, Greece.

Received: December 08, 2022; Accepted: January 03, 2023; Published: January 09, 2023

Abstract

Chronic kidney disease is a global public health problem, which, in combination with an aging population, is expected to increase its impact in the coming years. The aim of this research is to study the effect of the sociodemographic and clinical profile of hemodialysis patients on their quality of life, social support, fatigue and satisfaction from nursing care. A quantitative, primary, non-experimental survey was conducted using the questionnaires “Multidimensional Scale of Perceived Social Support”(a≥ 0.908),FAS (a≥ 0.658), Missoula-VITAS Quality of Life (a≥ 0.622) and nursing care (a = 0.944). The study involved 69 patients with dialysis of a University Hospital, with most having the disease for 0-10 years. The majority of the patients in the research are men, aged 51-80, married with 1-2 children, with an educational level up to that of High school, who live in a city and receive an income of 500-1,500 euros. Data analysis was performed at a significance level of 5%, using the parametric criteria independent samples t-test, ANOVA and the non-parametric Mann Whitney, Kruskal Wallis and Spearman. The necessary ethical issues were observed. Age affected social support (p <0.05) and fatigue (p<0.05). The educational level affected physical fatigue (p= 0.040) and spirituality (p= 0.037). Residence affected spirituality (p = 0.036) and nursing care (p = 0.039). Occupational status influenced social support from friends (p = 0.001). Years in dialysis affected social support (p ≤ 0.027), interpersonal relationships (p = 0.013) and physical fatigue (p = 0.027). It seems that age, educational level, place of residence, professional status and years of dialysis influence the research factors.

Keywords: Dialysis; Quality of life; Fatigue; Social support; Nursing care

Introduction

Hemodialysis is a time-consuming and expensive treatment and requires more restrictions on diet and fluid intake. Longterm hemodialysis causes loss of freedom, dependence on the caregiver, disruption of marriage, family, social life and reduction or lack of income. All these factors affect patients’ quality of life [1].

Terms like human development and social welfare are frequently used as equivalent or analogous terms. Quality of life (QOL) is considered as the interplay of various factors of social, health, economic and environmental conditions that cumulatively and often in unknown ways, interact to affect both human and social development at the level of the individual and societies. Current patterns of urban development are based on the ideas of imported Western countries and use capital and natural resource intensive systems. Capital intensity divides the urban population into rich and poor urbanites. Resource intensity is destroying the rural hinterland. The end result is that while there is an affluent class with a very high quality of life, the majority of urban dwellers have very poor environmental quality. Decision makers on the development strategy of urban centers often do not consider this human element. Population migration to urban centers, especially industrial cities, is driving the growth of metropolitan areas [2].

Perceptions of quality of life are influenced by urbanization and living standards, creating a perception that is limited to specific areas of human life. First, it directs attention to the positive aspects of people’s lives, thus contrasting with the deficit orientation of these disciplines. Second, it extends traditional objective measures of health, wealth, and social functioning to include subjective perceptions of well-being. Quality of life is the product of the interaction between social, health, economic and environmental conditions that affect human and social development. The notion that quality of life refers to an indefinite number of states and does not entail valuing life style [2].

Health-related quality of life (HRQoL) is a measure that reflects individuals’ subjective experiences of their health status. HRQoL systematically focuses on measuring the relationship between health and health status with quality of life (QoL). It is a dynamic multidimensional model and consists of three main dimensions: the physical, social and mental dimensions of health [3]. Despite the lack of consensus on the definition of QoL, it can be understood as satisfaction or happiness with life, focusing on the areas that the individual considers important. Likewise in the case of HRQOL, what is considered a health indicator is the evaluation of the person’s general physical condition, functional impairment, and ability to perform household activities, social interactions, cognitive function and emotional state in relation to their health status. HRQOL measurement tools can facilitate clinical decision-making, assess quality of care, assess population health needs, and help understand how the causes and effects of causes of health problems increase the effect of treatment on physical health, in work performance and personal life. Thus, improvements in QOL become as important as clinical-laboratory responses to interventions, expanding the field of therapeutic outcomes [4].

Health-related quality of life is a cultural concept as revealed by the differential association between HRQOL and clinical outcomes such as patient compliance or survival. HRQOL is recognized as a key health outcome for studies that assess the quality of health care, assess the impact of illness, and analyze cost-effectiveness. In addition, HRQOL has been shown to be clinically important in improving hemodialys is outcome in hemodialysis patients [5].

The aim of this research is to study the effect of the sociodemographic and clinical profile of hemodialysis patients on their quality of life, social support, fatigue and satisfaction from nursing care.

Method

Research design

A quantitative, primary, non-experimental survey was conducted including specific variables, such as quality of life, social support and fatigue among hemodialysis patients as well as the satisfaction from nursing care.

Sample

The research population is considered to be all dialysis patients in Greece. Regarding the sample, 69 patients on hemodialysis participated in the research with most to have the disease 0-10 years. The majority of patients are men, aged 51-80 years, married with 1-2 children, with educational level up to that of Lyceum, who live in a city and receive an income of 500-1,500 euros. The criteria for entering or excluding the sample were considered: 1) the conduct of the session of hemodialysis, 2) the age over 18 years, 3) the Greek language and 4) diagnosed with end-stage chronic kidney disease.

Questionnaires

For the needs of this research, 3 questionnaires were used: 1) “Multidimensional Scale of Perceived Social Support” [6], 2) Fatigue Assessment Scale (FAS) by Michielsen et al. [7] and 3) Missoula VITAS Quality of Life Index by Theofilou et al. [8]. It emerged from these questionnaires a questionnaire of 60 questions divided into 5 sections.

The 1st section includes 9 questions related to socio-demographic data of the patients, such as gender, age, marital status, number of children, education level, place of residence, employment, monthly income and years in hemodialysis.

The 2nd section refers to perceived social support which was measured according to the “Multidimensional Scale of Perceived Social Support” [6]. The questionnaire includes 12 questions on a 7-point Likert scale 1-7 (1= Strongly Disagree, 2=Strongly Disagree, 3=Disagree, 4=Neutral, 5=Agree, 6=Strongly agree, 7=Strongly agree), and 3 subsections of 4 questions about social support from others, from family and friends. The 3rd section refers to patient fatigue which was measured with the Fatigue Assessment Scale (FAS) questionnaire by Michielsen et al. [7]. The questionnaire includes 10 questions on a five-point Likert scale 1-5 (1= Never, 2=Sometimes, 3= Regularly, 4=Often, 5=Always) and 2 subsections of 5 questions about physical and mental fatigue.

The 4th section includes 16 questions about perceived quality of life of patients which was measured by the Missoula-VITAS Quality of Life questionnaire Index of Theofilou et al. [8]. The questionnaire includes 1 question about global quality of life five-point Likert scale 1-5 (1=Very poor, 2=Poor, 3=Average, 4=Good, 5=Very good) and 15 questions divided into 5 subsections of 3 of quality-of-life questions about symptoms, functioning, interpersonal relationships, wellness and spirituality. In each subsection the 1st question refers to evaluation (scale from -2 to +2), the 2nd to satisfaction (scale from -4 to 4) and the 3rd in importance (from 1 to 5).

The 5th section includes 13 questions on a five-point Likert scale from 1 to 5 (1= Not at all, 2=Little, 3=Moderate, 4=Quite a bit, 5=Too much), related to nursing care.

All procedures were performed in accordance with the ethical standards of the 1964 Declaration of Helsinki, as revised in 2000. Completing the questionnaires was voluntary and was done by the patients themselves. Before the procedure, all participants were informed about the purposes of the research, anonymity, voluntary withdrawal in case they felt uncomfortable and they were given a written consent form.

From Tables 3-4 it appears that in the "Physical fatigue" factor, Technological - University education graduates showed a lower average value (M.O.=2.49) compared to Primary School graduates (M.O.=3.23, p=0.029) and High School (M.O.=3.14, p=0.024).

Results

Table 1 presents the demographics of the respondents.73.9% (N=51) were men and 26.1% (N=18) were women. Regarding marital status, 66.7% (N=46) were married or cohabiting, 23.2% (N=16) single, 7.2% (N=5) widowed and2.9% (N=2) from divorcees. Regarding age, 34.8% (N=24) are 61-70 years old, 24.6% (N=17) 51-60,14.5% (N=10) 71-80, 10.1% (N=7) to 40, 10.1% (N=7) over 80 and 5.8% (N=4) 41-50 years old.What is the effect of demographic profile on levels of perceived social support, fatigue, quality of life and nursing care? In the present research question, the statistically significant results are presented.