Health status, quality of life, and the individual

JAMA ◽  
1994 ◽  
Vol 272 (8) ◽  
pp. 630-631 ◽  
Author(s):  
G. H. Guyatt
Keyword(s):  
Quality Of Life ◽  
Health Status ◽  
The Individual

scholarly journals Path Analysis on the Children’s Characteristics and Environmental on the Quality of Life of Children Aged 2-4 Years

2020 ◽  
Vol 12 (10) ◽  
pp. 69
Author(s):  
Heni P. Wahyuningsih ◽  
Bhisma Murti ◽  
Eny Lestari ◽  
Reviono Reviono
Keyword(s):  
Quality Of Life ◽  
Health Status ◽  
Breast Feeding ◽  
Data Retrieval ◽  
Exclusive Breast Feeding ◽  
Safe Water ◽  
Retrospective Cohort Studies ◽  
The Individual ◽  
The Impact

OBJECTIVE: Quality of life is a person's self-perception of the enjoyment and satisfaction of life. Health related quality of life (HRQOL) is multidimensional, which is the individual's perception of the impact of a person's health. Data from US News shows the quality of life of Indonesia is ranked at 40 from the 80 countries in the survey. The quality of life of children can be influenced by factors such as foster patterns, immunization status, breast feeding, no smoking area, and safe water. This research aims to determine the influence of exclusive feeding, immunization, foster patterns, no smoking are, and safe water to the health status and quality of life of children. METHOD: This research is a quantitative observational study with a research design of retrospective cohort studies. Population of this study is all toddlers aged 2-4 years old who reside in the village worthy of children (exposed groups) and ordinary villages (unexposed groups) in the region of Sleman regency. The large sample in this study was 350 respondents with multistage random sampling data retrieval techniques. FINDINGS: The quality of life of the children was directly affected by health status (b=0.006; SE=0.054; p<0.001), foster pattern (b=0.079; SE=0.055; p<0.001), and safe water (b=0.004; SE=0.145; p<0.001). Health status was affected by exclusive breast feeding, foster pattern, and safe water. Foster pattern was affected by safe water (b=0.056). CONCLUSION: The quality of life of the children is directly affected by health status, foster patterns, and safe water. The quality of life is indirectly affected by exclusive breast feeding.

Health Status, Quality of Life, and the Individual

JAMA ◽  
1994 ◽  
Vol 272 (8) ◽  
pp. 630 ◽  
Author(s):  
Gordon H. Guyatt
Keyword(s):  
Quality Of Life ◽  
Health Status ◽  
The Individual

scholarly journals ON THE QUESTION OF THE JUSTIFICATION OF REGIONAL POPULATION STANDARDS OF “QUALITY OF LIFE” RELATED WITH THE HEALTH OF CHILDREN AND ADOLESCENTS (ON THE EXAMPLE OF THE OMSK REGION)

2018 ◽  
Vol 97 (4) ◽  
pp. 337-341
Author(s):  
Olga A. Kozubenko ◽  
M. S. Turchaninova ◽  
E. A. Vilms ◽  
V. A. Shirinsky ◽  
I. A. Sokhoshko
Keyword(s):  
Quality Of Life ◽  
Health Status ◽  
Children And Adolescents ◽  
Physical Functioning ◽  
Life Questionnaire ◽  
Relative Distribution ◽  
Regional Population ◽  
Population Standards ◽  
The Individual

Currently, many developed countries have produced and applied population standards of quality of life, which are used as health status indices in formulating preventive measures and assessing their effectiveness. The study of children and adolescents quality of life is important, as it is one of the population health status indices. In this research, the population standards of adolescents quality of life were studied and justified on an example of Omsk region as a large administrative-territorial unit in the Western Siberia. The research was implemented in compliance with the methodology for the study quality of life. The general well-being quality of life questionnaire PedsQL 4.0. was used as the primary tools. We have investigated the quality of life of 427 students of secondary schools aged 13 to 17 years, residing in the city of Omsk and Omsk region. Among the surveyed were 183 boys and 244 girls. The median values and the 25th and 75th percentiles for the individual scales were: physical functioning (FF) to 87.5 (71.9-100.0) points, emotional functioning (EF) - 70.0 (50.0-85.0) points, social functioning (SF) - 95.0 (75.0-100.0) points, school life (SL) - 70.0 (55.0-90.0) points, psychosocial health (PH) - 76.7 (63.3-88.3) points and the total score (TS) was 81.5 (67.4-90.2) points. The peculiarities of formation of indices were studied depending on the gender of the subject, the area of residence and their state of health. The adolescents with a chronic disease in remission and attending the educational institution were determined to have the lower quality of life rates by reducing physical functioning. The relative distribution of quality of life indices for the individual scales of the questionnaire does not depend on the area of residence; there is an evidence of the existence of the formation of quality of life indices regularities and their relations among themselves. The results of the study are characterized by the sensitivity and reproducibility, which allowed designating the obtained values as regional population-based standards of quality of life.

Mental Health Status and Health-Related Quality of Life among Systemic Lupus Erythematosus (SLE) Patients in Thailand: A Multi-Site Study

2020 ◽  
Vol 103 (11) ◽  
pp. 1185-1193
Keyword(s):  
Quality Of Life ◽  
Mental Health ◽  
Health Status ◽  
Lupus Erythematosus ◽  
Self Esteem ◽  
Mental Health Status ◽  
Health Related Quality ◽  
Related Quality ◽  
Health Related

Background: The systemic lupus erythematosus (SLE) patients oftentimes suffer from both physical and psychosocial challenges that may lead to low health-related quality of life (HRQoL). However, limited research has been done in this area. Objective: To examined mental health status and HRQoL among SLE patients in Thailand. Materials and Methods: The present study was a cross-sectional study conducted at the rheumatology clinic of four major hospitals in Thailand. The paper-based questionnaire consisted of demographic, health history such as depression, anxiety, stress Scale (DASS-21), and the Rosenberg self-esteem scale (RSE), and the disease-specific Lupus Quality of Life scale (LupusQoL). Depending on the variable’s level of measurement such as categorical or continuous, Spearman’s Rho or Pearson’s product moment correlation coefficients were used to explore the relationships among the variables. Hierarchical multiple regression was used to identify the predictors of LupusQoL. Results: Among the 387 participants, many might have experienced depression, anxiety, and stress (30%, 51%, and 29%, respectively). Self-esteem among the participants was good (31.8 out of 40). All eight domains of LupusQoL were affected with intimate relationship domain being impacted the most. The overall LupusQoL was significantly associated with the number of prescribed medications (r=–0.23), depression (r=–0.70), anxiety (r=–0.58), stress (r=–0.67), and self-esteem (r=0.59), p<0.001. Significant predictors of the overall LupusQoL were mental health status (depression, anxiety, and stress) and self-esteem, F (3, 81)=43.10, p<0.001, adjusted R²=0.60. Conclusion: SLE patients should be holistically assessed in both physical and psychological aspects. In addition to proper medical treatments, healthcare providers should use a multidisciplinary team approach to resolve the patients’ psychosocial issues, which in turn, may increase the patients’ quality of life. Self-care education may be necessary to help the patients manage the condition and decrease the number of medications. Keywords: Mental health, Quality of life, SLE, Thailand

scholarly journals P139 What impact does JIA have on health-related quality of life over time and by gender?

Rheumatology ◽  
2020 ◽  
Vol 59 (Supplement_2) ◽  
Author(s):  
Andrew Smith ◽  
Bishma Saqib ◽  
Rebecca Lee ◽  
Wendy Thomson ◽  
Lis Cordingley
Keyword(s):  
Quality Of Life ◽  
Health Status ◽  
Child Health ◽  
Reference Population ◽  
Health Related Quality ◽  
Related Quality ◽  
Health Related ◽  
Over Time ◽  
Domain Scores

Abstract Background Juvenile idiopathic arthritis (JIA) is a heterogeneous group of arthritic conditions presenting in children and young people, in which physical limitations and associated complications can have detrimental effects on physical and psychosocial wellbeing. This study aims to investigate the impact of living with JIA on different aspects of health-related quality of life (HRQoL) and to explore how this changes over time, using data from the Childhood Arthritis Prospective Study (CAPS). Methods Longitudinal data collected as part of CAPS were analysed. HRQoL was assessed at baseline, 1 year and 3 years’ post-diagnosis using the Child Health Questionnaire (CHQ), a parent-completed form for children from 5 years of age. The CHQ measures physical, emotional and social components of child health status. Raw domain scores were transformed via algorithm into values ranging from 0-100, with higher scores indicating better health status. Mean (standard deviation) and median (interquartile range) for each domain were determined, both for the full cohort and by gender. Differences between median scores at baseline and 3 years were assessed using the Wilcoxon signed-rank test. Mean scores of each domain were visually compared with a reference population sample of healthy children from the United States. Results 184 participants completed the questionnaire at all 3 time points. At baseline, compared to the reference population, children with JIA scored lower in every domain although scores were closer between the 2 groups at 3 years. Median scores improved over time, the exception being the general health perceptions domain which decreased after baseline. Domains with the greatest improvement were physical functioning,“bodily pain and social-physical. The largest changes occurred from baseline to 1 year. Statistically significant differences between baseline and 3-year scores were found for all domains. Domain scores for male and female participants were very similar at baseline, though scores for male participants indicated slightly better health at 1 and 3 years for both physical and psychosocial domains. Conclusion JIA has significant impact on HRQoL, which improves within 3 years of diagnosis with the greatest improvement occurring within the first year. Physical health domains show greater improvement over time than psychosocial domains, although psychosocial scores were generally higher throughout the study. Male participants tend to score slightly higher than female participants in both physical and psychosocial domains after baseline. Further research should explore measurable patient, age or disease-related drivers of HRQoL. Disclosures A. Smith None. B. Saqib None. R. Lee None. W. Thomson None. L. Cordingley None.

Quality-of-Life Measurement in Advanced Cancer: Assessing the Individual

1999 ◽  
Vol 17 (11) ◽  
pp. 3603-3611 ◽  
Author(s):  
Dympna Waldron ◽  
Ciaran A. O'Boyle ◽  
Michael Kearney ◽  
Michael Moriarty ◽  
Desmond Carney
Keyword(s):  
Quality Of Life ◽  
Advanced Cancer ◽  
Internal Validity ◽  
Semistructured Interview ◽  
Incurable Cancer ◽  
Life Measurement ◽  
The Difference ◽  
The Individual ◽  
Very High

PURPOSE: Despite the increasing importance of assessing quality of life (QoL) in patients with advanced cancer, relatively little is known about individual patient's perceptions of the issues contributing to their QoL. The Schedule for the Evaluation of Individual Quality of Life (SEIQoL) and the shorter SEIQoL–Direct Weighting (SEIQoL-DW) assess individualized QoL using a semistructured interview technique. Here we report findings from the first administration of the SEIQoL and SEIQoL-DW to patients with advanced incurable cancer. PATIENTS AND METHODS: QoL was assessed on a single occasion using the SEIQoL and SEIQoL-DW in 80 patients with advanced incurable cancer. RESULTS: All patients were able to complete the SEIQoL-DW, and 78% completed the SEIQoL. Of a possible score of 100, the median QoL global score was as follows: SEIQoL, 61 (range, 24 to 94); SEIQoL-DW, 60.5 (range, 6 to 95). Psychometric data for SEIQoL indicated very high levels of internal consistency (median r = .90) and internal validity (median R2 = 0.88). Patients' judgments of their QoL were unique to the individual. Family concerns were almost universally rated as more important than health, the difference being significant when measured using the SEIQoL-DW (P = .002). CONCLUSION: Patients with advanced incurable cancer were very good judges of their QoL, and many patients rated their QoL as good. Judgments were highly individual, with very high levels of consistency and validity. The primacy given to health in many QoL questionnaires may be questioned in this population. The implications of these findings are discussed with regard to clinical assessment and advance directives.

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