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Wyszukujesz frazę "Quality of Life" wg kryterium: Temat


Tytuł:
Life satisfaction and self-efficacy in patients with stoma
Autorzy:
Bazaliński, D.
Sałacińska, I.
Więch, P.
Kózka, M.
Powiązania:
https://bibliotekanauki.pl/articles/1916649.pdf
Data publikacji:
2014
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Stoma
satisfaction
quality of life
Opis:
Introduction: There are many indications for a stoma surgery; however, most frequently it is the severity and progression of colorectal cancer. The result of surgical procedure is frequently a stoma. In view of the increasing prevalence of colorectal cancer and delaying stoma surgery particular attention should be paid to the aspects of quality of life and adaptation to a new life situation in patients with a stoma. Purpose: To evaluate satisfaction with life and management of difficult situations in people with the stoma. Materials and methods: The study included 200 people from three provinces: Podkarpackie, Małopolska, and Zachodniopomorskie. The study was performed by means of a diagnostic survey in a form of the author’s questionnaire and two standardized tools: the SWLS (satisfaction with life scale) and the GSES (generalized self-efficacy scale). A chi-square test for independence was used for a statistical analysis. Results: The research found that for 56.5% of the respondents a stoma formation had a strong negative impact on their functioning both in personal, family and social life. In the opinion of 12.5% of the respondents intestinal stoma was the reason for giving up work. It was also found that there was a correlation between the level of satisfaction with life and education - higher education favors a higher level of satisfaction with life. Conclusions: This study showed that there is a positive relationship between the level of life satisfaction and the sense of self-efficacy. The higher self-efficacy, the higher satisfaction with life among the respondents were found.
Źródło:
Progress in Health Sciences; 2014, 4, 2; 22-30
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life of osteoarthritis patients in the aspect of analgesic treatment
Autorzy:
Niczyporuk, M.
Kłossowska, J.
Kleszczewska, E.
Shpakou, A.
Knaś, M.
Powiązania:
https://bibliotekanauki.pl/articles/1918857.pdf
Data publikacji:
2019-08-26
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Osteoarthritis
analgesics
quality of life
Opis:
Introduction: Osteoarthritis an inflammatory process in the synovial membrane. These changes cause pain and joint deformities. Pharmacists can assess patients’ quality of life, which can be a good criterion for assessing analgesics treatment effectiveness and prevent the growing phenomenon of polypharmacy and self-treatment. Purpose: To answer these questions: 1) Is there a relationship between the quality of life of patients with osteoarthritis taking analgesics and those with osteoarthritis taking analgesics and implemented rehabilitation? 2) Do patients using analgesics practice polypharmacy? 3) Are patients with osteoarthritis the main consumers of painkillers? and 4) Does the use of analgesics affect the health-related quality of life of patients with osteoarthritis? Materials and methods: The study was conducted on 240 people who were divided into three groups: osteoarthritis, reference (generally healthy, occasionally taking analgesics), and control (generally healthy, no intake of analgesics). To assess the rise in analgesics consumption by patients with osteoarthritis and the phenomenon of polypharmacy, an original questionnaire was used. Results: There is a relationship between the quality of life of patients with osteoarthritis taking analgesics. Statistical analysis showed that in the years 2013-2015 the purchase of prescription analgesics and without a prescription systematically, significantly increased. Conclusions: Patients using analgesics unknowingly practice polypharmacy. In Ars Medica Pharmacies, analgesics purchases by patients with osteoarthritis grew significantly in the analyzed period, but they are not the main analgesics consumers. Use of analgesics by patients with osteoarthritis improves their health-related quality of life.
Źródło:
Progress in Health Sciences; 2019, 1; 36-44
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The effect of perceived social support on the quality of life of hemodialysis patients. A preliminary study.
Autorzy:
Theofilou, P.
Stefanidou, M.
Giannakopoulou, N.
Tzavella, F.
Zyga, S.
Tsironi, M.
Alikari, V.
Powiązania:
https://bibliotekanauki.pl/articles/1918921.pdf
Data publikacji:
2020-06-10
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
hemodialysis
quality of life
social support.
Opis:
Purpose: Recent studies have shown that the role of social support is a predictive factor influencing the course of the disease. The current study is focused on patients’ assessment of quality of life and the relationship of the latter with perceived social support. Materials and methods: A total sample of 40 hemodialysis patients voluntarily participated in this study. Participants were recruited from two clinics in Athens and have been under hemodialysis. The measures used were the Missoula- Vitas Quality of Life Index–15 and the Multidimensional Scale of Perceived Social Support. For the data analysis descriptive statistics, parametric Pearson r test and Non-parametric Spearman’s rho test were used. Statistical level was set up at 0.05. Results: The results of the current study provide good quality of life of hemodialysis patients and significant statistical significance between quality of life in several domains. Conclusions: This study concludes that the participants’ assessment of quality of life is poor regarding the well-being dimension. Also, perceived social support is significantly related to quality of life
Źródło:
Progress in Health Sciences; 2020, 10(1); 19-25
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life during the first year after breast cancer resection
Autorzy:
Kulesza-Bronczyk, B.
Dobrzycka, B.
Piekut, K.
Terlikowski, R.
Mackowiak-Matejczyk, B.
Wojno, A.
Terlikowski, SJ.
Powiązania:
https://bibliotekanauki.pl/articles/1916396.pdf
Data publikacji:
2014
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Breast cancer
quality of life
questionnaires
Opis:
Introduction: Quality of life can be determined by a number of factors, including subjective perception of various spheres of health and health-unrelated factors. Purpose: To compare the quality of life of women who had breast cancer one month and one year after mastectomy, and to verify the usefulness of health-related quality of life (HRQoL) scales in early identification of patients having problems in various functional spheres. Materials and methods: The study included the group of 110 mastectomized women. Quality of life of the participants was estimated with EORTC QLQ-C30 and EORTC QLQ-BR23 questionnaires. Results: Global health status (QoL) determined with the aid of the EORTC QLQ-C30 questionnaire turned out to be significantly higher in women surveyed one year after mastectomy than in those examined one month after the surgery (74.23 vs. 58.33, p<0.001). Moreover, the two groups of patients differed significantly in terms of physical, cognitive, social and role functioning scores. Most of the symptoms assessed were resolved within a year after the breast cancer surgery. No significant intergroup differences were revealed with regard to emotional and socioeconomic functioning or future perspective scores. Conclusions: Quality of life of most mastectomized women improves considerably within one year after the surgery. The use of quality of life instruments can be useful in early postoperative identification of patients who score low on functional and symptom scales. Such patients require support and/or psycho-oncological treatment during the early postoperative period. Quality of life of breast cancer patients during the early postoperative period can be a predictor of this parameter in a longer-term perspective.
Źródło:
Progress in Health Sciences; 2014, 4, 1; 124-129
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pelvic floor muscle disorders and women’s quality of life
Autorzy:
Stadnicka, G.
Łepecka-Klusek, C.
Pilewska-Kozak, A.B.
Powiązania:
https://bibliotekanauki.pl/articles/1917754.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Pelvic floor disorders
quality of life
sexuality
Opis:
Purpose: To characterize the symptoms of urinary incontinence of women suffering from pelvic organ disorders (POP) and the effect of these problems on quality of life (QoL). Materials and methods: 215 women from rural regions diagnosed with POP were examined. The research implemented the Life Satisfaction Questionnaire (LISAT-11), used to assess quality of life; the Sexual Quality of Life-Female (SQoL-F) questionnaire, which was employed to assess sexual activity; and the Gaudenz-Incontinence questionnaire, served to assess the occurrence of symptoms of urinary incontinence as well as to define the type of urinary incontinence and its degree of escalation. Results: The average age of the participants was 54.8 years. Most of the participants had urinary incontinence (159; 73.95%). Women with POP and symptoms of urinary incontinence achieved a lower indicator of the sexual function QoL (median - 61.00) when compared to those not suffering from urinary incontinence (median- 78.00). Differences between the groups were statistically significant (p=0.002). The general indicator of QoL for women with symptoms and those without symptoms of stress urinary incontinence (SUI) did not reveal any significant differences between the groups (p=0.643). Conclusions: Urinary incontinence in women with disorders of pelvic floor muscle functions has an insignificant effect on general QoL, whereas it has a decidedly negative impact on sexual function QoL.
Źródło:
Progress in Health Sciences; 2016, 6(1); 95-101
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life of patients with atrial fibrillation
Autorzy:
Ślifirczyk, A.
Michalczuk, T.
Piszcz, P.
Kierczuk, E.
Kowalenko, M.
Zalewski, R.
Krajewska-Kułak, E.
Powiązania:
https://bibliotekanauki.pl/articles/1918616.pdf
Data publikacji:
2018-06-18
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Patient
quality of life
atrial fibrillation
treatment
Opis:
Introduction: Atrial fibrillation (AF) is one of the most frequent arrhythmias. In Poland, there is a risk of developing AF in about 400,000 people. Atrial fibrillation occurs most frequently as a result of disorders of physiological automatism and afterdepolarization and triggered activity. The treatment strategy of AF is based on pharmacological treatment and procedures such as ablation or cardioversion. The quality of life as defined by the WHO is an individual perception of one's well-being. On the other hand, the assessment of the quality of life in illness is modified regarding health problems. Purpose: The main goal of the study was to get to know the quality of life of people with atrial fibrillation. Materials and methods: The research was carried out using a diagnostic survey, based on a survey among 100 patients diagnosed with AF. The place of the research was the Regional Specialist Hospital in Biała Podlaska, in the Emergency Department. Results: Increased morbidity was observed among women and people over the age of 60. The majority of patients with AF declared the quality of life at the medium level. The respondents most often followed medical recommendations. The majority of respondents did not follow healthy lifestyle rules, because as many as 68% of respondents did not do any physical activity and a significant part of the respondents smoked cigarettes and had an inflated BMI. Conclusion: AF affects the quality life by causing sadness, irritation and insomnia.
Źródło:
Progress in Health Sciences; 2018, 8(1); 88-92
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The quality of life of women suffering from polycystic ovary syndrome
Autorzy:
Stadnicka, G.
Łepecka-Klusek, C.
Kulesza-Brończyk, B.
Pilewska-Kozak, A.B.
Powiązania:
https://bibliotekanauki.pl/articles/1917498.pdf
Data publikacji:
2015
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Polycystic Ovary Syndrome
Women
Quality of Life
Opis:
Purpose: To assess how certain clinical symptoms of polycystic ovary syndrome (PCOS) affect the quality of life of women, their activity, and their sexual lives.Materials and methods: The World Health Organization quality of life questionnaire (WHOQOL-Bref) was used to assess the quality of life and health of 78 women diagnosed with PCOS, and the female sexual function questionnaire -28 (FSQ-28) was used to assess their sexual activity and associated disorders.Results: Among three groups of women with varying body mass indexes and aged26.93 years on average, significant differences (p<0.05) were found in quality of life. In individual domains of the WHOQOL-Bref, the median score of women with obesity was lower than that of women with normal body weight or with overweight. Women with symptoms of hirsutism showed lower quality of life than women without these symptoms, while womenwho had undergone treatment for 4–6 years experienced significantly worse quality of life than those who had undergone therapy for less than 3 or more than 6 years. In the various domains of sexual response, regression analysis showed a positive correlation (p <0 .05) between better quality of life and women’s sexual activity.Conclusions: Clinical symptoms of PCOS such as obesity and hirsutism affect women’s quality of life, as does the length of infertility treatment, whereas general quality of life affects the occurrence of disorders in women at particular stages of sexual response.
Źródło:
Progress in Health Sciences; 2015, 5, 2; 61-68
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life of children suffering from motor disabilities as evaluated by their parents
Autorzy:
Wojtkowski, J.
Sienkiewicz, D.
Okurowska-Zawada, B.
Paszko-Patej, G.
Konopka, A.
Okulczyk, K.
Średzińska, K.
Dmitruk, E.
Mirska, A.
Kułak, W.
Powiązania:
https://bibliotekanauki.pl/articles/1918580.pdf
Data publikacji:
2018-01-09
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Quality of life
motor disability
children
parents
Opis:
Purpose: We assessed the quality of life of children with motor disabilities in comparison with healthy children, as evaluated by their parents, using the CHQ-PF28 questionnaire (Child Health Questionnaire—Parent Form). Materials and methods: In a prospective study, we evaluated the quality of life of 105 children with motor disabilities. Results: Our research showed lower quality of life in the group of children with motor disabilities compared with controls, both in terms of physical and psychosocial health. Significant correlations between independent walking and physical functioning, general behavior, and mental health of children suffering from motor disabilities were found. According to the average indices of quality of life of children suffering from motor disabilities, depending on sex, the greatest differences occurred in behavior and change of health status, while the smallest differences in self-esteem and parental involvement, compared with controls. In the case of healthy children, the largest differences appeared in the perception of pain, behavior, and self-esteem; whereas, the smallest variations occurred in the change of health status and physical activity. Conclusion: Children suffering from motor disabilities demonstrate lower quality of life compared with healthy children.
Źródło:
Progress in Health Sciences; 2017, 7(2); 60-66
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Assessment of psychological distress and quality of life in lung cancer patients receiving chemotherapy: A single center experience
Autorzy:
Pigkou, K.
Alikari, V.
Papathanasiou, I.V.
Theophilou, P.
Lavdaniti, M.
Zyga, S.
Fradelos, E.C.
Powiązania:
https://bibliotekanauki.pl/articles/1918603.pdf
Data publikacji:
2018-06-18
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Lung cancer
psychological distress
quality of life
Opis:
Background: Lung cancer is one of the most common malignant diseases with high mortality. Patients diagnosed with lung cancer are most likely to exhibited psychiatric symptomatology while they experience poor quality of life. Purpose: To examine the relationship between psychological distress and quality of life (QoL) in lung cancer patients receiving chemotherapy. Methods: A cross sectional study was conducted in which 110 lung cancer patients were recruited to participate. Data was collected with an anonymous self-administrated question-naire consisted by three parts: a sheet concerning demographic information, the scales Missoula Vitas Quality of Life Index-15 and General Health Questionnaires (GHQ)-28. Results: Women accounted for 51.8% of the sample, 27.3% were ≥56 years old and 24.5% were in the age between 35-44. Moreover, 38.2% were high school graduates while 46.4% were married. Age, educational level, and marital status were found to be related to patients’ perceived QoL. QoL was found to be related to psychological variables for GHQ-28. Conclusions: Quality of life can be considered to be a result of disease and treatment, as perceived by the patient and is affected by factors such as injury, anxiety, perceptions and social opportunities. This has a direct effect on patients’ functioning and ability to self-care.
Źródło:
Progress in Health Sciences; 2018, 8(1); 122-129
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life and the level of knowledge and utilization of lymphedema prevention principles among mastectomized patients
Autorzy:
Kulesza-Bronczyk, B.
Dobrzycka, B.
Chrzanowska, MI.
Terlikowski, R.
Maćkowiak-Matejczyk, B.
Stadnicka, G.
Terlikowski, SJ.
Powiązania:
https://bibliotekanauki.pl/articles/1916354.pdf
Data publikacji:
2014
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
breast cancer
mastectomy
quality of life
lymphedema
prevention
Opis:
Introduction: Breast cancer is the most prevalent female malignancy in Poland. Oncological treatment and its adverse effects diminish quality of life of breast cancer patients, which is determined by a number of somatic, psychological and social factors. Purpose: To assess the quality of life and the level of knowledge and utilization of lymphedema prevention principles among women after surgical treatment of breast cancer. Materials and methods: The study included 145 breast cancer patients after radical mastectomy. The respondents were examined with the validated EORTC QLQ-BR23 questionnaire and a custom-designed survey. Results: Examination with the QLQ-BR23 questionnaire revealed that mastectomized women scored low on the body image scale. The most frequently reported ailments were arm and breast symptoms. While the respondents showed high level of knowledge with regards to lymphedema prevention, they poorly adhered to the prophylactic guidelines. The participants were well aware of the risk factors of lymphedema, and most of them declared avoidance of their harmful effects. Conclusions: Quality of life assessment should constitute an integral component of rehabilitation in every breast cancer patient, as mastectomy exerts significant effect on the outcome of perioperative period. Apart from specialist physiotherapy, also education of patients with regards to principles of lymphedema prevention and autotherapy constitutes an important component of complex management of lymphatic insufficiency.
Źródło:
Progress in Health Sciences; 2014, 4, 1; 110-117
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Burnout syndrome impacts on quality of life in nursing professionals: The contribution of perceived social support
Autorzy:
Fradelos, E.
Mpelegrinos, S.
Mparo, Ch.
Vassilopoulou, Ch.
Argyrou, P.
Tsironi, M.
Zyga, S.
Theofilou, P.
Powiązania:
https://bibliotekanauki.pl/articles/1916393.pdf
Data publikacji:
2014
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
burnout
quality of life
social support
nursing staff
Opis:
Purpose: To examine the impacts of burnout that has in health-related quality of life (QOL) in nursing staff in Greece. The association of social support with burnout and QOL is also investigated. Materials and methods: Individuals working in Mental and General Hospitals in the broader area of Athens participated in this study (N.139). The measurement tools include a) the Maslach Burnout Inventory (MBI), b) the SF-36 Health Survey and c. the Multidimensional Scale of Perceived Social Support. Burnout and QOL are expected to be related to the evaluation of social environment. Results: The results indicated the impacts that burnout has on quality of life and the positive effect of social support for nursing professionals in the levels of burnout. Conclusions: There is an association between burnout, quality of life and social support. Social support and socio-demographic factors appear to affect the levels of burnout to Psychiatric and General Hospital.
Źródło:
Progress in Health Sciences; 2014, 4, 1; 102-109
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The Relationship Between Depression and Quality of Life in Elderly Patients with Glaucoma
Autorzy:
Çavdar, R.N.
Türkleş, S.
Powiązania:
https://bibliotekanauki.pl/articles/1918942.pdf
Data publikacji:
2020
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
glaucoma
elderly patients
depression
quality of life
nursing
Opis:
Purpose: To examine the relationship between depression and quality of life in elderly patients with glaucoma. Materials and methods: The study was conducted as a descriptive and cross-sectional research. The sample of the work consists of 130 patients aged 60 years and over who were followed up at Mersin University Hospital Ophtalmology Department between 01 October 2016 and 31 March 2017. The data were gathered with Personal Information Form, Geriatric Depression Scale and Modifiye GLAU-QOL 17 Glaucoma Quality of life. Number, percentage, mean, Pearson Correlation, Student`s t test, ANOVA test, Tukey and Games-Howell statistic were used in the evaluation of the data. Results: The mean age of the patients was 67.9±7.27. The mean score of geriatric depression scale of the patients was 15,23±5,52. It was determined that 16,2% of the patiens had possible depression and 62,3% had definite depression. The median Glau–QOL-17 Glaucoma Quality of Life Questionnaire subcale scores of the patients were as follows: daily living (3,58±3,25), driving (3,23±2,53), worry (5,26±3,47), self-assesment (6,4±3,07), psychology (4,08±2,74), feeling oppressed (4,39±2,35) and taking responsibility (3,56±1,86). The mean total score was 34.44±15.29. There was a negative and statistically significant relationship between the age of the patients and the scores of geriatric depression and the scores of age and quality of life. Conclusions: Elderly patients with glaucoma are at a major risk for depression and their quality of life is negatively affected.
Źródło:
Progress in Health Sciences; 2020, 10(2); 55-64
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Psychological, physical, and social situation of patients with Hodgkin lymphoma undergoing radical chemoradiotherapy
Autorzy:
Hempel, D.
Politynska, B.
Danilewicz, A.
Sierko, E.
Wojtukiewicz, M.Z.
Powiązania:
https://bibliotekanauki.pl/articles/1917650.pdf
Data publikacji:
2015
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Hodgkin lymphoma
Quality of Life
Medical care
chemoradiotherapy
Opis:
Purpose: To assess the physical and psychosocial situation and needs of Polish patients with Hodgkin lymphoma (HL), who had undergone radical chemoradiotherapy.Materials and methods: 50 Hodgkin lymphoma patients were asked to complete an institution-developed questionnaire concerning their physical, emotional and social well-being, as well as their perceptions regarding the medical care they had received. Results:The physical and psychosocial quality of life of patients with HL was diminished by the disease and its treatment. The most frequently reported side effects of both chemo- and radiotherapy were fatigue and loss of taste. The observed symptoms were slight or moderate. Although 36% of participants reported feelings of depression and 52% - were concerned about their future functioning in society, more than half of patients reported that were happy (60%). 20% of respondents were unable to work at all, but more than half had some difficulties with their employment. 20-40% of the patients complained about having received insufficient dietary instructions and lack of information about the late adverse effects of treatment. Although the majority of respondents assessed the quality of medical care as very high emotional problems preferred to share with relatives (90%).Conclusions:Although the physical and psychosocial situation of HL patients may be affected by the disease and its treatment, for the majority of patients, these impediments did not cause serious deterioration in functioning. Medical care was positively assessed by the HL patients, but more emotional and informative support is needed to decrease patients’ anxiety regarding future functioning in society.
Źródło:
Progress in Health Sciences; 2015, 5, 2; 69-76
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The quality of life in parents raising children with an autism spectrum disorder from Poland, Belarus and France
Autorzy:
Ślifirczyk, A.
Krajewska - Kułak, E.
Brayer, A.
Sobolewski, M.
Maciorkowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/1917772.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
autism spectrum disorder
children
parents
quality of life
Opis:
Purpose: To assess the health-related quality of life (HRQL) in parents of children with autism spectrum disorder (ASD). Materials and methods: The sample consisted of 83 families with children with ASD, including 30 families from Poland, 25 from Belarus, and 28 from France. Parental HRQL was surveyed with the World Health Organization Quality of Life–BREF (WHOQOL–BREF) and KINDLR questionnaires. Results: This study showed that Polish parents reported the lowest quality of life according to the WHOQOL–BREF. Parents from Belarus reported slightly worse HRQL than parents from France, though other aspects of quality of life (e.g, social sphere, somatic sphere) did not differ significantly between these parents. Parents from Poland also reported lower HQOL according to the KINDLR questionnaire, while parents from Belarus had a higher HQRL in the mental, physical, and self-esteem domains compared to parents from Poland and France. Conclusion: Parents from Poland with children with ASD reported lower HRQL both on the WHOQOL–BREF and KINDL R questionnaires compared to parents from Belarus and France.
Źródło:
Progress in Health Sciences; 2016, 6(1); 102-107
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Life’s quality of chronically dialyzed children in Poland
Autorzy:
Juzyszyn, A.
Kunecka, D.
Musiał, B.
Powiązania:
https://bibliotekanauki.pl/articles/1917833.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Sick children
quality of life
renal replacement therapy
Opis:
Introduction: The paper presents the possibility of assessing the quality of life (QOL) of children on dialysis. Purpose: To evaluate the QOL depending on the health status of children on dialysis, to compare the subjective assessment of the QOL and to identify some of the factors independently affecting the QOL. Materials and methods: The study has been conducted on a group of 28 children on dialysis. Research tools: Poland abbreviated version of the survey assessing the quality of life of The World Health Organization Quality of Life (WHOQOL); survey constructed on the basis of the Polish version of Kidney Disease and Quality of LifeTM Short Form (KDQOL-SFTM) Version 1.2 and a questionnaire assessing QOL of children and adolescents with end-stage renal disease on dialysis and transplantation of kidneys by Rubik, Grenda, Jakubowska - Winecka and Dabrowska. Results: There were no significant differences in QOL between children treated with peritoneal dialysis and Hemodialisis (HD). While there is a strong correlation between the severity of depressive symptoms and the treatment's duration, financial status and parents' education. Conclusions: The phenomenon of reduced QOL must be counteracted. Medical pediatric staff of dialyze centers should especially pay attention to the problem of life’s quality, due to the intensity of disease’s impact on growing organism, should actively counteract the phenomena of its decrease by continuous therapeutic education of patient and his or her family.
Źródło:
Progress in Health Sciences; 2016, 6(2); 117-124
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł

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