Factors affecting the quality of life among Chinese rural general residents: a cross-sectional study

Public Health ◽  
2017 ◽  
Vol 146 ◽  
pp. 140-147 ◽  
Author(s):  
Y. Chen ◽  
G. Sun ◽  
X. Guo ◽  
S. Chen ◽  
Y. Chang ◽  
...  
PLoS ONE ◽  
2020 ◽  
Vol 15 (4) ◽  
pp. e0231346 ◽  
Author(s):  
Brita Roy ◽  
Judith R. L. M. Wolf ◽  
Michelle D. Carlson ◽  
Reinier Akkermans ◽  
Bradley Bart ◽  
...  

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Burcu Akpınar Söylemez ◽  
Özlem Küçükgüçlü ◽  
Merve Aliye Akyol ◽  
Ahmet Turan Işık

Abstract Background Quality of life (QoL) is a growing area of interest in dementia research. However, it remains a controversial topic. This study aimed to determine the QoL of people with Alzheimer’s disease (PwAD) and investigate the factors affecting patients’ and caregivers’ QoL scores. Methods A cross-sectional study design was used. A total of 98 home-dwelling PwADs and their primary caregivers were recruited in the study. Sociodemographic characteristics and QoL scores, activities of daily living (ADL) and instrumental ADL (IADL), Mini-mental State Examination (MMSE) scores, neuropsychiatric inventory (NPI), and NPI–distress were determined to assess the relevant outcomes. All statistical analyses were performed using SPSS version 22.0. Descriptive statistics, t-test, Pearson correlation, and multinomial regression were used for analysis. Results The patients’ ratings of their QoL were higher than those of the caregivers. Caregiver education, patients’ ADL, and IADL were associated with the patients’ score on the Quality of Life in Alzheimer’s Disease (QoL-AD) scale. In addition to these variables, MMSE, NPI, and NPI–distress were associated with the caregiver scores on QoL-AD. Conclusion From a clinical point of view, the proxy-rated scores of QoL cannot replace the self-ratings of the patients. This study suggests that both self- and proxy-rated QoL scores should be applied whenever possible. Focusing on the management of behavioral problems and supporting functionality and cognitive functions may be modifiable factors that may represent targets for intervention to improve the QoL. The findings of this study should also be used to design caregiver educational programs about the determinants of QoL.


Author(s):  
Junaid A. Ahangar ◽  
Samina Farhat ◽  
Rabbanie T. Wani

Background: Quality of life (QOL) is a broad, multidimensional concept that usually includes subjective evaluations of both positive and negative aspects of life. Very few studies have been carried out on QOLIE 31 in India and research in this area will identify factors affecting QOL. study was therefore conducted to determine the level of health related QOL of patients of epilepsy in a tertiary care teaching hospital. To evaluate patterns of the use of anti-epileptic drugs (AEDs) and their impact on the Quality of Life (QOL) in patients with epilepsy.Methods: The study was a hospital based cross sectional study conducted by the Department of Pharmacology in association with the Department of Medicine, Government Medical College, Srinagar. A total number of 134 patients, aged >18 years were studied for a period of one and a half years, January 2015-July 2016. QOLIE‑31 questionnaire was used for collecting data on health‑related QOL.Results: The mean overall QOLIE-31 score was 53 corresponding to a t-score of 44. Amongst the QOLIE-31 subscales, the highest mean score was the cognitive subscale (73.6) followed by medication effects (55.5) and social functions (52).Conclusions: It is evident from our study that there are many factors that influence QOL of people with epilepsy. Among them, type of drug therapy plays an important role. Adding clinical counselling and other interventions to address the physical, mental, psychological, social, and emotional aspects of health wellbeing is likely to achieve better health outcomes for epilepsy patients.


2016 ◽  
Vol 17 (1) ◽  
Author(s):  
Sa’ed H. Zyoud ◽  
Dala N. Daraghmeh ◽  
Diana O. Mezyed ◽  
Razan L. Khdeir ◽  
Mayas N. Sawafta ◽  
...  

Author(s):  
Orapan Fumaneeshoat ◽  
Thammasin Ingviya

Objective: To measure the Quality of Life (QoL) and Caregiver Burden Scale (CBS) of lung cancer patients’ caregivers and assess the associated factors. Material and Methods: This was a cross-sectional study. We interviewed lung cancer patients and their caregivers who were visiting the outpatient department of a tertiary hospital in Thailand. QoL was measured by the World Health Organization Quality of Life-BREF-THAI. CBS was measured by Zarit’s burden interview. The data were collected using the KoBoToolbox application. Multivariate ordinal logistic regression was used to assess associations between caregivers’ QoL and CBS with the dependent variables, including patient and caregiver factors. Results: Two hundred and four patients and 202 caregivers were included in the study. The only caregivers factor associated with lower QoL was younger age [odds ratio (OR)=0.33, 95% confidence interval (CI): 0.11-0.95)] while factors associated with better QoL were income (OR=3.91, 95% CI: 1.13-14.50) and being a child of the patient (OR=3.24, 95% CI: 1.02-11.30). The main caregivers factor associated with a lower CBS was being Muslim (OR=0.16, 95% CI: 0.05-0.52), and the main factor associated with a higher CBS was income (OR=6.12, 95% CI: 1.66-23.75). The patients factors affecting CBS were female (OR=0.36, 95% CI: 0.17-0.71), Barthel’s activity daily living (ADL) index (OR= 7.42, 95% CI: 1.99-28.65), and ≥2 years looking after a patient (OR=0.40, 95% CI: 0.18-0.88). Conclusion: The factors affecting caregivers’ QoL and CBS were their patients’ ADL and years with disease. Training on caring patients to maintain the patients’ ADL for caregivers should be provided. Health authorities should provide opportunities for patients to share their experience on how they live and cope with the symptoms of lung cancer.


Sign in / Sign up

Export Citation Format

Share Document