PURPOSE There is limited available research about the experiences of family caregivers and their care of family members with cancer. The purpose of this study was to explore the experience of distress among family caregivers. Further, this study explored what aspects of caring for family member contributed to the distress. METHODS Data were collected through in-depth interviews with thirteen family members primarily responsible for the care of the member with cancer. All interviews were audio-taped, transcribed, and analyzed with qualitative content analysis. RESULTS The findings showed that the patients' physical, psychological, socio-relational, and spiritual symptoms influenced their caregivers' distress. The four categories that emerged from the data included “focusing attention only on the patient battling with cancer,â€â€œbeing trapped in turmoil of complex emotions and feelings,â€â€œhaving had to endure alone,†and “hanging in there at the crossroads of life and death.†With respect to these categories, fourteen sub-categories were ultimately identified. CONCLUSION Based on this study, researchers need to focus more attention on, and explore such co-existing distress to develop an adequate support program for the family caregivers of cancer patients.
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PURPOSE The objective of the study was to identify impact of depression, fatigue, family support, and resilience on rehabilitation among cancer survivors. METHODS One hundred and twenty-four participants who visited an out-patient department were recruited from a university hospital in Korea. An inclusion criterion was no reported relapse following the primary cancer treatment. Data were collected from July 1st to August 31st, 2014. Data analysis included an independent t-test, ANOVA, Pearson correlation coefficients and multiple regression using the SPSS 19.0 program. RESULTS Rehabilitation of those with colon and breast cancer was significantly correlated with depression, fatigue, family support and resilience. In a regression analysis, cancer rehabilitation accounted for 79.2% of the variance of depression, fatigue, monthly household income and resilience. The most significant factor affecting the success of rehabilitation was depression (β=-0.39, p < .001). CONCLUSION The results of the study indicate the importance of managing depression for the successful rehabilitation of cancer survivors. Nurses should prioritize the development and implementation of effective interventions for the improvement of rehabilitation among cancer survivors.
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PURPOSE The purpose of this study was to describe and explore the adaptation process of patients with myelodysplastic syndrome (MDS). METHODS Using a grounded theory methodology, 15 interviews were performed with nine men and six women, 43-83 years of age, suffering from MDS. Data were analyzed using the constant comparative analysis method. RESULTS The core category emerged as “To do my best in uncertaintyâ€. MDS patients engaged in three stages: Panic, Active fighting against illness, and Putting down/Adaptation phase. Causal conditions were unexpected cancer diagnosis, endless painful treatment, and uncertainty. Contextual conditions were physical deterioration and differences in recovery. The central phenomenon of the illness adaptation process among the patients with MDS was powerlessness at the dead end. Action/Interaction strategies included dependence on the constant medical care, physical energy conservation, mind control and environmental control. Intervening conditions were social support and desire to live. Consequences were hope for recovery and tug-of-war from repetition of exacerbation and recuperation. CONCLUSION When caring for these patients, it is important to identify needs, allow patients to express what they want at that moment and support them in maintaining a daily life.
PURPOSE Subjective Attitudes toward cardiopulmonary resuscitation (CPR) can be diverse. The purpose of this study was to identify subjective attitudes toward CPR among hospital nurses working in emergency room and intensive care units. METHODS The Q methodology was used. The 42 Q-statements selected by each of the 38 participants were classified into a shape of normal distribution. The collected data were analyzed using a QUANL program. RESULTS Three types of attitudes emerged: ‘TypeI, CPR requires professionalism(medical personnel-centered)’, ‘Type II, CPR requires reality (patient-centered)’, and ‘Type III, CPR requires ethicality (human dignity-centered)’. CONCLUSION The findings suggest that nursing intervention programs for the three types should be developed. Mandatory repeat education programs for TypeI, Development of guidelines for the prohibition and termination of CPR for TypeII. Continuing education on wills and advance directives for TypeIII can be helpful.
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PURPOSE The aim of the study was to identify factors influencing quality of communication life of older adults in the community. METHODS Participants in this study were 128 older adults who registered at the community welfare center. The data were collected from September to October 2015 by using audiometer and three self-administered questionnaires including Korean Evaluation Scale for Hearing Handicap, Korean-Perceived Stress Scale, and Quality of Communication Life Scale. Mean minimal threshold of both ears was defined as 40dB and above for hearing handicap in this study. Data analysis included descriptive statistics, t-test, Pearson correlation coefficients, and hierarchical regression. RESULTS According to the screening test result from audiometer measurement, 53.9% of the participants were found to have hearing impairment. The main factors influencing quality of communication life in older adults were subjective hearing handicap of social domain and perceived stress. They explained about 41% of quality of communication life. CONCLUSION This study identified that subjective hearing handicap on social domain and self perceived stress in older adults were more important factors for their quality of communication life compared to physical hearing loss. Nurses caring for older people should include strategies to increases communication skills and to decrease communication related stress.
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PURPOSE The aim of this study was to identify gender and age differences in health status and health behaviors of community-dwelling older adults in an urban city. METHODS A convenience sample of 500 older people were recruited. Participants completed eight study instruments by face to face interview. The instruments were the Korea Instrumental Activities of Daily Living (K-IADL), Short Physical Performance Battery (SPPB), Body Mass Index (BMI), Mini Nutritional Assessment-Short Form, Stanford Research Instruments for Chronic Disease, Geriatric Depression Scale Short Form Korea version, EuroQol-5 Dimensions scale (EQ-5D), and the Study of Osteoporotic Fracture Frailty Index. RESULTS 71.6% were females and mean age of all participants was 74.4 years. Participants were divided into three age groups: 60 to 74 years (n=263, 52.6%), 75 to 84 years (n=207, 41.4%), and ≥85 years (n=30, 6.0%). Significant gender differences were found in educational level, marital status, family type, religion, perceived economic status, K-IADL, SPPB, grip strength, BMI, fatigue, smoking, drinking, communication with physicians and nurses, and EQ-5D. There were significant differences among the three age groups on educational level, marital status, family type, SPPB, grip strength, regular health check-up, communication with physicians and nurses, and frailty. CONCLUSION Gender difference should be taken into consideration more than age when policy and preventive programs for community-dwelling older adults in an urban city is developed.
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PURPOSE The purpose of this study was to describe the mediating effect of social support and its relationship between distress and quality of life (QoL) of elderly patients with gastric cancer. METHODS 186 elderly patients who visited an inpatient/outpatient at two cancer hospitals were recruited from May 30 to July 26, 2017. Distress, social support, and QoL were measured using structured questionnaires such as Distress Thermometer and Problem list, Perceived Social Support scale, and QoL scale for Korean patients with cancer. The mediating effects were analyzed by a multiple hierarchical regression. RESULTS Distress was found to have significant negative correlations with social support (r=-.47, p < .001) and QoL (r=-.58, p < .001). There was a positive correlation between social support and QoL (r=.72, p < .001). The influencing factors on QoL were education, recurrence, sleep, dietary problem, distress, and social support. These variables were explained 66% of the variance in QoL. The direct effect of distress on QoL was significant (β=-.24, p < .001) and the indirect effect of distress on QoL via social support was significant (z=-4.14, p < .001). CONCLUSION Based on this study findings, intervention programs directed at reducing distress by focusing on bolstering social support is recommended to improve QoL in elderly patients with gastric cancer.
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