Nurses should be involved in educating women about cervical cancer and Papanicolaou testing. By doing so, they can change the attitudes, knowledge, and beliefs of the women.
Objective:One of the most difficult challenges regarding hematopoietic stem cell transplantation in Turkey is finding donors for allogeneic transplantation candidates who do not have related donors. This study aims to determine whether there is any difference in the awareness of stem cell donation and transplantation between cancer and noncancer patients and their family caregivers. In addition, this study aims to determine the awareness of stem cell donation and transplantation in the entire study population.Methods:This descriptive study was conducted in Turkey using a data collection form comprising questions about demographics, stem cell transplantations, donations, and medical history. On analyzing the research data, variables were expressed as mean ± standard deviation and as numbers (n) and percentages (%). The Chi-square and Fisher's exact tests were performed to evaluate differences among cancer and noncancer diagnosed patients and their family members.Results:A total of 192 patients and 169 family caregivers participated in the study. In comparison with noncancer patients, cancer patients showed more awareness on what stem cell transplantation is, how lifesaving it is, and how to donate stem cells. Similarly, the family caregivers of cancer patients were more aware of what stem cell transplantation is and how to donate stem cells.Conclusions:The results of this study showed that cancer patients and their families were more aware of stem cell donation and transplantation; however, most of the patients and families did not know enough about the national registry program and how to donate stem cells.
Objective: The aim of this study was to explore the experiences of patients with myocardial infarction and their relatives. Methods: This qualitative and phenomenological study was conducted with 20 patients hospitalized due to the diagnosis of myocardial infarction and 15 relatives. A semi-structured interview form and data collection form including socio-demographic characteristics were used. The data of the study were collected using the in-depth individual interview method and were assessed using the phenomenological approach developed by Colaizzi. The researchers analyzed statements of the participants regarding their experiences and prepared categories and themes. Results: Three categories and seven themes emerged as a result of the data analysis. These categories included symptom experiences, views about death, transportation to health care facility. The statements of participants revealed that patients experienced various symptoms including sweating, chest pain, gastrointestinal system symptoms, shortness of breath, yellow and purple skin tone. It was also determined that they generally had a lack of knowledge about myocardial infarction symptoms, could not associate symptoms with myocardial infarction, attributed myocardial infarction to other matters, used various ineffective methods to cope with symptoms. The majority of the patients arrived at the health care facility by self-transport and some patients even drove themselves to the health care facility. Conclusion: Participants had a lack of knowledge about the symptoms of myocardial infarction and appropriate transport to the health care facility, for example, utilizing an ambulance. This, in turn, prolongs the period of prehospital delay that has an effect on the chance of survival and receiving an effective treatment.
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