No description available.

No description available.

Submitted by Rosina Valeria Lanzellotti Mattiussi Teixeira (rosina.teixeira@unisantos.br) on 2017-03-20T19:58:07Z No. of bitstreams: 1 Thais Laudares Soares Maia.pdf: 2383778 bytes, checksum: 63872173da6a935884954d9df67bf090 (MD5) / Made available in DSpace on 2017-03-20T19:58:07Z (GMT). No. of bitstreams: 1 Thais Laudares Soares Maia.pdf: 2383778 bytes, checksum: 63872173da6a935884954d9df67bf090 (MD5) Previous issue date: 2017-02-21 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / Cancer is a serious public health problem. The World Health Organization (WHO) considers in 27 million new cases of cancer by the year 2030 in the whole world. In Brazil, the frequent diagnose of cancer in advanced phase results in a delay of treatment and invalidate possibilities of cure. Nowadays, the Unique Health System (UHS) advocates to the patients with cancer, without possibilities of cure, the approach in palliative cares that is still recent, limited and little consolidated in health services. The study had as objective to analyse the strategies of confrontation and meanings of cancer without possibility of cure in users of outpatient oncology service from UHS. It was done a qualitative study with semi-structured interviews with 11 participants of both sexes, age from 18 years old and diagnosed with cancer without possibilities of cure. The results were analysed in the following reaction categories: 1) sadness and hope; 2) process of sickness; 3) ¿I don¿t want these words¿; 4) non-clinical context; 5) God¿s will; 6) family comfort; 7) sickness and losses; 8) organic and existential pain; 9) psychosocial aspects of sickness; and 10) eminence of death in health services. One identified the need of reflecting about the relational aspects and cares that envolve the patients without possibilities of cure, considering the advance of medicine and of technology and on the other hand, the need to rescue the human relation aspects between health professionals and patients. / O câncer é um grave problema de saúde pública. A Organização Mundial da Saúde (OMS) estima em 27 milhões de novos casos de câncer para o ano de 2030 em todo o mundo. No Brasil, o frequente diagnóstico de câncer em fase avançada resulta no atraso do tratamento e inviabiliza as possibilidades de cura. Atualmente, o Sistema Único de Saúde (SUS) preconiza aos pacientes com câncer, sem possibilidades de cura, a abordagem em cuidados paliativos, que ainda é recente, restrita e pouco consolidada nos serviços de saúde. O estudo teve como objetivo analisar as estratégias de enfrentamento e significados do câncer sem possibilidade de cura em usuários de um serviço ambulatorial de oncologia do SUS. Foi realizado estudo qualitativo com entrevistas semiestruturadas com 11 participantes de ambos os sexos, idade a partir de 18 anos e diagnosticados com câncer sem possibilidades de cura. Os resultados foram analisados nas seguintes categorias empíricas: 1) Tristeza e esperança; 2) processo de adoecimento; 3) ¿eu não quero essas palavras¿; 4) contexto não clínico; 5) vontade divina; 6) o conforto da família; 7) adoecimento e perdas; 8) dor orgânica e existencial; 9) aspectos psicossociais do adoecimento; e 10) a eminência da morte nos serviços de saúde. Identificou-se a necessidade de refletir sobre os aspectos relacionais e de cuidados que envolvem os pacientes sem possibilidades de cura, considerando o avanço da medicina e da tecnologia e, por outro lado, o necessário resgate aos aspectos humanísticos da relação entre profissionais de saúde e os pacientes.

This work is engaged in theme of orphan's agenda and care for orphans in region Prácheň in 18th century. First part this work is engaged in law limitation of orphan's position and insurance orphan's and guardian's charge in law codices. This part represents evolution of law position from Roman period until law codification of Pavel Kristian from Koldín. One of important factor for orphan's life was guardian, therefore is in this part also limitation for guardian's charge. Second part of work is engaged in position of orphans in Czech towns in 18th century. Work is in next chapters engaged in towns that were in property of family Schwarzenberg. In this chapter are this town introduce. In this part of work are further manners of leading of orphan's agenda and his regulating, then how intervened suzerain in leading of orphan's agenda. Also this chapter describe instruction for leading of orphan's agenda in manor Netolice, what is preserved in State regional archives in Třeboň. Fundamental chapters are engaged in orphan's agenda in a several towns in region Prácheň. This chapter above all engage in three kinds of orphan's agenda, then orphan's books, orphan's accounts and confronting of orphans. Orphan's books are introduced from towns Lhenice, Netolice, Volary and Bavorov. Orphan's accounts are introduced from towns Lhenice, Netolice, Volary and Záblatí and confrontig of orphans are introduced from towns Lhenice, Netolice and Volary. All kinds of orphan's agenda are presented in their formal aspect and also in contents aspect. Here is put down evolution of orphan's agenda and changes in their leading. All work goes out from wells, which are deposited in State district archives in Prachatice, State district archives in Strakonice and also in State regional archives in Třeboň. In Prachatice and Strakonice are depositing all kinds of orphan's agenda and this is important for comparing their method of leading.

The hospice volunteer is viewed as an integral member of a multidisciplinary team, with various roles directed at enhancing the quality of life of patients and their families. The purpose of this study is to provide an integrated picture of the hospice volunteer, their role, the human dimensions of this role and the impact this has on their lives as not much has been written in literature about this specific sub-group of hospice workers. The context of the study is a hospice in Gauteng where the researcher works as a volunteer. The ethnographic case study has been chosen as an appropriate research design as it explores the above phenomenon from the volunteers' point of view. The subjects are three volunteers who have been active at the hospice for at least twelve months. Evidence in terms of specific interviews and observations are used to draw conclusions. The interviews are based on a minimal number of open-ended questions. The primary method of analysis is the examination of transcripts from these in-depth interviews. A thematic analysis is carried out in which a detailed description of the emerging themes are given. Four major themes are identified and explored: Description of the role; The experience of being a volunteer; A way of coping; and The influence of the hospice culture. Sub-themes that emerge within each case study vary due to the individual nature of the experience of the role. Themes are explored in light of current theory and findings. This was to note the similarities and differences of this specific sub-group of volunteers compared to others found in the literature reviewed for this study. As there is a scarcity of literature pertaining specifically to hospice volunteers, the study depends mostly on writings pertaining to hospice staff and volunteers in general. A summary and integration of the core findings of the three case studies is given and their similarities and differences are explored. How some of the different themes interlink is also discussed. Although various sub-themes found in the individual case studies are significant to the individual cases, some of them can be incorporated into common themes when looking at the volunteers as a group. The strengths and limitations of the study are discussed as well as recommendations for the hospice organisation and further research. / Psychology / M.A. (Psychology)

The hospice volunteer is viewed as an integral member of a multidisciplinary team, with various roles directed at enhancing the quality of life of patients and their families. The purpose of this study is to provide an integrated picture of the hospice volunteer, their role, the human dimensions of this role and the impact this has on their lives as not much has been written in literature about this specific sub-group of hospice workers. The context of the study is a hospice in Gauteng where the researcher works as a volunteer. The ethnographic case study has been chosen as an appropriate research design as it explores the above phenomenon from the volunteers' point of view. The subjects are three volunteers who have been active at the hospice for at least twelve months. Evidence in terms of specific interviews and observations are used to draw conclusions. The interviews are based on a minimal number of open-ended questions. The primary method of analysis is the examination of transcripts from these in-depth interviews. A thematic analysis is carried out in which a detailed description of the emerging themes are given. Four major themes are identified and explored: Description of the role; The experience of being a volunteer; A way of coping; and The influence of the hospice culture. Sub-themes that emerge within each case study vary due to the individual nature of the experience of the role. Themes are explored in light of current theory and findings. This was to note the similarities and differences of this specific sub-group of volunteers compared to others found in the literature reviewed for this study. As there is a scarcity of literature pertaining specifically to hospice volunteers, the study depends mostly on writings pertaining to hospice staff and volunteers in general. A summary and integration of the core findings of the three case studies is given and their similarities and differences are explored. How some of the different themes interlink is also discussed. Although various sub-themes found in the individual case studies are significant to the individual cases, some of them can be incorporated into common themes when looking at the volunteers as a group. The strengths and limitations of the study are discussed as well as recommendations for the hospice organisation and further research. / Psychology / M.A. (Psychology)