scholarly journals Lived experiences and quality of life after gynaecological cancer—An integrative review

2019 ◽  
Vol 28 (9-10) ◽  
pp. 1393-1421 ◽  
Author(s):  
Ragnhild Johanne Tveit Sekse ◽  
Gail Dunberger ◽  
Mette Linnet Olesen ◽  
Maria Østerbye ◽  
Lene Seibæk
Geriatrics ◽  
2021 ◽  
Vol 6 (2) ◽  
pp. 60
Author(s):  
Kimberley Wilson ◽  
Arne Stinchcombe ◽  
Sophie M. Regalado

Canada has a unique socio-political history concerning the inclusion of lesbian, gay, bisexual, transgender, and queer (LGBTQ+) people. With aging populations, understanding diverse groups of older adults is paramount. We completed a systematic search and scoping review of research in Canada to quantify and articulate the scale and scope of research on LGBTQ+ aging. Our search identified over 4000 results and, after screening for relevance, our review focused on 70 articles. Five major themes in the literature on LGBTQ+ aging in Canada were identified: (1) risk, (2) HIV, (3) stigma, and discrimination as barriers to care, (4) navigating care and identity, (5) documenting the history and changing policy landscapes. Most of the articles were not focused on the aging, yet the findings are relevant when considering the lived experiences of current older adults within LGBTQ+ communities. Advancing the evidence on LGBTQ+ aging involves improving the quality of life and aging experiences for LGBTQ+ older adults through research.


2021 ◽  
Vol 26 (1) ◽  
pp. 58-62
Author(s):  
Jan Sunman

Purpose The purpose of this paper is to provide a commentary on the article by Rachel Forrester-Jones on the experiences of older carers of people with learning disabilities. Design/methodology/approach The commentary reflects on the themes identified in the original article, comparing its findings to the lived experiences of those taking part in older carers’ projects in Oxfordshire, England. Findings Similar broad themes were identified in both samples. Given these findings, the extent to which matters have changed, since the Valuing People work on older carers is considered. Originality/value The paper discusses policy and practice implications to improve the quality of life of older carers and their families and explores how the voice of older carers can be strengthened to enable them to shape practice and policy.


2017 ◽  
Vol 6 (3) ◽  
pp. 72
Author(s):  
Márcia Teles De Oliveira Gouveia ◽  
Hidelkarla Sales De Santana ◽  
Ana Maria Ribeiro Dos Santos ◽  
Girlene Ribeiro Da Costa ◽  
Márcia Astrês Fernandes

Objetivo: realizar busca de publicações científicas nas bases de dados sobre a qualidade de vida e o bem-estar do estudante universitário de enfermagem; descrever e analisar as perspectivas enfocadas na literatura. Metodologia: Revisão Integrativa da Literatura. Foram selecionados vinte e três estudos publicados entre 2010 e 2014, nas bases de dados Literatura Latino Americana e do Caribe de Informação em Ciências da Saúde, Medical Literature Analysis and Retrieval Sistem on-line e o Cumulative Index to Nursing and Allied Health Literature nos idiomas português, inglês e espanhol. Resultados: Observou-se que a qualidade de vida e o bem-estar encontram-se moderadamente bem na avaliação dos estudantes de enfermagem avaliados nos estudos, e que apesar dos estressores decorrentes do curso, os estudantes resolvem as situações estressantes com algumas técnicas de relaxamento e enfrentamento, mas também recorrendo ao uso de álcool e fumo. Os instrumentos utilizados nos estudos: WHOQOL-BREF, Inventário de Depressão de Beck e a Escala de Estresse Percebido. Conclusão: identificadas depressão, insônia, estresse e cansaço, decorrentes da vida acadêmica. Desse modo, importante às instituições e docentes estarem atentos para reconhecer precocemente os indicativos multidimensionais que afetam a qualidade de vida e o bem-estar dos seus estudantes, e implementar medidas preventivas.


2017 ◽  
Vol 18 (1) ◽  
pp. 186-202
Author(s):  
Lívia Cristina de Resende Izidoro ◽  
Tamires de Castro Vieira ◽  
Lizete Malagoni de Almeida Cavalcante Oliveira ◽  
Anamaria Alves Napoleão

2018 ◽  
Vol 12 (5) ◽  
pp. 1648-1664 ◽  
Author(s):  
Sabrina L. Dickey ◽  
Motolani E. Ogunsanya

The purpose of this integrative review was to explore the impact of prostate cancer (PCa) on the quality of life (QoL) and factors that contribute to the QoL for Black men with PCa. Prostate is recognized as the prevalent cancer among men in the United States. Compared to other men, Black men are diagnosed more frequently and with more advanced stages of PCa. Black men also experience disproportionately higher morbidity and mortality rates of PCa, among all racial and ethnic groups. The initial diagnosis of PCa is often associated with a barrage of concerns for one’s well-being including one’s QoL. As a result, men must contend with various psychosocial and physiological symptoms of PCa survivorship. Whittemore and Knafl’s integrative review method was utilized to examine empirical articles from the electronic databases of the Cumulative Index to Nursing and Allied Health Literature (CINAHL), PsycINFO, PubMed, Project Muse, and Google Scholar. The time frame for the literature was January 2005 to December 2016. A synthesis of the literature yielded 18 studies that met the inclusion criteria for the integrative review. A conceptual framework that examined QoL among cancer survivors identified four domains that measured the QoL among Black PCa survivors: (a) physical; (b) psychological; (c) social; and (d) spiritual well-being. Social well-being was the dominant factor among the studies in the review, followed by physical, psychological, and spiritual. Results indicate the need for additional studies that examine the factors impacting the QoL among Black PCa survivors, using a theoretical framework so as to develop culturally appropriate interventions for Black PCa survivors.


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