scholarly journals Women with high level of education, victims of the care of people with Alzheimer's

2020 ◽  
Vol 19 (2) ◽  
pp. 390-420
Author(s):  
Patricia Luque-Carrillo ◽  
Ignacio Morales-Cané ◽  
Juan Manuel Carmona-Torres ◽  
Roberto Manfredini ◽  
Mª Aurora Rodríguez Borrego ◽  
...  

Objetivo: Conocer la relación existente entre la tarea de cuidar a pacientes con Enfermedad de Alzheimer, el Género de los cuidadores y su nivel de formación académica. Método: Estudio descriptivo, como sujetos de estudio 69 personas diagnosticadas de Enfermedad de Alzheimer y sus respectivos cuidadores familiares. En los cuidadores se analizó: la edad, el género, el nivel de estudios, carga, depresión, nivel de ansiedad, calidad de vida y soledad social. En los pacientes se valoró la edad, género, nivel de dependencia y estado neuropsicológico. La recogida de datos se realizó en 2016. Entre otros análisis se realizó análisis de regresión logística.Resultados: Se obtuvo que los cuidadores con estudios superiores sufrían mayor carga, siendo mujeres en su mayoría. Mujeres con más probabilidad de presentar soledad social, altos niveles de ansiedad y peor calidad de vida que los hombres. La carga puede ser debida al gran número de responsabilidades y a la imposibilidad de combinarlas con el papel de cuidador. Se puede concluir que las mujeres llegan a ser víctimas del cuidado de personas con Enfermedad de Alzheimer. The aim of this job is to know the existing relationship between the task of caring patients with Alzheimer's disease, caregivers' gender and their level of academic studies. Descriptive study, 69 persons diagnosed with Alzheimer’s disease and their respective familiar caregivers as subjects of the study. Age, gender, academic level, burden, depression, anxiety level, quality of life and social loneliness have been measured in caregivers. Age, gender, dependency level and neuropsychological state have been measured in patients. Data collection was done in 2016. Logistic regression analysis was performed. Caregivers with high levels of academic studies suffer more burden, being women in their majority. They are more likely to present social loneliness and higher levels of anxiety and a worse quality of life than men. The burden may be due to a greater number of responsibilities to respond to, and to the inability to combine it with the role of caregiver. We can conclude that women become victims of caring Alzheimer' patients.

2010 ◽  
Vol 18 (1) ◽  
pp. 26-32 ◽  
Author(s):  
Keika Inouye ◽  
Elisete Silva Pedrazzani ◽  
Sofia Cristina Iost Pavarini ◽  
Cristina Yoshie Toyoda

This paper aimed to compare the reports of patients and caregivers about how they perceive quality of life (QoL) in general and each of its dimensions in elderly with Alzheimer’s Disease (AD). The participants were elderly diagnosed with AD (n=53) attended by the Exceptional Medication Program in a city in the interior of Sao Paulo; and their respective family caregivers. The QoL measures were obtained through the Quality of Life Assessment Scale on Alzheimer’s Disease. The results showed statistically significant differences in the “memory” (p<0.05) and “you in general” (p<0.005) dimensions. Regarding the final score, the average in the patient’s version was 29.32 points (sd=6.27), against 28.33 points (sd=5.58) in the family version, p>0.100. Although the relative and patient reports were not identical, the results pointed to a high level of consistency among information.


2004 ◽  
Vol 9 (1) ◽  
Author(s):  
Pieter M Heyns ◽  
Michelle Viljoen ◽  
Dirk C Odendaal

This study addresses the role of psychofortigenic factors in maintaining quality of life in elderly people diagnosed with either rheumatoid arthritis or Alzheimer's disease. Opsomming Hierdie studie handel oor die rol wat psigofortigene faktore speel in die handhawing van lewenskwaliteit deur bejaardes wat gediagnoseer is met rumatoïede artritis of Alzheimer se siekte. *Please note: This is a reduced version of the abstract. Please refer to PDF for full text.


2019 ◽  
Vol 13 (3) ◽  
pp. 811
Author(s):  
Thâmara Bezerra De Souza ◽  
Nathália Patricia Almeida Santos ◽  
Joyci Larissa Sousa Móta ◽  
Melliny Vibelly Da Silva ◽  
Nathália França Da Silva ◽  
...  

RESUMOObjetivo: analisar a importância do papel da Enfermagem em relação a mulheres portadoras de endometriose acometidas por depressão. Métodos: trata-se um estudo bibliográfico, tipo revisão integrativa, com busca nas bases de dados LILACS, BDENF, MEDLINE e IBECS. Selecionaram-se artigos trilíngues na íntegra, no período de 2008 a setembro de 2018. Coletaram-se as informações a partir de um instrumento, apresentaram-se os resultados por meio de figuras e os discutiram com a literatura. Resultados: selecionaram-se oito artigos para análise. Mostrou-se a importância do papel do enfermeiro no enfrentamento da endometriose associada aos distúrbios de depressão. Sabe-se que a endometriose afeta a vida cotidiana das mulheres, dificultando as suas atividades diárias, as suas relações pessoais e interferindo na sua capacidade reprodutiva. Compromete-se, ainda mais, a qualidade de vida à medida que os sintomas se tornam mais graves. Conclusão: conclui-se que, para melhorar a qualidade de vida da mulher portadora de endometriose, o enfermeiro deve garantir o conhecimento e o empoderamento das mulheres para que o sofrimento seja amenizado. Descritores: Endometriose; Assistência de Enfermagem; Depressão, Enfermagem; Qualidade de Vida; Saúde da Mulher;ABSTRACTObjective: to analyze the importance of the role of nursing in relation to women with endometriosis affected by depression. Methods: this is a bibliographical study, type integrative, with search in the LILACS, BDENF, MEDLINE and IBECS databases. Trilingual articles were selected in full, from 2008 to September 2018. Information was collected from an instrument, the results were presented by figures and discussed with the literature. Results: eight papers were selected for analysis. The importance of the role of nurses in coping with endometriosis associated with disorders of depression has been shown. It is known that endometriosis affects the daily life of women, hindering their daily activities, their personal relationships and interfering in their reproductive capacity. It further compromises quality of life as symptoms become more severe. Conclusion: it is concluded that, in order to improve the quality of life of women with endometriosis, nurses must guarantee the knowledge and empowerment of women so that suffering is reduced. Descriptors: Endometriosis; Nursing Care; Depression, Nursing; Quality of life; Woman's Health.RESUMENObjetivo: analizar la importancia del papel de la enfermería en relación a mujeres portadoras de endometriosis acometidas por depresión. Métodos: se trata de un estudio bibliográfico, tipo revisión integrativa, con búsqueda en las bases de datos LILACS, BDENF, MEDLINE e IBECS. Se seleccionaron artículos trilingües en su totalidad, en el período de 2008 a septiembre de 2018. Se recogen las informaciones a partir de un instrumento, se presentaron los resultados por medio de figuras y los discutieron con la literatura. Resultados: se seleccionaron ocho artículos para análisis. Se mostró la importancia del papel del enfermero en el enfrentamiento de la endometriosis asociada a los disturbios de depresión. Se sabe que la endometriosis afecta la vida cotidiana de las mujeres, dificultando sus actividades diarias, sus relaciones personales e interfiriendo en su capacidad reproductiva. Se compromete, aún más, la calidad de vida a medida que los síntomas se vuelven más graves. Conclusión: se concluye que, para mejorar la calidad de vida de la mujer portadora de endometriosis, el enfermero debe garantizar el conocimiento y el empoderamiento de las mujeres para que el sufrimiento sea amenizado. Descriptores: Endometriosis; Asistencia de Enfermería; Depresión, Enfermería; Calidad de Vida; Salud de la Mujer.


Author(s):  
Rosa Herminia Pastuña Doicela

Introducción: En la actualidad un gran número de adultos mayores es vulnerable a enfermedades crónicas y otras afecciones como la enfermedad de Alzheimer, por lo que el cuidado de estas personas representa un desafío. Objetivo: Analizar la calidad de vida de los cuidadores de personas con la enfermedad de Alzheimer. Métodos: Se realizó una revisión integrativa de la literatura científica, con una pregunta de investigación con el PICO: ¿Cuál es la Calidad de Vida de los cuidadores de personas con enfermedad de Alzheimer?, posteriormente se inició la búsqueda de artículos científicos en las siguientes bases de datos: Pub Med; Wef of Science (WOS); Bvs; SciELO y Scopus. Utilizando los siguientes DeCS: “Quality of life”, “Caregivers” y “Alzheimer Disease”, identificados inicialmente 343 artículos, de los cuales 15 fueron elegibles y 7 fueron seleccionados porque cumplieron con los criterios de inclusión y exclusión. Resultados: El cuidado de la persona con enfermedad de Alzheimer recae mayormente en las familias. La mayor parte de cuidadoras/es son mujeres, el cuidado es integral, continuo, con desgaste físico y psicológico, estos factores afectan negativamente en su calidad de vida y compromete su salud. Conclusiones: La calidad de vida del cuidador de personas con enfermedad de Alzheimer se ve comprometida, debido al aparecimiento de afecciones físicas, psicológicas, sociales y económicas, derivadas por el desgaste y la sobrecarga. Palabras clave: calidad de vida; cuidadores; enfermedad de Alzheimer; Atención de Enfermería   ABSTRACT Introduction: The new demographic transition because of the phenomenon of globalization has generated improvements in health care. Despite this, today a large number of older adults are vulnerable to chronic diseases and other conditions such as Alzheimer's disease, so caring for these people represents a challenge for their caregivers. Objective: Analyze the quality of life of caregivers of people with Alzheimer's disease. Methods: An integrative review of the scientific literature was carried out, for the formulation of the research question, the PICO format was used: What is the Quality of Life of caregivers of people with Alzheimer's disease? Subsequently, the search for scientific articles was started in the following databases: Pub Med; Wef of Science (WOS); Bvs; SciELO and Scopus. Using the following DeCS: "Quality of life", "Caregivers" and "Alzheimer Disease", associated with the Boolean operator "AND". 343 articles were initially identified, of which 15 were eligible and 7 were selected because they met the inclusion and exclusion criteria. Results: The care of the person with Alzheimer's disease falls mostly in families. The majority of caregivers are women, the care is integral, continuous, with physical and psychological wear, and these factors negatively affect their quality of life and compromise their health. Conclusions: The quality of life of the caregiver of people with Alzheimer's disease is compromised, due to the appearance of physical, psychological, social and economic conditions, derived from wear and tear and overload. Therefore, making the needs and problems derived from their visible role can contribute significantly to the development of comprehensive care interventions in this vulnerable population   Keywords: quality of life; caregivers; Alzheimer disease; Nursing care


2010 ◽  
Vol 51 (02) ◽  
pp. 72 ◽  
Author(s):  
Oscar Rosas Carrasco ◽  
Laura del Pilar Torres Arreola ◽  
María de Guadalupe Guerra Silla ◽  
Sara Torres Castro ◽  
Luis Miguel Gutiérrez Robledo

2019 ◽  
Vol 10 (3) ◽  
Author(s):  
Larissa Giovanna Cazella ◽  
Letícia Yamawaka De Almeida ◽  
Jaqueline Lemos De Oliveira ◽  
Ana Carolina Guidorizzi Zanetti ◽  
Jacqueline De Souza

Objetivo: analisar as características sociodemográficas associadas à percepção da qualidade de vida de mulheres atendidas na atenção primária. Metodologia: estudo transversal, quantitativo, desenvolvido com 113 mulheres em uma unidade de saúde do interior de São Paulo. Utilizou-se um questionário sociodemográfico e a versão abreviada do instrumento de avaliação de qualidade de vida. Para análise dos dados, foram empreendidos testes de associação. Resultados: a maioria das participantes era de classes sociais menos favorecidas e apresentava boa percepção de qualidade de vida e saúde. Os fatores renda, escolaridade e idade foram os mais relevantes na associação com a qualidade de vida. Conclusão: Apesar de mencionarem boa qualidade de vida e saúde, foram identificados piores resultados nos domínios físicos, psicológicos e meio ambiente.  Os achados reforçam a necessidade de que as ações de saúde estejam contextualizadas aos aspectos sociais/territoriais e vinculadas a políticas mais amplas de redução da vulnerabilidade social. WOMEN'S QUALITY OF LIFE AND ASSOCIATED SOCIO DEMOGRAPHIC CHARACTERISTICSObjective: to analyze the sociodemographic characteristics associated to the perception of the quality of life of the women attended in the Primary Health Care. Methodology: this cross-sectional quantitative study was carried out with 113 women aged 20 to 65 years in a health unit in the interior of São Paulo. A sociodemographic questionnaire and the abbreviated version of the WHOQOL-bref quality of life assessment instrument were used. For data analysis, association tests were undertaken. Results: the majority of participants were from less favored social classes and had a good perception of quality of life and health. The factors income, schooling and age were the most relevant in the association with quality of life. Conclusion: in view of the sociodemographic characteristics associated with quality of life in the present study, it is emphasized that health actions should be linked to broader policies to reduce social vulnerability, enabling empowerment strategies and, above all, increasing women's access to education and income.Descriptors: Quality of Life; Health Centers; Social Vulnerability; Women; Primary Health Care.CALIDAD DE VIDA DE LAS MUJERES Y LAS CARACTERÍSTICAS SOCIODEMOGRÁFICAS ASSOCIADASObjetivo: analizar las características sociodemográficas asociadas a la percepción de la calidad de vida de mujeres que acuden a atención primaria. Métodos: este estudio cuantitativo transversal se realizó con 113 mujeres de 20 a 65 años en una unidad de salud en el interior de São Paulo. Se utilizó un cuestionario sociodemográfico y la versión abreviada del instrumento de evaluación de calidad de vida WHOQOL-bref. Para el análisis de los datos, se realizaron pruebas de asociación. Resultados: la mayoría de los participantes provenían de clases sociales más bajas y tenían una buena percepción de la calidad de vida y la salud. Los factores ingresos, educación y edad fueron los más relevantes en asociación con la calidad de vida. Conclusión: en vista de las características sociodemográficas asociadas con la calidad de vida en el presente estudio, se enfatiza que las acciones de salud están vinculadas a políticas más amplias para reducir la vulnerabilidad social, permitiendo estrategias de empoderamiento y, sobre todo, aumentando el acceso de las mujeres a educación e ingresos.Descriptores: Calidad de Vida; Centros de Salud; Vulnerabilidad Social; Mujeres; Atención Primaria de Salud.


2015 ◽  
Vol 12 (4) ◽  
pp. 427-437 ◽  
Author(s):  
Sandrine Andrieu ◽  
Nicola Coley ◽  
Yves Rolland ◽  
Christelle Cantet ◽  
Catherine Arnaud ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document