scholarly journals Depressão e qualidade de vida em pacientes no pré e pós-transplante renal

2018 ◽  
Vol 12 (1) ◽  
pp. 203
Author(s):  
Patrícia Madruga Rêgo Barros ◽  
Ednaldo Cavalcante de Araújo ◽  
Luciane Soares de Lima

RESUMOObjetivo: analisar a ocorrência de depressão e a qualidade de vida em pacientes renais no pré e pós-transplante. Método: estudo quantitativo, descritivo, exploratório, de coorte transversal. Foram aplicados três instrumentos para a coleta de dados: um questionário para caracterização da amostra, o inventário Beck de depressão (BDI) e o questionário SF-36, para avaliação da qualidade de vida. A amostra foi composta por dois grupos, um de pacientes no pré-transplante renal (59 pacientes) e o outro de transplantados renais (63 pacientes), totalizando 122 pacientes. Resultados: a maioria dos pacientes, em ambos os grupos, não apresentava depressão, correspondendo a 88,9% dos transplantados e 79.6% de pacientes no pré-transplante. A qualidade de vida mostrou-se superior nos pacientes transplantados em relação aos que aguardavam o procedimento. Os domínios do questionário SF-36 que determinaram a melhor qualidade de vida nos pacientes transplantados foram capacidade funcional (p = 0,001), dor (p = 0,027), estado geral de saúde (p = 0,049) e vitalidade (p = 0,000). Conclusão: esse estudo mostrou uma baixa ocorrência de depressão nos pacientes tanto no pré, como no pós-transplante renal. A qualidade de vida mostrou-se superior no grupo de transplantados. Descritores: Depressão, Qualidade De Vida; Transplante de Órgãos; Doença Crônica.ABSTRACTObjective: to analyze the occurrence of depression and quality of life in renal patients before and after transplantation. Method: quantitative, descriptive, exploratory, cross-sectional study. Three instruments were used to collect data: a questionnaire for characterization of the sample, the Beck depression inventory  (BDI) and the SF-36 questionnaire, to evaluate the quality of life. The sample consisted of two groups: one in pre-transplant patients (59 patients) and the other in renal transplant patients (63 patients), totaling 122 patients. Results: the majority of patients, in both groups, did not present depression, corresponding to 88.9% of the transplanted patients and 79.6% of the pre-transplant patients. Quality of life was higher in transplant patients than in those awaiting the procedure. The SF-36 domains that determined the best quality of life in the transplanted patients were functional capacity (p = 0.001), pain (p = 0.027), general health status (p = 0.049) and vitality (p = 0.000). Conclusion: this study showed a low occurrence of depression in patients both in the pre- and post-renal transplantation. Quality of life was higher in the transplant group. Descriptors: Depression, Quality of Life; Organ Transplantation; Chronic Disease.RESUMENObjetivo: analizar la ocurrencia de depresión y la calidad de vida en pacientes renales en el pre y post-trasplante. Método: estudio cuantitativo, descriptivo, exploratorio, de cohorte transversal. Se aplicaron tres instrumentos para la recolección de datos: un cuestionario para la caracterización de la muestra, el inventario Beck de depresión (BDI) y el cuestionario SF-36, para la evaluación de la calidad de vida. La muestra fue compuesta por dos grupos, uno de pacientes en el pre-trasplante renal (59 pacientes) y el otro de trasplantados renales (63 pacientes), totalizando 122 pacientes. Resultados: la mayoría de los pacientes, en ambos grupos, no presentaba depresión, correspondiendo al 88,9% de los trasplantados y el 79.6% de pacientes en el pre-trasplante. La calidad de vida se mostró superior en los pacientes trasplantados en relación a los que esperaban el procedimiento. Los dominios del cuestionario SF-36 que determinaron la mejor calidad de vida en los pacientes trasplantados fueron capacidad funcional (p = 0,001), dolor (p = 0,027), estado general de salud (p = 0,049) y vitalidad (p = 0,000). Conclusión: este estudio mostró una baja ocurrencia de depresión en los pacientes tanto en el pre, como en el post-trasplante renal. La calidad de vida se mostró superior en el grupo de trasplantados. Descriptores: Depresión, Calidad de Vida; Trasplante de órganos; Enfermedad Crónica.

2020 ◽  
Vol 14 ◽  
Author(s):  
Débora Cristina Martins ◽  
Beatriz Maria dos Santos Santiago Ribeiro ◽  
Giovanna Brichi Pesce ◽  
Giordana Maronezzi da Silva ◽  
André Soares da Silva ◽  
...  

Objetivo: analisar a qualidade de vida e identificar doenças autorreferidas em mulheres de apenados. Método: trata-se de um estudo quantitativo, descritivo, transversal, com 349 mulheres de apenados em três penitenciárias. Coletaram-se os dados por meio de dois instrumentos. Analisaram-se as informações por meio da estatística descritiva e regressão linear múltipla. Resultados: consideraram-se inadequados os fatores relativos à qualidade de vida, sendo eles físico (42,1%), psicológico (21,2%), relações sociais (49%), meio ambiente (59%) e geral (53,3%). Constatou-se que a qualidade de vida inadequada se manteve associada a outras doenças (34,7%; p<0,054). Conclusão: torna-se necessário investir em ações estratégicas de promoção da saúde nesta população, pois ela é considerada vulnerável, com predisposição a doenças devido a comportamentos de risco e à qualidade de vida inadequada. Descritores: Saúde da Mulher; Qualidade de Vida; Doença; Populações Vulneráveis; Cuidados de Enfermagem; Fatores de Risco.AbstractObjective: to analyze the quality of life and identify self-reported diseases in women inmates. Method: this is a quantitative, descriptive, cross-sectional study with 349 women inmates in three prisons. Data was collected by two instruments. Information was analyzed using descriptive statistics and multiple linear regressions. Results: the factors related to quality of life were inadequate, being physical (42.1%), psychological (21.2%), social relations (49%), environment (59%) and general (53, 3%). Inadequate quality of life was found to be associated with other diseases (34.7%; p <0.054). Conclusion: it is necessary to invest in strategic health promotion actions in this population, as it is considered vulnerable, with a predisposition to disease due to risky behaviors and inadequate quality of life. Descriptors: Women's Health; Quality of life; Disease; Vulnerable Populations; Nursing Care; Risk Factors.ResumenObjetivo: analizar la calidad de vida e identificar enfermedades autoinformadas en mujeres de encarcelados. Método: este es un estudio cuantitativo, descriptivo, transversal, con 349 mujeres de encarcelados en tres cárceles. Los datos fueron recolectados por dos instrumentos. Las informaciones se analizaron mediante estadística descriptiva y regresión lineal múltiple. Resultados: los factores relacionados con la calidad de vida fueron inadecuados, siendo físicos (42.1%), psicológicos (21.2%), relaciones sociales (49%), ambiente (59%) y generales (53, 3%). Se comprobó que la calidad de vida inadecuada estaba asociada con otras enfermedades (34.7%; p <0.054). Conclusión: es necesario invertir en acciones estratégicas de promoción de la salud en esta población, ya que se considera vulnerable, con una predisposición a la enfermedad debido a conductas de riesgo y calidad de vida inadecuada. Descriptores: Salud de la Mujer; Calidad de Vida; Enfermedad; Poblaciones Vulnerables; Cuidados de Enfermería; Factores de Riesgo.


2021 ◽  
Vol 26 (1) ◽  
Author(s):  
Prachita P. Walankar ◽  
Vrushali P. Panhale ◽  
Kanchi M. Vyas

Abstract Background Functional ankle instability is a common musculoskeletal condition affecting the community. It is characterized by repetitive bouts of giving away, recurrent sprains, and sensation of instability leading to functional deficits in an individual. The present study aimed to assess the influence of kinesiophobia on physical function and quality of life in participants with functional ankle instability. A cross-sectional study was conducted in 30 participants with functional ankle instability. Kinesiophobia was assessed using the 17-item Tampa Scale of Kinesiophobia, physical function using the Foot and Ankle Ability Measure (FAAM) and the FAAM-Sport version (FAAM-S), and quality of life using SF-36. Results The TSK score showed a moderate negative correlation with FAAM-S (r = −0.5, p = 0.005) and a weak negative correlation with SF-36 physical component summary (r = −0.42, p = 0.02). However, TSK showed no significant correlation with FAAM-ADL and SF-36 mental component summary. Conclusion Increased fear of movement, reduced physical function, and health-related quality of life were observed in functional ankle instability individuals. Hence, evaluation of these parameters is imperative in these individuals.


2008 ◽  
Vol 126 (5) ◽  
pp. 252-256 ◽  
Author(s):  
Maristela Bohlke ◽  
Diego Leite Nunes ◽  
Stela Scaglioni Marini ◽  
Cleison Kitamura ◽  
Marcia Andrade ◽  
...  

CONTEXT AND OBJECTIVE: Quality of life (QoL) is considered important as an outcome measurement, especially for long-term diseases such as chronic renal failure. The present study searched for predictors of QoL in a sample of patients undergoing dialysis in southern Brazil. DESIGN AND SETTING: This was a cross-sectional study developed in three southern Brazilian dialysis facilities. METHODS: Health-related QoL of patients on hemodialysis or peritoneal dialysis was measured using the generic Short Form-36 (SF-36) health survey questionnaire. The results were correlated with sociodemographic, clinical and laboratory variables. The analysis was adjusted through multiple linear regression. RESULTS: A total of 140 patients were assessed: 94 on hemodialysis and 46 on peritoneal dialysis. The mean age was 54.2 ± 15.4 years, 48% were men and 76% were white. The predictors of higher (better) physical component summary in SF-36 were: younger age (β-0.16; 95% confidence interval, CI: -0.27 to -0.05), shorter time on dialysis (β-0.06; 95% CI: -0.09 to -0.02) and lower Khan comorbidity-age index (β 5.16; 95% CI: 1.7-8.6). The predictors of higher mental component summary were: being employed (β 8.4; 95% CI: 1.7-15.1), being married or having a marriage-like relationship (β 4.56; 95% CI: 0.9-8.2), being on peritoneal dialysis (β 4.9; 95% CI: 0.9-8.8) and not having high blood pressure (β 3.9; 95% CI: 0.3-7.6). CONCLUSIONS: Age, comorbidity and length of time on dialysis were the main predictors of physical QoL, whereas socioeconomic issues especially determined mental QoL.


2019 ◽  
Vol 13 ◽  
Author(s):  
Rafael Lemes de Aquino ◽  
Douglas Ataniel Alves Xavier ◽  
Meirielen Danubia Marra ◽  
Nubia Fernandes Fernandes Teixeira ◽  
Lorena Silva Vargas ◽  
...  

RESUMO Objetivos: avaliar a qualidade de vida de acadêmicos regularmente ativos em uma universidade; verificar se existe associação entre qualidade de vida e sintomas depressivos. Método: trata-se de estudo quantitativo, tipo transversal, aplicar-se-ão três questionários estruturados, autoaplicáveis para mensurar o nível da qualidade de vida e índice de depressão entre acadêmicos. Far-se-á a análise estatística descritiva, empregar-se-á o teste Liliefors e usar-se-ão o teste t de Student. Apresentar-se-ão os resultados em forma de figuras. Resultados esperados: realizar-se-á a correlação entre a qualidade de vida dos estudantes dos cursos de graduação da universidade e a incidência de fatores depressivos com o início da vida acadêmica. Descritores: Depressão; Vida Acadêmica; Qualidade de Vida; Universidade; Estudantes; Educação Superior.ABSTRACT Objectives: to evaluate the quality of life of academically active students in a university; to verify if there is an association between quality of life and depressive symptoms. Method: this is a quantitative cross-sectional study. Three structured, self-administered questionnaires will be applied to measure the level of quality of life and depression index among academics. The descriptive statistical analysis will be done, the Liliefors test will be used and the Student's t-test will be used. The results will be presented in the form of figures. Expected results: the correlation between the quality of life of undergraduate students of the university and the incidence of depressive factors with the beginning of academic life will be realized. Descriptors: Depression; Academic life; Quality of Life; Universities; Students; Education, Higher.RESUMEN Objetivos: evaluar la calidad de vida de los académicos regularmente activos en una universidad; comprobar si existe asociación entre calidad de vida y síntomas depresivos. Método: se trata de estudio cuantitativo, tipo transversal, se aplicarán tres cuestionarios estructurados, autoaplicables para medir el nivel de la calidad de vida e índice de depresión entre académicos. Se hará el análisis estadístico descriptivo, se empleará la prueba Liliefors y se utilizarán la prueba t de Student. Se presentarán los resultados en forma de figuras. Resultados esperados: se realizará la correlación entre la calidad de vida de los estudiantes de los cursos de grado de la universidad y la incidencia de factores depresivos con el inicio de la vida académica. Descriptores: Depresión; Vida académica; Calidad de Vida; Universidades; Estudiantes; Educación Superior.


2021 ◽  
Author(s):  
Geohana Hamoy-Jimenez ◽  
Hadiya Elahmar ◽  
Meg Mendoza ◽  
Raymond Kim ◽  
Vera Bril ◽  
...  

Abstract Background. There is limited data regarding gender differences in quality of life between women and men with Neurofibromatosis type 1. We aimed to study differences in quality of life domains between women and men with Neurofibromatosis type 1 living in Canada.Methods: This is a cross sectional study of adults with Neurofibromatosis type 1 attending a tertiary NF centre at Toronto General Hospital between January 2016 to December 2017. Demographic and clinical data were collected. We compared scores of generic measures (SF-36, EQ-5D-5L, pain interference) and a disease-specific measure (PedsQL-NF1 module) between women and men. We also assessed the relationship between disease visibility scored by an examiner (Ablon’s visibility index) and self-reported perceived physical appearance, stratified by gender.Results. One hundred and sixty-two participants were enrolled, 92 females and 70 males. Ablon’s index score 1 was in 43% and score 2 in 44%, while only 13% of patients had a score 3. Women had worse scores on the total PedsQL-NF1 scales, and also in the perceived physical appearance, anxiety and emotional health domains. In women, there was a significant association between Ablon’s index and perceived physical appearance, with lower scores with increments in Ablon’s class (ANOVA p<0.001). In men, there was no difference in self-reported physical appearance by Ablon’s index. There were no differences between men and women in the SF-36 or EQ-5D-5L scores.Conclusion. Women with NF1 reported worse NF1-related quality of life than men, with worse perceived physical appearance, anxiety, and mental health. Perceived physical appearance did not always correlate to disease visibility; therefore, healthcare providers should inquire about body image, physical appearance concerns, and mental health, especially among women with NF1.


2021 ◽  
Vol 15 (11) ◽  
pp. 3087-3089
Author(s):  
Rashida Jabeen ◽  
Kousar Perveen ◽  
Muhammad Afzal ◽  
Sadia Khan

Kidney transplantation is the famous and most important choice of treatment of renal replacement therapies (RRTs) because of its positive impact on morbidity, survival and cost. The health related quality of life is becoming important outcome. Quality of life is usually impaired in patients who have renal transplant because of renal transplant patients have anxiety, lack of social, physical and emotional support and diminished ability to take care of themselves. The basic purpose of renal transplantation is to achieve maximum quality of life with minimum side effects. Methods: A cross sectional study was conducted at Rukhsana Akhtar Bahria International Orchard Hospital Lahore after approval from institution board of university of Lahore. 36 patients were enrolled in study by using purposive sampling technique. After taking informed consent all Kidney transplant patients aged between 18 years to 60 years, visited the post-transplantation OPD and continuously in follow-up sessions were included in study. A validated and standard WHO questionnaire of “Kidney Disease and Quality of Life (KDQOL-36™)” was used for data collection. Data was entered and analyzed in SPSS version.21.Chi-square test was applied to find out significant association between qualitative variables. P -Value < 0.05will be considered as statistically significant. Results: Majority of patients were from 40-49 years 10(27.0%). Females were more as compared to men (20(55.6) vs 16(44.4%)). 10(27.8) patients can read and write and 8(22.2%) have done matriculation. More patients live in Urban area as compared to rural area(19(52.8%) vs 17(47.2%)).8(22.2%) patients have less than 1 year of post kidney transplantation time and 19(52.8%) have 1 to 3 years. All the seven domains of KDQOL show poor QOL. General Health, Physical function and physical and emotional function shows average QOL and Emotional, social, daily activities and overall KDQOL shows poor QOL. There was insignificant association with age, gender, education; residential area and Post kidney transplantation length of time (years)(p-value > 0.05). Conclusions: After renal transplantation HRQOL becomes very important factor. After kidney transplantation HRQOL depends on many factors. It was concluded from current study that the HRQOL was not as good as it should be. Over the period of transplantation time patient’s quality of life remain same. The society, government, family, and medical staff need to support patients so they can also improve their QOL. Key word: Renal Diseases, Kidney transplant, Quality of life, KDQOL-36


Author(s):  
Daniela Angerame Yela ◽  
Iuri de Paula Quagliato ◽  
Cristina Laguna Benetti-Pinto

Abstract Objective To describe clinical and sociodemographic characteristics of women with deep infiltrating endometriosis (DIE) and assess their quality of life (QOL) during 6 months of medical treatment. Methods A descriptive cross-sectional study of 60 women diagnosed with DIE either by surgery or image methods (ultrasound or magnetic resonance), who received clinical treatment for at least 6 months in the Universidade de Campinas, Campinas, state of São Paulo, Brazil. Both the SF-36 and the EHP-30 questionnaires were used to assess the quality of life. Results The mean age of the patients was 37.7 ± 6.0 years old, with 50% presenting dysmenorrhea; 57% dyspareunia; and 50% chronic pelvic pain. The SF-36 and the EHP-30 revealed impaired quality of life. In the SF-36, the worst domains were limitation due to emotional aspects (40.2 ± 43.1) and self-esteem and disposition (46.1 ± 24.8), whereas in the EHP-30 they were social well-being (50.3 ± 30.6); infertility (48.0 ± 36.3); and sexual intercourse (54.0 ± 32.1). Conclusion Although clinically treated, women with deep endometriosis present impairment in different domains of quality of life regardless of the questionnaire used for evaluation.


2019 ◽  
Vol 31 (4) ◽  
pp. 213-218 ◽  
Author(s):  
Nooshin Masoudian ◽  
Mohammad Sarmadi ◽  
Rasool Najafi ◽  
Fereshteh Najafi ◽  
Shirin Maleki

The purpose of this study was to investigate the relationship between Burden of Care and Quality of Life in informal home caregivers of stroke patients in Iran. Also we were trying to explore the factors that affect the burden of care. In this cross-sectional study, we have selected 62 informal home caregivers of the patients admitted to “the stroke outpatient unit of the neurology clinic” of the central hospital in Semnan province, Iran, to take part in the investigation. We interviewed them using the Caregiver Burden Inventory and SF-36 Questionnaire for assessing their quality of life. There was a negative and significant correlation between different aspects of quality of life and burden of care. In the bivariate regression model, being married and having lower levels of education (minimum years of schooling) were associated with higher levels of the burden. Our study shows that increasing burden of care in informal home caregivers reduces the quality of life in all domains. Thus, the results of this study indicate that an increase in the burden of caregiving on caregivers lowers their quality of life in all aspects; especially, caregivers who provide care to their spouses encountered more burden. Therefore, these caregivers must be in the center of interest while planning to reduce the burden of care.


2014 ◽  
Vol 77 (2) ◽  
pp. 128-134 ◽  
Author(s):  
Christiane Kugler ◽  
Christoph Bara ◽  
Thea von Waldthausen ◽  
Ina Einhorn ◽  
Burkhard Haastert ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document