Health-Related quality of life by 31-item Cervantes scale in breast cancer survivors undergoing adjuvant endocrine therapy

ABSTRACT Introduction Instruments to manage adverse effects of endocrine therapy with Aromatase inhibitors (AI) may improve adherence and persistence to treatment and Health-Related Quality of Life (HRQL). The 31-item Cervantes Scale (CS-31) is an HRQL questionnaire with particularities of the perimenopausal and postmenopausal period that could be an appropriate instrument to assess HRQL in Breast Cancer (BC) survivors. Objective This study aimed to perform additional validation of the CS-31 for BC survivors undergoing adjuvant endocrine therapy. Methods This prospective study was performed at three time points named T0, T1, and T2: initial, intermediate, and final follow-up period, respectively, totaling 24 months of follow-up. At each time point, the participants completed the CS-31, Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F), and Hospital Anxiety and Depression Scale (HADS). The internal consistency, construct validity, responsiveness analyses, and known-group validity of CS-31 were evaluated. Results This study included 89 postmenopausal women diagnosed with hormone receptor-positive early BC in adjuvant endocrine therapy with AI. The internal consistency was good (Cronbach's alpha = 0.89). Construct validity received a positive rating, with 100% of results consistent with prior hypotheses. A prospective improvement in HRQL was identified for the CS-31 Global Score and FACIT-F Total Score and for most of their domains. Furthermore, women with anxiety and depression by HADS presented worse HRQL by CS-31. Conclusion The authors identified that the CS-31 seems to be appropriate for use in oncology medical routine and may help to monitor adverse effects and HRQL of BC survivors during adjuvant endocrine therapy.

Burial or cremation? Factors associated with preferences among patients with cancer in Brazil: a cross-sectional study

ABSTRACT BACKGROUND: People living with life-limiting illnesses and their family caregivers consistently emphasize the importance of preparing for imminent death, with planned funerals being a common aspect of this preparation. Few studies have described the funeral rituals or post-mortem preferences of patients with cancer. OBJECTIVE: To evaluate the percentage of patients with cancer who wish to be cremated and to identify the factors associated with this preference. DESIGN AND SETTING: Cross-sectional study conducted at Barretos Cancer Hospital. METHODS: A total of 220 patients with cancer completed a Sociodemographic and Clinical Questionnaire, the Duke University Religiosity Index, and burial or cremation preferences. Binary Logistic Regression was performed to identify independent variables associated with cremation. RESULTS: Of the 220 patients, 25.0% preferred cremation and 71.4% preferred burial. Talks about death with family or close friends in their daily life (odds ratio, OR = 2.89; P = 0.021), patients that answered "other" (unsure, tends not be true and not true) for religious beliefs are what really lie behind my whole approach to life (OR = 20.34; P = 0.005), and education 9 to 11 years (OR = 3.15; P = 0.019) or ≥ 12 years (OR = 3.18; P = 0.024) were associated with cremation preference. CONCLUSION: Most patients with Cancer in Brazil prefer burial after death. Discussions about death, religious beliefs and involvement, and educational level seem to influence the preference for cremation. A deeper understanding of ritual funeral preferences and their associated factors may guide policies, services, and health teams in promoting the quality of dying and death.

Translation, Validity and Internal Consistency of the Quality of Dying and Death Questionnaire for Brazilian families of patients that died from cancer: a cross-sectional and methodological study

ABSTRACT BACKGROUND: The Quality of Dying and Death Questionnaire (QoDD) may prove to be an important evaluation tool in the Brazilian context, and, therefore, can contribute to a more precise evaluation of the dying and death process, improving and guiding the end-of-life patient care. OBJECTIVE: To translate and cross-culturally adapt the QoDD into Brazilian Portuguese and measure its validity (convergent and known-groups) and internal consistency DESIGN AND SETTING: A cross-sectional, methodological study was conducted at the Hospital de Câncer de Barretos, Brazil METHODS: A total of 78 family caregivers participated in this study. Semantic, cultural, and conceptual equivalences were evaluated using the content validity index. The construct validity was assessed through convergent validation and known groups analysis [presence of family members at the place of death; feel at peace with dying; and place of death (hospital versus home; hospital versus Palliative Care)]. Internal consistency was evaluated using Cronbach's alpha. RESULTS: The questionnaire was translated into Brazilian Portuguese and presented evidence of a clear understanding of its content. Cronbach's alpha values were ≥ 0.70, except for the domains of treatment preference (α = 0.686) and general concerns (α = 0.599). The convergent validity confirmed a part of the previously hypothesized correlations between the Palliative Care Outcome Scale-Brazil (POS-Br) total scores and the QoDD domain scores. The QoDD-Br domains could distinguish the patients who died in palliative care and general wards. CONCLUSION: The QoDD-Br is a culturally adapted valid instrument, and may be used to assess the quality of death of cancer patients.

Adaptação transcultural para o português brasileiro do questionário Pediatric Intensive Care Unit-Quality of Dying and Death / Cross-cultural adaptation and translation of the Pediatric Intensive Care Unit-Quality of Dying and Death into Brazilian Portuguese

RESUMO Objetivo: Traduzir e adaptar culturalmente o questionário Pediatric Intensive Care Unit-Quality of Dying and Death para o português do Brasil. Métodos: Realizou-se um processo de adaptação transcultural que incluiu equivalências conceitual, cultural e semântica. Esse processo foi composto de três etapas: Etapa 1 - autorização para realização da tradução e adaptação cultural; Etapa 2 - traduções independentes do inglês para o português do Brasil, síntese das traduções, retrotraduções e painel de especialistas; e Etapa 3 - pré-teste realizado com familiares cuidadores e equipe multiprofissional. Resultados: A avaliação pelo painel de especialistas resultou em concordância média de 0,8 em relação à equivalência semântica, cultural e conceitual. Os pré-testes de ambas as versões do questionário mostraram compreensão adequada dos participantes dos itens e opções de respostas. Conclusão: Após o processo de tradução e adaptação cultural da ferramenta Pediatric Intensive Care Unit-Quality of Dying and Death, as versões para cuidador e equipe multiprofissional foram consideradas culturalmente adaptadas, com boa compreensão dos itens por ambos os grupos. Os questionários incluem itens relevantes para avaliar o processo de morte e do morrer no ambiente de terapia intensiva e podem proporcionar mudanças no cuidado centrado no paciente e, principalmente, no familiar cuidador, perante a finitude de seus filhos.

ABSTRACT Objectives: To translate and culturally adapt the Pediatric Intensive Care Unit-Quality of Dying and Death questionnaire into Brazilian Portuguese. Methods: This was a cross-cultural adaptation process including conceptual, cultural, and semantic equivalence steps comprising three stages. Stage 1 involved authorization to perform the translation and cultural adaptation. Stage 2 entailed independent translation from English into Brazilian Portuguese, a synthesis of the translation, back-translation, and an expert panel. Stage 3 involved a pretest conducted with family caregivers and a multidisciplinary team. Results: The evaluation by the expert panel resulted in an average agreement of 0.8 in relation to semantic, cultural, and conceptual equivalence. The pretests of both versions of the questionnaire showed that the participants had adequate comprehension regarding the ease of understanding the items and response options. Conclusion: After going through the process of translation and cultural adaptation, the Pediatric Intensive Care Unit-Quality of Dying and Death caregiver and multidisciplinary team versions were considered culturally adapted, with both groups having a good understanding of the items. The questionnaires include relevant items to evaluate the process of death and dying in the intensive care setting, and suggest changes in care centered on patients and especially family caregivers, given the finitude of their children.

Prevalence of burnout and predictive factors among oncology nursing professionals: a cross-sectional study

ABSTRACT BACKGROUND: Burnout is a syndrome that mostly affects professionals working in contact with patients and their caregivers. In oncology care, nursing professionals are constantly required to provide emotional support for patients and their caregivers, throughout the process of becoming ill, suffering and dying. OBJECTIVE: To evaluate the prevalence and factors associated with burnout in a sample of nursing professionals at a cancer hospital. DESIGN AND SETTING: Cross-sectional study conducted at Hospital de Câncer de Barretos. METHODS: The study population comprised 655 nursing professionals. Burnout syndrome was assessed using the Maslach Burnout Inventory Human Service Survey. Univariate analysis and binary logistic regression models were used to identify independent predictors associated with burnout. RESULTS: Among 304 nursing professionals included in the study, 27 (8.9%) were classified as presenting burnout according to the two-dimensional criteria, and four (1.3%) were classified based on the three-dimensional criteria. Workplace characteristics were not associated with burnout, while single marital status (odds ratio, OR = 2.695; P = 0.037), perceived workplace stressors, such as impatience with colleagues (OR = 3.996; P = 0.007) and melancholy (OR = 2.840; P = 0.021) were considered to be predictors of burnout. Nursing professionals who would choose the profession again (OR = 0.214; P = 0.001) were least likely to present burnout. CONCLUSION: Perceived workplace stressors are strongly associated with burnout. Strategies focusing on restructuring of daily work processes and on activities that stimulate positive relationships are important for professionals' health because motivation to continue working in oncology nursing has a protective effect against burnout.

Validation of the Adolescent Barriers Questionnaire for use in Brazilian adolescents with cancer

Abstract Objective To translate, culturally adapt, and evaluate the psychometric properties of Adolescent Barriers Questionnaire for use in Brazilian adolescents with cancer aged 12 to 18 years, based on the original American Adolescent Barriers Questionnaire which was designed to measure the extent to which adolescents with cancer have concerns about reporting pain and using analgesics. Methods The study analyzed the psychometric properties reliability (internal consistency and test-retest) and validity (known groups and convergent) of Adolescent Barriers Questionnaire in adolescents between 12 and 18 years of age with a diagnosis of cancer who were using or who had used analgesic medication (opioid or not) in a pediatric public health institution. It was estimated 64 adolescents as sample size and the research was conclude with 48. Results Results of pre-test suggest good understanding (content validity index > 0.9). The internal consistency value Cronbach's α was 88%. The convergent validity values ranged between -0.400 and -0.450. Analysis of known groups showed that the instrument discriminated groups of patients with solid vs. hematologic tumors. The intraclass correlation coefficient obtained after retest was 0.863. Conclusion After the process of translations, validations and analysis of psychometric properties, the Brazilian Portuguese version of Adolescent Barriers Questionnaire could be considered culturally adapted, valid, and reliable for the Brazilian adolescent population with cancer aged 12 to 18 years and it can be useful in practical clinic, offering the health professionals the opportunity to understand which barriers the adolescent with cancer can encounter and offer, thus, all the support to overcome them.

Predictors of happiness and satisfaction with life in individuals from the Brazilian general population who use social networks: a cross-sectional study / Preditores de felicidade e satisfação com a vida em indivíduos da população geral brasileira que utilizam redes sociais: um estudo transversal / Predictores de felicidad y satisfacción con la vida en personas de la población brasileña general que usan redes sociales: un estudio transversal

Abstract: This study aimed to identify possible conditions associated with the perception of happiness and satisfaction with life in a sample of the Brazilian population who use social networks. This was a cross-sectional study with participants recruited online in five regions of Brazil via Facebook and WhatsApp. Data were collected from October 2015 to October 2016. The instruments used were the Pemberton Happiness Index, the Satisfaction with Life Scale, and a questionnaire regarding sociodemographic and clinical characteristics and issues potentially associated with the feeling of happiness. In total, 2,151 participants were included. A total of five variables exerted the greatest influence on higher levels of happiness and satisfaction with life in the multiple linear regression model, in the multiple logistic regression analysis, and in the decision tree model. Being satisfied with financial circumstances, having a positive self-evaluation of health, having frequent family gatherings, engaging in physical activity ≥ 3 times a week, and having no previous psychological/psychiatric diagnosis are variables that "seem" to positively influence Brazilians' perception of happiness and satisfaction with life. We identified some predictors of happiness and satisfaction with life, which were mainly related to the social activities and personal satisfaction of the participating individuals. Encouraging people to seek strategies for increasing levels of happiness and life satisfaction based on modifiable variables, such as those found, can be helpful in this context.

Resumo: O estudo teve como objetivo identificar possíveis condições associadas com a percepção de felicidade e satisfação de vida em uma amostra de indivíduos da população geral brasileira que usam redes sociais. O estudo transversal recrutou participantes via redes sociais nas cinco macrorregiões brasileiras, através do Facebook e do WhatsApp. Os dados foram coletados entre outubro de 2015 e outubro de 2016. Os instrumentos utilizados foram o Índice de Felicidade de Pemberton, Escala de Satisfação com a Vida e um questionário sobre características sociodemográficas e clínicas e questões potencialmente associadas com a sensação de felicidade. Foram incluídos 2.151 participantes. Cinco variáveis tiveram maior influência sob níveis mais altos de felicidade e de satisfação com a vida, de acordo com o modelo de regressão linear múltipla, análise de regressão logística multivariada e modelo de árvore de decisão. A satisfação com as circunstâncias financeiras, a autoavaliação da saúde positiva, reuniões familiares frequentes, atividade física ≥ 3 vezes por semana e ausência de diagnóstico psicológico ou psiquiátrico prévio são variáveis que "parecem" influenciar positivamente a percepção de felicidade e satisfação com a vida entre os brasileiros. Foram identificados alguns preditores de felicidade e satisfação com a vida, relacionados principalmente a atividades sociais e à satisfação pessoal. Uma medida útil nesse contexto é incentivar as pessoas a buscarem estratégias para elevar os níveis de felicidade e de satisfação com a vida baseadas nas variáveis modificáveis identificadas no estudo.

Resumen: El objetivo fue identificar posibles condiciones asociadas con la percepción de felicidad y satisfacción con la vida, en una muestra de individuos de la población general brasileña que utilizó redes sociales. Se trata de un estudio transversal, con participantes reclutados en línea en cinco regiones de Brasil, a través del Facebook y del WhatsApp. Los datos fueron recogidos entre octubre 2015 y octubre 2016. Los instrumentos usados fueron: el Índice de Felicidad de Pemberton, la Escala de Satisfacción con la Vida, y un cuestionario respecto a las características sociodemográficas y clínicas, así como asuntos potencialmente asociados con el sentimiento de felicidad. Se incluyeron a un total de 2.151 participantes. Cinco variables ejercieron la influencia más significativa en los mayores niveles de felicidad y satisfacción con la vida en el modelo de regresión múltiple, en los análisis de regresión logística múltiple y en el modelo de árbol de decisión. Estar satisfecho con las circunstancias financieras, tener una autoevaluación positiva de salud, reunirse frecuentemente con la familia, implicarse en actividades físicas ≥ 3 veces a la semana, y no contar diagnósticos previos psicológicos/psiquiátricos son variables que "parecen" influenciar positivamente la percepción de felicidad y satisfacción con la vida de los brasileños. Se identificaron algunos predictores de felicidad y satisfacción con la vida, lo que estaba principalmente relacionado con actividades sociales y satisfacción personal de los participantes brasileños. Fomentar que la gente busque estrategias para incrementar los niveles de felicidad y satisfacción con la vida, basados en variables modificables como las encontradas, puede ser útil en este contexto.

Analysis of the quality of life in patients submitted to oncological treatment of the head and neck / Análise da qualidade de vida em pacientes submetidos a tratamento oncológico de cabeça e pescoço

To evaluate the quality of life and the influence of sociodemographic and clinical variables in patients undergoing treatment for head and neck cancer. Method: Quantitative, cross-sectional study. Two instruments were used: sociodemographic and clinical questionnaire and the Functional Assessment Cancer Therapy Head Neck (FACT-HN). Results: 170 respondents, 60.6% male, 51.2% married, with laryngeal cancer being the most found (34.7%) of the total sample, 78.8% underwent surgical procedures. In FACT-HN, the variables that showed significance were: educational level, professional activity and salary income. Only in the subscale additional head and neck cancer specific concerns (HNSC) were significant: type of cancer, staging, chemotherapy and surgical treatment. Conclusions: The research contributes by showing that predictive factors of quality of life are also socioeconomic issues and not just clinical issues related to the therapeutic approach. Assistance planning is essential to provide support for rehabilitation and reintegration into society.

Objetivo: Avaliar a qualidade de vida e a influência de variáveis sociodemográficas e clínicas, nos pacientes submetidos ao tratamento de câncer de cabeça e de pescoço. Método: Estudo quantitativo, transversal. Foram utilizados dois instrumentos: questionário sociodemográfico e clínico e o instrumento Functional Assessment Cancer Therapy Head Neck (FACT-HN). Resultados: 170 entrevistados, 60,6% do sexo masculino, 51,2% casados, sendo o câncer de laringe o mais encontrado (34,7%) do total da amostra, 78,8% realizaram procedimento cirúrgico. No FACT-HN, as variáveis que apresentaram significância foram: nível educacional, atividade profissional e renda salarial. Apenas na subescala preocupações adicionais específicas do câncer de cabeça e pescoço (PACP) foram significativos: tipo de câncer, estadiamento, tratamento quimioterápico e cirúrgico. Conclusões: A pesquisa contribui ao evidenciar que fatores preditores de qualidade de vida são também questões socioeconômicas e não apenas questões clínicas relacionadas a abordagem terapêutica. O planejamento da assistência é fundamental para fornecer um suporte com vistas a reabilitação e reinserção na sociedade.

Do different pedagogical conceptions result in different quality of life levels?

SUMMARY OBJECTIVE The present study aims to compare medical students' quality of life (QoL) at two Brazilian institutions with different pedagogical conceptions. METHODS We studied students during the first four years of medical school at two institutions (one using active methodologies and small groups and the other using traditional lectures and large groups). We used a demographic questionnaire and the WHOQOL-BREF. RESULTS 820 medical students were included. No significant differences in quality of life were found in general, nor while evaluating the course phase, except for the physical WHOQOL, which was lower for 2nd-year students at the institution with traditional lectures, even when adjusted for gender. CONCLUSION Our findings revealed that, despite having very distinct pedagogical conceptions and characteristics, there were no significant differences in medical students' QoL scores between both institutions. These results are surprising and differ from our initial hypothesis, which expected better QoL for those using more active and student-centered methods.

RESUMO OBJETIVO O presente estudo tem como objetivo comparar a qualidade de vida (QV) de estudantes de medicina de duas instituições brasileiras com diferentes concepções pedagógicas. MÉTODOS Estudo comparativo incluindo estudantes do 1o ao 4o ano do curso de medicina de duas instituições no Brasil (uma usando metodologias ativas e pequenos grupos e a outra aulas expositivas tradicionais e grandes grupos). Utilizou-se um questionário demográfico e o instrumento WHOQOL-Bref. RESULTADOS Foram incluídos 820 estudantes de medicina. Nenhuma diferença significativa na qualidade de vida foi encontrada no geral e na avaliação por fase do curso, com exceção do WHOQOL físico, que mostrou ser mais baixo para os estudantes da da instituição com aulas tradicionais, mesmo quando ajustado para o gênero. CONCLUSÃO Nossos achados revelaram que apesar de terem concepções e características pedagógicas bem distintas, não se observaram diferenças significativas nos escores de QV dos estudantes de medicina das duas instituições. Esses resultados são surpreendentes e diferem da nossa principal hipótese, uma vez que esperávamos uma melhora de QV para aqueles que usam métodos mais ativos e centrados no estudante.

Qualidade de vida do idoso em tratamento oncológico / Quality of life in elderly oncological treatment

O câncer é uma doença de alta prevalência global com elevada taxa de mortalidade a partir dos trinta anos de idade, em especial, na população geriátrica. Os principais objetivos do diagnóstico de câncer e do programa de tratamento é curar ou prolongar a vida consideravelmente, e garantir a melhor qualidade de vida (QV) possível aos sobreviventes do câncer. Garantir boa QV tem sido um dos desafios das políticas públicas na área da gerontologia no mundo e no Brasil. Objetivo: revisar dados da literatura sobre a QV do idoso em tratamento oncológico. Metodologia: o método de pesquisa utilizado foi a revisão integrativa da literatura, que se fundamenta na prática baseada em evidências, utilizando como fonte de levantamento as bases de dados: LILACS, Scielo e MEDLINE/PubMed e os seguintes descritores: qualidade de vida (quality of life), câncer (neoplasms ou cancer), idosos (aged ou elderly) e tratamento (treatment). Foram incluídos artigos com resumos disponíveis que retratam a QV do paciente idoso com câncer e excluídos artigos que não tinha como enfoque principal o paciente idoso. Resultados: fatores como função emocional, social, cognitiva, dificuldades financeiras, assim como fatores relacionados aos efeitos colaterais dos tratamentos, interferem diretamente na qualidade de vida do idoso com câncer. Conclusão: vê-se a necessidade de uma avaliação global do paciente, realizada em conjunto entre as áreas de geriatria, oncologia e equipe multiprofissional, visando a um monitoramento para que o idoso consiga receber e seguir o tratamento sem complicações, possibilitando, assim, uma melhora da qualidade de vida.

Cancer is a global high-prevalence disease with high mortality rate from thirty years of age, especially in the geriatric population. The main goals of cancer diagnosis and treatment program is to cure or prolong life considerably, and ensure the best quality of life (QL) possible for cancer survivors. Ensure good QL has been one of the challenges of public policies in the field of gerontology in the world and in Brazil. Objective: to review the literature on QL of the elderly in cancer treatment. Methodology: the research method was an integrative literature review, which is based on evidence-based practice, using as a source of raising three databases: LILACS, Scielo and MEDLINE/PubMed and the following descriptors: quality of life, cancer, elderly and treatment. They included articles with abstracts available that depict the elderly patient QL with cancer and excluded articles that had as its main focus the elderly. Results: the results showed that factors such as emotional function, social, cognitive, financial difficulties, as well as factors related to the side effects of treatments, directly affect the quality of life of the elderly with cancer. Conclusion: it is necessary a comprehensive patient assessment, carried out jointly between the areas of geriatrics, oncology and multidisciplinary team, aiming to monitoring so that the elderly can receive and follow the treatment without complications, allowing a better quality of life.

Translation and cultural adaptation of the Breast Cancer Treatment Outcome Scale (BCTOS) into Brazilian Portuguese

SUMMARY BACKGROUND: Breast conservative treatment (BCT) is safe when it is performed in association with radiotherapy. The number of referral for BCT has increased, and it has become an important treatment modality. Patients who undergo BCT present some characteristics that are associated with better quality of life compared with patients who undergo mastectomy without reconstruction. Instruments that measure the quality of life specifically used in cases of BCT are limited. One of these instruments is the Breast Cancer Treatment Outcome Scale (BCTOS), which has not yet been translated into Brazilian Portuguese. It contains 22 questions and four domains (functional, aesthetic, breast sensitivity and oedema). METHODS: We performed the translation and cultural adaptation process using Beaton's and EORTC translations process. In summary, the translation process is based on Portuguese translation, translation summary, reverse translation into English, expert committee, pre-test (10 patients), questionnaire review and test of the final version (6 patients). RESULTS: All 16 patients were submitted to quadrantectomy and mammary radiotherapy. Lymphedema was present in 4, altered strength in 5, and altered shoulder mobility in 6 patients. Considering the questionnaire, the reconciled version determined change in 2 items. Pre-test evaluation showed difficulties in 3 patients, but the questionnaire did not change. Test evaluation showed no problems. CONCLUSION: The translation of BCTOS into Portuguese will help us to evaluate the quality of life in BCT patients evaluating treatment-related sequelae and may be useful for oncoplastic surgery evaluation.

RESUMO INTRODUÇÃO: O tratamento conservador da mama (TCM), desde que associado à radioterapia, é seguro. As indicações inicialmente utilizadas para o TCM se elevaram, sendo importante modalidade de tratamento. Novas modalidades, como a oncoplastia associada ao TCM, tornam-se cada vez mais presentes no cotidiano. Pacientes submetidas ao TCM apresentam alguns parâmetros associados a uma melhor qualidade de vida em relação às pacientes mastectomizadas sem reconstrução. Há limitados instrumentos de qualidade de vida a serem utilizados específicamente no TCM, sendo um deles o Breast Cancer Treatment Outcome Scale (BCTOS), questionário este não traduzido e adaptado para a língua portuguesa/Brasil. O BCTOS contém 22 perguntas e quatro domínios (funcional, estético, sensibilidade mamária e oedema). MÉTODOS: Realizamos a tradução e adaptação cultural utilizando a metodologia proposta por Beaton e pelo EORTC. Em resumo, consiste de tradução para o português, resumo da tradução, tradução reversa para o inglês, comitê de especialistas, pré-teste (dez pacientes), revisão do questionário e teste da versão final (seis pacientes). RESULTADOS: As 16 pacientes foram submetidas a quadrantectomia e radioterapia. Linfedema esteve presente em quatro, alteração da força em cinco e alteração da mobilidade em seis pacientes. Avaliando o questionário, a versão de conciliação modificou dois itens. O pré-teste mostrou dificuldades em três pacientes, mas o questionário não se alterou, fato que não se observou no teste final. CONCLUSÃO: A tradução do BCTOS para o português nos ajudará a avaliar a qualidade de vida em pacientes submetidas a tratamento conservador da mama, avaliando as sequelas relacionadas ao tratamento, podendo ser útil na avaliação da cirurgia oncoplástica.

Relationship between food perceptions and health-related quality of life in a prospective study with breast cancer patients undergoing chemotherapy

OBJECTIVE: To correlate the perceptions related to dietary intake with the domains and subscales of health-related quality of life (HRQL) in women with breast neoplasms receiving chemotherapy. METHODS: In this prospective study, 55 women with breast cancer were followed up during chemotherapy at three different times (T0, T1, T2). Before chemotherapy, perceptions related to food consumption were evaluated. HRQL was analyzed with the EORTC QLQ-C30 and Br23 instruments 21 days after each investigated cycle. The differences (T2-T0) in the subscales and HRQL domains were correlated with the differences (T2-T0) in the appetite scores. Spearman's correlation was used to verify a possible correlation between differences in functional and overall HRQL domains (T2-T0) and differences in appetite scores for certain foods and between the differences in some subscales of EORTC QLQ-C30 and Br23 (T2-T0) and differences in appetite scores for certain food groups (T2-T0). RESULTS: Correlations between pain and appetite for bitter taste and between an increased appetite for juices and pain intensification or fatigue were identified, and pain was correlated with an appetite for starchy foods. An appetite for vegetables, legumes and meat/eggs was correlated with physical function. The only significant correlation with social functions occurred between the appetite for sweet foods and these functions. We found a correlation between overall health, emotional function, social function and physical function and the appetite for juices. CONCLUSION: Chemotherapy alters the individual's relationship with food and, consequently, the individual's HRQL.

Translation and cultural adaptation of the Shame and Stigma Scale (SSS) into Portuguese (Brazil) to evaluate patients with head and neck cancer / Tradução e adaptação cultural da Shame and Stigma Scale (SSS) para a língua portuguesa (Brasil) para avaliação de pacientes com câncer de cabeça e pescoço

Abstract Introduction: Head and neck cancer is the sixth leading cause of death from cancer worldwide and its treatment may involve surgery, chemotherapy and/or radiation therapy. The surgical procedure may cause mutilating sequelae, that can alter patient self-image. Thus, head and neck cancer is often connected to the negative stigma with decreased quality of life. Few studies assess the social stigma and shame perceived by patients with head and neck cancer. Objective: To perform the translation and cultural adaptation of the Shame and Stigma Scale (SSS) into Portuguese (Brazil). Methods: Two independent translations (English into Portuguese) were carried out by two professionals fluent in the English language. After the synthesis of the translations, two independent back-translations (from Portuguese into English) were performed by two translators whose native language is English. All translations were critically assessed by a committee of experts consisting of five members. A sample of 15 patients answered the Brazilian Portuguese version of the SSS to carry out the pretest. At this step, the patients were able to suggest modifications and evaluate the understanding of the items. Results: There was no need to change the scale after this step. Based on the previous steps, we obtained the Portuguese (Brazil) version of the SSS, which was called "Escala de Vergonha e Estigma". Conclusion: The Portuguese (Brazil) version of the SSP was shown to be adequate to be applied to the population with HNC and, therefore, the psychometric properties of the tool will be evaluated during following steps.

Resumo Introdução: O câncer de cabeça e pescoço corresponde à sexta causa de morte por câncer no mundo; seu tratamento pode envolver cirurgia, quimio e/ou radioterapia, a cirurgia pode acarretar sequelas mutiladoras, pode alterar a autoimagem do paciente. Assim, o câncer de cabeça e pescoço é muitas vezes ligado ao estigma negativo, com diminuição da qualidade de vida. Poucos instrumentos avaliam o estigma social e a vergonha percebidos por pacientes com câncer de cabeça e pescoço. Objetivo: Traduzir e adaptar culturalmente a Shame and Stigma Scale (SSS) para o português/Brasil. Método: Fizeram-se duas traduções independentes (do inglês para o português) por dois profissionais fluentes na língua inglesa. Após a síntese das traduções, duas retrotraduções independentes (do português para o inglês) foram feitas por dois tradutores cuja língua materna é o inglês. Todas as traduções foram analisadas criticamente por um comitê de especialistas composto por cinco membros. Uma amostra de 15 pacientes respondeu à versão em português/Brasil da SSS para o pré-teste. Nessa etapa, os pacientes puderam sugerir modificações e avaliar o entendimento dos itens. Resultados: Não houve necessidade de alteração da escala após essa fase. A partir das etapas anteriores, obteve-se a versão em português/Brasil da SSS, denominada de Escala de Vergonha e Estigma. Conclusão: A versão em português/Brasil da SSS se mostrou apta para ser aplicada na população com câncer de cabeça e pescoço; portanto, as propriedades psicométricas do instrumento serão avaliadas na etapa seguinte.

ATYPICAL STERNAL PAIN IN A BREAST CANCER PATIENT MIMICKING ACUTE MYOCARDIAL INFARCTION / Dor esternal atípica no câncer de mama mimetizando infarto agudo do miocárdio

Radiation therapy on the left side of the chest, some chemotherapy drugs, and trastuzumab raise the risk of cardiac events. Acute chest pain associated with breast cancer is not common, but it is possible. Electrocardiogram, which can result normal in up to 80% of cases of infarction, and serial dosing of myocardial necrosis markers are fundamental for differential diagnosis. Total creatine kinase (CK), creatine kinase-MB fraction (CK-MB), and troponins are frequently used. We present the case of a patient with atypical chest pain associated with elevation of CK and CK-MB, whose evolution and complementary exams showed to be a thoracic tumor recurrence. We discuss the use of these markers for acute chest pain; possible differential diagnoses, the use of CKMB relative index and, particularly, the presence of macro CK in some breast cancer patients ­ which in the case herein presented was a marker of tumor progression.

A radioterapia do lado esquerdo do tórax, alguns quimioterápicos e o trastuzumabe elevam o risco de eventos cardíacos. A dor torácica aguda associada ao câncer de mama não é um evento frequente, mas é possível. No diagnóstico diferencial, faz-se necessário o eletrocardiograma, que pode ser normal em até 80% dos infartos, e a dosagem seriada de marcadores de necrose miocárdica, sendo frequentemente utilizados a creatinoquinase (CK) total, a creatinnoquinase fração MB (CK-MB) e as troponinas. Apresentamos o caso de uma paciente com dor torácica atípica associada à elevação sérica da CK e da CK-MB, sendo que a evolução e os exames complementares mostraram tratar-se de uma recorrência tumoral torácica. Discutem-se a utilização desses marcadores na dor torácica aguda, os diagnósticos diferenciais possíveis, a utilização do índice relativo CK-MB e, em especial, as macro CK presentes em algumas portadoras de câncer de mama, o que, nessa paciente, foi um marcador de progressão tumoral.

Relato de experiência sobre educação em saúde a idosos: percepção dos discentes / Experience report on health education in the elderly people: perception of students

Trata-se de um relato de experiência da percepção de discentes sobre ações educativas em saúde voltadas a idosos da casa de acolhida Remanso da Paz, Quixadá, CE. Foi desenvolvido pelos acadêmicos do curso de Farmácia do Centro Universitário Católica de Quixadá e realizado durante o mês de maio 2016. As experiências foram baseadas em orientação e aconselhamento sobre as medidas diárias frente a doenças crônicas, por meio de palestras, rodas de conversa, discussões, além da execução de teste de glicemia e verificação de pressão arterial para averiguação da terapia medicamentosa. Dentre os temas abordados destacam-se: uso racional de medicamentos, alimentação saudável, uso de preparações caseiras de plantas medicinais, diabetes e hipertensão e sedentarismo. Dessa forma, considerou-se a promoção da saúde como um processo que abrangeu a participação de toda a população no contexto do cotidiano do idoso e não apenas das pessoas sob risco de adoecer, evidenciando-se as ações desenvolvidas como essenciais na melhoria da qualidade de vida do idoso.

This is an experience report of perception of students on educational activities focused on health with the elderly people of the welcome home Remanso Peace, QuixadáCE. It was developed by students of the Pharmacy course at the University Catholic Center Quixadá held during the month of May 2016. The experiments were based on guidance and counseling on daily measures in the face of chronic diseases, through lectures, conversation circle, discussions, and the blood glucose test run and checking blood pressure for an investigation of drug therapy. Among the topics covered, there is the rational use of drugs, healthy eating, use of homemade herbal preparations, diabetes and hypertension and physical inactivity. Thus, health promotion is seen as a process that includes the participation of the entire population in the elderly everyday context and not just people at risk of becoming ill, showing that the actions undertaken are essential improving the quality of life of the elderly population.

Abordagem transcultural da qualidade de vida relacionada à saúde de pacientes com câncer / Transcultural approach to the health-related quality of life of cancer patients

Objetivo: comparar a qualidade de vida relacionada à saúde de pacientes com câncer em tratamento quimioterápico no Brasil e na Espanha. Métodos: estudo transversal, cuja coleta de dados ocorreu no Hospital de Câncer e Hospital Universitário, com os instrumentos de caracterização sociodemográfica European Organization for Research and Treatment of Cancer and Quality of Life Questionnaire-C30. Resultados: nos dois países predominaram sexo feminino, cor branca, estado civil casado, escolaridade fundamental, religião católica e a profissão não qualificados. Os escores de Qualidade de vida relacionada à saúde no Estado Geral de Saúde e as funções de Desempenho de papel e cognitiva foram maiores na amostra brasileira, enquanto que os sintomas de fadiga, dor, dispneia, insônia e diarreia foram mais presentes na população espanhola, com diferenças estatisticamente significantes. Conclusão: a qualidade de vida relacionada à saúde foi melhor entre os brasileiros. (AU)

Translation and cultural adaptation of the Functional Assessment of Chronic Illness Therapy - Cervical Dysplasia (FACIT-CD) to evaluate quality of life in women with cervical intraepithelial neoplasia / Tradução e adaptação cultural do Functional Assessment of Chronic Illness Therapy - Cervical Dysplasia (FACIT-CD) para avaliar qualidade de vida em mulheres com neoplasia intraepitelial cervical

ABSTRACT Objective To translate and perform the cultural adaptation of the tool Functional Assessment of Chronic Illness Therapy - Cervical Dysplasia (FACIT-CD) to the Portuguese language. Methods A descriptive cross-sectional study, with translation and cultural adaptation of the assessment tool performed according to international guidelines and the Functional Assessment of Chronic Illness Therapy (FACIT) protocol group. It involved eight experts, six from Brazil, one from Portugal and one from the United States. After translation and back-translation of the tool, the semantic analysis process was carried out. We randomly included 20 women aged between 18 and 70 years with altered cervical cytology exam, seen at the Department of Prevention and Gynecologic Oncology - Hospital de Câncer de Barretos. Results The sample consisted of women with low education level. In the first pre-test, ten women participated and half of them considered the questions CD1, CD2 and CD3 as difficult, because they did not understand the meaning of the term "pelvic area". The question CD5, "I worry about spreading the infection", was also considered difficult to understand by five women. After the reconsideration of the expert committee and FACIT group, the second pre-test was performed. At this stage, we concluded that the previously raised understanding problems had been solved. Conclusion The translated version of FACIT-CD in universal Portuguese language is equivalent to the original version in English and was easily understood by patients with cervical intraepithelial neoplasia.

RESUMO Objetivo Traduzir e adaptar o instrumento Functional Assessment of Chronic Illness Therapy - Cervical Dysplasia (FACIT-CD), para a língua portuguesa. Métodos Estudo descritivo, transversal, com metodologia de tradução e adaptação cultural de instrumento de avaliação, realizado por meio de diretrizes internacionais e seguindo o protocolo do grupo Functional Assessment of Chronic Illness Therapy (FACIT). Envolveu oito especialistas, sendo seis nativos do Brasil, um de Portugal e um dos Estados Unidos. Ao término do processo de tradução e retrotradução, deu-se início ao processo de análise semântica. Foram incluídas aleatoriamente 20 mulheres entre 18 e 70 anos com exame de citologia cervical alterado, atendidas no Departamento de Prevenção e Ginecologia Oncológica do Hospital de Câncer de Barretos. Resultados A amostra foi composta por mulheres com baixa escolaridade. No primeiro pré-teste participaram dez mulheres, sendo que a metade considerou as questões CD1, CD2 e CD3 difíceis por não compreenderem o significado do termo "região pélvica". A questão CD5, "Estou preocupada em disseminar a infecção", também foi considerada de difícil entendimento por cinco mulheres. Após as reconsiderações do comitê de especialistas e do grupo FACIT, foi realizado o segundo pré-teste. Nesta fase, pode-se concluir que os problemas de entendimento anteriores foram resolvidos. Conclusão A versão traduzida do FACIT-CD é equivalente à versão original em inglês e em língua portuguesa universal, sendo facilmente compreendida pelas pacientes com neoplasia intraepitelial cervical.

Consumo alimentar e estado nutricional de mulheres em quimioterapia / Food intake and the nutritional status of women undergoing chemotherapy

Resumo O objetivo deste estudo foi analisar o consumo alimentar e o estado nutricional de mulheres com câncer de mama (CM) em quimioterapia (QT). A avaliação dietética quantitativa foi realizada de acordo com as Dietary Reference Intakes (DRI) e a avaliação qualitativa pelo Índice de Qualidade da Dieta Revisado (IQD-R). Dentre o total de pacientes (n = 20), 60% (n = 12) apresentaram circunferência da cintura igual ou superior a 88 cm. Foi verificado 75% (n = 15) de indivíduos com excesso de peso. A média da ingestão de cálcio, cobre, ferro, fibra alimentar, magnésio, potássio, vitamina A, niacina, vitamina B6 e zinco encontrava-se abaixo da recomendação de ingestão adequada e o consumo de vitamina C, fósforo, manganês, sódio e tiamina encontrava-se acima. Quanto à análise do IQD-R, 80% (n = 16) das pacientes apresentaram uma “dieta que requer modificações”, enquanto que 20% (n = 4) apresentaram uma “dieta saudável”. Observou-se elevado excesso de peso, desequilíbrio na ingestão de micronutrientes e dieta que necessita melhorias. Dessa forma, a criação e a utilização de um protocolo de intervenção nutricional são de grande relevância para melhorar a dieta de pacientes com CM que realizam QT.

Abstract The objective behind this study was the analysis of food intake and the nutritional status of women with breast cancer (BC) undergoing chemotherapy (CT). The quantitative dietary evaluation was performed in accordance with Dietary Reference Intakes (DRI), whereas the qualitative evaluation was performed through the Brazilian Healthy Eating Index – Revised (BHEI-R).From among the total number of patients (n = 20), 60% (n = 12) presented waist circumference, equal to or higher than 88cm. It was noted that 75% (n = 15) individuals were overweight. The average intake for calcium, copper, iron, dietary fiber, magnesium, potassium, vitamin A, niacin, vitamin B6 and zinc, were found to be below adequate intake levels, while the intake of vitamin C, phosphorus, manganese, sodium and thiamine were all found to be above DRIs recommendations. As for the analysis of the BHEI-R, 80% (n = 16) of the patients presented a “diet that needs modifications”, while 20% (n = 4) presented a “healthy diet”. Noted from these observations was the presence of a high overweight rate, a discrepancy in the intake of micronutrients and a diet that needed improvements. In this manner, the establishment and use of a nutritional intervention protocol are very important when it comes to the improvement of the diet in patients with BC and who are undergoing CT.