Seguimiento Funcional hasta Seis Meses después de Sobrevivir a Cuidados Intensivos: Lecciones aprendidas de un Estudio Chileno Multicéntrico / Functional follow-up six months after surviving intensive care: lessons learned from a Chilean multicenter study

Introducción. Las tasas de retención en los estudios de seguimiento oscilan entre el 32 y 100%, demostrando el desafío que implica realizar estudios longitudinales de sobrevivientes de la unidad de cuidados intensivos (UCI). Objetivo. Identificar las estrategias implementadas y lecciones aprendidas en un estudio prospectivo multicéntrico de seguimiento de sobrevivientes de la UCI durante la pandemia. Métodos. Estudio post-hoc de las lecciones aprendidas mediante encuestas y entrevistas dirigidas a explorar la experiencia de los investigadores y coordinadores del estudio IMPACCT COVID-19, realizado en siete centros chilenos entre octubre 2020 y abril 2021 evaluando el síndrome post-cuidados intensivos de sobrevivientes hasta seis meses después. Resultados. Identificamos ocho lecciones: 1) selección de instrumentos de medición, 2) identificación de centros participantes, 3) aprobación del estudio, 4) financiamiento, 5) capacitación de evaluadores, 6) coordinación/aseguramiento de calidad, 7) reclutamiento y 8) seguimiento de pacientes. Incluso durante el primer año de pandemia, reclutamos 252 pacientes a una tasa de 1,4 pacientes/día con una retención del 48% a los 6 meses de seguimiento. El uso de redes académicas existentes y las estrategias de comunicación entre investigadores, coordinadores y evaluadores fueron aspectos positivos; mientras que la fidelización con evaluadores al egreso de la UCI y con pacientes durante el seguimiento son aspectos que deberían considerarse en futuros estudios. Conclusiones. Se evaluaron más de 250 pacientes en seis meses durante la pandemia, con tasas de retención post UCI acorde a la literatura. Futuros estudios debiesen optimizar los procesos de medición y de seguimiento para minimizar la pérdida de pacientes.

Background. Retention rates of follow-up studies range from 32 to 100%, demonstrating the challenge to conduct longitudinal studies of intensive care unit (ICU) survivors. Objective. To identify the strategies implemented and lessons learned in a multicenter prospective follow-up study of ICU survivors during pandemic times. Methods. Post-hoc study of lessons learned through surveys and interviews aimed at exploring the experience of the researchers and coordinators of the IMPACCT COVID-19 study. The original study was performed in seven Chilean sites between October 2020 and April 2021 evaluating the post-intensive care syndrome of survivors up to six-month follow-up. Results. We identified eight lessons: 1) selection of measurement instruments, 2) identification of participating sites, 3) Study approval, 4) funding, 5) evaluators training, 6) coordination/quality assurance, 7) recruitment, and 8) patient follow-up. Even during the first year of the pandemic, we recruited 252 patients at a rate of 1.4 patients/day with a retention rate of 48% at 6 months of follow-up. The use of existing academic networks and communication strategies between researchers, coordinators and evaluators were positive aspects; while evaluators fidelity at ICU discharge and patient engagement during follow-up are aspects should be considered. Conclusions. More than 250 patients were evaluated in six months during the pandemic, with post-ICU retention rates consistent with the literature. Future studies should optimize measurement and monitoring processes to minimize patient atrition.

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.

Prognostic Impact of Residual Moderate Mitral Regurgitation Following Valve-in-Valve Transcatheter Aortic Valve Implantation

ABSTRACT Introduction: The impact of mitral regurgitation (MR) on valve-in-valve transcatheter aortic valve implantation (VIV-TAVI) in patients with failed bioprostheses remains unclear. The purpose of this study was to assess the prognostic impact of residual moderate MR following VIV-TAVI. Methods: We retrospectively analyzed 127 patients who underwent VIV-TAVI between March 2010 and November 2021. At least moderate MR was observed in 51.2% of patients before the procedure, and MR improved in 42.1% of all patients. Patients with postoperative severe MR, previous mitral valve intervention, and patients who died before postoperative echocardiography were excluded from further analyses. The remaining 114 subjects were divided into two groups according to the degree of postprocedural MR: none-mild MR (73.7%) or moderate MR (26.3%). Propensity score matching yielded 23 pairs for final comparison. Results: No significant differences were found between groups before and after matching in early results. In the matched cohort, survival probabilities at one, three, and five years were 95.7% vs. 87.0%, 85.0% vs. 64.5%, and 85.0% vs. 29.0% in the none-mild MR group vs. moderate MR-group, respectively (log-rank P=0.035). Among survivors, patients with moderate MR had worse functional status according to New York Heart Association (NYHA) class at follow-up (P=0.006). Conclusion: MR is common in patients with failed aortic bioprostheses, and improvement in MR-status was observed in over 40% of patients following VIV-TAVI. Residual moderate MR after VIV-TAVI is not associated with worse early outcomes, however, it was associated with increased mortality at five years of follow-up and worse NYHA class among survivors.

Facilidades e dificuldades autorreferidas por trabalhadores de enfermagem para retorno ao trabalho após o diagnóstico de câncer / Self-reported facilities and difficulties by nursing workers for return to work after cancer diagnosis / Facilidades y dificultades autodeclaradas por trabajadores de enfermería para el regreso al trabajo después del diagnóstico de cáncer

Objetivo: analisar fatores facilitadores e dificultadores autorreferidos por trabalhadores da saúde para o retorno ao trabalho após o diagnóstico de câncer. Método: estudo descritivo transversal realizado com trabalhadores de enfermagem submetidos a tratamento de câncer, de dois hospitais públicos entre março e dezembro de 2019. Coletara-se dados sociodemográficos, do Índice para Capacidade de Trabalho e do Functional Assessment of Cancer Illness Therapy ­ General, analisados por estatística descritiva. Protocolo aprovado pelo Comitê de Ética em Pesquisa. Resultados: entre os participantes, 81,9% eram do sexo feminino e 54,6% técnicos de enfermagem. A dor foi o principal dificultador (81,9%) e, para todos, o apoio de chefes e colegas de trabalho o principal facilitador. Identificou-se excelente capacidade para o trabalho em 45,5% e qualidade de vida média de 56. Conclusão: para o retorno ao trabalho ser possível, é necessário oferecer suporte ao trabalhador, tanto em função dos efeitos do tratamento do câncer quanto da necessidade de apoio.

Objective: to analyze facilitating and hindering factors self-reported by health workers in returning to work after a cancer diagnosis. Method: cross-sectional descriptive study carried out with nursing workers undergoing cancer treatment in two public hospitals between March and December 2019. Sociodemographic data were collected, from the Work Capacity Index and the Functional Assessment of Cancer Illness Therapy ­ General, analyzed by descriptive statistics. Protocol approved by the Research Ethics Committee. Results: among the participants, 81.9% were female and 54.6% were nursing technicians. Pain was the main obstacle (81.9%) and, for everyone, support from bosses and co-workers was the main facilitator. Excellent work capacity was identified in 45.5% and an average quality of life of 56. Conclusion: for a return to work to be possible, it is necessary to offer support to the worker, both due to the effects of cancer treatment and the need of support.

Objetivo: analizar los factores facilitadores y obstaculizadores autodeclarados por trabajadores de la salud en el regreso al trabajo después de un diagnóstico de cáncer. Método: estudio descriptivo transversal realizado con trabajadores de enfermería en tratamiento oncológico, en dos hospitales públicos, entre marzo y diciembre de 2019. Se recolectaron datos sociodemográficos, del Functional Assessment of Cancer Illness Therapy ­ General (Evaluación Funcional de la Terapia para Enfermedad Oncológica), analizados mediante estadística descriptiva. El Comité de Ética en Investigación aprobó el Protocolo. Resultados: entre los participantes, el 81,9% consistía en mujeres y el 54,6% en técnicos de enfermería. El dolor fue el principal obstáculo (81,9%) y, para todos, el apoyo de jefes y compañeros de trabajo fue el principal facilitador. Se identificó una excelente capacidad de trabajo en un 45,5% y una calidad de vida promedio de 56. Conclusión: para que el retorno al trabajo sea posible, es necesario ofrecer soporte al trabajador, tanto por los efectos del tratamiento del cáncer como por la necesidad de apoyo.

Prevalence and Determinants of Long COVID among the COVID-19 Survivors: A Cross-sectional Study from A Rural Area of Maharashtra

Background: Most patients infected with the COVID-19 virus may experience long-term effects from COVID-19 infection, known as post-COVID or long COVID conditions. Long COVID may last for weeks, months or years and may limit ones day to day activities and needs health care. Aim & Objective: To study the prevalence and risk factors of long COVID among the COVID-19 survivors of a rural area of Maharashtra. Methods and Material: A Community-based cross-sectional study was conducted in adult subjects residing in Chanai village from Maharashtra who have had a history of COVID-19 and have passed more than 3 months since the diagnosis from May 2022 to June 2022. The interview of the study participants was conducted with the help of a pre-designed, semi-structured questionnaire for data collection. Statistical Analysis: Data was analyzed using Microsoft Excel 2010, Open EPI-Info version 3.01 updated on 2013/04/06. Data was presented in tables, graphical format, frequencies and percentages and the statistical association was shown using the chi- square test. Results: The majority of participants were males (59%), from 19 to 39 years of age group (57%), having fever as presenting symptom (83%), with mild COVID (13%), and required hospitalization (53%). Long COVID was associated with the elderly age group, male sex (27.1%), severe COVID presentation (88.2%) after 12 weeks, and those required intubation (80%). Conclusion: The prevalence of long COVID was 17.5%. Determinants associated with long COVID were the elderly age group, male sex, severe COVID presentation and who required intubation.

Hormonal profile of survivors of breast cancer with fatigue: A pilot study

Background & objectives: One of the most common problems experienced by breast cancer survivors (BCSs) is fatigue. There has been little research about the status of hormones in breast cancer patients as an aetiology of cancer-related fatigue (CRF). Hence, a pilot study was conducted to assess the levels of hormones such as thyroid, cortisol, dehydroepiandrosterone sulphate (DHEAS), oestrogen and progesterone in BCSs with fatigue. Methods: BCSs with complaints of fatigue were assessed using the Brief Fatigue Inventory (BFI) tool and evaluation of the hormone profiles was done in moderate-to-severe fatigued survivors. Data collected were analyzed to look for any association between fatigue and altered hormonal levels. Results: In this study, 56 per cent (n=62) of survivors experienced moderate-to-severe fatigue out of 110 patients reporting fatigue. Thyroid functions were deranged in 22 patients (35.48%). The thyroid stimulating hormone (TSH) levels were found to have a significant negative association with the severity of fatigue, (P<0.05). Twelve patients (19.35%) had reduced DHEAS levels suggestive of impaired hormone synthesis in the adrenal gland. Twenty two postmenopausal survivors (35.48%) had raised oestradiol levels. Interpretation & conclusions: The findings of this study suggest that the hormonal milieu, especially thyroid hormone and DHEAS may have a role in CRF experienced by BCSs and needs further exploration.

Validation into Spanish of a Scale to Detect the Post-intensive Care Syndrome / Validación al español de una escala para detectar el Síndrome Poscuidado Intensivo / Validação em espanhol de uma escala para detectar a Síndrome de Cuidados Pós-Intensivos

Objective. This work sought to validate the Spanish version of the scale Healthy Aging Brain-Care Monitor (HABC-M) scale as clinical tool to detect the Post-intensive Care Syndrome. Methods. Psychometric study, conducted in adult intensive care units from two high-complexity university hospitals in Colombia. The sample was integrated by 135 survivors of critical diseases with mean age of 55 years. The translation of the HABC-M was carried out through transcultural adaptation, evaluating content, face, and construct validity and determining the scale's reliability. Results. A replica was obtained of the HABC-M scale in its version into Spanish, semantically and conceptually equivalent to the original version. The construct was determined through confirmatory factor analysis (CFA), evidencing a three-factor model comprised of the subscales: cognitive (6 items), functional (11 items), and psychological (10 items), with a confirmatory factor index (CFI) of 0.99, a Tucker Lewis index (TLI) of 0.98, and an approximate root-mean-square error (RMSE) of 0.073 (90% CI: 0.063 ­ 0.084). Internal consistency was determined through Cronbach's alpha coefficient, obtaining 0.94, (95% CI 0.93 ­ 0.96). Conclusion. The Spanish of the HABC-M scale is a tool with adequate psychometric properties, validated and reliable to detect the Post-intensive Care Syndrome.

Objetivo. Validar la versión en español de la escala Healthy Aging Brain-Care Monitor (HABC-M) como herramienta clínica para la detección del síndrome poscuidado intensivo. Métodos. Estudio psicométrico, el cual se llevó a cabo en unidades de cuidado intensivo adulto de dos hospitales universitarios de alta complejidad en Colombia. La muestra fue integrada por un total de 135 sobrevivientes a enfermedades críticas con edad promedio de 55 años. La traducción del HABC-M se realizó mediante adaptación transcultural, evaluándose la validez de contenido, facial, constructo y determinándose la confiabilidad de la escala. Resultados. Se obtuvo una réplica de la escala HABC-M en su versión al español, semántica y conceptualmente equivalente a la versión original. El constructo se determinó a través de análisis factorial confirmatorio (AFC), evidenciando un modelo de tres factores compuesto por las subescalas: cognitiva (6 ítems), funcional (11 ítems) y psicológica (10 ítems), con un índice de factores confirmatorios (CFI) de 0.99, un índice de Tucker Lewis (TLI) de 0.98 y una raíz cuadrada del error cuadrático medio aproximado (RMSEA) de 0.073 (IC 90 %: 0.063 ­ 0.084). La consistencia interna se determinó mediante el coeficiente alfa de Cronbach, obteniendo e 0.94, (IC 95 % 0.93 ­ 0.96). Conclusión. La versión en español de la escala HABC-M es una herramienta con adecuadas propiedades psicométricas, válida y confiable para la detección del síndrome poscuidado intensivo.

Objetivo. Para validar a versão espanhola da escala Healthy Aging Brain-Care Monitor (HABC-M) como uma ferramenta clínica para a detecção da síndrome do cuidado pós-cuidado. Métodos. Estudo psicométrico, que foi realizado em unidades de terapia intensiva para adultos de dois hospitais universitários de alta complexidade na Colômbia. A amostra consistiu em 135 sobreviventes de doenças críticas. A tradução do HABC-M foi realizada por meio de adaptação transcultural, avaliando o conteúdo, facial e construção de validade e determinando a confiabilidade da escala. Resultados.Uma réplica da escala HABC-M foi obtida em sua versão em espanhol, semântica e conceitualmente equivalente à versão original. A construção foi determinada através da análise fatorial confirmatória, mostrando um modelo de três fatores composto pelas subescalas: cognitiva (6 itens), funcional (11 itens) e psicológica (10 itens), com um índice fator confirmatório (CFI) de 0.99, um índice de Tucker Lewis (TLI) de 0.98 e um erro médio quadrático aproximado da raiz (RMSEA) de 0.073 (90% CI: 0.063 ­ 0.084). A consistência interna foi determinada pelo coeficiente alfa do Cronbach, com de 0.94 (95 % CI 0.93 ­ 0.96). Conclusão. A versão espanhola da escala HABC-M é uma ferramenta com propriedades psicométricas adequadas, válida e confiável para a detecção da síndrome do pós-cuidado intensivo

The mediating effect of self-advocacy between posttraumatic growth and social isolation among female breast cancer survivors / 中国实用护理杂志

Objective:To explore the mediating effect of self-advocacy between posttraumatic growth and social isolation among female breast cancer survivors, so as to provide reference for the establishing nursing intervention strategies for social isolation.Methods:A random samplingsurvey was conducted, a total of 220 female breast cancer survivors from May to December 2021in Tianjin Cancer Hospital Airport Hospital were recruited by convenience sampling method. They were investigated by the general information questionnaire, General Alienation Scale, Posttraumatic Growth Inventory and Female Self-advocacy in Cancer Survivorship, respectively.Results:A total of 203 valid questionnaires were collected. The score of posttraumatic growth was (60.91 ± 12.04) points, self-advocacy was (59.56 ± 12.19) points, social isolation was (36.52 ± 7.79) points of female breast cancer survivors. The Posttraumatic Growth Inventory scores of each dimension in female breast cancer survivors were positively correlated with the scores of female self-advocacy of each dimension in cancer survivorship ( r values were 0.219-0.686, all P<0.01); each dimension of the General Alienation Scale scores were negatively correlated with the scores of Posttraumatic Growth Inventory and Female Self-advocacy in Breast Cancer Survivorship ( r values were -0.804 to -0.202, all P<0.01). The posttraumatic growth of female breast cancer survivors affected social alienation through self-advocacy, which showed the mediating effect of self-advocacy accounts for 32.8% of total effect. Conclusions:Self-advocacy plays a mediating role in the relationship between posttraumatic growth and social isolation. Nurses can improve the level of self-advocacy of female breast cancer survivors and promote posttraumatic growth, so as to decrease social isolation.

Content validity evidence of the Brazilian version of the Cognitive Symptom Checklist-Work-21 / Evidencia de validez de contenido de la versión brasileña del Cognitive Symptom Checklist-Work-21 / Evidências de validade de conteúdo da versão brasileira do Cognitive Symptom Checklist-Work-21

ABSTRACT Objective: to cross-culturally adapt and assess the content validity evidence of the Cognitive Symptom Checklist-Work-21 for the Brazilian context. Method: a psychometric study of cross-cultural adaptation, covering the stages of translation, reconciliation, back-translation, intercultural equivalence assessment and content validity evidence analysis, considering Content Validity Ratio parameters in breast cancer survivors. Results: the translations were equivalent to the original version. Colloquial expressions were modified, tense, verbal adjusted, and two items containing multiple commands were separated. The final version now contains 22 items, presenting semantic, conceptual, idiomatic and experimental equivalences. The pre-test indicated good understanding and ease in the response process. Conclusion: the final version was defined as "Lista de verificação de sintomas cognitivos relacionados ao trabalho - 22 itens", showing good linguistic equivalence and strong evidence of content validity in the Brazilian context.

RESUMEN Objetivo: realizar la adaptación transcultural y evaluar las evidencias de validez de contenido del Cognitive Symptom Checklist-Work-21 para el contexto brasileño. Método: estudio psicométrico de adaptación transcultural, abarcando las etapas de traducción, reconciliación, retrotraducción, evaluación de equivalencia intercultural y análisis de evidencias de validez de contenido, considerando parámetros de Content Validity Ratio en sobrevivientes de cáncer de mama. Resultados: las traducciones fueron equivalentes a la versión original. Se modificaron las expresiones coloquiales, se tensaron, se ajustaron las verbales y se separaron dos ítems que contenían múltiples comandos. La versión final ahora contiene 22 ítems, presentando equivalencia semántica, conceptual, idiomática y experimental. El pre-test indicó buena comprensión y facilidad en el proceso de respuesta. Conclusión: la versión final fue definida como "Lista de verificação de sintomas cognitivos relacionados ao trabalho - 22 itens", mostrando buena equivalencia lingüística y fuerte evidencia de validez de contenido en el contexto brasileño.

RESUMO Objetivo: realizar a adaptação transcultural e avaliar as evidências de validade de conteúdo do Cognitive Symptom Checklist-Work-21 para o contexto brasileiro. Método: estudo psicométrico de adaptação transcultural, abrangendo as etapas de tradução, reconciliação, retrotradução, avaliação de equivalência intercultural e análise das evidências de validade de conteúdo, considerando parâmetros de Content Validy Ratio em sobreviventes de câncer de mama. Resultados: as traduções demonstraram equivalência à versão original. Expressões coloquiais foram modificadas, o tempo verbal ajustado, e dois itens contendo múltiplos comandos foram separados. A versão final passou a conter 22 itens, apresentando equivalências semântica, conceitual, idiomática e experimental. Os valores de CVR mantiveram-se acima de 0,87. O pré-teste indicou boa compreensão e facilidade no processo de resposta. Conclusão: a versão final foi definida como "Lista de verificação de sintomas cognitivos relacionados ao trabalho - 22 itens", apresentando boa equivalência linguística e fortes evidências de validade de conteúdo no contexto brasileiro.

Transiciones en sobrevivientes de cáncer de mama frente al reintegro laboral: revisión integrativa / Transitions in breast cancer survivors regarding work return: integrative review

INTRODUCCIÓN: El cáncer de mama es una de las enfermedades más comunes entre las mujeres en todo el mundo. El tratamiento del cáncer de mama a menudo implica cirugía, radioterapia, quimioterapia y/o terapia hormonal, tratamientos que a largo plazo pueden generar efectos en las mujeres. Estas mujeres que han sido tratadas por cáncer de mama pueden enfrentar situaciones diversas al decidir retornar a su trabajo, debido entre otros a que pueden ser percibidas como menos productivas. OBJETIVO: Describir las transiciones que experimentan las sobrevivientes de cáncer de mama frente al reintegro laboral a través de una revisión integrativa. MATERIALES Y MÉTODOS: revisión integrativa de alcance descriptivo, a través de la identificación del problema, búsqueda de literatura, evaluación de datos, análisis de datos y presentación de resultados. Los términos de búsqueda utilizados fueron: "breast neoplasms" "breast cancer" "breast cancer survivor and, or y not "return to work". Las bases de datos utilizadas fueron Scielo, Pubmed, Scopus, según criterios de inclusión implementados en la búsqueda de literatura se encontraron 22 artículos que cumplieron con ello. RESULTADOS: Se identificaron temáticas que van en relación con las sobrevivientes de cáncer de mama que planean reincorporarse laboralmente, por lo general no se identifica un momento ni tiempo específico para que la sobreviviente tome la decisión de volver al trabajo después de pasar la enfermedad. CONCLUSIÓN: Es importante generar estudios donde el abordaje de los factores asociados al retorno laboral pueda ocasionar un impacto sobre la calidad de vida de la mujer sobreviviente y su relación con el retorno al trabajo, sobre todo aspectos relacionados con los efectos de los tratamientos.

INTRODUCTION: Breast cancer is one of the most common diseases among women worldwide. Breast cancer treatment often involves surgery, radiotherapy, chemotherapy and/or hormone therapy, treatments that can have long-term effects on women. These women who have been treated for breast cancer may face different situations when deciding to return to work, due to the fact that they may be perceived as less productive, among others. OBJECTIVE: To describe the transitions experienced by breast cancer survivors when faced with reemployment through an integrative review. MATERIALS AND METHODS: integrative review of descriptive scope, through the identification of the problem, literature search, data evaluation, data analysis and presentation of results. The search terms used were "breast neoplasms" "breast cancer" "breast cancer survivor and, or and not "return to work". The databases used were Scielo, Pubmed, Scopus, according to the inclusion criteria implemented in the literature search, 22 articles were found that complied with it. RESULTS: Themes that are related to breast cancer survivors who plan to return to work were identified, in general, a specific moment or time is not identified for the survivor to make the decision to return to work after passing the disease. CONCLUSION: It is important to generate studies where the approach to the factors associated with the return to work may have an impact on the quality of life of the surviving woman and its relationship with the return to work, especially aspects related to the effects of the treatments.

Physical activity of children with cancer during the COVID-19 pandemic: what were the most relevant studies published from August 2019 to July 2021? / Actividad física em niños con cáncer durante la covid-19: ¿cuáles fueron las publicaciones más relevantes entre agosto de 2019 y julio de 2021? / Atividade física de crianças com câncer durante a covid-19: o que foi publicado de mais relevante entre agosto de 2019 e julho de 2021?

ABSTRACT This study aims to investigate up-to-date scientific information about physical activity, COVID-19, and childhood cancer. This study is an integrative review. Research was conducted in the Science Direct database, using keywords in three different combinations. In total, 50 publications classified as the most relevant of each keyword combination were selected, 26 eligible publications were reached from August 2019 to July 2021, of which nine were duplicates. When exclusion criteria were applied, 11 complete studies were selected. The level of physical activity (PA) of children diagnosed with cancer or those who survived cancer is low. Changes due to the COVID-19 pandemic include the decrease in the level of PA and the increase in the use of technological devices. The minimum PA recommendations for this population vary but some evidence supports its importance and benefits in minimizing the adverse effects arising from cancer and from the performed medical treatment. Exercise-based interventions should be chosen and carried out considering the type of cancer and the stage of treatment the child is in due to the evidence of its effectiveness.

RESUMEN Este estudio tiene como objetivo investigar, en la base de datos ScienceDirect, la información científica actualizada sobre actividad física, COVID-19 y cáncer infantil, mediante una revisión integradora, en la cual se utilizaron las palabras clave en tres combinaciones diferentes. Se seleccionaron cincuenta publicaciones clasificadas como las más relevantes de cada combinación, y se alcanzaron 26 publicaciones elegibles en el periodo entre agosto de 2019 y julio de 2021, de las cuales nueve fueron textos duplicados. Al aplicar los criterios de exclusión, se seleccionaron 11 artículos completos. El nivel de actividad física (AF) de los niños diagnosticados de cáncer o supervivientes de cáncer es bajo, y entre los cambios provocados por la pandemia de la COVID-19 se encuentran la disminución del nivel de AF y el aumento en el uso de dispositivos tecnológicos. Las recomendaciones mínimas de AF para esta población varían entre sí, sin embargo, existe evidencia que respalda su importancia y los beneficios en la minimización de los efectos adversos derivados del propio cáncer y del tratamiento médico realizado. Las intervenciones basadas en ejercicios, para la cual ya existe evidencia de efectividad, deben elegirse y llevarse a cabo teniendo en cuenta el tipo de cáncer y la etapa de tratamiento en la que se encuentra el niño.

RESUMO O objetivo deste trabalho é investigar, na base de dados Science Direct, informações científicas sobre atividade física, covid-19 e câncer infantojuvenil, através de uma revisão integrativa, utilizando três combinações de palavras-chave. Cinquenta publicações mais relevantes de cada combinação de palavras-chave foram selecionadas, e chegou-se a 26 artigos elegíveis no período compreendido entre agosto de 2019 e julho de 2021, dos quais nove eram textos duplicados. Aplicando-se os critérios de exclusão, foram selecionados 11 estudos completos. Constatou-se que o nível de atividade física (AF) de crianças com câncer ou sobreviventes do câncer é baixo e que entre as mudanças causadas pela pandemia de covid-19 estão a diminuição do nível de AF e o aumento do uso de dispositivos tecnológicos. As recomendações mínimas de AF para essa população variam, entretanto há evidências que sustentam sua importância e seus benefícios ao minimizar os efeitos adversos oriundos do próprio câncer e do tratamento médico realizado. As intervenções baseadas em exercícios, para as quais já há evidência de eficácia, devem ser escolhidas e realizadas a partir do tipo de câncer e na fase do tratamento em que a criança está.

Plano de cuidados para sobreviventes de câncer de mama: tradução e validação / Plan de cuidados para sobrevivientes de cáncer de mama: traducción y validación / Care plan for breast cancer survivors: translation and validation

Resumo Objetivo Traduzir, adaptar transculturalmente e validar o conteúdo do Treatment Summary and Survivorship Care Plan (TSSCP-S) para sobreviventes brasileiras de câncer de mama. Métodos Estudo metodológico, quantitativo, executado de acordo com as etapas de tradução, compatibilização e retrotradução, construção de consenso de opiniões de um grupo de especialistas para a validação de conteúdo, de acordo com a Técnica Delphi e avaliação do usuário. Resultados O plano traduzido e adaptado transculturalmente foi avaliado por 10 profissionais, entre estes, enfermeiros, médicos, psicológos, nutricionista e fisioterapeuta, possuidores de titulação, produção científica, conhecimento e tempo de atuação na temática e o consenso foi obtido em duas rodadas. O instrumento apresentou coeficiente de validade de conteúdo de 83,3% na segunda rodada da Delphi. Na avaliação dos domínios conteúdo, clareza, utilidade, responsividade cultural e socioecológica, a concordância foi de 93,3%. O perfil sóciodemográfico e clínico das usuárias foi heterogêneo, contribuindo para os ajustes culturais necessários, com consenso final de 93,9%. Conclusão O plano de cuidados foi traduzido para o português do Brasil, adaptado transculturalmente e seus conteúdos foram validados, considerando as políticas de saúde nacionais.

Resumen Objetivo Traducir, adaptar transculturalmente y validar el contenido del Treatment Summary and Survivorship Care Plan (TSSCP-S) para sobrevivientes brasileñas de cáncer de mama. Métodos Estudio metodológico, cuantitativo, ejecutado de acuerdo con las etapas de traducción, compatibilización y retrotraducción, construcción de consenso de opiniones de un grupo de especialistas para la validación de contenido, de acuerdo con el método Delphi y evaluación del usuario. Resultados El plan traducido y adaptado transculturalmente fue evaluado por diez profesionales, entre ellos enfermeros, médicos, psicólogos, nutricionista y fisioterapeuta, con titulación académica, producción científica, conocimiento y tiempo de actuación en la temática, y el consenso se obtuvo en dos rondas. El instrumento presentó un coeficiente de validez de contenido del 83,3 % en la segunda ronda de Delphi. En la evaluación de los dominios contenido, claridad, utilidad, responsividad cultural y socioecológica, la concordancia fue del 93,3 %. El perfil sociodemográfico y clínico de las usuarias fue heterogéneo, lo que contribuye a los ajustes culturales necesarios, con consenso final del 93,9 %. Conclusión El plan de cuidados fue traducido al portugués de Brasil, adaptado transculturalmente y sus contenidos fueron validados, considerando las políticas sanitarias nacionales.

Abstract Objective To translate, cross-culturally adapt and validate the content of the Treatment Summary and Survivorship Care Plan (TSSCP-S) for Brazilian breast cancer survivors. Methods Methodological, quantitative study performed according to the steps of translation, compatibility and back-translation, construction of consensus of opinions in a group of experts for content validation, according to the Delphi technique and user evaluation. Results The translated and cross-culturally adapted plan was evaluated by ten professionals, including nurses, physicians, psychologists, nutritionists and physical therapists with a degree, scientific production, knowledge and time working on the subject. Consensus was obtained in two rounds. The instrument presented a content validity coefficient of 83.3% in the second round of Delphi. In the evaluation of content, clarity, usefulness, cultural and socioecological responsiveness domains, agreement was 93.3%. The sociodemographic and clinical profile of users was heterogeneous, contributing to the necessary cultural adjustments, with a final consensus of 93.9%. Conclusion The care plan was translated into Brazilian Portuguese, cross-culturally adapted and its contents were validated considering national health policies.

Estado emocional de los pacientes pos-COVID-19 en la Región Amazonas del Perú / Emotional Status of Post-COVID-19 Patients in the Amazonas Region of Peru

Introducción: La pandemia de la COVID-19 no solo ocasionó problemas de salud física, sino también alteraciones a nivel emocional en las personas que contrajeron esta enfermedad. Objetivo: Describir el estado emocional de los pacientes pos-COVID-19 de un distrito de la Región Amazonas del Perú. Métodos: Estudio descriptivo, correlacional y transversal, realizado en el distrito de Copallín, Región Amazonas, Perú, durante julio-noviembre de 2021. La población estuvo conformada por 245 pacientes pos-COVID-19, la muestra fue de 235 pacientes seleccionados por muestreo no probabilístico por conveniencia. Se aplicó el Cuestionario de DASS-21 (Depression Anxiety and Stress Scale - 21, por sus siglas al inglés) y la versión estandarizada al idioma castellano de Antúnez & Vinet, 2012. Para procesar la información se utilizó el programa Statistical Package for the Social Sciences versión 25, se usó la estadística descriptiva y la prueba Chi cuadrado de Pearson. Resultados: El 54,47 por ciento tiene entre los 18 y 29 años; 51,91 por ciento son mujeres; el 63,83 por ciento solteros. El 55,32 por ciento presenta depresión, el 56,60 por ciento tiene ansiedad en diferentes niveles y el 68,09 por ciento no presenta estrés. Además, el análisis correlacional reportó que la depresión se relaciona con la hospitalización (p = 0,001) y secuelas de la COVID-19 (p < 0,001); la ansiedad con grado de instrucción (p = 0,015), hospitalización (p < 0,001) y secuelas (p < 0,001); el estrés con grado de instrucción (p = 0,003) y secuelas (p < 0,001). Conclusiones: La mayoría de los pacientes pos-COVID-19 presentaron diferentes niveles de depresión y ansiedad, por lo cual se requiere de intervenciones efectivas para evitar consecuencias en la salud mental(AU)

Introduction: The COVID-19 pandemic not only caused physical health problems, but also emotional alterations in people who contracted this disease. Objective: To describe the emotional state of post-COVID-19 patients in a district of the Amazon Region of Peru. Methods: Descriptive, correlational and cross-sectional study, carried out in the district of Copallín, Amazonas Region, Peru, during July-November 2021. The population consisted of 245 post-COVID-19 patients, the sample was 235 patients selected by non-probabilistic convenience sampling. The DASS-21 Questionnaire (Depression Anxiety and Stress Scale - 21) and the standardized Spanish version of Antúnez & Vinet, 2012 were applied. The Statistical Package for the Social Sciences version 25 was used to process the information, and descriptive statistics and Pearson's Chi-square test were used. Results: 54.47 percent were between 18 and 29 years of age; 51.91 percent were women; 63.83 percent were single. 55.32 percent present depression, 56.60 percent have anxiety at different levels and 68.09 percent do not present stress. In addition, correlational analysis reported that depression is related to hospitalization (p = 0.001) and sequelae of COVID-19 (p < 0.001); anxiety with educational level (p = 0.015), hospitalization (p < 0.001) and sequelae (p < 0.001); stress with educational level (p = 0.003) and sequelae (p < 0.001). Conclusions: Most post-COVID-19 patients presented different levels of depression and anxiety, thus requiring effective interventions to avoid mental health consequences(AU)

Alteraciones Provocadas por el SARS-CoV-2 durante el 2020: Una Mirada a sus Secuelas. Revisión Narrativa / Alterations Caused by SARS-CoV-2 during 2020: A Look at its Aftermath. Narrative Review

Introducción. El 11 de marzo del 2020, la OMS declaró a la COVID-19 como pandemia. Hoy se han establecido diversas secuelas posteriores a la fase aguda por infección por SARS-CoV-2, y diversos autores han mostrado que esta enfermedad persiste en un gran número de personas luego de la fase aguda. Objetivo. Identificar y describir las características previas de pacientes que presentan secuelas post infección por COVID-19. Métodos. Se realizaron 2 búsquedas bibliográficas en diferentes bases de datos, donde se seleccionaron 15 artículos en total según criterios de inclusión y exclusión. Se hizo un análisis cualitativo de las referencias y fueron separadas según tipo de secuela reportada. Resultados. Dentro de las características demográficas de las personas que presentaron secuelas post infección por COVID-19 se encuentran la edad, sexo, comorbilidades preexistentes y, en algunos casos, el IMC. Dentro de las características clínicas se incluye la sintomatología presente en fase aguda, estado de gravedad, tiempo de estadio hospitalario, y resultados de exámenes imagenológicos y de laboratorio. Cada secuela fue especificada según el tipo asociado a alteración cardiovascular, músculo-esquelética, respiratoria y neurológica. Conclusión. La mayoría de los pacientes con secuelas tienen una edad media de 50 años, siendo las mujeres las que presentaron una mayor prevalencia. Los antecedentes de HTA y DM se encontraron en las cinco áreas analizadas, mientras que las enfermedades cardiovasculares y el EPOC sólo se encontraron en algunas secuelas. Los síntomas predominantes en la fase aguda de la enfermedad varían entre el grupo de secuelas neurológicas en comparación con los demás grupos.

Background. On March 11, 2020, WHO declared COVID-19 a pandemic. Today, several post-acute sequelae of SARS-CoV-2 infection have been established, but several authors have shown that this disease persists in many people after the acute phase. Objective. Identify and describe the previous characteristics of patients who present sequelae after infection with COVID-19. Methods. 2 bibliographic searches were performed in different databases, where a total of 15 articles were selected according to inclusion and exclusion criteria. A qualitative analysis of the references was made and they were separated according to the type of sequelae reported. Results. Among the demographic characteristics of the persons who presented sequelae after infection with COVID-19 were age, sex, pre-existing comorbidities, and in some cases BMI. The clinical characteristics include the symptoms present in the acute phase, state of severity, length of hospital stay, and results of imaging and laboratory tests. Each of them is specified according to the type of sequelae associated with cardiovascular, musculoskeletal, respiratory and neurological. Conclusion. The majority of patients with sequelae had a mean age of 50 years, with women presenting a higher prevalence. A history of hypertension and DM were found in all five areas analyzed, while cardiovascular disease and COPD were only found in some sequelae. The predominant symptoms in the acute phase of the disease varied among the neurological sequelae group compared to the other groups.

Sobrevivir al cáncer: Narrativas de un grupo de personas a partir de sus experiencias

Resumen: Objetivo: Comprender los significados que las personas que sobreviven al cáncer le dan a su vida después de este suceso. Método: Estudio realizado desde el paradigma naturalista con enfoque cualitativo; se aplicó el método biográfico de historia de vida, mediante entrevistas en profundidad a cinco sobrevivientes al cáncer. Se realizó análisis de contenido. Resultados: Emergieron cuatro categorías: el estigma del cáncer en la sobrevida; redes de apoyo para la sobrevida; cuidado de sí en la sobrevida, y trascendencia. Los datos permitieron alcanzar un mayor nivel de comprensión de sus necesidades y cómo están siendo atendidas por los prestadores de servicios de salud en Colombia. Conclusiones: Los sobrevivientes transforman sus cuidados hacia una perspectiva más integral y reinterpretan su nueva vida a partir de la reflexión y la creencia en Dios. En enfermería, los cuidados son orientados a acompañar los principales cambios en el continuo de la sobrevida que se dan desde el momento de la curación.

Resumo: Objetivo: Entender os significados que as pessoas que sobrevivem ao câncer dão às suas vidas após esse evento. Método: Um estudo baseado no paradigma naturalista com uma abordagem qualitativa, o método de história de vida biográfica foi aplicado através de entrevistas em profundidade com cinco sobreviventes de câncer. Foi realizada uma análise de conteúdo. Resultados: Quatro categorias emergiram: o estigma do câncer sobre a sobrevivência; redes de apoio à sobrevivência; autocuidado sobre a sobrevivência; e transcendência. Os dados permitiram um maior nível de compreensão de suas necessidades e de como eles estão sendo tratados pelos prestadores de serviços de saúde na Colômbia. Conclusões: Os sobreviventes transformam seus cuidados em uma perspectiva mais holística e reinterpretam sua nova vida com base na reflexão e na crença em Deus. Na enfermagem, o cuidado é orientado para acompanhar as principais mudanças na continuidade da sobrevivência que ocorrem a partir do momento da cura.

Abstract: Objective: Our aim was to understand cancer survivors' meanings of life after their cancer experience. Method: This was a biographical and qualitative study carried out from a naturalistic approach. We conducted in-depth interviews with five cancer survivors and analyzed the resulting content. Results: We found four categories: the stigma of cancer in survivorship; survivorship support networks; self-care in survivorship; and transcendence. The results gave us a greater understanding of survivors' needs and how they are being addressed by healthcare providers in Colombia. Conclusions: Cancer survivors shift towards a more holistic view of their health and transform the meaning of their life based on reflection and belief in God. Therefore, the nursing practice should focus on assisting them in these changes since healing.

Fear of cancer recurrence in informal caregivers of childhood cancer survivors / Miedo a la recurrencia del cáncer en cuidadores de supervivientes de cáncer infantil

Abstract Background Fear of cancer recurrence is one of the most distressing psychological consequences in cancer survivors and their informal primary caregivers (IPC). IPC of childhood cancer survivors (CCS) are often their mothers, which could intensify fear of cancer recurrence (FCR) and its impact on both IPC and CCS. However, the phenomenon has not been widely described in this specific population. Objective To summarize and analyze current evidence on the evaluation and management of FCR among IPC of CCS. Method A narrative review of studies included in four databases (PsycInfo, Medline, CINALH, and Web of Science) with no language or year of publication restrictions. Results Measures specifically developed to assess FCR among IPC of CCS comprising an interview and a questionnaire with initial psychometric evaluations and two short, online intervention programs based on cognitive-behavioral-contextual therapy were identified (ENGAGE and CASCAdE). Both have demonstrated acceptability in parents of CCS in high-income countries; preliminary evidence also exists of the effectivity of CASCAdE in reducing FCR. Discussion and conclusion Given the limitations of this area of psychological evaluation, the Fear of Cancer Recurrence Inventory, originally developed for adult cancer survivors, constitutes the most suitable tool for evaluating FCR among IPC of CCS. The CASCAdE program seems a promising intervention for IPC of CSS, although cultural adaptations, evaluations of its acceptability in low- and middle-income countries, and controlled studies in large samples are still required.

Resumen Antecedentes El miedo a la recurrencia del cáncer es una de las consecuencias psicológicas más angustiantes en los supervivientes y sus cuidadores primarios informales (CPI). Los CPI de supervivientes de cáncer infantil (SCI) a menudo son sus madres, lo que podría intensificar el miedo a la recurrencia (MR) y su impacto tanto a los CPI como a los SCI. Sin embargo, el fenómeno no se ha descrito ampliamente en esta población específica. Objetivo Resumir y analizar la evidencia actual sobre la evaluación y manejo del MR entre CPI de SCI. Método Se realizó una revisión narrativa de los estudios incluidos en cuatro bases de datos (PsycInfo, Medline, CINALH y Web of Science) sin restricciones de idioma o año de publicación. Resultados Se identificaron instrumentos desarrollados específicamente para evaluar MR entre CPI de SCI que comprenden una entrevista y un cuestionario, además de dos programas de intervención en línea basados en terapia cognitivo-conductual-contextual (ENAGE y CASCAdE). Ambos demostraron aceptabilidad en los padres de SCI en países de ingresos altos. También existe evidencia preliminar de la efectividad de CASCAdE en la disminución del MR. Discusión y conclusión Dadas las limitaciones de esta área de evaluación psicológica, el Inventario del Miedo a la Recurrencia del Cáncer, desarrollado originalmente para supervivientes adultos, constituye la herramienta más adecuada para evaluar MR en los CPI de SCI. El programa CASCAdE parece una intervención prometedora para CPI de SCI, aunque aún requiere adaptaciones culturales, evaluaciones de aceptabilidad en países de ingresos medio-bajos y estudios controlados con nuestras más grandes.

EXPLORING ACTUAL CAUSES OF SUICIDE: LIVED EXPERIENCE OF SUICIDE SURVIVORS IN KOLKATA, INDIA

Background: An increasing rate of suicide by different age groups of people is a grievous social problem in the world. India is not an exception. This study aims to identify the actual causes of suicide by analysing the lived experiences of suicide survivors and explore the preventive strategy. A phenomenological approach wa Methodology: s used. As study participants, nine suicide survivors selected through snowball sampling were face to face interviewed. The Results: lived experience of suicide survivors is summarized into four themes: the first theme is feelings during suicide attempts, the second theme is the perception of triggers, the third theme is behavioural changes and the fourth theme is expectations. At the time of attempting suicide or before it if people get support from society, and feel desired and loved they won't attempt suicide. Strong informal social connectedness to preve Conclusion: nt suicide is not only relevant but essential to prevention efforts.

High Residual Gradient Following a Self-Expandable Transcatheter Aortic Valve-in-Valve Implantation — Risk Factor Analysis, Outcomes, and Survival

Abstract Introduction: Transcatheter aortic valve-in-valve implantation (TAVI-ViV) can be associated with unfavorable hemodynamic outcomes. This study aimed to estimate the prevalence, identify the risk factors, and evaluate the outcomes and survival of patients with high residual gradients after TAVI-ViV. Methods: A total of 85 patients were included in the study. The cohort was divided into group A, with postprocedural mean pressure gradient (PG) ≥ 20 mmHg, and group B, with mean PG < 20 mmHg. Results: Postprocedural PG ≥ 20 mmHg was observed in 24.7% of the patients. In a univariate analysis, preoperative gradient, pre-existing patient-prosthesis mismatch (PPM), deep valve implantation, small degenerated valves, and an older generation of transcatheter aortic valves were found to be risk factors for high residual gradient. Multivariate analysis showed that preexisting maxPG > 60 mmHg, implantation level of 4 mm below neo-annulus, and degenerated valve size ≤ 23 mm were independent predictors of high residual gradient. There were no differences in early morbidity (myocardial infarction, pacemaker implantation, stroke, acute renal insufficiency) between groups. Kaplan-Meier estimated that the survival rate was comparable at one and five years regardless of postoperative gradient. Survivors with high residual mean gradient were significantly affected by a high New York Heart Association (NYHA) class. Conclusion: High residual transvalvular gradient after TAVI-ViV is not rare, but it does not significantly affect mortality. High residual mean gradient has a negative impact on NYHA functional class improvement after the procedure. High preoperative gradient, implantation level, and small failed bioprosthesis may predispose to increased residual gradient.

Management Strategies for Sexuality Complaints after Gynecologic Cancer: A Systematic Review / Estratégias para enfrentamento de queixas da sexualidade após câncer ginecológico: uma revisão sistemática

Abstract Objective To explore the main sexuality complaints of gynecologic cancer survivors after treatment and to identify the care strategies provided. Data Source Searches were conducted in six electronic databases: Scopus, Web of Science, LILACS, MEDLINE, PsychINFO, and EMBASE. Study Selection Articles published between 2010 and 2020 were selected and the following descriptors were used in the English language: female genital neoplasms and gynaecological cancer. The methodological quality of the studies used the Mixed Methods Appraisal Tool (MMAT). Data Collection The primary data extracted were: names of the authors, year of publication, country of origin, objective and type of study, data collection instrument, sample size and age range, types of cancer, and symptoms affected with the strategies adopted. Data Summary A total of 34 out of 2,536 screened articles were included. The main strategies found for patient care were patient-clinician communication, practices for sexuality care, individualized care plan, multiprofessional team support, and development of rehabilitation programs. For sexuality care, the most common practices are pelvic physiotherapy sessions and the use of vaginal gels and moisturizers. Conclusion The main complaints identified in the scientific literature were low libido and lack of interest in sexual activity, vaginal dryness, pain during sexual intercourse, and stenosis. Different care strategies may be adopted, such as follow-up with a multidisciplinary health team and sexual health rehabilitation programs, which could minimize these symptoms and ensure the quality of life of patients.

Resumo Objetivo Explorar as principais queixas da sexualidade com sobreviventes de câncer ginecológico após o tratamento e identificar as estratégias de cuidados prestados. Fonte dos Dados As buscas foram realizadas em seis bases eletrônicas: Scopus, Web of Science, LILACS, MEDLINE, PsychINFO e EMBASE. Seleção dos Estudos Foram selecionados artigos publicados entre 2010 e 2020 e os descritores utilizados (em inglês) foram female genital neoplasms e gynaecological cancer. A qualidade metodológica dos estudos utilizou a ferramenta Mixed Methods Appraisal Tool (MMAT). Coleta de Dados Os principais dados extraídos foram: nomes dos autores, ano de publicação, país de origem, objetivo e tipo de estudo, instrumento para coleta de dados, tamanho da amostra e faixa etária, tipos de câncer, os sintomas acometidos e as estratégias adotadas. Síntese dos Dados Dos 2,536 artigos identificados, 34 foram incluídos. As principais estratégias encontradas para os cuidados aos pacientes foram a comunicação paciente-médico, práticas para os cuidados sexuais, plano de cuidados individualizado, apoio a equipes multiprofissionais e desenvolvimento de programas de reabilitação. Para os cuidados de sexualidade, as práticas mais comuns são sessões de fisioterapia pélvica e o uso de géis vaginais e hidratantes. Conclusão As principais queixas identificadas na literatura científica foram baixa libido e falta de interesse na atividade sexual, secura vaginal, dor durante a relação sexual e estenose. Diferentes estratégias de cuidados podem ser adotadas, como o acompanhamento com uma equipe de saúde multidisciplinar e programas de reabilitação da saúde sexual, as quais poderiam minimizar estes sintomas e garantir a qualidade de vida dos pacientes.

Resignificación de la vida por parte de jóvenes sobrevivientes al cáncer hematológico / Resignification of Life by Young People Survivors of Hematologic Cancer

Introducción: Los jóvenes con enfermedades oncológicas enfrentan dificultades durante los períodos de diagnóstico, tratamiento y recuperación. Estos procesos complejos cargados de experiencias vitales inusitadas producen la transformación de su conciencia y los lleva a construir nuevos significados en la manera de comprender, relacionarse y actuar en el mundo que los rodea. Objetivo: Comprender el (re)significado de la vida a partir de la experiencia de los jóvenes que sobrevivieron al cáncer hematológico. Métodos: Estudio cualitativo, que utilizó la Teoría Fundamentada en Datos como metodología y el referencial de la Teoría de la Complejidad de Morin. Se realizaron entrevistas en profundidad a 12 adolescentes sobrevivientes de cáncer hematológico. El tamaño de muestra fue determinado al alcanzar nivel de saturación. El análisis fue simultáneo durante la recolección de los datos, mediante codificación abierta, axial y selectiva según lo señalan Strauss y Corbin. Resultados: Emergieron dos categorías: Reorganizando su vida por medio de cambios y aprendizajes para vencer al cáncer y, Asumiendo una mejor comprensión y compromiso con los demás y consigo mismo. Conclusiones: Las experiencias vividas por jóvenes sobrevivientes que padecen de cáncer modifican su forma de vivir y se tornan más comprensivos con el sufrimiento que ocasiona la enfermedad. Esta situación los hace más solidarios y comprometidos con su contexto social sobre todo con su familia y con pacientes oncológicos(AU)

Introduction: Young people with oncological diseases face difficulties during the periods of diagnosis, treatment and recovery. These complex processes loaded with unusual life experiences produce the transformation of their consciousness and lead them to construct new meanings in the way that they understand, relate and act in the world around them. Objective: To understand the (re)signification of life from the experience of young survivors of hematological cancer. Methods: A qualitative study was carried out, using the data driven theory as the methodology and Morin's complexity theory as the referent. In-depth interviews were conducted with twelve adolescent hematologic cancer survivors. The sample size was determined by reaching the saturation level. The analysis was simultaneous during data collection, using open, axial and selective coding according to Strauss and Corbin. Results: Two categories emerged: 1. reorganizing their life through changes and learning to overcome cancer and 2. assuming a better understanding and commitment to others and to themselves. Conclusions: The experiences lived by young cancer survivors modify their way of living as they become more understanding of the suffering caused by the disease. This situation makes them more supportive and committed to their social context, especially with their family and with cancer patients(AU)