scholarly journals CÂNCER INFANTIL: VIVÊNCIAS DE CRIANÇAS EM TRATAMENTO ONCOLÓGICO

2017 ◽  
Vol 7 (3/4) ◽  
pp. 51-55 ◽  
Author(s):  
Patrick Leonardo Nogueira Da Silva ◽  
Greice Carvalho Xavier ◽  
Valdira Vieira De Oliveira ◽  
Mirela Lopes De Figueredo ◽  
Patrícia Fernandes Do Prado ◽  
...  

Objetivo: conhecer a percepção da criança em tratamento oncológico sobre a vivência da doença. Metodologia: estudo descritivo, observacional, com abordagem qualitativa. Participaram sete crianças com câncer, mediante entrevista semiestruturada, cujos dados foram estudados por meio da análise de conteúdo. Resultados: foram identificadas quatro categorias: Impedimentos e limitações ao enfrentamento da doença; Brincando e aprendendo; Imaginando ser diferente o ambiente hospitalar; Vivenciando o medo e o desconforto dos procedimentos. Conclusão: o diagnóstico de câncer em crianças e a hospitalização são fatores que privam suas atividades rotineiras e lhes acarretam desconforto emocional e físico.Descritores: Enfermagem pediátrica, Serviço hospitalar de oncologia, Emoções manifestasCHILDHOOD CANCER: EXPERIENCES OF CHILDREN IN TREATMENT ONCOLOGICObjective: to know the child’s perception of cancer treatment on the experience of the disease. Methods: A descriptive, observational study with a qualitative approach. Participants were seven children with cancer through semi-structured interviews and data were analyzed using content analysis. Results: Four categories were identified: Impediments and limitations to cope with the disease; Playing and Learning; Imagining be different from the hospital environment; Experiencing fear and discomfort of procedures. Conclusion: The diagnosis of cancer in children and hospitalization are factors that deprive their routine activities and carry them emotional and physical discomfort.Descriptors: Pediatric nursing, Oncology service hospital, Expressed emotion.CÁNCER INFANTIL: EXPERIENCIAS DE LOS NIÑOS EN TRATAMIENTO ONCOLÓGICOObjetivo: conocer la percepción del niño en tratamiento del cáncer sobre la experiencia de la enfermedad. Métodos: Estudio descriptivo, observacional con un enfoque cualitativo. Los participantes fueron siete niños con cáncer a través de entrevistas semiestructuradas y los datos se analizaron mediante análisis de contenido. Resultados: Se identificaron cuatro categorías: Los impedimentos y limitaciones para hacer frente a la enfermedad; Jugar y aprender; Imaginando ser diferente del entorno del hospital; Experimentar el miedo y la incomodidad de los procedimientos. Conclusión: El diagnóstico de cáncer en niños y la hospitalización son factores que privan a sus actividades de rutina y los llevan malestar emocional y físico.Descriptores: Enfermería pediátrica, Servicio de oncología en hospital, Emoción expresada.

2015 ◽  
Vol 8 (7) ◽  
pp. 100 ◽  
Author(s):  
Masoud Bahrami ◽  
Paymaneh Shokrollahi ◽  
Shahnaz Kohan ◽  
Ghodratollah Momeni ◽  
Mozhgan Rivaz

<p><strong>INTRODUCTION:</strong> Domestic violence is a continual stressor that motivates its victim to react. The way a woman deals with her husband’s violence determine the consequence of the violent relationship. In the present study, a qualitative approach was employed to investigate women’s reactions to and ways of coping with domestic violence.</p><p><strong>METHOD:</strong> Semi-structured interviews were conducted in 2014 with 18 women who experienced domestic violence in an attempt to explain how women deal with domestic violence. After the interviews were transcribed word by word, they were explored in the form of meaningful units and encoded as subcategories and categories<strong> </strong>through inductive content analysis. The reliability and validity of the interviews were measured by an external supervisor.</p><p><strong>RESULTS: </strong>Two categories of reaction and coping were identified through content analysis: passive and non-normative measures and active measures. Passive and non-normative measures included the subcategories of harmful behaviors, retaliation, tolerance, and silence. Active measures included seeking help and advice, legal measures, leaving the spouse, positive and health promoting measures.</p><p><strong>CONCLUSION: </strong>In the present study, ways of coping with a husband’s violence among women experiencing domestic violence were divided into two categories: passive and non-normative measures and active measures. These categories confirmed the models of coping with stress in previous studies. Adopting an appropriate approach to dealing with domestic violence is affected by a woman’s capacity and beliefs, the dominant culture, intensity of the violence, available social and legal supports, and effectiveness of evaluation measures. To generalize service provision to victimized women, the type of coping and the reason for adopting the chosen approach need to be taken into account.</p>


2016 ◽  
Vol 15 (2) ◽  
Author(s):  
Tássia Regine de Morais Alves ◽  
Francisco Arnoldo Nunes de Miranda ◽  
Glauber Weder dos Santos Silva ◽  
Jovanka Bittencourt Leite de Carvalho ◽  
Cecília Nogueira Valença ◽  
...  

Aim:  To  understand  the  importance  and  the  difficulties  faced  by women  when  adhering  to  exclusive  breastfeeding.  Method:  This  is  an exploratory  and descriptive study, using a qualitative approach, in which semi-structured interviews were conducted with 14 women. Data treatment occurred by means of the content analysis, in the form of a thematic analysis. Results: Most women revealed knowing the importance and  benefits  of  breastfeeding  for  being  an  important  practice,  since  it  provides  good nourishment   and   aids   the   development   of   the   child.   The   aspects   that   benefit breastfeeding  women  were  made  explicit;  however,  these  were  given  less  focus  when compared to the aspects related to the baby's health. Conclusion: We should point out the  need  to  incorporate  practices  beyond  the  biological  dimension,  to  understand  the characteristics  of  each  woman  and  to  encourage  self-care  as  an  important  issue  for them.


2016 ◽  
Vol 15 ◽  
pp. 521
Author(s):  
Malena Storani Gonçalves Rosa ◽  
Ândrea Cardoso De Sousa

General  aim:  to  evaluate  whether  PET-Health  has  been  constituted as   a   possibility   with   regard  to   continuing   education   for   professionals/preceptors employed by the health services. Specific aims: to identify and characterize the actions of Pet-Health, recognized by preceptors as a form of continuing education. Method: This is  a  descriptive  and  evaluative  study using  a  qualitative approach, to  be  undertaken  in mental health services that make use of PET experience in Niterói/RJ. For data collection, semi-structured interviews will be conducted with professionals who act as PET-HEALTH preceptors  in  the  mental  health  network.  Information  processing  will  be  based  on content  analysis.  At  the  end  of  this  study,  benefits  pointing  to  the  power  that  shapes PET-Health with regard to continuing education are expected.


2009 ◽  
Vol 17 (1) ◽  
pp. 52-58 ◽  
Author(s):  
Júlia Trevisan Martins ◽  
Maria Lúcia do Carmo Cruz Robazzi

The purpose of this study was to investigate the feelings of suffering that Intensive Care Unit (ICU) nurses experience, and the strategies they use to face these feelings. It is a descriptive study using a qualitative approach and based on content analysis. The study used previous studies on Work Psychodynamics as complementary groundwork. Data collection occurred by means of semi-structured interviews, which were transcribed, categorized, and subcategorized. Results showed that suffering is related to: taking care of a young patient in critical condition, taking problems home, the patient's family, the team's work, and technology at work. As for the defense strategies used, emphasis is given to the search for strength in religion, promoting inter-relationships among team members, engaging in physical activity, and withdrawing from the patient.


Author(s):  
Michele Cristina Miyauti da Silva ◽  
Luís Carlos Lopes Júnior ◽  
Lucila Castanheira Nascimento ◽  
Regina Aparecida Garcia de Lima

ABSTRACT Objective: to investigate health professionals' knowledge about the concept, assessment and intervention in fatigue in children and adolescents with cancer. Method: exploratory study with qualitative approach, with 53 health professionals (10 nurses, 33 assistant nurses, 3 physicians, 3 nutritionists, 2 psychologists and 2 physical therapists). Semi structured interviews were held, which were recorded and analyzed by means of inductive thematic content analysis. Results: the data were organized around three themes: knowledge of health professionals about fatigue; identification of fatigue and interventions to relieve fatigue. Conclusion: the results indicate the health professionals' limited knowledge about fatigue, as well as the lack of investment in their training and continuing education. Most of all, the lack of research on the theme in the Brazilian context remains a barrier to support improvements in care for this symptom in children and adolescents with cancer.


2019 ◽  
Vol 28 ◽  
Author(s):  
Marinete Esteves Franco ◽  
Marina de Góes Salvetti ◽  
Suzana Cristina Teixeira Donato ◽  
Ricardo Tavares de Carvalho ◽  
Ednalda Maria Franck

ABSTRACT Objective: to understand the perception of dignity of patients in palliative care and to identify factors that may increase or decrease the sense of dignity. Method: an exploratory study with a qualitative approach, carried in a Palliative Care Center in São Paulo (Brazil), with the Chochinov’s Dignity Model as theoretical framework and content analysis as methodological framework. The participants of this study were 20 patients in palliative care, assessed through semi-structured interviews based on three questions: "What is dignity for you?", "What increases your dignity?", "What decreases your dignity?" The interviews were recorded with the patients’ authorization, from September to November 2017, and transcribed for content analysis. Results: the analysis of the perception of dignity allowed the identification of three categories: Correct person, Autonomy/independence and Socio-political factors. The factors that increased the sense of dignity were the following: Care, Independence/autonomy, Leisure/positive thinking/being with friends. And those that decreased it were the following: Behaviors/attitudes, Health status and Economic situation. Conclusion: the perception of dignity of patients in palliative care was influenced by health professionals and caregivers. Being a “correct person”, maintaining autonomy, being cared for and respected has increased the sense of dignity. Urban violence and the lack of compliance with accessibility policies have reduced the sense of dignity among palliative care patients.


2015 ◽  
Vol 77 (9) ◽  
Author(s):  
Fatin Filzahti Ismail ◽  
Rozilawati Razali

Software testing outsourcing is becoming attractive among organisations that desire to gain high quality products within reasonable cost while allowing testing experts to assure its quality. Despite these promising advantages however, organisations have yet to learn the factors that contribute to such projects’ success. The necessary planning and actions could not thus be taken towards the effort. Consequently, software testing outsourcing projects still fail. This study aimed to address this concern by collating the factors from previous research. The investigation continued by confirming the factors besides discovering other relevant factors from software testing practitioners. This study adopted qualitative approach where it employed semi-structured interviews involving five practitioners, who represented both client and vendor. The data were analysed using content analysis. The results show that there are two aspects to be considered, namely Process and People. The former contains nine factors and the latter comprises four factors. Each factor has specific elements, which delineates the characteristics or roles that it owns. The findings provide practitioners with understanding of conducting software testing outsourcing projects effectively.


Author(s):  
Zelia Breda ◽  
Adriana Santos ◽  
Tamara Kliček ◽  
Gorete Dinis

The segment of independent travelers has experienced big growth in recent years, not only worldwide but also in Portugal. This phenomenon, which is not recent, has been gaining momentum in recent times, with women playing an important role. This chapter explores the literature on solo female travel, seeking to understand the motivations, as well as the difficulties encountered during the journey. To this end, a qualitative approach was used, with semi-structured interviews being conducted to 24 Portuguese women. The content analysis of the interviews was done with the assistance of the WebQDA software. Results show that most women traveling alone are young, single, and childless, identifying themselves mostly as adventurous, outgoing, and independent. The lack of travel companion, the freedom of choice, the experience and adventure, and the escape from the daily routine are highlighted as motivations to travel alone. The main difficulties identified are loneliness, harassment, fear of walking alone at night or being robbed.


2015 ◽  
Vol 36 (1) ◽  
pp. 49-55 ◽  
Author(s):  
Michele Ebert ◽  
Elisiane Lorenzini ◽  
Eveline Franco da Silva

Childhood autism is characterized by severe and global impairment in several areas of human development and demands extensive care and dependence on the parents. The objective of this study was to understand the perceptions of mothers of children with autism regarding changes suffered by the child and their trajectories in search of an autism diagnosis. This is an exploratory descriptive study with a qualitative approach conducted with ten participant mothers. Data were collected in 2013 by means of semi-structured interviews. Thematic content analysis produced the following categories: perceptions of mothers as to changes in behaviour and/or development of their children; and trajectories of mothers in search of a diagnosis for their children. After the perception of changes in behaviour/development, mothers face an arduous trajectory of healthcare service utilization.


2018 ◽  
Vol 40 (5) ◽  
pp. 944-965 ◽  
Author(s):  
Lorna McWilliams ◽  
Caroline Swarbrick ◽  
Janelle Yorke ◽  
Lorraine Burgess ◽  
Carole Farrell ◽  
...  

AbstractThe risk of living with dementia and, separately, cancer, increases exponentially with age. However, to date, there is a paucity of research investigating the experiences of people living with both these conditions. This study used semi-structured interviews to explore the decision-making and treatment options for people who live with both dementia and cancer. In total, ten people living with both dementia and cancer (aged 39–93 years) and nine family carers were interviewed. Braun and Clarke's approach to thematic analysis was used together with framework matrices to organise the data. In this article four sequential and descriptive themes are presented. ‘Reaching a diagnosis of cancer’ describes the vital role that family carers play in encouraging the person with dementia to seek an explanation for their presenting (undiagnosed cancer) symptoms to their general practitioner. ‘Adjusting to the cancer diagnosis when living with dementia’ outlines a variety of emotional and practical responses to receiving news of the diagnosis. ‘Weighing up the cancer treatment options’ highlights the different decisions and circumstances that family carers and people living with both dementia and cancer are faced with post-diagnosis. ‘Undergoing cancer treatment’ shares the finding that cancer treatment decision-making was not straightforward and that people living with both dementia and cancer would often forget about their cancer and what procedures they had been through.


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