Pub Date : 2023-05-17DOI: 10.15253/2175-6783.20232483200
Isaura Emília Rodrigues Espinola, Lara Fernandes de Carvalho, D. F. D. Silva, José Madson Medeiros Souza, Fabiana Maria Rodrigues Lopes de Oliveira, José Uilson Ferreira Galindo Júnior, Keylla Talitha Fernandes Barbosa
Objective: to understand the perception of the LGBTQIA+ elderly person about social and programmatic vulnerability. Methods: qualitative study developed with ten elderly persons. The collection was done through an interview supported by a semi-structured instrument. Elderly people of both sexes and non-binary assisted in a reference center were included. We adopted content analysis through the thematic modality for data systematization. Results: human aging raised discussions about specific needs, such as sexuality. Treated as taboos, elderly individuals who belonged to sexual minority groups suffered double invisibility, especially in health services. Furthermore, the lack of social and family support resulted in psychological suffering and social vulnerability. Conclusion: through the reports, it is possible to identify important gaps in the assistance to the LGBTQIA+ elderly person, such as difficulty of access and generic health practices, which do not consider the particularities of this population, as well as discrimination and lack of spaces for coexistence. Contributions to practice: population aging raises discussions about the adequacy of health services in the face of the specific demands of the elderly, especially regarding sexuality and sexual and gender minorities.
{"title":"Aging and vulnerability: perspectives of LGBTQIA+ elderly persons","authors":"Isaura Emília Rodrigues Espinola, Lara Fernandes de Carvalho, D. F. D. Silva, José Madson Medeiros Souza, Fabiana Maria Rodrigues Lopes de Oliveira, José Uilson Ferreira Galindo Júnior, Keylla Talitha Fernandes Barbosa","doi":"10.15253/2175-6783.20232483200","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483200","url":null,"abstract":"Objective: to understand the perception of the LGBTQIA+ elderly person about social and programmatic vulnerability. Methods: qualitative study developed with ten elderly persons. The collection was done through an interview supported by a semi-structured instrument. Elderly people of both sexes and non-binary assisted in a reference center were included. We adopted content analysis through the thematic modality for data systematization. Results: human aging raised discussions about specific needs, such as sexuality. Treated as taboos, elderly individuals who belonged to sexual minority groups suffered double invisibility, especially in health services. Furthermore, the lack of social and family support resulted in psychological suffering and social vulnerability. Conclusion: through the reports, it is possible to identify important gaps in the assistance to the LGBTQIA+ elderly person, such as difficulty of access and generic health practices, which do not consider the particularities of this population, as well as discrimination and lack of spaces for coexistence. Contributions to practice: population aging raises discussions about the adequacy of health services in the face of the specific demands of the elderly, especially regarding sexuality and sexual and gender minorities.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86251270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-05-17DOI: 10.15253/2175-6783.20232483147
Stéffane Costa Mendes, Josenilson Bernardo da Silva, Marlene Menezes de Souza Teixeira, Maria do Socorro Bezerra Lopes
Objective: to investigate the actions of nurses in regard to lesbian and bisexual women in the context of the National Policy for the Integral Health of Lesbians, Gays, Bisexuals, Cross-Dressers and Transgender Persons. Methods: qualitative study involving 25 nurses from the Family Health Strategy, contacted via electronic means. We applied a form containing sociodemographic data and an investigation of actions in primary health care, as well as a thematic content analysis. Results: we found there are professional capacitation activities, embracing of demands, and enhanced interprofessional work. Nonetheless, there were shortcomings in the knowledge regarding health care towards lesbian and bisexual women. Conclusion: there are still prejudices, difficulty to access, and little attendance of lesbian and bisexual women in health services, as well as a deficit in the support to health actions and lack of monitoring. Contributions to practice: the importance of the scientific, professional, and social experiences stand out, regarding the need to humanize the care to lesbian and bisexual women. It is a supporting material for researchers and nursing professionals, enabling them to direct their care to a holistic and integral care to be provided to these women, in addition to being an encouragement to further comparative studies.
{"title":"Nursing actions in Primary Health Care to lesbian and bisexual women","authors":"Stéffane Costa Mendes, Josenilson Bernardo da Silva, Marlene Menezes de Souza Teixeira, Maria do Socorro Bezerra Lopes","doi":"10.15253/2175-6783.20232483147","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483147","url":null,"abstract":"Objective: to investigate the actions of nurses in regard to lesbian and bisexual women in the context of the National Policy for the Integral Health of Lesbians, Gays, Bisexuals, Cross-Dressers and Transgender Persons. Methods: qualitative study involving 25 nurses from the Family Health Strategy, contacted via electronic means. We applied a form containing sociodemographic data and an investigation of actions in primary health care, as well as a thematic content analysis. Results: we found there are professional capacitation activities, embracing of demands, and enhanced interprofessional work. Nonetheless, there were shortcomings in the knowledge regarding health care towards lesbian and bisexual women. Conclusion: there are still prejudices, difficulty to access, and little attendance of lesbian and bisexual women in health services, as well as a deficit in the support to health actions and lack of monitoring. Contributions to practice: the importance of the scientific, professional, and social experiences stand out, regarding the need to humanize the care to lesbian and bisexual women. It is a supporting material for researchers and nursing professionals, enabling them to direct their care to a holistic and integral care to be provided to these women, in addition to being an encouragement to further comparative studies.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89947910","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-05-17DOI: 10.15253/2175-6783.20232482832
José Vitor da Silva, Elaine Aparecida Rocha Domingues, F. Orlandi, E. V. D. Souza Júnior, Daniel Rodrigues Machado
Objective: to evaluate the relationship between bio sociodemographic characteristics and advanced activities of daily living in hospitalized elderly people. Methods: cross-sectional study. Two hundred hospitalized elderly people participated. The instruments were used: Mental Status Assessment Questionnaire, Bio-sociodemographic and Health Characterization Instrument and Advanced Activities of Daily Living Scale. Results: age impacted social (p=0.024), leisure (p=0.004), intellectual (p=0.017) and religious (p=0.047) activities. Regarding gender, men presented higher scores in leisure (p=0.046) and intellectual (p=0.002) activities; on the other hand, women obtained better scores in religious activities (p=0.001). The variables "family income", "physical disability" and "physical activity" were significantly associated with the global score. Conclusion: there was an association of the variables "age", "education", "family income", "physical disability", "physical activity practice" and "health status perception" with the global score of the scale. Most of the bio sociodemographic variables showed association with the Leisure Activities domain. Contributions to practice: the elucidation of factors that may be related to the performance of advanced activities in hospitalized elderly people can support the improvement of care.
{"title":"Association between bio-sociodemographic profile and advanced activities of daily living in hospitalized elderly people","authors":"José Vitor da Silva, Elaine Aparecida Rocha Domingues, F. Orlandi, E. V. D. Souza Júnior, Daniel Rodrigues Machado","doi":"10.15253/2175-6783.20232482832","DOIUrl":"https://doi.org/10.15253/2175-6783.20232482832","url":null,"abstract":"Objective: to evaluate the relationship between bio sociodemographic characteristics and advanced activities of daily living in hospitalized elderly people. Methods: cross-sectional study. Two hundred hospitalized elderly people participated. The instruments were used: Mental Status Assessment Questionnaire, Bio-sociodemographic and Health Characterization Instrument and Advanced Activities of Daily Living Scale. Results: age impacted social (p=0.024), leisure (p=0.004), intellectual (p=0.017) and religious (p=0.047) activities. Regarding gender, men presented higher scores in leisure (p=0.046) and intellectual (p=0.002) activities; on the other hand, women obtained better scores in religious activities (p=0.001). The variables \"family income\", \"physical disability\" and \"physical activity\" were significantly associated with the global score. Conclusion: there was an association of the variables \"age\", \"education\", \"family income\", \"physical disability\", \"physical activity practice\" and \"health status perception\" with the global score of the scale. Most of the bio sociodemographic variables showed association with the Leisure Activities domain. Contributions to practice: the elucidation of factors that may be related to the performance of advanced activities in hospitalized elderly people can support the improvement of care.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87061500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-05-17DOI: 10.15253/2175-6783.20232483042
F. Silva, Taysa do Nascimento Silva, Raphael Alves da Silva, Karina Ferreira da Silva, Ligia Maria de Almeida, D. Silva, Jael Maria de Aquino
Objective: to analyze, in the light of Callista Roy’s model, the pandemic implications of COVID-19 on the behavior and care of users assisted at a Child and Adolescent Psychosocial Care Center. Methods: a qualitative study, in which 13 family caregivers of users assisted at a Child and Adolescent Psychosocial Care Center participated. Data collection occurred through semi-structured interviews. Data analysis was performed through content analysis. Results: three categories emerged: The impact of social distancing on the behavior of children/adolescents assisted at the Child and Adolescent Psychosocial Care Center; Difficulties experienced by family caregivers with children/adolescents during the COVID 19 pandemic; Welcoming and support for children/adolescents and family members linked to the Child and Adolescent Psychosocial Care Center during the COVID-19 pandemic. Conclusion: children’s and adolescents’ care and behavior have undergone changes resulting from changes in social interaction and care at the Child and Adolescent Psychosocial Care Center. This scenario required adaptation and, through Callista Roy’s model, it was possible to better understand this adaptive process. Contributions to practice: this study allows us to better understand the problem and, consequently, improve the care offered by the team considering the reality presented.
{"title":"Repercussions of COVID-19 on the care and behavior of users of a Child and Adolescent Psychosocial Care Center","authors":"F. Silva, Taysa do Nascimento Silva, Raphael Alves da Silva, Karina Ferreira da Silva, Ligia Maria de Almeida, D. Silva, Jael Maria de Aquino","doi":"10.15253/2175-6783.20232483042","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483042","url":null,"abstract":"Objective: to analyze, in the light of Callista Roy’s model, the pandemic implications of COVID-19 on the behavior and care of users assisted at a Child and Adolescent Psychosocial Care Center. Methods: a qualitative study, in which 13 family caregivers of users assisted at a Child and Adolescent Psychosocial Care Center participated. Data collection occurred through semi-structured interviews. Data analysis was performed through content analysis. Results: three categories emerged: The impact of social distancing on the behavior of children/adolescents assisted at the Child and Adolescent Psychosocial Care Center; Difficulties experienced by family caregivers with children/adolescents during the COVID 19 pandemic; Welcoming and support for children/adolescents and family members linked to the Child and Adolescent Psychosocial Care Center during the COVID-19 pandemic. Conclusion: children’s and adolescents’ care and behavior have undergone changes resulting from changes in social interaction and care at the Child and Adolescent Psychosocial Care Center. This scenario required adaptation and, through Callista Roy’s model, it was possible to better understand this adaptive process. Contributions to practice: this study allows us to better understand the problem and, consequently, improve the care offered by the team considering the reality presented.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73542911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-04-12DOI: 10.15253/2175-6783.20232483089
Samara dos Santos Paiva, Erika Lorena Ramos de Oliveira Silva, Gisele Martins
Objective: to map the evidence on web-based technologies and their applicability in outpatient and home care in pediatric urology. Methods: this is a scoping review, with searches conducted in six databases, with no time limit, in Portuguese, English, and Spanish. Results: 2,200 articles were obtained, with 19 publications eligible for the final sample. The most used web-based technologies were telehealth and telemedicine (47.3%), online intervention programs (21.0%), and mobile apps (15.8%), with a lower rate of use of serious games, social media, and urination videos (5.3%), mostly in the home setting. Conclusion: the mapping of technological evidence in outpatient and home care in pediatric urology allowed us to identify the types of technology and their applications focused on self-management of symptoms and self-efficacy, for monitoring and follow-up of urologic care. Contributions to practice: the synthesized evidence contributes to an expanded, qualified, and innovative professional practice with the pediatric population with urinary and bowel symptoms, characteristics related to advanced nursing practice, in addition to favoring early diagnosis and greater therapeutic adherence, particularly by supporting interventions tailored to the needs of the pediatric patient and his family.
{"title":"Technological evidence for outpatient and home care in pediatric urology: a scoping review","authors":"Samara dos Santos Paiva, Erika Lorena Ramos de Oliveira Silva, Gisele Martins","doi":"10.15253/2175-6783.20232483089","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483089","url":null,"abstract":"Objective: to map the evidence on web-based technologies and their applicability in outpatient and home care in pediatric urology. Methods: this is a scoping review, with searches conducted in six databases, with no time limit, in Portuguese, English, and Spanish. Results: 2,200 articles were obtained, with 19 publications eligible for the final sample. The most used web-based technologies were telehealth and telemedicine (47.3%), online intervention programs (21.0%), and mobile apps (15.8%), with a lower rate of use of serious games, social media, and urination videos (5.3%), mostly in the home setting. Conclusion: the mapping of technological evidence in outpatient and home care in pediatric urology allowed us to identify the types of technology and their applications focused on self-management of symptoms and self-efficacy, for monitoring and follow-up of urologic care. Contributions to practice: the synthesized evidence contributes to an expanded, qualified, and innovative professional practice with the pediatric population with urinary and bowel symptoms, characteristics related to advanced nursing practice, in addition to favoring early diagnosis and greater therapeutic adherence, particularly by supporting interventions tailored to the needs of the pediatric patient and his family.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85226900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-04-12DOI: 10.15253/2175-6783.20232483199
Francisco Daniel Brito Mendes, Zaira de Andrade Lopes, A. M. Martins, Helder de Pádua Lima, M. F. Amorim
Objective: to understand the experiences of deprivation of freedom from the perspective of men and their implications to health care. Methods: qualitative study carried out with 10 men serving sentences on probation. Data collection was carried out in individual interviews using a semistructured questionnaire. Data was submitted to content analysis. Results: three categories emerged, which were: Crooked life: living before being deprived of freedom; Caged bird: being a man deprived of freedom; and Time bomb: health care in the prison system. The deprivation of freedom is an experience marked by the lack of safety, considering the health risks in the prison environment, the perception of participants of being vulnerable to disease, and the denial, on the part of the state, of the right to health. Since the access to health is not guaranteed, relatives were the most commonly responsible for organizing care. Conclusion: an unhealthy situation was found, with vulnerability to disease and denial of the right to health in the prison environment. Contributions to practice: this study contributed for sensitizing professionals who work in the prison system, emphasizing the importance of guaranteeing human rights during imprisonment.
{"title":"Experiences of deprivation of freedom from the perspective of men and its implications to health care","authors":"Francisco Daniel Brito Mendes, Zaira de Andrade Lopes, A. M. Martins, Helder de Pádua Lima, M. F. Amorim","doi":"10.15253/2175-6783.20232483199","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483199","url":null,"abstract":"Objective: to understand the experiences of deprivation of freedom from the perspective of men and their implications to health care. Methods: qualitative study carried out with 10 men serving sentences on probation. Data collection was carried out in individual interviews using a semistructured questionnaire. Data was submitted to content analysis. Results: three categories emerged, which were: Crooked life: living before being deprived of freedom; Caged bird: being a man deprived of freedom; and Time bomb: health care in the prison system. The deprivation of freedom is an experience marked by the lack of safety, considering the health risks in the prison environment, the perception of participants of being vulnerable to disease, and the denial, on the part of the state, of the right to health. Since the access to health is not guaranteed, relatives were the most commonly responsible for organizing care. Conclusion: an unhealthy situation was found, with vulnerability to disease and denial of the right to health in the prison environment. Contributions to practice: this study contributed for sensitizing professionals who work in the prison system, emphasizing the importance of guaranteeing human rights during imprisonment.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78828543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-04-12DOI: 10.15253/2175-6783.20232483087
Maísa Mara Lopes Macedo, Nayara Luiza Henriques, S. Deodato, E. D. Duarte
Objective: to describe how families experienced the care of children in chronic condition during the pandemic by COVID-19. Methods: qualitative study, guided by the Family Management Style Model, conducted with 24 families of children in chronic condition. The data, collected by telephone contact through semi-structured interviews, were submitted to thematic analysis. Results: data analysis resulted in three thematic categories: Changes in the routine of family members; Emotions triggered in family members and children due to the pandemic; and Implications of the pandemic by COVID-19 for the continuity of care. They highlighted: incorporation of hygiene care, social distancing concomitant to domestic and professional activities at home; and feelings of fear and concern about the children's health and development and the need for caregivers to provide rehabilitation and support for school activities. Conclusion: it was observed that the pandemic changed the family routine, produced negative feelings in families, modified care demands and compromised access to services. Contributions to practice: these results contribute to the identification of the repercussions of COVID-19 on families and children with chronic conditions and can help establish strategies to reduce the consequences of this pandemic and other future health emergencies.
{"title":"Family care of children with chronic conditions in the context of the pandemic by COVID-19","authors":"Maísa Mara Lopes Macedo, Nayara Luiza Henriques, S. Deodato, E. D. Duarte","doi":"10.15253/2175-6783.20232483087","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483087","url":null,"abstract":"Objective: to describe how families experienced the care of children in chronic condition during the pandemic by COVID-19. Methods: qualitative study, guided by the Family Management Style Model, conducted with 24 families of children in chronic condition. The data, collected by telephone contact through semi-structured interviews, were submitted to thematic analysis. Results: data analysis resulted in three thematic categories: Changes in the routine of family members; Emotions triggered in family members and children due to the pandemic; and Implications of the pandemic by COVID-19 for the continuity of care. They highlighted: incorporation of hygiene care, social distancing concomitant to domestic and professional activities at home; and feelings of fear and concern about the children's health and development and the need for caregivers to provide rehabilitation and support for school activities. Conclusion: it was observed that the pandemic changed the family routine, produced negative feelings in families, modified care demands and compromised access to services. Contributions to practice: these results contribute to the identification of the repercussions of COVID-19 on families and children with chronic conditions and can help establish strategies to reduce the consequences of this pandemic and other future health emergencies.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82219806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-04-12DOI: 10.15253/2175-6783.20232483198
Willian Martins de Araujo, Flávio Adriano Borges, Janaína Ferreira de Lima, Walkiria Jéssica de Araújo Silveira, José Francisco Sampaio Souza, N. Stofel, D. Carlos
Objective: to analyze nursing students' perceptions about their professional training for health care of LGBTQIA+ people. Methods: qualitative study, conducted with 19 nursing students through semi-structured interviews. Data were processed and worked through lexical analysis using IRaMuTeQ® software. Results: the textual corpus gave rise to two categories: professional nursing training on health of LGBTQIA+ people (subdivided into: curricular spaces addressing health of LGBTQIA+ people and Formative deficits for health care of LGBTQIA+ people) and Extracurricular spaces of professional training on health of LGBTQIA+ people (subdivided into: informal and extracurricular learning on health of LGBTQIA+ people and Work context and autonomy in learning about LGBTQIA+ health). Conclusion: addressing the health of LGBTQIA+ people in the training of nurses needs to expand beyond specific classes, which demands the creation of spaces within the curricular matrices that address the specificities required by this population, without, however, relegating them to extracurricular activities. Contributions to practice: problematization of the training of nurses for the health care of LGBTQIA+ people.
{"title":"Nursing students' perceptions of teaching health care to LGBTQIA+ people","authors":"Willian Martins de Araujo, Flávio Adriano Borges, Janaína Ferreira de Lima, Walkiria Jéssica de Araújo Silveira, José Francisco Sampaio Souza, N. Stofel, D. Carlos","doi":"10.15253/2175-6783.20232483198","DOIUrl":"https://doi.org/10.15253/2175-6783.20232483198","url":null,"abstract":"Objective: to analyze nursing students' perceptions about their professional training for health care of LGBTQIA+ people. Methods: qualitative study, conducted with 19 nursing students through semi-structured interviews. Data were processed and worked through lexical analysis using IRaMuTeQ® software. Results: the textual corpus gave rise to two categories: professional nursing training on health of LGBTQIA+ people (subdivided into: curricular spaces addressing health of LGBTQIA+ people and Formative deficits for health care of LGBTQIA+ people) and Extracurricular spaces of professional training on health of LGBTQIA+ people (subdivided into: informal and extracurricular learning on health of LGBTQIA+ people and Work context and autonomy in learning about LGBTQIA+ health). Conclusion: addressing the health of LGBTQIA+ people in the training of nurses needs to expand beyond specific classes, which demands the creation of spaces within the curricular matrices that address the specificities required by this population, without, however, relegating them to extracurricular activities. Contributions to practice: problematization of the training of nurses for the health care of LGBTQIA+ people.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89977078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-08DOI: 10.15253/2175-6783.20232481790
Isabelle Pereira da Silva, Iraktânia Vitorino Diniz, Luana Souza Freitas, Pétala Tuani Cândido de Oliveira Salvador, Helena Megumi Sonobe, Simone Karine da Costa Mesquita, I. F. Costa
Objective: to develop a mobile application to support self- -care for people with intestinal stomas. Methods: descriptive study of technological innovation, guided by Theory of Self-Care to organize the application´s content and production. Design Science Research that followed the steps: problem knowledge identified in practice; determination of the artifact objectives; development; demonstration. Before the technology development, a qualitative study was conducted to understand difficulties in self-care and a scope review to map the content. Two specialized professionals helped in the application development. Results: ostocuide application has 36 screens subdivided into menus: registration and record; feeding; self-care; stomas types; health care; laws; curiosities; contact and interactive questions. The application offers the diary function for photos and texts records about care performed with the stoma and the possibility of sending questions to researchers responsible for the application. Conclusion: the application was successfully developed and gathered resources that may collaborate with the self-care of people with intestinal stomas. Contributions to practice: the application can contribute to the population learning with intestinal stomas and to health education carried out by nurses.
{"title":"Development of a mobile application to support self-care for people with intestinal stomas","authors":"Isabelle Pereira da Silva, Iraktânia Vitorino Diniz, Luana Souza Freitas, Pétala Tuani Cândido de Oliveira Salvador, Helena Megumi Sonobe, Simone Karine da Costa Mesquita, I. F. Costa","doi":"10.15253/2175-6783.20232481790","DOIUrl":"https://doi.org/10.15253/2175-6783.20232481790","url":null,"abstract":"Objective: to develop a mobile application to support self- -care for people with intestinal stomas. Methods: descriptive study of technological innovation, guided by Theory of Self-Care to organize the application´s content and production. Design Science Research that followed the steps: problem knowledge identified in practice; determination of the artifact objectives; development; demonstration. Before the technology development, a qualitative study was conducted to understand difficulties in self-care and a scope review to map the content. Two specialized professionals helped in the application development. Results: ostocuide application has 36 screens subdivided into menus: registration and record; feeding; self-care; stomas types; health care; laws; curiosities; contact and interactive questions. The application offers the diary function for photos and texts records about care performed with the stoma and the possibility of sending questions to researchers responsible for the application. Conclusion: the application was successfully developed and gathered resources that may collaborate with the self-care of people with intestinal stomas. Contributions to practice: the application can contribute to the population learning with intestinal stomas and to health education carried out by nurses.","PeriodicalId":45440,"journal":{"name":"Rev Rene","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2023-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74818051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-03-08DOI: 10.15253/2175-6783.20232481786
Renata Ferreira de Araújo, Alexsandro Silva Coura, Isabella Joyce Silva de Almeida Carvalho, Rayssa Gabrielle da Costa Farias, Jamilly da Silva Aragão, Inácia Sátiro Xavier de França
Objective: to understand the perspective of nurses regarding the obstacles faced by physically disabled women in regard to cytopathological examinations. Methods: qualitative study with 11 nurses from Basic Health Units, including urban and rural areas. Data was processed and analyzed using the software IRAMUTEQ (R pour les Analyses Multidimensionnelles de Textes et de Questionnaires). Results: classes 1 and 5 were grouped into the class “Inadequate infrastructure”; class 2 was “Results of the collected exams”; class 3, “Feelings at the time of examination”; and 4 “Team training”. Conclusion: we revealed that women presented negative feelings during the examination, professionals lacked further training, there were no strategies to deal with the situation in the unit, and facilities were inadequate to attend the needs of the users. Contributions to practice: we demonstrated that it is essential to provide care to physically disabled women and carry out routine exams in this population. Furthermore, this study can give support to strategies to adapt and improve the knowledge of the workers who provide care.
目的:了解护士对残障妇女在细胞病理检查中遇到的障碍的看法。方法:对11名城乡基层卫生保健单位护士进行定性研究。使用IRAMUTEQ (R pour les Analyses Multidimensionnelles de Textes et de questionnaire)软件对数据进行处理和分析。结果:1级和5级被归为“基础设施不足”类;第二课是“收集的考试结果”;第三课“考试时的感受”;4 .“团队训练”。结论:我们发现妇女在检查过程中表现出消极情绪，专业人员缺乏进一步的培训，单位没有应对这种情况的策略，设施不足以满足用户的需求。对实践的贡献:我们证明了为身体残疾妇女提供护理和在这一人群中进行常规检查是至关重要的。此外，本研究可提供策略支持，以适应和提高护理工作者的知识。
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