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1.
Enferm. foco (Brasília) ; 15: 1-5, maio. 2024. ilus
Article Dans Portugais | LILACS, BDENF | ID: biblio-1553746

Résumé

Objetivo: Relatar a construção e implantação de painel de bordo, desenvolvido por enfermeiros e profissionais da tecnologia da informação, para gerenciamento do Protocolo de Prevenção de Lesão por Pressão. Métodos: Trata-se de um relato de experiência sobre a construção e implantação de painel de bordo informatizado para gerenciamento de protocolo em um hospital privado universitário, localizado no interior do estado de São Paulo. Resultados: A construção do painel de bordo foi dividida nas seguintes etapas: revisão e atualização do protocolo, construção do modelo eletrônico e implementação. A divulgação foi realizada pela Comissão de Prevenção de Lesão por Pressão. Conclusão: O painel de bordo possibilitou a visualização rápida e em tempo real dos riscos dos pacientes, intervenções propostas e efetividade das medidas de prevenção, além de promover a integração e empoderamento dos profissionais na gestão do cuidado. (AU)


Objective: To report the construction and implementation of a dashboard, developed by nurses and information technology professionals, to manage the Pressure Injury Prevention Protocol. Methods: This is an experience report on the construction and implementation of a computerized dashboard for protocol management in a private university hospital, located in the interior of the state of São Paulo. Results: The construction of the dashboard was divided into the following steps: review and update of the protocol, construction of the electronic model and implementation. The Pressure Injury Prevention Commission disclosed the tool. Conclusion: The dashboard enabled the quick and real-time visualization of patient risks, proposed interventions and effectiveness of prevention measures, in addition to promoting the integration and empowerment of professionals in the management of care. (AU)


Objetivo: Informar la construcción e implementación de un panel, desarrollado por enfermeras y profesionales de tecnologías de la información, para gestionar el Protocolo de Prevención de Lesiones por Presión. Métodos: Se trata de un informe de experiencia sobre la construcción e implementación de un panel computarizado para la gestión del protocolo en un hospital universitario privado, en el interior del estado de São Paulo. Resultados: La construcción del panel se dividió en los siguientes pasos: revisión y actualización del protocolo, construcción del modelo electrónico e implementación. La divulgación fue realizada por la Comisión de Prevención de Lesiones por Presión. Conclusión: El panel permitió la visualización rápida y en tiempo real de los riesgos del paciente, las intervenciones propuestas y la efectividad de las medidas de prevención, además de promover la integración y el empoderamiento de los profesionales en la gestión del cuidado. (AU)


Sujets)
Gestion du risque , Escarre , Sécurité des patients , Gestion de l'information en santé , Soins infirmiers
2.
Medisan ; 28(1)feb. 2024.
Article Dans Espagnol | LILACS-Express | LILACS | ID: biblio-1558503

Résumé

La utilización de herramientas tecnológicas en la docencia condiciona el desarrollo de nuevas destrezas intelectuales en los estudiantes, lo que les facilita la aplicación de estrategias de investigación, mejora sus capacidades de una forma integral, les ayuda a enfrentar las dificultades y exigencias del mundo y les permite adquirir un aprendizaje más significativo para poder desenvolverse en el ámbito socioeducativo. Con vistas a cumplir lo anterior, se desarrolló un repositorio institucional de recursos educativos abiertos para la Universidad Virtual de Salud, a partir del empleo de herramientas tecnológicas libres y de código abierto que permiten la estandarización e interoperabilidad entre cada uno de los repositorios establecidos en el Sistema Nacional de Salud, con lo cual se garantizará una lógica de organización académica.


The use of digital technologies in teaching determines the development of new intellectual skills in students, which facilitates the application of investigation strategies, improves their capabilities in an integral way, helps them face the difficulties and demands of the current world and allows them to acquire more significant learning to have a good performance in the socio-educational environment. With a view to fulfilling the above, an institutional repository of open educational resources was developed for the Virtual Health University, based on the use of free and open-source technology tools that allow the standardization and interoperability among each of the repositories established in the National Health System, which will guarantee logic of academic organization.

3.
Chinese Medical Ethics ; (6): 428-433, 2024.
Article Dans Chinois | WPRIM | ID: wpr-1031319

Résumé

Currently, the ethical review model for organ donation and transplantation in domestic hospitals is generally characterized by suddenness, unpredictability, tight time, difficulty in convening meetings and training committee members, as well as generally low quality and efficiency of ethical review, which cannot meet clinical needs and cause the waste of some scarce resources. The team of the Clinical Application Center of Human Organ Transplantation and the Ethics Committee of the First People’s Hospital of Kunming combine more than 10 years of review practice experience, as well as continuously explore and optimize the ethical review process and operating procedures for organ donation and transplantation. The special application has been approved and jointly developed with Soochow University and the Medical Ethics Committee of Fujian Province to build a full-process information software system management platform for organ ethical review of donation and transplantation, giving the full play the advantages of the review information system in improving work efficiency and review quality, facilitating full-process information management, and conducting online training and learning for committee members, with a view to providing a specialized practical model for addressing the difficulties and challenges related to ethical review of human organ donation and transplantation.

4.
Chinese Journal of Pharmacoepidemiology ; (4): 9-18, 2024.
Article Dans Chinois | WPRIM | ID: wpr-1023160

Résumé

As an increasing number of emerging anti-tumor drugs are approved and marketed,the imperative for clinical safety monitoring and risk information management has grown significantly.Drug-induced neuropathy associated with these drugs exhibit characteristics such as insidious onset,rapid progression,and challenging treatment,ultimately leading to treatment failures.Therefore,a comprehensive understanding of the risk of neuropathy induced by emerging anti-tumor drugs,coupled with risk surveillance and early warning,as well as management and reporting,can significantly reduce the incidence and severity of drug-related diseases.This paper provides a review of the neuropathy caused by emerging anti-tumor drugs,introduces the pharmacovigilance system and risk information management measures in clinical usage,aiming to provide a reference for guiding the rational clinical use and minimizing the incidence of drug-induced diseases.

5.
Rev. panam. salud pública ; 48: e9, 2024. tab, graf
Article Dans Anglais | LILACS-Express | LILACS | ID: biblio-1551021

Résumé

ABSTRACT This article points out deficiencies in present-day definitions of public health surveillance, which include data collection, analysis, interpretation and dissemination, but not public health action. Controlling a public health problem of concern requires a public health response that goes beyond information dissemination. It is undesirable to have public health divided into data generation processes (public health surveillance) and data use processes (public health response), managed by two separate groups (surveillance experts and policy-makers). It is time to rethink the need to modernize the definition of public health surveillance, inspired by the authors' enhanced Data, Information, Knowledge, Intelligence and Wisdom model. Our recommendations include expanding the scope of public health surveillance beyond information dissemination to comprise actionable knowledge (intelligence); mandating surveillance experts to assist policy-makers in making evidence-informed decisions; encouraging surveillance experts to become policy-makers; and incorporating public health literacy training - from data to knowledge to wisdom - into the curricula for all public health professionals. Work on modernizing the scope and definition of public health surveillance will be a good starting point.


RESUMEN En este artículo se señalan las deficiencias de las definiciones actuales de la vigilancia de salud pública, que incluyen la recopilación, el análisis, la interpretación y la difusión de los datos, pero no las medidas de salud pública. El control de un problema de salud pública de interés exige una respuesta de salud pública que vaya más allá de la difusión de información. No es deseable que la salud pública esté dividida por un lado en procesos de generación de datos (vigilancia de salud pública) y por otro en procesos de uso de datos (respuesta de salud pública), gestionados por dos grupos diferentes (expertos en vigilancia y responsables de la formulación de políticas). Ha llegado el momento de replantear la necesidad de modernizar la definición de la vigilancia de salud pública tomando como referencia el modelo mejorado de Datos, Información, Conocimiento, Inteligencia y Sabiduría de los autores. Entre las recomendaciones que se proponen se encuentran las de ampliar el alcance de la vigilancia de salud pública más allá de la difusión de información para que incluya también el conocimiento aplicable (inteligencia); instar a los expertos en vigilancia a que presten ayuda a los responsables de la formulación de políticas en la toma de decisiones basadas en la evidencia; alentar a los expertos en vigilancia a que se conviertan en responsables de la formulación de políticas; e incorporar la formación en conocimientos básicos de salud pública (desde los datos hasta los conocimientos y la sabiduría) en los planes de estudio de todos los profesionales de la salud pública. Un buen punto de partida será trabajar en la modernización del alcance y la definición de la vigilancia de salud pública.


RESUMO Este artigo aponta deficiências nas definições atuais de vigilância em saúde pública, que incluem coleta, análise, interpretação e disseminação de dados, mas não ações de saúde pública. O controle de um problema preocupante de saúde pública exige uma resposta de saúde pública que vá além da disseminação de informações. A saúde pública não deve ser dividida em processos de geração de dados (vigilância em saúde pública) e processos de uso de dados (resposta de saúde pública) gerenciados por dois grupos distintos (especialistas em vigilância e formuladores de políticas). É hora de repensar a necessidade de modernizar a definição de vigilância em saúde pública, inspirada no modelo aprimorado de Dados, Informações, Conhecimento, Inteligência e Sabedoria dos autores. Nossas recomendações incluem: expansão do escopo da vigilância em saúde pública para além da disseminação de informações, de modo a abranger conhecimentos acionáveis (inteligência); obrigatoriedade de que os especialistas em vigilância auxiliem os formuladores de políticas na tomada de decisões baseadas em evidências; incentivo para que os especialistas em vigilância se tornem formuladores de políticas; e incorporação de capacitação em letramento em saúde pública (partindo dos dados para o conhecimento e em seguida para a sabedoria) nos currículos de todos os profissionais de saúde pública. O trabalho de modernizar o escopo e a definição de vigilância em saúde pública será um bom ponto de partida.

6.
Rev. Esc. Enferm. USP ; 58: e20230340, 2024. tab
Article Dans Anglais | LILACS, BDENF | ID: biblio-1550651

Résumé

ABSTRACT Objective: to explore associations and gender differences between OHI-seeking (online health information seeking) behaviors and eHealth (electronic health) literacy among Chinese university students. Methods: Online questionnaires of eHealth literacy scale and OHI-seeking behaviors created in software Wenjunxing were used in this survey. Chi-squared tests, t-test, and Pearson correlation analysis were performed using SPSS for data analysis. Results: Among 5,383 participants, 72.4% were girls, 77.5% lived in rural areas, 51.2% majored in liberal arts, 76.6% with low education parents. The average C-eHEALS scores of boys and girls were 26.53 ± 5.861 and 26.84 ± 5.816, respectively, with no significant difference (P = 0.084). The top three OHI-seeking behaviors for boys and girls, as well as for the C-eHEALS low and high groups, were "finding information about physical exercises" "reading or sharing health information via social media" "finding information about nutrition and diet", all of which had significant gender and eHealth literacy differences. Conclusions: Gender and eHealth literacy differences should be focused for intervention when developing and implementing eHealth intervention training for parents and adolescents in schools and communities.


RESUMO Objetivo: Visa explorar associações e diferenças de gênero entre comportamentos de busca de OHI (busca de informações de saúde on-line) e letramento em e-Saúde (saúde eletrônica) entre estudantes universitários chineses. Métodos: Questionários on-line da escala de letramento em e-Saúde e comportamentos de busca de OHI criados no software Wenjunxing foram utilizados nesta pesquisa. Testes qui-quadrado, teste t e análise de correlação de Pearson foram realizados utilizando SPSS para análise de dados. Resultados: Dos 5.383 participantes, 72,4% eram meninas, 77,5% viviam em áreas rurais, 51,2% eram formados em artes liberais, 76,6% tinham pais com baixa escolaridade. As pontuações médias do C-eHEALS de meninos e meninas foram 26,53 ± 5,861 e 26,84 ± 5,816, respectivamente, sem diferença significativa (P = 0,084). Os três principais comportamentos de busca de IHO para meninos e meninas, bem como para os grupos baixo e alto do C-eHEALS, foram "encontrar informações sobre exercícios físicos"; "ler ou compartilhar informações de saúde através das redes sociais"; "encontrar informações sobre nutrição e dieta", todos com diferenças significativas de gênero e de letramento em e-Saúde. Conclusões: As diferenças de gênero e de letramento em e-Saúde devem ser focadas na intervenção ao desenvolver e implementar formação de intervenção em e-Saúde para pais e adolescentes em escolas e comunidades.


RESUMEN Objetivo: Explorar las asociaciones y las diferencias de género entre el comportamiento de búsqueda de OHI (información sanitaria en línea) y los conocimientos sobre e-Salud (salud electrónica) entre estudiantes universitarios chinos. Métodos: Se utilizaron cuestionarios en línea de la escala de conocimientos en e-Salud y conductas de búsqueda de OHI creadas con el software Wenjunxing. En el análisis de los datos, se utilizó el programa SPSS para llevar a cabo las pruebas de chi-cuadrado, pruebas t y análisis de correlación de Pearson. Resultados: De los 5.383 participantes, el 72,4% estaba formado por muchachas, el 77,5% vivía en zonas rurales, el 51,2% era licenciado en Humanidades y el 76,6% tenía padres con bajo nivel educativo. Las puntuaciones medias del C-eHEALS para chicos y chicas fueron 26,53 ± 5,861 y 26,84 ± 5,816, respectivamente, sin diferencias significativas (P = 0,084). Las tres conductas principales de búsqueda de la OHI para muchachos y muchachas, así como para los grupos de C-eHEALS bajo y alto, fueron "encontrar información sobre ejercicio físico"; "leer o compartir información sobre salud a través de las redes sociales"; "encontrar información sobre nutrición y dietas", todos ellos con diferencias significativas de género y de aprendizaje sobre e-Salud. Conclusiones: Las diferencias de género y de conocimientos en e-Salud deben centrarse en la intervención a la hora de desarrollar e implementar la formación en cibersalud para padres y adolescentes en escuelas y comunidades.


Sujets)
Humains , Éducation pour la santé , Compétence informationnelle en santé , Identité de genre , Étudiants , Gestion de l'information en santé
7.
Rev. bras. enferm ; 77(1): e20230358, 2024. tab, graf
Article Dans Anglais | LILACS-Express | LILACS, BDENF | ID: biblio-1559453

Résumé

ABSTRACT Objectives: to psychometrically validate the European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire EORTC QLQ-INFO25 instrument and identify the domains that influence patients' perception of the information received. Methods: a cross-sectional methodology with cancer patients in a Brazilian philanthropic hospital institution. Sociodemographic and clinical instruments, EORTC QLQ-C30, EORTC QLQ-INFO25 and Supportive Care Needs Survey - Short Form 34 were used. Analysis occurred using Cronbach's alpha coefficients, intraclass correlation, test-retest and exploratory factor analysis. Results: 128 respondents participated. Cronbach's alpha coefficient was 0.85. The test-retest obtained p-value=0.21. In the factor analysis, one item was excluded. Satisfaction with the information received was 74%, with three areas with averages below 70%. In open-ended questions, there was a greater desire for information. Conclusions: validity evidence was obtained with instrument reliability, consistency and stability. Respondents expressed satisfaction with the information received.


RESUMEN Objetivos: validar psicométricamente el instrumento European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire EORTC QLQ-INFO25 e identificar los dominios que influyen en la percepción del paciente sobre la información recibida. Métodos: metodología transversal con pacientes con cáncer en una institución hospitalaria filantrópica brasileña. Se utilizaron instrumentos sociodemográficos y clínicos, EORTC QLQ-C30, EORTC QLQ-INFO25 y Supportive Care Needs Survey - Short Form 34. El análisis se realizó mediante coeficientes alfa de Cronbach, correlación intraclase, prueba-reprueba y análisis factorial exploratorio. Resultados: participaron 128 encuestados. El coeficiente alfa de Cronbach fue de 0,85. La prueba-reprueba obtuvo p-valor=0,21. En el análisis factorial se excluyó un ítem. La satisfacción con la información recibida fue del 74%, con tres áreas con promedios inferiores al 70%. En las preguntas abiertas hubo mayor deseo de información. Conclusiones: se obtuvo evidencia de validación con confiabilidad, consistencia y estabilidad del instrumento. Los encuestados expresaron satisfacción con la información recibida.


RESUMO Objetivos: validar psicometricamente o instrumento da European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire EORTC QLQ-INFO25 e identificar os domínios que influenciam na percepção do paciente sobre as informações recebidas. Métodos: metodológico, transversal, com pacientes com câncer em instituição hospitalar filantrópica brasileira. Utilizaram-se instrumentos sociodemográficos e clínicos, EORTC QLQ-C30, EORTC QLQ-INFO25 e Supportive Care Needs Survey - Short Form 34. Análise ocorreu utilizando coeficientes alfa de Cronbach, correlação intraclasse, teste-reteste e análise fatorial exploratória. Resultados: participaram 128 respondentes. O coeficiente alfa de Cronbach foi de 0,85. O teste-reteste obteve p-valor=0,21. Na análise fatorial, foi excluído um item. A satisfação da informação recebida foi de 74%, com três domínios com médias inferiores a 70%. Nas questões abertas, evidenciou-se maior desejo por informações. Conclusões: evidências de validação foram obtidas com confiabilidade, consistência e estabilidade do instrumento. Os respondentes demonstraram satisfação com as informações recebidas.

8.
Educ. med. super ; 37(4)dic. 2023.
Article Dans Espagnol | LILACS-Express | LILACS | ID: biblio-1564462

Résumé

Introducción: La información y el conocimiento constituyen recursos estratégicos en las organizaciones ya que garantizan una efectiva toma de decisiones y mayor adaptabilidad a contextos cada vez más dinámicos y cambiantes. Objetivo: Proponer una herramienta diagnóstica para evaluar la comprensión de la Gestión de Información y el Conocimiento en el Centro Nacional de Información de Ciencias Médicas/Infomed. Métodos: Se realizó un análisis de las particularidades de la Gestión de Información y el Conocimiento en las organizaciones. Se caracterizó el Centro Nacional de Información de Ciencias Médicas/Infomed, teniendo en cuenta su objeto social, estructura y actividad informacional. Resultados: Se propone una herramienta ajustada a las características de dicha entidad para el diagnóstico de la comprensión de la Gestión de Información y el Conocimiento. Esta herramienta diagnóstica esboza cuatro divisiones estructurales para la recogida de información. Su concepción y diseño valoran, entre otros aspectos de interés, los elementos cognitivos y de comportamiento de los trabajadores de cara a los procesos de Gestión de Información y el Conocimiento. Conclusiones: Esta herramienta permite diagnosticar el estado de la comprensión de la Gestión de Información y el Conocimiento en el Centro Nacional de Información de Ciencias Médicas/Infomed, sobre la base de la importancia de la identificación y el desarrollo de estos procesos en la organización. También tiene en cuenta la necesidad de articular aquellos componentes de la gestión desde todos los niveles de la organización con el propósito de fomentar una cultura informacional.


Introduction: Information and knowledge are strategic resources in organizations, since they guarantee effective decision making and greater adaptability to increasingly dynamic and changing contexts. Objective: To propose a diagnostic tool for assessing the understanding of information and knowledge management at the Centro Nacional de Información de Ciencias Médicas/Infomed. Methods: An analysis was carried out of the particularities of information and knowledge management in organizations. Centro Nacional de Información de Ciencias Médicas/Infomed was characterized, taking into account its social purpose, structure and informational activity. Results: A tool adjusted to the characteristics of this entity is proposed for diagnosing the understanding of information and knowledge management. This diagnostic tool outlines four structural divisions for collecting the information. Its conception and design assess, among other aspects of interest, the cognitive and behavioral elements of the workers in the face of the information and knowledge management processes. Conclusions: This tool makes it possible to diagnose the state of understanding of information and knowledge management at Centro Nacional de Información de Ciencias Médicas/Infomed, based on the importance of identifying and developing these processes in the organization. It also takes into account the need to articulate those management components from all organizational levels and with the purpose of fostering an informational culture.

9.
Rev. cuba. inform. méd ; 15(2)dic. 2023.
Article Dans Espagnol | LILACS-Express | LILACS | ID: biblio-1536288

Résumé

Introducción: la Revista Cubana de Tecnología de la Salud, requiere un sistema de base de datos para el tratamiento de la información concerniente a los diferentes procesos de la gestión editorial. Esto es necesario en la automatización y a la vez humanización de la recolección, organización, procesamiento y presentación de los datos relacionados con los indicadores de evaluación de la calidad, los bibliométricos y los referentes con la indexación, por citar ejemplos. Objetivo: diseñar una base de datos para la Revista Cubana de Tecnología de la Salud. Métodos: se realizó una investigación aplicada de innovación tecnológica, en la que diseñó una base de datos relacional. Se emplearon métodos a nivel teórico y empíricos; entre ellos la entrevista para obtener una descripción detallada de las necesidades de la revista, y la modelación en la representación a través de modelos lógicos y conceptuales del universo de discurso. Resultados: la base de datos se diseñó mediante el modelo Entidad-Relación. Se obtuvieron el diagrama de entidad-relación y el esquema relacional de la base de datos. Se aplicó la teoría de la normalización para eliminar las redundancias. Conclusiones: quedó descrito el proceso de diseño de la base de datos con la cual la Revista Cubana de Tecnología de la Salud, podrá gestionar los datos de una forma centralizada y eficaz, de manera que se puedan aplicar en la evaluación de la gestión editorial y el desarrollo de estudios bibliométricos de la producción científica de la revista.


Introduction: The Cuban Journal of Health Technology requires a database system for the treatment of information concerning the different editorial management processes. This is necessary in the automation process and, at the same time, in the humanization of the collection, organization, processing, and presentation of the data related to the quality evaluation and bibliometric indicators, as well as those related to the indexing, to cite some examples. Objective: To design a database for the Cuban Journal of Health Technology. Methods: An applied research on technological innovation was carried out, in which a relational database was designed. Theoretical and empirical methods were used; among them, we can mention the interview to obtain a detailed description of the needs of the journal, and the representation modeling through logical and conceptual models of the universe of discourse. Results: The database was designed using the Entity-Relationship model. The entity-relationship diagram and the relational schema of the database were obtained. Normalization theory was applied to eliminate redundancies. Conclusions: The design process of the database that will allow the Cuban Journal of Health Technology to manage data in a centralized and efficient way was described, so that it can be applied to the evaluation of the editorial management and the development of bibliometric studies of the scientific production of the journal.

10.
Notas enferm. (Córdoba) ; 24(42): 26-33, nov.2023.
Article Dans Espagnol | LILACS, BDENF, UNISALUD, InstitutionalDB, BINACIS | ID: biblio-1527366

Résumé

Introducción: hacer el registro de los cuidados que la Enfermería proporciona diariamente a los pacientes, es una tarea esencial, tanto para dar una adecuada calidad sanitaria como para el desarrollo de la profesión. Objetivo: identificar la calidad de los registros electrónicos de Enfermería de un hospital de alta complejidad de la ciudad de Corrientes. Metodología: se realizó un estudio cuantitativo de tipo descriptivo transversal donde se revisaron 133 historias clínicas digitales mediante una herramienta adaptada y previamente validada. Resultados: de forma específica, la variable identificación del paciente obtuvo calidad buena, en cuanto al registro de la valoración se identificó que el 92% de las historias clínicas registraron menos de 6 indicadores, una calidad deficiente, y el 8% restante registró calidad regular, y la variable intervenciones obtuvo una calidad deficiente con un 87% de registro de los indicadores. Conclusión: en los resultados de la investigación se llegó a la conclusión de que, la calidad de los registros electrónicos de enfermería del servicio de terapia intensiva del hospital es de calidad deficiente respecto al registro electrónico del proceso enfermero[AU]


Introduction: recording the care that nursing provides daily to patients is an essential task, both for providing adequate health quality and for the development of the profession. Objective:to identify the quality of the electronic nursing records of a highly complex hospital in the city of Corrientes. Methodology: a cross-sectional descriptive quantitative study was carried out where 133 digital medical records were reviewed using an adapted and previously validated tool. Results: specifically, the patient identification variable obtained good quality, regarding the assessment record, it was identified that 92% of the medical records re-gistered less than 6 indicators, a poor quality, and the remaining 8% re-gistered regular quality, and the variable interventions obtained a poorquality with 87% registering the indicators. Conclusion: in the results of the investigation, it was concluded that the quality of the electronic nursing records of the hospital's intensive care service is of poor quality compared to the electronic record of the nursing process[AU]


Introdução: registrar os cuidados que a enfermagem presta diaria-mente aos pacientes é tarefa essencial, tanto para a prestação de uma saúde de qualidade adequada, quanto para o desenvolvimento da profissão. Objetivo: identificar a qualidade dos registros eletrônicos de enfermagem de um hospital de alta complexidade da cidade de Corrientes. Metodologia: realizouse um estudo quantitativo descritivo transversal onde foram revistos 133 prontuários digitais por meio de um instrumento adaptado e previamente validado. Resultados: especificamente, a variável identificação do paciente obteve qualidade boa, quanto ao registro de avaliação, identificouse que 92% dos prontuários registraram menos de 6 indicadores, a qualidade ruim, e os 8% restantes registraram qualidade regular, e a variável as intervenções obtiveram uma qualidade ruim com 87% registrando os indicadores. Conclusão: nos resultados da investigação concluiuse que a qualidade do prontuário eletrônico de enfermagem do serviço de terapia intensiva do hospital é de baixa qualidade em relação ao prontuário eletrônico do processo de enfermagem[AU]


Sujets)
Humains
11.
RECIIS (Online) ; 17(3): 650-667, jul.-set. 2023.
Article Dans Portugais | LILACS, ColecionaSUS | ID: biblio-1517720

Résumé

Este artigo é parte do relatório de pesquisa de opinião, quantitativa, executada pela Unesp em parceria com o Conselho Municipal de Políticas para Mulheres, de Bauru-SP, sobre a violência doméstica, de junho a agosto de 2020. A investigação não probabilística, de caráter descritivo, teve como método de coleta de dados o questionário on-line. Seu objetivo foi levantar opiniões de mulheres, de modo a oferecer parâmetros para subsidiar ações de comunicação e publicitação dos serviços promovidos pela Rede de Enfrentamento à violência contra a mulher nessa cidade. Seus resultados constituíram um insumo fundamental para a divulgação de direitos, leis, medidas protetivas, campanhas e informativos de prevenção, e de visibilidade aos serviços dessa Rede. Eles permitiram orientar estratégias de comunicação balizadas na opinião da comunidade, adequadas às demandas e às necessidades de cada região observada na pesquisa, que possibilitaram monitorar e avaliar a Rede de Enfrentamento


This article is part of a report based on a survey carried out by Unesp in partnership with the Municipal Council of Policies for Women, Bauru-SP on domestic violence, from June to August 2020. The non-prob-abilistic research, of descriptive nature, used the online questionnaire to collect data. The survey was con-ducted to find out woman opinions, in order to offer parameters to support communication and publicity actions for the service provided by a network for combating violence against women in that city. Its results enerated fundamental information for dissemination of rights, laws, protective measures, campaigns and prevention, among other ways of giving visibility to the service provided by that network. They made possi-ble to plan communication strategies based on the community opinion, appropriate to demands and pecu-liar needs for each region approached by the survey, which enabled to monitor and evaluate that network


Este artículo es parte del informe cuantitativo de encuesta de opinión realizada por la Unesp en alianza con el Consejo Municipal de Políticas para Mujeres, Bauru-SP, sobre violencia intrafamiliar, desde junio hasta agosto de 2020. La investigación no probabilística, de naturaleza descriptiva, utilizó el cuestionario online para obtener datos. Su objetivo fue conocer la opinión de mujeres, con el fin de ofrecer parámetros para auxiliar acciones de comunicación y divulgar los servicios promovidos por una red de afrontamiento a la violencia contra las mujeres en aquella ciudad. Sus resultados generaron informaciones fundamentales para la difusión de derechos, leyes, medidas de protección, campañas y prevención, y visibilidad a los servicios de esa red. Permitieron orientar estrategias de comunicación basadas en la opinión de la comunidad, adecuadas a las demandas y necesidades de cada región observada en la encuesta, que posibilitaron monitorizar y evaluar aquella red


Sujets)
Humains , Femmes , Violence domestique , Violence Contre les Femmes , Communication , Accès à l'information , Analyse de données , Équité de genre , COVID-19
12.
RECIIS (Online) ; 17(3): 469-487, jul.-set. 2023.
Article Dans Portugais | LILACS, ColecionaSUS | ID: biblio-1515948

Résumé

Aborda a tipologia documental em sistemas de informação digitais, compreendendo-a como metadado essencial na estrutura de transferência da informação entre serviços, sistemas e redes de atenção e inovação à saúde. Por meio de pesquisa de campo com gestores de dois hospitais federais do Rio de Janeiro, realiza prospecção e análise da gestão de sistemas de informação digitais em saúde. Os resultados revelaram que o emprego do conceito de Regime de Informação e de seus componentes analíticos permite-nos obter uma visão dos recursos informacionais, tecnológicos, humanos e normativos do sistema nacional de saúde, que integram o Sistema Único de Saúde. Destaca a tipologia documental como um dos elementos constituintes dos sistemas de informação nos serviços dos hospitais, cujas interconexões e articulações expressam os aspectos seletivos e decisórios das práticas e ações de informação


It addresses the document typology in digital information systems, understanding it as essential metadata in the structure of information transfer between attention and innovation health services, systems and networks. Through field research with managers of two federal hospitals in Rio de Janeiro, it prospects and analyzes the management of digital health information systems. The results revealed that the use of the concept of Information System and of its analytical components allows us to obtain a vision of the informational, technological, human and normative resources of the national health system, which are part of the Unified Health System. It highlights the documentary typology as one of the constituent elements of information systems in hospital services, whose interconnections and articulations express the selective and decision-making aspects of information practices and actions


Aborda como objeto la tipología documental en los sistemas de información digital, entendiéndola como un metadato esencial en la estructura de transferencia de información entre servicios, sistemas y redes de atención e innovación en salud. A través de una investigación de campo con gerentes de dos hospitales federales de Río de Janeiro, prospecta y analiza la gestión de los sistemas digitales de información en salud. Los resultados revelaran que la utilización del concepto de Régimen de Información y de sus componen-tes analíticos permítenos obtener una visión de los recursos informacionales, tecnológicos, humanos y normativos del sistema nacional de salud, que integram el Sistema Único de Salud. Destaca la tipología documental como uno de los elementos constitutivos de los sistemas de información cuyas interconexiones y articulaciones expresan los aspectos selectivos y decisorios de las prácticas y acciones informativas reali-zadas en este dominio


Sujets)
Humains , Gestion de l'information en santé , Services de santé , Recherche , Systèmes d'information , Hôpitaux
13.
Rev. enferm. Inst. Mex. Seguro Soc ; 31(3): 67-68, 10-jul-2023.
Article Dans Espagnol | LILACS, BDENF | ID: biblio-1518819

Résumé

La razón del ser y del saber que es objeto de estudio de la enfermería es el cuidado de las personas. Para garantizar la continuidad en el cuidado de las personas, el personal de enfermería realiza el enlace de turno en los diversos escenarios clínicos, durante el cual es imprescindible una actitud de compromiso, empatía y habilidad de comunicación efectiva para compartir ­transferir­ el estado de las personas que son sujetos de cuidados. Se han desarrollado herramientas que ayudan a reducir errores durante la transferencia de pacientes y el enlace de turno, como el protocolo Escuchar-escribir-leer-confirmar y la técnica SAER (Situación, antecedentes, evaluación y recomendaciones) o SBAR por sus siglas en inglés.


The entire purpose which is the object of study of nursing is the care of individuals. To guarantee continuity on this task, the nursing staff performs the shift change in the various clinical scenarios, during which an attitude of commitment, empathy and effective communication skills is essential to share ­transfer­ the status of the individuals under care. Tools that help reducing errors during patient transfer and shift change have been developed, such as the Listen-Write-Read-Confirm protocol, and the SBAR technique


Sujets)
Humains , Mâle , Femelle , Personnel infirmier/éthique , Transfert de patient/éthique , Soins/organisation et administration
14.
RECIIS (Online) ; 17(1): 47-66, jan.-marc. 2023.
Article Dans Portugais | LILACS | ID: biblio-1418672

Résumé

A pandemia da covid-19 tem desafiado a humanidade, com implicações alarmantes. Por essa razão, também há uma forte preocupação com a circulação de informações falsas que atrapalham a luta contra a doença e comprometem o cumprimento de orientações seguras para prevenção e tratamento da infecção. Neste artigo, analisamos as ações empregadas para combater esse tipo de conteúdo através do projeto Saúde sem Fake News do Ministério da Saúde, enquanto estava ativo, e propomos a elaboração de uma nova categorização das verificações classificadas pelo canal como "Isto é fake news!", a partir do conceito e da metodologia de desordem da informação. Como resultado, identificamos que o canal adotou uma postura reativa que se limitava a atestar a veracidade ou falsidade das verificações, sem problematizar as suas especificidades, ignorando os aspectos essenciais para o efetivo combate da desinformação


The covid-19 pandemic has challenged humanity, with alarming implications. Thus, there is also a strong concern about the circulation of false information that hinders the fight against the disease and compromise the fulfillment of safe guidelines for the prevention and the treatment of infection. In this article we analyze the actions to fight against this type of content through the Saúde sem Fake News project of the Ministry of Health, while it was active, and propose the formulation of a new categorization of the checks classified by the channel as "This is fake news!", based on the concept and the methodology of information disorder. As a result, we identified that the channel adopted a reactive stance that limited itself to attesting to the veracity or the falsity of the verifications, not questioning their specificities, ignoring essential aspects for the effective fight against misinformation


La pandemia de covid-19 ha desafiado a la humanidad, con implicaciones alarmantes. Por eso, también existe una fuerte preocupación por la circulación de informaciones falsas que dificultan la lucha contra la enfermedad y compromete el cumplimiento de pautas seguras para la prevención y el tratamiento de la infección. En este artículo analizamos las acciones utilizadas para combatir este tipo de contenido a través del proyecto Saúde sem Fake News del Ministerio de Salud, mientras estuvo activo, y proponemos la elaboración de una nueva categorización de las verificaciones clasificadas por el canal como "Esta es una información falsa!" basándonos en el concepto y la metodología del desorden de la información. Como re-sultado, identificamos que el canal adoptó una postura reactiva, limitada a certificar la veracidad o falsedad de las verificaciones, sin analizar sus especificidades, ignorando aspectos esenciales para la lucha eficaz contra la desinformación


Sujets)
Humains , COVID-19 , Désinformation , Santé publique , Communication , Information du Public , Diffusion de l'information , Communication sur la santé , Sources d'information
15.
Chinese Journal of Medical Instrumentation ; (6): 454-458, 2023.
Article Dans Chinois | WPRIM | ID: wpr-982264

Résumé

OBJECTIVE@#In order to record the whole life process information of medical equipment and improve the management efficiency, this study proposes an informatization scheme for the whole life cycle management of medical equipment.@*METHODS@#Relying on cloud-native, based on the software architecture of front-end and back-end separation, a mode of sub-account and sub-authority management of medical equipment was designed to integrate maintenance work orders, operation reports and other functions, and manage medical equipment data in a structured and platform-based manner.@*RESULTS@#Comparing the equipment failure rate, maintenance response time, and average inventory time per device before and after the system operation, the differences are statistically significant (P<0.05).@*CONCLUSIONS@#The system can realize the work collaboration of maintenance engineers, equipment users, and equipment management personnel, and can trace the information of the whole life cycle of the equipment.


Sujets)
Logiciel , Systèmes d'information
16.
World Science and Technology-Modernization of Traditional Chinese Medicine ; (12): 2287-2296, 2023.
Article Dans Chinois | WPRIM | ID: wpr-1019689

Résumé

Outpatient information management system is an important part of hospital information system,which plays an important role in hospital management,patient treatment,medical insurance reimbursement and settlement.This study integrated the application modes of big data,cloud computing,Internet of things and other cutting-edge technologies of artificial intelligence,focused on the intelligent decision support and whole-process simplified management of the diagnosis and treatment behavior of clinical TCM physicians,and developed a cloud intelligent TCM outpatient system for primary medical care.The system has intelligent medical functions such as intelligent prescription monitoring driven by the rule engine and intelligent recommendation of traditional Chinese medicine knowledge.It seamlessly connects with the intelligent four-diagnosis instrument for information collection and medical order input,and realizes the cloud storage,computing,distribution,management,service and outpatient process,multi-directional and convenient management mode.

17.
Chinese Journal of Medical Science Research Management ; (4): 62-66, 2023.
Article Dans Chinois | WPRIM | ID: wpr-995830

Résumé

Objective:To establish a standardized information management system (IMS) for preserving, managing, querying, and performing statistics on biospecimens and their clinical data, which is conducive to improving the utilization of biobank.Methods:Under the premise of ensuring operating environment and data security, a database-based data logic relationship model is created and applied to the IMS to manage and analyze biospecimens and their supporting clinical information of patients enrolled in the biobank of our center.Results:To ensure the establishment of the follow-up cohort, biospecimens and clinical information of inpatients and outpatients were continuously collected in the biobank of our center. Since December 2014, more than 270 000 biospecimens from inpatient, outpatient, and scientific research have been preserved. The IMS optimized by this model efficiently completes the basic work of the biobank. At the same time, the data can be queried jointly and in batches, and then converted into a report format for statistical analysis.Conclusions:The IMS of our center is suitable for application and popularization as a construction and management model for the hospital-level biobank, which meets the daily work of the biobank and diverse research needs, and provides a convenient platform and rich resources for the development of precision medicine.

18.
Chinese Journal of Medical Science Research Management ; (4): 67-70, 2023.
Article Dans Chinois | WPRIM | ID: wpr-995831

Résumé

Objective:To promote clinical innovation and patent transformation, Ningbo First Hospital built a medical device innovation and transformation management information platform to optimize the supply of clinical innovation and transformation resources and explore a new path of clinical innovation and transformation management.Methods:A series of processes of medical device innovation research, patent declaration, and transformation were managed by the cloud data platform based on Springboot micro-service architecture. The functions and practices of the medical device innovation and transformation management information platform were elaborated on in detail, and the problems in the platform construction were discussed.Results:The medical device innovation and transformation management information platform has been accepted and recognized by clinical care, enterprises, and third-party agents for shortening the research and development and transformation time of innovative projects.Conclusions:The medical device innovation and transformation management information platform can promote the output and achievement transformation of clinical innovative projects.

19.
Chinese Journal of Medical Science Research Management ; (4): 308-311, 2023.
Article Dans Chinois | WPRIM | ID: wpr-995874

Résumé

Objective:In the context of China′s increasing standardized management requirements of clinical research, this article aims to explore the management methods of investigator-initiated trials in the new period, to provide possible reference for other medical institutions dedicated to clinical research.Methods:According to the requirements set forth by the"Administrative Measures for Investigator-Initiated Trials in Medical and Health Institutions (Trial)", combined with the hospital management practice, experiences regarding the research management system construction and implementation, management system construction and its implementation effects are summarized and analyzed.Results:By exploring and summarizing the connotation of high-quality clinical research under the New Policy, tailored clinical research management system in our hospital was developed and implemented. And the hospital′s clinical research capability and level have been greatly improved, which enhancing the hospital academic influence, as well as its competence for serving the development of national and regional clinical research.Conclusions:Along with the rapid progress of clinical research, hospitals need to assure the compliance of national laws and regulations, and develop appropriate and applicable institutional management measures to empower the conduct of high quality clinical research.

20.
Chinese Journal of Blood Transfusion ; (12): 1159-1162, 2023.
Article Dans Chinois | WPRIM | ID: wpr-1003956

Résumé

【Objective】 To develop a mobile software application named " Component Assistant" and test for its performance in practical work, so as to address the difficulties and problems encountered during the management process of blood component preparation, such as communication and coordination in the workflow, personnel scheduling and workload arrangements. 【Methods】 The software was developed based on the daily work requirements and processes using Java language, and foreground-background separation technologies were employed to provide secure and reliable data support. 【Results】 The results of practical work verification showed that through this software, component preparation managers were able to real-time monitor blood collection situations, blood transfusion details, manage inventory levels, and summarize and review the details of the preparation process. Comparison of the usage sequence of this software, the average amount of blood prepared of employees has increased(198 bloodbag, /M), the workload of employees has increased(3.5, /M) and the rest time has been shortened(1 h, /M). 【Conclusion】 The innovation of this software lies in providing effective data support for matching the workload and personnel in component preparation operations, meeting the needs of blood component preparation management, and greatly improving work efficiency in this field.

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