Base de datos : IBECS
Búsqueda : F01.100.050 [Categoria DeCS]
Referencias encontradas : 340 [refinar]
Mostrando: 1 .. 10   en el formato [Largo]

página 1 de 34 va a la página                         

  1 / 340 IBECS  
              next record last record
selecciona
para imprimir
Fotocópia
Id: 173279
Autor: Arroyo González, Ainara.
Título: Salud física de la persona con trastorno mental grave: sensibilización a los profesionales de atención primaria / No disponible
Fuente: Inf. psiquiatr(231):67-83, ene.-mar. 2018. tab.
Idioma: es.
Resumen: El presente trabajo se propone recoger la opinión y actitudes de médicos, enfermeros y trabajadores sociales de los Centros de Atención Primaria (CAP) de Ibiza y Pacífico, pertenecientes al distrito de Retiro, sobre la atención que llevan a cabo en sus consultas a los pacientes con Trastorno Mental Grave (TMG), así como sensibilizar acerca de la problemática de la salud física y el estigma asociados. Esta acción se materializó a través de la aplicación de una encuesta anónima con formato de preguntas cerradas y abiertas que recoge la percepción general ante el paciente con TMG por parte del profesional de Atención Primaria (AP), la autopercepción de conocimientos o formación en materia de enfermedad mental y los problemas de salud física más comúnmente asociados, los recursos del entorno promotores de hábitos saludables y la coordinación existente entre dispositivos y niveles asistenciales. Tras el análisis descriptivo de los resultados, se pone de manifiesto: Que los profesionales de atención primaria tienen mucho que decir respecto a los pacientes con TMG a los que atienden. Que presentan actitudes de rechazo, miedo y estigma relacionadas con dificultades en el manejo por la falta de conocimientos y formación en salud mental así como de la comorbilidad física que presentan. Y que es necesario mejorar la coordinación entre dispositivos. Estos resultados fueron devueltos a los profesionales en una acción de sensibilización llevado a cabo en los CAP acerca del estado de salud física del paciente con TMG, de donde surgieron propuestas de coordinación y colaboración entre dispositivos para mejorar la atención del usuario y el cuidado de su salud física

The present work aims to collect the opinion and attitudes of doctors, nurses and social workers of the Primary Care Centers (PCC) of Ibiza and Pacific, belonging to the district of Retiro, about the care they carry out in their consultations to patients with Severe Mental Disorder (SMD), as well as raising awareness about the associated physical health problems. This action was materialized through the application of an anonymous survey in the form of closed and open questions that reflects the general perception of the patient with SMD by the Primary Care Professional (PCC), the self-perception of knowledge or training in the field of mental illness and the physical health problems most commonly associated, the resources of the environment promoting healthy habits and the existing coordination between devices and levels of care. After the descriptive analysis of the results, it becomes clear: That the primary care professionals have a lot to say about the patients with SMD that they attend. They present attitudes of rejection, fear and stigma related to difficulties in handling due to the lack of knowledge and training in mental health as well as the physical comorbidity they present. And also that it is necessary to improve the coordination between devices. These results were returned to the professionals in an awareness-raising action carried out in the CAPs about the physical health status of the patient with SMD, from which proposals for coordination and collaboration between devices emerged to improve the user's attention and care of their patients
Responsable: ES1.1
BNCS


  2 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 172796
Autor: Moreno Küstner, Berta; Bordallo Aragón, Antonio; Sepúlveda Muñoz, Jesús.
Título: Estudio psicométrico de un cuestionario sobre las actitudes de los médicos de atención primaria hacia la salud mental: Cuestionario MAPSAM-14 / Psychometrics properties of a questionnaire on the attitudes of general practitioners towards mental health (MAPSAM-14)
Fuente: An. psicol;34(2):258-263, mayo 2018. tab.
Idioma: es.
Resumen: Antecedentes: El objetivo de este estudio es la adaptación y el análisis de las propiedades psicométricas de un cuestionario para medir las opiniones y percepciones de los médicos de atención primaria hacia la salud mental. Método: Se trata de un estudio observacional, descriptivo y transversal. Han participado 145 médicos de atención primaria pertenecientes al área de referencia del Hospital Regional de Málaga, que contestaron un cuestionario de 25 items. Con dicho cuestionario se realizó un análisis factorial exploratorio y de consistencia interna. Resultados: Las condiciones de adecuación muestral y esfericidad se cumplieron de forma satisfactoria. En el análisis factorial se obtuvieron 3 dimensiones medidas por 14 items que explican el 55.1% de la varianza total: el cuestionario MAPSAM-14 (Cuestionario de Médicos de Atención Primaria y Salud Mental). Conclusiones: Este cuestionario puede ser una herramienta de rápida aplicación, válida y fiable, para conocer la satisfacción de los médicos de atención primaria respecto a su relación con los equipos de salud mental, sus creencias hacia la enfermedad mental y su percepción del nivel de formación en relación con la esquizofrenia y trastornos afines

Background: The aim of this study is to adapt and analyze the psychometric properties of a questionnaire on the perceptions of general practitioners towards mental health. Method: This is a descriptive crosssectional, observational study. A total of 145 general practitioners from the reference area of Malaga Regional Hospital answered this 25-item questionnaire; a factorial analysis was then conducted and its internal consistency reliability was tested. Results: The adequacy of sampling and sphericity were satisfactorily met. Three dimensions measured by 14 items were found in the factorial analysis explaining 55.1% of its variance: the MAPSAM-14 questionnaire. Conclusions: This questionnaire may be a proper tool with which to determine the satisfaction of general practitioners in relation to mental health services, their beliefs and stigma towards mental illness and their level of training in the field of schizophrenia and related disorders
Responsable: ES1.1
BNCS


  3 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 172703
Autor: Martínez-Serrano, Paloma; Palmar-Santos, Ana M; Solís-Muñoz, Montserrat; Pedraz-Marcos, Azucena; del Pliego-Pilo, Gema; Alarcón-Diana, M Paz; Álvarez-Plaza, Consuelo.
Título: Proceso de atención al parto en la muerte fetal tardía / Delivery care process in late fetal death
Fuente: Metas enferm;21(7):24-32, sept. 2018. tab, graf.
Idioma: es.
Resumen: Objetivo: analizar la evidencia disponible acerca del proceso de atención al parto en la muerte fetal tardía, que permita conocer la experiencia y las necesidades de madres y padres, y la experiencia y dificultades de los profesionales que atienden estos casos. Método: revisión narrativa de estudios cualitativos publicados desde 2005 hasta agosto de 2017 en las bases de datos Pubmed, Cinahl, Embase, Scielo, Cuiden y Lilacs en el campo de la muerte fetal tardía, atendiendo a su definición en el contexto español (a partir de 28 semanas de gestación) y en el internacional (a partir de la semana 24 de gestación). Se llevó a cabo un análisis temático de los artículos seleccionados, identificándose cuatro áreas temáticas en función a la experiencia de las madres y padres, por un lado, y dos áreas temáticas según la experiencia de los profesionales. Resultados: se seleccionaron siete artículos cualitativos (cuatro análisis de contenido, dos análisis fenomenológicos y una teoría fundamentada). Los temas identificados respecto a la experiencia de madres y padres estuvieron relacionados con un diagnóstico devastador, comienzo de la despedida, construcción de la maternidad y la paternidad, e impacto de la actuación de los profesionales. Los temas identificados en relación a la experiencia de los profesionales fueron impacto personal y profesional, y manejo del caso. Conclusiones: esta revisión pone de manifiesto tanto lo traumático de la experiencia de las madres y padres que sufren una pérdida fetal tardía como la afectación personal de los profesionales que les atienden, que presentan dificultades para afrontar adecuadamente el caso, y demandan formación específica para ayudar de forma eficiente en el proceso de duelo

Objective: to analyze the evidence available about the delivery care process in late fetal death, allowing to learn about the experience and needs of mothers and fathers, and the challenges for the professionals managing these cases. Method: a narrative review of qualitative studies published from 2005 to August, 2017 in the following databases: Pubmed, Cinahl, Embase, Scielo, Cuiden and Llilacs, on the area of late fetal death, according to its definition in the Spanish setting (from 28 gestation weeks onwards), and in the international setting (from week 24 of gestation). A themed analysis was conducted on the articles selected, and four theme areas were identified, based on the experience of mothers and fathers on one hand, and two theme areas according to the experience of professionals. Results: seven qualitative articles were selected: four content analyses, two phenomenological analyses, and one grounded theory. The themes identified regarding the experience of mothers and fathers were associated with a devastating diagnosis, the initial goodbye, building maternity and paternity, and the impact of the action by professionals. The themes identified associated with the experience of professionals were: personal and professional impact, and case management. Conclusions: this review shows the traumatic experience of mothers and fathers suffering a late fetal loss, as well as the personal impact on those professionals managing them, who will be faced with difficulties for addressing the case adequately, and demand specific training to help in the mourning process in an efficient way
Responsable: ES1.1
BNCS


  4 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 172673
Autor: Agra Tuñas, M del Carmen; Pérez Varela, Fátima; Bello Rama, Eva; Mato Guerra, Paula; Calviño Vieito, Nuria; Garrudo Díaz, Rubén; Pérez Rivas, Manuela; Rodríguez Núñez, Antonio.
Título: Cuidados intensivos pediátricos: calidad percibida por los progenitores / Pediatric Intensive Care: Quality perceived by parents
Fuente: Metas enferm;21(3):19-26, abr. 2018. tab, graf.
Idioma: es.
Resumen: Objetivo: evaluar la calidad de los cuidados realizados en la Unidad de Cuidados Intensivos Pediátrica (UCIP) desde la perspectiva de los familiares de los pacientes. Método: estudio transversal llevado a cabo en la UCIP del Hospital Clínico Universitario de Santiago de Compostela (A Coruña), entre el 01/01/2016 y el 25/01/2017. Se invitó a participar a los familiares de los niños que fueron dados de alta de la UCIP en ese periodo, solicitando que cumplimentaran el cuestionario EMPATHIC-30, que consta de 30 ítems distribuidos en cinco dimensiones. Se excluyeron los ingresos de menos de 24 horas, los fallecidos, los ingresos previos en los últimos seis meses y los casos de desconocimiento del idioma. Se entregaron un total de 308 encuestas. Se llevó a cabo un análisis descriptivo. Los datos se presentaron con media y desviación estándar (DE). Resultados: se recogieron 181 encuestas (58,8% de los casos posibles). El 63,5% fue cumplimentada por madres, el 26% fue un ingreso superior a siete días, el 32% traslados desde otro hospital y el 30,4% ingresos programados. Sobre una puntuación de 5, la media (DE) de satisfacción de los progenitores fue 4,5 (0,6). Respecto a las distintas dimensiones del cuestionario: organización de la unidad 4,7 (0,5), actitud de los profesionales 4,6 (0,7), cuidados y tratamiento 4,5 (0,7), información 4,4 (0,8) y participación familiar 4,3 (0,8). Los ítems peor valorados fueron el interés del personal por las preocupaciones de los padres 3,9 (1,2) y la participación de los progenitores en la toma de decisiones 3,9 (1,2). Conclusiones: los progenitores de los niños ingresados en la UCIP valoran de forma muy positiva la calidad de los cuidados y la atención llevada a cabo por los profesionales. Sin embargo, se debería mejorar la actitud y empatía de los profesionales, además de fomentar la participación de la familia en los procesos de toma de decisiones

Objectives: to assess the quality of care offered at the Paediatric Intensive Care Unit (PICU) from the perspective of patient's relatives. Method: a transversal study conducted at the PICU of the Hospital Clínico Universitario de Santiago de Compostela (A Coruña), between January, 1st, 2016 and January, 25th, 2017. The relatives of children discharged from the PICU within this period were invited to take part, and they were requested to complete the EMPATHIC-30 questionnaire, which consists in 30 items distributed into five dimensions. The study excluded hospitalizations < 24 hours, deaths, previous admissions in the past six months, and those cases with lack of knowledge of the language. Overall, 308 surveys were handed out. There was a descriptive analysis, and data were presented with mean and standard deviation (SD). Results: there was a collection of 181 surveys (58.8% of all likely cases); of these, 63.5% were completed by mothers, and 26% were for hospitalizations >7 days, 32% were referrals from other hospitals, and 30.4% were scheduled hospitalizations. On a 5 score, the mean (SD) satisfaction of parents was 4.5 (0.6). Regarding the different dimensions in the questionnaire, the scores were: unit organization: 4.7 (0.5), attitude of professionals: 4.6 (0.7), care and treatment: 4.5 (0.7), information: 4.4 (0.8), and family involvement: 4.3 (0.8). The worse rated items were: Interest by the staff for parents' concerns: 3.9 (1.2), and parents' involvement in decision making: 3.9 (1.2). Conclusions: parents of children admitted in the PICU rate very positively the quality of care conducted by professionals. However, there should be an improvement in the attitude and empathy by professionals, and family involvement should be encouraged in terms of decision making processes
Responsable: ES1.1
BNCS


  5 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 172253
Autor: Ríos Zambudio, Antonio.
Título: Proyecto colaborativo internacional donante / International collaborative donor project
Fuente: Cir. Esp. (Ed. impr.);96(2):69-75, feb. 2018. graf, tab, ilus.
Idioma: es.
Resumen: El grupo de investigación Proyecto Colaborativo Internacional Donante (PCID) surge en el año 1996 en España con el objetivo de potenciar la investigación en el campo de la donación y el trasplante de órganos, liderado por cirujanos españoles. Durante este período han desarrollado los cuestionarios del PCID, tanto el de actitud hacia la donación de cadáver como de vivo, que son los cuestionarios más utilizados en publicaciones en revistas indexadas. Ha sido el grupo impulsor de estudios estratificados representativos de las poblaciones a estudio y de la realización de análisis estadísticos multivariantes en el campo de las investigaciones psicosociales en la donación y el trasplante de órganos. Las principales aportaciones del grupo se centran en el análisis de los profesionales de centros sanitarios y en grupos emigrantes emergentes. En los últimos años, se han extendido los estudios a Estados Unidos, Latinoamérica (principalmente México) y Europa (AU)

The International Donor Collaborative Project (PCID) research group was created in 1996 in Spain with the aim of promoting research in the field of organ donation and transplantation, led by Spanish surgeons. During this period they have developed the questionnaires of the PCID, both the attitude towards cadaver and live donation, which are the most used questionnaires in publications in indexed journals. They have been the driving group of stratified studies representative of the populations under study, and of the performance of multivariate statistical analyzes in the field of psycho-social research in organ donation and transplantation. The main contributions of the group focus on the analysis of health center professionals and emerging migrant groups. In recent years, studies have been extended to the United States, Latin America (mainly Mexico) and Europe (AU)
Responsable: ES1.1
BNCS


  6 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 171856
Autor: Tegegn, Henok Getachew; Abdela, Ousman Abubeker; Mekuria, Abebe Basazn; Bhag Avathula, Akshaya Srikanth; Ayele, Asnakew Achaw.
Título: Challenges and opportunities of clinical pharmacy services in Ethiopia: a qualitative study from healthcare practitioners' perspective
Fuente: Pharm. pract. (Granada, Internet);16(1):0-0, ene.-mar. 2018. tab.
Idioma: en.
Resumen: Background: Currently, clinical pharmacists have in-depth therapeutic knowledge and scientific skills to act as drug therapy experts in healthcare settings. Objective:The aim of this study was to assess the opportunities and challenges of clinical pharmacy services from the health practitioners' perspective in University of Gondar (UOG) hospital Ethiopia. Methods: A qualitative study was performed using face-to-face in-depth interviews with health practitioners who were directly involvedin clinical pharmacy services (clinical pharmacists, physicians, and nurses) in UOG hospital. Results: A total of 15 health professionals from various specialties were interviewed to express their views towards clinical pharmacists' competencies and identified challenges and opportunities regarding their clinical services. Based on inter-viewees report,the opportunities for clinical pharmacists includes acceptance of their clinical services among health specialties, new government policy and high patient load in hospital. However, inadequacy of service promotions, lack of continuity of clinical pharmacy services in wards, poor drug information services, lack of commitment, lack of confidence among clinical pharmacists, conflict of interest due to unclear scope of practice, and absence of cooperation with health workers were some of the challenges identified by the interviewees. Conclusion: We identified health professionals working in UOG hospital are receptive towards clinical pharmacy services, but identified some of the potential challenges that needed to be focused to strengthen and promote clinical pharmacy services. Further, the opportunities at hand also need to be utilized astutely to boost the services (AU)

No disponible
Responsable: ES1.1
BNCS


  7 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 171853
Autor: Saade, Sylvia; Ghazala, Fatima; Farhat, Ali; Hallit, Souheil.
Título: Attitudes towards continuous professional development: a study of pharmacists in Lebanon
Fuente: Pharm. pract. (Granada, Internet);16(1):0-0, ene.-mar. 2018. tab.
Idioma: en.
Resumen: Objective: To investigate the views and assess motivation, attitudes of pharmacists in Lebanon towards mandatory continuous education (CE), its transition to Continuous Professional Development (CPD), and identify barriers to participation in CPD. Methods: A cross-sectional observational study, conducted between February and May 2017, enrolled 591 pharmacists. The questionnaire used in this study was developed after an extensive literature review and based on previous similar studies in different countries. Results: Half of the pharmacists who completed the questionnaire agreed that all the factors that were mentioned in the questionnaire motivated completing CPD, whereas 55.4% felt confident that CPD meets their needs. 78.4% felt confident in their abilities to assess what they have learned. 71.6% felt confident in their abilities to assess what additional CPD activity may be necessary. The majority of the pharmacists agreed that accessibility of group learning activities location/distance) (69.6%), job restrictions (76.3%) and lack of time (80.6%) were the most essential barriers against participation in CPD. Motivation was significantly and positively correlated with attitude (r= 0.718), but negatively correlated with barriers (r= -0.243). Attitude was significantly and negatively correlated with barriers (r= -0.120). Conclusion: Our findings contribute to informing the forward pathway for the profession. Attitude and motivation to CPD were positive in this study. Accessibility of group learning activities due to distance and location, job restrictions and lack of time were the major barriers to participation in CPD. Potential solutions can be sought to address these issues (AU)

No disponible
Responsable: ES1.1
BNCS


  8 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Id: 171708
Autor: Rabanaque Mallén, Gloria; Robles Pellitero, Sandra; Borrell Gascón, Adoración; Orozco Mossi, Nuria.
Título: Actitud de los médicos de familia ante los cuidados paliativos en zonas rurales sin cobertura de unidad de hospitalización a domicilio / The attitude of family practitioners to palliative care in rural areas with no domiciliary hospitalisation coverage
Fuente: Med. paliat;25(2):94-104, abr.-jun. 2018. ilus, tab.
Idioma: es.
Resumen: Objetivo: Analizar la aptitud y actitud de los médicos de familia de zonas rurales sin cobertura de unidades de hospitalización a domicilio (UHD) ante los cuidados paliativos (CP). Aportar evidencia sobre los condicionantes que determinan la aplicación de los CP en el medio rural de la zona a estudio. Método: Estudio observacional, transversal, cualitativo. Encuesta semiestructurada de 27 preguntas y entrevista telefónica a todos los médicos de atención primaria y continuada de una comarca de 27 pueblos, dispersos geográficamente y alejados del hospital, administradas por tutores y médicos residentes de un centro rural docente en 2014 que dieron su consentimiento, con cuestionario piloto previo. Resultados: Participan 27 de los 30 médicos; 3 rehúsan colaborar. La edad media es de 53,3 años y la moda de 58; tienen una media de 24,2 (8-40) años de ejercicio profesional y de 18,4 (2-40) años en el medio rural. La isócrona hasta el hospital oscila entre 20 y 75min. La población es envejecida, con un alto porcentaje de personas que viven solas. El 70 por mil de médicos (19) asumen los CP (5-10 pacientes de media/año), conocen los recursos del Departamento para CP. Solo 1/3 los utilizan. Un 54 por mil creen tener conocimientos y preparación suficiente para abordarlos. El 70 por mil de médicos informan al paciente, cuentan con su opinión para la toma de decisiones y atienden al duelo; un 18 por mil no lo hacen y solo informan a la familia y/o cuidador principal; el 11 por mil nunca informan. La mayoría considera importante ayudar a bien morir en el domicilio si es deseo del paciente y la familia. Apuntan como problemas: deficiente coordinación con la atención especializada, desconocimiento de recursos, carencia de medios, aislamiento, desinformación, falta de destrezas, inadecuada gestión de la consulta, necesidad de implementar la visita domiciliaria. Conclusiones: Existe variabilidad en las creencias, actitud y aptitud entre los médicos rurales frente al abordaje de CP, condicionando desigualdad sociosanitaria en función del lugar de residencia y médico asignado de los pacientes, siendo necesario implementar programas de sensibilización y formación para los médicos de familia (AU)

Objective: To analyse the aptitude, attitude of rural family doctors in rural regions without domiciliary hospitalisation (DH) towards palliative care (PC). To show evidence of the factors determining the application of PC in the rural area under study. Method: An observational, qualitative, cross-sectional study. A semi-structured survey of 27 questions and telephone interviews of all the doctors of primary and ongoing care in a region of 27 geographically dispersed villages, distant from a hospital, led by medical tutors and residents from the Rural Educational Centre in 2014. Previous pilot questionnaire. Results: Twenty-seven of the 30 physicians participated. Mean age 53.3 years, mode 58; mean of 24.2 (8-40) years of professional practice; 18.4 (2-40) years in rural areas. The isochronal distance to the hospital ranged between 20 to 75min. The population was aging, with a high percentage of people living alone. Two thirds of the family physicians (19) covered PC (5-10 patients/year), and knew the department's resources for PC. Only 1/3 used them. Half believed they had the knowledge and skills to manage them. Two thirds of the physicians informed the patients and took their opinions into account for decision making, and provided bereavement support. Nearly all of them informed the family and/or main carer, 3 never informed. The majority considered it important to offer assistance towards dying well at home if this was the patient's and their family's wish. They pointed out problems such as the deficient coordination with specialised care, lack of knowledge of resources, lack of means, isolation, misinformation, lack of skills, inadequate management at medical consultation, and the need to implement the domiciliary visit. Conclusions: There is a variation in beliefs, attitude and aptitude between rural doctors towards the approach to palliative care, which results in socio-sanitary inequalities with regard to place of residence, and doctors allocated to patients. It is necessary to implement sensitization and training programmes for family doctors (AU)
Responsable: ES1.1
BNCS


  9 / 340 IBECS  
              first record previous record next record last record
selecciona
para imprimir
Fotocópia
Texto completo SciELO España
Id: 169843
Autor: Gabriel, Carmen Silvia; Bogarin, Denise Franzé; Mikael, Sabrina; Cummings, Greta; Bernardes, Andrea; Gutierrez, Larissa; Caldana, Graziela.
Título: Perspectiva de las enfermeras brasileñas sobre el impacto de la Acreditación Hospitalaria / Perspectiva dos Enfermeiros Brasileiros sobre o Impacto da Acreditação Hospitalar / Brazilian Nurses' Perspective on the Impact of Hospital Accreditation
Fuente: Enferm. glob;17(49):381-394, ene. 2018. tab.
Idioma: es.
Resumen: El estudio tuvo como objetivo identificar el impacto de los programas de acreditación hospitalaria desde la perspectiva de las enfermeras. Este es un estudio cuantitativo, descriptivo, exploratorio, que tuvo lugar en hospital general privado acreditado con excelencia (Nivel III, el más alto) por la Organización Nacional de Acreditación. La recolección de datos se realizó mediante un cuestionario tipo Likert compuesto por siete escalas relacionadas con: la calidad de los resultados; El uso de los recursos humanos; la calidad de la planificación estratégica; Gestión de la Calidad; El uso de datos relacionados con la satisfacción del paciente; Participación del personal; Y los beneficios de la acreditación. Los resultados muestran que las enfermeras se dieron cuenta de las mejoras resultantes del proceso de acreditación en las siguientes áreas: planificación estratégica de la calidad; Gestión de la Calidad; Utilización de los datos relacionados con la satisfacción del paciente y la participación del personal con la calidad del hospital. Por el contrario, el proceso de acreditación no resultó en desarrollos en relación al tiempo dado a las enfermeras para preparar y probar mejoras de la calidad y también para el uso de los recursos humanos, especialmente en lo que se refiere a las recompensas y estrategias de reconocimiento. Llegamos a la conclusión de que las enfermeras tienen un papel clave en la consecución del proceso de acreditación y, por tanto, las recompensas y las estrategias de reconocimiento precisan ser mejor desarrolladas y puestas en práctica y las enfermeras necesitan tener tiempo suficiente para realizar actividades relacionadas con el proceso de acreditación (AU)

O estudo objetivou identificar o impacto dos programas de acreditação hospitalar do ponto de vista dos enfermeiros. Trata-se de um estudo quantitativo, descritivo, exploratório, realizado em hospital geral privado credenciado com Excelência (Nível III, o mais alto) pela Organização Nacional de Acreditação. A coleta de dados foi realizada por meio de um questionário de tipo Likert composto por sete escalas relacionadas a: Resultados de qualidade; Utilização de recursos humanos; Planejamento estratégico de qualidade; Gestão da Qualidade; Uso de dados relacionados à satisfação do paciente; Envolvimento do pessoal; E os benefícios da acreditação. Os resultados mostram que os enfermeiros perceberam melhorias como resultado do processo de acreditação nas seguintes àreas: Planejamento estratégico de qualidade; Gestão da Qualidade; uso de dados relacionados à satisfação do paciente e envolvimento do pessoal com qualidade hospitalar. Inversamente, o processo de acreditação não resultou em desenvolvimentos em relação ao tempo dado aos enfermeiros para planejar e testar melhorias de qualidade, e também em relação à utilização de recursos humanos, especialmente no que se refere a recompensas e estratégias de reconhecimento. Concluímos que os enfermeiros têm um papel fundamental na realização do processo de acreditação e, portanto, as recompensas e as estratégias de reconhecimento precisam ser melhor desenvolvidas e implementadas e os enfermeiros precisam ter tempo suficiente para realizar atividades relacionadas ao processo de acreditação (AU)

This study aimed to identify the impact of hospital accreditation programs from the nurses' perspective. This quantitative, descriptive, exploratory study was performed in a private general hospital. This institution is accredited with Excellence (Level III, the highest) by the Brazilian National Accreditation Organization. Data collection was conducted using a Likert-type questionnaire consisting of seven scales related to: quality results; human resources utilization; strategic quality planning; quality management; use of data related to patient satisfaction; staff involvement; and benefits of accreditation. The results show that nurses perceived improvements as outcome of the accreditation process in the following areas: strategic quality planning; quality management; use of data related to patient satisfaction; and staff involvement with hospital quality. Inversely, the accreditation process have not result in developments in relation to the time given to nurses to plan for and test quality improvements, and also in relation to human resources utilization, especially concerning rewards and recognition strategies. We concluded that nurses have a key role in accomplishment of the accreditation process and therefore rewards and recognition strategies need to be better developed and implemented, and nurses need to be given adequate time for performing activities related to the accreditation process (AU)
Responsable: ES1.1
BNCS


  10 / 340 IBECS  
              first record previous record
selecciona
para imprimir
Fotocópia
Id: 169522
Autor: Setiadi, Adji P; Wibowo, Yosi; Irawati, Sylvi; Setiawan, Eko; Presley, Bobby; Gudka, Sajni; Wardhani, Ari S.
Título: Indonesian pharmacists' and pharmacy students' attitudes towar ds collaboration with physicians
Fuente: Pharm. pract. (Granada, Internet);15(4):0-0, oct.-dic. 2017. tab.
Idioma: en.
Resumen: Background: Recent implementation of national health coverage and the increasing health burden in Indonesia require health professionals, including pharmacists, to work more collaboratively to improve access and quality of health care. Nevertheless, relatively little is known about Indonesian pharmacists' attitude towards collaboration. Objective: To assess and compare the attitude of Indonesian pharmacy students and pharmacists towards collaboration with physicians. Methods: A survey of 95 pharmacy students (Universitas Surabaya) and 114 pharmacists (public health facilities in East Java) in Indonesia was conducted using the validated questionnaire, Scale of Attitudes Toward Physician-Pharmacist Collaboration (SATP2C), which was translated in Bahasa Indonesia. The questionnaire contained 16 items which were based on a 4-point Likert scale. Descriptive statistics were used to summarise the responses, (i.e., individual scores, factor scores and total scores). Results: Response rates of 97.9% and 65.8% were reported for students and pharmacists, respectively. The mean total score of SATP2C among Indonesian students and pharmacists were 56.53 versus 56.77, respectively; indicating positive attitudes toward collaboration. Further analysis of each item of SATP2C confirmed the positive attitudes in which mean and median scores of ≥3 were reported for most items in both groups. Significant differences between students and pharmacists were found regarding the following items: (i) 'there are many overlapping areas of responsibility between pharmacists and physicians' (3.28 versus 2.89, respectively; p<0.001), (ii) 'pharmacist should clarify a physician's order' (3.54 versus 3.71, respectively; p=0.046); and (iii) 'physicians should consult with pharmacists about adverse reactions or refractory to drug treatment' (3.60 versus 3.44, respectively; p=0.022). Conclusions: Indonesian pharmacists reported positive attitudes toward collaboration with physicians. Further research is needed to understand other factors contributing in translating those positive attitudes into actual practice, and thus, providing a good foundation for policy makers, researchers and practitioners to support pharmacist-physician collaboration in Indonesia (AU)

No disponible
Responsable: ES1.1
BNCS



página 1 de 34 va a la página                         
   


Refinar la búsqueda
  Base de datos : Formulario avanzado   
Buscar por : Formulario libre    Formulario básico

    Buscar en el campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPS/OMS - Centro Latinoamericano y del Caribe de Información en Ciencias de la Salud