Vivencias e impacto en la calidad de vida de personas con COVID persistente / Experiences and impact on the quality of life of people with long COVID

Objetivo: Explorar las vivencias de las personas con COVID persistente en el País Vasco transcurrido más de 1 año desde el inicio de la pandemia, con el fin de comprender su impacto en la salud y en el ámbito social, así como detectar posibles áreas de mejora en la asistencia que reciben estas personas con el fin de desarrollar programas de salud que apoyen su recuperación. Método: Estudio cualitativo fenomenológico. Como técnica de recogida de datos se realizaron entrevistas en profundidad hasta la saturación del discurso. Se incluyeron pacientes mayores de edad con sintomatología de COVID persistente con un tiempo de evolución mayor de 12 semanas. El contacto con los/las pacientes se realizó a través del Colectivo COVID Persistente de Euskadi. Las entrevistas se realizaron y grabaron con la aplicación ZOOM. Se realizó una trascripción literal de las entrevistas y posteriormente un análisis temático, identificando las primeras unidades de significado y asignando códigos que se agruparon después en las diferentes categorías. Resultados: Participaron 20 pacientes. Del análisis de los discursos emergieron tres categorías principales: 1) afectación/impacto en la calidad de vida de los/las pacientes; 2) detección de mejoras en la asistencia sanitaria; y 3) aspectos que reconfortan. Conclusiones: Este estudio evidencia el importante impacto en la calidad de vida que sufren estas personas. Es necesario diseñar políticas sanitarias que favorezcan el abordaje personalizado, integral y multidisciplinario de tales pacientes. (AU)

Objective: To explore the experiences of people with persistent COVID in the Basque Country more than a year after the start of the pandemic, in order to understand the health and social impact it has, as well as to detect possible areas for improvement in the care that these people receive in order to develop health programms to support their recovery. Method: Qualitative phenomenological study. In-depth interviews will be carried out as a data collection technique until saturation of the discourse. Patients of legal age who present persistent COVID symptomatology with an evolution time of more than 12 weeks were included. Contact with the patients was made through the Basque Long COVID Collective. The interviews were carried out and recorded through the ZOOM application. After the literal transcription of the interviews, the thematic analysis will be carried out, identifying the first units of meaning and assigning codes that will later be grouped into the different categories. Results: 20 patients participated. A total of three main categories emerged from the analysis of the discourses: 1) affecting/impacting patients’ quality of life; 2) identifying improvements in healthcare; and 3) comforting aspects. Conclusions: This study shows the significant impact on the quality of life suffered by these people. It is necessary to design health policies that favour a personalised, comprehensive and multidisciplinary approach to these patients. (AU)

Impacto de la primera ola de Covid-19 en el estudiantado de cuarto curso de grado de enfermería de la Escuela Universitaria de Enfermería de Vitoria-Gasteiz / Impact of first wave covid-19 on fourth course nursing students in vitoria-gasteiz´s university school of nursing

Introducción: La pandemia de Covid-19 ocasionó una situación sanita ria grave que provocó la suspensión de las prácticas clínicas en la titulación de Enfermería. Como alternativa a ellas, el estudiantado de 4º curso realizó, en un Call Center, actividades de atención tele fónica y consejo sanitario para personas afectadas por la pandemia, con un con trato laboral de auxilio sanitario. Objetivo: conocer las experiencias vividas por el estudiantado de cuarto curso de la Es cuela Universitaria de Enfermería de Vi toria-Gasteiz participantes en el Call Center durante la primera ola de la pan demia COVID-19. Metodología: estudio cualitativo fenomenológico, donde se realizaron entrevistas en profundidad hasta la saturación del discurso. Resul tados: surgieron tres categorías de análi sis: la valoración del contrato de Auxilio Sanitario en un Call Center como alter nativa, las emociones identificadas en el estudiantado y la necesidad de apoyo psicológico al incorporarse a la actividad profesional. Conclusiones: la participa ción en el Call Center provocó en el es tudiantado diferentes emociones que tu vieron repercusión en su desarrollo pro fesional y se puso de manifiesto la im portancia del apoyo psicológico en una situación similar (AU)

Introduction: Covid-19 pandemic caused a serious health situation that induced the stopping of clinical practices in the Nursing degree. As an alternative, the 4thcourse students did in a Call Cen ter, phone attention and sanitary advice for people affected with Covid-19 and were provided with a labour contract as Sanitary Aid. Objective: to know the ex periences lived by the 4thcourse stu dents of the University School of Nursing of Vitoria-Gasteiz in the Call Center du ring the first wave of Covid-19 pandemic. Methodology: a qualitative phe nomenological study, with deep inter views until saturation. Results: three ca tegories arose in the analysis: the as sessment of the Sanitary Aid contract in a Call Center as an alternative, the iden tified in the student feelings and expe rience and the need of support on joining the labour force. Conclusions: Joining the Call center triggered different feelings in the students that affected their professio nal behavior and showed the evidence of psychological supporting a similar situa tion (AU)

[Experiences and impact on the quality of life of people with long COVID]. / Vivencias e impacto en la calidad de vida de personas con COVID persistente.

OBJECTIVE: To explore the experiences of people with persistent COVID in the Basque Country more than a year after the start of the pandemic, in order to understand the health and social impact it has, as well as to detect possible areas for improvement in the care that these people receive in order to develop health programms to support their recovery. METHOD: Qualitative phenomenological study. In-depth interviews will be carried out as a data collection technique until saturation of the discourse. Patients of legal age who present persistent COVID symptomatology with an evolution time of more than 12 weeks were included. Contact with the patients was made through the Basque Long COVID Collective. The interviews were carried out and recorded through the ZOOM application. After the literal transcription of the interviews, the thematic analysis will be carried out, identifying the first units of meaning and assigning codes that will later be grouped into the different categories. RESULTS: 20 patients participated. A total of three main categories emerged from the analysis of the discourses: 1) affecting/impacting patients' quality of life; 2) identifying improvements in healthcare; and 3) comforting aspects. CONCLUSIONS: This study shows the significant impact on the quality of life suffered by these people. It is necessary to design health policies that favour a personalised, comprehensive and multidisciplinary approach to these patients.

A questionnaire development to assess the social representation of nurses in the Basque Country: a psychometric assessment.

Background: Only a few Spanish studies have explored how nurses are seen by society and no validated tools exist for this purpose in the scientific literature. Objectives: The aim was create and evaluate the psychometric characteristics of a questionnaire that explored the social representation of nursing in social and health care. Methods: Qualitative and quantitative methods were used to develop the questionnaire and the first version was created based on existing studies. A three-round Delphi technique was used that involved nurses, doctors, journalists and a politician. The pilot questionnaire was then tested and retested with 23 journalism students, with an interval of 10-14 days between the two phases. After further modifications, the questionnaire was sent to all the third and fourth year journalism students at the University of the Basque Country. Principal component factor analysis was used to identify the key components for the questionnaire. Results: A total of 141 third and fourth year journalism students took part in the study. The internal consistency of the 43-item perception section of the questionnaire had a Cronbach's alpha value of 0.90. The 42.7% agreed or strongly agreed that nursing was an eminently scientific profession and 26.3% agreed or strongly agreed with the statement that nurses were presented in the media as health educators and disseminators. Just under a fifth (19.9%) agreed with the statement that society was aware of the competencies that nurses required. Conclusions: The questionnaire provided the first validated tool that allowed researchers to assess how nursing, and all of its areas of professional development, were perceived by society. This could enable studies to assess the evolution of the profession over time and between different socio-cultural contexts.

Modelling the risk of hospital admission of lab confirmed SARS-CoV-2-infected patients in primary care: a population-based study.

The objectives of this study are to develop a predictive model of hospital admission for COVID-19 to help in the activation of emergency services, early referrals from primary care, and the improvement of clinical decision-making in emergency room services. The method is the retrospective cohort study of 49,750 patients with microbiological confirmation of SARS-CoV-2 infection. The sample was randomly divided into two subsamples, for the purposes of derivation and validation of the prediction rule (60% and 40%, respectively). Data collected for this study included sociodemographic data, baseline comorbidities, baseline treatments, and other background data. Multilevel analyses with generalized estimated equations were used to develop the predictive model. Male sex and the gradual effect of age were the main risk factors for hospital admission. Regarding baseline comorbidities, coagulopathies, cancer, cardiovascular diseases, diabetes with organ damage, and liver disease were among the five most notable. Flu vaccination was a risk factor for hospital admission. Drugs that increased risk were chronic systemic steroids, immunosuppressants, angiotensin-converting enzyme inhibitors, and NSAIDs. The AUC of the risk score was 0.821 and 0.828 in the derivation and validation samples, respectively. Based on the risk score, five risk groups were derived with hospital admission ranging from 2.94 to 51.87%. In conclusion, we propose a classification system for people with COVID-19 with a higher risk of hospitalization, and indirectly with it a greater severity of the disease, easy to be completed both in primary care, as well as in emergency services and in hospital emergency room to help in clinical decision-making.Registration: ClinicalTrials.gov Identifier: NCT04463706.

Percepciones y vivencias de escolares de 7 a 8 años del País Vasco durante la alerta sanitaria COVID-19 / Perceptions and experiences of 7-8 year old schoolchildren in the Basque Country during the COVID-19 health alert

Objetivo: Explorar las experiencias y las vivencias de escolares de 7-8 años en una situación excepcional de alerta sanitaria en la que se han aplicado a la población estrictas medidas de confinamiento. Método: Estudio cualitativo exploratorio a través del análisis de ilustraciones realizadas por 71 escolares de 7-8 años de edad. El análisis se llevó a cabo según el marco teórico de Rose. Se realizó análisis descriptivo de los datos sociodemográficos. Resultados: Del análisis del contenido emergieron cinco categorías: 1) sentimientos de tristeza y miedo; 2) importancia del núcleo familiar, seguridad y protección; 3) hábitos de vida sedentarios durante el confinamiento; 4) infraestructuras de las viviendas y desigualdades sociales (la vida tras una ventana); y 5) respuesta social, lucha colectiva y de los/las profesionales de la salud. Conclusiones: La situación de pandemia de COVID-19 y las medidas estrictas de confinamiento han tenido un importante impacto en la población escolar, que es la que ha vivido las mayores restricciones. La infraestructura del hogar se ha mostrado como un claro diferenciador que ahonda en las desigualdades sociales y el impacto que la situación tiene en los/las escolares. Es necesario ampliar los estudios acerca del impacto psicosocial que esta situación va a tener a largo plazo en su salud física y mental. (AU)

Objective: To explore the experiences of schoolchildren in an exceptional health alert situation in which strict confinement measures have been applied to the population. Method: Qualitative exploratory study through the analysis of illustrations carried out by schoolchildren aged 7 to 8. The analysis was carried out according to Rose's theoretical framework. Descriptive analysis of socio-demographic data was performed. Results: Five categories emerged from the analysis of the content: 1) feelings of sadness and fear; 2) importance of the family nucleus, safety and protection; 3) sedentary living habits during confinement; 4) housing infrastructure and social inequalities (life through a window); and 5) social response, collective struggle and through health professionals. Conclusions: The COVID-19 pandemic situation and the strict confinement measures have had a significant impact on the school population, who had experienced the greatest restrictions. Household infrastructure has been shown to be a clear differentiator that deepens social inequalities and the impact that the situation has on school children. More studies are needed on the long-term psychosocial impact of this situation on their physical and mental health.

[Perceptions and experiences of 7-8 year old schoolchildren in the Basque Country during the COVID-19 health alert]. / Percepciones y vivencias de escolares de 7 a 8 años del País Vasco durante la alerta sanitaria COVID-19.

OBJECTIVE: To explore the experiences of schoolchildren in an exceptional health alert situation in which strict confinement measures have been applied to the population. METHOD: Qualitative exploratory study through the analysis of illustrations carried out by schoolchildren aged 7 to 8. The analysis was carried out according to Rose's theoretical framework. Descriptive analysis of socio-demographic data was performed. RESULTS: Five categories emerged from the analysis of the content: 1) feelings of sadness and fear; 2) importance of the family nucleus, safety and protection; 3) sedentary living habits during confinement; 4) housing infrastructure and social inequalities (life through a window); and 5) social response, collective struggle and through health professionals. CONCLUSIONS: The COVID-19 pandemic situation and the strict confinement measures have had a significant impact on the school population, who had experienced the greatest restrictions. Household infrastructure has been shown to be a clear differentiator that deepens social inequalities and the impact that the situation has on school children. More studies are needed on the long-term psychosocial impact of this situation on their physical and mental health.

Clinical and Economic Impact of Wound Care Using a Polyurethane Foam Multilayer Dressing.

OBJECTIVE: To study the impact of a newly introduced dressing on efficiency and quality of care in routine clinical practice in a Spanish community setting. DESIGN AND SETTING: An ambispective multicenter observational study was conducted in 24 primary care centers and 6 nursing homes in 4 different Spanish regions. The study was carried out between November 2017 and March 2019. PATIENTS AND INTERVENTION: A total of 128 wounds in 94 patients (primary care, n = 79; nursing home, n = 15) were analyzed before and 4 weeks after switching to the study dressing. OUTCOME MEASURES: Frequency of dressing changes; secondary outcomes were change in the mean wound area and weekly cost and patient and provider satisfaction. MAIN RESULTS: The mean number of dressing changes was significantly reduced with the study dressing from 3.14 ± 1.77 changes per week to 1.66 ± 0.87 (P < .001), a 47.1% reduction in frequency. Wound area significantly reduced from 9.90 ± 19.62 cm to 7.10 ± 24.33 cm. In addition, a 58.7% reduction in weekly costs was achieved with the intervention. Patients and providers agreed that their satisfaction with wound care improved. CONCLUSIONS: The use of the study dressing in routine clinical practice could lead to a major improvement in both efficiency and quality of wound care. Its use could reduce wound care-related costs through improvements in healing and a reduced frequency of dressing changes. It also enhanced the wound care experience from the perspective of both patients and providers.

Witnessed resuscitation of adult and paediatric hospital patients: An umbrella review of the evidence.

OBJECTIVE: To examine the research evidence about whether families were allowed to witness cardiopulmonary resuscitation on hospitalised adult and paediatric patients; and the views of patients, families and health professionals, about witnessed cardiopulmonary resuscitation. DESIGN: An umbrella review methodology of systematic reviews with sufficient methodological quality. REVIEW METHODS: Papers published in Spanish and English between, 1 January 2009 and 31 December 2018 were considered. The following databases were searched: PubMed, CINAHL, Web of Science, Scopus, Cochrane Central Register of Controlled Trials, PsycInfo, Embase, the Central Supplier Database and the Joanna Briggs Institute, Evidence-based Practice Database. Two independent reviewers assessed the papers for methodological quality employing instruments from the Joanna Briggs Institute. Critical appraisal, extraction and synthesis were carried out, employing the established methods for umbrella reviews and the protocol was registered in the International Prospective Register of Systematic Reviews (PROSPERO number CRD42019145610). RESULTS: The search identified 12 systematic reviews with moderate-to-high quality, which covered 110 original papers. Habitually, health professionals expressed controversial views and showed some reluctance to let families be present during cardiopulmonary resuscitation. In contrast, family members felt strongly that they should be present and patients agreed. Key factors that facilitated witnessed cardiopulmonary were a formal institutional policy, educating health professionals, and designating a health professional to support the family. Educational and cultural backgrounds influenced healthcare professionals' experiences and their attitudes towards witnessed cardiopulmonary resuscitation. In general, Anglo-Saxon countries showed greater support for this practice. These included the United States, which was the country that dominated the literature on this subject. CONCLUSIONS: The best available evidence supports allowing the family to be present during cardiopulmonary resuscitation. It is necessary to include this practice in educational curricula and to train emergency personnel in its implementation. Culturally sensitive policies need to be designed, and the public to be aware of their right to be present.

Accesibilidad de las mujeres sordas al sistema público sanitario del País Vasco / Accessibility of deaf women to the public health system of the Basque Country (Spain)

OBJETIVO: Explorar cuáles son las percepciones y las vivencias de las mujeres sordas en relación con la accesibilidad al Sistema de Salud Público Vasco (Osakidetza). Como objetivo secundario, explorar la experiencia de estas mujeres acerca de la violencia de género. MÉTODO: Estudio cualitativo con diseño exploratorio. La selección de las informantes se realizó mediante muestreo intencional. Se invitó a participar a mujeres sordas a través de la Federación de Personas Sordas de Euskadi. Se desarrollaron cuatro grupos de discusión entre octubre de 2013 y julio de 2014, con una duración media de 90-120 minutos. Estos grupos fueron grabados en vídeo para su posterior transcripción literal, en la que participó el Servicio de Intérpretes de Lengua de Signos de Euskadi. Se realizó un análisis temático. RESULTADOS: Surgen tres categorías principales: 1) sentimientos de discriminación y limitación del principio de autonomía; 2) barreras y facilitadores en la accesibilidad al sistema sanitario; y 3) vulnerabilidad de las mujeres sordas como consecuencia de la falta de comunicación. CONCLUSIONES: Las mujeres sordas continúan presentando dificultades para el acceso al sistema sanitario en nuestro contexto. Los resultados de este estudio pueden ser un punto de partida para el desarrollo de políticas sanitarias y de protocolos institucionales

OBJECTIVE: To explore what are the perceptions and experiences of deaf women in relation to accessibility to the Basque Public Health System (Osakidetza). As a secondary objective, explore the experience of these women about gender violence. METHOD: A qualitative study with exploratory design is developed. The selection of the informants was carried out through intentional sampling. Deaf women were invited to participate through the Federation of Deaf People of the Basque Country. Four discussion groups were developed between October 2013 and July 2014, with duration of 90-120 minutes. The discussion groups were recorded in video for their later literal transcription in which the service of interpreters of sign language of Euskadi participated. Thematic analyses carried out. RESULTS: Three main categories arise: 1) feelings of discrimination and limitation of the principle of autonomy; 2) barriers and facilitators in the accessibility to the health system; and 3) vulnerability of deaf women as a result of the lack of communication. CONCLUSIONS: Nowadays, deaf women continue having difficulties in accessing to the health system in our context. The results of this study can be the starting point for the development of health policies and institutional protocols

Eficiencia de un apósito innovador en la cura de heridas: reducción de la frecuencia de cambio y del coste semanal por paciente / The efficiency of an innovative dressing in wound healing: reduction of change frequency and weekly cost per patient

OBJETIVOS: Evaluar el impacto en la frecuencia de cambio de apósito y en el coste del tratamiento de las heridas que tiene la utilización de un apósito de espuma hidrocelular con indicador de cambio y capa enmascaradora de exudado, y valorar la satisfacción del paciente y la opinión del profesional de enfermería con el apósito de estudio frente a los tratamientos previos. METODOLOGÍA: Estudio observacional, ambispectivo, multicéntrico, realizado en atención primaria y sociosanitaria, en cuatro regiones de España. Participaron pacientes con heridas exudativas, en las que se fuera a sustituir apósitos previos por el apósito del estudio (ALLEVYN Life) según práctica clínica habitual. En cada región, se recogieron y analizaron características de las heridas (antigüedad, localización, tratamientos anteriores, área de la herida), frecuencia de cambio de apósito, coste semanal por paciente (apósitos utilizados y tiempo de enfermería dedicado a curas), satisfacción del paciente y opinión del profesional de enfermería. RESULTADOS: Se incluyó un total de 128 heridas (Galicia: 29; País Vasco: 30; Extremadura: 25, y Comunidad Valenciana: 44). Tras 4 semanas de uso del apósito del estudio se redujo significativamente la frecuencia de cambio (29-58%) y el coste semanal por paciente (apósitos utilizados: 11-61%; apósitos + tiempo de enfermería: 27-59%). En la mayoría de regiones, la reducción del área fue superior al 30%. La experiencia global de los pacientes mejoró con el apósito de estudio frente al tratamiento previo, y fue buena o muy buena en el 60-78% de los casos. En todas las regiones, el profesional de enfermería consideró los apósitos ALLEVYN Life superiores en rendimiento global, indicación de idoneidad de cambio y enmascaramiento del exudado. CONCLUSIONES: El uso del apósito con indicador de cambio y capa enmascaradora disminuyó la frecuencia de cambio de apósito, lo que permitió prolongar los intervalos entre visitas y reducir costes asociados. Al mismo tiempo, mejoró la opinión del profesional de enfermería, y aumentó la satisfacción del paciente

OBJECTIVES: To assess the impact on the dressing change frequency and cost of wound management of using a hydrocellular foam dressing with change indicator and exudate masking layer, and to evaluate the patient's satisfaction and nurse's opinion of the study dressing versus previous treatments. METHODS: Observational, ambispective, multicenter study conducted in primary care and social health care, in four regions of Spain. Patients with acute or chronic exuding wounds, in which previous dressings were to be replaced by the study dressing (ALLEVYN Life) according to usual clinical practice, participated. In each region, wound characteristics (evolution period, location, previous dressings, wound area), dressing change frequency, weekly cost per patient (dressings used and nursing time spent), patient satisfaction and nursing staff opinion were collected and analysed. RESULTS: A total of 128 wounds were included (Galicia: 29; Basque Country: 30; Extremadura: 25; and Valencia: 44). After four weeks of use of the study dressing the frequency of change (29-58%) and the weekly cost per patient were significantly reduced (dressings used: 11-61%; dressings + nursing time: 27-59%). In most regions, the area reduction was more than 30%. The overall patient satisfaction with the study dressing was improved, being good or very good in 60-78% of cases. In all regions, nurses considered ALLEVYN Life dressings superior in overall performance, indication of change adequacy and exudate masking. CONCLUSIONS: The use of the dressing with change indicator and masking layer decreased the frequency of dressing changes, allowing for longer intervals between visits and reducing associated costs. At the same time, they improve the opinion of the nursing staff, and increased patient satisfaction

The advocacy role of nurses in cardiopulmonary resuscitation.

BACKGROUND: The decision whether to initiate cardiopulmonary resuscitation may sometimes be ethically complex. While studies have addressed some of these issues, along with the role of nurses in cardiopulmonary resuscitation, most have not considered the importance of nurses acting as advocates for their patients with respect to cardiopulmonary resuscitation. RESEARCH OBJECTIVE: To explore what the nurse's advocacy role is in cardiopulmonary resuscitation from the perspective of patients, relatives, and health professionals in the Basque Country (Spain). RESEARCH DESIGN: An exploratory critical qualitative study was conducted from October 2015 to March 2016. Thematic analysis was used to analyse the data. PARTICIPANTS: Four discussion groups were held: one with patients and relatives (n = 8), two with nurses (n = 7 and n = 6, respectively), and one with physicians (n = 5). ETHICAL CONSIDERATIONS: Approval was obtained from the Basque Country Clinical Research Ethics Committee. FINDINGS: Three significant themes were identified: (a) accompanying patients during end of life in a context of medical dominance, (b) maintaining the pact of silence, and (c) yielding to legal uncertainty and concerns. DISCUSSION: The values and beliefs of the actors involved, as well as pre-established social and institutional rules reduced nurses' advocacy to that of intermediaries between the physician and the family within the hospital environment. On the contrary, in primary health care, nurses participated more actively within the interdisciplinary team. CONCLUSION: This study provides key information for the improvement and empowerment for ethical nursing practice in a cardiac arrest, and provides the perspective of patients and relatives, nurses and physicians.

[Accessibility of deaf women to the public health system of the Basque Country (Spain)]. / Accesibilidad de las mujeres sordas al sistema público sanitario del País Vasco.

OBJECTIVE: To explore what are the perceptions and experiences of deaf women in relation to accessibility to the Basque Public Health System (Osakidetza). As a secondary objective, explore the experience of these women about gender violence. METHOD: A qualitative study with exploratory design is developed. The selection of the informants was carried out through intentional sampling. Deaf women were invited to participate through the Federation of Deaf People of the Basque Country. Four discussion groups were developed between October 2013 and July 2014, with duration of 90-120minutes. The discussion groups were recorded in video for their later literal transcription in which the service of interpreters of sign language of Euskadi participated. Thematic analyses carried out. RESULTS: Three main categories arise: 1) feelings of discrimination and limitation of the principle of autonomy; 2) barriers and facilitators in the accessibility to the health system; and 3) vulnerability of deaf women as a result of the lack of communication. CONCLUSIONS: Nowadays, deaf women continue having difficulties in accessing to the health system in our context. The results of this study can be the starting point for the development of health policies and institutional protocols.

Presencia de familiares durante la reanimación cardiopulmonar: perspectivas de pacientes, familiares y profesionales de la salud en el País Vasco / Presence of relatives during cardiopulmonary resuscitation: Perspectives of health professionals, patients and family in the Basque Country

Objetivo: Explorar la percepción acerca de la presencia de familiares durante la reanimación cardiopulmonar (RCP) en pacientes adultos, de los propios pacientes y familiares, enfermeras y médicos. Diseño: Se desarrolló un estudio cualitativo exploratorio y un análisis temático. Emplazamiento: Atención Primaria, Atención Hospitalaria y Servicio de Emergencias del Servicio Vasco de Salud. Participantes: La selección de los participantes se realizó a través de muestreo intencional. Se desarrollaron 4 grupos de discusión: uno de pacientes y familiares, 2 de enfermeras y uno de médicos. Método: Se realizó un análisis temático. Se utilizaron técnicas de triangulación entre investigadores e investigador-informante. Se utilizó el programa informático Open Code 4.1. Resultados: Se identificaron 3 categorías significativas: impacto de la actuación en la familia; peso de la responsabilidad ética y legal; poder, lugar donde sucede la parada y supuestos culturales. Conclusiones: La RCP es un constructo social influido por los valores de los contextos socioculturales específicos. En este estudio, los pacientes y familiares describieron temor y resistencia a presenciar la RCP. Por su parte, los profesionales sanitarios consideran que su decisión reviste complejidad, siendo necesario valorar cada caso de forma independiente e integrando a pacientes y familiares en la toma de decisiones. Como líneas de investigación futuras sería recomendable profundizar sobre la experiencia subjetiva de familiares que hayan presenciado la RCP y el impacto de los elementos contextuales y socioculturales en sus percepciones

Objective: To determine the perception of nurses, doctors, patients and family or relatives being present during cardiopulmonary resuscitation (CPR) in adult patients. Design: A qualitative exploratory study and thematic analysis were developed. Site: Primary Care, Hospital Care and Emergency Service of the Basque Health Service. Participants.The selection of the participants was made through intentional sampling. Four focus groups were developed: one of patients and family, 2 of nurses, and one of physicians. Method: Thematic analysis was performed. Triangulation techniques were used between investigators and investigator-participant member. The Open code 4.1 statistics software was used. Results: Three significant categories were identified: the impact on the family; the weight of ethical and legal responsibility; power, place of death, and cultural assumptions. Conclusions: CPR is a social construct influenced by values which are situated in specific socio-cultural contexts. In this study, patients and family members describe the fear and resistance to being present during CPR. Health professionals consider that their decision is complex, and each case must be assessed independently, and patients and relatives must be integrated into decision-making. Future research should explore in greater depth the subjective experience of relatives who have witnessed CPR and the impact of contextual and sociocultural elements from the perspectives of relatives

Postoperative pain management in a surgical unit in a Basque Country hospital: a best practice implementation project.

OBJECTIVES: The objective of this project was to implement evidence-based recommendations for post-surgical pain management and improve quality of care for patients. INTRODUCTION: Inadequate approaches to postoperative pain can lead to the pain becoming chronic, which has an impact on the patient's quality of life. The focus of this project was to implement evidence-based recommendations to improve the effect or outcome of post-surgical pain management strategies and improve quality of care. METHODS: This implementation project was undertaken in a surgical unit of a tertiary hospital. The clinical audit was developed in three phases using the Joanna Briggs Institute Practical Application of Clinical Evidence System and Getting Research into Practice audit and feedback tools for promoting change in healthcare practices and improving quality of care. A baseline audit was conducted with 27 patients that identified the barriers and strategies needed to improve the assessment and management of postoperative pain. Two follow-up audits audits were conducted, each comprising 40 patients. RESULTS: The baseline audit revealed the need to increase health education for patients and, or, their families on managing postoperative pain, with a special emphasis on non-pharmacological measures. This education was not recorded in the patients' medical histories at baseline and the aim was to rectify this.In follow-up audits, 100% of patients received individually tailored education about postoperative pain and its management. CONCLUSIONS: The aims and main objectives of the present project were achieved, including improvements in the quality of health education related to pain and the recording of pain data. In addition, variations in the clinical practice related to the management of post-surgical pain decreased.

Nursing knowledge of and attitude in cardiopulmonary arrest: cross-sectional survey analysis.

BACKGROUND: Nurses are often the first to activate the chain of survival when a cardiorespiratory arrest happens. That is why it is crucial that they keep their knowledge and skills up-to-date and their attitudes to resuscitation are very important. The main aim of this study was to analyse whether the level of theoretical and practical understanding affected the attitudes of nursing staff. METHODS: A questionnaire was designed using the Delphi technique (three rounds). The questionnaire was adjusted and it was piloted on a test-retest basis with a convenience sample of 30 registered nurses. The psychometric characteristics were evaluated using a sample of 347 nurses using Cronbach's alpha. Descriptive analysis was performed to describe the sociodemographic variables and Spearman's correlation coefficient to assess the relationship between two scale variables. Pearson's chi-squared test has been used to study the relationship between two categorical variables. Wilcoxon Mann Whitney test and the Kruskal-Wallis test were performed to establish relationships between the demographic/work related characteristics and the level of understanding. RESULTS: The Knowledge and Attitude of Nurses in the Event of a Cardiorespiratory Arrest (CAEPCR) questionnaire comprised three sections: sociodemographic information, theoretical and practical understanding, and attitudes of ethical issues. Cronbach's alpha for the internal consistency of the attitudes questionnaire was 0.621. The knowledge that nurses self-reported with regard to cardiopulmonary arrest directly affected their attitudes. Their responses raised a number of bioethical issues. CONCLUSIONS: CAEPCR questionnaire is the first one which successfully linked knowledge of cardiopulmonary resuscitation to the attitudes towards ethical issues Health policies should ensure that CPR training is mandatory for nurses and all healthcare workers, and this training should include the ethical aspects.