Revistas
Revista:
NURSE EDUCATION TODAY
ISSN 0260-6917
Vol. 106
Año 2021
Págs.105001
BACKGROUND: Cultural sensibility is an important concept linked to the achievement of cultural competence. Health professionals must first improve their cultural sensibility to become culturally competent and to be able to offer competent care to culturally diverse populations. Aim To develop and psychometrically test the Cultural Sensibility Scale for Nursing (CUSNUR), a cultural sensibility scale that can be used in nursing for the achievement of competencies needed to care for culturally diverse populations.
DESIGN AND METHODS: The cross-sectional survey was conducted over two stages. The first stage involved the cross-cultural and discipline-specific adaptation of an existing scale addressing this concept in the field of law using the reverse translation method. Second, validation of the scale was carried out from October 2016-June 2017 by studying the psychometric properties of the questionnaire through an analysis of content acceptability and reliability and through exploratory factor analysis (EFA).
RESULTS: The questionnaire was designed to be clear, easy to understand, and of adequate length, and experts involved in content validation agreed that the scale meets these criteria. A total of 253 nursing students participated in the validation stage. Four factors were identified from the EFA: (1) patient and health professional behaviours, (2) self-assessments, (3) self-awareness, and (4) cultural influence. Two items were excluded. Factorial saturation is adequate for all factors (>0.30). The Cronbach alpha was measured as 0.75.
CONCLUSIONS: This study presents the first version of the CUSNUR and demonstrates that the scale is valid and reliable.
Revista:
NURSE EDUCATION TODAY
ISSN 0260-6917
Vol. 101
Año 2021
Págs.104879
Education in palliative care is a required competence for the nursing degree.Pedagogical strategies in palliative care are mainly aimed at promoting an understanding of patients with advanced disease. Phenomenological texts are stories intended to evoke lived experiences and help understand these complex situations. However, there is no evidence regarding the experience of reading phenomenological texts in nursing. The aim of this study is to determine what impact nursing students have when reading a phenomenological text about the experience of people living with advanced cancer. The students¿ writings showed that reading the phenomenological text caused them to reflect and feel moved and challenged. The impact on the students is grouped into three categories: the experience of the corporeality of patients makes students aware of the importance of the body; the disease as an individual transformative process challenges students; and the experiences of advanced cancer
patients make students aware of the importance of how they care for patients and their families. The reading of a phenomenological text on the experience of living with advanced cancer is innovative and may be a teaching method that promotes care focused on the person with advanced illness, key aspect for student¿s competency in clinical practice.
Revista:
CLINICAL NURSING RESEARCH
ISSN 1054-7738
Vol. 30
N° 5
Año 2021
Págs.579 - 590
Living with chronic illness has an impact on the family's wellbeing and quality of life. An integrative review was conducted to identify and analyse the existing scales that evaluate the process of living with chronic illness or related factors of daily living from the family perspective. A search was developed in Medline, CINAHL, PsycINFO, Cochrane Library, Cuiden and Scielo databases until May 2019. From 5,344 identified articles, 13 studies were eligible for inclusion. 16 scales were identified and assessed constructs related to the concept of living with chronic illness, including quality of life; perceptions and needs; life satisfaction and well-being; impact; and psychological adjustment to the disease. However, these scales do not measure the family process of living with chronic illness from a comprehensive perspective. This review highlights the need to develop and validate a scale that evaluates the multidimensional nature of living with chronic illness from the family perspective.
Revista:
QUALITATIVE HEALTH RESEARCH
ISSN 1049-7323
Vol. 30
N° 8
Año 2020
Págs.1143 - 1155
Abstract
Literature suggests that it is possible to live well with advanced cancer but little is known about the process. In this article, we present a secondary analysis of experiences of living with advanced cancer (n=22) that refines the theory of ¿Living Well with Chronic Illness¿ for a different context and population. The refined theory explains the experience of living well with advanced cancer illuminating a five phase iterative process: struggling, accepting, living with advanced cancer, sharing the illness experience, and reconstructing life. These five phases revolve around the core concept of Awareness of Dying, which varied from awareness of the possibility of dying, to accepting the possibility of dying, to acceptance that ¿I am dying.¿ Awareness of Dying led to a focus on living well with advanced cancer and movement towards living a life rather than living an illness.
Revista:
INTERNATIONAL PRACTICE DEVELOPMENT JOURNAL
ISSN 2046-9292
Vol. 2
N° 9
Año 2019
Págs.1 - 8
Background: Registered nurses are increasingly expected to provide person-centred end-of-life care. However, there is a gap between patients¿ needs and the capacity of nurses to meet the existing recommendations on provision of this care. Identifying the relevant barriers and facilitators can inform the development of strategies to support person-centred nursing.
Aim: To identify registered nurses¿ perceived barriers and facilitators in terms of providing person-centred end-of-life care.
Method: A scoping review was conducted according to the 2005 guidelines proposed by Arksey and O`Malley. The databases Medline, CINAHL, PsycINFO, Cochrane, Web of Science and Embase were searched using the period 2000 to 2018. Empirical studies, literature reviews and studies focusing on the experiences of generalist nurses providing end-of-life care were included. The selected articles were independently reviewed by two researchers.
Results: A total of 2,126 publications were identified, with 26 retained after applying the eligibility criteria. Four barriers to providing person-centred care were identified: knowledge of end-of-life care; communication skills; coping strategies; and teamwork. Three main facilitators were identified: knowing the person in a holistic way; nurses¿ self-knowledge; and the development of a good nurse-person relationship. Organisational and managerial support also emerged to be important. These findings are reflected in the construct of McCormack and McCance¿s
Revista:
MEDICINA PALIATIVA
ISSN 1134-248X
Vol. 25
N° 2
Año 2018
Págs.105 - 113
La esclerosis lateral amiotrófica (ELA) afecta a diferentes aspectos de la vida de las personas y por ello, el objetivo de este estudio es conocer la calidad de vida relacionada con la salud (CVRS) de estos enfermos. Se realizó una revisión narrativa de los artículos de los últimos 10 años. La estrategia de búsqueda incluyó las palabras clave «esclerosis lateral amiotrófica» y «calidad de vida relacionada con la salud» y sus sinónimos traducidos al inglés y se aplicó en Cochrane, Cinahl, Pubmed, PsycInfo y Dialnet. Se incluyeron 9 artículos tras aplicar los criterios de selección. Se analizó el nivel de evidencia que generan los artículos utilizando como referencia las indicaciones de la «US Agency of Health Research and Quality» y posteriormente se analizaron los resultados de los estudios agrupándolos por áreas temáticas. Se identificaron un total de 3 áreas clave: la importancia de las necesidades emocionales, sociales y físicas de los pacientes con ELA; la presencia del cuidador y la CVRS de los enfermos; y los tipos de afrontamiento que pueden ayudar en la CVRS. La dimensión física es la que obtiene peores resultados de CVRS, pero dado que las dimensiones sociales y emocionales están también afectadas menos significativamente, la puntuación global de la CVRS permanece estable. La familia y el entorno del paciente surgen como aspecto clave a considerar en la atención a estos pacientes.
Revista:
PALLIATIVE & SUPPORTIVE CARE
ISSN 1478-9523
Vol. 16
N° 1
Año 2018
Págs.73-79
ICS ATLANTES
The PDI has intrinsic therapeutic value and is useful in clinical practice, and it is also a way of examining issues related to dignity and the meaning of life within the context of advanced-stage illness. There is a need for studies that examine patient experiences through a PDI-based intervie
Revista:
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN 0885-3924
Vol. 56
N° 6
Año 2018
Págs.E137
Revista:
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN 0885-3924
Vol. 56
N° 6
Año 2018
Págs.E87 - E88
Revista:
REVISTA ROL DE ENFERMERIA
ISSN 0210-5020
Vol. 1
N° 40
Año 2017
Págs.16 - 24
INTRODUCCIÓN. Conocer cómo los pacientes conviven con un proceso crónico es necesario para proporcionar un cuidado individualizado e integral. En la actualidad, no existe ninguna escala validada que evalúe la convivencia con un proceso crónico, como es la enfermedad de Parkinson. OBJETIVOS. Los objetivos fueron: 1) definir el concepto Convivencia con un proceso crónico; 2) diseñar una escala de medición del grado de convivencia en pacientes con un proceso crónico, y en concreto, con la enfermedad de Parkinson. METODOLOGÍA. Se llevaron a cabo dos pasos metodológicos. Respecto al primero, se realizó un análisis del concepto Convivencia con un proceso crónico, a través del método evolutivo de Rodgers. El segundo paso metodológico fue el diseño de la escala, a través de la guía propuesta por DeVellis. RESULTADOS. A través del análisis de concepto se identificó que la Convivencia con un proceso crónico es un proceso complejo, dinámico, cíclico y multidimensional compuesto por los atributos de Aceptación, Afrontamiento, Automanejo, Integración y Adaptación. En cuanto a los resultados del diseño de la escala, se desarrolló una medida autocumplimentada, con cinco opciones de respuesta, tipo Likert y 27 ítems. CONCLUSIONES. La escala diseñada, es una medida innovadora y de interés potencial clínico que permite identificar qué factor o factores hacen que la persona conviva mejor o peor con la enfermedad y, consecuentemente, intervenir de manera integral, acorde con las necesidades indi
Revista:
AQUICHAN
ISSN 1657-5997
Vol. 17
N° 3
Año 2017
Págs.241 - 242
Revista:
GEROKOMOS
ISSN 1134-928X
Vol. 28
N° 1
Año 2017
Págs.25 - 29
Las caídas son ¿acontecimientos involuntarios que hacen perder el
equilibrio y dar con el cuerpo en la tierra u otra superficie firme que lo
detenga¿. Las caídas recurrentes (presencia de dos o más caídas en un año)
constituyen un problema frecuente en centros residenciales, y predisponen
a las personas mayores a sufrir incapacidad, dependencia y múltiples
enfermedades. La aplicación de medidas de prevención puede disminuir
notablemente su incidencia y, por tanto, sus consecuencias.
El objetivo de este trabajo es identificar qué intervenciones de enfermería
pueden ayudar a prevenir caídas recurrentes en las personas mayores
institucionalizadas, y minimizar el impacto emocional que ocasionan estos
episodios. Para ello, se desarrolla un caso clínico y, tras el análisis de la
evidencia científica, se proponen intervenciones para evitar la recurrencia de
un episodio de caída y sus consecuencias. El análisis de este caso se estructura
en valoración de riesgo de caídas recurrentes e intervenciones de prevención
de las mismas. Y, a su vez, cada apartado se divide en aspectos físicos y
emocionales. La literatura especializada refleja que la valoración del riesgo
de caídas es clave para implantar un plan de cuidados. Conocer los factores
de riesgo intrínsecos y extrínsecos ayudará a los profesionales a diseñar
intervenciones de prevención. Asimismo, se ha identificado el impacto
emocional que producen las caídas en los pacientes y se proponen algunas
intervenciones para aliviarlo.
Revista:
MEDICINA PALIATIVA
ISSN 1134-248X
Vol. 23
N° 1
Año 2016
Págs.52
Revista:
PALLIATIVE MEDICINE
ISSN 0269-2163
Vol. 31
N° 6
Año 2016
Págs.492 - 509
Background:
Dignity therapy is psychotherapy to relieve psychological and existential distress in patients at the end of life. Little is known about its effect.
Aim:
To analyse the outcomes of dignity therapy in patients with advanced life-threatening diseases.
Design:
Systematic review was conducted. Three authors extracted data of the articles and evaluated quality using Critical Appraisal Skills Programme. Data were synthesized, considering study objectives.
Data sources:
PubMed, CINAHL, Cochrane Library and PsycINFO. The years searched were 2002 (year of dignity therapy development) to January 2016. `Dignity therapy¿ was used as search term. Studies with patients with advanced life-threatening diseases were included.
Results:
Of 121 studies, 28 were included. Quality of studies is high. Results were grouped into effectiveness, satisfaction, suitability and feasibility, and adaptability to different diseases and cultures. Two of five randomized control trials applied dignity therapy to patients with high levels of baseline psychological distress. One showed statistically significant decrease on patients¿ anxiety and depression scores over time. The other showed statistical decrease on anxiety scores pre¿post dignity therapy, not on depression. Nonrandomized studies suggested statistically significant improvements in existential and psychosocial measurements. Patients, relatives and professionals perceived it improved end-of-life experience.
Conclusion:
Evidence suggests that dignity therapy is beneficial. One randomized controlled trial with patients with high levels of psychological distress shows DT efficacy in anxiety and depression scores. Other design studies report beneficial outcomes in terms of end-of-life experience. Further research should understand how dignity therapy functions to establish a means for measuring its impact and assessing whether high level of distress patients can benefit most from this therapy.
Revista:
NPJ PARKINSON'S DISEASE
ISSN 2373-8057
Vol. 2
N° UNSP 16022
Año 2016
Understanding how a person lives with a chronic illness, such as Parkinson's disease (PD), is necessary to provide individualized care and professionals role in person-centered care at clinical and community levels is paramount. The present study was aimed to analyze the psychometric properties of the Living with Chronic Illness-PD Scale (EC-PC) in a wide Spanish-speaking population with PD. International cross-sectional study with retest was carried out with 324 patients from four Latin American countries and Spain. Feasibility, acceptability, scaling assumptions, reliability, precision, and construct validity were tested. The study included 324 patients, with age (mean +/- s.d.) 66.67 +/- 10.68 years. None of the EC-PC items had missing values and all acceptability parameters fulfilled the standard criteria. Around two-third of the items (61.54%) met scaling assumptions standards. Concerning internal consistency, Cronbach's alpha values were 0.68-0.88; item-total correlation was 40.30, except for two items; item homogeneity index was 40.30, and inter-item correlation values 0.14-0.76. Intraclass correlation coefficient for EC-PC stability was 0.76 and standard error of measurement (s.e.m.) for precision was 8.60 (for a EC-PC s.d. = 18.57). EC-PC presented strong correlation with social support (r(S) = 0.61) and moderate correlation with life satisfaction (r(S) = 0.46). Weak and negligible correlations were found with the other scales.
Revista:
PARKINSONISM AND RELATED DISORDERS
ISSN 1353-8020
Vol. 25
Año 2016
Págs.52 - 57
Introduction: To explore the psychometric attributes of a new Satisfaction with Life Scale (SLS-6) in a wide Spanish-speaking population with Parkinson's disease (PD).
Methods: This was an international, cross-sectional study. Several rater-based and patient-reported outcomes measures for evaluation of PD (e.g., Scales for Outcomes in Parkinson's Disease-Motor) and other constructs (e.g., Duke-UNC Functional Social Support Questionnaire, Scale for Living with Chronic Illness) were applied together with the SLS-6. Acceptability, scaling assumptions, reliability, precision, and construct validity were tested.
Results: The study included 324 patients from five countries, with age (mean ± standard deviation) 66.67 ± 10.68 years. None of the SLS-6 items had missing values and all acceptability parameters fulfilled the standard criteria. Scaling assumptions allowed the calculation of a summary index from items 2 to 6, complementary to the global evaluation (item 1). For these five items, Cronbach's alpha was 0.85; the corrected item¿total correlation 0.53¿0.73; inter-item correlation, 0.45¿0.70, with an item homogeneity index of 0.55. The standard error of measurement, based on Cronbach's alpha for a single observation, was 3.48. SLS-6 correlations were moderate to strong (rs ¿ 0.35) with the patient-reported outcomes and weak to moderate with the rater-based assessments used in the study. The SLS-6 total score was significantly different according to PD severity levels establised
Revista:
EUROPEAN JOURNAL OF CANCER CARE
ISSN 0961-5423
Vol. 25
N° 4
Año 2016
Págs.551 - 569
The aim of the study was to understand the experience of people living with advanced-stage cancer through literature. The search included The Cochrane Library, PubMed, PsycInfo, CINAHL and Cuiden. Thirteen studies were included. A qualitative meta-synthesis was conducted. One thread emerged from the thematic synthesis: the desire to live as normally as possible, despite being aware of the proximity of death. Three themes also emerged: "a process that is unique" with its four sub-themes; "support network" and "health context," each of them having two sub-themes. This study concludes that living with advanced-stage cancer is a unique and complex process which has both positive and negative aspects. The review provides a comprehensive view of the experience, which considers the importance of the support network and the health context in which the person lives. In this study, "normalcy" is the adjustment to the new reality and living as closely as possible to the way one lived before the disease, while developing a new relationship with being finite and death. A better understanding of the experience of living with advanced-stage cancer will help health professionals to identify the needs of the patients in order to plan individual, high-quality care.
Revista:
REVISTA DE NEUROLOGIA
ISSN 0210-0010
Vol. 61
N° 10
Año 2015
Págs.447 - 453
Revista:
ANALES DEL SISTEMA SANITARIO DE NAVARRA
ISSN 1137-6627
Vol. 38
N° 3
Año 2015
Págs.439 - 452
A quarter of the people with heart failure are at an advanced stage of the disease, during which they experience numerous common and distressing symptoms that have an impact on all spheres of their life. In this context, there is a need for frequent assessment and clinical monitoring of patients. The aim of this review is to identify the instruments used in assessing patients with advanced heart failure. For the purposes of this study, any type of questionnaire, scale or functional test used to assess some aspect of these patients was considered to be an instrument. Forty-nine tools were identified that make it possible to assess symptoms, psychological, cognitive and spiritual aspects and quality of life. The information provided on the most used instruments and their availability and applicability is a first step for their possible integration into daily clinical practice. Thus, professionals who work with these patients can improve the identification of specific needs, enabling their subsequent management and monitoring.
Revista:
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN 0885-3924
Vol. 50
N° 6
Año 2015
Págs.874-81
The Spanish version of the PDI showed adequate psychometric properties when tested with advanced cancer patients. This research provides a three-factor alternative in Spanish to the PDI.
Revista:
ENFERMERIA (MONTEVIDEO)
ISSN 1688-8375
Vol. 4
N° 2
Año 2015
Págs.10 - 11
Titulo completo de la Revista: Enfermería: Cuidados Humanizados. Su ISSN es: 1688-8375.
Revista:
ANALES DEL SISTEMA SANITARIO DE NAVARRA
ISSN 1137-6627
Vol. 38
N° 2
Año 2015
Págs.225-234
Todos los participantes (n=40) completaron el estudio. La consistencia interna con el alpha de Cronbach fue de 0,71 y la armonía interjueces obtuvo un índice de Kappa moderado y bueno en la mayoría de los ítems (k=0,4-0,81) excepto en ¿lengua y encía¿ (k=0,33-0,37). La validez concurrente con la escala de la mucositis dela OMS fue aceptable (r=0,458). Todas las enfermeras (n=6) consideraron que la escala era fácil de entender y útil en la práctica clínica. Los pacientes dijeron que no les pareció incómoda la valoración de la boca con la escala.Conclusiones. La versión española dela OAG es un instrumento válido y fiable en pacientes con cáncer. Es una escala fácil de usar en la práctica clínica y bien aceptada por los pacientes.
Revista:
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN 0885-3924
Vol. 47
N° 1
Año 2014
Págs.189 - 197
The high responsiveness confirms the value of the MDAS for ongoing delirium assessment. Two differentiated factor loadings point to a potential future need for MDAS subscales
Revista:
REVISTA ESPAÑOLA DE CARDIOLOGIA
ISSN 0300-8932
Vol. 67
N° Supl 1
Año 2014
Págs.272
Revista:
CUADERNOS DE BIOETICA
ISSN 0328-8390
Vol. 25
N° 84
Año 2014
Págs.243-256
Todos los modelos incluidos en esta revisión proporcionan a los profesionales de la salud un punto de partida para la reflexión e incorporación de prácticas que traten de preservar la dignidad social de los pacientes con enfermedad terminal. Uno de los modelos identificados ha sido aplicado a la práctica clínica con resultados positivos
Revista:
METAS DE ENFERMERIA
ISSN 1138-7262
Vol. 17
N° 4
Año 2014
Págs.49-54
Revista:
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
ISSN 0885-3924
Vol. 45
N° 1
Año 2013
Págs.129-36
The ESAS-r is a valid instrument with adequate psychometric characteristics. This version is preferred by patients with advanced cancer. The Spanish version of the ESAS-r can, therefore, replace the use of the ESAS.
Revista:
MEDICINA PALIATIVA
ISSN 1134-248X
Vol. 20
N° 4
Año 2013
Págs.143-149
El ESAS puede considerarse como un instrumento de referencia para la evaluación sintomática de los pacientes con cáncer avanzado en espa¿nol.
Revista:
European Journal of Palliative Care
ISSN 1352-2779
Vol. 19
N° 2
Año 2012
Págs.77 - 81
The Edmonton Symptom Assessment System (ESAS) is one of the most widely used instruments in the assessment of palliative care and advanced cancer patients. It has been used internationally in clinical practice and research.
Revista:
European Journal of Cancer
ISSN 0959-8049
Vol. 47
N° 12
Año 2011
Págs.1863 -1872
Conclusion ESAS is a valid, reliable, responsive and feasible instrument with adequate psychometric properties when tested on Spanish advanced cancer patients..
Revista:
Journal of Palliative Medicine
ISSN 1096-6218
Vol. 14
N° 1
Año 2011
Págs.4 - 5
Revista:
Anales del Sistema Sanitario de Navarra
ISSN 1137-6627
Vol. 34
N° 1
Año 2011
Págs.63-72
