11 results on '"Rocafort-Gil J"'
Search Results
2. Consideraciones de la Organización Médica Colegial para el desarrollo de los cuidados paliativos en España
- Author
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Gómez Sancho, M., Altisent Trota, R., Bátiz Cantera, J., Ciprés Casasnovas, L., Corral Collantes, P., González Fernández, J.L., Herranz Martínez, J.A., Rocafort Gil, J., and Rodríguez Sendín, J.J.
- Published
- 2010
- Full Text
- View/download PDF
3. Cuidados al Paciente y su Familia al Final de la Vida: La Anticipación Compasiva
- Author
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Pérez Bret, E., Altisent Trota, R., Rocafort Gil, J., and Jaman Mewes, P.
- Abstract
El final de la vida va acompañado de sufrimiento y penalidades que pueden ser aliviados en las unidades de Cuidados Paliativos (CP) con una atención compasiva. El objetivo de este trabajo consiste en describir el concepto de “anticipación compasiva” como una forma de cuidar al paciente y a su familia al final de la vida desde la perspectiva tanto de los profesionales, profesores y estudiantes de las ciencias de la salud, como de las personas con enfermedad avanzada y sus familiares. Se ha empleado para ello una metodología cualitativa. Los datos se recogieron a través de entrevistas en profundidad y de grupos focales, siendo analizados y codificados usando la técnica de la teoría fundamentada. Se obtuvo la aprobación de un Comité de Ética. La muestra intencionada fue de 29 participantes: pacientes y familiares de pacientes con enfermedad avanzada, profesionales asistenciales de CP y expertos en bioética, profesores universitarios y estudiantes de Ciencias de la Salud. Los datos se recogieron en un Hospital de CP en Madrid, España. Los participantes valoran positivamente la anticipación compasiva de los profesionales que supone estudiar y reflexionar sobre las posibles complicaciones que pueden derivarse de la situación de enfermedad avanzada que padece el enfermo y dialogar con él acerca de las posibles actuaciones al respecto. El artículo concluye que la compasión es una virtud que implica adelantarse a las necesidades de los pacientes para que el enfermo pueda tomar decisiones compartidas acertadas. Es lo que se denomina anticipación compasiva. Son necesarios ulteriores estudios que profundicen en las características de la anticipación compasiva y cómo desarrollarla de forma óptima en los pacientes al final de la vida. End of life is frequently accompanied by suffering and hardships that can be alleviated in the Palliative Care (PC) units by applying compassionate advance care. It is the aim of this paper to describe the concept of "compassionate advance care" as a way of caring for the patient and his family at the end of life from the perspective of both professionals, teachers and students of the health sciences, and persons with advanced disease and their families. A qualitative methodology was used. Data were collected through in-depth interviews and focus groups, and analysed and coded using the theory of Grounded Theory. Approval of an Ethics Committee was obtained. The intentional sample consisted of 29 participants, who were patients and relatives of patients with advanced disease, PC professionals and experts in bioethics, university professors and Health Sciences students. Data were collected in a PC Hospital in Madrid, Spain. The participants positively valued the compassionate advance care provided by professionals: analysing and reflecting on possible complications that may arise from the advanced disease situation suffered by the patient and establishing a dialogue with him about possible actions in this regard. The paper concludes that compassion is a virtue that implies anticipating the needs of patients, thus allowing the patient to make the right shared decisions. This is what the term Compassionate Advance Care Planning entails. Further studies are needed to delve into the characteristics of compassionate Advance Care Planning and how to optimally implement it in patients at the end of life. To admit the opposite is to enter a spiral where the dignity of the human being would become an object of weighting with respect to another value, which, in a hypothetical conflict could be postponed by another. However, Palliative Care takes into account the social dimension of the end of life of the human being. They take care of the sick human being in its entirety. That is why they are the option most in line with the dignity of the human being at the end of his life.
- Published
- 2019
4. PLANIFICACIÓN ANTICIPADA DE CUIDADOS EN RESIDENCIAS DE MAYORES: REVISIÓN NARRATIVA
- Author
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Sánchez-Ortiz, M., Forcano-García, M., López-Pérez, M., Altisent-Trota, R., and Rocafort-Gil, J.
- Abstract
La planificación anticipada de cuidados (PAC) es un proceso deliberativo que ayuda a los pacientes a definir objetivos y preferencias sobre la atención y tratamientos futuros en momentos que tengan limitada su capacidad de decisión. Este estudio tiene como objetivo analizar los modelos de planificación anticipada de cuidados en residencias. Hemos examinado los trabajos publicados en Cochrane, PubMed y Embase. Se incluyeron un total de 26 artículos, con un sumatorio de personas mayores que asciende hasta 44.131. Se identificaron los tipos de intervención (entrevistas, videos, talleres, documentación, etc.) y sus resultados derivados de la aplicación. En conclusión, ninguno de los trabajos implementa un modelo de intervención estandarizado. Las intervenciones incluyen la toma de decisiones sobre traslados, órdenes de reanimación y la adecuación de esfuerzo terapéutico (antibioterapia, nutrición, sueroterapia, etc). Otros resultados incluyen las barreras de implementación: tiempo y formación.
- Published
- 2024
- Full Text
- View/download PDF
5. Declaración sobre la atención médica al final de la vida: Working group on Medical care at the end of life
- Author
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Gómez Sancho, M., Altisent Trota, R., Bátiz Cantera, J., Ciprés Casasnovas, L., Corral Collantes, P., González Fernández, J.L., Herranz Martínez, J.A., Rocafort Gil, J., and Rodríguez Sendín, J.J.
- Published
- 2010
6. Declaración sobre la atención médica al final de la vida
- Author
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Gómez Sancho, M., primary, Altisent Trota, R., additional, Bátiz Cantera, J., additional, Ciprés Casasnovas, L., additional, Corral Collantes, P., additional, González Fernández, J.L., additional, Herranz Martínez, J.A., additional, Rocafort Gil, J., additional, and Rodríguez Sendín, J.J., additional
- Published
- 2010
- Full Text
- View/download PDF
7. The quality of life concept among Palliative Care professionals,El concepto de calidad de vida en los profesionales de Cuidados Paliativos
- Author
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Alvaro Sanz Rubiales, Blanco Toro, L., Librada Flores, S., Julián Caballero, M. M., Del Valle Rivero, M. L., and Rocafort Gil, J.
8. [Advance care planning in nursing homes: scoping review].
- Author
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Sánchez-Ortiz M, Forcano-García M, López-Pérez M, Altisent-Trota R, and Rocafort-Gil J
- Subjects
- Humans, Aged, Homes for the Aged organization & administration, Nursing Homes organization & administration, Advance Care Planning
- Abstract
Advance care planning is a deliberative process that aims to help patients define goals and preferences for future care and treatment at a times when they have limited decision-making capacity. This study aims to analyze models of advance care planning in elderly individuals living in nursing homes. We reviewed papers published in Cochrane, PubMed and Embase. A total of 26 studies were selected, including a total of 44,131 people over 65 years of age. We analyzed the types of intervention (interviews, videos, workshops, documentation, etc.) and their results derived from the application. We conclude that no study implements a standardized intervention model. These interventions include decision-making (transfers to hospital, resucitation orders) and the adequacy of therapeutic effort (antibiotherapy, nutrition, serotherapy, etc.). Other outcomes are implementation barriers (time and training)., (Copyright © 2024 SEGG. Publicado por Elsevier España, S.L.U. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
9. [Care for the Patient and his Family at the end of Life: Compassionate Advance Care Planning].
- Author
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Pérez Bret E, Altisent Trota R, Rocafort Gil J, and Jaman Mewes P
- Subjects
- Humans, Advance Care Planning, Empathy, Family, Terminal Care standards
- Abstract
End of life is frequently accompanied by suffering and hardships that can be alleviated in the Palliative Care (PC) units by applying compassionate advance care. It is the aim of this paper to describe the concept of "compassionate advance care" as a way of caring for the patient and his family at the end of life from the perspective of both professionals, teachers and students of the health sciences, and persons with advanced disease and their families. A qualitative methodology was used. Data were collected through in-depth interviews and focus groups, and analysed and coded using the theory of Grounded Theory. Approval of an Ethics Committee was obtained. The intentional sample consisted of 29 participants, who were patients and relatives of patients with advanced disease, PC professionals and experts in bioethics, university professors and Health Sciences students. Data were collected in a PC Hospital in Madrid, Spain. The participants positively valued the compassionate advance care provided by professionals: analysing and reflecting on possible complications that may arise from the advanced disease situation suffered by the patient and establishing a dialogue with him about possible actions in this regard. The paper concludes that compassion is a virtue that implies anticipating the needs of patients, thus allowing the patient to make the right shared decisions. This is what the term Compassionate Advance Care Planning entails. Further studies are needed to delve into the characteristics of compassionate Advance Care Planning and how to optimally implement it in patients at the end of life. To admit the opposite is to enter a spiral where the dignity of the human being would become an object of weighting with respect to another value, which, in a hypothetical conflict could be postponed by another. However, Palliative Care takes into account the social dimension of the end of life of the human being. They take care of the sick human being in its entirety. That is why they are the option most in line with the dignity of the human being at the end of his life.
- Published
- 2019
10. [Qualitative research about euthanasia concept, between Spanish doctors].
- Author
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Cuervo Pinna MÁ, Rubio M, Altisent Trota R, Rocafort Gil J, and Gómez Sancho M
- Subjects
- Humans, Physicians, Spain, Euthanasia, Qualitative Research, Suicide, Assisted
- Abstract
Background and Objectives: The decriminalisation of euthanasia and assisted medical suicide has generated a continuous debate. The terminological confusion is one of the main difficulties in obtaining medical practice consensus. The objective of this study was to determine whether the terms of Euthanasia and physician assisted suicide are used with the same meaning by doctors in Extremadura (Spain)., Material and Method: A qualitative study was conducted using two focus groups in which doctors from different specialties who attended a large number of terminal patients participated. No other focus group was required due to saturation. The sessions were tape recorded and transcribed by two experts in qualitative methodology. Atlas.ti software was used for the analysis. We were advised by the "Health Care at the end of life" Group of the Organizacion Médica Colegial of Spain., Results: Terminological confusion was verified in: 1) The mixture of etymological, functional and social concepts, 2) the term Passive Euthanasia, 3) the association between euthanasia and physician assisted suicide, 4) the confusion with the equivalent "wish to hasten death", and 5) the difficulty of differentiating sedation with Euthanasia. There was consensus on some aspects: a) Full voluntariness, b) the condition of terminal illness, and c) the condition of unbearable symptoms., Conclusions: Conceptual variability persists in relation to the concept of Euthanasia, and is particularly noticeable in the persistence of the concept of passive euthanasia. It would be desirable to achieve a common language to assign a precise meaning to these words to help doctors in their professional practice., (Copyright © 2015 SECA. Published by Elsevier Espana. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
11. [Palliative care support teams and the commitment of primary care teams to terminally ill patients in their homes].
- Author
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Rocafort Gil J, Herrera Molina E, Fernández Bermejo F, Grajera Paredes María ME, Redondo Moralo MJ, Díaz Díez F, and Espinosa Rojas JA
- Subjects
- Humans, Primary Health Care statistics & numerical data, Program Evaluation, Spain, Terminally Ill, Home Care Services statistics & numerical data, Palliative Care statistics & numerical data, Patient Care Team statistics & numerical data
- Abstract
Objective: To find out if the activity of palliative care support teams (PCST) does not negatively influences the performance of the primary care "care of terminally ill patients" service., Participants: Terminally ill patients cared for at home., Design: Multicentre observational study., Main Measurements: The observed variable is the increase in the number of registered patients in primary care, and the number of patients covered between the years 2002 and 2003 and the 4 intervention variables are: total visits, joint visits, assessments, and teaching sessions., Results: The number of patients covered in 2002 was 41.19%, increasing to 45.44% in 2003. The activity rate of the PCST for each 100 000 inhabitants was 526 home visits in 2003, 86.15 joint visits, 313.68 professional assessments, and 23.14 teaching sessions. The joint visits and the teaching sessions were strongly associated with an improvement in the coverage of primary care (Pearson correlation of 0.784 and 0.759, respectively). The total visits were moderately associated (0.525) and the assessments were weakly associated (0.245)., Conclusions: Joint visits and teaching sessions of a PCST are associated to an increase in the activity of primary care teams. Assessments and total visits did not have a negative influence.
- Published
- 2006
- Full Text
- View/download PDF
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