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1.
Nurse Educ Today ; 70: 77-86, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30170152

RESUMEN

BACKGROUND: In the face of rapid digitalisation and ever-higher educational requirements for healthcare professionals, it is important that health science teachers possess the relevant core competences. The education of health science teachers varies internationally and there is no consensus about the minimum qualifications and experience they require. OBJECTIVE: The aim of this systematic review was to describe the health science teachers' competences and the factors related to it. DESIGN: Systematic review of original quantitative studies. DATA SOURCES: Four databases were selected from which to retrieve original studies: Cinahl (Ebsco), PubMed, Medic, Eri (ProQuest). REVIEW METHODS: The systematic review used PICOS inclusion criteria. Original peer-reviewed quantitative studies published between 1/2007 and 1/2018 were identified. Screening was conducted by two researchers separately reading the 1885 titles, 600 abstracts, and 63 full-texts that were identified, and then agreed between them. Critical appraisal was performed using the JBI MAStARI evaluation tool. The data was extracted and then analysed narratively. RESULTS: The core competences of health science teachers include areas of knowledge, skills and attitudes. Health science teachers evaluate their own competence as high. Only in relation to entrepreneurship and leadership knowledge was evaluated to be average. The most common factors influencing competence were teachers' title/position, healthcare experience, research activities, age, academic degree and for which type of organisation they work. CONCLUSION: It is important to identify the core competencies required by health science teachers in order to train highly competent healthcare professionals. Based on the findings of this systematic review we suggest that teachers should be encouraged to gain university education and actively participate in research, and that younger teachers should have opportunities to practice the relevant teaching skills to build competence.


Asunto(s)
Competencia Clínica , Conocimientos, Actitudes y Práctica en Salud , Empleos en Salud/normas , Enseñanza , Atención a la Salud , Educación de Postgrado , Humanos , Liderazgo
2.
Scand J Pain ; 6(1): 33-40, 2015 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-29911591

RESUMEN

Background Research has emphasised the essential role of psychosocial risk factors in chronic pain. In practice, pain is usually verified by identifying its physical cause. In patients without any distinct pathology, pain is easily defined as imaginary pain. The aim of this qualitative study was to explore the invisibility of chronic pain, from the patients' perspective. Methods Thirty-four participants with chronic pain were interviewed. The mean age of the participants was 48 years, and 19 of them were women. For 21 of the participants, the duration of pain was more than five years, and most of the participants had degenerative spinal pain. The transcribed interviews were analysed using Giorgi's four-phase phenomenological method. Results The participants' chronic pain was not necessarily believed by health care providers because of no identified pathology. The usual statements made by health care providers and family members indicated speculation, underrating, and denial of pain. The participants reported experience of feeling that they had been rejected by the health care and social security system, and this feeling had contributed to additional unnecessary mental health problems for the participants. As a result from the interviews, subthemes such as "Being disbelieved", "Adolescents' pain is also disbelieved", "Denying pain", "Underrating symptoms", "The pain is in your head", "Second-class citizen", "Lazy pain patient", and "False beliefs demand passivity" were identified. Conclusions In health care, pain without any obvious pathology may be considered to be imaginary pain. Despite the recommendations, to see chronic pain as a biopsychosocial experience, chronic pain is still regarded as a symptom of an underlying disease. Although the holistic approach is well known and recommended, it is applied too sparsely in clinical practice. Implications The Cartesian legacy, keeping the mind and body apart, lives strong in treatment of chronic pain despite recommendations. The biopsychosocial approach seems to be rhetoric.


Asunto(s)
Dolor Crónico/psicología , Adulto , Femenino , Humanos , Entrevistas como Asunto , Masculino , Persona de Mediana Edad , Relaciones Médico-Paciente , Investigación Cualitativa
3.
Chronic Illn ; 11(2): 156-67, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25330917

RESUMEN

OBJECTIVES: Chronic pain may disable the body, depress the mind and ruin the quality of life. The aim of this study was to use the participants' personal experiences to explore the meaning of the experience of chronic pain and to find successful ways to manage chronic pain. METHODS: Thirty-four participants with chronic pain were interviewed. The transcribed interviews were analysed using Giorgi's phenomenological method consisting of four phases: (1) reading the transcriptions several times, (2) discriminating meaning units, (3) collecting meaning units into groups and (4) the synthesis. RESULTS: The participants stated that the key to managing chronic pain was to reconsider the individual meaning of the experience of pain. As a result of the interviews, seven subthemes were found based on the 'Negativity of chronic pain', namely, 'State of reflection', 'Reconsidering values', 'Acceptance of pain', 'Support network', 'Altered self', 'Joys in life' and 'Pain dissociation'. CONCLUSIONS: Pain is an aversive sensation, which leads to the conclusion that the meaning of the experience is also negative, but it can be reversed. In clinical practice, the focus should be on revising the subjective meaning of pain in order to manage pain and to restore positivity in personal life.


Asunto(s)
Adaptación Psicológica , Dolor Crónico/psicología , Adulto , Anciano , Actitud Frente a la Salud , Femenino , Humanos , Masculino , Persona de Mediana Edad , Investigación Cualitativa , Calidad de Vida/psicología
4.
Disabil Rehabil ; 37(4): 363-71, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-24856637

RESUMEN

PURPOSE: The aim of this qualitative study was to explore participants' perspectives on the effects of chronic pain on the psychophysical unity. METHODS: Thirty-four chronic pain outpatients were interviewed, and the transcribed interviews were analysed with Giorgi's four-phase phenomenological method. The mean age of the participants was 48 years, and 19 of them were women. For 21 of the participants, the pain duration was more than 5 years, and most had degenerative spinal pain. RESULTS: The results of this whole research project indicated that the phenomenon chronic pain consisted of four essential themes: Pain affects the whole person, invisibility, negativity, and dominance of pain. This study concentrates only on one theme "Chronic pain affects the whole person", in which were found eight subthemes in the interviews. The strongest argument made by the participants was not the physical pain itself but the psychosocial consequences, such as distress, loneliness, lost identity, and low quality of life which were their main problems. CONCLUSIONS: In multidisciplinary holistic rehabilitation, it is essential to take care of the patient's psychological distress. A potential source of psychosocial symptoms may be the subjective responses to experience of chronic pain due to the subjective meanings of pain. Implications for Rehabilitation About chronic pain Pain is an experience, not only an aversive sensation. Intensity of pain describes only the sensation, not the experience of pain. In chronic pain, the main complaint may be not the physical pain, but the distress. In rehabilitation, the patient needs to be taken as a whole person. Multidisciplinary rehabilitation, including patient counselling should be the fundamental part of treatment. In rehabilitation, the individual meaning of chronic pain needs to be disclosed.


Asunto(s)
Dolor Crónico/psicología , Dolor Crónico/rehabilitación , Adaptación Psicológica , Adulto , Anciano , Femenino , Necesidades y Demandas de Servicios de Salud , Humanos , Entrevistas como Asunto , Soledad , Masculino , Persona de Mediana Edad , Investigación Cualitativa , Calidad de Vida , Sensación , Apoyo Social
5.
Musculoskeletal Care ; 12(3): 141-9, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24425247

RESUMEN

BACKGROUND: Chronic pain is not only a physical disorder, but also a complex combination of biopsychosocial symptoms affecting each other. When in chronic pain, the patient's entire body becomes a source of pain, and eventually the pain occupies the patient's mind and entire life. The aim of the present study was to examine the life experience and management of chronic pain from the patient's perspective. METHODS: Thirty-four participants with chronic pain were interviewed. For 21 of the participants, the duration of pain was more than five years. Most of the participants had degenerative spinal pain. The transcribed interviews were analysed using Giorgi's four-phase phenomenological method. RESULTS: The results indicated that chronic pain impaired the participant's psychosocial well-being by controlling thoughts and making life itself painful. When life is filled with pain, the entire life is seen through pain. Continuity, unpredictability and the fear of the pain decreased quality of life. As a result of the interviews, the following subthemes were identified, based on the essential theme of 'the dominance of chronic pain': namely: 'pain is the master', 'life is not worth living', 'contextual pain' and 'waiting and hoping'. CONCLUSIONS: Chronic pain may decrease the quality of the patient's life to such an extent that it may be regarded as not worth living. Multidisciplinary management of chronic pain may lead to a better health status and diminish the adverse consequences of chronic pain.


Asunto(s)
Dolor Crónico/psicología , Emociones , Calidad de Vida/psicología , Valor de la Vida , Adaptación Psicológica , Adulto , Anciano , Dolor Crónico/complicaciones , Dolor Crónico/terapia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Autoimagen , Factores Socioeconómicos , Factores de Tiempo
6.
Disabil Rehabil ; 35(4): 306-14, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22726109

RESUMEN

PURPOSE: Acceptance has been discovered to be successful in improving quality of life when adjusting to chronic pain. Instead of avoiding and controlling the pain, the goal is to confront the pain and to live a value directed life. Thus far, there has not been an instrument in Finnish to assess the acceptance of chronic pain. This study aimed at translating the Chronic Pain Acceptance Questionnaire-(CPAQ)-into Finnish and assessing its reliability and validity. METHOD: Eighty-one persons with different types of chronic pain responded to the CPAQ, the Beck Depression Inventory (BDI), RAND-36 and questions of sociodemographic and pain-related variables. RESULTS: The responders' ages varied from 16 to 83 years (mean = 48.5 years) and 63% of them were women. For 55% of the participants, the pain had lasted more than 4 years and 63% from the sample had chronic pain in the low back or lower extremities. In test-retest analysis, the interclass correlation coefficient (ICC ) values were good, 0.81-0.87. Internal consistency was very good (α = 0.86). There was no floor-ceiling effect in the Finnish version of CPAQ. Correlation was found between both subscales of the CPAQ and every domain of the RAND-36 (r = 0.23; 0.68) and the BDI (r = -0.24; -0.62). Education, age, pain avoidance, social support and pain intensity correlated with either one of the subscales or total CPAQ. CPAQ revealed no association between fear of pain and pain duration. CONCLUSIONS: In conclusion, the Finnish version of the CPAQ is a reliable and valid method for measuring chronic pain acceptance.


Asunto(s)
Adaptación Psicológica , Actitud Frente a la Salud , Dolor Crónico/psicología , Desamparo Adquirido , Psicometría/métodos , Encuestas y Cuestionarios/normas , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Ansiedad/etiología , Dolor Crónico/etnología , Cultura , Depresión/etiología , Femenino , Finlandia , Humanos , Masculino , Persona de Mediana Edad , Dimensión del Dolor/métodos , Escalas de Valoración Psiquiátrica , Psicometría/estadística & datos numéricos , Calidad de Vida/psicología , Reproducibilidad de los Resultados , Índice de Severidad de la Enfermedad , Apoyo Social , Factores Socioeconómicos , Traducción , Adulto Joven
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