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1.
Rev Esp Salud Publica ; 922018 Jun 25.
Article in Spanish | MEDLINE | ID: mdl-29938691

ABSTRACT

OBJECTIVE: Polio affects the quality of life of those who have suffered from it and causes health problems including the post-polio syndrome. The main goals of this work were to know the patients perspective of how they have been affected by the disease and establish the knowledge of post-polio syndrome among patients and primary health care professionals. METHODS: Interpretive qualitative research based on the Grounded Theory carried out in two health-care centers in the city of Malaga, one of them with care-rural clinics. Four focal groups were established with the participation of thirteen patients and two focus groups with twenty-six professional participants. Intentional sampling is performed until saturation. The analysis follows an inductive strategy using the Atlas Ti5.2 software. RESULTS: The people affected by polio reports their personal histories of suffering counteracted by strong family support and an active coping attitude, marked by great effort exertion, willpower and endurance. These people made a positive assessment of their lives minimising the limitations. They presented compatible symptoms with post-polio syndrome, which remain unidentified due to the lack of knowledge of it among patients and health-care professionals. The health care provided was considered deficient due to several causes as for instance lack of involvement, communication problems. CONCLUSIONS: The day-to-day polio experience is focused on personal overcoming with major roles played by family support, difficult relationships with the healthcare system and lack of knowledge of the post-polio syndrome.


OBJETIVO: La polio afecta a la calidad de vida de las personas que la han padecido y ocasiona problemas de salud entre los que se encuentra el síndrome postpolio. Los objetivos de este estudio fueron conocer la perspectiva de pacientes sobre cómo les ha afectado la enfermedad y describir el conocimiento sobre el síndrome postpolio de pacientes y profesionales de atención primaria. METODOS: Investigación cualitativa interpretativa basada en la Teoría Fundamentada, realizada en dos centros de salud de la ciudad de Málaga, uno de ellos con consultorios rurales. Se realizaron cuatro grupos focales con participación de trece pacientes y dos grupos focales con veintiséis profesionales participantes. Muestreo intencional hasta saturación. El análisis siguió una estrategia inductiva con ayuda del programa Atlas Ti 5.2. RESULTADOS: Los pacientes relataron una historia personal de sufrimiento, contrarrestada por un fuerte apoyo familiar y afrontamiento activo (categoría central), marcado por el sobreesfuerzo, la superación y una alta resiliencia. Realizaron una valoración positiva de sus vi- das, minimizando las limitaciones. Presentaron síntomas compatibles con el síndrome postpolio, no identificado por el gran desconocimiento de pacientes y profesionales. La atención sanitaria fue considerada deficitaria (falta de implicación y problemas de comunicación). CONCLUSIONES: La vivencia de la polio está centrada en la superación personal, con gran relevancia del apoyo familiar, las difíciles relaciones con el sistema sanitario y el desconocimiento del síndrome postpolio.


Subject(s)
Poliomyelitis/diagnosis , Poliomyelitis/therapy , Postpoliomyelitis Syndrome/diagnosis , Postpoliomyelitis Syndrome/therapy , Adaptation, Psychological , Aged , Communication , Family Health , Female , Focus Groups , Health Knowledge, Attitudes, Practice , Health Personnel , Humans , Male , Middle Aged , Patient Participation , Poliomyelitis/psychology , Postpoliomyelitis Syndrome/psychology , Primary Health Care , Qualitative Research , Quality of Life , Software , Spain
2.
Rev. esp. salud pública ; 92: 0-0, 2018. ilus, tab, graf
Article in Spanish | IBECS | ID: ibc-177586

ABSTRACT

Fundamentos: La polio afecta a la calidad de vida de las personas que la han padecido y ocasiona problemas de salud entre los que se encuentra el síndrome postpolio. Los objetivos de este estudio fueron conocer la perspectiva de pacientes sobre cómo les ha afectado la enfermedad y describir el conocimiento sobre el síndrome postpolio de pacientes y profesionales de atención primaria. Métodos: Investigación cualitativa interpretativa basada en la Teoría Fundamentada, realizada en dos centros de salud de la ciudad de Málaga, uno de ellos con consultorios rurales. Se realizaron cuatro grupos focales con participación de trece pacientes y dos grupos focales con veintiséis profesionales participantes. Muestreo intencional hasta saturación. El análisis siguió una estrategia inductiva con ayuda del programa Atlas Ti 5.2. Resultados: Los pacientes relataron una historia personal de sufrimiento, contrarrestada por un fuerte apoyo familiar y afrontamiento activo (categoría central), marcado por el sobreesfuerzo, la superación y una alta resiliencia. Realizaron una valoración positiva de sus vidas, minimizando las limitaciones. Presentaron síntomas compatibles con el síndrome postpolio, no identificado por el gran desconocimiento de pacientes y profesionales. La atención sanitaria fue considerada deficitaria (falta de implicación y problemas de comunicación). Conclusiones: La vivencia de la polio está centrada en la superación personal, con gran relevancia del apoyo familiar, las difíciles relaciones con el sistema sanitario y el desconocimiento del síndrome postpolio


Backgrounds: Polio affects the quality of life of those who have suffered from it and causes health problems including the post-polio syndrome. The main goals of this work were to know the patients perspective of how they have been affected by the disease and establish the knowledge of post-polio syndrome among patients and primary health care professionals. Methods: Interpretive qualitative research based on the Grounded Theory carried out in two health-care centers in the city of Malaga, one of them with care-rural clinics. Four focal groups were established with the participation of thirteen patients and two focus groups with twenty-six professional participants. Intentional sampling is performed until saturation. The analysis follows an inductive strategy using the Atlas Ti5.2 software. Results: The people affected by polio reports their personal histories of suffering counteracted by strong family support and an active coping attitude, marked by great effort exertion, willpower and endurance. These people made a positive assessment of their lives minimising the limitations. They presented compatible symptoms with post-polio syndrome, which remain unidentified due to the lack of knowledge of it among patients and health-care professionals. The health care provided was considered deficient due to several causes as for instance lack of involvement, communication problems. Conclusions: The day-to-day polio experience is focused on personal overcoming with major roles played by family support, difficult relationships with the healthcare system and lack of knowledge of the post-polio syndrome


Subject(s)
Humans , Poliomyelitis/epidemiology , Postpoliomyelitis Syndrome/epidemiology , Sickness Impact Profile , Primary Health Care , Quality of Life , Social Support , Poliomyelitis/history , Diagnosis, Differential
3.
Aten. prim. (Barc., Ed. impr.) ; 41(9): 493-500, sept. 2009. tab, ilus
Article in Spanish | IBECS | ID: ibc-76979

ABSTRACT

Objetivo. Analizar la experiencia de mujeres que sufren violencia de género desde su propio punto de vista. Identificar los factores relacionados con el mantenimiento o la ruptura de la situación. Diseño. Investigación cualitativa interpretativa. Perspectiva fenomenológica.EmplazamientoEstudio multicéntrico en 6 centros de salud urbanos de Málaga.ParticipantesMujeres que sufren violencia de género. Estos casos se detectaron en atención primaria y las mujeres reconocieron su situación (maltrato percibido).MétodosTécnica de relato biográfico mediante entrevista entre la mujer informante y la trabajadora social, de forma audiograbada y transcrita. Asimismo, se utilizó la teoría fundamentada de Glasser y Strauss, la codificación abierta y axial, y el programa ATLAS-TI 5.2.ResultadosSe analizaron 35 relatos. La vivencia del maltrato fue descrita mediante la metáfora del «torbellino» (ceguera, aislamiento, indefensión, sufrimiento, destino, dependencia, fantasías y círculos viciosos). Ésta se relacionó con el término «aguantar»: valores inculcados, ideal de familia, incertidumbre, anulación, fracaso personal, amor, falta de apoyos, imagen de sí misma y pública, protección a los hijos, miedos múltiples y aspectos materiales. Las mujeres identifican 2 tipos de «salidas» con distintas repercusiones según la participación en la toma de decisiones: una activa y otra pasiva. El término «salir» se relacionó con: situaciones límite, hartazgo, intervención de los hijos, ruptura del ideal de familia y pérdida del miedo. Salir es un proceso de cambio o un «camino». No siempre se da el apoyo institucional y se valora más el apoyo emocional que el legal. Conclusiones. Las mujeres definen «aguantar» y «salir» como estados cualitativamente distintos, con intervención de múltiples factores personales y culturales, y definen un «camino» o proceso entre ambos, que puede ser distinto según el grado de protagonismo de la mujer en la toma de decisiones (AU)


Objectives. To analyse the experience from the point of view of women who have suffered domestic violence. To identify factors related to continuing or resolving the problem.DesignQualitative interpretative research from a phenomenological perspective.Population sampleWomen, detected in primary care, who have suffered domestic violence and have recognised the problem, and who accepted to participate in this research.Multicentre StudySix health centres in the city of Malaga.Methods and techniquesThe technique used is the biographical narration using individual open interviews between social workers and women. This narration was tape-recorded and verbatim transcribed to written text. Grounded theory. Qualitative analysis was made with ATLAS-TI 5.2.OutcomesA total of 35 narrations were analysed. The abuse situation was described as “whirl-wind” metaphor (blindness-isolation-helplessness-suffering-destiny-dependence-fantasies -about love, protection, happiness, change- and vicious circles). Enduring experience is reported to be related to several factors: inculcated gender values, family-ideal, uncertainty, annulment, personal failure sensation, love, support defects, self-image, children protection, multiple fears and material aspects. They identified two types of “exit”: passive and active with different mechanisms and repercussions. Exit experience is related to: limit situations, children intervention, family ideal attempts, and fear-loss. Leaving is a transitional process or “pathway”. Institutional support is not always guaranteed and emotional support is better evaluated than a legal one.ConclusionsEnduring and coming out are reported as two qualitatively different states, which involve many cultural and personal factors. There is a gap between these two states with a process that varies depending on the involvement of the women in decision-making(AU)


Subject(s)
Humans , Female , Pregnancy , Adult , Middle Aged , Aged , Violence , Domestic Violence , Violence Against Women , Sex Offenses , Primary Health Care , Multicenter Studies as Topic , Case Reports
4.
Aten Primaria ; 41(9): 493-500, 2009 Sep.
Article in Spanish | MEDLINE | ID: mdl-19446925

ABSTRACT

OBJECTIVES: To analyse the experience from the point of view of women who have suffered domestic violence. To identify factors related to continuing or resolving the problem. DESIGN: Qualitative interpretative research from a phenomenological perspective. POPULATION SAMPLE: Women, detected in primary care, who have suffered domestic violence and have recognised the problem, and who accepted to participate in this research. MULTICENTRE STUDY: Six health centres in the city of Malaga. METHODS AND TECHNIQUES: The technique used is the biographical narration using individual open interviews between social workers and women. This narration was tape-recorded and verbatim transcribed to written text. Grounded theory. Qualitative analysis was made with ATLAS-TI 5.2. OUTCOMES: A total of 35 narrations were analysed. The abuse situation was described as "whirl-wind" metaphor (blindness-isolation-helplessness-suffering-destiny-dependence-fantasies -about love, protection, happiness, change- and vicious circles). Enduring experience is reported to be related to several factors: inculcated gender values, family-ideal, uncertainty, annulment, personal failure sensation, love, support defects, self-image, children protection, multiple fears and material aspects. They identified two types of "exit": passive and active with different mechanisms and repercussions. Exit experience is related to: limit situations, children intervention, family ideal attempts, and fear-loss. Leaving is a transitional process or "pathway". Institutional support is not always guaranteed and emotional support is better evaluated than a legal one. CONCLUSIONS: Enduring and coming out are reported as two qualitatively different states, which involve many cultural and personal factors. There is a gap between these two states with a process that varies depending on the involvement of the women in decision-making.


Subject(s)
Spouse Abuse/psychology , Adaptation, Psychological , Adult , Aged , Female , Humans , Middle Aged
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