Inhaloterapia en pacientes pediátricos con fibrosis quística
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Fecha
2018
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Universidad de Guayaquil. Facultad de Ciencias Médicas. Carrera de Tecnología Médica
Resumen
La presente investigación fue sobre la enfermedad de fibrosis quística,
sus principales características y problemas que causan en el sistema
respiratorio. Este estudio fue efectuado en el hospital “Dr. Francisco De Icaza
Bustamante”, en donde a través del método cuantitativo se realizaron
encuestas a los licenciados en terapia respiratoria, que junto con los registros
de análisis de datos, se adquirió una población de 84 pacientes, además para la
obtención de la muestra se emplearon criterios de inclusión y exclusión,
resultando un total de 20 pacientes con diagnóstico de fibrosis quística, donde
se observó ciertas complicaciones y síntomas que suelen presentar a medida
que transcurre el proceso de la enfermedad. Basándose en ésta información se
realizó la elaboración de una guía de inhaloterapia dirigida a terapeutas
respiratorios, referente al adecuado manejo de dispositivos empleados en
terapia inhalatoria.
Overview this research was about disease cystic fibrosis, its main characteristics and problems caused by the respiratory system. This study was carried out at the hospital "Dr. Francisco De Icaza Bustamante", in where surveys were conducted through the quantitative method to graduates in respiratory therapy, which together with the records of data analysis, acquired a population of 84 patients, in addition to obtaining the sample used inclusion and exclusion criteria, resulting in a total of 20 patients with a diagnosis of cystic fibrosis, where certain complications and symptoms that usually appear during the process of the disease. Based on this information we have developed a guide for inhalotherapy directed to respiratory therapists relating to the proper management of devices used in inhalation therapy
Overview this research was about disease cystic fibrosis, its main characteristics and problems caused by the respiratory system. This study was carried out at the hospital "Dr. Francisco De Icaza Bustamante", in where surveys were conducted through the quantitative method to graduates in respiratory therapy, which together with the records of data analysis, acquired a population of 84 patients, in addition to obtaining the sample used inclusion and exclusion criteria, resulting in a total of 20 patients with a diagnosis of cystic fibrosis, where certain complications and symptoms that usually appear during the process of the disease. Based on this information we have developed a guide for inhalotherapy directed to respiratory therapists relating to the proper management of devices used in inhalation therapy
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Inhaloterapia, Fibrosis quística, Pediatría, Hospital del Niño Francisco de Icaza Bustamante, Cantón Guayaquil, Ecuador