dc.contributor.advisor | Hernández Álvarez, Erick Mario | |
dc.contributor.author | Navarrete Rueda, Nury Nicole | |
dc.date.accessioned | 2023-06-09T19:37:07Z | |
dc.date.available | 2023-06-09T19:37:07Z | |
dc.date.issued | 2023 | |
dc.identifier.uri | http://dspace.utb.edu.ec/handle/49000/14377 | |
dc.description | Pulmonary Fibrosis is a pathology belonging to the group of interstitial diseases which causes scarring, increased thickness of the lung tissue and inflammation of the lung parenchyma, and the damage caused by this disease is irreversible for which adequate treatment is required. for a good management of the pathology, which delays the advance of the damage and alleviates symptoms such as cough, dyspnea, myalgia and arthralgia. It is diagnosed by performing a set of tests such as control chest X-ray where diffuse bibasal hilar infiltrates are evident plus an increase in the cardiac silhouette and volume loss in the left lung. An alteration in the restrictive pattern was identified through spirometry. Once diagnosed, treatments such as respiratory therapy and oxygen therapy should be implemented. | es_ES |
dc.description | Pulmonary Fibrosis is a pathology belonging to the group of interstitial diseases which causes scarring, increased thickness of the lung tissue and inflammation of the lung parenchyma, and the damage caused by this disease is irreversible for which adequate treatment is required. for a good management of the pathology, which delays the advance of the damage and alleviates symptoms such as cough, dyspnea, myalgia and arthralgia. It is diagnosed by performing a set of tests such as control chest X-ray where diffuse bibasal hilar infiltrates are evident plus an increase in the cardiac silhouette and volume loss in the left lung. An alteration in the restrictive pattern was identified through spirometry. Once diagnosed, treatments such as respiratory therapy and oxygen therapy should be implemented. | es_ES |
dc.description.abstract | La Fibrosis Pulmonar es una patología perteneciente al grupo de enfermedades intersticiales la cual causa cicatrices, aumento del grosor del tejido pulmonar e inflamación del parénquima pulmonar, siendo que los daños causados por esta enfermedad son irreversibles por los cual se precisa de un tratamiento adecuado para un buen manejo de la patología, que retrase el avance de los daños y alivie los síntomas como tos, disnea, mialgia y artralgia. Se diagnostica realizando un conjunto de exámenes como radiografía de torax de control donde se evidencia infiltrados difusos para hiliares bibasales más aumento de la silueta cardiaca y perdida de volumen en pulmón izquierdo. Se identifico a través de la espirometría una alteración en el patrón restrictivo , una vez diagnosticada se deberá implementar tratamientos como la Terapia respiratoria y oxigenoterapia. | es_ES |
dc.format.extent | 30 p. | es_ES |
dc.language.iso | es | es_ES |
dc.publisher | Babahoyo: UTB-FCS, 2023 | es_ES |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Ecuador | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ec/ | * |
dc.subject | Fibrosis Pulmonar | es_ES |
dc.subject | Terapia respiratoria | es_ES |
dc.subject | Cicatrices | es_ES |
dc.subject | Inflamación | es_ES |
dc.subject | Tos seca | es_ES |
dc.title | Intervención del terapista respiratorio en paciente masculino de 55 años con fibrosis pulmonar. | es_ES |
dc.type | bachelorThesis | es_ES |