Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista

The increased survival of patients with cystic fibrosis (CF) resulted in the appearance of new pulmonary and non-pulmonary complications. Even though subjects with CF present with inflammatory pulmonary changes at birth, several pathogens such as Staphyloccocus aureus, Haemophilus influenzae and Pse...

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Autores principales:	Vega-Briceño,Luis E, Guiraldes C,Ernesto, Sánchez D,Ignacio
Lenguaje:	Spanish / Castilian
Publicado:	Sociedad Médica de Santiago 2006
Materias:	Cystic fibrosis Respiratory insufficiency Respiratory tract infectious
Acceso en línea:	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006000300016
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spelling	oai:scielo:S0034-988720060003000162006-05-02Fibrosis quística: enfrentando la transición desde el pediatra hacia el internistaVega-Briceño,Luis EGuiraldes C,ErnestoSánchez D,Ignacio Cystic fibrosis Respiratory insufficiency Respiratory tract infectious The increased survival of patients with cystic fibrosis (CF) resulted in the appearance of new pulmonary and non-pulmonary complications. Even though subjects with CF present with inflammatory pulmonary changes at birth, several pathogens such as Staphyloccocus aureus, Haemophilus influenzae and Pseudomona aeruginosa contribute to the progression of pulmonary injury. Clinical presentations vary according to patient age; even though mild forms exist, patients with severe forms, develop respiratory insufficiency and end-stage disease at an early stage. Today, new diagnostic and therapeutic tools, increase the possibility of an early diagnosis and of greater survival. Successful management will depend on the timely selection of adequate antimicrobials, the use of pancreatic enzyme supplementation and early institution to respiratory physiotherapy. The transition from pediatric care to adult care must occur according to development of each patient. This timing must be flexible and there should be a constant communication and coordination within the different specialists in internal medicine. Thus, it is crucial to recognize the disease progression as a continuous process, giving the appropriate physiologic support and evaluating the needs of the patient and close relativesinfo:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.134 n.3 20062006-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006000300016es10.4067/S0034-98872006000300016
institution	Scielo Chile
collection	Scielo Chile
language	Spanish / Castilian
topic	Cystic fibrosis Respiratory insufficiency Respiratory tract infectious
spellingShingle	Cystic fibrosis Respiratory insufficiency Respiratory tract infectious Vega-Briceño,Luis E Guiraldes C,Ernesto Sánchez D,Ignacio Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
description	The increased survival of patients with cystic fibrosis (CF) resulted in the appearance of new pulmonary and non-pulmonary complications. Even though subjects with CF present with inflammatory pulmonary changes at birth, several pathogens such as Staphyloccocus aureus, Haemophilus influenzae and Pseudomona aeruginosa contribute to the progression of pulmonary injury. Clinical presentations vary according to patient age; even though mild forms exist, patients with severe forms, develop respiratory insufficiency and end-stage disease at an early stage. Today, new diagnostic and therapeutic tools, increase the possibility of an early diagnosis and of greater survival. Successful management will depend on the timely selection of adequate antimicrobials, the use of pancreatic enzyme supplementation and early institution to respiratory physiotherapy. The transition from pediatric care to adult care must occur according to development of each patient. This timing must be flexible and there should be a constant communication and coordination within the different specialists in internal medicine. Thus, it is crucial to recognize the disease progression as a continuous process, giving the appropriate physiologic support and evaluating the needs of the patient and close relatives
author	Vega-Briceño,Luis E Guiraldes C,Ernesto Sánchez D,Ignacio
author_facet	Vega-Briceño,Luis E Guiraldes C,Ernesto Sánchez D,Ignacio
author_sort	Vega-Briceño,Luis E
title	Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
title_short	Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
title_full	Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
title_fullStr	Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
title_full_unstemmed	Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
title_sort	fibrosis quística: enfrentando la transición desde el pediatra hacia el internista
publisher	Sociedad Médica de Santiago
publishDate	2006
url	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006000300016
work_keys_str_mv	AT vegabricenoluise fibrosisquisticaenfrentandolatransiciondesdeelpediatrahaciaelinternista AT guiraldescernesto fibrosisquisticaenfrentandolatransiciondesdeelpediatrahaciaelinternista AT sanchezdignacio fibrosisquisticaenfrentandolatransiciondesdeelpediatrahaciaelinternista
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Fibrosis quística: enfrentando la transición desde el pediatra hacia el internista

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