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Idiopathic Pulmonary Fibrosis in Switzerland: Diagnosis and Treatment.
Respiration ; 93(5): 363-378, 2017.
Article en En | MEDLINE | ID: mdl-28343230
Idiopathic pulmonary fibrosis (IPF) is a severe progressive and irreversible lung disease. Novel antifibrotic drugs that slow disease progression are now available. However, many issues regarding patient management remain unanswered, such as the choice between available drugs, their use in particular subgroups and clinical situations, time of treatment onset, termination, combination or switch, or nonpharmacologic management. To guide Swiss respiratory physicians in this evolving field still characterized by numerous areas of uncertainty, the Swiss Working Group for interstitial and rare lung diseases of the Swiss Respiratory Society provides a position paper on the diagnosis and treatment of IPF.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Idiopática Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Respiration Año: 2017 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Pulmonar Idiopática Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline Límite: Humans Idioma: En Revista: Respiration Año: 2017 Tipo del documento: Article País de afiliación: Suiza