Guidelines for the medical treatment of idiopathic pulmonary fibrosis
Arch Bronconeumol. 2017 May;53(5):263-269.
doi: 10.1016/j.arbres.2016.12.011.
Epub 2017 Mar 11.
[Article in
English,
Spanish]
Affiliations
- 1 Servicio de Neumología, Hospital Clínic, Barcelona, España; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), España. Electronic address: [email protected].
- 2 Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), España; Unidad Funcional del Intersticio Pulmonar (UFIP), Servicio de Neumología, Hospital Universitario de Bellvitge-Instituto de Investigación Biomédica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, España.
- 3 Servicio de Neumología, Hospital Universitario de Canarias, Santa Cruz de Tenerife, España.
- 4 Servicio de Neumología, Complejo Asistencial Universitario de León, León, España.
- 5 Servicio de Neumología, Hospital de la Santa Creu i Sant Pau, Barcelona, España.
- 6 Servicio de Neumología, Consorcio Hospital General Universitario de Valencia, Valencia, España.
- 7 Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), España; Servicio de Neumología, Hospital Universitario Virgen del Rocío, Sevilla, España.
- 8 Servicio de Neumología, Hospital Universitario de La Princesa, Universidad Autónoma de Madrid, Madrid, España.
Abstract
Idiopathic pulmonary fibrosis is defined as chronic fibrosing interstitial pneumonia limited to the lung, with poor prognosis. The incidence has been rising in recent years probably due to improved diagnostic methods and increased life expectancy. In 2013, the SEPAR guidelines for the diagnosis and treatment for idiopathic pulmonary fibrosis were published. Since then, clinical trials and meta-analyses have shown strong scientific evidence for the use of pirfenidone and nintedanib in the treatment of idiopathic pulmonary fibrosis. In 2015, the international consensus of 2011 was updated and new therapeutic recommendations were established, prompting us to update our recommendation for the medical treatment of idiopathic pulmonary fibrosis accordingly. Diagnostic aspects and non-pharmacological treatment will not be discussed as no relevant developments have emerged since the 2013 guidelines.
Keywords:
Fibrosis pulmonar idiopática; Idiopathic pulmonary fibrosis; Nintedanib; Pirfenidona; Pirfenidone; Tratamiento; Treatment.
Copyright © 2017 SEPAR. Publicado por Elsevier España, S.L.U. All rights reserved.
MeSH terms
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Adrenal Cortex Hormones / therapeutic use
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Disease Progression
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Disease-Free Survival
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Evidence-Based Medicine
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Gastroesophageal Reflux / complications
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Gastroesophageal Reflux / therapy
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Gastrointestinal Diseases / chemically induced
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Humans
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Hypertension, Pulmonary / complications
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Idiopathic Pulmonary Fibrosis / complications
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Idiopathic Pulmonary Fibrosis / drug therapy*
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Indoles / adverse effects
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Indoles / therapeutic use
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Meta-Analysis as Topic
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Pulmonary Emphysema / complications
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Pyridones / adverse effects
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Pyridones / therapeutic use
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Randomized Controlled Trials as Topic
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Societies, Medical / standards
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Spain
Substances
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Adrenal Cortex Hormones
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Indoles
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Pyridones
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pirfenidone
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nintedanib