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[Expert Knowledge and Supporting Advice for the Clinical Use of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis]. / Erfahrungen und unterstützende Hinweise zur Anwendung von Nintedanib bei Patienten mit idiopathischer Lungenfibrose.
Behr, J; Günther, A; Kreuter, M; Koschel, D; Prasse, A; Pfeifer, M; Costabel, U.
Afiliação
  • Behr J; Asklepios Fachkliniken München-Gauting und Medizinische Klinik V, Klinikum der Ludwig-Maximilians-Universität München.
  • Günther A; Med. Klinik II, Klinische Forschergruppe "Lungenfibrose", Universitätsklinikum Gießen und Marburg.
  • Kreuter M; Lungenfachklinik Waldhof-Elgershausen, Greifenstein.
  • Koschel D; Zentrum für seltene und interstitielle Lungenerkrankungen, Pneumologie und Beatmungsmedizin, Thoraxklinik, Universitätsklinikum Heidelberg, Mitglied des Deutschen Zentrums für Lungenforschung.
  • Prasse A; Abteilung Pneumologie, Fachkrankenhaus Coswig, Zentrum für Pneumologie, Allergologie, Beatmungsmedizin und Thoraxchirurgie.
  • Pfeifer M; Klinik für Pneumologie, Medizinische Hochschule Hannover und Deutsches Zentrum für Lungenforschung BREATH.
  • Costabel U; Fraunhofer Institut ITEM Hannover.
Pneumologie ; 71(9): 567-579, 2017 Sep.
Article em De | MEDLINE | ID: mdl-28772332
ABSTRACT
In October 2016, a group of German IPF experts were invited by Boehringer Ingelheim to meet in Frankfurt with the aim, (a) to discuss relevant aspects of the management and treatment of idiopathic pulmonary fibrosis (IPF) using nintedanib; and, (b) to provide supportive advice for daily clinical practice with nintedanib. The resulting information compiled in this document is confined to practical issues regarding the use of nintedanib in patients with IPF. Where different therapeutic options were available, the choice of IPF medication was not discussed and the experts alluded to current guidelines for the diagnosis and treatment of IPF.The participants discussed a comprehensive spectrum of clinical questions related to 10 different topics, including patient-related aspects at initiation of IPF therapy, the treatment of anticoagulated IPF patients, and the handling of nintedanib-related adverse events such as gastrointestinal side effects and elevated liver enzymes. In addition, the experts evaluated therapeutic options for IPF patients with continuous disease progression, clinical scenarios that justify discontinuation of nintedanib treatment, and therapeutic options for IPF patients with an acute exacerbation or severe infection. Finally, the participants discussed the handling of nintendanib before/after elective surgical intervention (e. g. lung transplantation) and the current evidence for antifibrotic combination therapy in patients with IPF.For each topic discussed, the resulting information incorporates published evidence from clinical trials. In case of insufficient or lacking evidence, the experts have formulated recommendations based on their personal clinical experience and evaluation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Competência Clínica / Fibrose Pulmonar Idiopática / Indóis Tipo de estudo: Guideline Limite: Humans Idioma: De Revista: Pneumologie Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Competência Clínica / Fibrose Pulmonar Idiopática / Indóis Tipo de estudo: Guideline Limite: Humans Idioma: De Revista: Pneumologie Ano de publicação: 2017 Tipo de documento: Article