Behr J, Günther A, Kreuter M, Koschel D, Prasse A, Pfeifer M, Costabel U
Asklepios Fachkliniken München-Gauting und Medizinische Klinik V, Klinikum der Ludwig-Maximilians-Universität München.
Med. Klinik II, Klinische Forschergruppe "Lungenfibrose", Universitätsklinikum Gießen und Marburg.
Pneumologie. 2017 Sep;71(9):567-579. doi: 10.1055/s-0043-109856. Epub 2017 Aug 3.
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.
2016年10月,勃林格殷格翰邀请了一批德国特发性肺纤维化(IPF)专家齐聚法兰克福,目的如下:(a)讨论使用尼达尼布治疗特发性肺纤维化(IPF)的相关管理和治疗方面;(b)为尼达尼布的日常临床应用提供支持性建议。本文汇总的信息仅限于尼达尼布在IPF患者中使用的实际问题。在有不同治疗选择的情况下,未讨论IPF药物的选择,专家们提及了IPF诊断和治疗的现行指南。参与者讨论了一系列与10个不同主题相关的临床问题,包括IPF治疗开始时与患者相关的方面、抗凝IPF患者的治疗以及尼达尼布相关不良事件(如胃肠道副作用和肝酶升高)的处理。此外,专家们评估了疾病持续进展的IPF患者的治疗选择、证明停用尼达尼布治疗合理的临床情况以及急性加重或严重感染的IPF患者的治疗选择。最后,参与者讨论了择期手术干预(如肺移植)前后尼达尼布的处理以及IPF患者抗纤维化联合治疗的现有证据。对于所讨论的每个主题,所得信息纳入了临床试验的已发表证据。在证据不足或缺乏的情况下,专家们根据个人临床经验和评估提出了建议。