Suppr超能文献

特发性肺纤维化的循证治疗策略。

Evidence-based treatment strategies in idiopathic pulmonary fibrosis.

机构信息

Asklepios Fachkliniken München Gauting, Dept of Internal Medicine V, Comprehensive Pneumology Center, University of Munich, Munich, Germany.

出版信息

Eur Respir Rev. 2013 Jun 1;22(128):163-8. doi: 10.1183/09059180.00001013.

Abstract

Recently updated guidelines have provided revised recommendations, based on the GRADE criteria, for the diagnosis and pharmacological and non-pharmacological management of patients with idiopathic pulmonary fibrosis (IPF). Cochrane reviews are also a highly respected and reliable source of evidence-based information that identify and analyse all available data of overall treatment effects from appropriate studies. A recent update of one Cochrane review failed to identify any new evidence supporting the use of corticosteroids in IPF. Another review of data from 15 randomised controlled studies of non-steroid agents for the treatment of IPF identified two trials of interferon-γ-1b suitable for analysis. However, the pooled analysis revealed no treatment effect in terms of survival. A further meta-analysis of three phase III studies of pirfenidone treatment in IPF patients suggested a significant increase in progression-free survival. The interpretation of recent international and national European guideline updates and treatment recommendations, available clinical data from published and ongoing trials investigating potential pharmacological agents, and the individual patient's preferences, must be considered in the clinical management of this disease.

摘要

最近更新的指南根据 GRADE 标准,为特发性肺纤维化(IPF)患者的诊断以及药物和非药物治疗提供了修订建议。Cochrane 评价也是一种非常受尊重且可靠的循证信息来源,它可以识别和分析所有来自适当研究的关于整体治疗效果的可用数据。最近对一项 Cochrane 评价的更新未能发现任何支持在 IPF 中使用皮质类固醇的新证据。另一项对 15 项关于非甾体药物治疗 IPF 的随机对照研究数据的评价确定了两项适合分析的干扰素-γ-1b 试验。然而,汇总分析显示在生存方面没有治疗效果。对三项吡非尼酮治疗 IPF 患者的 III 期研究的进一步荟萃分析表明,无进展生存期有显著增加。在这种疾病的临床管理中,必须考虑最近的国际和国家欧洲指南更新和治疗建议的解释、已发表和正在进行的潜在药物治疗试验的临床数据以及个体患者的偏好。

相似文献

5
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
8
Recommendations on treatment for IPF.特发性肺纤维化治疗建议。
Respir Res. 2013;14 Suppl 1(Suppl 1):S6. doi: 10.1186/1465-9921-14-S1-S6. Epub 2013 Apr 16.

引用本文的文献

5
: WNT signalling in chronic lung diseases.慢性肺部疾病中的WNT信号传导
Thorax. 2017 Aug;72(8):746-759. doi: 10.1136/thoraxjnl-2016-209753. Epub 2017 Apr 17.

本文引用的文献

5
10
Non-steroid agents for idiopathic pulmonary fibrosis.用于特发性肺纤维化的非甾体类药物。
Cochrane Database Syst Rev. 2010 Sep 8(9):CD003134. doi: 10.1002/14651858.CD003134.pub2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验