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The prognostic role of Gender‐Age‐Physiology system in idiopathic pulmonary fibrosis patients treated with pirfenidone

机译:性别时代生理体系对吡法酮治疗特发性肺纤维化患者的预后作用

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摘要

Abstract Introduction Gender, age, physiology (GAP) system have proven to be an easy tool for predicting disease stages and survival in idiopathic pulmonary fibrosis (IPF) patients. Objective To validate mortality risk as determined by the GAP system in a real‐life multicentre IPF population treated with pirfenidone. Methods The study included patients who received pirfenidone for at least 6?months. The GAP calculator and the GAP index were determined. The primary outcome was all‐cause mortality. The prognostic accuracy of the GAP system was evaluated with respect to calibration and discrimination. Results and Conclusion Sixty‐eight IPF patients were enrolled in the study. The median follow‐up was 2.4 years (range 0.1‐7.4 years). A total of 22 deaths as first event (32%) and of 10 lung transplantation (15%) were recorded. The cumulative incidence of mortality at 1, 2 and 3 years was 10.4%, 22.4% and 38.4%, respectively. The differences between the predicted and observed mortality were not significant for the GAP index while the observed mortality become comparable to that predicted by the GAP calculator only in the third year of follow‐up. The C‐index for the GAP index was 0.74 (95% CI 0.57‐0.93) while the C‐statistic value for the GAP calculator was 0.77 (95% CI 0.59‐0.95).
机译:摘要介绍性别,年龄,生理学(间隙)系统已被证明是预测特发性肺纤维化(IPF)患者的疾病阶段和生存的简单工具。目的验证死亡率风险,由Pirfenidone治疗的真实多期型IPF人群中的差距系统确定。方法该研究包括接受Pirfenidone至少6个月的患者。确定间隙计算器和间隙指数。主要结果是全导致死亡率。基于校准和辨别,评估了间隙系统的预后精度。结果和结论六十八个IPF患者参加了研究。中位随访2.4岁(范围0.1-7.4岁)。记录了总共22例死亡(32%)和10次肺移植(15%)。 1,2和3岁的死亡率的累积发生率分别为10.4%,22.4%和38.4%。预测和观察到的死亡率之间的差异对于间隙指数并不重要,而观察到的死亡率与间隙计算器仅在后续三年中预测的相当。间隙指数的C折射率为0.74(95%CI 0.57-0.93),而间隙计算器的C统计值为0.77(95%CI 0.59-0.95)。

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  • 来源
    《The clinical respiratory journal.》 |2019年第3期|共8页
  • 作者单位

    U.O. di Pneumologia e Terapia Semi‐Intensiva Respiratoria – Servizio di Fisiopatologia Respiratoria;

    U.O. di Pneumologia e Terapia Semi‐Intensiva Respiratoria – Servizio di Fisiopatologia Respiratoria;

    Department of PulmonologyUniversity Hospital of Cattinara Azienda Ospedaliero‐Universitaria;

    U.O. di Pneumologia Dipartimento dell’Apparato Respiratorio e del ToraceOspedale G.P. Morgagni –L;

    Regional Referral Centre for Rare Lung DiseaseUniversity of Catania A.O.U. Policlinico‐Vittorio;

    Respiratory Unit Department of Health ScienceUniversity of Milano Bicocca AO San GerardoMonza;

    Respiratory Unit Policlinico Tor Vergata Department of “Systems MedicineUniversity of Rome “Tor;

    Center for Rare Lung DiseasesUniversity Hospital Policlinico di ModenaModena Italy;

    Department of Medicine – DIMEDUniversity of PadovaPadova Italy;

    Respiratory Diseases and Lung Transplant Unit Department of Internal and Specialist;

    UOC II Pneumotisiologia Scuola di specializzazione in malattie respiratorie Università degli Studi;

    UOS Interstiziopatie Polmonari Az Osp. S. Camillo‐ForlaniniRoma Italy;

    Department of PulmonologyUniversity Hospital of Cattinara Azienda Ospedaliero‐Universitaria;

    Department of PulmonologyUniversity Hospital of Cattinara Azienda Ospedaliero‐Universitaria;

    Department of Clinical and Biological Sciences Interstitial and Rare Lung Disease Unit AOU San;

    U.O. di Pneumologia Dipartimento dell’Apparato Respiratorio e del ToraceOspedale G.P. Morgagni –L;

    Regional Referral Centre for Rare Lung DiseaseUniversity of Catania A.O.U. Policlinico‐Vittorio;

    Respiratory Unit Department of Health ScienceUniversity of Milano Bicocca AO San GerardoMonza;

    Respiratory Unit Policlinico Tor Vergata Department of “Systems MedicineUniversity of Rome “Tor;

    Center for Rare Lung DiseasesUniversity Hospital Policlinico di ModenaModena Italy;

    Department of Medicine – DIMEDUniversity of PadovaPadova Italy;

    Respiratory Diseases and Lung Transplant Unit Department of Internal and Specialist;

    UOC II Pneumotisiologia Scuola di specializzazione in malattie respiratorie Università degli Studi;

    UOS Interstiziopatie Polmonari Az Osp. S. Camillo‐ForlaniniRoma Italy;

    Department of Molecular and Translational MedicineUniversity of BresciaBrescia Italy;

    Department of Clinical and Biological Sciences Interstitial and Rare Lung Disease Unit AOU San;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 呼吸系及胸部疾病;
  • 关键词

    antifibrotic therapies; idiopathic pulmonary fibrosis; mortality; prognosis; staging; survival;

    机译:抗纤维化疗法;特发性肺纤维化;死亡率;预后;分期;生存;

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