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2
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Respir Med. 2006 Oct;100(10):1734-41. doi: 10.1016/j.rmed.2006.02.004. Epub 2006 Mar 20.
3
High-dose acetylcysteine in idiopathic pulmonary fibrosis.高剂量乙酰半胱氨酸治疗特发性肺纤维化
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Registry of the International Society for Heart and Lung Transplantation: twenty-second official adult lung and heart-lung transplant report--2005.国际心肺移植学会登记处:2005年第二十二次成人肺和心肺移植官方报告
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Exercise testing determines survival in patients with diffuse parenchymal lung disease evaluated for lung transplantation.运动试验可确定接受肺移植评估的弥漫性实质性肺疾病患者的生存率。
Respir Med. 2005 Nov;99(11):1431-9. doi: 10.1016/j.rmed.2005.03.007.
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Double-blind, placebo-controlled trial of pirfenidone in patients with idiopathic pulmonary fibrosis.吡非尼酮治疗特发性肺纤维化患者的双盲、安慰剂对照试验。
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Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia.在纤维化间质性肺炎中,生理学指标比病理学指标更能预测生存率。
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9
Six-minute walk, maximal exercise tests: reproducibility in fibrotic interstitial pneumonia.六分钟步行试验、最大运动试验:在纤维化间质性肺炎中的可重复性
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10
The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis.定时步行试验作为特发性肺纤维化严重程度和生存率的一项指标。
Eur Respir J. 2005 Jan;25(1):96-103. doi: 10.1183/09031936.04.00137203.

六分钟步行距离可预测特发性肺纤维化患者在等待名单上的生存情况。

Six-minute-walk distance predicts waiting list survival in idiopathic pulmonary fibrosis.

作者信息

Lederer David J, Arcasoy Selim M, Wilt Jessie S, D'Ovidio Frank, Sonett Joshua R, Kawut Steven M

机构信息

Department of Medicine, College of Physicians and Surgeons, Joseph L. Mailman School of Public Health, Columbia University, New York, New York 10032, USA.

出版信息

Am J Respir Crit Care Med. 2006 Sep 15;174(6):659-64. doi: 10.1164/rccm.200604-520OC. Epub 2006 Jun 15.

DOI:10.1164/rccm.200604-520OC
PMID:16778159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2648057/
Abstract

RATIONALE

Functional studies may be useful to predict survival in idiopathic pulmonary fibrosis (IPF). Various cutoffs of 6-min-walk distance (6MWD) have been suggested to identify patients at a high risk of death.

OBJECTIVES

To examine the association between 6MWD and survival in patients with IPF listed for lung transplantation, and to identify sensitive and specific cutoffs for predicting death at 6 mo.

METHODS

We performed a retrospective cohort study of 454 patients classified as having IPF listed for lung transplantation with the United Network for Organ Sharing between June 30, 2004 and July 22, 2005.

MEASUREMENTS AND MAIN RESULTS

Lower 6MWD was associated with an increased mortality rate (p value for linear trend < 0.0001). Patients with a walk distance less than 207 m had a more than fourfold greater mortality rate than those with a walk distance of 207 m or more, despite adjustment for demographics, anthropomorphics, FVC % predicted, pulmonary hypertension, and medical comorbidities (adjusted rate ratio, 4.7; 95% confidence interval, 2.5-8.9; p < 0.0001). 6MWD was a significantly better predictor of 6-mo mortality than was FVC % predicted (c-statistic = 0.73 vs. 0.59, respectively; p = 0.02).

CONCLUSIONS

Lower 6MWD was strongly and independently associated with an increased mortality rate for wait-listed patients classified as having IPF. 6MWD was a better predictor of death at 6 mo than was FVC % predicted.

摘要

理论依据

功能研究可能有助于预测特发性肺纤维化(IPF)患者的生存率。已提出多种6分钟步行距离(6MWD)的临界值来识别死亡风险高的患者。

目的

研究6MWD与等待肺移植的IPF患者生存率之间的关联,并确定预测6个月时死亡的敏感且特异的临界值。

方法

我们对2004年6月30日至2005年7月22日期间被器官共享联合网络分类为等待肺移植的454例IPF患者进行了一项回顾性队列研究。

测量指标与主要结果

较低的6MWD与死亡率增加相关(线性趋势p值<0.0001)。步行距离小于207米的患者死亡率比步行距离为207米或更长的患者高出四倍多,尽管对人口统计学、人体测量学、预测的FVC%、肺动脉高压和合并症进行了调整(调整后的率比为4.7;95%置信区间为2.5-8.9;p<0.0001)。6MWD对6个月死亡率的预测明显优于预测的FVC%(c统计量分别为0.73和0.59;p=0.02)。

结论

较低的6MWD与被分类为IPF的等待名单上患者的死亡率增加密切且独立相关。6MWD对6个月时死亡的预测优于预测的FVC%。