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预测终末期囊性纤维化患者的生存率。

Predicting survival in end-stage cystic fibrosis.

作者信息

Ketchell Robert I, Roughton Michael, Agent Penny, Gyi Khin, Hodson Margaret E

机构信息

Department of Cystic Fibrosis, Royal Brompton and Harefield NHS Foundation Trust, Sydney Street, London SW3 6NP, UK.

出版信息

Respir Med. 2009 Oct;103(10):1441-7. doi: 10.1016/j.rmed.2009.04.025. Epub 2009 Jul 16.

DOI:10.1016/j.rmed.2009.04.025
PMID:19615875
Abstract

The natural history of cystic fibrosis (CF) is unpredictable and the optimal timing for lung transplantation in end-stage disease uncertain. Predicting survival based on FEV1 alone remains controversial and therefore the aim of this study was to assess the value of walk test performance in pre-transplant assessment. Retrospective review of adult patients with end-stage CF who underwent transplant assessment between 1988 and 2004 including a documented walk test on room air, but who died before transplant. The six-minute walk test (6MWT) was used between 1988 and 1993 and the shuttle walk test (SWT) thereafter, the two cohorts were therefore individually assessed. A total of 121 patients were identified. The median (IQR) survival in patients performing SWT (n=77) and 6MWT (n=44) was 363 days (226, 566) and 433 days (232, 844), respectively, with survival in both cohorts significantly associated with pre-test (resting) heart rate (HR) (p<0.03), but not distance walked, pre-test SpO2, FEV1 or BMI. It was predicted that 85% of patients performing SWT with a resting HR of 120 bpm, 70% of those with a HR of 109 bpm (cohort median) but only 25% with a HR of 72 bpm would die within 500 days. Distance walked in the SWT was significantly related to pre-test HR (p<0.01), SpO2 (p<0.01) and Borg score (p=0.016) when performing linear regression. Only pre-test HR remained significant when performing multiple regression. Resting heart rate was the only consistent parameter in this study at predicting a high risk of dying on the transplant waiting list.

摘要

囊性纤维化(CF)的自然病史不可预测,终末期疾病进行肺移植的最佳时机也不确定。仅根据第一秒用力呼气量(FEV1)预测生存率仍存在争议,因此本研究的目的是评估步行试验表现在移植前评估中的价值。对1988年至2004年间接受移植评估的成年终末期CF患者进行回顾性研究,这些患者均有在室内空气中进行步行试验的记录,但在移植前死亡。1988年至1993年使用六分钟步行试验(6MWT),此后使用往返步行试验(SWT),因此对这两组分别进行评估。共确定了121例患者。进行SWT(n = 77)和6MWT(n = 44)的患者的中位(四分位间距)生存期分别为363天(226,566)和433天(232,844),两组患者的生存期均与试验前(静息)心率(HR)显著相关(p<0.03),但与步行距离、试验前血氧饱和度(SpO2)、FEV1或体重指数(BMI)无关。据预测,静息心率为120次/分钟的SWT患者中有85%、心率为109次/分钟(队列中位数)的患者中有70%、但心率为72次/分钟的患者中只有25%会在500天内死亡。进行线性回归时,SWT中的步行距离与试验前HR(p<0.01)、SpO2(p<0.01)和博格评分(p = 0.016)显著相关。进行多元回归时,只有试验前HR仍然显著。在本研究中,静息心率是预测移植等待名单上高死亡风险的唯一一致参数。

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Predicting survival in end-stage cystic fibrosis.预测终末期囊性纤维化患者的生存率。
Respir Med. 2009 Oct;103(10):1441-7. doi: 10.1016/j.rmed.2009.04.025. Epub 2009 Jul 16.
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The 12-min walk test as an assessment criterion for lung transplantation in subjects with cystic fibrosis.12分钟步行试验作为囊性纤维化患者肺移植的评估标准。
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Six-minute walking test in cystic fibrosis adults with mild to moderate lung disease: comparison to healthy subjects.成年囊性纤维化轻度至中度肺部疾病患者的六分钟步行试验:与健康受试者的比较。
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The six-minute walk test: a guide to assessment for lung transplantation.六分钟步行试验:肺移植评估指南
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Long-term outcome of lung transplantation for cystic fibrosis--Danish results.囊性纤维化肺移植的长期结果——丹麦的研究结果。
Eur J Cardiothorac Surg. 2004 Dec;26(6):1180-6. doi: 10.1016/j.ejcts.2004.08.015.
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[Reproducibility of the shuttle walk test in children with cystic fibrosis].
Rev Mal Respir. 2003 Nov;20(5 Pt 1):711-8.
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Use of the peak heart rate reached during six-minute walk test to predict individualized training intensity in patients with cystic fibrosis: validity and reliability.使用六分钟步行试验中达到的峰值心率来预测囊性纤维化患者的个体化训练强度:有效性和可靠性。
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True survival benefit of lung transplantation for cystic fibrosis patients: the Zurich experience.囊性纤维化患者肺移植的真正生存获益:苏黎世的经验
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Clinical Outcomes and Prognostic Factors in a Cohort of Adults With Cystic Fibrosis: A 7-Year Follow-Up Study.成年囊性纤维化患者队列的临床结局及预后因素:一项7年随访研究
Respir Care. 2016 Feb;61(2):192-9. doi: 10.4187/respcare.04097. Epub 2015 Dec 29.
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Body mass index as a predictor of survival in adults with cystic fibrosis referred for lung transplantation.体重指数作为接受肺移植的成年囊性纤维化患者生存情况的预测指标。
J Heart Lung Transplant. 1998 Nov;17(11):1097-103.

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