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囊性纤维化肺部恶化后未能恢复到基线肺功能。

Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation.

机构信息

Department of Pediatrics, American Family Children's Hospital, 600 Highland Avenue, Madison, WI 53792-9988, USA.

出版信息

Am J Respir Crit Care Med. 2010 Sep 1;182(5):627-32. doi: 10.1164/rccm.200909-1421OC. Epub 2010 May 12.

Abstract

RATIONALE

Patients with cystic fibrosis periodically experience pulmonary exacerbations. Previous studies have noted that some patients' lung function (FEV(1)) does not improve with treatment.

OBJECTIVES

To determine the proportion of patients treated for a pulmonary exacerbation that does not recover to spirometric baseline, and to identify factors associated with the failure to recover to spirometric baseline.

METHODS

Cohort study using the Cystic Fibrosis Foundation Patient Registry from 2003-2006. We randomly selected one pulmonary exacerbation treated with intravenous antibiotics per patient and compared the best FEV(1) in the 3 months after treatment with the best FEV(1) in the 6 months before treatment. Recovery to baseline was defined as any FEV(1) in the 3 months after treatment that was greater than or equal to 90% of the baseline FEV(1). Multivariable logistic regression was used to estimate associations with the failure to recover to baseline FEV(1).

MEASUREMENTS AND MAIN RESULTS

Of 8,479 pulmonary exacerbations, 25% failed to recover to baseline FEV(1). A higher risk of failing to recover to baseline was associated with female sex; pancreatic insufficiency; being undernourished; Medicaid insurance; persistent infection with Pseudomonas aeruginosa, Burkholderia cepacia complex, or methicillin-resistant Staphylococcus aureus; allergic bronchopulmonary aspergillosis; a longer time since baseline spirometric assessment; and a larger drop in FEV(1) from baseline to treatment initiation.

CONCLUSIONS

For a randomly selected pulmonary exacerbation, 25% of patients' pulmonary function did not recover to baseline after treatment with intravenous antibiotics. We identified factors associated with the failure to recover to baseline, allowing clinicians to identify patients who may benefit from closer monitoring and more aggressive treatment.

摘要

背景

囊性纤维化患者会周期性地经历肺部恶化。先前的研究表明,一些患者的肺功能(FEV1)在治疗后并未得到改善。

目的

确定接受肺部恶化治疗后无法恢复至肺活量基线的患者比例,并确定与无法恢复至肺活量基线相关的因素。

方法

使用 2003-2006 年囊性纤维化基金会患者登记处进行队列研究。我们随机选择每位患者的一次静脉抗生素治疗的肺部恶化,并将治疗后 3 个月的最佳 FEV1 与治疗前 6 个月的最佳 FEV1 进行比较。恢复至基线定义为治疗后 3 个月的任何 FEV1 均大于或等于基线 FEV1 的 90%。使用多变量逻辑回归来估计与无法恢复至基线 FEV1 相关的因素。

测量和主要结果

在 8479 次肺部恶化中,有 25%未能恢复至基线 FEV1。无法恢复至基线 FEV1 的风险较高与女性;胰腺功能不全;营养不良;医疗补助保险;持续感染铜绿假单胞菌、洋葱伯克霍尔德菌复合菌或耐甲氧西林金黄色葡萄球菌;变应性支气管肺曲霉病;从基线肺活量评估到治疗开始的时间间隔较长;以及 FEV1 从基线到治疗开始时的下降幅度较大。

结论

对于随机选择的肺部恶化,25%的患者在接受静脉抗生素治疗后肺功能未恢复至基线。我们确定了与无法恢复至基线相关的因素,这使临床医生能够识别出可能需要更密切监测和更积极治疗的患者。

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本文引用的文献

1
Return of FEV1 after pulmonary exacerbation in children with cystic fibrosis.
Pediatr Pulmonol. 2010 Feb;45(2):127-34. doi: 10.1002/ppul.21117.
2
Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations.
Am J Respir Crit Care Med. 2009 Nov 1;180(9):802-8. doi: 10.1164/rccm.200812-1845PP. Epub 2009 Sep 3.
4
Persistent methicillin-resistant Staphylococcus aureus and rate of FEV1 decline in cystic fibrosis.
Am J Respir Crit Care Med. 2008 Oct 15;178(8):814-21. doi: 10.1164/rccm.200802-327OC. Epub 2008 Jul 31.
5
Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosis.
Chest. 2007 Aug;132(2):562-8. doi: 10.1378/chest.06-2888. Epub 2007 Jul 23.
6
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.
J Pediatr. 2007 Aug;151(2):134-9, 139.e1. doi: 10.1016/j.jpeds.2007.03.006. Epub 2007 Jun 22.
7
Predictors of mortality in adults with cystic fibrosis.
Pediatr Pulmonol. 2007 Jun;42(6):525-32. doi: 10.1002/ppul.20619.
8
Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis.
Thorax. 2007 Apr;62(4):360-7. doi: 10.1136/thx.2006.060889.
9
Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis.
Am J Respir Crit Care Med. 2006 Dec 1;174(11):1211-20. doi: 10.1164/rccm.200603-423OC. Epub 2006 Sep 7.
10
Cystic fibrosis pulmonary exacerbations.
J Pediatr. 2006 Feb;148(2):259-64. doi: 10.1016/j.jpeds.2005.10.019.

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