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哮喘患者局部支气管内过敏原激发试验的安全性问题

Safety aspects of local endobronchial allergen challenge in asthmatic patients.

作者信息

Krug N, Teran L M, Redington A E, Gratziou C, Montefort S, Polosa R, Brewster H, Howarth P H, Holgate S T, Frew A J, Carroll M P

机构信息

Immunopharmacology Group, University Medicine, Southampton General Hospital, United Kingdom.

出版信息

Am J Respir Crit Care Med. 1996 Apr;153(4 Pt 1):1391-7. doi: 10.1164/ajrccm.153.4.8616571.

Abstract

Local endobronchial allergen challenge is being increasingly used to investigate the role of allergic inflammation in asthma. However, little information is available about the safety of this procedure and the changes induced in airway physiology. BAL and biopsy were performed at 10 min and at 4 to 6 h, or 24 h after segmental allergen challenge in 49 patients with atopic asthma. Two hours after challenge, FEV1 was reduced from 97.6 +/- 13.9 (mean +/- SD) to 83.4 +/- 21.7% predicted. FEV1 remained reduced at 4 to 6 h (87.7 +/- 20.4%), but it had nearly returned to baseline by 24 h (93.2 +/- 14.0%). When endobronchial challenge was combined with BAL and biopsy, the initial fall in FEV1 was slightly greater (from 101.8 +/- 14.2 to 78.5 +/- 13.6%). Bronchial responsiveness to methacholine was measured in 10 subjects, and it showed a twofold increase 24 h after local challenge and lavage. Significant changes in FEV1 and methacholine PC20 were still detectable 72 h after challenge. Widespread wheezing occurred in 29% of the subjects, but none of the them had to be admitted to hospital. We conclude that local endobronchial allergen challenge, although producing measurable changes in airway physiology, is in general well tolerated and is an acceptable method to investigate airway pathophysiologic processes in patients with mild to moderate asthma.

摘要

局部支气管内过敏原激发试验越来越多地用于研究变应性炎症在哮喘中的作用。然而,关于该操作的安全性以及气道生理学所诱导的变化,目前可用信息很少。对49例特应性哮喘患者进行节段性过敏原激发试验后10分钟、4至6小时或24小时,进行了支气管肺泡灌洗(BAL)和活检。激发试验后两小时,第一秒用力呼气量(FEV1)从预测值的97.6±13.9(平均值±标准差)降至83.4±21.7%。FEV1在4至6小时时仍降低(87.7±20.4%),但到24小时时已几乎恢复至基线水平(93.2±14.0%)。当支气管内激发试验与BAL和活检相结合时,FEV1的初始下降幅度略大(从101.8±14.2降至78.5±13.6%)。对10名受试者测量了对乙酰甲胆碱的支气管反应性,结果显示局部激发试验和灌洗后24小时反应性增加了两倍。激发试验72小时后,FEV1和乙酰甲胆碱PC20仍有显著变化。29%的受试者出现广泛哮鸣音,但他们中无人需要住院治疗。我们得出结论,局部支气管内过敏原激发试验虽然会在气道生理学上产生可测量的变化,但总体耐受性良好,是研究轻至中度哮喘患者气道病理生理过程的一种可接受的方法。

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