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痰液嗜酸性粒细胞增多能否预测难治性哮喘患儿对全身用糖皮质激素的反应?

Does sputum eosinophilia predict the response to systemic corticosteroids in children with difficult asthma?

作者信息

Lex Christiane, Jenkins Gavin, Wilson Nicola M, Zacharasiewicz Angela, Erin Ed, Hansel Trevor T, Bush Andrew, Payne Donald N R

机构信息

Department of Paediatric Respiratory Medicine, Imperial College of Science, Technology and Medicine at the Royal Brompton Hospital and National Heart and Lung Institute, London, United Kingdom.

出版信息

Pediatr Pulmonol. 2007 Mar;42(3):298-303. doi: 10.1002/ppul.20570.

Abstract

Little evidence exists to guide the management of children with difficult asthma. The aim of this study was to determine whether children with difficult asthma, associated with sputum eosinophilia, are more likely to benefit from further treatment with high-dose systemic corticosteroids, compared to those without sputum eosinophilia. Induced sputum was obtained from 20 children aged between 8 and 15 years with difficult asthma before and after a systemic corticosteroid trial (prednisolone 40 mg/day for 14 days or a single 80 mg dose of intramuscular triamcinolone). Subjects were defined as "eosinophilic" if the baseline sputum eosinophil percentage was > or = 2.5% or "non-eosinophilic" if < 2.5%. Clinical response to the corticosteroid trial was assessed using spirometry and clinical data and defined by an increase in pre-bronchodilator forced expiratory volume in 1 sec (FEV1) > 9% predicted and/or an overall subjective improvement. Seventeen children had evidence of satisfactory adherence to the systemic corticosteroid treatment; eight of these were "eosinophilic" and nine were "non-eosinophilic" subjects. Following the trial there was a similar clinical improvement in both groups, with FEV1 increasing in both the "eosinophilic" and "non-eosinophilic" groups (median change in FEV1 16 [range 5-54]% vs. 12.5 [1-29]% predicted). Sputum eosinophils fell in the "eosinophilic" group (median 17.5 [range 3-37]% vs. 0 [0-23]%, P = 0.054), with no change in the "non-eosinophilic" group (0 [0-2]% vs. 0 [0-1]%, P = 0.12). Sputum neutrophils did not change in either the "eosinophilic" (22.5 [5-50]% vs. 25 [0-91]%) or the "non-eosinophilic" group (27.5 [0-96] vs. 44 [9-96]%). In conclusion children with difficult asthma may benefit clinically from high-dose systemic corticosteroids even in the absence of sputum eosinophilia.

摘要

几乎没有证据可用于指导难治性哮喘儿童的治疗。本研究的目的是确定与痰液嗜酸性粒细胞增多相关的难治性哮喘儿童,与无痰液嗜酸性粒细胞增多的儿童相比,是否更有可能从高剂量全身性皮质类固醇的进一步治疗中获益。在进行全身性皮质类固醇试验(泼尼松龙40mg/天,共14天或单次80mg剂量的肌肉注射曲安奈德)之前和之后,从20名年龄在8至15岁的难治性哮喘儿童中获取诱导痰。如果基线痰液嗜酸性粒细胞百分比≥2.5%,则受试者被定义为“嗜酸性粒细胞性的”;如果<2.5%,则定义为“非嗜酸性粒细胞性的”。使用肺活量测定法和临床数据评估对皮质类固醇试验的临床反应,并通过支气管扩张剂前1秒用力呼气量(FEV1)增加>预测值的9%和/或总体主观改善来定义。17名儿童有证据表明对全身性皮质类固醇治疗依从性良好;其中8名是“嗜酸性粒细胞性的”受试者,9名是“非嗜酸性粒细胞性的”受试者。试验后两组临床改善情况相似,“嗜酸性粒细胞性的”组和“非嗜酸性粒细胞性的”组FEV1均增加(FEV1的中位数变化分别为预测值的16[范围5 - 54]%和12.5[1 - 29]%)。“嗜酸性粒细胞性的”组痰液嗜酸性粒细胞减少(中位数17.5[范围3 - 37]%对0[0 - 23]%,P = 0.054),“非嗜酸性粒细胞性的”组无变化(0[0 - 2]%对0[0 - 1]%,P = 0.12)。“嗜酸性粒细胞性的”组(22.5[5 - 50]%对25[0 - 91]%)和“非嗜酸性粒细胞性的”组(27.5[0 - 96]对44[9 - 96]%)痰液中性粒细胞均无变化。总之,即使没有痰液嗜酸性粒细胞增多,难治性哮喘儿童在临床上也可能从高剂量全身性皮质类固醇中获益。

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