哮喘患儿的依从性、气道炎症和肾上腺抑制

L. Selby, A. Jamalzadeh, P. Hall, A. Bush, Sammy Ndlovu-Dawika, S. Saglani, L. Fleming
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摘要

简介:正常成人吸入皮质类固醇(ICS)的全身吸收量大于哮喘患者[Lancet 2000;356:556-61]。在儿童中,ICS不可预测地引起肾上腺抑制。我们假设,在气道阻塞和炎症较严重的哮喘儿童中,给予一定剂量的ICS对肾上腺抑制作用较小。方法:单中心前瞻性队列研究4-16岁儿童处方≥400微克/天倍氯米松(BDP)当量。使用电子监测装置(EMD)测量12周的依从性。采用低剂量Synacthen试验(LDSST)(300纳克/m2,给药后15、20、25、30和35分钟前测定血清皮质醇)评估肾上腺功能。结果:33例患儿中LDSST异常14例(42%)。LDSST正常的患者血嗜酸性粒细胞和FeNO均显著升高。在LDSST正常的人群中,预测FEV1%的趋势较低,在测试前一周有较高的累积ICS暴露趋势。结论:尽管测试前一周的ICS累积剂量较高,但血嗜酸性粒细胞计数和FeNO升高的儿童肾上腺功能正常。肾上腺功能正常者有降低FEV1的趋势。我们推测,在哮喘患儿中,肾上腺抑制与ICS剂量对气道炎症水平的适宜性有关,而不是绝对剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adherence, airway inflammation and adrenal suppression in children with asthma
Introduction: Systemic absorption of inhaled corticosteroids (ICS) is greater in normal adults than asthmatics [Lancet 2000;356:556-61]. In children, ICS unpredictably cause adrenal suppression. We hypothesized that adrenal suppression for a given ICS dose is less in asthmatic children with worse airway obstruction and inflammation. Methods: Single centre prospective cohort study of children aged 4-16 years prescribed ≥400µg/day beclomethasone (BDP) equivalent. Adherence was measured with an electronic monitoring device (EMD) for 12 weeks. Adrenal function was assessed using the low dose Synacthen test (LDSST) (300 nanograms/m2, serum cortisol taken before then 15, 20, 25, 30 and 35 minutes post administration). Results: 33 children were recruited, 14 (42%) had abnormal LDSST. Those with normal LDSST had significantly higher blood eosinophils and significantly higher FeNO. There was a trend for FEV1% predicted to be lower in those with normal LDSST with a trend to higher cumulative ICS exposure in the week prior to testing. Conclusion: Despite a higher cumulative dose of ICS in the week prior to testing, children with elevated blood eosinophil count and FeNO had normal adrenal function. There was a trend to lower FEV1 in those with normal adrenal function. We speculate that in children with asthma, adrenal suppression relates to the appropriateness of ICS dosage for the level of airway inflammation, rather than absolute dose.
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