Kapoor Upender, Tayal Girish, Mittal S K, Sharma V K, Tekur Uma
Department of Pharmacology, Lok Nayak Hospital, New Delhi, India.
Indian J Pediatr. 2003 Dec;70(12):965-8. doi: 10.1007/BF02723822.
The study was undertaken with the aim to determine correlation between the initial plasma cortisol level and severity of asthma attack and the response to standard treatment for acute exacerbation of bronchial asthma in pediatric age group.
The study was performed in 33 asthmatic patients between 5-12 years of age, presenting to pediatric emergency with acute exacerbation of bronchial asthma. None of the patients included in the present study was on steroids. Venous blood sample for determination of plasma cortisol level was taken and patients were nebulized with salbutamol every 20 minutes, up to 1 hour. The patients who failed to respond even after three nebulizations were labeled as nonresponders and repeat venous blood sample for plasma cortisol estimation was taken before giving injection hydrocortisone. In responders sample was taken 1 hour after last nebulization.
The mean plasma cortisol value at the time of admission in responders (12.42 +/- 1.9 microg/dl) was not found to be significantly different from that in nonresponders (13.1 +/- 2.74 microg/dl). Children with severe attack of asthma had significantly higher plasma cortisol levels both at the time of admission (p=0.03) and at the end of study (p=0.001), as compared to patients with moderate attack. The mean percentage change in plasma cortisol levels in nonresponders was an increase of 80.65 +/- 60.64%, whereas, in responders it decreased by 16.49 +/- 21.7% and this difference was statistically significant (p<0.05).
The hypothalamo pituitary adrenal axis functions normally in asthmatic patients, producing a rise in cortisol levels corresponding to degree of stress; and from initial cortisol level alone, it cannot be predicted, whether a patient will respond to beta-2 agonist (salbutamol) nebulization alone or will require exogenous corticosteroids.
本研究旨在确定儿童年龄组支气管哮喘急性加重期初始血浆皮质醇水平与哮喘发作严重程度之间的相关性以及对标准治疗的反应。
对33例5至12岁因支气管哮喘急性加重期就诊于儿科急诊的哮喘患者进行研究。本研究纳入的患者均未使用类固醇。采集静脉血样本以测定血浆皮质醇水平,患者每20分钟接受一次沙丁胺醇雾化吸入,持续1小时。即使经过三次雾化吸入仍无反应的患者被标记为无反应者,并在给予氢化可的松注射前再次采集静脉血样本以评估血浆皮质醇。有反应者在最后一次雾化吸入后1小时采集样本。
有反应者入院时的平均血浆皮质醇值(12.42±1.9微克/分升)与无反应者(13.1±2.74微克/分升)相比,差异无统计学意义。与中度发作的患者相比,重度哮喘发作的儿童在入院时(p = 0.03)和研究结束时(p = 0.001)的血浆皮质醇水平均显著更高。无反应者血浆皮质醇水平的平均百分比变化增加了80.65±60.64%,而有反应者则下降了16.49±21.7%,这种差异具有统计学意义(p<0.05)。
哮喘患者下丘脑-垂体-肾上腺轴功能正常,皮质醇水平随应激程度升高;仅根据初始皮质醇水平无法预测患者是否仅对β-2激动剂(沙丁胺醇)雾化吸入有反应或是否需要外源性皮质类固醇。