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Peak flow variation in childhood asthma: correlation with symptoms, airways obstruction, and hyperresponsiveness during long term treatment with inhaled corticosteroids

机译:儿童哮喘的峰值流量变化:与 长期症状,气道阻塞和反应过度 吸入糖皮质激素治疗

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摘要

BACKGROUND—Guidelinesfor asthma management focus on treatment with inhaled corticosteroidsand on home recording of peak expiratory flow (PEF). The effect ofmaintenance treatment with inhaled corticosteroids on PEF variation andits relation to other parameters of disease activity were examined in102 asthmatic children aged 7-14 years.
METHODS—During 20 months of treatment with inhaled salbutamol, with or without inhaledbudesonide (600 µg daily), forced expiratory volume in one second(FEV1), the dose of histamine required to provoke a fall inFEV1 of more than 20% (PD20), the percentage of symptom free days, and PEF variation were assessed bimonthly. PEFvariation was computed as the lowest PEF as a percentage of the highestPEF occurring over 14 days, the usual way of expressing PEF variationin asthma self-management plans. For each patient using inhaledcorticosteroids within subject correlation coefficients (ρ) werecomputed of PEF variation to the percentage of symptom free days,FEV1, and PD20.
RESULTS—PEF variationdecreased significantly during the first two months of treatment withinhaled corticosteroids and then remained stable. The same pattern wasobserved for symptoms and FEV1. In contrast,PD20 histamine continued to improve throughout the whole follow up period. In individual patients predominantly positive associations of PEF variation with symptoms, FEV1, andPD20 were found, but the ranges of these associations were wide.
CONCLUSIONS—Duringtreatment with inhaled corticosteroids the changes in PEF variationover time show poor concordance with changes in other parameters ofasthma severity. When only PEF is monitored, clinically relevantdeteriorations in symptoms, FEV1, or PD20 maybe missed. This suggests that home recording of PEF alone may not besufficient to monitor asthma severity reliably in children.


机译:背景—哮喘管理的指南侧重于吸入皮质类固醇的治疗以及峰值呼气流量(PEF)的家庭记录。在102名7-14岁的哮喘儿童中,研究了吸入糖皮质激素维持治疗对PEF变化的影响及其与疾病活动性其他参数的关系。方法—在吸入或不吸入布地奈德(每天600 µg)吸入沙丁胺醇的20个月治疗期间,在一秒钟内强迫呼气量(FEV1),引起FEV1下降超过20%(PD20)所需的组胺剂量,每两个月评估无症状天数百分比和PEF变化。 PEF变异计算为在14天中发生的最低PEF占最高PEF的百分比,这是哮喘自我管理计划中表达PEF变异的常用方式。对于每位使用吸入糖皮质激素的患者,应计算受试者的PEF变化与无症状天数,FEV1和PD20的百分比之间的相关系数(ρ)。结果—在治疗的头两个月内,吸入皮质类固醇的PEF变化显着降低,然后保持稳定。症状和FEV1观察到相同的模式。相反,PD20组胺在整个随访期间持续改善。在个别患者中,发现PEF变异与症状,FEV1,PD20呈正相关,但这些关联的范围很广。结论—吸入性糖皮质激素治疗期间,PEF随时间的变化显示与哮喘严重程度其他参数的变化不一致。当仅监测PEF时,可能会忽略症状,FEV1或PD20的临床相关恶化。这表明仅在家中记录PEF可能不足以可靠地监测儿童的哮喘严重程度。

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