Purokivi Minna, Koskela Heikki, Koistinen Tiina, Peuhkurinen Keijo, Kontra Kirsi Maarit
Department of Respiratory Medicine, Kuopio University Hospital, Kuopio, Finland.
Clin Respir J. 2010 Apr;4(2):67-73. doi: 10.1111/j.1752-699X.2009.00146.x.
Bronchial provocation tests may be utilised to monitor the efficacy of the corticosteroid treatment. Unfortunately, these measurements necessitate good patient cooperation during the spirometry. Coughing during such tests is related to the degree of the bronchoconstriction and occurs involuntarily, i.e. independent of patient cooperation. This study aimed to evaluate the utility of a hypertonic histamine challenge-induced cough in assessing the efficacy of inhaled corticosteroid treatment.
A total of 16 steroid-naïve asthmatics and 10 non-asthmatic, symptomatic controls received 800-microg beclomethasone (Beclomet Easyhaler(R), Orion Ltd., Orion Pharma, Helsinki, Finland) via powder inhaler per day for 8 weeks. Videoed inhalation challenge with hypertonic histamine solution was performed before and after the treatment. Symptom questionnaire was completed before both challenges. The airway responsiveness to hypertonic histamine was expressed as the cumulative number of coughs divided by the final histamine concentration administered [coughs/concentration ratio (CCR)] and as the provocative concentration of histamine to induce a 20% fall in FEV(1)(PC(20)).
CCR [geometric mean; 95% confidence interval (CI)] of the asthmatic subjects decreased from 494 (209-1168) to 73.6 (29.8-182) coughs per mg/mL (P = 0.002). Their PC(20) levels were 1.31 (1.07-1.60) and 1.91 (1.33-2.74) mg/mL over the treatment period (P = 0.01). The symptom frequency also decreased significantly in the asthmatics (P = 0.039). There were no significant changes in PC(20) level, in CCR level or in symptom frequency in non-asthmatic subjects during the treatment.
Hypertonic histamine challenge-induced cough and PC(20) are sensitive measures in assessing the treatment effect in asthma. The cough response may be especially useful in subjects who cannot perform spirometry reliably.
支气管激发试验可用于监测皮质类固醇治疗的效果。不幸的是,这些测量需要患者在肺活量测定过程中良好的配合。在此类测试中咳嗽与支气管收缩程度相关,且不由自主地发生,即与患者配合无关。本研究旨在评估高渗组胺激发诱导的咳嗽在评估吸入性皮质类固醇治疗效果中的作用。
总共16名未使用过类固醇的哮喘患者和10名有症状的非哮喘对照者,每天通过干粉吸入器吸入800微克倍氯米松(Beclomet Easyhaler(R),Orion Ltd.,Orion Pharma,芬兰赫尔辛基),持续8周。在治疗前后进行高渗组胺溶液的视频吸入激发试验。在两次激发试验前均完成症状问卷。气道对高渗组胺的反应性以咳嗽累积次数除以最终给予的组胺浓度表示[咳嗽/浓度比(CCR)],并以诱导第一秒用力呼气容积(FEV(1))下降20%的组胺激发浓度(PC(20))表示。
哮喘患者的CCR[几何平均数;95%置信区间(CI)]从每毫克/毫升494(209 - 1168)次咳嗽降至73.6(29.8 - 182)次咳嗽(P = 0.002)。在整个治疗期间,他们的PC(20)水平分别为1.31(1.07 - 1.60)和1.91(1.33 - 2.74)毫克/毫升(P = 0.01)。哮喘患者的症状频率也显著降低(P = 0.039)。在治疗期间,非哮喘患者的PC(20)水平、CCR水平或症状频率均无显著变化。
高渗组胺激发诱导的咳嗽和PC(20)是评估哮喘治疗效果的敏感指标。咳嗽反应对于无法可靠进行肺活量测定的受试者可能特别有用。