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Assessment of inhaled corticosteroid treatment response in asthma using hypertonic histamine challenge-induced cough.

机译:使用高渗组胺激发诱发的咳嗽评估吸入性糖皮质激素治疗哮喘的反应。

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BACKGROUND AND AIMS: 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. METHODS: A total of 16 steroid-naive 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)). RESULTS: 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. CONCLUSIONS: 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.
机译:背景与目的:支气管激发试验可用于监测皮质类固醇治疗的疗效。不幸的是,这些测量需要在肺活量测定期间患者良好的配合。在这种测试过程中,咳嗽与支气管收缩程度有关,并且是非自愿发生的,即独立于患者的配合。这项研究旨在评估高渗组胺激发引起的咳嗽在评估吸入性糖皮质激素治疗疗效中的效用。方法:每天通过粉末吸入器对总共16名初治类固醇的哮喘患者和10名非哮喘,有症状的对照患者每天通过粉末吸入器接受800微克倍氯米松(Beclomet Easyhaler(R),Orion Ltd.,Orion Pharma,芬兰赫尔辛基)。在治疗前后用高渗组胺溶液进行视频吸入激发。在两个挑战之前都完成了症状问卷。气道对高渗组胺的反应性表示为咳嗽的累积次数除以最终给药的组胺最终浓度[咳嗽/浓度比(CCR)],以及引起FEV(1)(PC)下降20%的组胺激发浓度。 (20))。结果:CCR [几何平均值;哮喘受试者的95%置信区间(CI)从每mg / mL咳嗽494(209-1168)降至73.6(29.8-182)(P = 0.002)。在治疗期间,其PC(20)水平为1.31(1.07-1.60)和1.91(1.33-2.74)mg / mL(P = 0.01)。哮喘患者的症状频率也显着降低(P = 0.039)。在治疗期间,非哮喘患者的PC(20)水平,CCR水平或症状频率无明显变化。结论:高渗组胺激发引起的咳嗽和PC(20)是评估哮喘治疗效果的敏感措施。咳嗽反应在不能可靠地进行肺活量测定的受试者中尤其有用。

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