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标准化支气管过敏原激发试验的可重复性

Reproducibility of standardized bronchial allergen provocation test.

作者信息

Frølund L, Madsen F, Svendsen U G, Weeke B

出版信息

Allergy. 1986 Jan;41(1):30-6. doi: 10.1111/j.1398-9995.1986.tb00271.x.

Abstract

Standardized bronchial allergen provocation was performed twice (with an interval of median 14 days (range 14-44)) in 19 extrinsic, well-defined asthmatic patients to study the reproducibility of the bronchial response. Smoking and medications were strictly withheld prior to the provocation. Ten-fold increasing concentrations of allergen solution 0.9 ml were inhaled by tidal volume breathing for 5 min at 10-min intervals. The actual dose given was expressed by the concentration of the solution used. Forced expiratory volume in the first second (FEV1) was used to determine responses, and the provocation continued until an allergen concentration (allergen PC20) was reached which caused at least 20% decrease of the post-saline FEV1. All provocations were followed by a bronchial reaction within clinically acceptable limits. The reproducibility was high, evaluated by the Spearman rank correlation coefficient Rho = 0.90 (P less than 0.01). It is concluded that bronchial provocation with allergens performed as outlined in this study represents a reproducible test which can be applied in routine allergy diagnostics, and in further investigations concerning specific bronchial reactivity.

摘要

对19名明确诊断为外源性哮喘的患者进行了两次标准化支气管过敏原激发试验(间隔时间中位数为14天,范围为14 - 44天),以研究支气管反应的可重复性。激发试验前严格禁止吸烟和使用药物。以潮气量呼吸,每隔10分钟吸入0.9毫升浓度递增10倍的过敏原溶液,持续5分钟。实际给予的剂量以所用溶液的浓度表示。用第一秒用力呼气量(FEV1)来确定反应,激发试验持续进行,直至达到导致盐水激发后FEV1至少下降20%的过敏原浓度(过敏原PC20)。所有激发试验后,支气管反应均在临床可接受范围内。通过Spearman等级相关系数Rho = 0.90(P < 0.01)评估,可重复性很高。得出结论,按照本研究所述进行的过敏原支气管激发试验是一种可重复的试验,可应用于常规过敏诊断以及有关特定支气管反应性的进一步研究。

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