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[雾化器单次给药吸入性支气管舒张剂对重度支气管哮喘急性加重患者的药效学]

[Pharmacodynamics of inhalation broncholytic agents introduced in a single dose by nebulizer in patients with severe exacerbation of bronchial asthma].

作者信息

Tsoĭ A N, Apkhipov V V

出版信息

Ter Arkh. 2002;74(3):17-21.

Abstract

AIM

To study pharmacodynamics and safety of inhalatory beta-2-adrenostimulators and M-cholinolytics given via nebulizer in patients with severe exacerbation of bronchial asthma (BA).

MATERIAL AND METHODS

The study covered 78 patients with severe exacerbation of BA (mean age--48.6 +/- 15.0 years). The patients were randomized into 4 groups: 23, 20, 18 and 17 patients, respectively. They were treated with: ventolin nebuly (2.5 mg), berodual (0.25 mg ipratropium bromide and 0.5 mg phenoterol), atrovent (0.5 mg), berotek (1.0 mg by nebulizer Pulmo-Aide 56501). Efficiency and safety of the treatment was assessed by the data of external respiration function, arterial blood gases and ECG each 30 min for 3 hours.

RESULTS

In patients with severe exacerbation of BA pharmacodynamics of all the studied drugs was characterized by less duration and potency of the action. Salbutamol and berotek were effective for 180 min, atrovent--for 30-60 min. Inhalation broncholytics had no such serious side effects as prolongation of corrected interval Q-T or onset of arrhythmia. Berotek demonstrated longer action on heart rate than salbutamol.

CONCLUSION

Severe complication of BA is treated more effectively with combination of beta 2-adrenomimetic with atrovent.

摘要

目的

研究雾化吸入β2肾上腺素能激动剂和M胆碱能阻滞剂对重度支气管哮喘(BA)加重期患者的药效学及安全性。

材料与方法

该研究纳入78例重度BA加重期患者(平均年龄48.6±15.0岁)。患者随机分为4组,分别为23例、20例、18例和17例。他们接受以下治疗:万托林雾化液(2.5毫克)、可必特(0.25毫克异丙托溴铵和0.5毫克非诺特罗)、爱全乐(0.5毫克)、博利康尼(通过Pulmo - Aide 56501雾化器给药1.0毫克)。在3小时内,每隔30分钟通过肺功能、动脉血气和心电图数据评估治疗的有效性和安全性。

结果

在重度BA加重期患者中,所有研究药物的药效学特点是作用持续时间较短且效力较低。沙丁胺醇和博利康尼的有效时间为180分钟,爱全乐为30 - 60分钟。吸入性支气管扩张剂没有出现如校正QT间期延长或心律失常发作等严重副作用。博利康尼对心率的作用时间比沙丁胺醇长。

结论

β2肾上腺素能激动剂与爱全乐联合使用治疗重度BA并发症的效果更佳。

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