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急性重症哮喘患者的沙丁胺醇血浆浓度。

Plasma concentrations of salbutamol in acute severe asthmatics.

作者信息

Lewis L D, McLaren M, Essex E, Cochrane G M

机构信息

Department of Thoracic Medicine, Guy's Hospital, London, UK.

出版信息

Aust N Z J Med. 1990 Jun;20(3):204-7. doi: 10.1111/j.1445-5994.1990.tb01019.x.

Abstract

We studied prospectively 11 asthmatic patients presenting to the Accident and Emergency department with acute asthma. (Four patients reported historically that they were taking some form of oral salbutamol as part of their maintenance therapy.) Standard cardiovascular and respiratory parameters and plasma salbutamol concentrations were measured before and one hour after treatment with five milligrams of nebulised salbutamol. The median plasma salbutamol concentration before treatment was below the level of detection of the assay (less than 3 micrograms.l-1) with a range from less than 3 micrograms.l-1 to 34.6 micrograms.l-1. One hour post treatment the median plasma salbutamol concentration was 7.4 micrograms.l-1 (range less than 3.0 micrograms.l-1 to 56.0 micrograms.l-1) p less than 0.05. (Wilcoxons test). Correlations were investigated between the measured pretreatment physiological variables and pre-treatment plasma salbutamol concentrations. None were found to be significant. Similar analysis of the measured post-treatment physiological variables and post-treatment plasma salbutamol concentrations again revealed no significant correlations. However, a significant negative correlation was noted between the change in plasma salbutamol concentration with treatment and the change in respiratory rate (Rs = -0.56, p = 0.04). If asthmatics do indeed use high doses of inhaled beta-2-agonists (salbutamol) in an attempt to abort an acute attack (as many clinicians suspect), little, if any, of the drug appears to reach the systemic circulation. In this study the administration of five milligrams of nebulised salbutamol to acute asthmatics did not produce excessive increases in plasma salbutamol concentration, even in those patients taking oral salbutamol as part of their maintenance therapy.

摘要

我们对11名因急性哮喘到急诊部就诊的哮喘患者进行了前瞻性研究。(4名患者既往报告称,他们正在服用某种形式的口服沙丁胺醇作为维持治疗的一部分。)在用5毫克雾化沙丁胺醇治疗前及治疗后1小时,测量标准心血管和呼吸参数以及血浆沙丁胺醇浓度。治疗前血浆沙丁胺醇浓度中位数低于检测水平(低于3微克/升),范围为低于3微克/升至34.6微克/升。治疗后1小时,血浆沙丁胺醇浓度中位数为7.4微克/升(范围低于3.0微克/升至56.0微克/升),p<0.05。(威尔科克森检验)。研究了测量的治疗前生理变量与治疗前血浆沙丁胺醇浓度之间的相关性。未发现有显著相关性。对测量的治疗后生理变量与治疗后血浆沙丁胺醇浓度进行的类似分析再次显示无显著相关性。然而,血浆沙丁胺醇浓度随治疗的变化与呼吸频率的变化之间存在显著负相关(Rs = -0.56,p = 0.04)。如果哮喘患者确实使用高剂量吸入β2激动剂(沙丁胺醇)试图终止急性发作(正如许多临床医生所怀疑的那样),那么几乎没有药物似乎能进入体循环。在本研究中,给急性哮喘患者使用5毫克雾化沙丁胺醇,即使在那些将口服沙丁胺醇作为维持治疗一部分的患者中,也不会使血浆沙丁胺醇浓度过度升高。

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