Higham M A, Sharara A M, Wilson P, Jenkins R J, Glendenning G A, Ind P W
Department of Medicine (Respiratory Division), Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Thorax. 1997 Nov;52(11):975-80. doi: 10.1136/thx.52.11.975.
Salbutamol is the most widely prescribed short acting beta 2 agonist and salmeterol is the first long acting inhaled beta 2 agonist. The dose equivalence of salmeterol and salbutamol is disputed. Estimates of weight-for-weight dose ratio have ranged from 1:2 to 1:16. A study was undertaken to clarify the true dose ratio.
The bronchoprotection afforded against repeated methacholine challenge by inhaled salmeterol 25 micrograms and 100 micrograms and salbutamol 100 micrograms and 400 micrograms was compared in a randomised, double blind, placebo controlled, crossover trial. Subjects were 16 stable asthmatics with a baseline forced expiratory volume in one second (FEV1) of > or = 65% predicted, screening concentration provoking a fall in FEV1 of 20% (PC20FEV1) of < or = 8mg/ml, and a shift in PC20FEV1 of more than two doubling concentration steps following inhalation of salbutamol 400 micrograms. On five separate occasions subjects underwent methacholine challenge before and 30 and 120 minutes after drug administration. PD20FEV1 was calculated for each challenge. FEV1 at 90 minutes after drug administration was also recorded.
Bronchoprotection afforded by salmeterol was increased at 120 minutes compared with 30 minutes and protection by salbutamol was decreased. Protection by both doses of salmeterol was similar to salbutamol 100 micrograms at 30 minutes but significantly greater at 120 minutes. FEV1 at 90 minutes was significantly greater after salmeterol 100 micrograms than after placebo, but there were no other significant differences between treatments. Maximal observed protection was equivalent for salmeterol 100 micrograms and salbutamol 400 micrograms.
The data are compatible with a weight-for-weight dose ratio for salmeterol:salbutamol of < or = 1:4.
沙丁胺醇是处方最广泛的短效β2激动剂,沙美特罗是首个长效吸入型β2激动剂。沙美特罗与沙丁胺醇的等效剂量存在争议。按重量计算的剂量比估计值在1:2至1:16之间。开展了一项研究以明确真正的剂量比。
在一项随机、双盲、安慰剂对照、交叉试验中,比较了吸入25微克和100微克沙美特罗以及100微克和400微克沙丁胺醇对重复吸入乙酰甲胆碱激发试验的支气管保护作用。研究对象为16名病情稳定的哮喘患者,其一秒用力呼气量(FEV1)基线值≥预测值的65%,激发FEV1下降20%的筛查浓度(PC20FEV1)≤8mg/ml,且吸入400微克沙丁胺醇后PC20FEV1的变化超过两个倍增浓度步长。在五个不同时间点,受试者在给药前、给药后30分钟和120分钟接受乙酰甲胆碱激发试验。计算每次激发试验的PD20FEV1。同时记录给药后90分钟的FEV1。
与30分钟时相比,沙美特罗在120分钟时提供的支气管保护作用增强,而沙丁胺醇的保护作用减弱。两种剂量沙美特罗的保护作用在30分钟时与100微克沙丁胺醇相似,但在120分钟时显著更强。100微克沙美特罗给药后90分钟的FEV1显著高于安慰剂,但各治疗组之间无其他显著差异。观察到的最大保护作用在100微克沙美特罗和400微克沙丁胺醇之间相当。
数据表明沙美特罗与沙丁胺醇按重量计算的剂量比≤1:4。