Pedersen F, Perrild H, Rasmussen S L, Skovsted L
Eur J Clin Pharmacol. 1984;26(6):669-73. doi: 10.1007/BF00541923.
Serum levels of T4, T3 rT3 and resin T3 uptake were followed for 5 days in 40 patients with acute myocardial infarction (AMI) allocated to early treatment either with alprenolol or placebo. There was a significant fall in T3 (P less than 0.05) and an increase in rT3 (P less than 0.05) without any significant difference between the alprenolol - (n = 19) and placebo - (n = 21) treated groups. The risk of missing a further 20% change in se-T3 and se-rT3 after alprenolol compared to placebo treatment (beta) was less than 0.10 and less than 0.50, respectively. In patients with a severe clinical course, the fall in T3 and increase in rT3 was significantly greater than in patients without complications. No change in T4 was observed either with respect to the clinical course nor following alprenolol. The data suggest that alprenolol can be given in the acute phase of myocardial infarction without causing any additional disturbance in the serum levels of T3 and T4.
对40例急性心肌梗死(AMI)患者进行了为期5天的随访,这些患者被分配接受阿普洛尔或安慰剂的早期治疗,观察其血清T4、T3、反T3(rT3)水平及树脂T3摄取率。T3水平显著下降(P<0.05),rT3水平升高(P<0.05),阿普洛尔治疗组(n = 19)和安慰剂治疗组(n = 21)之间无显著差异。与安慰剂治疗相比,阿普洛尔治疗后血清T3(se-T3)和血清rT3(se-rT3)再有20%变化的漏诊风险(β)分别小于0.10和小于0.50。在临床过程严重的患者中,T3的下降和rT3的升高显著大于无并发症的患者。无论临床过程如何,T4均未观察到变化,阿普洛尔治疗后也未观察到T4变化。数据表明,在心肌梗死急性期给予阿普洛尔不会引起血清T3和T4水平的任何额外紊乱。