Paciaroni E, Luca C
Cardiology Department, I.N.R.C.A. Institute, Ancona, Italy.
Eur Heart J. 1991 Oct;12(10):1076-80. doi: 10.1093/oxfordjournals.eurheartj.a059840.
A transdermal nitroglycerin (TNG) patch (10 mg.24 h-1), using a daily overnight 8-h free interval, was assessed by means of a multicentre trial in 96 elderly patients with stable angina (age greater than or equal to 65 years). The main entry requirement was a reproducible exercise-induced ST depression (greater than or equal to 1 mm) appearing at a load of 60 to 90 W, during an incremental bicycle ergometer test (10 W.min-1). During the study only one other antianginal drug and sublingual TNG tablets were allowed. The protocol consisted of a run-in period (mean 10 days), followed by a double-blind, randomized, parallel, placebo-controlled 28-day phase and a single-blind active treatment phase of the same duration. The exercise test parameters, the number of spontaneous anginal attacks and any unwanted effects were evaluated at the end of every study phase. In the double-blind phase, no ergometric values changed with placebo while transdermal TNG significantly improved total workload and double product by 36.4% and 7.7% at the maximal workload respectively and by 49.8% and 13.5% at the time to onset of 1 mm ST depression respectively and reduced ST depression (-58.8%) at the equivalent baseline workload. Anginal attacks decreased by 61.5% and 30.8% with TNG patch and placebo respectively. A similar trend was seen at the end of the single-blind active treatment period in patients who had received placebo in the double-blind phase. Nine patients failed to complete the study; six for unwanted effects (four in the active group and two in the placebo group) and three for other reasons.(ABSTRACT TRUNCATED AT 250 WORDS)
采用每日夜间8小时无药间隔的透皮硝酸甘油(TNG)贴片(10毫克/24小时),通过一项多中心试验对96例老年稳定型心绞痛患者(年龄大于或等于65岁)进行了评估。主要入选标准是在递增式自行车测力计试验(10瓦/分钟)中,在60至90瓦负荷时出现可重复的运动诱发ST段压低(大于或等于1毫米)。研究期间仅允许使用另一种抗心绞痛药物和舌下含服TNG片。试验方案包括一个导入期(平均10天),随后是一个为期28天的双盲、随机、平行、安慰剂对照阶段以及一个为期相同的单盲活性治疗阶段。在每个研究阶段结束时评估运动试验参数、自发性心绞痛发作次数和任何不良反应。在双盲阶段,安慰剂组的测力计值无变化,而透皮TNG在最大负荷时分别使总工作量和双乘积显著提高36.4%和7.7%,在出现1毫米ST段压低时分别提高49.8%和13.5%,并在等效基线工作量时降低ST段压低(-58.8%)。TNG贴片组和安慰剂组的心绞痛发作分别减少61.5%和30.8%。在双盲阶段接受安慰剂的患者,在单盲活性治疗期结束时也出现了类似趋势。9例患者未完成研究;6例因不良反应(活性组4例,安慰剂组2例),3例因其他原因。(摘要截短于250字)