Marten W, Weiss M, Haase W
Curr Med Res Opin. 1984;9(2):96-106. doi: 10.1185/03007998409109566.
An open, multi-centre clinical trial was carried out in 537 hospital patients and 2138 general practice patients to evaluate the efficacy and tolerance of isosorbide 5-mononitrate in the treatment of angina pectoris. Prior to entry into the trial, angina attack frequency and acute glyceryl trinitrate consumption were assessed during previous, in most cases unsatisfactory, anti-anginal therapy. After a treatment-free washout period of 3 days, graded multi-stage exercise testing was performed and then treatment started with 20 mg isosorbide mononitrate 3-times per day. Exercise testing was repeated after 14 days' therapy and, in the case of the hospital patients, also 4 to 5 hours after the first dose of isosorbide mononitrate. At the end of the 14-day treatment period, angina attack frequency and glyceryl trinitrate consumption were again assessed. Similar results were obtained for both hospital and general practice patients. Changing to isosorbide mononitrate resulted in a marked reduction in angina frequency, with complete elimination of angina attacks in approximately half of the patients; nocturnal angina, present in approximately 20% of the patients during previous therapy, virtually disappeared during isosorbide mononitrate therapy. Exercise tolerance and performance improved in the majority of patients, with a marked increase in the number of patients able to exercise to the level at which some symptom other than angina pectoris caused them to stop. ST-depression during exercise and exercise-induced arrhythmias also showed clear reductions during isosorbide mononitrate therapy. Tolerance to isosorbide mononitrate was good, the expected 'nitrate headaches' being the only common side-effect reported. The results were such that continuation of treatment with isosorbide mononitrate after the trial was recommended by the attending physician in 77% of the hospital patients and 87% of the general practice patients.
一项开放性、多中心临床试验在537名住院患者和2138名全科患者中开展,以评估5-单硝酸异山梨酯治疗心绞痛的疗效和耐受性。在进入试验之前,在之前大多数情况下效果不佳的抗心绞痛治疗期间,评估心绞痛发作频率和急性硝酸甘油消耗量。经过3天的无治疗洗脱期后,进行分级多阶段运动试验,然后开始每日3次服用20毫克单硝酸异山梨酯进行治疗。治疗14天后重复运动试验,对于住院患者,在首次服用单硝酸异山梨酯后4至5小时也进行重复试验。在14天治疗期结束时,再次评估心绞痛发作频率和硝酸甘油消耗量。住院患者和全科患者均获得了相似的结果。改用单硝酸异山梨酯后心绞痛频率显著降低,约一半患者的心绞痛发作完全消除;夜间心绞痛在之前治疗期间约20%的患者中出现,在单硝酸异山梨酯治疗期间几乎消失。大多数患者的运动耐量和表现有所改善,能够运动到除心绞痛以外的某些症状导致他们停止运动水平的患者数量显著增加。在单硝酸异山梨酯治疗期间,运动期间的ST段压低和运动诱发的心律失常也明显减少。对单硝酸异山梨酯的耐受性良好,所报告的唯一常见副作用是预期的“硝酸盐头痛”。结果表明,77%的住院患者和87%的全科患者的主治医生建议在试验后继续使用单硝酸异山梨酯进行治疗。