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地尔硫䓬对与动脉粥样硬化相关的慢性稳定型心绞痛的长期疗效:对平板运动试验的影响

Long-term efficacy of diltiazem in chronic stable angina associated with atherosclerosis: effect on treadmill exercise.

作者信息

Pool P E, Seagren S C

出版信息

Am J Cardiol. 1982 Feb 18;49(3):573-7. doi: 10.1016/s0002-9149(82)80014-3.

Abstract

Short-term efficacy of diltiazem in prolonging exercise end points in patients with chronic stable atherosclerosis-associated angina has been demonstrated. The safety and efficacy of diltiazem were examined in a placebo-controlled exercise study over 4 months (eight patients) and subsequently at 12 to 16 months (six patients). Three end points were evaluated: (1) time to onset of angina or fatigue if angina were eliminated; (2) time to 1 mm S-T segment depression or termination of exercise if S-T depression were eliminated; and (3) time to termination of exercise (2+ angina or fatigue). All end points were significantly prolonged over the medium-term 4 month study and decreased again significantly with return to placebo. Maximal effect occurred at 3 months with the first end point increasing from a mean +/- standard error of the mean of 7.2 +/- 1.2 to 10.2 +/- 0.9 minutes (p less than 0.01), the second end point from 8.0 +/- 0.9 to 10.3 +/- 1.0 minutes (p less than 0.01), and the third end point from 9.6 +/- 1.3 to 11.9 +/- 0.8 minutes (p less than 0.05). At 12 to 16 months efficacy was again present. Comparisons for 3 month peak effect with 12 to 16 month long-term effect and subsequent final placebo period were, respectively: first end point, 10.5 +/- 1.3, 9.4 +/- 1.0 and 6.6 +/- 1.7 minutes; second end point, 11.0 +/- 1.3, 10.2 +/- 1.2 and 6.3 +/- 0.7 minutes; and third end point, 12.1 +/- 1.0, 11.0 +/- 1.0 and 9.2 +/- 1.5 minutes. No significant adverse effects of hematologic abnormalities were noted.

摘要

已证实地尔硫䓬在延长慢性稳定型动脉粥样硬化相关性心绞痛患者运动终点方面的短期疗效。在一项为期4个月的安慰剂对照运动研究中(8例患者)以及随后12至16个月时(6例患者)对地尔硫䓬的安全性和疗效进行了检查。评估了三个终点:(1)出现心绞痛或疲劳的时间(如果心绞痛消失);(2)出现1毫米ST段压低或运动终止的时间(如果ST段压低消失);(3)运动终止的时间(2级以上心绞痛或疲劳)。在为期4个月的中期研究中,所有终点均显著延长,恢复使用安慰剂后又再次显著缩短。最大效应出现在3个月时,第一个终点从平均±平均标准误7.2±1.2分钟增加到10.2±0.9分钟(p<0.01),第二个终点从8.0±0.9分钟增加到10.3±1.0分钟(p<0.01),第三个终点从9.6±1.3分钟增加到11.9±0.8分钟(p<0.05)。在12至16个月时再次出现疗效。3个月峰值效应与12至16个月长期效应以及随后最终安慰剂期的比较分别为:第一个终点,10.5±1.3、9.4±1.0和6.6±1.7分钟;第二个终点,11.0±1.3、10.2±1.2和6.3±0.7分钟;第三个终点,12.1±1.0、11.0±1.0和9.2±1.5分钟。未观察到血液学异常的显著不良反应。

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