首页> 外文期刊>Journal of the American College of Cardiology >Incidence of dyspnea and assessment of cardiac and pulmonary function in patients with stable coronary artery disease receiving ticagrelor, clopidogrel, or placebo in the ONSET/OFFSET study.
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Incidence of dyspnea and assessment of cardiac and pulmonary function in patients with stable coronary artery disease receiving ticagrelor, clopidogrel, or placebo in the ONSET/OFFSET study.

机译:在ONSET / OFFSET研究中,接受替卡格雷,氯吡格雷或安慰剂治疗的稳定冠心病患者的呼吸困难发生率以及心肺功能评估。

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OBJECTIVES: We prospectively assessed cardiac and pulmonary function in patients with stable coronary artery disease (CAD) treated with ticagrelor, clopidogrel, or placebo in the ONSET/OFFSET (A Multi-Centre Randomised, Double-Blind, Double-Dummy Parallel Group Study of the Onset and Offset of Antiplatelet Effects of AZD6140 Compared With Clopidogrel and Placebo With Aspirin as Background Therapy in Patients With Stable Coronary Artery Disease) study. BACKGROUND: Ticagrelor reduces cardiovascular events more effectively than clopidogrel in patients with acute coronary syndromes. Dyspnea develops in some patients treated with ticagrelor, and it is not known whether this is associated with changes in cardiac or pulmonary function. METHODS: In all, 123 stable aspirin-treated CAD patients randomly received either ticagrelor (180 mg load, then 90 mg twice daily; n=57), clopidogrel (600 mg load, then 75 mg daily; n=54), or placebo (n=12) for 6 weeks in a double-blind, double-dummy design. Electrocardiography, echocardiography, serum N-terminal pro-brain natriuretic peptide, and pulmonary function tests were performed before (baseline) and 6 weeks after drug administration and/or after development of dyspnea. RESULTS: After drug administration, dyspnea was reported by 38.6%, 9.3%, and 8.3% of patients in the ticagrelor, clopidogrel, and placebo groups, respectively (p<0.001). Most instances were mild and/or lasted<24 h, although 3 patients discontinued ticagrelor because of dyspnea. Eight of 22 and 17 of 22 ticagrelor-treated patients experiencing dyspnea did so within 24 h and 1 week, respectively, after drug administration. In all treatment groups, and in ticagrelor-treated patients with dyspnea, there were no significant changes between baseline and 6 weeks in any of the cardiac or pulmonary function parameters. CONCLUSIONS: Dyspnea is commonly associated with ticagrelor therapy, but was not associated in this study with any adverse change in cardiac or pulmonary function. (A Multi-Centre Randomised, Double-Blind, Double-Dummy Parallel Group Study of the Onset and Offset of Antiplatelet Effects of AZD6140 Compared With Clopidogrel and Placebo With Aspirin as Background Therapy in Patients With Stable Coronary Artery Disease [ONSET/OFFSET]; NCT00528411).
机译:目的:我们前瞻性评估了接受替加格雷,氯吡格雷或安慰剂治疗的稳定冠心病(CAD)患者在开始/偏移时的心肺功能(多中心随机,双盲,双假人平行分组研究与阿司匹林作为背景疗法的氯吡格雷和安慰剂相比,AZD6140抗血小板作用的起效和失调研究)。背景:替卡格雷在急性冠脉综合征患者中比氯吡格雷更有效地减少了心血管事件。接受替格瑞洛治疗的某些患者会出现呼吸困难,目前尚不清楚这是否与心脏或肺功能的改变有关。方法:总共123例接受阿司匹林治疗的稳定的CAD患者随机接受替卡格雷(180 mg,然后90 mg每天两次; n = 57),氯吡格雷(600 mg,然后75 mg每天; n = 54)或安慰剂(n = 12)双盲,双假人设计持续6周。在给药前(基线)和给药后6周和/或发生呼吸困难后,进行了心电图,超声心动图,血清N末端脑钠肽和肺功能测试。结果:在替卡格雷,氯吡格雷和安慰剂组中,服药后呼吸困难的患者分别占38.6%,9.3%和8.3%(p <0.001)。大多数病例为轻度和/或持续<24小时,尽管3例患者因呼吸困难而中断了替卡格雷的治疗。接受替卡格雷治疗的22例患者中有8例发生呼吸困难,22例中有17例分别在给药后24小时和1周内。在所有治疗组中,在替卡格雷洛治疗的呼吸困难患者中,在基线和第6周之间,任何心脏或肺功能参数均无显着变化。结论:呼吸困难通常与替格瑞洛治疗相关,但在这项研究中与心脏或肺功能的任何不良变化无关。 (多中心,双盲,双假性平行组研究AZD6140与氯吡格雷和安慰剂联合阿司匹林作为背景治疗稳定型冠心病患者的抗血小板作用的起效和抵消[ONSET / OFFSET]; NCT00528411)。

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