Age-Dependent Therapeutic Effects of Once-Daily Molsidomine Used as an Add-On Treatment in Patients with Stable Angina pectoris

R. Messin, Fabienne Carreer-Bruhwyler, C. Dubois, J. Famaey, J. Géczy
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引用次数: 3

Abstract

Background: A once-daily 16-mg-dose formulation of molsidomine (Coruno® tablets) was recently developed for the chronic treatment of angina pectoris. It required efficacy and safety testing. Objective: The objective of the present study was to compare the efficacy and tolerability of Coruno with that of the currently prescribed twice-daily 8-mg dose of molsidomine (Corvatard® tablets), using them as add-on therapies in patients with stable angina pectoris aged either less or more than 75 years. Methods: 133 patients (including 55 elderly patients of at least 75 years) received molsidomine 8 mg twice daily (M8) for at least 1 month as add-on therapy before enrollment. The study itself consisted of a 1-week period during which patients went on with M8, followed by a 4-week period during which M8 was replaced by molsidomine 16 mg once daily (M16). The frequency of anginal attacks and short-acting nitroderivative consumption for symptomatic relief were measured, and the quality of life was assessed by validated questionnaires. Results: M16 significantly reduced the incidence of anginal attacks in elderly patients compared with M8. The same significant benefit was not observed in younger patients. A nonsignificant decrease in the consumption of nitroderivatives for pain relief was recorded in both age groups. From 3 weeks of treatment, M16 did not induce more drug-related adverse events than M8. It had no significant effect on blood pressure, heart rate or ECG. Conclusions: M16 was as safe and effective as M8 in controlling angina, reducing the frequency of anginal attacks even more in the elderly compared with the younger patient group.
每日一次莫西多明作为稳定型心绞痛患者附加治疗的年龄依赖性治疗效果
背景:最近开发了一种每日一次16毫克剂量的莫西多明制剂(Coruno®片)用于慢性心绞痛的治疗。它需要功效和安全性测试。目的:本研究的目的是比较Coruno的疗效和耐受性与目前处方的每日两次8毫克剂量的莫西多明(Corvatard®片),将其作为75岁以下或75岁以上的稳定型心绞痛患者的附加治疗。方法:133例患者(包括55例75岁以上的老年患者)在入组前接受莫西多明8mg,每日2次(M8),至少1个月作为附加治疗。研究本身包括1周,在此期间,患者继续使用M8,随后4周,在此期间,M8被莫西多明16 mg每日一次(M16)代替。测量心绞痛发作频率和用于缓解症状的短效硝基衍生物用量,并通过有效问卷评估生活质量。结果:与M8相比,M16可显著降低老年患者心绞痛发作的发生率。在年轻患者中没有观察到同样的显著益处。在两个年龄组中,用于缓解疼痛的硝基衍生物的消费量均无显著下降。从治疗3周开始,M16没有比M8引起更多的药物相关不良事件。它对血压、心率和心电图没有显著影响。结论:M16在控制心绞痛方面与M8一样安全有效,与年轻患者组相比,M16更能降低老年患者心绞痛发作的频率。
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