Banning A P, Ramsey M W, Jones E A, Evans W, Carolan G, Jones C H, Henderson A H
Department of Cardiology, University of Wales College of Medicine, Cardiff, UK.
Eur J Clin Pharmacol. 1996;51(2):133-8. doi: 10.1007/s002280050173.
Diuretics, angiotensin converting enzyme inhibitors and digoxin have become "standard" triple therapy for many patients with chronic cardiac failure. Flosequinan increases exercise duration and improves symptoms when added to standard triple therapy. Despite intensive study, the clinical pharmacology of flosequinan remains uncertain.
The University Hospital of Wales, a Regional Cardiac Centre.
Twenty four patients with chronic heart failure who remained symptomatic despite standard therapy including ACE inhibitors.
A double-blind placebo-controlled parallel group study of 100 mg daily of flosequinan. We measured changes in exercise duration using cardiorespiratory exercise testing and changes in large artery distensibility using Doppler ultrasound.
Exercise duration after 8 weeks flosequinan treatment was significantly greater than following placebo treatment. The flosequinan-related increase in exercise duration (+14%) was associated with a significant reduction in VE/VCO2 slope (-16%). Brachial-radial pulse wave velocities were unaltered by flosequinan treatment.
Our results confirm that flosequinan improves exercise duration in patients with chronic heart failure. They suggest that this observed beneficial effect is independent of any change in large artery distensibility and that in the presence of ACE inhibitors, this improvement may be independent of any vasodilating action of flosequinan. Although this study confirms the beneficial symptomatic effects of flosequinan in chronic cardiac failure, clinical trials have subsequently demonstrated an overall increase in mortality in patients treated with 100 mg flosequinan daily. This has resulted in the withdrawal of flosequinan from routine clinical use.
利尿剂、血管紧张素转换酶抑制剂和地高辛已成为许多慢性心力衰竭患者的“标准”三联疗法。在标准三联疗法基础上加用氟司喹南可增加运动持续时间并改善症状。尽管进行了深入研究,但氟司喹南的临床药理学仍不明确。
威尔士大学医院,一家地区心脏中心。
24例慢性心力衰竭患者,尽管接受了包括血管紧张素转换酶抑制剂在内的标准治疗,但仍有症状。
一项双盲安慰剂对照平行组研究,每日服用100毫克氟司喹南。我们使用心肺运动试验测量运动持续时间的变化,并使用多普勒超声测量大动脉扩张性的变化。
氟司喹南治疗8周后的运动持续时间显著长于安慰剂治疗后。氟司喹南使运动持续时间增加(+14%),同时伴有VE/VCO2斜率显著降低(-16%)。氟司喹南治疗未改变肱桡脉搏波速度。
我们的结果证实氟司喹南可改善慢性心力衰竭患者的运动持续时间。结果表明,观察到的这种有益作用与大动脉扩张性的任何变化无关,并且在使用血管紧张素转换酶抑制剂的情况下,这种改善可能与氟司喹南的任何血管舒张作用无关。尽管本研究证实了氟司喹南对慢性心力衰竭有有益的症状改善作用,但随后的临床试验表明,每日服用100毫克氟司喹南的患者总体死亡率有所增加。这导致氟司喹南退出常规临床应用。