Kloner Robert A, Mitchell Malcolm, Emmick Jeffrey T
Division of Cardiovascular Medicine, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Am J Cardiol. 2003 Nov 6;92(9A):37M-46M. doi: 10.1016/s0002-9149(03)00074-2.
To determine the effects of tadalafil on the cardiovascular system, safety assessments were performed on a database of >4000 subjects who received tadalafil in >60 clinical pharmacology, phase 2, phase 3, and open-label studies. In healthy subjects, tadalafil resulted in small changes in blood pressure, which are not believed to be clinically relevant. Daily administration of tadalafil 20 mg for 26 weeks in healthy male subjects or patients with mild erectile dysfunction resulted in blood pressure changes similar to those observed after placebo administration. In patients with coronary artery disease (CAD), tadalafil administration before nitrate administration resulted in small decreases in blood pressure. The resulting mean maximal change in standing systolic blood pressure (SBP) after coadministration of sublingual nitroglycerin in patients with chronic stable angina was -36 mm Hg for tadalafil 5 mg, -31 mm Hg for tadalafil 10 mg, and -28 mm Hg for placebo. In addition, a larger number of men had a standing SBP <85 mm Hg after coadministration of sublingual nitroglycerin and tadalafil 5 mg (p <0.001 vs placebo) or tadalafil 10 mg (p <0.01 vs placebo) compared with coadministration with placebo. In patients with chronic stable angina taking doses of isosorbide mononitrate on a long-term basis, the mean maximal change in standing SBP was -23 mm Hg for placebo, -23 mm Hg for tadalafil 5 mg, and -26 mm Hg for tadalafil 10 mg. In a study of older subjects (>or=55 years of age) with no overt evidence of CAD, the resulting mean maximal change in standing SBP after coadministration of sublingual nitroglycerin was -25 mm Hg for tadalafil 10 mg, -29 mm Hg for sildenafil 50 mg, and -25 mm Hg for placebo. Cardiac mortality rates in tadalafil studies are consistent with the expected rate in this male population. Across all studies, the incidence rate of myocardial infarction was low in tadalafil-treated patients (0.43 per 100 patient-years) compared with patients who received placebo (0.6 per 100 patient-years), and the incidence rate was comparable to that observed in the age-standardized male population (0.60 per 100 patient-years). The incidence rate of presumed thrombotic strokes in tadalafil studies (0.27 per 100 patient-years) is comparable to the expected rate in this patient population. The data presented herein suggest that tadalafil can be safely used by healthy subjects and by patients with cardiovascular diseases. As with sildenafil, the use of tadalafil is contraindicated in patients receiving nitrate therapy because of the potential for significant hypotensive effects.
为确定他达拉非对心血管系统的影响,对一个包含4000多名受试者的数据库进行了安全性评估,这些受试者在60多项临床药理学、2期、3期及开放标签研究中接受了他达拉非治疗。在健康受试者中,他达拉非导致血压出现微小变化,一般认为这些变化不具有临床相关性。在健康男性受试者或轻度勃起功能障碍患者中,每日服用20 mg他达拉非,持续26周,其血压变化与服用安慰剂后观察到的变化相似。在冠状动脉疾病(CAD)患者中,在服用硝酸盐之前服用他达拉非会导致血压小幅下降。在慢性稳定型心绞痛患者中,舌下含服硝酸甘油与他达拉非5 mg合用时,站立位收缩压(SBP)的平均最大变化为-36 mmHg;与他达拉非10 mg合用时为-31 mmHg;与安慰剂合用时为-28 mmHg。此外,与安慰剂合用相比,更多男性在舌下含服硝酸甘油与他达拉非5 mg(与安慰剂相比,p<0.001)或他达拉非10 mg(与安慰剂相比,p<0.01)合用时,站立位SBP<85 mmHg。在长期服用单硝酸异山梨酯的慢性稳定型心绞痛患者中,站立位SBP的平均最大变化为:安慰剂组为-23 mmHg,他达拉非5 mg组为-23 mmHg,他达拉非10 mg组为-26 mmHg。在一项针对无明显CAD证据的老年受试者(≥55岁)的研究中,舌下含服硝酸甘油与他达拉非10 mg合用时,站立位SBP的平均最大变化为-25 mmHg;与西地那非50 mg合用时为-29 mmHg;与安慰剂合用时为-25 mmHg。他达拉非研究中的心脏死亡率与该男性人群的预期死亡率一致。在所有研究中,他达拉非治疗患者的心肌梗死发病率较低(每100患者年0.43例),低于接受安慰剂治疗的患者(每100患者年0.6例),且发病率与年龄标准化男性人群中观察到的发病率相当(每100患者年0.60例)。他达拉非研究中推测的血栓性中风发病率(每100患者年0.27例)与该患者人群的预期发病率相当。本文提供的数据表明,健康受试者和心血管疾病患者可以安全使用他达拉非。与西地那非一样,由于可能产生显著降压作用,正在接受硝酸盐治疗的患者禁用他达拉非。