Ward A, Brogden R N, Heel R C, Speight T M, Avery G S
Drugs. 1983 Dec;26(6):468-502. doi: 10.2165/00003495-198326060-00002.
Amrinone is a bipyridine derivative with positive inotropic effects and vasodilatory properties. However, in the clinical setting of congestive heart failure, the relative contribution of these factors remains a matter of conjecture. Its mode of action appears to be related to alterations in extracellular and intracellular calcium balance, probably mediated by increased levels of tissue cyclic adenosine monophosphate and possibly involving a sodium-dependent pathway. Clinical experience has mostly been short term and is limited to a relatively small number of patients with severe congestive heart failure, refractory to conventional treatment. Amrinone rapidly improves cardiac performance by decreasing systemic vascular resistance (afterload), decreasing the determinants of left ventricular filling pressure (preload) and improving the cardiac contractility. Improvements in exercise performance and clinical symptomatology occur without an increase in heart rate or decrease in mean arterial pressure. Amrinone has been compared with dopamine, dobutamine, pirbuterol and prazosin in preliminary short terms studies in patients with severe congestive heart failure, although more studies are needed before any relative clinical advantages or disadvantages can be ascribed to amrinone. Initial experience suggests that the addition of vasodilators such as hydralazine and isosorbide dinitrate to amrinone therapy may confer additional haemodynamic benefits. Preliminary medium term studies suggest that tolerance to the haemodynamic effects of amrinone does not usually occur, but long term studies are needed to determine whether amrinone alters the normal progression of the disease and whether overall mortality is affected. Amrinone has usually been administered as intravenous bolus doses (totalling 1.5 to 3.6 mg/kg/day) and/or continuous intravenous infusion, with varied results. Generally, an oral dose greater than the intravenous dose is required to achieve an equivalent level of response. Reversible, usually asymptomatic, thrombocytopenia occurs in about 20% of patients treated with amrinone. Arrhythmias and gastrointestinal disturbances have been reported, but wider clinical experience is required to determine the side effect profile of the drug.
氨力农是一种具有正性肌力作用和血管舒张特性的双吡啶衍生物。然而,在充血性心力衰竭的临床环境中,这些因素的相对作用仍存在争议。其作用方式似乎与细胞外和细胞内钙平衡的改变有关,可能是由组织环磷酸腺苷水平升高介导的,并且可能涉及一条钠依赖性途径。临床经验大多是短期的,并且仅限于相对少数对传统治疗无效的严重充血性心力衰竭患者。氨力农通过降低全身血管阻力(后负荷)、降低左心室充盈压的决定因素(前负荷)和改善心脏收缩力,迅速改善心脏功能。运动能力和临床症状得到改善,而心率没有增加或平均动脉压没有降低。在对严重充血性心力衰竭患者进行的初步短期研究中,已将氨力农与多巴胺、多巴酚丁胺、吡布特罗和哌唑嗪进行了比较,不过在能够确定氨力农的任何相对临床优势或劣势之前,还需要更多的研究。初步经验表明,在氨力农治疗中添加血管扩张剂如肼屈嗪和硝酸异山梨酯可能会带来额外的血流动力学益处。中期初步研究表明,通常不会出现对氨力农血流动力学效应的耐受性,但需要进行长期研究以确定氨力农是否会改变疾病的正常进展以及是否会影响总体死亡率。氨力农通常以静脉推注剂量(总计1.5至3.6毫克/千克/天)和/或持续静脉输注的方式给药,结果各不相同。一般来说,需要口服大于静脉剂量才能达到等效的反应水平。在用氨力农治疗的患者中,约20%会出现可逆的、通常无症状的血小板减少症。已报告有心律失常和胃肠道紊乱,但需要更广泛的临床经验来确定该药物的副作用情况。