Clissold S P, Brogden R N
Drugs. 1985 Jun;29(6):489-530. doi: 10.2165/00003495-198529060-00002.
Piretanide is a potent 'loop' diuretic whose principal site of action is in the thick ascending limb of the loop of Henle. When administered orally or intravenously to healthy volunteers it rapidly increases diuresis and electrolyte excretion, and the effects are short-lived. In comparative studies, piretanide has generally been found to be 5 to 7 times more potent than frusemide (furosemide) but only one-tenth as potent as bumetanide, on a weight-for-weight basis. Piretanide 6 to 12 mg/day, in conventional or sustained release formulations, has been shown to significantly lower elevated blood pressure in a large proportion of patients with mild to moderate hypertension. Comparative trials of up to 3 months duration indicate that at this dosage piretanide is of comparable antihypertensive efficacy as hydrochlorothiazide 50 to 100 mg/day, but has significantly less effect on serum potassium levels. Short term studies in patients with oedema caused by renal, hepatic or cardiac failure demonstrated that piretanide 6 to 9 mg is of similar diuretic potency as frusemide 40 mg and bumetanide 1 mg. In medium term trials in patients with congestive heart failure piretanide 6 mg/day produced equivalent symptomatic improvement as frusemide 40 mg/day. When used to treat oedema caused by liver disease, piretanide 12 to 24 mg/day was successful in only about 50% of patients, but spironolactone added to the treatment regimen greatly increased the response rate. Generally, piretanide has been well-tolerated in clinical trials, although the conventional tablet formulation has caused a relatively high incidence of acute adverse effects--these were greatly reduced with the introduction of the sustained release formulation. Serum concentrations of most electrolytes have not shown any consistent adverse trends and hyperuricaemia and hypokalaemia have been encountered infrequently. Thus, piretanide appears to offer an effective alternative to other 'loop' diuretics for the treatment of oedematous diseases and to hydrochlorothiazide for the management of mild to moderate hypertension. However, its relative place in therapy remains to be clarified with wider clinical experience.
吡咯他尼是一种强效的“袢”利尿剂,其主要作用部位在髓袢升支粗段。给健康志愿者口服或静脉注射后,它能迅速增加尿量和电解质排泄,且作用持续时间短。在比较研究中,按重量计算,吡咯他尼的效力通常比呋塞米(速尿)强5至7倍,但仅为布美他尼的十分之一。常规或缓释制剂的吡咯他尼6至12毫克/天已被证明能使很大一部分轻度至中度高血压患者的血压显著降低。长达3个月的比较试验表明,在此剂量下,吡咯他尼的降压效果与50至100毫克/天的氢氯噻嗪相当,但对血清钾水平的影响明显较小。对肾、肝或心力衰竭引起水肿的患者进行的短期研究表明,6至9毫克的吡咯他尼与40毫克的呋塞米和1毫克的布美他尼利尿效力相似。在充血性心力衰竭患者的中期试验中,6毫克/天的吡咯他尼产生的症状改善与40毫克/天的呋塞米相当。用于治疗肝病引起的水肿时,12至24毫克/天的吡咯他尼仅在约50%的患者中取得成功,但在治疗方案中添加螺内酯可大大提高有效率。一般来说,吡咯他尼在临床试验中耐受性良好,尽管常规片剂制剂引起的急性不良反应发生率相对较高——随着缓释制剂的引入,这些不良反应大大减少。大多数电解质的血清浓度未显示出任何一致的不良趋势,高尿酸血症和低钾血症很少见。因此,吡咯他尼似乎为治疗水肿性疾病提供了一种有效的替代其他“袢”利尿剂的药物,为治疗轻度至中度高血压提供了一种替代氢氯噻嗪的药物。然而,随着更广泛的临床经验,其在治疗中的相对地位仍有待明确。