McClellan K J, Wiseman L R, Wilde M I
Adis International Limited, Auckland, New Zealand.
Drugs Aging. 1998 Jan;12(1):76-86. doi: 10.2165/00002512-199812010-00007.
Midodrine is a prodrug which undergoes enzymatic hydrolysis to the selective alpha 1-adrenoceptor agonist desglymidodrine after oral administration. Oral midodrine significantly increases 1-minute standing systolic blood pressure compared with placebo. The drug also improves standing time and energy level and clinical symptoms of orthostatic hypotension including dizziness, light-headedness and syncope. Comparative studies have shown midodrine to have similar efficacy to dihydroergotamine mesylate, norfenefrine, fludrocortisone and etilefrine, and to be more effective than dimetofrine and ephedrine in patients with orthostatic hypotension. Midodrine is well tolerated, with the most commonly reported adverse events being piloerection, pruritus, paraesthesias, urinary retention and chills. The risk of supine hypertension, which is associated with midodrine therapy in up to 25% of patients, can be reduced by taking the final daily dose at least 4 hours before bedtime. Thus, oral midodrine is an effective therapeutic option for the management of various forms of orthostatic hypotension. This well-tolerated agent is likely to be useful in conjunction with standard nonpharmacological care.
米多君是一种前体药物,口服后经酶水解成为选择性α1肾上腺素能受体激动剂去甘米多君。与安慰剂相比,口服米多君可显著提高站立1分钟时的收缩压。该药还能延长站立时间、提升精力水平,并改善体位性低血压的临床症状,如头晕、头重脚轻和晕厥。比较研究表明,米多君与甲磺酸双氢麦角胺、去甲麻黄碱、氟氢可的松和乙苯福林疗效相似,且在体位性低血压患者中比二甲福林和麻黄碱更有效。米多君耐受性良好,最常报告的不良事件为竖毛、瘙痒、感觉异常、尿潴留和寒战。高达25%的患者使用米多君治疗会出现仰卧位高血压风险,可通过在睡前至少4小时服用最后一剂日剂量来降低该风险。因此,口服米多君是治疗各种类型体位性低血压的有效治疗选择。这种耐受性良好的药物可能与标准非药物治疗联合使用会很有用。