Gutman Lawrence B, Wilson Ben J
University of Calgary, Cumming School of Medicine, Calgary, Canada.
J Popul Ther Clin Pharmacol. 2017 Aug 23;24(3):e45-e50. doi: 10.22374/1710-6222.24.3.4.
Midodrine is an oral, peripherally acting alpha-adrenergic agonist. After gaining Food and Drug Administration (FDA) approval in 1996 for orthostatic hypotension, its use has evolved to target vasoplegic conditions such as intradialytic hypotension in the end-stage renal disease population, refractory ascites in cirrhotic patients to support diuresis, and in hepatorenal syndrome. Upon oral ingestion, the drug undergoes enzymatic hydrolysis to an active metabolite, desglymidodrine. Its use has been well tolerated at 2.5 mg, 5 mg, and 10 mg oral doses. The most frequently occurring side effects relate directly to its sympathomimetic profile and include piloerection, scalp pruritis, generalized paresthesias, and urinary retention. The vasoplegic profile of sepsis would be a potential target for midodrine therapy. While its use to mediate recovery from septic shock has been suggested, there is a paucity of clinical data supporting its use. Such therapy may be uniquely appropriate in septic patients who are not candidates for intensive care unit (ICU) level of care.
米多君是一种口服的外周作用性α-肾上腺素能激动剂。1996年获得美国食品药品监督管理局(FDA)批准用于治疗体位性低血压后,其应用范围已扩展至治疗血管麻痹性疾病,如终末期肾病患者的透析中低血压、肝硬化患者难治性腹水以辅助利尿,以及肝肾综合征。口服后,该药物经酶水解转化为活性代谢产物去甘米多君。其口服剂量为2.5毫克、5毫克和10毫克时耐受性良好。最常见的副作用直接与其拟交感神经作用有关,包括竖毛、头皮瘙痒、全身感觉异常和尿潴留。脓毒症的血管麻痹状态可能是米多君治疗的潜在靶点。虽然有人提出使用米多君来介导感染性休克的恢复,但支持其使用的临床数据很少。这种治疗方法可能特别适用于不适合入住重症监护病房(ICU)的脓毒症患者。