Gilden J L
Department of Medicine, Chicago Medical School, Illinois.
Int Angiol. 1993 Jun;12(2):125-31.
Neurogenic orthostatic hypotension is a severely disabling condition due to deficient peripheral vasoconstrictor tone in response to the upright position and is characterized by a decrease in blood pressure upon standing associated with symptoms of lightheadedness, dizziness, visual "white-out", weakness, lack of energy, near syncope or even syncope. Previous pharmacologic treatment of neurogenic orthostatic hypotension has been problematic. Midodrine, a new specific alpha-1-agonist has been shown to produce arteriolar constriction and decrease in venous pooling via a constriction of venous capacitance vessels. Therefore, a recent multicenter study evaluated the safety and efficacy of midodrine therapy in 97 patients with neurogenic orthostatic hypotension due to various etiologies: Shy Drager syndrome (No. 18); Bradbury Eggleston syndrome (idiopathic orthostatic hypotension) (No. 20); diabetic autonomic neuropathy (No. 27); Parkinson's disease (No. 22); and miscellaneous (No. 10). Following one week of placebo therapy, the patients were randomized into 4 groups for a 4 week period of time; placebo, 2.5 mg, 5 mg, or 10 mg three times daily. The BE/SDS subgroup demonstrated a 27 +/- 8% (22 mmHg) increase in standing systolic blood pressure for the 10 mg dose. Diabetics achieved a significant increase at 5 mg. Similar increases were observed for the entire group on the 10 mg dose (p < 0.001). Symptoms or fainting, blurred vision, improved energy level, standing time, and depressed feelings were also significantly improved even at lower doses (p < 0.05 or less). Side effects were mild. Therefore, midodrine is an effective and safe agent for the treatment of neurogenic orthostatic hypotension.
神经源性直立性低血压是一种严重致残的病症,其原因是对直立姿势的外周血管收缩张力不足,其特征是站立时血压下降,并伴有头晕、眩晕、视觉“白茫茫”、虚弱、乏力、接近晕厥甚至晕厥等症状。先前对神经源性直立性低血压的药物治疗一直存在问题。米多君是一种新型特异性α-1激动剂,已被证明可通过收缩静脉容量血管产生小动脉收缩并减少静脉淤血。因此,最近一项多中心研究评估了米多君治疗97例因各种病因导致的神经源性直立性低血压患者的安全性和有效性:夏伊-德雷格综合征(18例);布拉德伯里-埃格尔斯顿综合征(特发性直立性低血压)(20例);糖尿病自主神经病变(27例);帕金森病(22例);以及其他(10例)。在接受一周的安慰剂治疗后,患者被随机分为4组,为期4周;安慰剂组、每日三次服用2.5毫克、5毫克或10毫克组。BE/SDS亚组显示,10毫克剂量组站立收缩压升高27±8%(22毫米汞柱)。糖尿病患者在5毫克剂量时血压显著升高。整个组在10毫克剂量时也观察到类似的升高(p<0.001)。即使在较低剂量下,症状或昏厥、视力模糊、能量水平改善、站立时间和抑郁情绪也有显著改善(p<0.05或更低)。副作用轻微。因此,米多君是治疗神经源性直立性低血压的一种有效且安全的药物。