Nappi C, Colace G, Di Carlo C, Affinito P, Ruotolo C, Montemagno R, Farace M J, Mailland F, Di Renzo G F
Department of Gynecological Endocrinology, School of Medicine, University of Turin, Italy.
Gynecol Endocrinol. 1993 Jun;7(2):129-33. doi: 10.3109/09513599309152492.
The aim of the present study was to evaluate the efficacy and tolerability of the dopamine agonist drug dihydroergocryptine in the suppression of puerperal lactation. A single blind and placebo-controlled study was performed. A total of 90 postpartum women was acutely or repeatedly treated with dihydroergocryptine at different doses in order to investigate the efficacy of this drug in the suppression of puerperal lactation and to find the optimum dose for therapy. Prolactin levels, mammary symptomatology and rebound effects were monitored during the repeated treatment and also 1 and 8 days after drug discontinuation. With acute administration, dihydroergocryptine significantly reduced prolactin levels only at the dose of 10 mg and not at 5 mg. With repeated administration, a daily dose of 15 mg was more effective than 10 mg in reducing prolactin levels and in suppressing puerperal lactation. No side-effects occurred during the treatment. These results suggest that dihydroergocryptine might be considered an effective drug in the suppression of puerperal lactation.
本研究的目的是评估多巴胺激动剂药物双氢麦角隐亭在抑制产后泌乳方面的疗效和耐受性。进行了一项单盲、安慰剂对照研究。总共90名产后妇女接受了不同剂量的双氢麦角隐亭急性或重复治疗,以研究该药物在抑制产后泌乳方面的疗效,并找到治疗的最佳剂量。在重复治疗期间以及停药后1天和8天监测催乳素水平、乳腺症状和反跳效应。急性给药时,双氢麦角隐亭仅在10毫克剂量时显著降低催乳素水平,而在5毫克剂量时则无此效果。重复给药时,每日15毫克剂量在降低催乳素水平和抑制产后泌乳方面比10毫克剂量更有效。治疗期间未出现副作用。这些结果表明,双氢麦角隐亭可能被认为是一种抑制产后泌乳的有效药物。