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培高利特与溴隐亭治疗高催乳素血症的疗效与安全性比较。

A comparison of the efficacy and safety of pergolide and bromocriptine in the treatment of hyperprolactinemia.

作者信息

Lamberts S W, Quik R F

机构信息

Department of Medicine, Erasmus University, Rotterdam, The Netherlands.

出版信息

J Clin Endocrinol Metab. 1991 Mar;72(3):635-41. doi: 10.1210/jcem-72-3-635.

Abstract

UNLABELLED

Pergolide is a synthetic ergoline derivative with highly potent long-acting PRL-lowering activity, allowing therapy of hyperprolactinemia with a once daily administration of the drug. The results of two open-label, randomized controlled multicenter clinical trials are reported. Pergolide (taken once a day), was compared with bromocriptine (taken two to four times daily) regarding efficacy and safety in the reduction of PRL levels, the cessation of galactorrhea and amenorrhea, the improvement in sexual function, and tumor shrinkage in hyperprolactinemia without (trial I; 61 patients) and with radiologically evident pituitary tumors (trial II; 96 patients). Both drugs were equally effective in lowering PRL levels in both trials. A median optimal dose of 50 micrograms pergolide and 5 mg bromocriptine/day suppressed PRL levels in the 61 patients of trial I by more than 80%. During the 24-week investigational period galactorrhea disappeared in 96% and 87% of patients, whereas menstruation returned in 90% and 96% of patients, respectively. An equally high efficacy (optimal median dose: 75-100 micrograms pergolide, 7.5-10 mg bromocriptine daily) was observed in trial II, although the resumption of menses was less frequent than in the patients of trial I (50% and 58% of patients, respectively). Sexual dysfunction improved similarly on both drugs in about half the patients. In addition, tumor shrinkage occurred to a similar extent with both drugs. A high incidence of adverse events was noted especially at the initiation of therapy with both compounds: nausea, dizziness, vomiting, asthenia, headache, and decrease in blood pressure occurred at a similar incidence and extent during the use of pergolide and bromocriptine. Patients in trial I treated with pergolide reported a slightly higher incidence of fever, vasodilatation, and flu syndrome.

CONCLUSIONS

in these 24-week studies comprising a total of 157 hyperprolactinemic patients, a once daily administration of pergolide was shown to be as safe and effective as the two to four times daily ingestion of bromocriptine. Longer-acting dopamine agonists like pergolide that can be taken once daily, are likely to increase the ease to adherence to the therapeutic regimen. This might result in a higher compliance to medical treatment of hyperprolactinemia.

摘要

未标注

培高利特是一种合成麦角林衍生物,具有高效长效降低催乳素(PRL)的活性,每日服用一次该药物即可治疗高催乳素血症。本文报告了两项开放标签、随机对照的多中心临床试验结果。比较了培高利特(每日服用一次)与溴隐亭(每日服用2 - 4次)在降低PRL水平、停止溢乳和闭经、改善性功能以及高催乳素血症患者(试验I;61例患者)和有影像学证据的垂体瘤患者(试验II;96例患者)肿瘤缩小方面的疗效和安全性。在两项试验中,两种药物降低PRL水平的效果相当。试验I的61例患者中,培高利特的中位最佳剂量为50微克/天,溴隐亭为5毫克/天,可使PRL水平降低超过80%。在24周的研究期间,试验I中96%的患者溢乳消失,试验II中为87%;试验I中90%的患者月经恢复,试验II中为96%。试验II中观察到同样高的疗效(中位最佳剂量:培高利特75 - 100微克/天,溴隐亭7.5 - 10毫克/天),尽管月经恢复的频率低于试验I的患者(分别为50%和58%)。约一半患者使用两种药物后性功能改善情况相似。此外,两种药物导致肿瘤缩小的程度相似。尤其在两种药物治疗开始时不良事件发生率较高:使用培高利特和溴隐亭期间,恶心、头晕、呕吐、乏力、头痛和血压下降的发生率及程度相似。试验I中接受培高利特治疗的患者报告发热、血管扩张和流感综合征的发生率略高。

结论

在这两项共纳入157例高催乳素血症患者的24周研究中,每日服用一次培高利特与每日服用2 - 4次溴隐亭的安全性和有效性相当。像培高利特这样每日服用一次的长效多巴胺激动剂可能会增加患者对治疗方案的依从性,这可能会提高高催乳素血症的药物治疗依从性。

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