Weingrill C O, Mussio W, Moraes C R, Portes E, Castro R C, Lengyel A M
Department of Medicine, Escola Paulista de Medicina, Sao Paulo, Brazil.
Fertil Steril. 1992 Feb;57(2):331-5. doi: 10.1016/s0015-0282(16)54840-7.
To compare the effect of Parlodel SRO (Sandoz, Basel, Switzerland), a long-acting oral bromocriptine, to Parlodel (Sandoz) and to study the chronic effects of Parlodel SRO.
The study was twofold: (1) random, double-blind and (2) open.
Patients were studied in an academic environment.
Hyperprolactinemic patients were selected. Sixteen patients were treated during 1 month. Ten patients completed the 1-year follow-up.
Parlodel SRO or Parlodel was administered during 1 month (first 15 days: 5 mg/d; afterwards: 10 mg/d). Parlodel SRO was given during 1 year in variable doses (maximal 20 mg/d).
Prolactin (PRL) levels, clinical improvement, and side effects were evaluated.
After 1 month, 63% of the patients in both groups had normal PRL and 43% had menses. Side effects were similar. After 1 year all patients except one had normal PRL levels, and 89% were ovulating.
The efficacy, tolerability, and long duration of action of Parlodel SRO make it an excellent alternative for the treatment of hyperprolactinemic patients.
比较长效口服溴隐亭Parlodel SRO(瑞士巴塞尔山德士公司生产)与Parlodel的疗效,并研究Parlodel SRO的长期效应。
该研究分为两部分:(1)随机、双盲;(2)开放试验。
在学术环境中对患者进行研究。
选取高泌乳素血症患者。16名患者接受了为期1个月的治疗。10名患者完成了1年的随访。
给予Parlodel SRO或Parlodel治疗1个月(前15天:5毫克/天;之后:10毫克/天)。给予Parlodel SRO治疗1年,剂量可变(最大20毫克/天)。
评估泌乳素(PRL)水平、临床改善情况和副作用。
1个月后,两组中63%的患者PRL水平正常,43%的患者月经来潮。副作用相似。1年后,除1名患者外,所有患者的PRL水平均正常,89%的患者排卵。
Parlodel SRO的疗效、耐受性和长效作用使其成为治疗高泌乳素血症患者的极佳选择。