首页> 外文OA文献 >Single dose cabergoline versus bromocriptine in inhibition of puerperal lactation: randomised, double blind, multicentre study. European Multicentre Study Group for Cabergoline in Lactation Inhibition.
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Single dose cabergoline versus bromocriptine in inhibition of puerperal lactation: randomised, double blind, multicentre study. European Multicentre Study Group for Cabergoline in Lactation Inhibition.

机译:单剂量卡麦角林与溴隐亭抑制产后泌乳:随机,双盲,多中心研究。卡麦角林抑制泌乳的欧洲多中心研究小组。

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摘要

OBJECTIVE--To compare the efficacy and safety of a single dose of 1 mg of cabergoline with that of bromocriptine 2.5 mg twice daily for 14 days in the inhibition of puerperal lactation. DESIGN--Prospective, randomised, double blind, parallel group, multicentre study. SETTING--University of hospital departments of obstetrics and gynaecology in different European countries. SUBJECTS--272 puerperal women not wishing to lactate (136 randomised to each drug). INTERVENTIONS--Women randomised to cabergoline received two 0.5 mg tablets of cabergoline and one placebo tablet within 27 hours after delivery and then placebo twice daily for 14 days. Those randomised to bromocriptine received 2.5 mg of bromocriptine and two placebo tablets within 27 hours and then 2.5 mg of bromocriptine twice daily for 14 days. MAIN OUTCOME MEASURES--Success of treatment (complete or partial) according to milk secretion, breast engorgement, and breast pain; rebound symptomatology; serum prolactin concentrations; and number of adverse events. RESULTS--Complete success was achieved in 106 of 136 women randomised to cabergoline and in 94 of 136 randomised to bromocriptine and partial success in 21 and 33 women respectively. Rebound breast symptomatology occurred respectively in five and 23 women with complete success up to day 15 (p less than 0.0001). Serum prolactin concentrations dropped considerably with both drugs from day 2 to day 15; a prolactin secretion rebound effect was observed in women treated with bromocriptine. cabergoline and 36 receiving bromocriptine (p = 0.054), occurring most during the first treatment day. CONCLUSION--A single 1 mg dose of cabergoline is at least as effective as bromocriptine 2.5 mg twice daily for 14 days in preventing puerperal lactation. Because of the considerably lower rate of rebound breast activity and adverse events and the simpler administration schedule cabergoline should be the drug of choice for lactation inhibition.
机译:目的-比较单剂量1 mg卡麦角林和2.5 mg溴隐亭每日两次,连续14天在抑制产褥期泌乳方面的功效和安全性。设计-前瞻性,随机,双盲,平行分组,多中心研究。地点-欧洲不同国家/地区的妇产科医院大学。受试者-272名不希望哺乳的产妇(每种药物随机分配136名)。干预措施-随机分配给卡麦角林的妇女在分娩后27小时内接受两片0.5毫克卡麦角林片剂和一剂安慰剂片剂,然后每天两次安慰剂,共14天。那些随机分配至溴隐亭的患者在27小时内接受2.5 mg溴隐亭和两片安慰剂片,然后每天2.5次服用2.5 mg溴隐亭,共14天。主要观察指标-根据乳汁分泌,乳房充血和乳房疼痛来治疗(全部或部分)成功;反弹症状血清催乳素浓度;和不良事件的数量。结果-随机分配给卡麦角林的136名女性中有106名获得了完全成功,随机分配有溴隐亭的136名女性中有94名分别获得了21和33名女性的完全成功。直到第15天,分别有5例和23例女性发生了反弹性乳房症状,完全成功(p小于0.0001)。从第2天到第15天,两种药物的血清催乳素浓度均显着下降。在溴隐亭治疗的妇女中观察到催乳素分泌反弹作用。卡麦角林和36接受溴隐亭(p = 0.054),发生在第一治疗日的大部分时间。结论-单次卡麦角林1 mg的剂量在预防产褥期泌乳方面至少每天两次与溴隐亭2.5 mg一样有效,持续14天。由于乳房反弹和不良反应的发生率相当低,并且卡麦角林的给药方案更简单,因此应选择抑制泌乳的药物。

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