1993
DOI: 10.1111/j.1365-2265.1993.tb02372.x
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The efficacy and tolerability of long‐term cabergoline therapy in hyperprolactinaemic disorders: an open, uncontrolled, multicentre study

Abstract: The results provide evidence for the long-term effectiveness and safety of cabergoline in the treatment of hyperprolactinaemia. Its ability to normalize PRL and restore gonadal function compares favourably with reported data on reference compounds while its tolerability profile and simple administration schedule offer potential advantages in terms of patient acceptability.

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Cited by 61 publications
(26 citation statements)
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“…The weekly dosage of cabergoline was reported to be 0.5-3.0 mg with the maximum dose being less than 3.5 mg/wk in most institutions of Western countries (4 -7, 9 -17). For instance, three independent investigators ͓Webster et al (4,10), Muratori et al (12), and Colao et al (7,13,(15)(16)(17)͔ used 0.5-1.0, 0.5-3.0, and 0.5-3.5 mg/wk. Cabergoline at doses greater than 4 mg/wk has rarely been used to treat hyperprolactinemia.…”
Section: Discussionmentioning
confidence: 98%
“…The weekly dosage of cabergoline was reported to be 0.5-3.0 mg with the maximum dose being less than 3.5 mg/wk in most institutions of Western countries (4 -7, 9 -17). For instance, three independent investigators ͓Webster et al (4,10), Muratori et al (12), and Colao et al (7,13,(15)(16)(17)͔ used 0.5-1.0, 0.5-3.0, and 0.5-3.5 mg/wk. Cabergoline at doses greater than 4 mg/wk has rarely been used to treat hyperprolactinemia.…”
Section: Discussionmentioning
confidence: 98%
“…Significant decreases in serum PRL levels occur in as many as 95% of hyperprolactinemic women during chronic cabergoline treatment at a dose of 1 mg twice weekly (202). In a multicenter, randomized, 24-wk trial conducted in 459 hyperprolactinemic women (203), cabergoline induced normal PRL levels in 83% compared with 59% with bromocriptine; ovulatory cycles or pregnancies were recorded in 72% vs. 52%, and side effects were less frequent, less severe, and shorter lived.…”
Section: Cabergolinementioning
confidence: 97%
“…In head-to-head randomized, prospective comparison studies (202), retrospective analyses (207), and general clinical experience, cabergoline has been shown to be more effective in lowering PRL levels to normal, reducing tumor size, and having less adverse effects. As noted below, patients are less likely to be resistant to the therapeutic effects of cabergoline; furthermore, most patients found to be resistant to bromocriptine subsequently respond to cabergoline.…”
Section: E Conclusion With Regard To Medical Therapymentioning
confidence: 97%
“…However, up to 12% of these patients did not tolerate the drug in therapeutic doses because of side effects and 5-10% of patients showed only minimal or no response after bromocriptine therapy (8,9). Cabergoline, a long-acting dopamine agonist, has been shown to be more effective (83%) (8) than bromocriptine with a marked reduction in adverse effects (7,8,(10)(11)(12)(13)(14)(15). Thus, cabergoline and also quinagolide started to progressively replace bromocriptine in the medical therapy of prolactinomas during the last decade (16)(17)(18)(19)(20).…”
Section: Introductionmentioning
confidence: 99%