Literature DB >> 2188044

[Terguride in hyperprolactinemia--experiences with 5 patients].

C Wüster1, A Scholz, A Schmelzle, R Horowski, R Ziegler.   

Abstract

Hyperprolactinemia can successfully be treated by dopaminagonists such as bromocriptin or lisuride. About 10% of patients complain about side effects like orthostatic hypotension, nausea or vomiting, which may lead to discontinuation of treatment. We therefore conducted a study using terguride--a new dopaminagonist--in 5 patients with hyperprolactinemia and intolerable side effects under conventional treatment. Terguride is the transdihydroderivative of lisuride (Dopergin). We treated 5 patients, 2 men with macroprolactinoma and 3 women with microprolactinoma with terguride. The mean duration of treatment was 15.6 months (7-37 months). Patients were treated with up to 5 mg terguride daily. All 5 patients had a marked initial decrease of elevated prolactin levels 8 h after administration of 0.25 mg terguride orally. Three patients became normoprolactinemic after sufficient increase of the dose of terguride, 2 female patients with a microprolactinoma got eumenorrhoeic thereafter. The treatment with terguride was tolerated without side effects by all patients. There were no significant changes of the examined parameters of clinical chemistry nor the other pituitary hormones. Results of cranial computertomography did not change in 4 patients, one patient had tumor progression. Tergurid as a dopaminagonist is an effective inhibitor of prolactin with little side effects and thus a useful drug in the treatment of hyperprolactinemia.

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Year:  1990        PMID: 2188044     DOI: 10.1007/bf01650889

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  8 in total

1.  Rapid regression of macroprolactinomas by the new dopamine partial agonist terguride.

Authors:  K J Gräf; D Köhler; R Horowski; R Dorow
Journal:  Acta Endocrinol (Copenh)       Date:  1986-04

2.  Long term suppression of prolactin concentrations after bromocriptine induced regression of pituitary prolactinomas.

Authors:  K W Hancock; J S Scott; J T Lamb; R M Gibson; C Chapman
Journal:  Br Med J (Clin Res Ed)       Date:  1985-01-12

3.  Dual action on central dopamine function of transdihydrolisuride, a 9, 10-dihydrogenated analogue of the ergot dopamine agonist lisuride.

Authors:  H Wachtel; R Dorow
Journal:  Life Sci       Date:  1983-01-24       Impact factor: 5.037

4.  Suppression of puerperal lactation by terguride. A double-blind study.

Authors:  P L Venturini; R Horowski; V Fasce; M Valenzano; C Ferreri; G Badino; E Rainer; A Scholz; L De Cecco
Journal:  Gynecol Obstet Invest       Date:  1988       Impact factor: 2.031

5.  Chronic treatment of pathological hyperprolactinemia and acromegaly with the new ergot derivative terguride.

Authors:  D Dallabonzana; A Liuzzi; G Oppizzi; R Cozzi; G Verde; P Chiodini; E Rainer; R Dorow; R Horowski
Journal:  J Clin Endocrinol Metab       Date:  1986-10       Impact factor: 5.958

6.  Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study.

Authors:  M E Molitch; R L Elton; R E Blackwell; B Caldwell; R J Chang; R Jaffe; G Joplin; R J Robbins; J Tyson; M O Thorner
Journal:  J Clin Endocrinol Metab       Date:  1985-04       Impact factor: 5.958

7.  Effect of the new ergot derivative terguride on plasma PRL and GH levels in patients with pathological hyperprolactinemia or acromegaly.

Authors:  D Dallabonzana; A Liuzzi; G Oppizzi; G Verde; P G Chiodini; R Dorow; R Horowski
Journal:  J Endocrinol Invest       Date:  1985-04       Impact factor: 4.256

8.  Terguride--a new dopamine agonist drug: a comparison of its neuroendocrine and side effect profile with bromocriptine.

Authors:  E Ciccarelli; R Touzel; M Besser; A Grossman
Journal:  Fertil Steril       Date:  1988-04       Impact factor: 7.329

  8 in total

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