Literature DB >> 3791649

Parenteral bromocriptine in the treatment of hormonally active pituitary tumours.

G Benker, B Gieshoff, O Freundlieb, R Windeck, H M Schulte, I Lancranjan, D Reinwein.   

Abstract

Eleven patients with PRL and three with GH-secreting pituitary adenomas were treated with a single intramuscular injection of 50 mg of bromocriptine retard (Parlodel, LA (long-acting)). There was a marked PRL suppression in 9 prolactinoma patients, in four for a period of at least 6 weeks. In one patient with acromegaly GH plasma levels decreased into the normal range. The size of the pituitary adenoma diminished considerably, as shown by CT scan, in three out of the 9 responding patients with prolactinoma and in the above acromegalic patient. Visual fields normalized within 14 d in one patient with a PRL-secreting macroadenoma and bitemporal hemianopsia who also had CT scan-documented shrinkage of the tumour. There were no side-effects except slight hypotension in two and local tenderness at the injection site in one patient; these symptoms disappeared without treatment. It is concluded that bromocriptine retard is a safe and effective therapeutic tool for shrinking hormonally active pituitary tumours in selected patients. Due to its good tolerance and the rapid hormonal and clinical improvement it may be also considered as the best therapeutic approach to initiate the treatment of PRL- and/or GH-secreting pituitary tumours.

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Year:  1986        PMID: 3791649     DOI: 10.1111/j.1365-2265.1986.tb03279.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  9 in total

Review 1.  Positron emission tomography applied in the study of pituitary adenomas.

Authors:  C Muhr; M Bergström
Journal:  J Endocrinol Invest       Date:  1991-06       Impact factor: 4.256

Review 2.  Therapeutic applications of bromocriptine in endocrine and neurological diseases.

Authors:  K Y Ho; M O Thorner
Journal:  Drugs       Date:  1988-07       Impact factor: 9.546

3.  Cabergoline: a first-choice treatment in patients with previously untreated prolactin-secreting pituitary adenoma.

Authors:  S Cannavò; L Curtò; S Squadrito; B Almoto; A Vieni; F Trimarchi
Journal:  J Endocrinol Invest       Date:  1999-05       Impact factor: 4.256

Review 4.  Control of prolactin secretion.

Authors:  G Benker; C Jaspers; G Häusler; D Reinwein
Journal:  Klin Wochenschr       Date:  1990-12-04

5.  A randomized cross-over study comparing cabergoline and quinagolide in the treatment of hyperprolactinemic patients.

Authors:  D A De Luis; A Becerra; M Lahera; J I Botella; C Varela
Journal:  J Endocrinol Invest       Date:  2000 Jul-Aug       Impact factor: 4.256

6.  Long-acting bromocriptine for the acute treatment of large macroprolactinomas.

Authors:  A Zarate; C Moran; R Miranda; M Loyo; M Medina; M E Fonseca
Journal:  J Endocrinol Invest       Date:  1987-06       Impact factor: 4.256

7.  Evaluation of a repeatable depot-bromocriptine preparation(Parlodel LAR) for the treatment of acromegaly.

Authors:  U Plöckinger; H J Quabbe
Journal:  J Endocrinol Invest       Date:  1991-12       Impact factor: 4.256

8.  A cross-over study with the two novel dopaminergic drugs cabergoline and quinagolide in hyperprolactinemic patients.

Authors:  M Giusti; E Porcella; A Carraro; M Cuttica; S Valenti; G Giordano
Journal:  J Endocrinol Invest       Date:  1994-01       Impact factor: 4.256

9.  Long-term treatment of acromegalic patients with repeatable parenteral depot-bromocriptine.

Authors:  C Jaspers; R Haase; H Pfingsten; G Benker; D Reinwein
Journal:  Clin Investig       Date:  1993-07
  9 in total

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