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1.
Eur J Clin Nutr ; 59 Suppl 1: S77-80, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16052199

ABSTRACT

BACKGROUND: Most of the national colleges of general practitioners (GPs) do not have their own dietary/nutritional tools, and GPs and nurses do not have the time, knowledge, or skills to advise their patients about desirable dietary practices. OBJECTIVE: To assess the usefulness of a simple and practical guide on healthy diet to be used by European GPs and nurses. DESIGN: A postal survey was mailed to 171 GPs and nurses from 12 European countries to obtain information about the usefulness of a guide on healthy diet developed by EUROPREV. RESULTS: The perception of health professionals is that the main source of information on healthy diet for the population was the media. In all, 95% of GPs and nurses reported that the guide was useful; 93, 95, and 82% reported that the concepts were concise, easy to understand, and realistic, respectively. Also, 77% reported that the type of counselling recommended was feasible and could be applied, 94% reported that the implementation measures proposed could be effective and 88% reported that the Traditional Mediterranean Diet Pyramid is useful, but some concerns about the content were mentioned. CONCLUSIONS: GPs and nurses from Europe think that a practical guide on healthy diet developed by EUROPREV could be used to advise patients in primary care, although the Traditional Mediterranean Diet Pyramid should be modified.


Subject(s)
Attitude of Health Personnel , Diet/standards , Nurses/psychology , Physicians, Family/psychology , Primary Health Care , Adult , Education, Nursing , Europe , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Mass Media , Middle Aged , Patient Education as Topic , Physicians, Family/education , Postal Service , Surveys and Questionnaires
2.
J Reprod Med ; 36(10): 717-21, 1991 Oct.
Article in English | MEDLINE | ID: mdl-1683403

ABSTRACT

Cabergoline, a new dopaminergic drug with a long-lasting prolactin inhibitory effect, was investigated at different single oral doses administered to puerperas who wished to inhibit their lactation. The study was prospective, randomized and double blind and included 140 puerperas divided into three groups of 40 women each treated with cabergoline and one group of 20 women who received a placebo. The tested doses were 1.0, 0.75 and 0.5 mg, administered orally within 24 hours after delivery. Prolactin levels were measured immediately before drug administration and then after 6 and 12 hours as well as on days 2, 3, 4, 5 and 14 after delivery. At those times the subjects were examined for milk secretion, breast engorgement, pain and possible side effects. In cases of symptoms requiring treatment, an additional 1 mg of cabergoline was administered. Complete inhibition of lactation up to day 14 was obtained in 90.2% of the women given 1 mg, 62.5% of those given 0.75 mg, 45% of those given 0.5 mg and 20% of those given a placebo. Four subjects experienced mild and transient side effects.


Subject(s)
Dopamine Agents/therapeutic use , Ergolines/therapeutic use , Lactation/drug effects , Postpartum Period , Prolactin/blood , Administration, Oral , Breast/drug effects , Cabergoline , Dopamine Agents/administration & dosage , Dopamine Agents/adverse effects , Double-Blind Method , Drug Tolerance , Ergolines/administration & dosage , Ergolines/adverse effects , Female , Humans , Placebos , Prolactin/metabolism , Prospective Studies , Regression Analysis
3.
J Clin Endocrinol Metab ; 69(4): 725-8, 1989 Oct.
Article in English | MEDLINE | ID: mdl-2570790

ABSTRACT

Cabergoline (CAB) is a new oral dopaminergic compound showing a very long-lasting PRL-lowering activity and reported to be well tolerated. The efficacy and tolerability of chronic treatment with CAB in 30 female hyperprolactinemic patients, aged 18-52 yr (6 microadenomas, 3 macroadenomas, and 21 functional hyperprolactinemias), were studied. In a group of 10 patients who received CAB (0.8 mg once weekly or 0.4 mg twice weekly) for 8 weeks PRL levels normalized while on treatment and remained normal (8 patients) or greatly reduced (1 patient) for 1-2 months after discontinuation of the drug. Twenty-six patients underwent chronic treatment (6-12 months) with an initial dose of 0.5 mg once weekly, subsequently increased to 1-2 mg in 10 patients and decreased in the other 2. Due to severe side-effects CAB was discontinued in 3 patients, in 1, 8, and 12 weeks. A significant reduction of PRL levels was already observed after the first week of treatment (mean +/- SEM basal values, 90.1 +/- 13.3 vs. 29.5 +/- 6.3 micrograms/L; P less than 0.001). Twenty-two patients had normal PRL levels in 1-36 weeks (mean, 6 weeks) with 0.5-2 mg CAB. Twenty-two patients resumed regular menses; 2 patients became pregnant after 3-11 months of treatment. Thirteen patients complained of side-effects (nausea, hypotension, headache, gastric pain, dizziness, and weakness) that disappeared with time in 10 of them. The comparison with a previous bromocriptine treatment regimen in 20 patients had shown that the number of patients requiring discontinuation of the latter drug was significantly higher (7 vs. 3 patients; P less than 0.001). However, 2 patients who needed to discontinue CAB were able to tolerate bromocriptine therapy. A computed tomographic scan performed after 12 months of therapy in 7 patients showed a significant reduction (50%) of the adenoma in 5. In conclusion, our results show that CAB is a well tolerated new dopamine agonist with long-lasting activity that represents an advance in chronic medical treatment of hyperprolactinemic conditions.


Subject(s)
Dopamine Agents/therapeutic use , Ergolines/therapeutic use , Hyperprolactinemia/drug therapy , Adenoma/drug therapy , Adenoma/metabolism , Adenoma/surgery , Adult , Amenorrhea/chemically induced , Bromocriptine/adverse effects , Bromocriptine/therapeutic use , Cabergoline , Ergolines/adverse effects , Female , Humans , Hyperprolactinemia/blood , Hyperprolactinemia/etiology , Pituitary Neoplasms/drug therapy , Pituitary Neoplasms/metabolism , Pituitary Neoplasms/surgery , Prolactin/blood , Prolactin/metabolism
4.
Fertil Steril ; 52(3): 412-5, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2570719

ABSTRACT

Different weekly doses (400 to 3,000 micrograms) of the new, long-acting dopamine agonist Cabergoline (Farmitalia Carlo Erba, Milan, Italy) were given to 11 hyperprolactinemic women with pituitary tumor. Pituitary computerized tomography (CT) scans were performed before the start of treatment and after 3 (n = 5), 6 (n = 3), and 9 (n = 3) months of Cabergoline administration. Plasma prolactin (PRL) was determined in blood samples collected before and at weekly intervals during Cabergoline administration. Cabergoline induced marked inhibition of PRL secretion in conjunction with a CT demonstration of reduction in the pituitary tumor size in all patients. The potent, long-lasting PRL inhibitory effect of Cabergoline and the absence of side effects typical of dopaminergic compounds suggest that the use of this drug is advantageous over others in the medical treatment of hyperprolactinemia.


Subject(s)
Antineoplastic Agents/therapeutic use , Dopamine Agents/therapeutic use , Ergolines/therapeutic use , Pituitary Neoplasms/drug therapy , Prolactinoma/drug therapy , Adolescent , Adult , Antineoplastic Agents/administration & dosage , Cabergoline , Dopamine Agents/administration & dosage , Ergolines/administration & dosage , Female , Humans , Pituitary Neoplasms/diagnostic imaging , Prolactin/blood , Prolactinoma/diagnostic imaging , Time Factors , Tomography, X-Ray Computed
5.
J Clin Endocrinol Metab ; 68(6): 1201-6, 1989 Jun.
Article in English | MEDLINE | ID: mdl-2656736

ABSTRACT

Cabergoline, a new orally active dopaminergic drug with an extremely long-lasting PRL-lowering effect, was given to 48 hyperprolactinemic women for 3-18 months (median, 8 months) at doses varying between 0.2-3 mg/week administered one to three times weekly. Serum PRL levels declined to normal in 41 women, 30 of whom received 0.2-1 mg cabergoline once weekly, 8 received 0.2-0.5 mg twice weekly, and 3 received 0.4-0.6 mg 3 times weekly. Five women had slightly supranormal serum PRL levels while receiving 0.3-0.6 mg once weekly, but the dose was not increased because the lower dose had produced the desired clinical benefit. Two women had 50% reductions in their serum PRL levels, but remained hyperprolactinemic while receiving 2-3 mg cabergoline weekly. Among 30 amenorrheic women, 28 had resumption of menses, the exceptions being 2 hypopituitary women, presumptive evidence of ovulation was available in 21. Marked tumor shrinkage occurred after 3-month treatment in 5 of the 6 women who had macroprolactinomas. Only 4 women had side-effects during the first weeks of treatment, and these vanished despite continued cabergoline administration at the same or reduced, but still effective, doses. In a short term, double blind study, cabergoline at 3 different schedules (0.4 mg twice weekly, 0.2 mg 4 times weekly, and 0.4 mg 3 times weekly for 3 weeks, followed by 0.4 mg twice weekly) or placebo was given to a total of 24 hyperprolactinemic women (6 in each subgroup) for 8 weeks, with weekly evaluation of serum PRL levels and side-effects. All 3 cabergoline schedules, but not placebo, induced significant reductions in serum PRL concentrations during the 8-week treatment period. Mild transient side-effects occurred in 7 drug-treated patients (nausea in 5; dizziness in 3). We conclude that cabergoline is effective treatment for hyperprolactinemia. Its efficacy, tolerability, and long duration of action may make it the drug of choice for patients with hyperprolactinemia.


Subject(s)
Ergolines/therapeutic use , Hyperprolactinemia/drug therapy , Prolactin/blood , Administration, Oral , Adolescent , Adult , Cabergoline , Clinical Trials as Topic , Dose-Response Relationship, Drug , Double-Blind Method , Ergolines/administration & dosage , Female , Humans , Hyperprolactinemia/blood , Middle Aged , Pituitary Neoplasms/diagnostic imaging , Pituitary Neoplasms/drug therapy , Placebos , Prolactinoma/diagnostic imaging , Prolactinoma/drug therapy , Radiography
6.
Clin Endocrinol (Oxf) ; 30(3): 315-21, 1989 Mar.
Article in English | MEDLINE | ID: mdl-2574083

ABSTRACT

It is known that dopaminergic neurotransmission is involved in the control of PRL, TSH and GH secretion. Cabergoline (CAB) is a new ergolinic derivative with a long-acting dopaminergic activity. We evaluated 11 women with pathological hyperprolactinaemia before and during sub-acute CAB treatment (0.8-1.2 mg/p.o.; 8 weeks). Simultaneous administration of TRH (200 micrograms i.v.) and GHRH 1-44 (50 micrograms i.v.) were carried out before and after 4, 8 and 10 week intervals from the beginning of CAB treatment. Basal PRL levels (2453.5 +/- S.E. 444.5 mU/l) were significantly reduced during CAB administration (week 4: 164.5 +/- 66.5 mU/l; week 8: 168.0 +/- 66.5 mU/l; P less than 0.01) and no variations were observed 2 weeks after drug discontinuation (week 10: 210.0 +/- 98.0 mU/l). PRL percentage change after TRH was increased by CAB (P less than 0.05). No variation in basal and TRH-stimulated TSH levels was found during CAB administration. A slight increase in GH basal levels (3.0 +/- 0.6 mU/l) was found after weeks 4 (6.4 +/- 2.0 mU/l) and 10 (5.8 +/- 1.6 mU/l) (P less than 0.05). GH response to GHRH was significantly enhanced (ANOVA: P less than 0.01) during sub-acute CAB treatment. A positive correlation was found between GH secretory area and weeks of CAB therapy (P less than 0.01). Our data show that CAB is very effective in lowering PRL secretion in hyperprolactinaemia, and is able to modify PRL and GH responses after TRH and GHRH. The increasing trend in GH basal and GHRH-stimulated GH levels seems to indicate that CAB can override the central dopaminergic tone which is operative in hyperprolactinaemia.


Subject(s)
Dopamine Agents/therapeutic use , Ergolines/therapeutic use , Hyperprolactinemia/drug therapy , Adult , Cabergoline , Female , Growth Hormone/blood , Growth Hormone-Releasing Hormone/pharmacology , Humans , Hyperprolactinemia/blood , Middle Aged , Prolactin/blood , Stimulation, Chemical , Thyrotropin/blood , Thyrotropin-Releasing Hormone/pharmacology , Time Factors
7.
Int J Androl ; 11(2): 93-100, 1988 Apr.
Article in English | MEDLINE | ID: mdl-3372047

ABSTRACT

Gonadal function was elevated in 80 male heroin and/or methadone addicts by measuring basal plasma levels of follicle stimulating hormone (FSH), luteinizing hormone (LH), prolactin (PRL) and testosterone. In 41 subjects semen analyses were also undertaken. Three groups were distinguished consisting of 15 heroin addicts, 42 undergoing methadone treatment but continuing to take heroin, and 23 taking only methadone. All patients had normal plasma levels of FSH, LH and testosterone. Prolactin levels were normal in all subjects except for the 15 heroin addicts, in whom they were significantly higher than in controls (P less than 0.025). Semen analyses from all of the heroin addicts and from the dual heroin-methadone users were abnormal, whereas only 10 out of 22 (45%) of the methadone takers were pathological. In all cases asthenospermia was one of the abnormalities (100%). Twenty-four per cent also showed teratospermia and hypospermia and 17% showed oligozoospermia. Such seminal pathology, especially of forward motility, even in combination with normal hormone levels, might be an early indication of heroin toxicity to the male reproductive tract.


Subject(s)
Heroin Dependence/physiopathology , Methadone , Opioid-Related Disorders/physiopathology , Testis/physiopathology , Adolescent , Adult , Gonadotropins, Pituitary/blood , Humans , Male , Semen/cytology , Sperm Count/drug effects , Sperm Motility , Testosterone/blood
8.
Zentralbl Gynakol ; 106(24): 1572-81, 1984.
Article in German | MEDLINE | ID: mdl-6532018

ABSTRACT

100 women have been asked using a psychologic open-answer-questionnaire containing items regarding the woman's distinctive features, her pregnancy delivery, puerperium and breastfeeding. Mainly there is a positive relationship to the growing fetus in cases of unwanted pregnancy, too. The highest degree of motivation is reached in the moment of the first contact between mother and newborn.


Subject(s)
Labor, Obstetric , Maternal Behavior , Mother-Child Relations , Pregnancy , Attitude , Breast Feeding , Female , Humans , Infant, Newborn , Patient Education as Topic/methods , Physician-Patient Relations , Social Environment
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