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1.
Arch Gynecol Obstet ; 277(1): 25-30, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17618446

RESUMO

OBJECTIVE: Women with polycystic ovary syndrome (PCOS) have multiple risk factors for cardiovascular disease. The cardiovascular risk marker homocysteine (Hcy) is elevated in women with PCOS. This prospective study investigated the effect of oral contraceptives containing ethinyl estradiol-cyproterone acetate (EE-CA) on serum Hcy levels in women with PCOS. STUDY DESIGN: A total of 30 women with PCOS were enrolled in this prospective study. The diagnosis of PCOS was made according to the criteria of the Rotterdam PCOS consensus workshop group. All women took oral contraceptives containing EE/CA (35 microg/2 mg) for 3 months. Serum samples for Hcy, lipid profile and hormones were obtained during the early follicular phase (days 3-5) of the spontaneous or progestin-induced bleeding at baseline, and after the third treatment cycle. RESULTS: Three months of EE-CA therapy significantly decreased the Hcy levels from 55.97 +/- 16.04 to 54.03 +/- 16.15 (P = 0.01). A significant correlation was observed between the Hcy and total and free testosterone levels (r = 0.44, P = 0.015 and r = 0.46, P = 0.001 respectively). CONCLUSIONS: Although the decrease in Hcy levels with EE-CA therapy was statistically significant, further studies are necessary to determine the clinical benefit of this treatment.


Assuntos
Antagonistas de Androgênios/uso terapêutico , Acetato de Ciproterona/uso terapêutico , Estrogênios/uso terapêutico , Etinilestradiol/uso terapêutico , Homocisteína/sangue , Síndrome do Ovário Policístico/tratamento farmacológico , Adulto , Anticoncepcionais Orais Hormonais/uso terapêutico , Combinação de Medicamentos , Feminino , Fase Folicular , Humanos , Lipídeos/sangue , Obesidade/sangue , Síndrome do Ovário Policístico/sangue , Estudos Prospectivos , Testosterona/sangue
2.
Aust N Z J Obstet Gynaecol ; 47(5): 410-4, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17877601

RESUMO

BACKGROUND: Misoprostol has been shown to increase colonic activity and decrease colonic transit time in chronic constipation patients. AIMS: The aim of this prospective, randomised, double-blind study was to examine the effectiveness of rectally administered misoprostol on inducing intestinal motility after gynaecological surgery. METHODS: Eighty women who underwent hysterectomy were divided randomly into three groups. Group A received misoprostol 200 microg rectally while group B received 400 microg rectal misoprostol after surgery before leaving the operating room. Patients in group C received no drugs. Bowel sounds in four quadrants were checked every hour and possible side-effects of misoprostol like nausea, vomiting, and distension were evaluated. The time interval between surgery and flatus pass and the need of analgesics were noted. Statistical analyses were done with Mann-Whitney U-test and chi2 tests where available. RESULTS: The time between surgery and presence of bowel sounds in four quadrants were similar in all groups (2.7 +/- 1.6, 2.9 +/- 1.2, 2.8 +/- 1.3 h, for groups A, B, and C, respectively). No difference was observed in flatus pass time. The incidence of nausea was significantly increased in group B compared to controls (P < 0.01). Additional analgesic need was significantly higher in groups A and B when compared to controls (P < 0.05 and P < 0.01, for groups A and B, respectively). CONCLUSION: Rectally administered misoprostol does not improve intestinal motility in the early postoperative period and thus, it is not effective in providing early oral food intake. On the contrary, it causes distention that requires additional analgesics and vomiting that naturally limits oral diet intake.


Assuntos
Motilidade Gastrointestinal/efeitos dos fármacos , Histerectomia/reabilitação , Misoprostol/farmacologia , Cuidados Pós-Operatórios , Administração Retal , Adulto , Método Duplo-Cego , Ingestão de Alimentos , Feminino , Humanos , Tempo de Internação , Pessoa de Meia-Idade , Misoprostol/administração & dosagem , Estudos Prospectivos , Fatores de Tempo
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