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1.
Fertil Steril ; 96(2): 445-451.e1, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21722894

RESUMO

OBJECTIVE: To investigate whether an insulin sensitizer has any effect on amenorrhea and clinical and biochemical hyperandrogenism in Chinese women with polycystic ovarian syndrome (PCOS). DESIGN: Randomized controlled double-blind trial. SETTING: A tertiary referral center, Hong Kong. PATIENT(S): Chinese women who fulfilled the Rotterdam criteria of PCOS (n = 70). INTERVENTION(S): Rosiglitazone 4 mg daily for the first month followed by 4 mg twice daily for 11 months. MAIN OUTCOME MEASURE(S): Menstrual status as well as clinical and biochemical hyperandrogenism. RESULT(S): There is a significantly higher rate of regular menses among the treatment arm (16 [50.0%] of 32 vs 4 [11.8%] of 34) at 6 months and the improvement appeared to be sustained (10 [41.7%] of 24 vs 6 [20.0%] of 30) at 12 months. There was no change in the acne and hirsutism scores as well as serum T levels in both arms. CONCLUSION(S): We found a possible benefit in menstrual cyclicity but a lack of improvement in hyperandrogenism in our Chinese population. CLINICAL TRIAL REGISTRATION NUMBER: ChiCTR-TRC-09000670 (Chinese Clinical Trial Registry).


Assuntos
Amenorreia/tratamento farmacológico , Hiperandrogenismo/tratamento farmacológico , Hipoglicemiantes/uso terapêutico , Síndrome do Ovário Policístico/tratamento farmacológico , Tiazolidinedionas/uso terapêutico , Adulto , Amenorreia/sangue , Amenorreia/etnologia , Amenorreia/fisiopatologia , Povo Asiático , Distribuição de Qui-Quadrado , Método Duplo-Cego , Feminino , Hong Kong/epidemiologia , Humanos , Hiperandrogenismo/sangue , Hiperandrogenismo/etnologia , Hiperandrogenismo/fisiopatologia , Hipoglicemiantes/efeitos adversos , Ciclo Menstrual/efeitos dos fármacos , Efeito Placebo , Síndrome do Ovário Policístico/sangue , Síndrome do Ovário Policístico/etnologia , Síndrome do Ovário Policístico/fisiopatologia , Rosiglitazona , Testosterona/sangue , Tiazolidinedionas/efeitos adversos , Fatores de Tempo , Resultado do Tratamento , Adulto Jovem
2.
Eur J Obstet Gynecol Reprod Biol ; 125(2): 206-10, 2006 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-16139416

RESUMO

OBJECTIVE: To evaluate the pregnancy outcomes of two policies of timing of induction of labor for post-term pregnancies. STUDY DESIGN: It is a retrospective study in a University obstetric unit from 1997 to 2002. Five thousand eight hundred and ninety-two singleton, cephalic pregnancies with gestational age at delivery at or more than 41 completed weeks were studied. They were divided into two groups. Group A included women who delivered from January 1997 to February 1999 when the policy of the department was to induce labor for post-maturity at 42 weeks of gestation. Group B included those delivered between March 1999 and December 2002 when the timing of induction for post-term was advanced to 41 weeks. The intrapartum characteristics, delivery and perinatal outcomes were analyzed by Student's t-test and Chi-square test for continuous and categorical variables, respectively. RESULTS: Two thousand one hundred and seventy-six women were studied in Group A and 3716 in Group B. Twenty-nine percent of these pregnancies in Group A required induction of labor whereas 20.3% were for post-term. In Group B, 58% of pregnancies had labor induction and 55% for post-maturity. For the pregnancies undergoing induction of labor for post-term, both the duration of labor (P<0.001) and the need of intrapartum epidural analgesia were increased (OR 1.3, 95% CI: 1.0-1.6) in Group B. However, there was no significant difference in the mode of delivery, apgar scores and stillbirths between the two study periods. CONCLUSION: Compared to routine induction at 42 weeks, induction at 41 weeks is associated with a significantly higher risk of use of medical interventions and associated complications, with no observable benefits.


Assuntos
Idade Gestacional , Criança Pós-Termo , Trabalho de Parto Induzido , Feminino , Hong Kong , Humanos , Recém-Nascido , Trabalho de Parto Induzido/métodos , Trabalho de Parto Induzido/estatística & dados numéricos , Gravidez , Estudos Retrospectivos , Resultado do Tratamento
3.
Hum Reprod ; 20(12): 3355-9, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16096322

RESUMO

BACKGROUND: When compared with the conventional surgical evacuation for the treatment of miscarriage, medical evacuation has been largely accepted as an effective and safe management. However, there is a lack of data on the long-term reproductive outcome of these two treatment modalities, which is crucial in patient counselling. The current study evaluates and compares the long-term fertility and pregnancy outcome following these two treatments. METHODS: A cohort of 604 women enrolled in a previous randomized controlled trial comparing medical and surgical evacuation for miscarriage were followed up prospectively by telephone interview at a median of 6 (range 4-9) years using a structured questionnaire. RESULTS: A total of 423 women were contacted and four declined to participate (response rate 69.4%). Of these, 261 women (131 medical and 130 surgical evacuations) had attempted to become pregnant since the miscarriage. There were no differences in their baseline characteristics including age, reproductive and contraceptive history. The natural conception rates were the same (97.7%, P = 0.99) and the cumulative pregnancy rates were similar between groups, being 60 and 80% at 12 and 24 months respectively. The median time-to-pregnancy was 8 months in both groups (P = 0.97) and the subsequent live birth rates (85.2 versus 88.2%, P = 0.72) resulting from the immediate pregnancy following previous treatment were similar. CONCLUSIONS: The long-term conception rate and pregnancy outcome are not different following medical or surgical evacuation for miscarriage. Women should be reassured that their long-term fertility potential will not be compromised after medical treatment.


Assuntos
Aborto Espontâneo/tratamento farmacológico , Aborto Espontâneo/cirurgia , Abortivos não Esteroides/efeitos adversos , Adulto , Estudos de Coortes , Dilatação e Curetagem/efeitos adversos , Feminino , Humanos , Misoprostol/efeitos adversos , Gravidez , Taxa de Gravidez , Inquéritos e Questionários , Telefone , Fatores de Tempo , Resultado do Tratamento
4.
Acta Obstet Gynecol Scand ; 83(4): 319-25, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15005776

RESUMO

Guillain-Barré syndrome (GBS) complicating pregnancy is a rare event. Reports before the mid-1980s suggested that GBS in pregnancy carries a high maternal morbidity and mortality. However, it is uncertain whether availability of active treatment such as plasmapheresis and intravenous immunoglobulin together with advancement in intensive care has improved maternal outcome. This review examines the maternal and fetal outcomes of GBS complicating pregnancy reported in the recent English literature.


Assuntos
Síndrome de Guillain-Barré/terapia , Complicações na Gravidez/terapia , Resultado da Gravidez , Analgesia Obstétrica , Anestesia Obstétrica , Parto Obstétrico , Feminino , Síndrome de Guillain-Barré/diagnóstico , Síndrome de Guillain-Barré/etiologia , Humanos , Gravidez , Complicações na Gravidez/diagnóstico , Complicações na Gravidez/etiologia
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