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1.
JBRA Assist Reprod ; 28(1): 21-26, 2024 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-38224580

RESUMO

OBJECTIVE: hCG is commonly used as an ovulation trigger in IVF. Its usage is associated with OHSS. GnRH agonist is an alternative to hCG and is associated with reduced incidence of OHSS. This study compared the cycle outcomes of GnRH agonists with hCG as an ovulation trigger in IVF cycles. METHODS: The medical notes of 209 IVF cycles receiving GnRH agonist and hCG as ovulation trigger over 18 months were reviewed in this retrospective study. The number and quality of mature oocytes, the number and quality of embryos, pregnancy rates, and outcomes were compared using Independent T-test or One-way ANOVA for normal distribution. The Mann-Whitney test or Kruskal-Wallis test was used for not normally distributed. p<0.05 was considered statistically significant. RESULTS: The cycle outcomes of 107 GnRH agonist-trigger and 102 hCG-trigger were compared. The MII oocytes retrieved and 2PN count was significantly higher in the GnRH agonist trigger group (p<0.001). Clinical pregnancy rate and ongoing pregnancy were higher in the GnRH agonist trigger group but were not statistically significant. The GnRH agonist trigger group was associated with low OHSS than the hCG trigger group (n=2(1.9%) and n=12(11.8%) respectively, p=0.004). CONCLUSION: GnRH agonist trigger is an option as a final maturation trigger in high-responder women undergoing IVF or ICSI cycles.


Assuntos
Síndrome de Hiperestimulação Ovariana , Feminino , Humanos , Gravidez , Gonadotropina Coriônica/uso terapêutico , Fertilização , Fertilização in vitro , Hormônio Liberador de Gonadotropina , Malásia/epidemiologia , Oócitos , Síndrome de Hiperestimulação Ovariana/epidemiologia , Síndrome de Hiperestimulação Ovariana/prevenção & controle , Ovulação , Indução da Ovulação , Estudos Retrospectivos , Centros de Atenção Terciária
2.
BMJ Case Rep ; 15(2)2022 Feb 08.
Artigo em Inglês | MEDLINE | ID: mdl-35135794

RESUMO

A young adult patient with 46XX congenital adrenal hyperplasia (CAH) presented with recurrent painful haematuria. CAH was diagnosed at birth following ambiguous genitalia. Hormonal treatment was started, female gender was assigned and feminising genitoplasty was planned, however the patient was lost to follow-up. Gender dysphoria started to occur during childhood which prompted the family to raise the patient as a boy. He eventually identified himself as a male. Examination revealed a male phenotype with severely virilised genitalia. Imaging studies confirmed the presence of uterus with low confluent urogenital sinus. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed, and the troublesome symptoms were cured.


Assuntos
Hiperplasia Suprarrenal Congênita , Transtornos do Desenvolvimento Sexual , Hiperplasia Suprarrenal Congênita/complicações , Hiperplasia Suprarrenal Congênita/cirurgia , Transtornos do Desenvolvimento Sexual/complicações , Transtornos do Desenvolvimento Sexual/cirurgia , Feminino , Genitália , Genitália Feminina , Humanos , Histerectomia , Masculino
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