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2.
Twin Res Hum Genet ; 9(2): 279-84, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16611499

RESUMO

Pregnancy outcome and characteristics of women who conceive following subfertility treatment remains a subject of great interest. We analyzed these variables among 199 women who delivered a registerable twin birth compared with 1773 women who delivered a naturally conceived twin birth in a population-based obstetric cohort drawn from around Oxford, England. Treatment was restricted to conceptions involving simple ovulation induction only. Treated mothers were of significantly higher social class and older, more likely to deliver girls and to be delivered by cesarean section, and significantly less likely to be smokers at the time of antenatal booking and to have delivered previous pregnancies. Pregnancy outcome was similar between the two groups for most measures, with the exception of birthweight which was lower in treated twins, though not significantly so. Overall the results are reassuring with respect to outcome in twin pregnancies following simple ovulation induction.


Assuntos
Infertilidade Feminina/terapia , Indução da Ovulação , Resultado da Gravidez , Gravidez , Adulto , Fatores Etários , Peso ao Nascer , Feminino , Fertilização , Humanos , Infertilidade Feminina/epidemiologia , Masculino , Resultado da Gravidez/epidemiologia , Fatores Socioeconômicos
4.
BMJ ; 325(7358): 239, 2002 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-12153918

RESUMO

OBJECTIVE: To determine effects of five years of treatment with an oral continuous combined regimen of 2 mg 17beta-oestradiol and 1 mg norethisterone acetate on endometrial histology in postmenopausal women. DESIGN: Follow up study in postmenopausal women. SETTING: 31 menopause clinics in the United Kingdom. PARTICIPANTS: 534 postmenopausal women, all with an intact uterus, who had completed nine months of treatment with oral continuous combined 2 mg 17beta-oestradiol and 1 mg norethisterone acetate agreed to take part in a long term follow up study. Women were assigned to different groups on the basis of the treatment status immediately before entering the original study: 360 women had taken sequential oestrogen-progestogen hormone replacement therapy, 164 had taken no hormone replacement therapy, and 10 had taken unopposed oestrogen therapy. METHODS: Endometrial aspiration specimens were taken before the women started the continuous combined regimen, after 9 and 24-36 months, and at the end of the five year treatment period or on withdrawal from the study. MAIN OUTCOME MEASURE: Results of endometrial histology. RESULTS: The duration of treatment with continuous combined hormone replacement therapy was 4.4 (range 1.1-5.9) years. Data on endometrial specimens were available for 526 women after nine months of treatment, 465 women after 24-36 months of treatment, and 398 women who completed the five years treatment (345 women) or were withdrawn between the two latter visits for biopsies (53 women). No cases of endometrial hyperplasia or malignancy were detected at biopsy; 69% of women had an endometrium classified as atrophic or unassessable on completion of the study or withdrawal from it. Before the continuous combined therapy was started, complex hyperplasia was detected in 21 women who had taken sequential hormone replacement therapy before the study and in one who had taken unopposed oestrogen. All of these women had normal results on histological examination of endometrial tissue after nine months of treatment with continuous combined hormone replacement therapy, and hyperplasia did not recur after up to five years of treatment. CONCLUSIONS: Long term treatment (for up to five years) with continuous combined hormone replacement therapy containing oestradiol 2 mg and norethisterone 1 mg daily was associated with neither endometrial hyperplasia nor malignancy. In women who had complex hyperplasia during previous sequential or unopposed regimens, the endometrium returned to normal during treatment with continuous combined hormone replacement therapy. These findings provide reassurance about the long term safety of this continuous combined regimen in terms of the endometrium.


Assuntos
Anticoncepcionais Orais Combinados/efeitos adversos , Hiperplasia Endometrial/induzido quimicamente , Estradiol/efeitos adversos , Terapia de Reposição Hormonal/efeitos adversos , Noretindrona/análogos & derivados , Noretindrona/efeitos adversos , Administração Oral , Adulto , Idoso , Anticoncepcionais Orais Combinados/administração & dosagem , Hiperplasia Endometrial/patologia , Estradiol/administração & dosagem , Feminino , Seguimentos , Humanos , Assistência de Longa Duração , Pessoa de Meia-Idade , Noretindrona/administração & dosagem , Acetato de Noretindrona , Pós-Menopausa , Estudos Prospectivos
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