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1.
Akush Ginekol (Sofiia) ; 46(3): 3-7, 2007.
Artigo em Búlgaro | MEDLINE | ID: mdl-18018774

RESUMO

A retrospective study with 79 pregnant women was conducted. All of them were diagnosed as spontaneous abortion. The patients were separated in two group and the women have been treated in two schemes--51%--Utrogestan and 49%--Utrogestan and Profasi. The medication was applied only into the first trimester of the pregnancy. The duration of the therapy was 15.0 +/- 12.34 days. The mean gestational age in this study was 7.6 +/- 3.0 gestational weeks. Women with a first pregnancy and spontaneous abortion were excluded from the study. The number of this hormonal treated pregnancy was 2.84 +/- 1.13. 10.2% of the followed women had 3 and more than 3 miscarriages. The followed group of women was historically and clinically heterogenic. For that reason we think that many other factors could play a role in the optimum outcome of this pregnancy. The criteria for positive result we accepted the vital embryo/fetus on the time of dehospitalization. From these pregnancy only 3 terminated with miscarriage--3.79%. The rest of 96.2% went at home with intact pregnancy. The authors try to find a theoretical support for use of micronized progesterone Utrogestan--there could be some changes in the cellular and humoral immunity at repeated abortions, related to the change of the cytokine production. It could be find an ability to realize a readjustment of the endocrine system of the mother and to control the immune reaction in the fetoplacental unit.


Assuntos
Aborto Habitual/tratamento farmacológico , Gonadotropina Coriônica/uso terapêutico , Progesterona/uso terapêutico , Aborto Habitual/epidemiologia , Aborto Habitual/imunologia , Adulto , Formação de Anticorpos/efeitos dos fármacos , Gonadotropina Coriônica/administração & dosagem , Esquema de Medicação , Combinação de Medicamentos , Feminino , Humanos , Imunidade Celular/efeitos dos fármacos , Gravidez , Resultado da Gravidez/epidemiologia , Primeiro Trimestre da Gravidez , Progesterona/administração & dosagem , Estudos Retrospectivos
2.
Akush Ginekol (Sofiia) ; 43(5): 47-54, 2004.
Artigo em Búlgaro | MEDLINE | ID: mdl-15518286

RESUMO

A case of successful pregnancy outcome is reported in a patient with 3 preceding severe placental abruptions with intrauterine fetal death and caesarean deliveries. In the course of the current pregnancy heterozygosity for R506Q mutation of factor V (Leiden) was diagnosed in 26 weeks of gestation [w.g.] and low molecular weight heparin [LMWH] therapy initiated. Maternal condition was stable until delivery and all laboratory findings were within normal range. The fetus was followed up by ultrasound biometry and Doppler blood flow studies. From 28 w.g. on NST and biophysical profile were included. An emergency caesarean section was performed in 34 w.g. because of contractions not responding to tocolysis. The newborn was in good condition with weight and length corresponding to the 10th centile for gestational age [g.a]. Histologic study of the placenta showed anemic infarctions and recent haemorrhages in the basal and the chorionic plate. The initiation of LMWH therapy in the case reported was late (26 w.g.). By that moment there was already evidence of impaired fetal growth with fetal biometry corresponding to the 10th centile for g.a. After LMWH therapy was started no further slow down of fetal growth was registered. Successful pregnancy outcome may be related not only to LMWH therapy but also to other factors like active fetal monitoring after 28 w.g. and the emergency caesarian delivery immediately after the onset of uterine contractions. Patients with past obstetric history of severe preeclampsia, placental abruption or fetal growth restriction have to be screened for hereditary or acquired thrombophilia. If a thrombophillic state is present early LMWH therapy has to be considered. It is aimed to prevent anaemic placental infarctions and thrombotic complications.


Assuntos
Descolamento Prematuro da Placenta/prevenção & controle , Fator V/genética , Morte Fetal/prevenção & controle , Heparina de Baixo Peso Molecular/uso terapêutico , Descolamento Prematuro da Placenta/genética , Adulto , Cesárea , Feminino , Morte Fetal/genética , Monitorização Fetal , Heparina de Baixo Peso Molecular/administração & dosagem , Heterozigoto , Humanos , Mutação Puntual , Gravidez , Resultado da Gravidez
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