RESUMEN
Despite generalisation of anti-D immunoprophylaxis, RhD allo-immunisation still remains the major cause of severe haemolytic disease of the fetus and of the newborn (HDFN). The routine follow up of pregnant women comprises: the ABO/D, Rh/Kell red cells typing and the search for irregular antibodies. In case of anti-D immunisation, the paternal Rh phenotype, when known, provides useful information regarding the probability for the fetus to have inherited the D antigen and thereby to be exposed to the risk of HDFN. The antibody titre, which is predictive of possible in vivo haemolysis, must be interpreted in the light of the previous obstetric history, and can lead to the decision of invasive amniocentesis. Then the measurement of the optical density (deltaOD450 nm) and the fetal RhD typing can be realised on amniotic fluid. New molecular techniques make it possible now to demonstrate the presence of fetal DNA in maternal plasma. These methods lying on non invasive procedures could advantageously be applied to the genotyping of fetal RHD during pregnancy. The present paper aims to discuss the predictive values of RHD fetal genotype in maternal plasma of RhD negative mothers. The ante-partum management of immunised pregnant women is reviewed in the light of this new molecular approach combined to Doppler ultrasonography of the fetal middle cerebral artery. This non invasive method for determining fetal RHD genotype could be systematically proposed to all RhD negative pregnant women for a better targeted prenatal follow-up and an increased efficacy of RhD prophylaxis.
Asunto(s)
Diagnóstico Prenatal/métodos , Isoinmunización Rh/diagnóstico , Algoritmos , Femenino , Humanos , EmbarazoRESUMEN
Nowadays, the management of ectopic pregnancy should be codified as often as possible. Two types of treatment are possible. One surgical and the other medical. Our study is concerned with a series of 97 patients hospitalized for suspicion of ectopic pregnancy for whom the risk factors and treatment were analyzed. Our conclusion is that the medical treatment should be more frequently proposed and surgery should prefer the conservative treatment whenever it is still possible.
Asunto(s)
Embarazo Ectópico/terapia , Abortivos no Esteroideos , Gonadotropina Coriónica/análisis , Toma de Decisiones , Dilatación y Legrado Uterino , Trompas Uterinas/cirugía , Femenino , Humanos , Dispositivos Intrauterinos , Laparoscopía , Metotrexato/uso terapéutico , Embarazo , Embarazo Ectópico/tratamiento farmacológico , Embarazo Ectópico/cirugía , Embarazo Tubario/tratamiento farmacológico , Embarazo Tubario/cirugía , Embarazo Tubario/terapia , Recurrencia , Estudios Retrospectivos , Factores de Riesgo , Fumar/efectos adversos , Ultrasonografía PrenatalRESUMEN
Since the beginning of RHD genotyping in maternal plasma, no Rh D positive baby was diagnosed RHD negative in our institution. Genotyping from circulating DNA in maternal plasma is as efficient as genotyping on amniocyts but without the associated risks. We propose a prophylactic injection based on fetal genotyping RHD in maternal blood with 300 microg anti-D immunoglobulin at 28 weeks of amenhorrea in all of Rh D negative pregnant women whitch fetuses positive RHD.
Asunto(s)
Sangre Fetal/química , Embarazo/sangre , Atención Prenatal , Sistema del Grupo Sanguíneo Rh-Hr/genética , ADN/sangre , Exones/genética , Femenino , Estudios de Seguimiento , Genotipo , Humanos , Factores Inmunológicos/uso terapéutico , Recién Nacido , Masculino , Valor Predictivo de las Pruebas , Isoinmunización Rh/prevención & control , Sistema del Grupo Sanguíneo Rh-Hr/análisis , Globulina Inmune rho(D)/uso terapéutico , Sensibilidad y EspecificidadRESUMEN
OBJECTIVES: To evaluate the predictive value of RHD fetal genotype in maternal plasma of Rh D negative mothers after 10 weeks of gestation in a clinical use. MATERIAL AND METHOD: Prospective, comparative study between fetal RHD genotyping in maternal plasma, with amplification of exons 4,5,10 of the RHD gene, by real-time multiplex PCR, and Rh D serology at birth, in 218 pregnancy and their 223 babies, between November 2002 and 2004. RESULTS: Combining the amplification of three exons, the concordance rate of fetal Rh D genotyping in maternal plasma and baby phenotyping at delivery was 100%. Four women whose the babies were Rh D negative were positive for RHD exon 10 during pregnancy. This positivity was, in three cases, correlated with the presence of RHDpsi pseudogene and in last case, with a haplotype Cdes (r's). RHD genotyping was performed for five twin pregnancies. CONCLUSION: Multiplex PCR using maternal plasma provides perfect prenatal prediction of fetal RHD gene. These results confirm that this non invasive procedure is the preferred method for assessing Rh D fetal status in Rh negative mothers. Using this method for two years in routine practice has led us to modify our management scheme for sensitized Rh D-negative pregnant women.