Prenatal diagnosis and management of nonimmune hydrops fetalis

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Abstract

We examined the incidence, aetiological factors and outcome in 40 cases of nonimmune hydrops fetalis (NIH) and suggest a rational approach to management. The incidence of NIH was 1 in 830 deliveries during the last 10-year period. In spite of extensive antenatal and postnatal investigation no cause could be established in 14 (35%) cases. A probable aetiological factor was found in 65% of cases. These included viral infection (7), cardiovascular (6), twin-to-twin transfusion (3), chromosomal abnormality (3), other malformation syndromes (4), renal dysplasia (1), laryngeal atresia (1) and severe fetomaternal haemorrhage (1). Five of the 40 fetuses survived, 2 treated antenatally for tachyarrhythmia, 2 had spontaneous resolution and the fifth fetus had repeated intrauterine transfusions because of human parvovirus B19-induced anaemia. After diagnosis of nonimmune hydrops fetalis, early referral to a tertiary centre is to be encouraged for investigation and provision of intensive perinatal care. Investigation allows parents to be counselled appropriately that the mortality is no longer 100% and a steadily growing number may be amenable to some form of fetal therapy.

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APA

Swain, S., Cameron, A. D., McNay, M. B., & Howatson, A. G. (1999). Prenatal diagnosis and management of nonimmune hydrops fetalis. Australian and New Zealand Journal of Obstetrics and Gynaecology. Royal Australian and New Zealand College of Obstetricians and Gynaecologists. https://doi.org/10.1111/j.1479-828X.1999.tb03398.x

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