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DOI 10.1159/000086809

Медицинская библиотека · Fetal diagnosis and therapy · 2005

Reassuring fetal middle cerebral artery doppler velocimetry in alloimmunised pregnancies: neonatal outcomes without invasive procedures.

Abdel-Fattah Sherif A, Shefras Julia, Kyle Phillipa M, Cairns Pamela, Hunter Alyson, Soothill Peter W

Клиническое исследованиеСтатьяПеревод в очереди

Аннотация

OBJECTIVE

To assess the neonatal outcome in red blood cell alloimmunised pregnancies at increased risk of fetal anaemia where invasive testing was avoided based on reassuring middle cerebral artery (MCA) Doppler velocity results.

METHODS

We included 28 alloimmunised pregnant women at significant risk of fetal or neonatal anaemia who did not have invasive testing because of reassuring MCA Doppler velocimetry. Women requiring invasive testing or intrauterine transfusion were excluded. Outcome measures were admission to neonatal intensive care unit, cord haemoglobin and bilirubin levels and neonatal therapy.

RESULTS

Ten neonates (36%) were anaemic at birth while 18 (64%) had normal haemoglobin. Seven neonates (25%) did not require any form of neonatal therapy, 10 (36%) had phototherapy only, 7 (25%) required exchange transfusions and 4 (14%) top-up transfusions. There were no treatment-related complications. Mean cord haemoglobin was 13.9 g/dl (range 7-18.9) and mean bilirubin was 84.1 micromol/l (range 29-192).

CONCLUSION

Avoiding invasive procedures in pregnancies at risk of fetal anaemia by relying on reassuring MCA Doppler velocimetry did not result in life-threatening fetal or neonatal morbidities. The extent of neonatal therapy was acceptable. The routine use of this test can lead to less unnecessary invasive procedures in at-risk fetuses.

Для цитирования: Abdel-Fattah Sherif A, Shefras Julia, Kyle Phillipa M, Cairns Pamela, Hunter Alyson, Soothill Peter W. Reassuring fetal middle cerebral artery doppler velocimetry in alloimmunised pregnancies: neonatal outcomes without invasive procedures.. Fetal diagnosis and therapy. 2005. DOI: 10.1159/000086809.

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