Prediction of the rate of decline in fetal hemoglobin levels between first and second transfusions in red cell alloimmune disease


Autoria(s): Nishie, Estela Naomi; Liao, Adolfo Wenjaw; Brizot, Maria de Loudes; Assuncao, Renata A.; Zugaib, Marcelo
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Objective To determine variables that predict the rate of decline in fetal hemoglobin levels in alloimmune disease. Method Retrospective review of singleton pregnancies that underwent first and second intrauterine transfusions for treatment of fetal anemia because of maternal Rh alloimmunization in a tertiary referral center. Results Forty-one first intrauterine transfusions were performed at 26.1?weeks (standard deviation, SD, 4.6), mean volume of blood transfused was 44.4?mL (SD 23.5) and estimated feto-placental volume expansion was 51.3% (SD 14.5%). Between first and second transfusion, hemoglobin levels reduced on average 0.40?g/dl/day (SD 0.25). Stepwise multiple regression analysis demonstrated that this rate significantly correlated with hemoglobin levels after the first transfusion, the interval between both procedures, and middle cerebral artery systolic velocity before the second transfusion. Conclusion The rate of decline in fetal hemoglobin levels between first and second transfusions in alloimmune disease can be predicted by a combination of hemoglobin levels after the first transfusion, interval between both procedures, and middle cerebral artery systolic velocity before the second transfusion. (C) 2012 John Wiley & Sons, Ltd.

Identificador

PRENATAL DIAGNOSIS, HOBOKEN, v. 32, n. 12, supl. 1, Part 6, pp. 1123-1126, DEC, 2012

0197-3851

http://www.producao.usp.br/handle/BDPI/41574

10.1002/pd.3966

http://dx.doi.org/10.1002/pd.3966

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

PRENATAL DIAGNOSIS

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #PEAK-SYSTOLIC-VELOCITY #PREVIOUS INTRAUTERINE TRANSFUSIONS #DOPPLER ULTRASOUND #ANEMIA #MANAGEMENT #DIAGNOSIS #FETUS #GENETICS & HEREDITY #OBSTETRICS & GYNECOLOGY
Tipo

article

original article

publishedVersion