Ferrazzi Enrico Maria

Prof. Dr. Ferrazzi Enrico Maria

1. Department of Mother, Child and Neonate, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, 20122 Milan MI, Italy
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orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2020 in Ultrasound in Obstetrics & Gynecology
Verified
Journal Article
Closed access
PDF file
CLChristoph Lees
Christoph Lees
TST. Stampalija
T. Stampalija
ABAhmet Alexander Baschat
Ahmet Alexander Baschat
FCF. da Silva Costa
F. da Silva Costa
FMFerrazzi Enrico Maria
Ferrazzi Enrico Maria
JUJ. Unterscheider
J. Unterscheider

10 January 2022 in American Journal of Obstetrics and Gynecology
Verified
Journal Article
Closed access
CLChristoph Lees
Christoph Lees
RRRoberto Romero
Roberto Romero
TSTamara Stampalija
Tamara Stampalija
ADAndrea Dall'Asta
Andrea Dall'Asta
GDGreggory R. DeVore
Greggory R. DeVore
KHKurt Hecher
Kurt Hecher

1 October 2020 in European Journal of Obstetrics & Gynecology and Reproductive Biology
Verified
Journal Article
Closed access
FMFerrazzi Enrico Maria
Ferrazzi Enrico Maria
GTGiulia Tiso
Giulia Tiso
DMDaniela Di Martino
Daniela Di Martino

1 January 2018 in American Journal of Obstetrics and Gynecology
Verified
Journal Article
Closed access
FMFerrazzi Enrico Maria
Ferrazzi Enrico Maria
TSTamara Stampalija
Tamara Stampalija
Lorenzo MonastaLorenzo Monasta
Lorenzo Monasta
DMDaniela Di Martino
Daniela Di Martino
SVSharona Vonck
Sharona Vonck
WGWilfried Gyselaers
Wilfried Gyselaers

9 June 2013 in BioMed Research International
Verified
Journal Article
Open access
PDF file
VFVassilios Fanos
Vassilios Fanos
Luigi AtzoriLuigi Atzori
Luigi Atzori
KMKarina Makarenko
Karina Makarenko
GMGian Benedetto Melis
Gian Benedetto Melis
FMFerrazzi Enrico Maria
Ferrazzi Enrico Maria
Metabolomics in maternal-fetal medicine is still an “embryonic” science. However, there is already an increasing interest in metabolome of normal and complicated pregnancies, and neonatal outcomes. Tissues used for metabolomics interrogations of pregnant women, fetuses and newborns are amniotic fluid, blood, plasma, cord blood, placenta, urine, and vaginal secretions. All published papers highlight the strong correlation between biomarkers found in these tissues and fetal malformations, preterm delivery, premature rupture of membranes, gestational diabetes mellitus, preeclampsia, neonatal asphyxia, and hypoxic-ischemic encephalopathy. The aim of this review is to summarize and comment on original data available in relevant published works in order to emphasize the clinical potential of metabolomics in obstetrics in the immediate future.

17 June 2020 in Ultrasound in Obstetrics & Gynecology
Verified
Journal Article
Open access
PDF file
TSTamara Stampalija
Tamara Stampalija
JTJ. Thornton
J. Thornton
NMN. Marlow
N. Marlow
RNR. Napolitano
R. Napolitano
ABA. Bhide
A. Bhide
KMK. Myklestad
K. Myklestad
Objectives: To explore the association between fetal umbilical and middle cerebral artery (MCA) Doppler abnormalities and outcome in late preterm pregnancies at risk of fetal growth restriction.Methods: This was a prospective cohort study of singleton pregnancies at risk of fetal growth restriction at 32 + 0 to 36 + 6 weeks of gestation, enrolled in 33 European centers between 2017 and 2018, in which umbilical and fetal MCA Doppler velocimetry was performed. Pregnancies were considered at risk of fetal growth restriction if they had estimated fetal weight and/or abdominal circumference (AC) < 10th percentile, abnormal arterial Doppler and/or a fall in AC growth velocity of more than 40 percentile points from the 20‐week scan. Composite adverse outcome comprised both immediate adverse birth outcome and major neonatal morbidity. Using a range of cut‐off values, the association of MCA pulsatility index and umbilicocerebral ratio (UCR) with composite adverse outcome was explored.Results: The study population comprised 856 women. There were two (0.2%) intrauterine deaths. Median gestational age at delivery was 38 (interquartile range (IQR), 37–39) weeks and birth weight was 2478 (IQR, 2140–2790) g. Compared with infants with normal outcome, those with composite adverse outcome (n = 93; 11%) were delivered at an earlier gestational age (36 vs 38 weeks) and had a lower birth weight (1900 vs 2540 g). The first Doppler observation of MCA pulsatility index < 5th percentile and UCR Z‐score above gestational‐age‐specific thresholds (1.5 at 32–33 weeks and 1.0 at 34–36 weeks) had the highest relative risks (RR) for composite adverse outcome (RR 2.2 (95% CI, 1.5–3.2) and RR 2.0 (95% CI, 1.4–3.0), respectively). After adjustment for confounders, the association between UCR Z‐score and composite adverse outcome remained significant, although gestational age at delivery and birth‐weight Z‐score had a stronger association.Conclusion: In this prospective multicenter study, signs of cerebral blood flow redistribution were found to be associated with adverse outcome in late preterm singleton pregnancies at risk of fetal growth restriction. Whether cerebral redistribution is a marker describing the severity of fetal growth restriction or an independent risk factor for adverse outcome remains unclear, and whether it is useful for clinical management can be answered only in a randomized trial. © 2020 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of the International Society of Ultrasound in Obstetrics and Gynecology.