Objective: To describe the incidence, clinical features and perinatal outcome of late onset growth restriction (FGR) associated with genetic syndromes or aneuploidy, structural malformation, or congenital infection. Methods: Retrospective multicenter cohort study conducted at four tertiary maternity hospitals in Italy. We included singleton pregnancies between 32+0 and 36+6 weeks of gestation with either abdominal circumference or estimated fetal weight <10 percentile for gestational age or a reduction by over 50 percentiles of abdominal circumference from an ultrasound scan performed between 18 and 32 weeks of gestation. The study group included pregnancies where FGR was associated with a genetic syndrome or aneuploidy, structural malformation, or congenital infection, i.e. anomalous late-onset FGR; the control group consisted of pregnancies with structurally and genetically normal late-onset FGR. Composite adverse perinatal outcome was defined by the presence of any among stillbirth, Apgar score <7 at 5 minutes, NICU admission, need for respiratory support at birth, neonatal jaundice and neonatal hypoglycemia. Results: Overall, 1246 pregnancies complicated by late-onset FGR were included, of which 120 (9.6%) were allocated to the anomalous late-onset FGR group. Of these, 11 (0.9%) had a genetic syndrome or aneuploidy, 105 (8.4%) isolated structural malformation, and 4 (0.3%) congenital infection. The most frequent structural defects associated with late-onset anomalous FGR were genitourinary malformations (28/105, 26.7%), and skeletal anomalies (21/105, 20%). Compared to the non-anomalous group, anomalous late onset FGR fetuses were associated with an increased incidence of composite adverse perinatal outcome (58.3% vs 35.9%; p<0.01). Anomalous late-onset FGR newborns showed a higher frequency of need for respiratory support at birth (25.8% vs 9.0%; p<0.001), intubation (10.0% vs 1.1%; p<0.01), intensive care unit (NICU) admission (43.3% vs 22.2% p<0.01) and longer length of hospital stay (24 (4-250) days vs 11 (2-59) days, p<0.01). Conclusions: Most pregnancies complicated by anomalous late-onset FGR fetuses are associated with structural malformations. Anomalous late-onset FGR fetuses are associated with an increased incidence of complications at birth and NICU admission and a longer length of hospital stay compared to isolated late-onset FGR fetuses. This article is protected by copyright. All rights reserved.

Dall'Asta, A., Stampalija, T., Mecacci, F., Ramirez Zegarra, R., Sorrentino, S., Minopoli, M., et al. (2022). Incidence, clinical features and perinatal outcome in anomalous fetuses with late-onset growth restriction: cohort study. ULTRASOUND IN OBSTETRICS & GYNECOLOGY [10.1002/uog.24961].

Incidence, clinical features and perinatal outcome in anomalous fetuses with late-onset growth restriction: cohort study

Rizzo, G;
2022-05-30

Abstract

Objective: To describe the incidence, clinical features and perinatal outcome of late onset growth restriction (FGR) associated with genetic syndromes or aneuploidy, structural malformation, or congenital infection. Methods: Retrospective multicenter cohort study conducted at four tertiary maternity hospitals in Italy. We included singleton pregnancies between 32+0 and 36+6 weeks of gestation with either abdominal circumference or estimated fetal weight <10 percentile for gestational age or a reduction by over 50 percentiles of abdominal circumference from an ultrasound scan performed between 18 and 32 weeks of gestation. The study group included pregnancies where FGR was associated with a genetic syndrome or aneuploidy, structural malformation, or congenital infection, i.e. anomalous late-onset FGR; the control group consisted of pregnancies with structurally and genetically normal late-onset FGR. Composite adverse perinatal outcome was defined by the presence of any among stillbirth, Apgar score <7 at 5 minutes, NICU admission, need for respiratory support at birth, neonatal jaundice and neonatal hypoglycemia. Results: Overall, 1246 pregnancies complicated by late-onset FGR were included, of which 120 (9.6%) were allocated to the anomalous late-onset FGR group. Of these, 11 (0.9%) had a genetic syndrome or aneuploidy, 105 (8.4%) isolated structural malformation, and 4 (0.3%) congenital infection. The most frequent structural defects associated with late-onset anomalous FGR were genitourinary malformations (28/105, 26.7%), and skeletal anomalies (21/105, 20%). Compared to the non-anomalous group, anomalous late onset FGR fetuses were associated with an increased incidence of composite adverse perinatal outcome (58.3% vs 35.9%; p<0.01). Anomalous late-onset FGR newborns showed a higher frequency of need for respiratory support at birth (25.8% vs 9.0%; p<0.001), intubation (10.0% vs 1.1%; p<0.01), intensive care unit (NICU) admission (43.3% vs 22.2% p<0.01) and longer length of hospital stay (24 (4-250) days vs 11 (2-59) days, p<0.01). Conclusions: Most pregnancies complicated by anomalous late-onset FGR fetuses are associated with structural malformations. Anomalous late-onset FGR fetuses are associated with an increased incidence of complications at birth and NICU admission and a longer length of hospital stay compared to isolated late-onset FGR fetuses. This article is protected by copyright. All rights reserved.
30-mag-2022
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/40 - GINECOLOGIA E OSTETRICIA
English
CGH-array
aneuploidy
congenital malformation
fetal growth restriction
perinatal outcome
respiratory complication
Dall'Asta, A., Stampalija, T., Mecacci, F., Ramirez Zegarra, R., Sorrentino, S., Minopoli, M., et al. (2022). Incidence, clinical features and perinatal outcome in anomalous fetuses with late-onset growth restriction: cohort study. ULTRASOUND IN OBSTETRICS & GYNECOLOGY [10.1002/uog.24961].
Dall'Asta, A; Stampalija, T; Mecacci, F; Ramirez Zegarra, R; Sorrentino, S; Minopoli, M; Ottaviani, C; Fantasia, I; Barbieri, M; Lisi, F; Simeone, S; Castellani, R; Fichera, A; Rizzo, G; Prefumo, F; Frusca, T; Ghi, T
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/301153
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