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Short-term outcome of periviable small-for-gestational-age babies: is our counseling up to date?
A R Lawin-O'Brien1, A Dall'Asta1,2, C Knight3
1Centre for Fetal Care, Queen Charlotte's and Chelsea Hospital, Imperial College Healthcare, London, UK.
Insights
Most periviable small-for-gestational-age (SGA) fetuses are caused by placental issues. Outcomes for these fetuses are better than often assumed, with survival linked to delivery timing.
Area of Science:
- Perinatal medicine
- Fetal development
- Neonatal outcomes
Background:
- Limited data exists for counseling and managing periviable small-for-gestational-age (SGA) fetuses.
- Understanding the causes of SGA is crucial for predicting outcomes.
Purpose of the Study:
- To investigate the short-term outcomes of periviable SGA fetuses.
- To determine the relationship between SGA causes and fetal outcomes.
Main Methods:
- Retrospective study of 245 viable singleton pregnancies with severely small fetuses (abdominal circumference ≤ 3rd percentile) between 22 and 25 weeks' gestation.
- Data included fetal biometry, placental anomalies, Doppler studies, and neonatal outcomes.
- Cases were classified by suspected cause: uteroplacental insufficiency, placental damage, viral infection, or unclassified.
Main Results:
- 82% of SGA cases were attributed to uteroplacental causes.
- Overall survival to the neonatal period was 41%; 36% had in-utero demise, 9% died neonatally, and 14% were terminated.
- The interval from diagnosis to delivery was longer for survivors (8.1 weeks) compared to those who died neonatally (4.5 weeks).
Conclusions:
- Nearly 90% of periviable SGA cases stem from uteroplacental insufficiency or intraplacental damage.
- Fetal survival is associated with gestational age at delivery.
- Outcomes for periviable SGA fetuses can be more favorable than anticipated, with some reaching term.
Objective:
There are limited data for counseling on and management of periviable small-for-gestational-age (SGA) fetuses. We therefore aimed to investigate the short-term outcome of periviable SGA fetuses in relation to the likely underlying cause.
Methods:
This was a retrospective study of data from three London tertiary fetal medicine centers obtained between 2000 and 2015. We included viable singleton pregnancies with a severely small fetus, defined as those with an abdominal circumference ≤ 3rd percentile, identified between 22 + 0 and 25 + 6 weeks' gestation. Data obtained included fetal biometry, presence of placental anomalies, uterine and fetal Doppler and neonatal outcome. We excluded cases with structural abnormalities, proven or suspected abnormal karyotype or genetic syndromes. Cases were classified according to the suspected underlying cause of the small fetal size into one of the following categories: uteroplacental insufficiency, evidence of placental damage with normal uterine artery Doppler, viral infection, or unclassied.
Results:
There were 245 cases included in the study. Of these, at diagnosis of SGA, 201 (82%) were categorized as uteroplacental cause, 13 (5%) as suspected placental cause, one (0.4%) as suspected viral cause and 30 (12%) could not be assigned to any of these categories. Overall, 101 (41%) cases survived the neonatal period; 89 (36%) underwent in-utero fetal demise, 22 (9%) died neonatally and 33 (14%) pregnancies were terminated. The diagnosis-to-delivery interval was 8.1 weeks in those that survived and 4.5 weeks in those that died neonatally.
Conclusions:
Almost 90% of periviable SGA cases are associated with uteroplacental insufficiency or intraplacental damage. Survival is related to gestational age at delivery, with outcomes better than might be assumed at diagnosis and some pregnancies reaching term. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.
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