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Customized birth weight percentiles for identification of SGA short statue
Corinna Melanie Held1, Andreas Krebs2, Dirk Manfred Olbertz3,4
1Department of Pediatrics and Adolescent Medicine, Schwarzwald-Baar-Klinikum, Villingen-Schwenningen, Germany.
Insights
Customized percentiles identify more small for gestational age (SGA) infants but do not increase the diagnosis of persistent short stature (SGA-SS) requiring growth hormone therapy compared to conventional methods.
Area of Science:
- Pediatrics
- Neonatology
- Endocrinology
Background:
- 10-15% of small for gestational age (SGA) children develop persistent short stature (SGA-SS), potentially benefiting from growth hormone therapy.
- Customized percentiles, incorporating maternal factors, may improve the identification of at-risk newborns.
Purpose of the Study:
- To evaluate if customized birth weight percentiles impact the diagnosis of SGA-SS and subsequent therapy decisions.
- To compare the frequency of SGA-SS diagnosis using conventional versus customized percentile definitions.
Main Methods:
- Analysis of birth data from 1321 infants (gestational age ≥30 weeks) using conventional and customized birth weight percentiles.
- Assessment of growth data at 2 and 4 years to identify persistent short stature (SGA-SS) in SGA infants.
Main Results:
- Customized percentiles identified more SGA infants (11.9%) than conventional ones (9.8%).
- Forty-one infants of high-weight mothers were exclusively identified by customized percentiles.
- Persistent short stature (SGA-SS) diagnosis at 2-4 years showed minimal difference between the two percentile methods.
Conclusions:
- Customized percentiles increase the classification of SGA infants based on birth weight.
- These customized methods do not appear to identify more cases of postnatal growth failure (SGA-SS) than conventional approaches.
Objectives:
About 10-15 % of small for gestational age (SGA) children have persistent short stature (SGA-SS) and may benefit from growth hormone therapy. Customized percentiles that consider maternal height and weight, among other factors, appear to more accurately identify pathologically small newborns at higher risk of perinatal morbidity. We aim to determine whether the consideration of maternal height and weight in definition of SGA has an impact on the frequency of SGA-SS diagnosis and potential therapy.
Methods:
Birth data of 1321 infants with a gestational age of ≥30 weeks of gestation were analyzed using both conventional percentiles and customized birth weight percentiles, the latter incorporating maternal height and weight. Growth data at 2 and 4 years of age were analyzed for the presence of persistent short stature (SGA-SS) in infants born SGA.
Results:
Using the conventional birth weight percentiles, 129 (9.8 %) newborns are classified as SGA compared to 158 (11.9 %) using the customized percentiles. Forty-one infants of high-weight mothers were identified using only the customized classification. Twelve infants born to low-weight mothers were identified by conventional classification only. At 2 and 4 years of age, seven children had persistent short stature. The diagnosis of SGA-SS differed in only one case between the conventional and customized birth weight percentiles.
Conclusions:
Customized percentiles classify more children as SGA based on their birth weight but do not appear to identify more children with postnatal growth failure than do conventional percentiles.
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