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Screening for fetal growth disorders by clinical exam in the era of obesity
OBJECTIVE: To evaluate the performance of clinical estimation of fetal weight as a screening test for fetal growth disorders and then to estimate the effect of maternal body mass index (BMI) on its screening efficiency. STUDY DESIGN: This was a retrospective cohort study of patients referred for thi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640749/ https://www.ncbi.nlm.nih.gov/pubmed/23079776 http://dx.doi.org/10.1038/jp.2012.130 |
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author | GOETZINGER, Katherine R. TUULI, Methodius G. ODIBO, Anthony O. ROEHL, Kimberly A. MACONES, George A. CAHILL, Alison G. |
author_facet | GOETZINGER, Katherine R. TUULI, Methodius G. ODIBO, Anthony O. ROEHL, Kimberly A. MACONES, George A. CAHILL, Alison G. |
author_sort | GOETZINGER, Katherine R. |
collection | PubMed |
description | OBJECTIVE: To evaluate the performance of clinical estimation of fetal weight as a screening test for fetal growth disorders and then to estimate the effect of maternal body mass index (BMI) on its screening efficiency. STUDY DESIGN: This was a retrospective cohort study of patients referred for third trimester ultrasound for the indication of “size unequal to dates”. Patients with medical co-morbidities which may alter their a priori risk for fetal growth disorders were excluded. The incidence of fetal growth disorders as well as amniotic fluid disturbances was determined for each group and then compared across maternal BMI categories of <25 kg/m(2), 25-30 kg/m(2), ≥30 kg/m(2), and ≥40 kg/m(2). To evaluate the accuracy of clinical estimation of fetal weight in predicting fetal growth disorders, the sensitivity, specificity, positive predictive value, negative predictive value, likelihood ratios, as well as number needed to scan (NNS) was calculated and compared across BMI categories. RESULTS: Of 51,366 patients, 1,623 were referred for the indication of size > dates and 1,543 for the indication of size < dates. The incidence of fetal growth disorders in each referral group was low and was not significantly different across BMI categories. The sensitivity and specificity were 9.7% and 96.6% for predicting neonatal birth weight (BW) >90(th)%ile and 13.5% and 96.7% for predicting BW <10(th)%ile. The NNS to detect one neonate with a BW <10(th)%ile ranged from 5-19 while the NNS to detect one neonate with a BW >90(th)%ile ranged from 6-13 across BMI categories. CONCLUSION: Overall, clinical estimation of fetal weight yields a low detection rate of fetal growth abnormalities; however, its screening efficiency is not adversely impacted by maternal BMI. |
format | Online Article Text |
id | pubmed-3640749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-36407492013-11-01 Screening for fetal growth disorders by clinical exam in the era of obesity GOETZINGER, Katherine R. TUULI, Methodius G. ODIBO, Anthony O. ROEHL, Kimberly A. MACONES, George A. CAHILL, Alison G. J Perinatol Article OBJECTIVE: To evaluate the performance of clinical estimation of fetal weight as a screening test for fetal growth disorders and then to estimate the effect of maternal body mass index (BMI) on its screening efficiency. STUDY DESIGN: This was a retrospective cohort study of patients referred for third trimester ultrasound for the indication of “size unequal to dates”. Patients with medical co-morbidities which may alter their a priori risk for fetal growth disorders were excluded. The incidence of fetal growth disorders as well as amniotic fluid disturbances was determined for each group and then compared across maternal BMI categories of <25 kg/m(2), 25-30 kg/m(2), ≥30 kg/m(2), and ≥40 kg/m(2). To evaluate the accuracy of clinical estimation of fetal weight in predicting fetal growth disorders, the sensitivity, specificity, positive predictive value, negative predictive value, likelihood ratios, as well as number needed to scan (NNS) was calculated and compared across BMI categories. RESULTS: Of 51,366 patients, 1,623 were referred for the indication of size > dates and 1,543 for the indication of size < dates. The incidence of fetal growth disorders in each referral group was low and was not significantly different across BMI categories. The sensitivity and specificity were 9.7% and 96.6% for predicting neonatal birth weight (BW) >90(th)%ile and 13.5% and 96.7% for predicting BW <10(th)%ile. The NNS to detect one neonate with a BW <10(th)%ile ranged from 5-19 while the NNS to detect one neonate with a BW >90(th)%ile ranged from 6-13 across BMI categories. CONCLUSION: Overall, clinical estimation of fetal weight yields a low detection rate of fetal growth abnormalities; however, its screening efficiency is not adversely impacted by maternal BMI. 2012-10-18 2013-05 /pmc/articles/PMC3640749/ /pubmed/23079776 http://dx.doi.org/10.1038/jp.2012.130 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article GOETZINGER, Katherine R. TUULI, Methodius G. ODIBO, Anthony O. ROEHL, Kimberly A. MACONES, George A. CAHILL, Alison G. Screening for fetal growth disorders by clinical exam in the era of obesity |
title | Screening for fetal growth disorders by clinical exam in the era of obesity |
title_full | Screening for fetal growth disorders by clinical exam in the era of obesity |
title_fullStr | Screening for fetal growth disorders by clinical exam in the era of obesity |
title_full_unstemmed | Screening for fetal growth disorders by clinical exam in the era of obesity |
title_short | Screening for fetal growth disorders by clinical exam in the era of obesity |
title_sort | screening for fetal growth disorders by clinical exam in the era of obesity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640749/ https://www.ncbi.nlm.nih.gov/pubmed/23079776 http://dx.doi.org/10.1038/jp.2012.130 |
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