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Local References for Ultrasound-Estimated Fetal Weight Based on 2,211 Singleton Pregnancies in the City of Curitiba, South of Brazil

Referências locais para o peso fetal estimado por ultrassom baseado em 2.211 gestações únicas na cidade de Curitiba, Sul do Brasil

Abstract

Objective

To develop reference curves of estimated fetal weight for a local population in Curitiba, South of Brazil, and compare them with the curves established for other populations.

Methods

An observational, cross-sectional, retrospective study was conducted. A reference model for estimated fetal weight was developed using a local sample of 2,211 singleton pregnancies with low risk of growth disorders and well-defined gestational age. This model was compared graphically with the Hadlock and Intergrowth 21st curves.

Results

Reference curves for estimated fetal weight were developed for a local population. The coefficient of determination was R2 = 99.11%, indicating that 99.11% of the fetal weight variations were explained by the model. Compared with Hadlock curves, the 50th, 90th, and 97th percentiles in this model were lower, whereas the 10th percentile nearly overlapped, and the 3rd percentile was slightly higher in the proposed model. The percentiles were higher in the proposed model compared with the Intergrowth 21st curves, particularly for the 3rd, 10th, and 50th percentiles.

Conclusion

We provide a local reference curve for estimated fetal weight. The proposed model was different from other models, and these differences might be due to the use of different populations for model construction.

Keywords
fetal weight; prenatal ultrasonography; growth charts; percentiles; reference curves

Resumo

Objetivo

Desenvolver curvas de referência para o peso fetal estimado em uma população de Curitiba, Sul do Brasil, e compará-las com curvas estabelecidas para outras populações.

Métodos

Foi realizado um estudo observacional, transversal e retrospectivo. Um modelo de referência para o peso fetal estimado foi desenvolvido usando uma amostra local de 2.211 gestações únicas de baixo risco de distúrbios do crescimento e idade gestacional bem definida. Este modelo foi comparado graficamente com as curvas de Hadlock e Intergrowth 21st.

Resultados

As curvas de referência para o peso fetal estimado foram desenvolvidas para uma população local. O coeficiente de determinação foi de R2 = 99,11%, indicando que 99,11% das variações do peso fetal foram explicadas pelo modelo. Em comparação com as curvas de Hadlock, os percentis 50, 90, e 97 neste modelo foram inferiores, enquanto o percentil 10 quase se sobrepôs, e o percentil 3 foi ligeiramente superior no modelo proposto. Os percentis foram maiores no modelo proposto em comparação com as curvas do Intergrowth 21st, particularmente para os percentis 3, 10, e 50.

Conclusão

Fornecemos uma curva de referência local para o peso fetal estimado. O modelo proposto foi diferente de outros modelos, e essas diferenças podem ser devido ao uso de diferentes populações para a construção do modelo.

Palavras-chave
peso fetal; ultrassonografia pré-natal; curvas de crescimento; percentis; curvas de referência

Introduction

Changes in intrauterine growth and prematurity are the major determinants of neonatal morbidity and mortality.11 Madan A, Holland S, Humbert JE, Benitz WE. Racial differences in birth weight of term infants in a northern California population. J Perinatol. 2002;22(03):230–235. Doi: 10.1038/sj.jp.7210703
https://doi.org/10.1038/sj.jp.7210703...
Intrauterine growth restriction (IUGR), a condition in which a fetus cannot reach its biological growth potential,22 Gordijn SJ, Beune IM, Thilaganathan B, Papageroghiou A, Baschat AA, Baker PN, et al. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol. 2016;48 (03):333–339. Doi: 10.1002/uog.15884
https://doi.org/10.1002/uog.15884...
is strongly associated with perinatal morbidity and mortality and acute fetal distress. It is estimated that 1 to 2% of neonatal deaths worldwide are a direct result of IUGR in term newborns.33 Lawn JE, Cousens S, Zupan J; Lancet Neonatal Survival Steering Team. 4 million neonatal deaths: when? Where? Why?. Lancet. 2005;365(9462):891–900. Doi: 10.1016/S0140-6736(05)71048-5
https://doi.org/10.1016/S0140-6736(05)71...
In addition, there is a correlation between IUGR and delayed neurodevelopment44 Arcangeli T, Thilaganathan B, Hooper R, Khan KS, Bhide A. Neurodevelopmental delay in small babies at term: a systematic review. Ultrasound Obstet Gynecol. 2012;40(03):267–275. Doi: 10.1002/uog.11112
https://doi.org/10.1002/uog.11112...
and chronic diseases in adulthood, including chronic arterial hypertension, type II diabetes mellitus, and cardiovascular diseases.55 United Nations Children’s Fund, World Health Organization. Low Birthweight: Country, Regional and Global Estimates. New York: UNICEF; 2004 Macrosomic or large-for-gestational-age fetuses present higher risk of intrauterine death and adverse perinatal outcomes, such as shoulder dystocia, humeral and clavicular fracture, brachial plexus and facial palsy, asphyxia, meconium aspiration, hypoglycemia, neonatal hyperbilirubinemia, hypertrophic cardiomyopathy, and prolonged stay in intensive care units.66 Amorim MMR, Leite DFB, Gadelha TGN, Muniz AGV, Melo ASO, Rocha AM. Rev Bras Ginecol Obstet. 2009;31(05):241–248. Doi: 10.1590/S0100-72032009000500007
https://doi.org/10.1590/S0100-7203200900...
Therefore, the adequate identification of these fetuses is crucial for prenatal management and for determining the optimal time for delivery.

Some studies have provided reference charts for fetal biometric parameters, although there are discrepancies in median values and percentile curves.77 Romano-Zelekha O, Freedman L, Olmer L, Green MS, Shohat T; Israel Network for Ultrasound in Obstetrics and Gynecology. Should fetal weight growth curves be population specific? Prenat Diagn. 2005;25(08):709–714. Doi: 10.1002/pd.1194
https://doi.org/10.1002/pd.1194...
,88 Jacquemyn Y, Sys SU, Verdonk P. Fetal biometry in different ethnic groups. Early Hum Dev. 2000;57(01):1–13. Doi: 10.1016/s0378- 3782(99)00049-3
https://doi.org/10.1016/s0378-3782(99)00...
These differences may be due to racial, maternal, biological, and demographic factors99 Gardosi J, Chang A, Kalyan B, Sahota D, Symonds EM. Customised antenatal growth charts. Lancet. 1992;339(8788):283–287. Doi: 10.1016/0140-6736(92)91342-6
https://doi.org/10.1016/0140-6736(92)913...
as well as to methodological failure in published studies.1010 Ioannou C, Talbot K, Ohuma E, Sarris I, Villar J, Conde-Agudelo A, Papageorghiou AT. Systematic review of methodology used in ultrasound studies aimed at creating charts of fetal size. BJOG. 2012;119(12):1425–1439. Doi: 10.1111/j.1471-0528.2012.03451.x
https://doi.org/10.1111/j.1471-0528.2012...

The data published by the Brazilian Institute of Geography and Statistics in the 2010 census1111 Instituto Brasileiro de Geografia e Estatística. Censo demográfico 2010: características gerais da população, religião e pessoas com deficiência. Rio de Janeiro: IBGE; 2012 indicated that 47.7% of Brazilians are classified as white, 43.1% as mixed race, 7.6% as black, 1.05% as Asian, and 0.43% as indigenous people. Therefore, almost 50% of the Brazilian population can be considered of mixed race. In the city of Curitiba, 78% of the population are white, 2.8% are black, 1.3% are Asian, and 16% are of mixed race,1212 Instituto Paranaense de Desenvolvimento Econômico e Social. Caderno estatístico: município de Curitiba. Curitiba: IPARDES; 2012 evidencing ethnic variations even within a single country. In Brazil, the most used reference is that published by Hadlock et al,1313 Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology. 1991;181 (01):129–133. Doi: 10.1148/radiology.181.1.1887021
https://doi.org/10.1148/radiology.181.1....
which is based on a predominantly Caucasian and middle-class population comprising 392 pregnant women.

Based on this information, we developed a reference curve for the city of Curitiba, South of Brazil, using data obtained from 2,211 tests conducted in a population classified as having a low risk of fetal growth disorders.

Methods

The present observational, cross-sectional and retrospective study was approved by the research ethics committee of the Hospital of Universidade Federal do Paraná (UFPR) on March 30, 2016 under Opinion No. 1.470.703.

For developing the estimated fetal weight reference curve, pregnant women at gestational weeks 14 to 41 were subjected to routine ultrasound examination at a private clinic in Curitiba from March 2011 to March 2015. The examinations were conducted by 10 medical specialists in fetal medicine using GE ultrasound devices models Voluson 730 Expert and Voluson S6 (GE Medical System, Zipf, Austria).

The inclusion criteria were low-risk pregnant women with a singleton gestation and well-defined gestational age, confirmed by the date of the last menstrual period, when the difference between this date and first trimester ultrasound was less than 5 days, or by the measurement of the crown-to-rump length (CRL) in an examination conducted before the gestational age of 13 weeks and 6 days. Multiple pregnancies, fetuses with congenital malformations or chromosomal abnormalities, congenital infections, fetal deaths, and pregnant women with diseases associated with fetal growth disorders (chronic arterial hypertension, gestational hypertension, preeclampsia, previous or gestational diabetes mellitus, chronic renal disease, chronic pulmonary disease, cyanotic heart disease, alcohol abuse, smoking, systemic lupus erythematosus, antiphospholipid syndrome, and thrombophilia)as well as those who were living in high altitudes were excluded.

A total of 8,447 examinations were conducted in 2,211 patients. Gestational age in weeks and days and fetal weight in grams (estimated by Hadlock's formula: Log10weight=1.35960.00386×AC×FL+0.0064×HC+0.00061×BPD×AC+0.0424×AC+0.174×FL, in which AC is abdominal circumference, FL is femoral length, HC is head circumference, and BPD is biparietal diameter) were recorded in a Microsoft Excel 2007 worksheet (Microsoft Corporation, Redmond, WA, USA).

For the inclusion of only one examination per pregnant woman and for obtaining homogeneity in the examinations, the Linear Integer Programming technique and LINGO 13 software (LINDO Systems Inc., Chicago, IL, USA) together with Microsoft Excel 2007 were used. The technique was executed a second time for the remaining examinations. The first sample was used to create the curve (training sample), and the second one was used to validate the model (test sample).

The protocol developed by Altman and Chitty1414 Altman DG, Chitty LS. Charts of fetal size: 1. Methodology. Br J Obstet Gynaecol. 1994;101(01):29–34. Doi: 10.1111/j.1471- 0528.1994.tb13006.x
https://doi.org/10.1111/j.1471-0528.1994...
was used to calculate the estimated fetal weight curves and correlate fetal weight (in grams) with gestational age (in weeks and days). One of the protocol's recommendations is that reference percentiles be calculated using cross-sectional studies, that is, with one observation per fetus. The standard deviation of the weight was modeled as a function of the gestational period. The quality of the model was evaluated by considering the coefficient of determination and analyzing the residues of the adjusted model. The model was estimated using the training dataset and validated in the second dataset. The generated model was compared graphically with the Hadlock model1313 Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology. 1991;181 (01):129–133. Doi: 10.1148/radiology.181.1.1887021
https://doi.org/10.1148/radiology.181.1....
because the latter is the most commonly used. The generated model was also compared with the curve of the Intergrowth 21st project,1515 Stirnemann J, Villar J, Salomon LJ, Ohuma E, Ruyan P, Altman DG, et al; International Fetal andNewborn Growth Consortiumfor the 21st Century (INTERGROWTH-21st); Scientific Advisory Committee; Steering Committees; INTERGROWTH-21st; INTERBIO-21st; Executive Committee; In addition for INTERBIO 21st; Project Coordinating Unit; Data Analysis Group; Data Management Group; In addition for INTERBIO 21st; Ultrasound Group; In addition for INTERBIO-21st; Anthropometry Group; In addition for INTERBIO-21st; Laboratory Processing Group; Neonatal Group; Environmental Health Group; Neurodevelopment Group; Participating countries and local investigators; In addition for INTERBIO-21st; In addition for INTERBIO-21st. International estimated fetal weight standards of the INTERGROWTH-21st Project. Ultrasound Obstet Gynecol. 2017;49(04):478–486. Doi: 10.1002/uog.17347
https://doi.org/10.1002/uog.17347...
a prescriptive curve of how growth should occur under optimal conditions, which was designed for international use.

Results

A sample of 2,211 ultrasound examinations was generated, one for each pregnant woman, of which 1,836 (83%) were white, 310 (14%) were mixed race, 44 (2%) were black, and 21 (1%) were Asian. There was adequate distribution across the 28 weeks of gestation analyzed (14 to 41 weeks of gestation) and a standard deviation of 0.173. We believe that the majority of the pregnant women had moderate/high socioeconomic status, because the ultrasound examinations were performed in a private clinic and all ultrasound examinations were private or covered by health insurance. The distribution of the examinations is presented in Table 1.

Table 1
Frequencies of cases at each gestational age

The model was executed a 2nd time using the remaining 6,236 examinations. This 2nd execution used the same extraction method to generate a second sample with 1,957 examinations. The first sample was used to create the curve (training sample), whereas the second sample was used to validate the curve (test sample).

The gestational periods and fetal weights determined for the 2,211 examinations were considered for assessing the correlation between the gestational week and estimated fetal weight on ultrasound. The estimation of the model considered the gestational period in weeks as the explanatory variable and the natural logarithm of fetal weight on ultrasound as the response variable. The best fit was obtained using a quadratic model given by the following equation: ln̂weight=0.6034575+0.3320483.week0.003589055.week2. The estimated weight of each fetus according to the gestation period is given by: stimatedweight=e0.6034575+0.3320483.week0.003589055.week2.

The standard deviation of fetal weight was modeled according to the gestational period, as proposed by Altman and Chitty.1414 Altman DG, Chitty LS. Charts of fetal size: 1. Methodology. Br J Obstet Gynaecol. 1994;101(01):29–34. Doi: 10.1111/j.1471- 0528.1994.tb13006.x
https://doi.org/10.1111/j.1471-0528.1994...
For this estimation, the absolute values of the residues obtained with the model presented above were considered. The best ratio obtained for estimating the standard deviation was quadratic. Below is the model used for estimating the standard deviation of fetal weight as a function of the gestational week.

SD ̂ = π 2 0 . 099235 0 . 002235 . week + 0 . 000046 . week 2

Therefore, the scores for each case were calculated using the following equation:

score = ln weight ln ̂ weight SD ̂

The model's coefficient of determination was R2= 99.11%, indicating that 99.11% of fetal weight variations were explained by the model. Fig. 1 shows the results of fetal weights and gestational periods of the evaluated cases. The adjusted curve correlating fetal weight and gestational period with a 95% confidence interval for the individual observations is also shown. The fetal weights in each gestational week for each percentile (3rd, 5th, 10th, 50th, 90th, 95th, and 97th) are shown in Table 2.

Table 2
Percentiles of estimated fetal weight (grams) at each gestational age

Fig. 1
Fetal estimated weight and gestational ages of the evaluated cases. The adjusted curve correlating fetal weight and gestational period with a 95% confidence interval for the individual observations is also shown.

Fig. 2 shows the calculated scores based on the above equation, together with the values of the standardized normal distribution (-1.64; 1.64), which indicates the range corresponding to 90% of the area under the curve of this distribution. For the model data, 89.5% of the scores were within this range, indicating a good adherence to the model. This percentage was 89% in the tested dataset, indicating a very good reproducibility of the model for estimating weights using data that were not used in the adjustment.

Fig. 2
Calculated scores at a confidence interval of 90%.

Fig. 3 shows the calculated values based on the above equation together with the values of the standardized normal distribution (-1.96; 1.96), which indicate the range corresponding to 95% of the area under the curve of this distribution. For the model data, 94.1% of the scores were within this range, indicating good adherence to the model. This percentage was 94% in the tested dataset, indicating very good reproducibility of the model for estimating weights using data that were not used in the adjustment.

Fig. 3
Calculated scores at a confidence interval of 95%.

The proposed model was compared graphically with the Hadlock references and the curves developed in the Intergrowth 21st project (Fig. 4).

Fig. 4
Proposed, Hadlock, and Intergrowth 21st models according to fetal estimated weight—Curves for the 3rd, 10th, 50th, 90th and 97th percentiles.

Additionally, the proposed model was compared graphically with the Fetal Medicine Foundation (FMF),1616 Nicolaides KH, Wright D, Syngelaki A, Wright A, Akolekar R. Fetal Medicine Foundation fetal and neonatal population weight charts. Ultrasound Obstet Gynecol. 2018;52(01):44–51. Doi: 10.1002/uog.19073
https://doi.org/10.1002/uog.19073...
and the World Health Organization (WHO),1717 Kiserud T, Piaggio G, Carroli G, Widmer M, Carvalho J, Neerup Jensen L, et al. TheWorld Health Organization fetal growth charts: a multinational longitudinal study of ultrasound biometricmeasurements and estimated fetal weight. PLoS Med. 2017;14(01): e1002220. Doi: 10.1371/journal.pmed.1002220
https://doi.org/10.1371/journal.pmed.100...
models (Fig. 5).

Fig. 5
Proposed, Fetal Medicine Foundation, and World Health Organization models according to fetal estimated weight—Curves for the 10th, 50th, 90th percentiles.

Discussion

We have developed reference curves for estimated fetal weight for a local population based on the hypothesis that these curves were different from those established for other populations. The distribution of racial population was in agreement with the data from the last local census,1212 Instituto Paranaense de Desenvolvimento Econômico e Social. Caderno estatístico: município de Curitiba. Curitiba: IPARDES; 2012 despite being a population with moderate/high socioeconomic status from a private service. The proposed model was constructed after excluding gestations at risk of growth disorders and by including normal fetuses, thus defining a reference curve.

Following the recommendation of Altman and Chitty,1414 Altman DG, Chitty LS. Charts of fetal size: 1. Methodology. Br J Obstet Gynaecol. 1994;101(01):29–34. Doi: 10.1111/j.1471- 0528.1994.tb13006.x
https://doi.org/10.1111/j.1471-0528.1994...
each fetus was included only once because the inclusion of multiple observations of the same fetus would characterize a growth curve, and, in this case, the effective sample size tends to be the number of fetuses and not the number of observations. Although our data were collected retrospectively, the use of Linear Integer Programming allowed us to select only one observation for each fetus, with homogeneous distribution across the evaluated gestational weeks. The use of this technique also allowed evaluating the reproducibility of the model in a population that was not included in the study, and the results indicated that reproducibility was very good in this population. Another advantage of the selected sample is that all patients had first trimester ultrasonography data for adequate determination of gestational age.

A disadvantage of the retrospective nature of the study is that it did not allow confirming whether a factor that could affect fetal growth was truly absent. Another limitation was that there was no standardization of data collection or blinding of the measurements on the screen of the ultrasound devices for the examiner, and this limitation might interfere with the obtained values. Moreover, the obtained curves might be affected by the fact that some examinations might have been requested by clinical indication because of suspected pathological growth. However, we believe that the influence of this factor, if present, is minimal because an overrepresentation of fetuses that were small for gestational age (SGA) and/or with IUGR or large for gestational age (LGA) in this sample would result in lower percentile values at the lower limit and an increase in curve percentiles, respectively, in contrast with what we observed by comparing our curves with other reference curves.

Compared with the Hadlock curves,1313 Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology. 1991;181 (01):129–133. Doi: 10.1148/radiology.181.1.1887021
https://doi.org/10.1148/radiology.181.1....
the 50th, 90th, and 97th percentiles in the proposed model were lower than those found by Hadlock, whereas the 10th percentile almost overlapped, and the 3rd percentile was slightly higher in our model. With regard to the curves of Intergrowth 21st 15 the 3rd, 10th, and 50th percentiles were higher in our model. Additionally, the proposed model was also compared with the Fetal medicine Foundation (FMF)1616 Nicolaides KH, Wright D, Syngelaki A, Wright A, Akolekar R. Fetal Medicine Foundation fetal and neonatal population weight charts. Ultrasound Obstet Gynecol. 2018;52(01):44–51. Doi: 10.1002/uog.19073
https://doi.org/10.1002/uog.19073...
and World health Organization (WHO)1717 Kiserud T, Piaggio G, Carroli G, Widmer M, Carvalho J, Neerup Jensen L, et al. TheWorld Health Organization fetal growth charts: a multinational longitudinal study of ultrasound biometricmeasurements and estimated fetal weight. PLoS Med. 2017;14(01): e1002220. Doi: 10.1371/journal.pmed.1002220
https://doi.org/10.1371/journal.pmed.100...
curves showing slight differences. While the 10th percentile was similar for the proposed and the WHO models, the FMF model was higher. With regarding to the 90th percentile, the proposed model was lower. Therefore, the use of all five models in the same population would result in different fetal classifications for estimated fetal weight and could reflect differences in the populations used for constructing the references.

Two Brazilian studies developed estimated fetal weight curves based on local populations1818 Cecatti JG, Machado MR, dos Santos FF, Marussi EF. [Curve of normal fetal weight values estimated by ultrasound according to gestation age]. Cad Saude Publica. 2000;16(04):1083–1090. Doi: 10.1590/s0102-311X2000000400026
https://doi.org/10.1590/s0102-311X200000...
,1919 Araujo Júnior E, Martins Santana EF, Martins WP, et al. Reference charts of fetal biometric parameters in 31,476 Brazilian singleton pregnancies. J Ultrasound Med. 2014;33(07):1185–1191. Doi: 10.7863/ultra.33.7.1185
https://doi.org/10.7863/ultra.33.7.1185...
in the cities of São Paulo and Campinas, which are both located in the southeast of Brazil, and both found that the mean values were slightly lower than those presented by Hadlock et al.1313 Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology. 1991;181 (01):129–133. Doi: 10.1148/radiology.181.1.1887021
https://doi.org/10.1148/radiology.181.1....
A similar result was also observed in the model proposed in the current study for higher percentiles, but it was not observed in the 3rd and 10th percentiles, demonstrating that local variations might occur within a single country. Addressing these small differences may be important for adequately diagnosing growth disorders. Therefore, evaluating the performance of these curves in the populations for which they were developed is essential to assess whether they are in fact more adequate than the curves currently in use.

Conclusion

In summary, we provide reference curves for estimated fetal weight for a local population living in the city of Curitiba, South of Brazil. The differences relative to the Hadlock and Intergrowth 21st Project curves may reflect differences in the populations on which the models were based. The implications of these differences for prenatal management and perinatal outcome could not be assessed in this study, and further research is needed to assess the application of these models to local populations for determining such implications.

References

  • 1
    Madan A, Holland S, Humbert JE, Benitz WE. Racial differences in birth weight of term infants in a northern California population. J Perinatol. 2002;22(03):230–235. Doi: 10.1038/sj.jp.7210703
    » https://doi.org/10.1038/sj.jp.7210703
  • 2
    Gordijn SJ, Beune IM, Thilaganathan B, Papageroghiou A, Baschat AA, Baker PN, et al. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol. 2016;48 (03):333–339. Doi: 10.1002/uog.15884
    » https://doi.org/10.1002/uog.15884
  • 3
    Lawn JE, Cousens S, Zupan J; Lancet Neonatal Survival Steering Team. 4 million neonatal deaths: when? Where? Why?. Lancet. 2005;365(9462):891–900. Doi: 10.1016/S0140-6736(05)71048-5
    » https://doi.org/10.1016/S0140-6736(05)71048-5
  • 4
    Arcangeli T, Thilaganathan B, Hooper R, Khan KS, Bhide A. Neurodevelopmental delay in small babies at term: a systematic review. Ultrasound Obstet Gynecol. 2012;40(03):267–275. Doi: 10.1002/uog.11112
    » https://doi.org/10.1002/uog.11112
  • 5
    United Nations Children’s Fund, World Health Organization. Low Birthweight: Country, Regional and Global Estimates. New York: UNICEF; 2004
  • 6
    Amorim MMR, Leite DFB, Gadelha TGN, Muniz AGV, Melo ASO, Rocha AM. Rev Bras Ginecol Obstet. 2009;31(05):241–248. Doi: 10.1590/S0100-72032009000500007
    » https://doi.org/10.1590/S0100-72032009000500007
  • 7
    Romano-Zelekha O, Freedman L, Olmer L, Green MS, Shohat T; Israel Network for Ultrasound in Obstetrics and Gynecology. Should fetal weight growth curves be population specific? Prenat Diagn. 2005;25(08):709–714. Doi: 10.1002/pd.1194
    » https://doi.org/10.1002/pd.1194
  • 8
    Jacquemyn Y, Sys SU, Verdonk P. Fetal biometry in different ethnic groups. Early Hum Dev. 2000;57(01):1–13. Doi: 10.1016/s0378- 3782(99)00049-3
    » https://doi.org/10.1016/s0378-3782(99)00049-3
  • 9
    Gardosi J, Chang A, Kalyan B, Sahota D, Symonds EM. Customised antenatal growth charts. Lancet. 1992;339(8788):283–287. Doi: 10.1016/0140-6736(92)91342-6
    » https://doi.org/10.1016/0140-6736(92)91342-6
  • 10
    Ioannou C, Talbot K, Ohuma E, Sarris I, Villar J, Conde-Agudelo A, Papageorghiou AT. Systematic review of methodology used in ultrasound studies aimed at creating charts of fetal size. BJOG. 2012;119(12):1425–1439. Doi: 10.1111/j.1471-0528.2012.03451.x
    » https://doi.org/10.1111/j.1471-0528.2012.03451.x
  • 11
    Instituto Brasileiro de Geografia e Estatística. Censo demográfico 2010: características gerais da população, religião e pessoas com deficiência. Rio de Janeiro: IBGE; 2012
  • 12
    Instituto Paranaense de Desenvolvimento Econômico e Social. Caderno estatístico: município de Curitiba. Curitiba: IPARDES; 2012
  • 13
    Hadlock FP, Harrist RB, Martinez-Poyer J. In utero analysis of fetal growth: a sonographic weight standard. Radiology. 1991;181 (01):129–133. Doi: 10.1148/radiology.181.1.1887021
    » https://doi.org/10.1148/radiology.181.1.1887021
  • 14
    Altman DG, Chitty LS. Charts of fetal size: 1. Methodology. Br J Obstet Gynaecol. 1994;101(01):29–34. Doi: 10.1111/j.1471- 0528.1994.tb13006.x
    » https://doi.org/10.1111/j.1471-0528.1994.tb13006.x
  • 15
    Stirnemann J, Villar J, Salomon LJ, Ohuma E, Ruyan P, Altman DG, et al; International Fetal andNewborn Growth Consortiumfor the 21st Century (INTERGROWTH-21st); Scientific Advisory Committee; Steering Committees; INTERGROWTH-21st; INTERBIO-21st; Executive Committee; In addition for INTERBIO 21st; Project Coordinating Unit; Data Analysis Group; Data Management Group; In addition for INTERBIO 21st; Ultrasound Group; In addition for INTERBIO-21st; Anthropometry Group; In addition for INTERBIO-21st; Laboratory Processing Group; Neonatal Group; Environmental Health Group; Neurodevelopment Group; Participating countries and local investigators; In addition for INTERBIO-21st; In addition for INTERBIO-21st. International estimated fetal weight standards of the INTERGROWTH-21st Project. Ultrasound Obstet Gynecol. 2017;49(04):478–486. Doi: 10.1002/uog.17347
    » https://doi.org/10.1002/uog.17347
  • 16
    Nicolaides KH, Wright D, Syngelaki A, Wright A, Akolekar R. Fetal Medicine Foundation fetal and neonatal population weight charts. Ultrasound Obstet Gynecol. 2018;52(01):44–51. Doi: 10.1002/uog.19073
    » https://doi.org/10.1002/uog.19073
  • 17
    Kiserud T, Piaggio G, Carroli G, Widmer M, Carvalho J, Neerup Jensen L, et al. TheWorld Health Organization fetal growth charts: a multinational longitudinal study of ultrasound biometricmeasurements and estimated fetal weight. PLoS Med. 2017;14(01): e1002220. Doi: 10.1371/journal.pmed.1002220
    » https://doi.org/10.1371/journal.pmed.1002220
  • 18
    Cecatti JG, Machado MR, dos Santos FF, Marussi EF. [Curve of normal fetal weight values estimated by ultrasound according to gestation age]. Cad Saude Publica. 2000;16(04):1083–1090. Doi: 10.1590/s0102-311X2000000400026
    » https://doi.org/10.1590/s0102-311X2000000400026
  • 19
    Araujo Júnior E, Martins Santana EF, Martins WP, et al. Reference charts of fetal biometric parameters in 31,476 Brazilian singleton pregnancies. J Ultrasound Med. 2014;33(07):1185–1191. Doi: 10.7863/ultra.33.7.1185
    » https://doi.org/10.7863/ultra.33.7.1185

Publication Dates

  • Publication in this collection
    18 May 2020
  • Date of issue
    Apr 2020

History

  • Received
    17 Jan 2019
  • Accepted
    09 Mar 2020
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