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Original Article

Fetal heart biventricular diameter/foot length index as a diagnostic marker of fetal macrosomia in the second and third trimester of pregnancy

ORCID Icon, & ORCID Icon
Article: 2183751 | Received 20 Jan 2022, Accepted 16 Feb 2023, Published online: 27 Feb 2023

Abstract

Purpose

Fetal macrosomia may have serious effects on both mother and newborn, so it is important to correctly evaluate the fetal weight before delivery. Fetal routine biometry, height of the fundus of uterus, interventricular septal thickness seems to be very good but still not perfect. In our study the relation between fetal biventricular (AP) diameter and fetal foot length was elaborated in the 2nd and 3rd trimester of pregnancy.

Material and methods

The analyzed group (n = 423 fetuses) was divided into 2 subgroups: a control group (n = 109 fetuses) with normal biometry, normal heart anatomy and normal cardiac function, no extracardiac malformation, no extracardiac anomalies, gestational age ranged from 17.5 to 37.1 weeks of gestation, born at term with birth weight 3000–3600 g, and a study group (n = 314 fetuses) with gestational age 17.5–39.5 weeks. Among the study group there were 20 patients (n = 20 fetuses) with macrosomia defined as a neonatal birth weight of greater than or equal to 4000 g. The control group was used to generate normograms on fetal AP, foot length and AP/Foot Index. The Statistica 13.3 and Excel 365 software were used to calculate the sensitivity, specificity, positive predictive value and negative predictive values.

Results

In control group, the mean biventricular fetal heart (AP) measurement was 23 mm (12.9 mm–38 mm), the mean foot length was 43 mm (24 mm–71 mm), and the mean AP/Foot Index was 0.52 (0.40–0.65). The value of the AP/Foot Index in the second trimester of the control group was 0.53, whereas the AP/Foot Index in the third trimester of pregnancy was 0.51. The use of standard fetal biometry resulted in the prediction of macrosomia in 20%, whereas the AP/Foot index in addition to standard fetal biometry enabled the detection of 65% of macrosomia.

Conclusions

The AP/Foot Index higher than 0.52 has greater sensitivity and negative predictive value to detect macrosomia compared to standard ultrasound fetal biometry.

Introduction

Ultrasound examination is a noninvasive tool used for advanced evaluation of the anatomy and function of fetuses [Citation1]. By definition, macrosomia is a fetal or newborn body weight greater than or equal to 4000 g [Citation2]. Nevertheless, some authors argue that macrosomia occurs when the fetal weight assessed by ultrasound or the birth weight of a newborn is 4500 g [Citation3]. A standard ultrasound assessment of the fetal body weight includes the measurement of the abdominal circumference, femur length and fetal head (biparietal diameter and head circumference) [Citation4].

Factors such as previous episodes of fetal macrosomia, maternal obesity, maternal age and height, and maternal diseases, mainly diabetes, excessive weight gain and prolonged duration of pregnancy may lead to fetal macrosomia [Citation5]. The diagnosis of fetal macrosomia is important to arrange further procedures, including cesarean section to reduce the risk of shoulder dystocia and plexus paralysis [Citation6].

The already used markers for the prediction of fetal weight such as fetal biometry, height of the fundus of uterus and interventricular septal thickness seem to be good but not perfect [Citation7]. There are still fetuses whose weight is underestimated in the 3rd trimester.

Can fetal foot be a good potential diagnostic marker of fetal macrosomia? The size of the heart is considered to be equal to the size of the fist [Citation8], however it is very difficult to find and measure fetal hand. According to Leonardo Da Vinci, the foot should be two times bigger than the size of the heart [Citation9]. Therefore, the analysis of the AP/Foot Index in healthy fetuses and in cases of macrosomia seems to be reasonable.

Materials and methods

This study focused on the elaboration of a new marker for better prediction of the fetal macrosomia and was performed based on the data retrieved from 2016 to 2020 from our unit computer database (Fetal Pathology of the Medical University of Lodz). The total number of 423 fetuses was divided into 2 groups: a control group (n = 109) fetuses who presented normal biometry, normal cardiac anatomy (NHA), normal heart study, normal cardiac function (NHS), no extracardiac malformation (ECM) and no extracardiac anomalies (ECA) and their gestational age ranged from 17.5 weeks to 37.1 weeks of gestation and were born at term with a birth weight of 3000–3600 g. The fetuses were used to generate normal ranges of the fetal AP, foot length and AP/Foot Index. The study group (n = 314) had gestational age ranged from 17.5 weeks to 39.5 weeks of gestation and presented normal biometry, normal cardiac anatomy (NHA), normal heart study, normal cardiac function (NHS), no extracardiac malformation (ECM) and no extracardiac anomalies (ECA). Among the study group there were 20 fetuses (20/314 = 6.4%) with macrosomia defined as neonatal birth weight more than or equal to 4000 g. In this study, the definition of macrosomia as weight greater than or equal to 4000 g was applied.

The ultrasound examinations were performed with the use of the Voluson E10, Philips and Voluson Expert ultrasound machines with convex transabdominal transducers.

The transverse diameter of the heart (AP) was measured in short axis of the fetal chest in the 4-chamber view at end-diastole with the calipers placed on the outer wall of the heart. The results of the AP measurements are presented in . The measurements of both AP and fetal foot were performed two times by one ultrasound specialist. This provided a uniform measurement data.

Figure 1. Measurement of fetal heart biventricular diameter (AP) in relation to gestational age in a control group (n = 109) of healthy fetuses with Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

Figure 1. Measurement of fetal heart biventricular diameter (AP) in relation to gestational age in a control group (n = 109) of healthy fetuses with Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

Interobserver and intraobserver variations were not analyzed. The first author (W.S.) performed an analysis of the collected data.

The fetal foot was measured from the most posterior tip of the foot to the end of the first or second toe in the longitudinal plane and the results of the measurements were presented in . Heart biventricular diameter (AP in mm) and fetal foot length (foot in mm) were retrieved from the last prenatal ultrasound examination before the delivery in cases having more than one visit. AP to foot index was calculated and presented in . The gestational age used to generate all the figures were referred to gestational age evaluated based on fetal biometry.

Figure 2. Measurement of fetal foot length in relation to gestational age in a control group of 109 healthy fetuses (Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies) with a trend line. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

Figure 2. Measurement of fetal foot length in relation to gestational age in a control group of 109 healthy fetuses (Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies) with a trend line. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

Figure 3. Measurement of the fetal heart AP to foot index (AP/Foot Index) in relation to gestational age in a control group of 109 healthy fetuses (Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies) with a trend line. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

Figure 3. Measurement of the fetal heart AP to foot index (AP/Foot Index) in relation to gestational age in a control group of 109 healthy fetuses (Normal Heart Anatomy, no Extracardiac malformations, no Extracardiac anomalies) with a trend line. Data from the Department of Diagnoses and Prevention of Fetal Malformations, Medical University of Lodz of 2016–2020. Gestational age in weeks.

The data on standard ultrasound biometry included the analysis of the estimated fetal weight, which was obtained by the measurement of the fetal BPD, HC, AC, and FL. The EFW values were automatically calculated by the built-in modules in the ultrasound machine software.

Linear regression analysis was based on Microsoft Statistical analysis. The Statistica 13.3 and Excel 365 software were used to calculate the sensitivity, specificity, positive predictive value and negative predictive value.

Results

Fetal heart biventricular diameter (AP) in mm from 17.5 week of gestation to 37.1 week of gestation in the control group of healthy fetuses is presented in .

The results presented in demonstrate an upward trend in fetal heart biventricular diameter (AP) with the gestational age (in terms of weeks of gestation). The heart diameter (AP) in healthy fetuses (with normal biometry, normal cardiac anatomy and function, without extracardiac malformation and extracardiac anomalies observed) during pregnancy from the 17.5 week of gestation to the 37.1 week of gestation demonstrated the minimum value of 12.9 mm at 17th week of gestation, maximum value of 38 mm at term and the median value was 23 mm.

Measurement of the fetal foot in mm from 17.5 week of gestation to 37.1 week of gestation in the control group of healthy fetuses is presented in .

The results presented in demonstrate an upward trend in fetal foot size with the gestational age (in terms of weeks of gestation). The size of the foot in healthy fetuses (with normal biometry, cardiac structure and function, without extracardiac malformation and extracardiac anomalies observed) during pregnancy from the 17.5 week of gestation to the 37.1 week of gestation was on average 43 mm, with the minimum value of 24 mm at 17th week of gestation, maximum value of 71 mm at term and the median value of 43 mm.

Measurement of the fetal AP to foot index (AP/F index) in mm from 17.5 week of gestation to 37.1 week of gestation in the study group is presented in .

The results presented in demonstrate a virtually constant value of the fetal AP to foot index in relation to the gestational age (in terms of weeks of gestation). This index in healthy fetuses (with normal biometry, cardiac structure and function, without extracardiac malformation and extracardiac anomalies observed) during pregnancy from the 17.5 week of gestation to the 37.1 week of gestation demonstrated minimum value of 0.40, maximum value of 0.65 and median and average value of 0.52.

The value of the AP/Foot Index in the second trimester of the control group was 0.53, whereas the AP/Foot Index in the third trimester of pregnancy was 0.51. The value for both the second and third trimester was 0.52.

This value was accepted as a reference value for the analysis of 20 fetuses with macrosomia (). Based on routine fetal ultrasound biometry only 4 fetuses (20%) were predicted to be macrosomic. Based on the AP/Foot Index, 13 (65%) of fetuses could be predicted as fetal macrosomia.

Table 1. Fetuses with a birth weight of more than or equal to 4000 g with the AP and foot measurements and the AP/Foot Index calculated and compared with fetal estimated weight based on ultrasound calculations.

The fetal AP/Foot Index used for the detection of fetal macrosomia showed 65% of sensitivity and 97.62% of specificity compared to standard biometry, which demonstrated 20% of sensitivity and 94.56% of specificity ().

Table 2. Statistical analysis for fetal AP/Foot Index with values exceeding 0.52 compared to LGA fetuses detected based on ultrasound according to fetal biometry.

The fetuses with a neonatal birth weight of more than or equal to 4000 g are presented in below.

Discussion

In prenatal ultrasound, it is important to correctly evaluate the fetal weight, and especially to detect fetal macrosomia as it may have serious effects on both mother and newborn [Citation1]. Proper diagnosis helps to take appropriate prevention. The already used ultrasound markers for prediction of fetal weight such as fetal biometry, height of the fundus of uterus, amniotic fluid index and interventricular septal thickness seem to be good however insufficient predictors [Citation2–5,Citation7].

Fetal macrosomia may have an effect on the child’s obesity in the postnatal life. Fetuses with a weight of 3400–3499 g show a statistically significant increase in the risk of obesity in childhood [Citation10]. According to Oçer et al. when fetal weight in the fetal biometry assessed by ultrasound during prenatal examinations exceeds 3400 g, this value should be considered a cutoff line for suspected fetal macrosomia in patients without diabetes [Citation11]. In patients with diabetes, blood glucose control and the use of targeted treatment may reduce the risk of macrosomia [Citation10–13]. The other very important maternal factors which may lead to the development of macrosomia in fetus include maternal age, BMI, blood pressure, PAPP-A, BhCG and PlGF levels, fetal CRL and uterine artery PI [Citation14]. Recently, some studies have suggested that the analysis of the umbilical vein flow may constitute a useful marker for the prediction of fetal macrosomia [Citation15].

Another very important risk factor for macrosomia is maternal obesity. There is a relationship between maternal BMI and the birth of LGA (large for gestational age) newborn [Citation12]. If the fetus weight is more than 4000 g, there is an increased risk of complications related to delivery. Birth weight of more than 4500 g increases the risk factors for newborns health complications, whereas birth weight of more than 5000 g increases the risk of neonatal death [Citation16].

The measurement of fetal biventricular diameter (AP) is very easy and is clinically important due to the fact that it can help in the assessment of fetal condition [Citation17,Citation18]. The obtained results are generally correlated to gestational age [Citation19]. The minimum value of the fetal heart anterior-posterior (AP) measurement in our research was 12.9 mm and maximum value of AP was 38 mm at term. These values reflect the summary data presented in other studies [Citation20,Citation21].

The size of the heart is considered to be equal to the size of the fist of an adult [Citation8]. According to Leonardo Da Vinci first observation, the foot is much longer than the hand [Citation9], therefore the foot is larger than the heart and probably twice as big as the heart. This paper was aimed at verifying this hypothesis based on our own data.

The measurement of fetal foot length during daily ultrasound examinations is relatively easy and can be an additional useful marker for the evaluation of many conditions related to pregnancy [Citation5,Citation22–24]. It may constitute an additional marker for the assessment of fetal gestational age and thus the weight [Citation6,Citation23,Citation25,Citation26]. The produced tables of measurements of fetal foot and fetal heart AP can constitute reference tables for daily ultrasound practice [Citation11,Citation27,Citation28].

In our study, we presented a new biometric marker that could be used in addition to standard ones to focus on fetuses who might be out of normal weight range [Citation29]. We analyzed the AP/Foot Index in relation to macrosomia in a period from the 15.6 week of gestation because the studied anatomical structures are developed quite well and can be easily observed during ultrasound examination.

The fetal foot was measured from the most posterior tip of the foot to the end of the first or second toe [Citation30,Citation31]. The choice of the toe depended on the length of the toe – we decided to choose the longest one. It was important to provide an appropriate projection and make sure that the foot is not bent or somehow deformed due to the fact that it could affect the results of our index [Citation30,Citation32]. The results obtained in this study confirmed that the measurement of the fetal heart AP and foot and then the calculation of the AP/Foot Index in the second and third trimester of pregnancy seems to have a higher sensitivity and specificity compared to standard ultrasound biometry (ultrasound measurement of fetal BPD, HC, AC, FL). According to the majority of recommendations, including ISUOG, the measurement of fetal length, so far, is not recommended. It is only recommended to visualize fetal upper and lower limbs to make sure that they are present [Citation29]. However, our index, which is relatively simple and easy to obtain, could be used in daily practice. The main limitation of this study is a small group of patients, which is due to the fact that measurement of the fetal foot is not easy.

Our promising results still require further validation by conducting prospective studies on a larger group of fetuses, probably only in the 3rd trimester to be able to answer the question of how early enough we could detect fetal macrosomia using the Heart/Foot index. As an additional marker to the already existing ones, this index may be a very useful and promising marker for better prediction of fetal macrosomia.

Conclusions

The range of the fetal heart to foot index (AP/Foot Index) was 0.40 (min.)–0.65 (max.) with a median value of 0.52. The inclusion of the fetal heart to foot index, in addition to standard fetal biometry, enabled the detection of 65% of cases of macrosomia.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

The author(s) reported there is no funding associated with the work featured in this article.

References

  • Respondek-Liberska M. Sonographic markers of genetic syndromes. Przegląd Chirurgii Dziecięcej. 2009;4(2–3):29–41.
  • Gaudet L, Ferraro ZM, Wen SW, et al. Maternal obesity and occurrence of fetal macrosomia: a systematic review and meta-analysis. Biomed Res Int. 2014;2014:640291.
  • Bérard J, Dufour P, Vinatier D, et al. Fetal macrosomia: risk factors and outcome. A study of the outcome concerning 100 cases >4500 g. Eur J Obstet Gynecol Reprod Biol. 1998;77(1):51–59.
  • Vintzileos AM, Campbell WA, Rodis JF, et al. Fetal weight estimation formulas with head, abdominal, femur, and thigh circumference measurements. Am J Obstet Gynecol. 1987;157(2):410–414. PMID: 3618691.
  • Hansen JP. Older maternal age and pregnancy outcome: a review of the literature. Obstet Gynecol Surv. 1986;11:726.
  • Degani S, Peleg D, Bahous K, et al. Fetal weight estimation for prediction of fetal macrosomia: does additional clinical and demographic data using pattern recognition algorithm improve detection? J Prenat Med. 2008;2(1):1–5.
  • Szmyd B, Biedrzycka M, Karuga FF, et al. Interventricular septal thickness as a diagnostic marker of fetal macrosomia. J Clin Med. 2021;10(5):1–6.
  • Fakoya AOJ, Otohinoyi DA, Marcelle T, et al. The palm-heart diameter: a prospective simple screening tool for identifying heart enlargement. Open Access Maced J Med Sci. 2017;5(7):818–824.
  • Smith D. How to think like Da vinci. London: Michael O'Mara Books Limited; 2015.
  • Henriksen T. The macrosomic fetus: a challenge in current obstetrics. Acta Obstet Gynecol Scand. 2008;87(2):134–145.
  • Oçer F, Kaleli S, Budak E, et al. Fetal weight estimation and prediction of fetal macrosomia in non-diabetic pregnant women. Eur J Obstet Gynecol Reprod Biol. 1999;83(1):47–52.
  • Ehrenberg HM, Mercer BM, Catalano PM. The influence of obesity and diabetes on the prevalence of macrosomia. Am J Obstet Gynecol. 2004;191:964–968.
  • Suhonen L, Hiilesmaa V, Kaaja R, et al. Detection of pregnancies with high risk of fetal macrosomia among women with gestational diabetes mellitus. Acta Obstet Gynecol Scand. 2008;87:940–945.
  • Gasiorowska A, Zawiejska A, Dydowicz P, et al. Maternal factors, ultrasound and placental function parameters in early pregnancy as predictors of birth weight in low-risk populations and among patients with pre-gestational diabetes. Ginekol Pol. 2019;90(7):388–395.
  • Rizzo G, Mappa I, Bitsadze V, et al. The added value of umbilical vein flow in predicting fetal macrosomia at 36 weeks of gestation: a prospective cohort study. Acta Obstet Gynecol Scand. 2021;100(5):900–907.
  • Boulet SL, Alexander GR, Salihu HM, et al. Macrosomic births in the United States: determinants, outcomes, and proposed grades of risk. Am J Obstet Gynecol. 2003;188(5):1372–1378.
  • Thakur V, Fouron JC, Mertens L, et al. Diagnosis and management of fetal heart failure. Can J Cardiol. 2013;29(7):759–767.
  • Bromley B, Estroff JA, Sanders SP, et al. Fetal echocardiography: accuracy and limitations in a population at high and low risk for heart defects. Am J Obstet Gynecol. 1992;166(5):1473–1481.
  • Gembruch U, Shi C, Smrcek JM. Biometry of the fetal heart between 10 and 17 weeks of gestation. Fetal Diagn Ther. 2000;15(1):20–31.
  • Sylwestrzak O, Respondek-Liberska M. Echocardiographic methods of fetal heart size assessment-heart to chest area ratio and transversal heart diameter. Prenat Cardiol. 2018;8(1):20–23.
  • Respondek M, Respondek A, Huhta JC, et al. 2D echocardiographic assessment of fetal heart size in the 2nd and 3rd trimester of uncomplicated pregnancy. Eur J Obstet Gynecol Reprod Biol. 1992;44(3):185–188.
  • Mercer BM, Sklar S, Shariatmadar A, et al. Fetal foot length as a predicator of gestational age. Amer J Obstet Gynecol. 1987;156:350–355.
  • Usta A, Usta CS, Yildiz A, et al. Frequency of fetal macrosomia and the associated risk factors in pregnancies without gestational diabetes mellitus. Pan Afr Med J. 2017;26:62.
  • Manjunatha B, Nithin M, Sameer S. Cross sectional study to determine gestational age by metrical measurements of foot length. Egypt J Forensic Sci. 2012;2:11–17.
  • Drey EA, Kang MS, McFarland W, et al. Improving the accuracy of fetal foot length to confirm gestational duration. Obstet Gynecol. 2005;105(4):773–778.
  • Hern WM. Correlation of fetal age and measurements between 10 and 26 weeks of gestation. Obstet Gynecol. 1984;63:26–32.
  • Geldenhuys E, Coldrey J, Wright C, et al. Fetal foot length at delivery as a tool for determining gestation length in non-macerated stillbirths. Int J Gynaecol Obstet. 2017;138(1):107–112.
  • Bogers H, Rifouna MS, Cohen-Overbeek TE, et al. First trimester physiological development of the fetal foot position using three-dimensional ultrasound in virtual reality. J Obstet Gynaecol Res. 2019;45(2):280–288.
  • Recommendations of the Ultrasound Section of the Polish Society of Gynecologists and Obstetricians on ultrasound screening in uncomplicated pregnancy – 2015. DOA: 13.08.2021.
  • Stevens K, Elia J, Kaneshiro B, et al. Updating fetal foot length to gestational age references: a chart review of abortion cases from 2012 to 2014. Contraception. 2020;101(1):10–13.
  • Shalev E, Weiner E, Zuckerman H, et al. Reliability of sonographic measurement of the fetal foot. J Ultrasound Med. 1989;8(5):259–262.
  • Ermito S, Dinatale A, Carrara S, et al. Prenatal diagnosis of limb abnormalities: role of fetal ultrasonography. J Prenat Med. 2009;3(2):18–22.