CORRELATION OF PLACENTAL THICKNESS ESTIMATED BY ULTRASONOGRAPHY WITH GESTATIONAL AGE IN THE SECOND AND THIRD TRIMESTER OF PREGNANCY

Document Type : Original Article

Authors

Department of Obstetrics and Gynecology, Faculty of Medicine Al-Azhar University

Abstract

Background: Normal development of placenta during gestation is necessary for supporting of a healthy fetus. On the other hand, any impairment in its development may have a profound impact on fetal development and pregnancy outcome.
Objective: To study the placental thickness by ultrasonography in relation to gestational age (GA).
Patient and Methods: The present prospective study was conducted on 100 pregnant females attending antenatal clinics in both Damanhour Educational Hospital and Eldelngat central Hospital in the period from August 2018 to August 2019. The placental thickness in mm was measured at the level of cord insertion site. Placental thickness was calculated from the echogenic chorionic plate to placental myometrial interface near the mid-placental portion.
Results: There was a positive correlation between increase in placental thickness (mm) in total sample, 2nd trimester, and 3rd trimester and GA, as GA increase Placental thickness increase.
Conclusion: Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of gestational age because of its linear correlation. Therefore, it can be used as an additional sonographic tool in correlating gestational age in cases where last mestrual period (LMP) is not known and in detecting patients developing intrauterine growth retardation (IUGR).

Keywords


CORRELATION OF PLACENTAL THICKNESS ESTIMATED BY ULTRASONOGRAPHY WITH GESTATIONAL AGE IN THE SECOND AND THIRD TRIMESTER OF PREGNANCY

By

Hamada Ali Abou Zeid, Mofeed Fawzy Mohamed and Wael Soliman Taha

Department of Obstetrics and Gynecology, Faculty of Medicine Al-Azhar University

E-mail: hamadaabouzeid@gmail.com

ABSTRACT

Background: Normal development of placenta during gestation is necessary for supporting of a healthy fetus. On the other hand, any impairment in its development may have a profound impact on fetal development and pregnancy outcome.

Objective: To study the placental thickness by ultrasonography in relation to gestational age (GA).

Patient and Methods: The present prospective study was conducted on 100 pregnant females attending antenatal clinics in both Damanhour Educational Hospital and Eldelngat central Hospital in the period from August 2018 to August 2019. The placental thickness in mm was measured at the level of cord insertion site. Placental thickness was calculated from the echogenic chorionic plate to placental myometrial interface near the mid-placental portion.

Results: There was a positive correlation between increase in placental thickness (mm) in total sample, 2nd trimester, and 3rd trimester and GA, as GA increase Placental thickness increase.

Conclusion: Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of gestational age because of its linear correlation. Therefore, it can be used as an additional sonographic tool in correlating gestational age in cases where last mestrual period (LMP) is not known and in detecting patients developing intrauterine growth retardation (IUGR).

Keywords: Gestational age, Placental thickness, Intrauterine growth retardation.

 

 

INTRODUCTION

     Obstetric ultrasonography offers the tools to estimate fetal weight and assess placental size (Mull et al., 2018). Placental thickness is the easiest placental dimension measure. Yet, little is known about the “normal” placental thickness as measured by sonography. Historically, a placenta of greater than 4 cm in thickness has been regarded as abnormal and associated with various poor outcomes (Sersam et al., 2016).

     Placental thickness is very much related to fetal development and may be a key in perinatal outcome at term placenta is approximately 3 cm thick and measures 15-25 cm in diameter (BaGhel et al., 2015). A ‘warning limit’ of placental diameter of 18 cm and placental thickness of 2 cm at 36 weeks predict low birth weight neonates (Abdelhamid et al., 2019). Small placentas are associated with preeclampsia, chromosomal abnormalities, severe maternal diabetes mellitus, chronic fetal infections and intrauterine growth restriction (BaGhel et al., 2015). The placentas over 4 cm thick at term have been observed in conditions like diabetes mellitus, perinatal infections and hydrops fetalis (Vinodha, 2016).

     The incidence of perinatal morbidity and mortality was considerably higher among gravid with thick placenta, related to higher rates of fetal anomalies and higher rates of both small for gestational age and large for gestational age neonates at term (Norris et al., 2015).

     Increased placental thickness is not diagnostic of any specific disorder but may contribute to the management of fetus at risk. The gestational age is frequently overestimated or underestimated, as many people are unaware of LMP and irregular menstrual cycle (Batstone et al., 2012).

PATIENTS AND METHODS

     The present prospective study was conducted on 100 pregnant females attending antenatal clinics in both Damanhour Educational Hospital and Eldelngat central Hospital in the period from August 2018 to August 2019 after taking ethical committee clearance from Institutional Ethical Committee. The study was explained to the study population, and a written consent was obtained from each patient.

Inclusion criteria:

     Singleton pregnancy, gestational age more than 13week, known last menstrual period, a history of regular menstruation, and age group of 20 - 35 years.

Exclusion criteria:

     Gestational hypertension, diabetes mellitus, hydrops fetalis, congenital malformations, twins, polyhydramnios, last menstrual period not known irregular menstrual period, abnormal placenta, and poor visualization of placenta.

      The placental thickness in mm was measured at the level of cord insertion site. Placental thickness was calculated from the echogenic chorionic plate to placental myometrial interface near the mid-placental portion. All placental measurements were taken during the relaxed phase of the uterus as contractions can spuriously increase the placental thickness.

     Placental thickness value, in mm, was calculated by averaging the three best measurements for each case.

     Umbilical artery color Doppler was used for further reconfirmation of the site of umbilical cord insertion. The placental thickness was measured trans-abdominally by using Madison color Doppler scanner with a 3.5-MHz convex transducer placing it perpendicularly to the plane of the placenta.

Statistical analysis of the data:

     Data were fed to the computer and analyzed using IBM SPSS software package version 20.0. (Armonk, NY: IBM. Corp) Qualitative data were described using number and percent. The Kolmogorov-Smirnov test was used to verify the normality of distribution. Quantitative data were described using range (minimum and maximum), mean, standard deviation and median. Significance of the obtained results was judged at the 5% level.


 

RESULTS

 

 

     In the present study, age of patients ranged between 20.0 – 35.0 years with a mean age of 29.35 ± 2.94 years in the present study. Patients <25 were 6 (6.0%), Patients 25 – 30 were 58 (58.0 %), and Patients >30 were 36 (36.0 %). GA ranged between 18.0 – 38.0 weeks with a mean age of 28.34 ± 4.44 weeks in the present study. Patients ≤26 (2nd trimester) were 30 (30%) and Patients >26 (3rd trimester) were 70 (70.0 %) (Table 1).


 

Table (1):   Distribution of the studied cases according to age, GA and Placental thickness

Age

No.

%

<25

6

6.0

25 – 30

58

58.0

>30

36

36.0

Min. – Max.

20.0 – 35.0

Mean ± SD.

29.35 ± 2.94

GA

No.

%

≤26 (2nd trimester)

30

30.0

>26 (3rd trimester)

70

70.0

Min. – Max.

18.0 – 38.0

Mean ± SD.

28.34 ± 4.44

Placental thickness (mm)

No.

%

<30

4

4.0

≥30

96

96.0

Min. – Max.

25.0 – 43.0

Mean ± SD.

36.03 ± 3.29

 

 

     In the present study, there was a positive correlation between increase in Placental thickness (mm) in Total sample, 2nd trimester, and 3rd trimester and GA, as GA increase Placental thickness increase.  The mean GA ≤26 was 34.93 ± 3.57 and mean GA >26 were 36.50 ± 3.07. As GA increase Placental thickness increase.  In our study, a significant positive correlation is seen between placental thickness and the gestational age (Table 2).

 

 

(Table 2):   Correlation between GA and Placental thickness

Placental thickness (mm)

GA

r

p

Total sample

0.413*

<0.001*

2nd trimester

0.714*

<0.001*

3rd trimester

0.242*

0.044*

r: Pearson coefficient

 

 

DISCUSSION

     The placenta is a fetal organ which provides the physiologic link between a pregnant woman and the fetus. The placenta develops from the chorionic villi at the implantation site at about the fifth week of gestation and by the ninth or tenth week, the diffuse granular echo texture of the placenta is clearly apparent at sonography (Amy Jnah and Trembath, 2019).

     Placental thickness appears to be a promising parameter for estimation of GA of the fetus because of increase in placental thickness with GA (Korzeniewski et al., 2016).

     In the present study, there was a positive correlation between increase in Placental thickness (mm) in Total sample, 2nd trimester, and 3rd trimester and GA, as GA increase Placental thickness increase.  The mean GA ≤26 was 34.93 ± 3.57 and mean GA >26 were 36.50 ± 3.07. As GA increase Placental thickness increase.  Accurate determination of gestational age has become important for deciding the appropriate time for termination of the pregnancy as well as to monitor the fetal growth during the entire period of pregnancy. In addition to the routine fetal biometry parameters, various studies were done trying to deduce a relationship between the placental thickness and gestational age and the estimated fetal weight (Mathai et al., 2013).

     A fairly linear increase in mean placental thickness with gestational age was observed in correlation analysis studies conducted to determine the relationship between placental thickness and gestational age (Mahale et al., 2018). The value of the mean placental thickness increased with advancing gestational age, almost matching from the 22nd to the 35th week and 27 to 33 weeks (Kakumanu et al., 2018). Significant positive correlations between placental thickness and estimated fetal weight in the second and third trimesters (p<0.05) in a non-IUGR group were also demonstrated (Mathai et al., 2013). A positive correlation, with increasing placental volume with increasing gestational age, was also observed, but it remained reduced in the growth-restricted fetuses (Krishna and Bhalerao, 2011). The usefulness of this relationship between placental thickness and growth parameters is that subnormal placental thickness for a gestational age may be the earliest indication of fetal growth retardation (Mathai et al., 2013).

     In our study, a significant positive correlation is seen between placental thickness and the ultra sonographic gestational age. (Babiker and Eisa, 2014) compared the fetal age progress and the placenta thickness in pregnant women. In a cross sectional descriptive study, one thousand pregnant women with mean age of 29 years old, were examined by ultrasound imaging. In the (12th -25th), (26th -36th) and (37th -40th) Weeks the GA were; 18.9 ± 4.2, 33.2 ± 2.9 and 38.1± 0.89 respectively. While the placenta thickness measurements were; 23.1mm ± 5.5, 35.0 mm ± 6.2 and 39.6 mm ± 7.0 respectively for the same periods. The highest frequency of placenta grading was Grade2 which is (36.0% of 1000). The highest frequency of placental location was Anterior Fundal which is (22.1% of 1000). There was strong statistical association between the increasing of placenta thickness and the GA, P = 0.000. The placenta thickness measurements can be carried on consideration with the other GA measurements parameters.

     Placental thickness ranged between 25.0 – 43.0 mm with a mean thickness of 36.03 ± 3.29 in the present study. Patients <30 were (4%) and Patients ≥30 were 96 (96.0 %). This study revealed a maximum placental thickness of 39.26 ± 5.69 mm at 40 weeks. This value is similar to that of (Ville and Bault, 2016) in the United States who reported that normal placenta never exceeded 40 mm in thickness throughout pregnancy. A slightly lower value of 37.5 mm at 39 weeks was reported by (Ali, 2018). This shows that race apparently has no influence on placenta measurements.

CONCLUSION

      It can be concluded that, Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of gestational age because of its linear correlation. Therefore, it can be used as an additional sonographic tool in correlating gestational age in cases where last mestrual period (LMP) is not known and in early detecting patients developing intrauterine growth retardation (IUGR).

REFERENCES

  1. Abdelhamid, A. N., Sayyed, T. M., Shahin, A. H. E., and Zerban, M. A. (2019): Correlation between second and third trimester placental thickness with ultra sonographic gestational age. Menoufia Medical Journal, 32(4): 1406-1410.
  2. Ali, R. K. E. (2018): A Study of Relationship between Placental Thickness and Fetal Age In 3rd trimester in Sudanese Women. Sudan University of Science and Technology, 110(3): 231-234.
  3. Amy Jnah, D. and Trembath, A. N. (2019): Fetal and neonatal physiology for the advanced practice nurse: Springer Publishing Company, 24(4):25-29.
  4. Babiker, M. S. and Eisa, R. A. (2014): Placenta thickness measurements during gestational age progress. Journal of Applied Medical Sciences, 3(6):31-37.
  5. BaGhel, P., Bahel, V., Paramhans, R., Sachdev, P. and Onkar, S. (2015): Correlation of placental thickness estimated by ultrasonography with gestational age and fetal outcome. Indian Journal of Neonatal Medicine and Research, 3(5): 19-24.
  6. Batstone, G. F., Blair, A. W. and Slater, J. M. (2012): A Handbook of Pre-Natal Paediatrics for Obstetricians and Pediatricians: Springer Science and Business Media, 5(9): 211-220.
  7. Kakumanu, P. K., Kondragunta, C. and GandraNR, Y. H. (2018): Evaluation of placental thickness as an ultrasonographic parameter for estimating gestational age of the fetus in 2nd and 3rd trimesters. International Journal of Contemporary Medicine Surgery and Radiology, 3(1): 128-132.
  8. Korzeniewski, S. J., Romero, R., Chaiworapongsa, T., Chaemsaithong, P., Kim, C. J., Kim, Y. M. and Yeo, L. (2016): Maternal Plasma Angiogenic Index-1 (PlGF/sVEGFR-1) is a Biomarker for the Burden of Placental Lesions Consistent with Uteroplacental Under perfusion: a Longitudinal Case-Cohort Study. American Journal of Obstetrics and Gynecology, 214(5): 629-621.
  9. Krishna, U., and Bhalerao, S. (2011): Placental insufficiency and fetal growth restriction. The Journal of Obstetrics and Gynecology of India, 61(5): 505-511.
  10. Mahale, N., Mitra, M., Mahale, A., Fernandes, M., and Ullal, S. (2018): Placental thickness and its correlation with gestational age and foetal growth parameters. Italian Journal of Obstetrics and Gynecology, 40(1): 33-41.
  11. Mathai, B. M., Singla, S. C., Nittala, P. P., Chakravarti, R. J., and Toppo, J. N. (2013): Placental thickness: its correlation with ultra sonographic gestational age in normal and intrauterine growth-retarded pregnancies in the late second and third trimester. The Journal of Obstetrics and Gynecology of India, 63(4): 230-233.
  12. Mulla, B. M., Noor, N., James-Todd, T., Isganaitis, E., Takoudes, T. C., Curran, A. and Brown, F. M. (2018): Continuous glucose monitoring, glycemic variability, and excessive fetal growth in pregnancies complicated by type 1 diabetes. Diabetes Technology and Therapeutics, 20(6): 413-419.
  13. Norris, T., Johnson, W., Farrar, D., Tuffnell, D., Wright, J., and Cameron, N. (2015): Small for gestational age and large for gestational age thresholds to predict infants at risk of adverse delivery and neonatal outcomes.  BMJ Open, 5(3): 67-73.
  14. Sersam, L. W., Abdul-Razzak, Z. Z., and Mohammed, S. Y. (2016): Second and Third Trimester Placental Thickness: Correlation with Placental and Birth Weights. Iraqi Postgraduate Medical Journal, 15(4): 42-46.
  15. Ville, Y. G., and Bault, J.-P. (2016): 13 Prenatal Diagnoses of Fetal Malformations by Ultrasound. Genetic disorders and the fetus, 5(4): 121-126.
  16. Vinodha, M. (2016): Ultra sonographic Placental Thickness: Its Correlation to Gestational Age. ESIC Medical College and PGIMSR, Chennai, 7(5): 438-443.


دراسة الإرتباط بین سمک المشیمة المقدر بواسطة الموجات الفوق صوتیة مع العمر الجنینی فی الثلث الثانی والثالث من الحمل

حمادة علی أبوزید، مفید فوزی محمد، وائل سلیمان طه

قسم التولید وأمراض النساء، کلیة الطب جامعة الأزهر

خلفیة البحث: إن النمو الطبیعی للمشیمة أثناء الحمل ضروری لنمو جنین سلیم وقد یکون لأی ضعف فی نموالمشیمه  تأثیراً عمیقاً على نمو الجنین ونتائج الحمل.

الهدف من البحث: دراسة الإرتباط بین سمک المشیمة المقدر بواسطة الموجات الفوق صوتیة مع العمر الجنینی فی الثلث الثانی والثالث من الحمل.

المریضات و طرق البحث: أجریت الدراسة على 100 سیدة حامل فی عیادات ما قبل الولادة فی کل من مستشفى دمنهور التعلیمی ومستشفى الدلنجات المرکزی فی الفترة من أغسطس 2018 إلى أغسطس 2019. وقد تم قیاس سمک المشیمة بواسطة الموجات الفوق صوتیة عند مستوی إدخال الحبل السری بالقرب من منتصف المشیمة.

نتائج البحث: هناک إرتباط إیجابی بین الزیادة فی سمک المشیمة فی العینة الکلیة والعمر الجنینی، حیث أنه کلما زاد العمر الجنینی زاد سمک المشیمة.

الاستنتاج: یمکن إستخدام سمک المشیمة بواسطة الموجات الفوق صوتیة کمؤشر دقیق فی تقییم العمر الجنینی بسبب إرتباطه الخطی.کما یمکن إستخدامه کأداة إضافیة للتصویر بالموجات فوق الصوتیة فی ربط العمر الجنینی فی الحالات التی تکون فیها فترة الدورة الشهریة الأخیرة غیر معروفة وفی إکتشاف المریضات اللاتى تصبن بتخلف النمو داخل الرحم.

  1. REFERENCES

    1. Abdelhamid, A. N., Sayyed, T. M., Shahin, A. H. E., and Zerban, M. A. (2019): Correlation between second and third trimester placental thickness with ultra sonographic gestational age. Menoufia Medical Journal, 32(4): 1406-1410.
    2. Ali, R. K. E. (2018): A Study of Relationship between Placental Thickness and Fetal Age In 3rd trimester in Sudanese Women. Sudan University of Science and Technology, 110(3): 231-234.
    3. Amy Jnah, D. and Trembath, A. N. (2019): Fetal and neonatal physiology for the advanced practice nurse: Springer Publishing Company, 24(4):25-29.
    4. Babiker, M. S. and Eisa, R. A. (2014): Placenta thickness measurements during gestational age progress. Journal of Applied Medical Sciences, 3(6):31-37.
    5. BaGhel, P., Bahel, V., Paramhans, R., Sachdev, P. and Onkar, S. (2015): Correlation of placental thickness estimated by ultrasonography with gestational age and fetal outcome. Indian Journal of Neonatal Medicine and Research, 3(5): 19-24.
    6. Batstone, G. F., Blair, A. W. and Slater, J. M. (2012): A Handbook of Pre-Natal Paediatrics for Obstetricians and Pediatricians: Springer Science and Business Media, 5(9): 211-220.
    7. Kakumanu, P. K., Kondragunta, C. and GandraNR, Y. H. (2018): Evaluation of placental thickness as an ultrasonographic parameter for estimating gestational age of the fetus in 2nd and 3rd trimesters. International Journal of Contemporary Medicine Surgery and Radiology, 3(1): 128-132.
    8. Korzeniewski, S. J., Romero, R., Chaiworapongsa, T., Chaemsaithong, P., Kim, C. J., Kim, Y. M. and Yeo, L. (2016): Maternal Plasma Angiogenic Index-1 (PlGF/sVEGFR-1) is a Biomarker for the Burden of Placental Lesions Consistent with Uteroplacental Under perfusion: a Longitudinal Case-Cohort Study. American Journal of Obstetrics and Gynecology, 214(5): 629-621.
    9. Krishna, U., and Bhalerao, S. (2011): Placental insufficiency and fetal growth restriction. The Journal of Obstetrics and Gynecology of India, 61(5): 505-511.
    10. Mahale, N., Mitra, M., Mahale, A., Fernandes, M., and Ullal, S. (2018): Placental thickness and its correlation with gestational age and foetal growth parameters. Italian Journal of Obstetrics and Gynecology, 40(1): 33-41.
    11. Mathai, B. M., Singla, S. C., Nittala, P. P., Chakravarti, R. J., and Toppo, J. N. (2013): Placental thickness: its correlation with ultra sonographic gestational age in normal and intrauterine growth-retarded pregnancies in the late second and third trimester. The Journal of Obstetrics and Gynecology of India, 63(4): 230-233.
    12. Mulla, B. M., Noor, N., James-Todd, T., Isganaitis, E., Takoudes, T. C., Curran, A. and Brown, F. M. (2018): Continuous glucose monitoring, glycemic variability, and excessive fetal growth in pregnancies complicated by type 1 diabetes. Diabetes Technology and Therapeutics, 20(6): 413-419.
    13. Norris, T., Johnson, W., Farrar, D., Tuffnell, D., Wright, J., and Cameron, N. (2015): Small for gestational age and large for gestational age thresholds to predict infants at risk of adverse delivery and neonatal outcomes.  BMJ Open, 5(3): 67-73.
    14. Sersam, L. W., Abdul-Razzak, Z. Z., and Mohammed, S. Y. (2016): Second and Third Trimester Placental Thickness: Correlation with Placental and Birth Weights. Iraqi Postgraduate Medical Journal, 15(4): 42-46.
    15. Ville, Y. G., and Bault, J.-P. (2016): 13 Prenatal Diagnoses of Fetal Malformations by Ultrasound. Genetic disorders and the fetus, 5(4): 121-126.
    16. Vinodha, M. (2016): Ultra sonographic Placental Thickness: Its Correlation to Gestational Age. ESIC Medical College and PGIMSR, Chennai, 7(5): 438-443.