ULTRASONOGRAPHIC MEASUREMENT OF PLACENTAL THICKNESS AS A PREDICTOR OF FETAL BIRTH WEIGHT

Document Type : Original Article

Authors

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

Abstract

Background: The human placenta develops with the principal function of providing nutrients and oxygen to the fetus.
Objective: to determine the normal sonographically measured placental thickness in millimeters from 18 week onwards and to determine the correlation between measurement and estimated fetal weight.
Patients and methods: This prospective observational study was conducted on 100 pregnant women aged between 18 and 35 years at Obstetrics and Gynecology Department, Edfu General Hospital from October 2018 to January 2020. After Institutional Ethics Committee approval all recruited women were observed for baseline demographic and obstetric data including age, parity and past medical events at first antenatal visit. All women provided an informed written consent and underwent ultrasound evaluation of placental thickness at 18 to 40 weeks of gestation.
Results: The mean placental thickness at 2nd trimester was 24.67±3.3 and mean Birth weight (g) was 3044.7±523.1 with range of (2200-4000).
Conclusion: Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of fetal weight because of its linear correlation.

Main Subjects


ULTRASONOGRAPHIC MEASUREMENT OF PLACENTAL THICKNESS AS A PREDICTOR OF FETAL BIRTH WEIGHT

By

Hisham A. Hussein, Ismail M. El-Garhy and Abd El-Monsef A. Sedek

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

Corresponding author: Hisham A. Hussein;

Mobile: 01061106522; E-mail: obshesham@gmail.com

ABSTRACT

Background: The human placenta develops with the principal function of providing nutrients and oxygen to the fetus.

Objective: to determine the normal sonographically measured placental thickness in millimeters from 18 week onwards and to determine the correlation between measurement and estimated fetal weight.

Patients and methods: This prospective observational study was conducted on 100 pregnant women aged between 18 and 35 years at Obstetrics and Gynecology Department, Edfu General Hospital from October 2018 to January 2020. After Institutional Ethics Committee approval all recruited women were observed for baseline demographic and obstetric data including age, parity and past medical events at first antenatal visit. All women provided an informed written consent and underwent ultrasound evaluation of placental thickness at 18 to 40 weeks of gestation.

Results: The mean placental thickness at 2nd trimester was 24.67±3.3 and mean Birth weight (g) was 3044.7±523.1 with range of (2200-4000).

Conclusion: Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of fetal weight because of its linear correlation.

Keywords: Estimated fetal weight, Placental thickness, umbilical cord insertion, sonographic.

 

 

INTRODUCTION

     Normal fetal growth is a critical component of a healthy pregnancy and influences the long-term health of the offspring. Common adult diseases such as type 2 diabetes and cardiovascular conditions have been linked to abnormal fetal growth, particularly fetal growth restriction (FGR). Diagnosis and management are complicated by the use of ambiguous terminology and a lack of uniform diagnostic criteria. Size alone is not an indication of a complication. As a result of this confusion, under intervention and over intervention can occur (Zhang et al., 2016).

     Fetal growth and development is one of the most important issues an obstetrician caring for the well-being of the fetus and the mother needs to address. This is because a normally growing fetus with its size within the normal limits means fewer complications during its prenatal and postnatal stages. It also means fewer complications in its infant and childhood stages. In addition, it also indicates a potentially healthy, intelligent, and well-grown adult. Any abnormality in fetal growth, whether growth restriction or growth acceleration, is a cause for worry as such abnormalities are usually associated with the risk of prenatal and postnatal morbidity and mortality. Therefore, prenatal diagnosis of these conditions is very important to the physician concerned, because it can help him/her to decide not only the time, but also the mode of delivery. This in turn reduces the risk (Sharma et al., 2016).

     Growth is a time-dependent change of bodily dimensions. The human fetus grows at a particularly rapid rate and this is important because a principle of developmental biology is that organisms are more susceptible to injury during periods of fast growth (Tarca et al., 2018).

     Birth weight has been used extensively as a parameter to characterize the appropriateness of fetal growth and, to date, remains the most frequently used index to assess size as a proxy to growth. Therefore, in clinical practice, many obstetricians rely on the assessment of sonographic estimation of fetal weight to evaluate fetal size and growth (Milner and Arezina, 2018).

     A number of surrogate markers of placental function, including maternal serum analyses and uterine artery Doppler velocimetric indices, have been investigated as early screening tests for these adverse pregnancy outcomes; however, most predictive models including various combinations of surrogate markers have a poor positive predictive value, largely rendering them inadequate standalone screening tests (Salavati et al., 2016).

     A correlation between placental weight and fetal birth weight at the time of delivery has long been established. Additionally, pregnancies affected by IUGR and preeclampsia often manifest a placental weight below the 10th per-centile for gestational age (Cantonwine et al., 2016). Variations in gross placental morphologic characteristics have also been associated with decreased birth weight and other adverse pregnancy outcomes (Cooley et al., 2013).

     The aim of this study was to determine the normal sonographically measured placental thickness in millimeters from 18 week onwards, and to determine the correlation between measurement and the estimated fetal weight.

PATIENTS AND METHODS

     The study had been conducted at Obstetrics and Gynecology Department, Edfu General Hospital.

     This was a prospective observational study which included 100 pregnant women from October 2018 to January 2020.

     The study included women with singleton pregnancy, gestational age between 18– 40 weeks of gestation, with known last menstrual period and a history of regular menstruation.

     Patients with gestational hypertension, diabetes mellitus, Intrauterine growth restriction, hydropes fetalis, congenital malformation, twins, polyhydramnios, last menstrual period not known, irregular menstrual period, abnormal placental and poor visualization of placenta., placental with variation in insertion of umbilical cord were excluded.

     Written consents were taken from all patients before starting the study with counseling about risk and benefit of study.

     Patients were subjected to complete history taking, examination and sonographic technique of placental thickness measurement.

Statistical Analysis:

     Data were collected, coded, entered and analyzed using Microsoft Excel software. Data were then imported into Statistical Package for the Social Sciences (SPSS version 20.0) software for analysis. According to the type of data, qualitative were represented as number and percentage, quantitative continues group were represented by mean ± SD, the following tests were used to test differences for significance; Linear regression and ANOVA tests were used followed by Post-hoc test. Correlation by Pearson's correlation or Spearman's. P value was set at


 

RESULTS

 

 

     Mean of Placental thickness 2nd trimester was 24.67±3.3with range of (18-32), mean of Placental thickness 3nd trimester was 36.83±7.3with range of (29-57), mean of biparietal diameter 2nd trimester was 60.1±8.1with range of (46.4-70.8), mean of femur length 2nd trimester was 44.5±6.9 with range of (32.7-53.8), mean of abdominal circumferance2nd trimester was 199.6±29.9 with range of (149.1-239), mean of head circumference 2nd trimester 230.3±30.1 with range of (176.8-266.1). Mean of biparietal diameter 3rd trimester was 82.12±5.9 with range of (73.5-90.5), mean of femur length 3rd trimester was 64.1±5.6 with range of (56.1-72.3), mean of abdominal circumference 3rd trimester was 287.2. ±26.3with range of (250-326.1), mean of head circumference 3rd trimester 305.3±20.2with range of (275.5-333.3). Mean Birth weight (g) was 3044.7±523.1 with range of (2200-4000) and mean Placental weight was 511±64 with range of (290-630) (Table 1).


 

 

 

 

 

 

 

 

 

 

 

 

 

Table (1):   Second trimesteric placental thickness, EFW, birth weight, and placental weight

Variables

 

Placental thickness 2nd trimester:

Mean ± SD

Range

10th percentile

90th percentile

24.67±3.3

18-32

20.0

28.5

Biparietal diameter 2nd trimester:

Mean ± SD

Range

60.1±8.1

46.4-70.8

Femur length 2nd trimester:

Mean ± SD

Range

44.5±6.9

32.7-53.8

Abdominal circumference 2nd trimester:

Mean ± SD

Range

199.6±29.9

149.1-239

Head circumference 2nd trimester

Mean ± SD

Range

230.3±30.1

176.8-266.1

Placental thickness 3nd trimester:

Mean ± SD

Range

10th percentile

90th percentile

36.83±7.3

29-57

30.0

52.0

Biparietal diameter 3nd trimester:

Mean ± SD

Range

82.12±5.9

73.5-90.5

Femur length 3nd trimester:

Mean ± SD

Range

64.1±5.6

56.1-72.3

Abdominal circumference 3nd trimester:

Mean ± SD

Range

287.2. ±26.3

250-326.1

Head circumference 3rd trimester

Mean ± SD

Range

305.3±20.2

275.5-333.3

Birth weight (g)

Mean ± SD

Range

3044.7±523.1

2200-4000

Placental weight

Mean ± SD

Range

520.36±52.15

290-630

 

 

     There was significant relation between placental thickness second trimester and fetal birth weight, also there is high significant relation between placental thickness second trimester and placental weight (Table 2).

 

 

 

Table (2):   Relation between placental thickness second trimester and fetal birth weight and placental weight

Placental thickness

 

 

 

Variables

Abnormal thin placenta less than 10th percentile (N=5)

Normal placental thickness (N=44)

Abnormal Increased thickness of placenta more than 90th percentile (N=5)

P value

Fetal birth weight (g)

Mean ± SD

2751.5±322.6

3324.1±377.9

2800±833.7

< 0.003

Placental weight(g)

Mean ± SD

462.2±49.2

532.3±37.2

452.5±102

<0.001

F is for ANOVA test.

 

 

     There was significant relation between placental thickness second trimester and fetal birth weight, also there is significant relation between placental thickness second trimester and placental weight (Table 3).

 

 

Table (3):   Relation between placental thickness 3rd trimester and fetal birth weight and placental weight

Placental thickness

 

Variables

Abnormal thin placenta (N=3)

Normal placental thickness (N=39)

Abnormal Increased thickness of placenta (N=4)

P value

Fetal birth weight (g)

Mean ± SD

2751.5±322.6

3305.2±361.9

3060±458

0.032

Placental weight(g)

Mean ± SD

462.2±49.2

530.5±35.6

483.6±112.4

< 0.016

 

 

     There was significant positive correlation between 2nd trimester placental thickness and fetal birth weight, placental weight and APGAR score. There was significant positive correlation between 3rd trimester placental thickness and fetal birth weight, placental weight and APGAR score (Table 4).

 

 

Table (4):   Correlation between 2nd and 3rd trimester placental thickness and fetal birth weight, placental weight and APGAR score

P

r

2nd trimester placental thickness

Variables

<0.05

0.354

fetal birth weight

<0.05

0.332

placental weight

<0.05

0.423

APGAR score*

P

r

3rd trimester placental thickness

Variables

<0.05

0.319

fetal birth weight

<0.05

0.28

placental weight

<0.05

0.414

APGAR score*

r is correlation coefficient of Pearson's correlation, * is for spearman's correlation

 

     Changes in fetal weight can be predicted by placental thickness 2nd trimester by 12.5 %, also changes in fetal weight can be predicted by placental thickness 3rd trimester by 10 %. Changes in placental weight can be predicted by placental thickness 2nd trimester by 11%, also changes in fetal weight can be predicted by placental thickness 3rd trimester by 7.8 % (Table 5).

 

 

Table (5):   Linear regression of placental thickness 2nd trimester and 3rd trimester for prediction of fetal birth weight and placental weight

Fetal birth weight

Variables

B

SE

Beta

Significance

R 2

placental thickness 2nd trimester

51.1

19.5

0.354

<0.05

0.125

placental thickness 3rd trimester

36.4

15.6

0.319

<0.05

0.1

 

Placental weight

Variables

B

SE

Beta

Significance

R 2

placental thickness 2nd trimester

5.4

2.2

0.332

<0.05

0.11

placental thickness 3rd trimester

3.6

1.8

0.28

<0.05

0.078

B, regression coefficient; SE, standard error, R 2 Coefficient of determination

 

 

DISCUSSION

     A healthy baby at term is the product of three important factors: a healthy mother, normal genes, and good placental implantation and growth. The placenta is the most important but unfortunately often ignored organ. A normally functioning placenta is required for normal fetal growth and development. It has been historically documented that placental weight in a normal pregnancy at term is about one-fifth of the fetal weight (Nagpal et al., 2018).

     Normal placental function and structure are required for normal growth and development of the fetus. Placental thickness is the simplest measurement of placental size and can be measured at any center equipped with ultrasound machine. The correlation of placental thickness with gestational age has been documented by many observers (Quant et al., 2016).

     The study was a prospective observational study in 100 pregnant women.

     The main results of the study were as following:

     Our study show that there mean age is 25±3.1with range of (20-30), mean weight 78±12 with range of (55-115), mean height 1.7±0.07 with range of (1.55-1.78) and mean BMI is 27.1±3.7 with range of 18.8-38.9.

     This coped with the study of Nagpal et al. (2018) who studied role of ultrasonographic placental thickness in prediction of fetal outcome and reported that the majority of the women were in age group of 19–23 years. The mean height of women in our study was 154.2±4.56 cm, and the mean BMI was 21.85±1.60 kg/m. Afrakhteh et al. (2013) reported that the age range was 16 to 42 years.

     Similar finding in our study was conducted by Kakumanu et al. (2018) who studied evaluation of placental thickness as an ultrasonographic parameter for estimating gestational age of the fetus in 2nd and 3rd trimesters. They reported that a greater number of patients were in 20-25 years of age (48.0%), followed by 26-30 years (39.30%).

     Sonographically thick placentae were associated with maternal diabetes mellitus, hypertension, fetal hydrops, and other abnormalities (Balla et al., 2014).

     Sersam et al. (2016) reported that maternal parameters were evaluated in the second trimester of the pregnancy, the mean weight was 69.08±8.11 kg, and the mean body mass index was 26.81± 3.49 kg/m2, with mean BMI gain of 1.15± 0.56 kg/m2, while the mean of placental thickness measured by ultrasound was 2.44±0.57 cm. The pregnant women were also assessed in the third trimester, the mean weight was 73.05±7.74 Kg, and the mean body mass index was 28.36±3.42 kg/m2, with mean gain of 2.7±0.83 kg/m2, while the mean placental thickness measured using ultrasound was 3.58±0.59 cm, and mean thickness change between the second and third trimester was 1.14± 0.38.

     The present study showed that 46% of cases had a normal vaginal delivery, and 54% of cases had cesarean section. This coped with the study of Afrakhteh et al. (2013) who reported that 18% of mothers had history of previous disease including diabetes, hypertension, thyroid disease and infertility. Two cases of intrauterine fetal demise occurred in the study group. No cases of hydrops fetalis or a specific infectious disease (syphilis, cytomegalovirus infection, toxoplasmosis, schistosomiasis) were reported. The delivery mode was normal vaginal (NVD) in 59% and cesarean in 41%. Baby Apgar score of less than 3, 3 to 7 and greater than 7 were observed in 2%, 9.3% and 88.7% newborns respectively.

     Also, this coped with the study of Nagpal et al. (2018) who reported that the mean placental thickness at 32 and 36 weeks were 33.45 ± 1.62 and 35.7 ± 2.08 mm. In our study, placentae with thickness (determined by antenatal ultrasound) below 10th percentile (\mean - 2SD) were considered as abnormally thin placentae. Also placentae with thickness more than 95th percentile ([mean 2SD) were considered as abnormally thick placentae. Placental thickness between 10th and 95th percentile was considered normal at 32 and 36 weeks (The pregnant women were divided according to placental thickness—those with thin, normal and thick placenta.

     Nagpal et al. (2018) reported that biometric parameters were (r = 0.67 at 32 weeks and r = 0.735 at 36 weeks). Also, there was a strong positive correlation between placental thickness and birth weight according to Pearson’s correlation analysis.

     This coped with the study of Afrakhteh et al., (2013) who reported that there was a significant positive correlation between placental thickness and birth weight in the second and third trimesters. However, no correlation was observed with placental thickness change. Placental weight did not correlate with both second and third trimester’s placental thickness.

     Sersam et al. (2016) reported that a significant positive correlation was found between placental thickness and birth weight in the second and third trimesters. Also our results partially agreed with those reported by Balla et al. (2014) who found a linear relation between maternal age and placental thickness, in the second and third trimesters, but disagreed with those reported by Miwa et al. (2014) who noted a lack of relation between placental thickness and maternal age. No relation between placental thickness and gestational age has been documented by Appiah (2018).

     A weak positive correlation was observed between placental thickness in the second and third trimesters and birth weight, mainly in birth weight. This was also observed by Afrakhteh et al. (2013). Still, we didn’t find a relation between thick placenta and low or high birth weights. This might be explained by small sample size in our study.

     This disagreed with the findings by Elchalal et al. (2012), who reported a higher percentage of thick placentas in birth weight at term above 4000 gm or less than 2500 gm.

     Schwartz et al. (2012) studied two-dimensional sonographic placental measurements in singleton pregnancies between 18 and 24 weeks, and found that mean placental thickness and diameter were significantly smaller in small-for-gestational-age infants.

     There was a significant positive correlation between 2nd trimester placental thickness and fetal birth weight, placental weight and APGAR score

     Nagpal et al. (2018) reported that fetal outcome was compromised when placental thickness was 10th percentile (31.1 mm), with good Apgar scores in 25% babies and poor Apgar scores in 75% babies. NICU admissions were there in 75% cases. Fetal outcome was compromised when placental thickness was 95th percentile at 36 weeks (39.9 mm), with good Agar scores in 20% babies and poor Apgar scores in 80% babies. All the babies were admitted to NICU.

     The present study showed that linear regression of placental thickness in 2nd trimester and 3rd trimester for prediction of placental weight showed that Placental weight can be predicted by placental thickness in 2nd trimester by 11%, and in 3rd trimester by 7.8 %. Changes in fetal weight can be predicted by placental thickness 2nd trimester by 12.5 %. Also changes in fetal weight can be predicted by placental thickness 3rd trimester by 10%.

     Schneider et al. (2010) reported that regression analysis yielded linear mathematical relationships between estimated fetal weight and placental thickness in the second and third trimesters, but the marked variations in fetal weights corresponding to particular placental thickness limit the usefulness of this relationship.

     Mathai et al. (2013) noted that regression analysis yielded linear equations of relationship with placental thickness and gestational age in both groups.

     Adeyekun et al. (2015) found a mean placental thickness of 22.6 mm at 15 weeks gestation to 39.2 mm at 39 weeks. The mean estimated fetal weight ranged from 147.0 g at 15 weeks to 3187.4 g at 39 weeks gestation. The correlation and probability values were 0.668 and 0.000 respectively.

CONCLUSION

     Placental thickness measured at the level of umbilical cord insertion can be used as an accurate sonographic indicator in the assessment of fetal weight because of its linear correlation.

REFERENCES

  1. Adeyekun, A. A. and Ikubor, J. E. (2015): Relationship between two-dimensional ultrasound measurement of placental thickness and estimated fetal weight. Sahel Medical Journal, 18(1): 4-10.‏
  2. Afrakhteh, M., Moeini, A., Taheri, M. S. and Haghighatkhah, H.R. (2013): Correlation between placental thickness in the second and third trimester and fetal weight. Revista Brasileira de Ginecologia e Obstetrícia, 35(7): 317-322.‏
  3. Appiah PK. (2018): Relationship between the morphology of placenta, Umbilical cord and Perinatal Outcome. Kwame Nkrumah University of Science and Technology.
  4. Balla, EAA., Ahmed, MS., Ayad, CE. and Ahmed, AS. (2014): Prediction of fetal growth by measuring the placental thickness using ultrasonography. Journal of Gynecology and Obstetrics, 2:26-31.
  5. Cantonwine, D.E., Ferguson, K.K., Mukherjee, B., Chen, Y. H., Smith, N.A., Robinson, J.N., Doubilet, P.M., Meeker, J.D. and McElrath, T.F. (2016): Utilizing longitudinal measures of fetal growth to create a standard method to assess the impacts of maternal disease and environmental exposure. PloS one, 11(1): e0146532.
  6. Cooley, SM., Donnelly, JC, Walsh T, McMahon C, Gillan J. and Geary MP. (2013): The correlation of ultrasonographic placental architecture with placental histology in the low-risk primigravid population. J Perinat Med Mar., 21:1-5.
  7. Elchalal, U., Ezra, Y., Levi, Y., Bar-Oz, B., Yanai, N., Intrator, O. and Nadjari, M. (2012): Sonographically thick placenta: a marker for increased perinatal risk–a prospective cross-sectional study. Placenta, 21:268–72.
  8. Kakumanu, P.K., Kondragunta, C., Gandra, N. R. and Yepuri, 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): 128-32.‏
  9. Mathai, B. M., Singla, S. C., Nittala, P. P., Chakravarti, R. J. and Toppo, J. N. (2013): Placental thickness: its correlation with ultrasonographic 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.‏

10. Milner, J. and Arezina, J. (2018): The accuracy of ultrasound estimation of fetal weight in comparison to birth weight: A systematic review. Ultrasound (Leeds, England): 26(1): 32–41.

11. Miwa, I., Sase, M., Torii, M., Sanai, H., Nakamura, Y. and Ueda, K. (2014): A thick placenta: a predictor of adverse pregnancy outcomes. Springer plus, 3(1):1-4.

12. Nagpal, K., Mittal, P. and Grover, S. B. (2018): Role of Ultrasonographic Placental Thickness in Prediction of Fetal Outcome: A Prospective Indian Study. The Journal of Obstetrics and Gynecology of India, 1-6.‏

13. Quant, H. S., Sammel, M. D., Parry, S. and Schwartz, N. (2016): Second-trimester 3‐dimensional placental sonography as a predictor of small-for-gestational-age birth weight. Journal of Ultrasound in Medicine, 35(8): 1693-1702.

14. Salavati, N., Sovio, U., Mayo, R. P., Charnock-Jones, D. S. and Smith, G. C. S. (2016): The relationship between human placental morphometry and ultrasonic measurements of utero-placental blood flow and fetal growth. Placenta, 38: 41-48.

15. Schneider, A., Hommel, G. and Blettner, M. (2010): Linear regression analysis: part 14 of a series on evaluation of scientific publications. Deutsches Ärzteblatt International, 107(44): 776.

16. Schwartz N, Wang E and Parry S. (2012): Two-dimensional sonographic placental measurements in the prediction of small for gestational age infants. Ultrasound Obstet Gynaecol, 40(6):674–9.

17. 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 Academic Scientific Journal, 15(2): 185-193.

18. Sharma, D., Shastri, S. and Sharma, P. (2016): Intrauterine Growth Restriction: Antenatal and Postnatal Aspects. Clinical medicine insights. Pediatrics, 10: 67–83.

19. Tarca, A. L., Romero, R., Gudicha, D. W., Erez, O., Hernandez-Andrade, E., Yeo, L. and Hassan, S. (2018): A new customized fetal growth standard for African American women: the PRB/ NICHD Detroit study. American Journal of Obstetrics and Gynecology, 218(2): S679-S691.‏

20. Zhang, J., Li, H., Wang, F., Qin, H. and Qin, Q. (2016): Prenatal Diagnosis of Abnormal Invasive Placenta by Ultrasound: Measurement of Highest Peak Systolic Velocity of Subplacental Blood Flow. Ultrasound in medicine and biology, 44(8): 1672-1678.

 

قياس سمک المشيمة باستخدام الموجات فوق الصوتية کمؤشر على وزن الجنين

هشام أحمد علي حسين، إسماعيل محمد طلعت الجارحي، عبد المنصف عبد الحميد صديق

قسم أمراض النساء والتوليد، کلية الطب، جامعة الأزهر

E-mail: obshesham@gmail.com

خلفية البحث: تتطور المشيمة البشرية مع الوظيفة الرئيسية لتوفير المغذيات والأکسجين للجنين. کان الهدف من هذه الدراسة هو تقييم العلاقة بين سمک المشيمة مع وزن الجنين المقدر.

الهدف من البحث: تحديد سُمک المشيمة الطبيعي المقاس بالموجات فوق الصوتية بالملليمتر من 18 أسبوعًا وما بعد ذلک وتحديد علاقة هذا القياس بالوزن المقدر للجنين.

المريضات وطرق البحث: شملت هذه الدراسة 100 سيدة حامل تتراوح أعمارهم بين 18 و 35 سنة. بعد موافقة لجنة الأخلاقيات المؤسسية، وقد لوحظ جميع النساء المعينات للبيانات الديموجرافية والتوليدية الأساسية بما في ذلک العمر وعدد مرات الولادة والأحداث الطبية السابقة في أول زيارة سابقة للولادة. قدمت جميع النساء موافقة خطية مستنيرة وخضعت لتقييم الموجات فوق الصوتية لسمک المشيمة في 18 إلى 40 أسبوعًا من الحمل.

نتائج البحث: کان متوسط سُمک المشيمة فى الثلث الثاني 24.67 ± 3.3 ومتوسط وزن المولود (جم) 3044.7 ± 523.1 مع مدى (2200-4000).

الاستنتاج: يُعتبر وزن الجنين المقدر أحد العناصر المهمة في رعاية ما قبل الولادة حيث يلعب التصوير بالموجات فوق الصوتية دورًا مهمًا. يمکن استخدام سمک المشيمة الذي يتم قياسه على مستوى إدخال الحبل السري کمؤشر صوتي دقيق في تقييم وزن الجنين بسبب ارتباطه الخطي.

الکلمات الدالة : سمک المشيمة – الموجات فو الصوتية – وزن الجنين .

  1. REFERENCES

    1. Adeyekun, A. A. and Ikubor, J. E. (2015): Relationship between two-dimensional ultrasound measurement of placental thickness and estimated fetal weight. Sahel Medical Journal, 18(1): 4-10.‏
    2. Afrakhteh, M., Moeini, A., Taheri, M. S. and Haghighatkhah, H.R. (2013): Correlation between placental thickness in the second and third trimester and fetal weight. Revista Brasileira de Ginecologia e Obstetrícia, 35(7): 317-322.‏
    3. Appiah PK. (2018): Relationship between the morphology of placenta, Umbilical cord and Perinatal Outcome. Kwame Nkrumah University of Science and Technology.
    4. Balla, EAA., Ahmed, MS., Ayad, CE. and Ahmed, AS. (2014): Prediction of fetal growth by measuring the placental thickness using ultrasonography. Journal of Gynecology and Obstetrics, 2:26-31.
    5. Cantonwine, D.E., Ferguson, K.K., Mukherjee, B., Chen, Y. H., Smith, N.A., Robinson, J.N., Doubilet, P.M., Meeker, J.D. and McElrath, T.F. (2016): Utilizing longitudinal measures of fetal growth to create a standard method to assess the impacts of maternal disease and environmental exposure. PloS one, 11(1): e0146532.
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