Prognosis of the End of Obstetrical Newborn-Born to EHS Nouar Fadela “Preliminary Results”

Article Information

Bouabida D*, Zelmat S, Belalaoui I

Oran Faculty of Medicine, Oran University 1, Oran, Algeria

*Corresponding Author: Bouabida D, Oran Faculty of Medicine, Oran University 1, Oran, Algeria

Received: 09 February 2021; Accepted: 25 February 2021; Published: 05 March 2021


Bouabida D, Zelmat S, Belalaoui I. Prognosis of the End of Obstetrical Newborn-Born to EHS Nouar Fadela “Preliminary Results”. Journal of Pediatrics, Perinatology and Child Health 5 (2021): 039-045.

View / Download Pdf Share at Facebook


Introduction: Performing a cesarean section at term or near term disrupts the normal cardiorespiratory adaptation of the newborn.

Objective: To study the neonatal prognosis of the delivery of newborns.

Materials and Methods: This is a cross-sectional, descriptive and analytical study; carried out at the “Nouar Fadéla neonatal service” during the period from April 15, 2015 to March 15, 2017 inclusive. The study looked at risk factors, the mode of delivery and perinatal complications.

Results: 6741 deliveries were performed. 889 newborn mothers were included in this study. For maternal characteristics: on average, mothers were 30 ± 5.70 years old and had a BMI of 27.4 ± 4.9 kg/m2. The upper route was the main outcome of the delivery of macrosome newborns. For the characteristics of newborns: the birth weight (PN) varied between 4000 gr and 5900 gr with an average PN of: 4172 ± 339 gr. Neonatal morbidity by route of delivery is dominated respectively by: hypoglycemia in 19.3%; deep hematomas in 3.8% and brachial plexus palsy (PPB) in 2.1%. Lethality was noted in 0.9% of cases.

Conclusion: The vaginal delivery is the main mode of delivery. However, shoulder dystocia is the main complication requiring management of childbirth by experienced obstetricians.


Cardiorespiratory adaptation, Pregnancy, Obstetrical newborn, Delivery

Cardiorespiratory adaptation articles; Pregnancy articles; Obstetrical newborn articles; Delivery articles

Article Details

1. Introduction

Performing a cesarean section at term or near term (especially before labor) is a clearly identified risk factor for the onset of respiratory distress in the newborn. This way of delivery disrupts the normal cardiorespiratory adaptation of the newborn objective: to study the neonatal prognosis of macrosome delivery.

2. Methods

Retrospective and analytical descriptive study including 324 macrosomes at term during the period from January 1, 2015 to December 31, 2015 at the neonatology department of EHS NOUAR FADELA. The study looked at risk factors, mode of delivery as well as fetal perinatal complications. We compared these results to the results of a eutrophic full-term birth weight control group during the same period. Variable analysis was performed using SPSS version 9.0 software. The results were expressed as mean ± standard deviation. The student test to compare the means. The differences observed are considered significant when p was less than 0.05.

3. Results

On average, the mothers were 30 ± 5.70 years old; measured 1.63 m ± 6.49; the mean term of 38.82 ± 1.31, parity of 2.32 ± 1.18 and BMI of 27.45 ± 4.96 kg/m2. During pregnancy, they gained an average of 9.99 ± 7.43 kg with significant differences.

Mothers Characteristics


N = 425


No Macrosomes

N = 464


Meaning Threshold


Age: Years 

30.60 ± 5.7

30.08 ± 6.30


Medium Term (Sa)

38.82 ± 1.3

38.57 ± 1.18



2.32 ± 1.1

2.00 ± 1.09


Weight Before Pregnancy (Kg) 

73.64 ± 13

67.47 ± 12.5


Size (cm) 

163.85 ± 6.4

162.39 ± 6.25

= 0.001

Bmi (Kg/m2

27.45 ± 4.9

25.56 ± 4.50


Weight During Pregnancy (Kg) 

83.63 ± 14

76.36 ± 13.0


Weight Gain (Kg) 

9.99 ± 7.4

8.89 ± 6.29

= 0.018

Table 1: Maternal characteristics.



N = 425

No Macrosomes

N = 464

OR [95% CI]

Meaning threshold






Abortion (Abrt)





1.3 [0.89 - 1.89]


Death in utero (MIU)





0.93 [0.5 - 1.76]


Gestational Diabetes





2.26 [1.54 - 3.31]


Chronic diabetes





2.59 [1.22 - 5.52]


Arterial hypertension (hypertension)





1.24 [0.87 - 1.76]


Macrosomia history





5.18 [3.66 - 7.29]


Table 2: Maternal ATCD.

The antecedent of macrosomia (40% versus 11.4%): (p <0.0001) is the most characteristic antecedent in our studied population with a risk multiplied by 5.18 with a significant difference (P<0.0001) follow-up of gestational diabetes (20.7% vs 10.3%): p < 0.0001 and chronic diabetes (5.4% vs 2.2%) (p = 0.01).

3.1 Characteristics of New Born

The male sex (72.9%) is more frequent than the female sex (27.1%). This difference is statistically significant with (p <0.0001) compared to eutrophic NNs with a relative risk multiplied by 2. The birth weight (PNN) varied between 4000g and 5900g with an average PNN of: 4172 ± 339 gram vs the birth weight of the controls varied between 2380g and 3800g with an average PNN of: 3296 ± 278 gram (p <0.0001). The mean bw of macrosome newborns was: 35.82 ± 1.26 vs. controls was 34 ± 1.10 cm (p <0.0001). The mean size of the newborn macrosomes was: 51 ± 2.31 cm vs the controls was 48.7 ± 2.12 cm (p <0.0001).

3.2 Evolution of Labor and Decision of the Method of Delivery

The majority of deliveries of NN macrosomes were by the upper route, i.e. 314 cases (73.3%) vs. 111 cases (26.1%) by the base route with a significant difference (p = 0.005) (Table 3).

3.3 Complications of Nn in Relation to the Path of Delivery of Macrosomes

In the low route, compared to the high route outcome; traumatic complications are dominated in macrosomes by brachial plexus palsy (p = 0.042) followed by BSS (p = 0.01) (Table 4).






Meaning Threshold













Table 3: Distribution of newborns by route of delivery.

Route of Delivery


High channel Basic channel

N (%)

Meaning threshold


Hypoglycemia (<0.40 gr/l) 

64 (20.4)

18 (16.2)


Hypocalcaemia (<80 mg/l)

6 (1.9)

1 (0.9)



29 (9.2)

16 (14.4)



1 (0.3%)

0 (0)


Perinatal Asphyxia

44 (14)

10 (9)


Respiratory Distress

34 (8)

8 (1.8)


Hypertrophic Cardiomyopathy (CMH)

3 (1)

0 (0)


Brachial Plexus Palsy (PPB)

4 (1.3)

5 (4.5)


Clavicle Fracture

2 (0.9)

1 (0.6)


Humeral Fracture

4 (1.3) 

1 (0.9)


Serum Blood Lump BSS

21 (14.4)

16 (6.7)



12 (3.8)

4 (3.6)



2 (0.6)

2 (1.8)


Table 4: Complications of NN over the route of delivery of macrosomic.

4. Discussion

Our hospital prevalence is 6.3%. Our results remain close to those found by the majority of studies; on the other hand, some authors report a higher frequency [1, 2]. This increase may be linked to a higher maternal weight gain during pregnancy, to the increase in the frequency of maternal obesity and diabetes, and diet. However, other authors report a lower frequency, especially in African countries. These variations in frequency between series could be explained by: the size of the sample, insufficient follow-up, lack of healthy lifestyle during pregnancy as well as low socio-economic level [3, 4]. Compared to literature data, age and multiparity were not statistically significant as a risk factor in our study. Exceeding the term was observed in 32% of mothers with emacrosomes, which is consistent with most studies. This can be explained by: lack of an early ultrasound for dating the pregnancy, imprecision of the date of the last period and the irregular nature of prenatal consultations [1, 5, 6]. As for the 25% rate of obesity cases found in our series, it is similar to that observed in the literature [7]. And the risk of giving birth to a macrosome is multiplied by 2 in pregnant women who are overweight and obese. While in the literature this risk is multiplied by 3 with a weight gain interval varying between 12-18 Kg [8]. In our series, the weight gain was 15 kg and the risk is multiplied by 2. The excessive weight gain can be explained by a modification of the maternal metabolism because it is dependent on food, thus explaining the macrosomia by anabolism [9, 10].

Regardless of the type of diabetes, our results match those of the literature, but the percentage of gestational diabetes in our series is higher compared to studies. This can be explained mainly by the ethnic and genetic variations of the populations, but also, to a lesser extent, by the diversity of the strategies and screening methods used [9, 11] the antecedent of macrosomia is the most implicated factor. However, its pathophysiology has not yet been elucidated, which confirms that a woman who has given birth to a macrosome most often recurs with a risk multiplied by six (OR = 6). And in our series , this is multiplied by 4 [11-13].

Male predominance has been reported by most authors, with a relative risk multiplied by 2, and our results agree with most studies. For this, hypotheses have been proposed to explain why girls are born lighter than boys. Wilkin and Murphy have suggested that the gender specific genes affecting insulin sensitivity are responsible for the difference between the birth weights of the two sexes [14-16]. According to them, the female fetus is genetically more resistant to insulin and less sensitive to the trophic effects of insulin and is therefore smaller [11, 17, 18, 19]. The majority of macrosomal childbirths were eutocic (73.9% vs. 65.7% controls) via the upper route with a significant difference. This rate of cesarean section in the macrosome group is high compared to that found by most studies, therefore, macrosomia increases the risk of cesarean section (p = 0.005). This rate varies according to the studies [20, 21, 22]. As evidenced by the majority of Moroccan series, the delivery of a macrosome is first spontaneous.The use of forceps is rare, unlike in European and American countries, where the use of forceps is more frequent [20, 23-24].

The morbidity and neonatal mortality of newborns macrosomes related to the delivery route:

Our results had shown a significantly higher rate of cesarean section in mothers of macrosomes than in mothers of eutrophic patients 73% vs 49.3% statistically significant (p = 0.005). This rate of cesarean section in the macrosome group is identical to that found in the literature [24, 25]. Cesarean sections were in 95 (30.1%) prophylactic cases for estimated fetal weight (3900-5300g). This attitude aims to reduce fetal morbidity by some authors [26, 27]; while several studies have shown that vaginal delivery is a more reasonable alternative to elective caesarean section [28]. The American College of Obstetric Gynecology has suggested carrying out a prophylactic cesarean delivery for any suspicion of macrosomia with PFE ≥ 5000g in non-diabetic women and ≥ 4500g in cases of diabetes [29].

In our study, the upper pathway in macrosomes is dominated by metabolic complications, namely hypoglycemia 64 cases (20.4%) followed by perinatal asphyxia 44 cases (14%), and respiratory distress 34 cases (8%). Complications according to the low channel is at the macrosomic are dominated s by traumatic complications such as paralysis of the brachial plexus 5 cases (4.5%) and blood serum bump (6.7%). The neonatal morbidity linked to the delivery of a macrosome is not negligible. It is dominated by lesions of the brachial plexus (p = 0.042) and sero-blood bumps (p = 0.01). The latter are formidable and quite frequent in our series. They reflect the existence of a fetopelvic disproportion. This is in line with the results found by other  authors. This morbidity seems to be linked to a lack of early management of high-risk pregnancies, especially in cases of fetopelvic disproportion. Added to this is the delay in evacuations from peripheral centers and the quality of prenatal consultation.

5. Conclusion

Vaginal delivery is the primary mode of delivery in macrosomia. There is no indication for systematic caesarean section in the event of a fetal weight exceeding 4 kg. However, shoulder dystocia constitutes the main neonatal complication of childbirth by natural means requiring childbirth management by experienced obstetricians.


  1. Grossetti E, Beucher G, Regeasse A, et al. Obstetric Complications Of Morbid Obesity. J Gynecol Obstet Biol Reprod 33 (2004): 739-744.
  2. Koyanagi AI, Jun Zhang, Amarjargal Dagvadorj, et al. Macrosomia In 23 Developing Countries: An Analysis of a Multicountry, Facility-Based, Cross-Sectional survey. Lancet 381 (2013): 476-483.
  3. Fatnassi R, Ragmoun H, Marzougui L, et al. Risk factors and materno-fetal prognosis of foetal macrosomia: comparative study of 820 cases. Pan African Medical Journal 28 (2017): 126.
  4. Panel P, De Meus JB, Yanolopoulos B, et al. Childbirth Of The Big Child. J.Gynecol. Obstet. Biol. Reprod 20 (1991): 729-736.
  5. Matthew C, Neil J, John P. Risk Factors For Macrosomia A Ditz Clinical Consequence: A Study Of 350,311 Pregnancies. Eur J Obstet Gynecol Reprod Biol 111 (2003): 9-14.
  6. Coulibaly Etienne Y. Childbirth Of A Large Fetus At Chu Gabrieltoure: Risk Factors And Materno-Fetal Prognosis. Medical Thesis (2008-2009).
  7. Ballard Jl, Rosenn B, Khoury JC, et al. Diabetic Fetal Macrosomia: Significance Of Disproportionate Growth. J Pediatr 122 (1993): 115-119.
  8. World Health Organization (Who): Recommended Definition Terminology And Format For Statistical Tables Related To The Perinatal Period And Rise Of A New Certification For Cause Of Perinatal Deaths. Modifications Recommended By Figo As Amended, October 14, 1976. Acta Obstet Gynecol Scand 56 (1977): 347.
  9. Ben-Haroush A, Yogev Y, Hod M. Epidemiology Of Gestational Diabetes Mellitus And Its Association With Type 2 Diabetes Diabet. Med 21 (2004): 103-113.
  10. Mimouni N. Epidemiological Profile Of Newborns Of Diabetic Mothers In The Neonatology Service Of Mother-Child Ehs Of Tlemcen Berrandou, Medical Thesis (2015).
  11. Wilkin TJ, Murphy MJ. The Gender Insulin Hypothesis: Why Girls Are Born Lighter Than Boys, And The Implication Of Insulin Resistance. Int J Obes 30 (2006): 1056-1061.
  12. Dolo A. Delivery Of The Large Fetus In The Obstetric Gynecology Department Of The University Hospital Center At Point G. Apropos Of 205 Cases Thes. Med.: Bamako (2001).
  13. Magnin G. Childbirth Of The Big Child. Prat Childbirth J Lansac G Bodyeds Vilerbanne Simep Edn (1989): 149.
  14. Ørskou J, Henriksen TB, Kesmodel U, et al. Maternal Characteristics And Lifestyle Factors And The Risk Of Delivering High Birth Weight Infants. Obstetrics And Gynecology 102 (2003): 115-120.
  15. Cuifang F, Tingting H, Fangfang C, et al. And All paternal Factors To The Offspring Birth Weight: The 829 birth Cohort Study. Int J Clin Exp Med 8 (2015): 11370-11378.
  16. Gerard G Nahum, Harold Stanislaw. Relationship Of Paternal Factors To Birth Weight. The Journal Of Reproductive Medicine 48 (2003): 963-968.
  17. Fettah Meriem. Full Term Fetal Macrosomia (About 340 Cases) These Presented And Publicly Supported. Morocco (2016).
  18. Andersen J, Watt J, Olson J, et al. Perinatal Brachial Plexus Palsy. Paediatrics & Child Health 11 (2006): 93-100.
  19. Aisha Salim Said. Risk Factors And Outcomes Of Fetal Macrosomia In A Tertiary Center In Tanzania: A Case-Control Study. Bmc Pregnancy And Childbirth 16 (2016): 243.
  20. Cisse Sanogo A. Epidemiological-Clinical Study Of Fetal Macrosomia At The Reference Health Center Of The Commune II These Med. Bamako (2009).
  21. Battaglia FC, Meschia G. Fetal Nutrition. Annu Revnutr 8 (1988): 43-61.
  22. Kabali C and Werler MM. Pre-Pregnant Body Mass Index, Weight Gain, And The Risk of Delivering Large Babies Among Non-Diabetic Mothers. International Journal Of Gynecology And Obstetrics: The Official Organ Of The International Federation Of Gynecology And Obstetrics 97 (2007): 100-104.
  23. Frederick IO, Williams MA, Sales AE, et al. Pre-Pregnancy Body Mass Index, Gestational Weight Gain, And Other Maternal Characteristics In Relation To Infant Birth Weight. Maternal And Child Health Journal 12 (2008): 557-567.
  24. Phelan JP, Eglinton GS, Horenstein JM, et al. Previous Cesarean Birth - Trial Of Labor In Women With Macrosomic Infants. J Reprod Med 29 (1984): 36-40.
  25. Merlob P, Hod M. Short-Term Implications: The Neonate. In Eds.: Hod M, Jovanovic L, Di Renzo GC, et al. Textbook Of Diabetes And Pregnancy. 2nd Informa, London (2008).
  26. Cuifang Fan, Tingting Huang, Fangfang Cui, et al. Paternal Factors To The Offspring Birth Weight: The 829 Birth Cohort Study. Int J Clin Exp Med 8 (2015): 11370-11378.
  27. Aisha Salim Said, Karim Premji Manji. Risk Factors And Outcomes Of Fetal Macrosomia In A Tertiary Center In Tanzania: A Case-Control Study. BMC Pregnancy and Childbirth 243 (2016).
  28. Lips Comb K, Gregory K. The Outcomes Of Macrosomic Infants Weighing At Least 4500 Grams: Los Angeles Country + University Of Southern California Experience. Obstet Gynecol 85 (1995): 558-564.
  29. Panel P, De Meus JB, Yanolopoulos B, et al. Delivery Of The Big Child. Jgynecol. Obstet. Biol. Reprod 20 (1991): 729-736.

© 2016-2024, Copyrights Fortune Journals. All Rights Reserved