1. Introduction

OJOG

Open Journal of Obstetrics and Gynecology

2160-8792

Scientific Research Publishing

10.4236/ojog.2020.10110147

OJOG-104514

Articles

Medicine&Healthcare

Neonatal Outcome of Induced Prematurity for Severe Preeclampsia in Four Great Kinshasa Maternities

Olive

Yalala Ambambula

¹^*Andy

Muela Mbangama

¹Therese

Biselele

²Rashid

Rahma Tozin

¹Dieudonné

Mushengezi Sengeyi

Department of Pediatrics, University Clinics of Kinshasa, Kinshasa, DR Congo

Department of Obstetrics and Gynecology, University Clinics of Kinshasa, Kinshasa, DR Congo

06112020

10111637164325, September 202027, November 2020 30, November 2020

2014

This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

Severe preeclampsia (SPE) is associated with fetal complications including intrauterine growth retardation (IUGR), prematurity and in utero fetal death. Its treatment remains child birth that often is planned before term. However, this attitude can lead to fetal complications related to prematurity. Several studies on preeclampsia have already been studied in the DRC and several aspects have already been realized, but to date, the neonatal outcome has not yet been addressed. Methods: This is cross-sectional study performed in four public hospitals in Kinshasa (Democratic Republic of Congo). We included 400 cases of induced prematurity (IP) for SPE; the analysis compared pregnant women who gave birth before 34 weeks of amenorrhea (WA) and those after 34 WA. The comparison of the proportions was made by the Chi - square test and the calculation of Means by the Student’s test. The significance level was set at P < 0.05. Objective: To determine the frequency of induced prematurity for severe preeclampsia (SPE), to identify the indications and to evaluate neonatal outcome. Results: The IP frequency for SPE was 46.2%. The retro placental hematoma was the most indication in pregnancies before 34 WA 24.9%, while high blood pressure 54.5% in the after 34 WA group. In utero death was more common in pregnant women who gave birth before 34 weeks 25.4%; chronic fetal distress was elevated in the after 34 WA group 19.5%. Neonatal infection was more common in the group after 34 WA 49.4%, while respiratory distress 39.6%, intra and periventricular hemorrhage 19.5% and neonatal death 39.6% were more in group before 34 WA. Conclusion: Prematurity induced for SPE is related to a poor neonatal prognosis.

Preeclampsia Induced Prematurity Neonatal Outcome

1. Introduction

Severe preeclampsia (SPE) is associated with fetal complications including intrauterine growth retardation (IUGR), prematurity and in utero fetal death [1]. Its treatment remains childbirth that often is planned before term [2]. However, this attitude can lead to fetal complications related to prematurity [3].

According to WHO, preterm birth is defined as any childbirth occurring between 22 and 37 weeks of age [4]. In Low-income countries like the DRC, childbirth is premature when it occurs between 28 and 37 weeks of age [5]. Its prevalence varies between 60/1000 and 120/1000 of live births in developed countries [4]. In Europe, it is 8% and in the USA it represents 12% [6]. This last high rate is essentially represented by induced prematurity. In Africa, the situation is complicated, particularly in Low-income countries like those in sub-Saharan Africa, which alone account for 22% of premature births [3]. In the DRC, prematurity accounts for 15% [5] and University Hospital of Kinshasa is 40% [7].

We can classify prematurity in “extremely premature” when the delivery occurs before 28 WA; “high prematurity” when childbirth is between 28 SA and 32 WA; “moderate prematurity” when the delivery occurs between 33 WA and 36 WA.

In prematurity in general, there is a problem of immaturity of all organs anatomically and functionally. Nevertheless, what is most feared are the pulmonary problems and the appearance of motor sequel following cortical attacks. Other complications may include cerebral hemorrhage, hypothermia, hypoglycemia and hypocalcaemia [2]. Prematurity in the context of SPE is generally induced (iatrogenic decided by the medical team when the continuation of the pregnancy is threatening for the mother and/or the fetus) contrary to the spontaneous prematurity (which intervenes in the context of spontaneous work delivery) [6].

Several studies on preeclampsia have already been studied in the DRC and several aspects have already been realized, but to date the neonatal outcome has not yet been addressed that is the reason why we initiate this study which aims to determine frequency of induced prematurity for SPE; to identify indications of is induced prematurity and to evaluate its neonatal prognosis.

2. Methods

Our study is cross-sectional, conducted in the severe preeclampsia who gave birth in the context of IP and their newborns in four public maternities in the city of Kinshasa namely: The University Hospitals of Kinshasa, the Ngaliema Clinic, the Saint Joseph Hospital and the Provincial General Hospital of Reference of Kinshasa. The study period was from January 2013 to December 2017. The women were then divided into 2 groups: those who gave birth before 34 WA and those who gave birth after 4 WA.

2.1. Inclusion Criteria

We included in the study:

Pregnant women who had preeclampsia during the study period;

Preterm infants born from these women from the 28^th week to the 37^th in a single fetal pregnancy.

2.2. Exclusion Criteria

Pregnancies of less than 28 weeks and more than 37 completed weeks;

All situations that may lead to prematurity: multiple pregnancies, urinary tract infection, malaria, Premature rupture of membranes (PRM), etc.

Statistical analyzes: The Student’s T test was used for the comparison of the means while the Chi-square was used for the comparison of the proportions. The significance level was set at P ≤ 0.05.

2.3. Statistical Calculations

Data were entered using Microsoft Excel 2007 software and exported to SPSS 21.0 for analysis. For normally distributed parametric data, comparisons of averages were made using t-test and comparisons of proportions with chi-square test.

Pearson’s correlation test between biologic markers was used to seek potential associations with oxidative stress. Testing was stated significant at P ≤ 0.05.

This study has been designed and financed by our own funds.

2.4. Ethical Considerations

This project was prepared according to the Declaration of Helsinki and was agreed by Ethics Committee of Department of Obstetrics and Gynecology, University clinics of Kinshasa.

3. Results

During the period from January 2013 to December 2017, 23,945 deliveries were recorded, including 2192 cases of preeclampsia (9.1%) including 1503 cases of severe preeclampsia; and 1012 cases of preterm delivery (4.2%). We noted 400 cases of induced prematurity for severe preeclampsia, which represents a frequency of 1.7% of all deliveries, 18.3% of cases of preeclampsia and 39.5% of cases of preterm delivery.

Table 1 shows that the mean age of the study group was 29.5 ± 6.8 years. The majority were married and primipara. The mean pregnancy age at diagnosis of PE was 32 ± 3.01 weeks. The diagnosis of severe preeclampsia was early, at 30.8 ± 2.7 WA in the group of pregnant women who gave birth before 34 WA compared to the group who gave birth after 34 WA with a highly significant difference (P < 0.001). Furthermore, no statistically significant difference was noted when comparing the other features.

The most frequent indications of induced prematurity were persistence of high blood pressure figures with 49.3% followed by eclampsia with 18.8% and retro placental hematoma (RPH) with 17.8%.

Table 1 Indications of Induced Prematurity (IP)

Indication of IP	Premature ≥ 34 WA		Premature < 34 WA		Total		p
Indication of IP	Number	%	Number	%	Number	%	p
SPE (HBP↗)	126	54.5	71	42	197	49.3
Eclampsia	43	18.6	32	18.9	75	18.8
Retroplanetal hematoma	29	12.6	42	24.9	71	17.8
Eclamptic Prodrome	21	9.1	15	8.9	36	9	<0.05
Chronic fetal distress	11	4.8	8	4.7	19	4.8
Hellp Syndrome	1	0.4	1	0.6	2	0.5
Total	231	100	169	100	400	100

RPH was significantly more prevalent in the gestational group who gave birth before the 34th week of gestation (24.9% vs. 12.6% P < 0.05), whereas persistence of high blood pressure in the pregnant group who delivered from the 34th week (54.5% vs 42%, P < 0.05) (Table 2).

Table 2 Fetal complications of severe preeclampsia

Fetal complications	Premature ≥ 34 WA		Premature < 34 WA		Total		P
Fetal complications	Number	%	Number	%	Number	%	P
Oligohydramnios	64	27.7	37	21.9	101	25.3	0.114
DIU	29	12.6	43	25.4	72	18	<0.002
CFD	45	19.5	22	13	67	16	<0.05

Oligohydramnios (25.3%), Death in utero (DIU) (18%) and chronic fetal distress (16%) are the fetal most common complications of the SPE. DIU was a more common complication before 34 WA (34.4% vs 12.6%, P < 0.002), while CFD was more found after 34 weeks (19.5% vs 13%, P < 0.05).

Table 3 shows that infants born with premature labor induced had, as frequent complications, neonatal infection (40.3%), respiratory distress (34.5%), neonatal death (26.5%), neonatal hypoglycemia (21.3%) and Cerebral meningeal hemorrhage (CMH) (13.5%), comparing the group of pregnant women who gave birth prematurely from the 34th week to those who gave birth before 34 weeks, only neonatal infection was significantly more common in the first group (49.4% vs 27.8%, P < 0. 001) while neonatal complications significantly more frequent in the second group were respiratory distress (39.6% vs 30.7% P < 0.05), neonatal death (39.6% vs 16.9%, P < 0.001) and cerebral meningeal hemorrhage 9.1% vs 19.5%, P < 0.003).

4. Discussion

The frequency of prematurity induced for severe preeclampsia was 46.2%. It is higher than that reported by the WHO that was 40% in 2013 [8]. This difference could be explained by the lack of regular monitoring of prenatal consultation in our communities. The same reasons are incriminated for the results found by Diguisto et al. [9] who report that 2.5% of these births occurred after a tripping or caesarean section before labor.

Our frequency is lower than that reported by Nvondo [10] in Cameroon which noted a rate of 65%. This difference could be explained by the fact that in our study we excluded all the other pathologies as well as all the other circumstances which can lead to prematurity (the PRM, the malaria, the urinary infection, multiple pregnancies...).

Table 3 Neonatal outcome of severe preeclampsia

Neonatal Complications	Premature ≥ 34 WA		Premature < 34 WA		Total		P
Neonatal Complications	Number	%	Number	%	Number	%	P
Neonatal Infection	114	49.4	47	27.8	161	40.3	<0.001
Respiratory Distress	71	30.7	67	39.6	138	34.5	<0.05
Neonatal death	39	16.9	67	39.6	106	26.5	<0.001
NN Hypoglycemia	51	22.1	34	20.1	85	21.3	0.365
CMH	21	9.1	33	19.5	54	13.5	<0.003
NN Icterus	4	1.7	2	1.2	6	1.5	0.497

In our series, 95.2% of the indications of onset were of maternal origin (SPE, eclampsia, RPH and eclamptic prodromes) versus 4.8% fetal origin (CFD). This result is contrary to that found by Fournier [8] where 51% of indications were of maternal origin against 41% of fetal origin and 8% of mixed origin. This difference could be explained by the fact that the socio-economic level is very low in our environment, the recording of the fetal heart rate is not done as expected due to lack of financial means and/or apparatus equipped with option Doppler ultrasound

In our study, premature neonates had neonatal infection, respiratory distress and neonatal death complications in 40.3%, 34.5% and 26.5%, respectively. Comparing the group of pregnant women who gave birth prematurely from 34 WA who gave birth before 34 WA, only neonatal infection was significantly more common in the first group (49.4% vs 27.8%, P < 0.001) while neonatal complications significantly more frequent in the second group were respiratory distress (39.6% vs 30.7%: P < 0.05), neonatal death (39% vs 16.9%: P < 0.001) and CMH (19.5% vs 9.1%, P < 0.001). This result is similar to that found by Hilal et al. [2] who noted that respiratory distress had a frequency of 38%.

Neonatal death was estimated at 26.5% in our study. This frequency is close to one found by Tchaoun et al. [11] which was 28%.

5. Conclusions

The frequency of induced prematurity was 4.2% of births and 46.2% in cases of SPE; induced Prematurity for SPE avoids in utero death, exposes newborns to the complications of prematurity: The main indications are the persistence of high blood pressure while HRP was the most frequent indication in the group of pregnant women having given birth before 34 weeks; “the neonatal outcome was poor with 26.5% of deaths due to neonatal infection, respiratory distress and metabolic disorders (hypoglycemia); premature infants who were born from 34 WA had more neonatal infection than those before 34 WA while those born before 34 WA had more respiratory distress, neonatal death and CMH.

Neutropenia, sepsis and prolongation of the duration of ventilation could not be observed in our due to the lack of holistic management in our setting.

Our study shows that the neonatal prognosis is poorer for newborns before 34 WA, hence the advantage of prolonging the pregnancy until at least 34 WA if the maternal-fetal condition allows it.

Author’s Contributions

All the authors contributed from the conception to the final writing of the article.

Acknowledgements

The authors thank the Heads of Service of the four maternities concerned for the facilities granted for the data collection as well as Dr. Charles UMESUMBU SHAKU for the English translation.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

Cite this paper

Ambambula, O.Y., Mbangama, A.M., Biselele, T., Tozin, R.R. and Sengeyi, D.M. (2020) Neonatal Outcome of Induced Prematurity for Severe Preeclampsia in Four Great Kinshasa Maternities. Open Journal of Obstetrics and Gynecology, 10, 1637-1643. https://doi.org/10.4236/ojog.2020.10110147

References1

Ancel

,et al. (2010)National Epidemiological Study for Enhanced Knowledge of Care and Subsequent Development of Very Premature Children Epipage 2, 5-7.

Ozkan, H., Cetinkaya, M. and Koksal, N. (2012) Increased Incidence of Bronchopulmonary Dysplasia in Pretem Infants Exposed to Preeclampsia. The Journal of Maternal-Fetal & Neonatal Medicine, 25, 2681-2685. https://doi.org/10.3109/14767058.2012.708371

Ravi, T., Henning, H., Wiebecke, S., Bernhard, R., Tuelay, C., Karumanchi, A., et al. (2016) Removal of Soluble Fms-Like Tyrosine Kinase-1 by Dextran Sulfate Apheresis in Preeclampsia. Journal of the American Society of Nephrology, 27, 903-913. https://doi.org/10.1681/ASN.2015020157

Cetinkayo, M., et al. (2010) Neonatal Outcomes of Premature Infant Born to Preeclamptic Mothers. The Journal of Maternal-Fetal & Neonatal Medicine, 23, 425-430. https://doi.org/10.3109/14767050903184173

Jelin, A.C., Chengy, W., Shaffer, B.L. and Kairel, A. (2010) Early Onset PE and Neonatal Outcomes. The Journal of Maternal-Fetal & Neonatal Medicine, 23, 389-392. https://doi.org/10.3109/14767050903168416

Bosso

,et al. (2015)Tendances dans la survie f&#339tale et infantile après prééclampsie JAMA 296, 1357-1362.

Shrestha, S., Paudel, S., Parajuli, P. and Khagi, B.R. (2017) Neonatal Outcome of Mothers with Pregnancy Induced Hypertension in Antenatal Ward of Kathmandu Medical College and Teaching Hospital. Birat Journal of Health Sciences, 2, 255-259. https://doi.org/10.3126/bjhs.v2i3.18937

Fournier

,et al. (2010)rématurité spontanée ou induite, quelle influence sur l’avenir du nouveau-né Gynecology and Obsetrics 34, 1-2.

Weymuller, V., Diguisto, C., Guellier, C. and Perrotin, F. (2016) Practice Indicated Preterm Birth in a Type 3 Maternity. Journal de Gynécologie Obstétrique et Biologie de la Reproduction, 45, 724-730. https://doi.org/10.1016/j.jgyn.2015.08.012

Nvondo, N. (2016) Facteur de risque et devenir hospitalier des nouveau-nés prématurés à l’hopital Gynécologique et Pédiatrique de Yaoundé. Journal de Pédiatrie et de puériculture, 23, 67.

Tchaoun, B.A., Salefou, K., Hounkpure, F.M. and Chlobé, M. (2012) Prise en charge de la prééclampsie sévère dans l’hopital Universitaire de Parakou. Vol. 17, No. 2.