Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Filter by Categories
Case Report
Case Series
Editorial
Journal Review
Journal Summary
Letter to Editor
Letter to the Editor
Original Article
Review Article
Summary
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Filter by Categories
Case Report
Case Series
Editorial
Journal Review
Journal Summary
Letter to Editor
Letter to the Editor
Original Article
Review Article
Summary
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Filter by Categories
Case Report
Case Series
Editorial
Journal Review
Journal Summary
Letter to Editor
Letter to the Editor
Original Article
Review Article
Summary
View/Download PDF

Translate this page into:

Original Article
35 (
2
); 105-109
doi:
10.25259/KPJ_21_2020

Perinatal outcomes of hypertensive disorders of pregnancy

Department of Pediatrics, Kempegowda Institute of Medical Sciences Hospital, Bengaluru, Karnataka, India.

*Corresponding author: Dr. Muragesh Awati, Department of Pediatrics, Kempegowda Institute of Medical Sciences Hospital, VV Puram, Bengaluru - 560 004 Karnataka, India. dr.murageshawati@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Srinivasa S, Awati M. Perinatal outcomes of hypertensive disorders of pregnancy. Karnataka Paediatr J 2020;35(2):105-9.

Abstract

Objectives:

Hypertensive disorders of pregnancy (HDP) are multisystem diseases, which include chronic (preexisting) hypertension, gestational hypertension, pre-eclampsia, eclampsia, and pre-eclampsia superimposed on chronic hypertension. These disorders may complicate 5%–10% of all pregnancies and are leading causes of maternal and perinatal mortality and morbidity worldwide. This study was done to assess the incidence of HDP and perinatal outcomes in comparison to normal pregnancy. The objectives of this study were to assess the incidence of HDP and its correlation with perinatal outcome.

Materials and Methods:

Eighty patients were enrolled for the study, Group A (cases) – 40 patients of HDP and Group B (controls) – 40 normotensive controls, these 40 normotensive controls were properly matched with Group A with respect to age and gestational age. The collected data were analyzed with IBM SPSS statistics software 23.0 Version XVII.

Results:

In Group A, 45% were gestational hypertensive patients, 35% were pre-eclamptic patients, 12.5% eclampsia, and 7.5% chronic hypertension. Perinatal morbidity and mortality were increased in HDP when compared with age and gestational age-matched controls. Perinatal mortality was seen in 10% in Group A. In Group B(controls) there were no perinatal mortalities.

Conclusion:

The study demonstrated that high parity, low gestational age, lack of antenatal care, having eclampsia, pre-delivery onset of HDP, vaginal delivery, low fetal birth weight, and maternal death were independent predictors of perinatal mortality. The majority of perinatal mortality predictors were also predictors of stillbirths. The strong association of perinatal mortality with eclampsia (a late complication of HDP in the majority) and lack of antenatal care is an indirect evidence for the delay in the utilization of obstetric services.

Keywords

Hypertensive disorders of pregnancy
Perinatal outcome
Birth weight
Apgar

INTRODUCTION

Hypertensive disorders of pregnancy (HDP) are the most significant problem in obstetrics. The incidence of pre-eclampsia in hospital practice in India varies from 5% to 15% and that of eclampsia about 1.5%.[1] The incidence of HDP varies in the range of 1–35%.[2] They represent one of the most common problems of pregnancy and lead to increased maternal and perinatal morbidity and mortality. Pre-eclampsia is a multisystem and multifactorial disease and causes cellular death. The objectives of this study were to assess the incidence of HDP and its correlation with perinatal outcome.

Definitions

Gestational hypertension

Blood pressure of more than 140/90 mmHg after 20 weeks in previously normotensive women and hypertension resolves by 12 weeks postpartum.

Pre-eclampsia

Hypertension with proteinuria ( ≥300 mg/day or persistent dipstick 1+ or urine protein:creatinine ratio ≥0.3) or thrombocytopenia (platelet <100,000/μL), renal insufficiency (creatinine >1.1 mg/dl), liver involvement (serum transaminase levels twice normal), cerebral symptoms (headache, visual disturbances, convulsion), and pulmonary edema.

Chronic hypertension

Blood pressure more than 140/90 mmHg before pregnancy or before 20 weeks gestation or both.

Eclampsia

In women with pre-eclampsia, a convulsion that cannot be attributed to another cause is termed as eclampsia.

MATERIALS AND METHODS

Study was conducted in the Department of Pediatrics in Kempegowda Institute of Medical Sciences, Bangalore, for a period of 18 months. The study comprised 80 pregnant women. Forty patients with HDP (Group A) were included for the study, and the results were compared with 40 normotensive patients (Group B). It was purposive sampling.

Inclusion criteria

Forty pregnant women diagnosed with HDP admitted under Obstetrics and Gynecology department in Kempegowda Institute of Medical Sciences (Group A). Results in Group A were compared with 40 normotensive patients and they were selected according to the age of the patient and gestational age of the cases at the time of delivery for proper matching.

Exclusion criteria

In Group A and Group B, patients with medical comorbidities such as diabetes mellitus, liver disorder, renal disease, and cardiovascular disease were excluded from the study.

METHODOLOGY

After taking, informed written consent from all the patients’ demographic features such as age, gestation, and parity were recorder on structured data collection sheet. A detailed medical history of all participants was taken to ensure that they fulfill the inclusion criteria for the study. This was followed by a thorough physical examination of every case and control. Blood pressure of all participants was measured using manual mercury sphygmomanometer twice for each patient at an interval of 15–20 min and then after 2 h of rest, before labeling them as normotensive or with hypertensive disorder of pregnancy.

Statistical data analysis

The collected data were analyzed with IBM SPSS statistics software 23.0 Version. To describe about the data descriptive statistics frequency analysis, percentage analysis was used for categorical variables. To find the significant difference between the bivariate samples in independent groups, the Unpaired sample t-test was used. To find the significance in categorical data, Chi-square test was used similarly if the expected cell frequency is <5 in 2×2 tables; then, the Fisher’s exact was used. In all the above statistical tools, the probability value 0.05 is considered as significant level.

RESULTS

A total of 80 cases were studied of which, Group A (cases): 40 patients with hypertensive disorder of pregnancy and Group B (controls): 40 normotensive pregnant women.

In our study group, the majority of the patients belong to 21–25 years age group (age was matched with Group A and Group B for proper matching). The youngest being 18 years and the oldest is 37 years [Table 1].

Table 1: Distribution of Group A and Group B according to age.
Age (years) Group A (Cases) Group B (Controls)
18–20 8 (20.0%) 3 (7.5%)
21–25 16 (40.0%) 21 (52.5%)
26–30 11 (27.5%) 13 (32.5%)
Above 30 5 (12.5%) 3 (7.5%)

In Group A (cases), the majority were primigravidas constituting 52.5 %. In Group B (controls), the majority were multigravidas constituting 67.5% [Table 2].

Table 2: Distribution of Group A and Group B according to gravidity.
Gravida Group A (Cases) Group B (Controls)
Multi 19 (47.5%) 27 (67.5%)
Primi 21 (52.5%) 13 (32.5%)

Controls were selected according to the gestational age of cases for proper matching. Majority of the patients were between the gestational age of 37 and 39+6 weeks gestation in both Group A and Group B [Table 3].

Table 3: Distribution of Group A and Group B according to gestational age.
Gestational age (weeks) Group A (Cases) Group B (Controls)
≤33+6 10 (25%) 8 (20%)
34–36+6 13 (32.5%) 10 (25%)
37–39+6 14 (35%) 18 (45%)
≥40 3 (7.5%) 4 (10%)

Majority of the cases were diagnosed with gestational hypertension followed by pre-eclampsia and 5 were cases of eclampsia. Among 14 pre-eclampsia cases, 5 were cases of severe pre-eclampsia [Table 4].

Table 4: Distribution of cases according to various types of hypertensive disorders of pregnancy.
Group A – Cases (n=40) Frequency Percentage
Gestational hypertension 18 45
Preeclampsia 14 35
Chronic hypertension 3 7.5
Eclampsia 5 12.5
Total 40 100

In Group A (cases), among five patients of eclampsia 3 had intrauterine death, other two babies were shifted to neonatal intensive care unit (NICU), of which one baby died on day 6 (neonatal death) due to preterm complication. In Group A (cases), among five patients of eclampsia three had intrauterine death, other two babies were shifted to NICU, of which one baby died on day 6 (neonatal death) due to preterm complication [Table 5].

Table 5: Comparison of Group A and Group B according to perinatal outcome.
Perinatal outcome Group A (Cases) Group B (controls)
Intrauterine growth restriction-preterm 13 (32.5%) 2 (5%)
Intrauterine growth restriction-term 6 (15%) 0
Intrauterine fetal death 3 (7.5%) 0
Neonatal death 1 (2.5%) 0

dications of elective lower segment cesarean section (LSCS) among cases and controls were previous LSCS not willing for trial of labor after previous cesarean, previous 2 LSCS, malpresentation, cephalopelvic disproportion, etc. In Group A (cases), maximum percentage was seen in emergency LSCS. In Group B (controls), maximum percentage of patients delivered vaginally [Table 6].

Table 6: Comparison of Group A and Group B according to mode of delivery.
Mode of delivery Group A (Cases) Group B (Controls)
Emergency lower segment cesarean section 19 (47.5%) 11 (27.5%)
Elective lower segment cesarean section 9 (22.5%) 10 (25%)
Vaginal delivery 12 (30.0%) 19 (47.5%)

In Group A (cases), only seven babies were more than 3 kg, whereas, in Group B (controls), 13 babies were more than 3 kg. In Group B (controls), none of the babies were <1 kg, whereas in Group A (cases) 3 babies were <1 kg [Table 7].

Table 7: Comparison of birth weight among Group A and Group B.
Birth weight Group A (Cases) Group B (Controls)
≤999 g 3 (7.5%) 0%
1000–1999 g 13 (32.5%) 7 (17.5%)
2000–2999 g 17 (42.5%) 20 (50%)
≥3000 g 7 (17.5%) 13 (32.5%)

In Group A, among five cases of eclampsia, three had intrauterine fetal demise. In Group B, only two babies had APGAR of <7/10, whereas, in Group A, there were nine babies of APGAR <7/10. All these APGAR represent 1 min APGAR score [Table 8].

Table 8: Comparison of Apgar score among Group A and Group B.
Apgar Group A (cases) Group B (controls)
7–10 31 (77.5%) 38 (95%)
4–6 6 (15%) 2 (5%)
0–3 3 (7.5%) 0
Total 40 40

In Group A, there were three intrauterine fetal demises; hence, among 37 babies, 24 babies were admitted in NICU. NICU admissions were maximum (64.9%) in Group A, whereas, in Group B, it was only 25% [Table 9].

Table 9: Comparison of neonatal intensive care unit admission among Group A and Group B.
Neonatal intensive care unit admission Group A (cases) Group B (controls)
No 13 (35.1%) 30 (75%)
Yes 24 (64.9%) 10 (25%)

DISCUSSION

There are numerous pathophysiological abnormalities in HDP. These changes occur in large extent and are translated into a full clinical presentation of pre-eclampsia, during late pregnancy. In this study, controls were selected after proper matching with the cases with respect to the age of the patient and gestational age at the time of delivery. In Group A and Group B, maximum percentage of patients were in the age group of 21–25 years, with the mean age of 25. According to Hazari et al., mean age among cases were 23 and among controls were 25.[3] In Group A, primigravidas were more compared to multigravidas, constituting 52.5% and 47.5%, respectively, which are consistent with various other studies. Primigravida is a proven risk factor for HDP. According to Sajith, 2014, the highest incidence of hypertension was occurred in primigravida patients (53.8%).[4] Hansen reported a two- to three-fold increase in the incidence in primigravida, and this was supported by Chesley.[5] Sibai and his association recently reconfirmed the high risk of developing of pregnancy induced hypertension in primigravidas.[6-8] Most common hypertensive disorder of pregnancy found in this study was gestational hypertension followed by pre-eclampsia, which is consistent with FOGSI which states that approximately two-third of HDP are due to gestational hypertension and preeclampsia and one-third are due to chronic hypertension. The total number of intrauterine deaths in the study were 3 (7.5 %) due to eclampsia. One case of neonatal death on day 6 of life was due to preterm complications. Perinatal mortality in my study was 10%. The mean birth weight of babies in Group A (cases) was 2.21 and standard deviation of 0.87; the mean birth weight of babies in Group B (controls) was 3.01 and standard deviation of 0.43. The magnitude of fetal growth restriction is more in Group A (cases) than Group B. In this study, in Group A (cases), 12 delivered vaginally (30 %) and 28 by cesarean section (70%). In Group B (controls), 19 delivered vaginally (47.5%) and 21 by cesarean section (52.5%). In the study by M.R. Dutta, Luna Pant (2002), 45% were vaginal deliveries, and cesarean section rate was 62 %. Iqbal et al. reported an incidence of cesarean as 43% and vaginal as 57 %. In Group A (cases), 55% were preterm deliveries and remaining were term. An observational study on maternal and neonatal outcome in Thrissur Medical college, conducted in 2017 by Kennady G et al. showed 52.4% preterm.[9] In Group A, only seven babies were more than 3 kg, whereas, in Group B, 13 babies were more than 3 kg. In Group B, none of the babies were <1 kg, whereas, in Group A, there were three babies. In Group A, there were 19 fetal growth restriction babies, whereas, in group B, there were only two cases of fetal growth restriction suggesting that IUGR is a common finding in HDP as seen by Odegard et al.[10] In Group A, among five cases of eclampsia, three had intrauterine fetal demise. In Group B, only two babies had APGAR of <7/10, whereas, in Group A, there were nine babies of APGAR <7/10. Limitations of our study – the sample size was small (as patients in Group A [cases] were selected only with HDP and patients with other comorbidities like diabetes, liver disorder, renal disease and cardiovascular disorders were excluded from the study), we did not correlate the levels of the parameter in different classification of HDP and its complications.

CONCLUSION

HDP are common in India. The basic management objectives included obstetric management, adequate fetal surveillance, antihypertensive management, anticonvulsant therapy, safe analgesia, anesthetic management of labor, and anesthesia for delivery. ISSHP recommends that women with established strong clinical risk factors for preeclampsia be treated, ideally before 16 weeks but definitely before 20 weeks with low-dose aspirin (75–162 mg/d as studied in randomized controlled trials). In normal pregnancy, there is decreased blood pressure response to pressor substances, but in pre-eclampsia, there is marked response to vasopressin, norepinephrine, and angiotensin. This response of arterial system leads to generalized vasoconstriction and hypertension in preeclampsia. These alterations secondarily lead to many pathophysiological changes which adversely affect maternal and fetal wellbeing. Such cases need special attention with early detection and referral to higher center with better facilities of NICU set up to reduce the complications and mortality. Hypertensive disorders remain among the most significant and intriguing unsolved problems in obstetrics. In further studies, it is critical to find early diagnostic markers which are also cost effective, markers which help us to know the prognosis, effective interventions, and preventions of HDP which are particularly important to reduce maternal and perinatal complications and ensure both pregnant women and neonates to be healthy and safe.

In Group A and Group B, maximum percentages of patients were in the age group of 21–25 years, with the mean age of 25. In Group A, primigravidas were more compared to multigravidas, constituting 52.5% and 47.5%, respectively, whereas, in Group B, multigravidas were more compared to primigravidas constituting 67.5% and 32.5%, respectively. Most common hypertensive disorder of pregnancy found in this study was gestational hypertension followed by preeclampsia. The total number of intrauterine deaths in the study were 3 (7.5%) due to eclampsia. One case of neonatal death on day 6 of life due to preterm complication. Perinatal mortality in my study was 10%. The mean birth weight of babies in Group A (cases) was 2.21 and standard deviation of 0.87; the mean birth weight of babies in Group B (controls) was 3.01 and standard deviation of 0.43 In this study, in Group A (cases), 12 delivered vaginally (30%) and 28 by cesarean section (70%). In Group B (controls), 19 delivered vaginally (47.5%) and 21 by cesarean section (52.5%). In Group A, only seven babies were more than 3 kg, whereas, in Group B, 13 babies were more than 3 kg. In Group B, none of the babies were <1 kg, whereas, in Group A, there were three babies. In Group A, there were 19 fetal growth restriction babies, whereas in Group, B there were only two cases of fetal growth restriction. In Group B, only two babies had APGAR of <7/10, whereas, in Group A, there were nine babies of APGAR <7/10.

Declaration of patient consent

Patient’s consent not required as patients identity is not disclosed or compromised.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

  1. , . Eclampsia in India through the decades. J Obstet Gynaecol India. 2016;66:172-6.
    [CrossRef] [PubMed] [Google Scholar]
  2. . Hypertensive Disorders in Pregnancy New York: Appleton-Century-Crofts; .
    [Google Scholar]
  3. , , . Study of Serum hepatic enzymes in preeclampsia. Int J Curr Med Appl Sci. 2014;2:1-8.
    [Google Scholar]
  4. . Incidence of pregnancy induced hypertension and prescription pattern of antihypertensive drugs in pregnancy. Int J Pharma Sci Res. 2014;6:164-6.
    [Google Scholar]
  5. , . Hepatic fibrinogen deposits in pre-eclampsia, Immunofluorescent evidence. N Engl J Med. 1976;295:578-82.
    [CrossRef] [PubMed] [Google Scholar]
  6. . Calcium supplementation during pregnancy reduces risk of high blood pressure, pre-eclampsia and premature birth compared with placebo? Evid Based Med. 2011;16:40-1.
    [CrossRef] [PubMed] [Google Scholar]
  7. , . Risk factors for pre-eclampsia in a large cohort of Latin American and Caribbean women. BJOG. 2000;107:75-83.
    [CrossRef] [PubMed] [Google Scholar]
  8. , , , , , . Outcomes in hypertensive disorders of pregnancy in the North Indian population. Int J Womens Health. 2013;5:101-8.
    [CrossRef] [PubMed] [Google Scholar]
  9. , . Maternal and neonatal outcomes in pregnancy induced hypertension: An observational study. Clin Exp Obstet Gynecol. 2017;44:110-2.
    [Google Scholar]
  10. , , , , . Preeclampsia and fetal growth. Obstet Gynecol. 2000;96:950-5.
    [CrossRef] [Google Scholar]
Show Sections