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Prevalence, placenta development, and perinatal outcomes of women with hypertensive disorders of pregnancy at Komfo Anokye Teaching Hospital

  • Stephen Poku Awuah ,

    Contributed equally to this work with: Stephen Poku Awuah, Isaac Okai, Emmanuel Amankwah Ntim, Kweku Bedu-Addo

    Roles Data curation, Formal analysis, Methodology, Writing – original draft

    Affiliation Department of Physiology, School of Medicine and Dentistry, KNUST, Kumasi, Ghana

  • Isaac Okai ,

    Contributed equally to this work with: Stephen Poku Awuah, Isaac Okai, Emmanuel Amankwah Ntim, Kweku Bedu-Addo

    Roles Conceptualization, Project administration

    Affiliation Department of Anatomy, School of Medicine and Dentistry, KNUST, Kumasi, Ghana

  • Emmanuel Amankwah Ntim ,

    Contributed equally to this work with: Stephen Poku Awuah, Isaac Okai, Emmanuel Amankwah Ntim, Kweku Bedu-Addo

    Roles Supervision, Writing – review & editing

    Affiliation Department of Physiology, School of Medicine and Dentistry, KNUST, Kumasi, Ghana

  • Kweku Bedu-Addo

    Contributed equally to this work with: Stephen Poku Awuah, Isaac Okai, Emmanuel Amankwah Ntim, Kweku Bedu-Addo

    Roles Conceptualization, Methodology, Supervision, Writing – review & editing

    kwekuba@yahoo.com

    Affiliation Department of Physiology, School of Medicine and Dentistry, KNUST, Kumasi, Ghana

Abstract

Background

One of the most common medical problems associated with pregnancy is hypertension. Hypertensive disorders of pregnancy (HDP), which has been attributable to abnormal placentation may have adverse effects on both mother and foetus if left unchecked. The objective of this study was to determine the prevalence of this condition and its effect on placental morphology as well as maternal and perinatal outcomes.

Materials and methods

This was a prospective case-control study, conducted at Komfo Anokye Teaching Hospital (KATH), Ghana between February 2018 and July 2018. The progression of pregnancy in normotensive and hypertensive pregnant women, and the eventual perinatal outcomes were closely followed. Statistical analysis was performed using IMB-SPSS version 23. Associations were considered significant at p values of ≤ 0.05.

Results

From a total of 214 deliveries recorded during the period of study, 84 (39.25%) were hypertensives. Forty four (52%) of the hypertensives had preeclampsia, 28 (33.3%) had gestational hypertension, 6 (7.1%) had eclampsia, 4 (4.8%) had chronic hypertension, and 2 (2.4%) had preeclampsia superimposed on chronic hypertension. The frequency of placental haematoma, placental infarction, and placental calcification in the normotensives were significantly (p = 0.001) lower than that of the hypertensives. The mean placental weight (p = 0.01), placental volume (p = 0.001), placental diameter (p = 0.03), and placental thickness (p = 0.001) of the normotensives were significantly higher than those of the hypertensives. The number of normotensives in whom labour was induced, who had their babies delivered by caesarean section, and who were admitted after they had given birth were significantly (p = 0.001) lower than that of hypertensives who underwent similar procedures. No stillbirths were recorded in the normotensives compared with four in the hypertensives. The number of babies delivered to the normotensives who were admitted to the NICU was significantly (p = 0.001) lower than those delivered by hypertensives.

Conclusion

There was a high prevalence of hypertensive disorders of pregnancy in the study site. Pregnant women who developed HDP are at a risk of developing placental abnormalities that adversely affected perinatal outcomes. These adverse effects can be curtailed by embarking on a vigorous health education drive.

Introduction

The nurturing and survival of the foetus is dependent on normal physiological changes that are associated with pregnancy. These adaptive changes which are reflected in biochemical parameters are different in the non-pregnant state [1] and become very significant during complications of pregnancy. Hypertension is one of the medical problems that mostly affect pregnant women and it remains an important cause of both maternal and foetal morbidity/mortality. Studies show that 10–15% of pregnancies will be complicated by high blood pressure [2, 3]. Up to about one-quarter of all antenatal admissions will be hypertensive related cases [2]. Over the last century, maternal mortality rates in high-income countries have steadily declined [4]. Every year about 70,000 women die and there are half a million stillbirths or neonatal deaths owing to hypertensive disorders of pregnancy (HDP)–the vast majority being in the developing world [5]. The identification of the disorder and its effective treatment play a beneficial role in pregnancy outcomes for the mother and the foetus, and hence a reduction in both maternal and perinatal mortality. Hypertensive disorders are associated with low birth weight, fetal growth restriction and prematurity which greatly contribute to perinatal morbidity and mortality [6, 7]. Many pregnancy complications that are associated with high foetal morbidity and mortality have shown gross deviations from the normal placental morphology and anatomy [8, 9]. With the placenta serving as the image for the health status of the mother and foetus, complications like hypertension in pregnancy has reflected in the placenta in a significant way, either microscopically or macroscopically [10, 11].

Pregnancies that are complicated by hypertension have been known to record higher incidence of neonatal morbidity compared to pregnancies with normal blood pressure. Pregnancies with hypertensive disorders are prone to a higher risk of preterm deliveries and low birth weights compared to healthy pregnancies [12]. The risk of HDP occurs mostly among mothers affected with severe chronic hypertension as well as those with superimposed preeclampsia on chronic hypertension [13]. The objective of this was to determine the prevalence of HDP, the morphological variations of human placenta in HDP, and maternal and neonatal outcomes in HDP.

Materials and methods

This was a prospective case-control study, conducted at the maternity block of Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghana, during the period of February 2018 to July 2018. Samples for the study were collected following approval from the Research and Development Unit, KATH and the Committee on Human Research, Publication and Ethics (CHRPE)-KNUST. With a total of 338 pregnant women evaluated, 214 participants with complete records were available for analysis during this study period. While ensuring confidentiality, the study protocol was explained to each individual in detail and those who gave either written or verbal informed consent were included in the study. Informed consent was obtained from the guardian or next of kins of study participants who had difficulty giving informed consent because of their health status. Patients were also informed that non participation or withdrawal from the study would have no effect on the standard management of their respective medical treatment at the hospital. The Patients’ obstetric history were reviewed and those with blood pressure ≥140/90 mm Hg, with or without proteinuria diagnosed after the 20th week of gestation, who developed hypertension within 48 hours after delivery, with absence of other serious diseases or congenital malformations, and with singleton pregnancy, were included in the study. Mothers with associated medical problems other than hypertension and those without antenatal records were excluded from the study.

The mothers with hypertensive disorders of pregnancy were divided into five groups according to the classification system developed by the Working Group of the national high blood pressure education program [14]. These are chronic hypertension, gestational hypertension, preeclampsia, eclampsia, and preeclampsia superimposed on chronic hypertension.

Maternal parameters recorded/measured included the age of participants, body mass index, the final blood pressure reading before and after delivery, parity, occupation and level of income, educational level, ethnicity, other previous obstetric medical history, and booking status. Blood pressure of participants were recorded as a clinical routine using OMRON (HEM-907) digital-portable automated blood pressure recorder with the woman sitting down and the feet resting on a flat surface. The third trimester blood pressure of participants were measured on three different visits before delivery. Also, the blood pressure of participants were measured after delivery. The mode of delivery (vaginal or caesarean section), maternal presentation, and the degree of tear of maternal perineum were also recorded.

The detailed assessment of placenta was accurately done using freshly delivered placentae from both the HDP group (hypertensive mothers) and the control group (normotensive mothers) at the labour ward, A1 HDU, and the theatre. Placentae were obtained soon after delivery using a clean placenta bowl or kidney dish. Each placenta sample was labelled with ID number that corresponded with the number indicated for their respective newborn and the mother.

Inspection of placenta was done to see if there was any torn tissue to suggest retained tissue. The foetal membranes were then inspected along the edges of the placenta. The foetal surface of each placenta was examined thoroughly, the state of membranes as well as the presence of any chorionic or subamniotic haematoma were noted. Examination of maternal surface was also done for the presence of retroplacental haematoma, calcification and infarction. The umbilical cord insertion types and cord vessel numbers, along with any umbilical cord abnormalities were recorded. The cord length was measured with Dritz C150 fiberglass measuring tape (Prym consumer USA Inc.).

Freshly delivered placentae were weighed at the ward using a highly sensitive mechanical kitchen scale (Zhongshan Camry Electronic Co. Model: KCH) graduated from 0–5 kg. The foetal surface of each placenta was well cleaned and then placed on a clean white rectangular board and the placental shape was observed and described as either round, oval, or irregular. The measurement of placenta diameter was done using a Dritz C150 fiberglass measuring tape (Prym consumer USA Inc.). Four different angles of each placenta were measured and the mean determined. This was done due to the fact that many of the placentae upon examination were not round in shape but rather ovoid or irregular in shape (particularly hypertensive placentae) making it impossible to take a single reading. The thickness of placenta was determined using the toothpick method [15]. This was done by piercing the placentae from the chorionic plate to the basal plate at both the centre and near the edge, with each placenta placed on the foetal surface. The values were transferred onto a clear ruler 30 cm/12 inches (Helix China Inc.) calibrated in centimetres and their averages computed to determine the placental thickness. The water displacement method was adopted in measuring the placenta volume using a calibrated one-litre beaker. With this method, the actual volume of placenta was determined as, Volume = Vol2 –Vol1, where Vol2 is for final volume (placenta volume + water volume) and Vol1 is for water volume only.

Gestational age was expressed as beginning from the last date of menstruation proven by preliminary examination with ultrasound scan. On the basis of gestational age, the infants were categorized into 3 groups: Term infants were those with gestational age between 37 to 42 weeks, preterm babies included infants with gestational age <37 weeks and post term babies had gestational age >42 weeks. Low birth weight (LBW) was specified for birth weight (BW) <2.5 kg, very low birth weight (VLBW) as BW <1.5 kg, and extremely low birth weight (ELBW) as BW <1 kg [16]. The standard body length was defined as length of baby ranging from 46.9 to 54.9 cm [17]. The standard head circumference was defined as circumference of the head of baby ranging from 33 to 37 cm [18]. The standard abdominal circumference was defined as the circumference of the abdomen of baby ranging from 31 to 33 cm [16].

Data was analyzed using Statistical Package for Social Sciences (SPSS) version 23.0. Statistical analysis was performed with student t-test, and chi-square test. P value equal to or less than 0.05 was considered statistically significant.

Results

Eighty four (39.25%) out of the 214 study population had hypertensive disorders of pregnancy (HDP). This indicates 393 out of every 1,000 patients had HDP. Of the 84 deliveries with hypertensive disorders of pregnancy, 28 (33.3%) had gestational hypertension, 44 (52.4%) had preeclampsia, 6 (7.1%) had eclampsia, 4 (4.8%) had chronic hypertension, and 2 (2.4%) had preeclampsia superimposed on chronic hypertension (Fig 1).

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Fig 1. Distribution of cases HDP group according to type of hypertension.

https://doi.org/10.1371/journal.pone.0233817.g001

The mean age of the hypertensives was 29.85 years. Among the hypertensives, 31 (36.9%) were in the age group 30–34 years, and 25 (29.8%) were in the age group 25–29 years. There was a significant difference in weight (p = 0.001) and height (p = 0.025) between the hypertensives and normotensives, but the difference in BMI observed between them was not significant (p = 0.090) (Table 1). The study showed that 42 (50.0%) of the hypertensives and 57 (43.8%) normotensives were obese.

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Table 1. Distribution according to maternal age, weight, height, and BMI.

https://doi.org/10.1371/journal.pone.0233817.t001

Forty-eight (57.2%) of the hypertensives were multiparous, 19 (22.6%) primiparous and the remaining 17 (20.2%) were nulliparous, while 59 (45.4%) of the normotensives were multiparous, 32 (26.4%) were primiparous, and the remaining 39 (17%) were nulliparous. There was no significant difference in maternal parity between the hypertensives and normotensives (p = 0.324) (Table 2).

Majority (67.9%) of women with hypertensive disorders of pregnancy presented to the hospital (KATH) with headache as the chief complaint. Rare symptoms that were observed from some of the patients were abdominal pain and swollen feet. The high BP readings that were recorded in all the women with HDP persisted throughout the pregnancy period ie from the time of diagnosis to delivery. There was a slight or gradual decrease after delivery. During their hospitalization, the increases in diastolic blood pressure (DBP) corresponded with the systolic blood pressure (SBP) for both groups. The SBP was used as the major preliminary criteria for identifying the HDP group. There was a significant difference in the mean systolic BP (p = 0.001) and pulse rate (p = 0.001) of the hypertensives and normotensives before and after delivery (Table 3). The averages for the minimum and maximum values, and mean of third trimester systolic BP of participants measured on three different visits in each study group before delivery after delivery are indicated in Table 3.

Women with chronic hypertension had a positive family history of hypertension and their high BP was present either pre-pregnancy or at <20+0 weeks’ gestation. Gestational hypertensive women recorded high BP at ≥20+0 weeks’ gestation. A large number of patients with preeclampsia (especially severe forms) presented with nausea and vomiting, epigastric pain, and visual disturbances like blindness. The eclampsia patients had the symptoms of preeclampsia associated with either mild or severe seizures. Pregnant women diagnosed of chronic hypertension with superimposed preeclampsia had chronic high BP with proteinuria, and a retrogression of blood pressure control. Women with eclampsia recorded the highest mean systolic BP (180.67 mm Hg), followed by those with preeclampsia superimposed on chronic hypertension (178.50 mm Hg), and the least was recorded in chronic hypertensive women (157.50 mm Hg). The mean systolic BP that was recorded for each of the 5 HDP subtypes were comparatively higher than that of the normotensive mothers (Table 4).

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Table 4. Systolic BP readings of study participants.

https://doi.org/10.1371/journal.pone.0233817.t004

The number of hypertensives in whom labour was induced, who had their babies delivered by caesarean section, and who were admitted after they had given birth, were significantly (p = 0.001) higher than that of normotensives who underwent similar procedures (Table 5). Four stillbirths were recorded in the hypertensives compared to zero in the normotensives. The number of babies delivered by the hypertensives who were admitted to the NICU was significantly (p = 0.001) higher than those delivered by normotensives. There was however, no significant differences in preterm deliveries, foetal presentation, and degree of maternal tear, between the two groups (Table 5).

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Table 5. Delivery outcomes of study participants.

https://doi.org/10.1371/journal.pone.0233817.t005

The frequency of placental haematoma, placental infarction, and placental calcification in the hypertensives were significantly (p = 0.001) higher than that of the normotensives. Thirty (35.7%) of the placentae of the hypertensives were round shaped, compared to 103 (79.2%) of the normotensives. Forty one (48.8%) of the placentae of the hypertensives were oval shaped, compared to 16 (12.3%) of the normotensives. The number of irregular shaped placentae were 13 (15.5%) and 11 (8.5%) for the hypertensives and normotensives respectively (Table 6).

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Table 6. Gross morphology of placenta of study participants.

https://doi.org/10.1371/journal.pone.0233817.t006

The mean placental weight (p = 0.01), placental volume (p = 0.001), placental diameter (p = 0.03), and placental thickness (p = 0.001) of the hypertensives were significantly lower than those of the normotensives (Table 7).

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Table 7. Placental indices of the participants.

https://doi.org/10.1371/journal.pone.0233817.t007

Thirty one (36.9%) placentae of the hypertensives had central cord insertion, 28 (33.3%) were eccentric, 23 (27.4%) were marginal, and 2 (2.4%) were velamentous. Eighty five (65.4%) of the placentae of the normotensives had eccentric cord insertion, 21 (16.2%) were central, 22 (16.9%) were marginal and 2 (1.5%) were velamentous. Although majority of the umbilical cords from both groups had 3 vessels, the mean number of umbilical cords that had 3 vessels were significantly (p = 0.001) lower in the hypertensives, compared to the normotensives (Table 8).

Majority (53.6%) of the umbilical cords of the hypertensives were short while majority (61.5%) of the umbilical cords of the normotensives had normal lengths. The mean cord length of the hypertensives (39.11±13.05 cm) was significantly lower than that of the normotensives (51.01±16.13 cm) (p = 0.001) (Table 8).

The mean birth weights, birth lengths, head circumferences, and abdominal circumferences of the neonates of the hypertensives were significantly lower than that of the neonates of the normotensives (p = 0.001) (Table 9). Additionally, the Apgar score at the 5th minute of birth of neonates of the hypertensives was significantly lower than that of the neonates of the normotensives (p = 0.001) (Table 9).

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Table 9. Neonatal indices of study participants.

https://doi.org/10.1371/journal.pone.0233817.t009

Discussion

HDP has become a major health issue worldwide, and the prevalence varies from one country to another as well as in different institutions. This study showed a HDP prevalence of 39.25% at Komfo Anokye Teaching Hospital (KATH) during the study period. There has been a reported incidence of 1.5% to 22% of all pregnancies, which is dependent upon the population sampled and the definitions used [1923]. The variation may be due to differences in genetic factors, socioeconomic status, racial differences, and some other demographic features such as maternal age and parity [2123]. Another reason might be the differences in terminologies used in the study methodologies. Pregnancy Induced Hypertension (PIH) for instance, has led to a significant debate with misleading account in HDP prevalence, rendering the term PIH obsolete and no longer recommended in literature [19]. Prevalence rates of 21.4%, 17%, and 16.8% have been recorded at Korle-bu Teaching Hospital in Ghana, in a tertiary referral heath facility in Nigeria, and in North West Ethiopia respectively [2426].

The prevalence of HDP with respect to age-group distribution was at its peak in women of 40 years and over (many of them being chronic hypertensives), and the lowest number was recorded for mothers who were 19 years or below. Other studies found the highest and lowest proportion of women with HDP between 25–29 years and ≥40 years respectively [7], results inconsistent with that of the present study. Other researchers have reported an increased risk of HDP like preeclampsia in younger women who were 21 years or below [27, 28].

Most of the women with hypertensive disorders of pregnancy in this study were multiparous (parity of 3 or more), followed by primiparous women. This is similar to some studies that found a higher prevalence of HDP among women with grand multiparity (5 or more) [7, 29]. From this study, the mean of third trimester Systolic BP of participants measured on three different visits before and after delivery was significantly (p = 0.001) higher in hypertensive mothers than normotensive mothers, a result similar to findings of other studies [30, 31]. Some investigators have found that women with HDP had a mid-trimester decrease, which was followed by a progressive rise in both systolic BP and diastolic BP between 30–45 days postpartum [32, 33]. The factors influencing the development of high blood pressure may differ depending on the particular type of hypertensive disorder, the study population (ethnicity or race), family history of the individual [34], life style and eating habit of the individual [35], and most importantly the age and parity of the pregnant woman [36].

From the antenatal history, mothers who had higher BMI at the beginning of pregnancy or were overweight or obese during gestation, showed higher SBP and DBP values in all gestational trimesters until delivery. Contrary to the findings of this study, some previous studies have found underweight pregnant women to be at risk of hypertension development which result in delivery of preterm infants [37, 38]. Higher maternal weight before pregnancy increases the risk of late fetal death, although it protects against the delivery of a small-for-gestational-age infant [39].

In this study, most of the placentae (48.8%) of the hypertensives were oval in shape, while most of the placentae (79.2%) of the normotensives were round in shape, a finding similar to that of other studies [11, 40, 41]. One study found no significant difference (p > 0.05) between the number of different placental shapes of the hypertensives and normotensives [42], and another study found that the shape of placentae from both hypertensives and normotensives were either oval or round [43]. The significantly high incidence of placental haematoma in hypertensives compared with the normotensives in this study is consistent with the findings of other studies [6, 44]. A study has found an association between placental haematoma and low Apgar score and also an association between larger haematomas and IUFD, due in part to separation of a considerable part of the villi from the utero placental circulation [45].

The number of placentae with infarction was significantly (p = 0.001) higher in the hypertensives than the normotensives in this study. This is consistent with the results obtained by other studies [40, 46, 47]. Placental infarcts are known to have an adverse effect on growth and development of the newborns [47].

The present study also observed a significantly high placental calcification in the hypertensives compared to the normotensives. This is similar to the findings of a study which concluded that the foetal outcome in terms of birth weight of newborns to mothers having PIH and calcification of placentae was poor when compared to the control group [48]. Another study found no significant difference in the incidence of calcification in the hypertensives and normotensives [49]. It is noteworthy that calcification that is seen in the placenta shows an evidence of placental senescence or degeneration [50].

The mean placental weight, volume, thickness, and diameter for hypertensives were significantly lower than that of the control group in the present study (p < 0.05). Similar outcomes in placental parameters have been reported by other studies [11, 41, 5154]. This study results suggest that placental weight may be a good predictor of newborn weight, because a significant linear correlation was observed for both the hypertensives (r = 0.579, p = 0.001) and the normotensives (r = 0.630, p = 0.001). Similar relations have been shown by other researchers [8, 55, 56]. The present study recorded a significant (p < 0.001) reduction in the mean central thickness of placentae in the hypertensives compared to the normotensives. This finding is consistent with that of other studies [5762]. The results for placental volume obtained in this study was similar to that obtained by other studies [6365].

Majority of the umbilical cord lengths in the hypertensive mothers were significantly short compared to that of the normotensives in this study. Short umbilical cord lengths are associated with a high rate of foetal abnormalities, such as abdominal wall defects and defects in the extremities and spine [66]. They are also associated with unsatisfactory foetal state, central nervous system complications, and low Apgar and IQ scores [67]. A normal umbilical cord has two arteries and a vein and is covered by Wharton’s jelly. Changes may sometimes occur during pregnancy that result in abnormal number of umbilical cord vessels [68]. The number of umbilical cords with three vessels in the hypertensives was significantly lower compared to the that of the normotensives in this study. Almost 30% of the umbilical cords of the hypertensives had less than 3 vessels compared to only 7% of the normotensives. The result of the present study is contrary to that of Saha et al. (2014) [69] who found 3 vessels in all their samples.

The umbilical cord insertion site to the placenta can be central, eccentric, marginal (battledore), or velamentous (membranous). More than 90% of term placentae insertions are central or eccentric. Marginal cord insertion (MCI) and velamentous cord insertions (VCI) are classified as abnormal placental cord insertions (PCI). VCI occurs in approximately 1% of singleton pregnancies and MCI in approximately 7% [66]. Eighty one percent of the umbilical cord insertions in the normotensives in this study were either central or eccentric compared to 70.2% in the hypertensives. The frequency of marginal and velamentous cord insertions was higher in the hypertensives. This finding is similar but not to the same degree as that of other studies [70, 71]. Abnormalities of the umbilical cord, related to morphology, placental insertion, number of vessels and primary tumors, can influence the perinatal outcome and may be associated with other fetal anomalies and aneuploidies [68].

The number of preterm deliveries for the hypertensive and normotensive mothers in the present study was not significantly different. A result contrary to that of Yadav et al. (1997) [72] who recorded significantly high numbers of preterm deliveries among the hypertensives compared to the normotensives. The need to induce labour or perform a caesarean section on the mothers was significantly higher (p = 0.001) in the hypertensives than the normotensives. The still birth rate was also significantly higher (p = 0.012) in the hypertensives. These findings are similar to that of Yadav et al. (1997) [72]. The number of babies born to hypertensives who needed NICU care was significantly higher compared to those of the normotensives, results similar that of other studies [7274]. It must be stated however that the frequencies in the present study were at times higher or lower than that of these studies.

The present study showed that the foetal development rate of hypertensives could be affected by adverse maternal and placental factors. The mean birth weight, baby length, abdominal circumference, and head circumference of neonates of the hypertensives were significantly (p = 0.001) lower compared to the normotensives in this study. Similar findings of LBW babies were observed in other studies [11, 40, 41, 75]. The APGAR scores after five minutes of delivery was significantly (p≥0.001) lower in infants of the hypertensives compared to the infants of the normotensives. This is consistent with the findings of other studies [74, 76].

Conclusion

The study found a high prevalence of hypertensive disorders of pregnancy at the study site. Those suffering from this condition were at a high risk of having placental abnormalities that would impact negatively on maternal and perinatal outcomes. Early detection and management of HDP should be instituted to forestall such outcomes.

Acknowledgments

The authors wish to appreciate the support of the Heads and nurses of various units of the Department of Obstetrics and Gynaecology of Komfo Anokye Teaching Hospital, Kumasi, Ashanti Region and all participants who voluntarily participated in the study.

References

  1. 1. Tran H.A. (2005). Biochemical tests in pregnancy. Australian Prescriber, (28)98: 107.
  2. 2. Nelson S. and Greer I. (2006). Hypertensive disorders of pregnancy: preventative-, immediate- and long term management. Expert Review of Pharmacoeconomics & Outcomes Research, 6(5): 541–54. pmid:20528501
  3. 3. Allen V., Joseph K. S., Murphy K. E., Magee L.A. and Ohlsson A. (2004). The effect of hypertensive disorders in pregnancy on small for gestational age and stillbirth: a population based study. BMC Pregnancy and Childbirth 4: 17. pmid:15298717
  4. 4. Nathan H. L., Seed P. T., Hezelgrave N. L., De Greeff A., Lawley E., Conti-Ramsden F., et al. (2018). Maternal and perinatal adverse outcomes in women with pre-eclampsia cared for at facility-level in South Africa: a prospective cohort study. J Glob Health, 8(2): 020401 pmid:30140431
  5. 5. Arulkumaran S (2016). Foreword: The Figo Textbook of Pregnancy Hypertension An evidence-based guide to monitoring, prevention and management. Eds: Magee L.A., M D, von Dadelszen P., Stones W., and Mathai M. Published by The Global Library of Women’s Medicine 9 Provost Court London NW3 4SR
  6. 6. Tangirala S. and Kumari D. (2015). Placental morphology in hypertensive disorders and its correlation to neonatal outcome. IAIM, 2(11): 35–38.
  7. 7. Adu-Bonsaffoh K., Oppong S.A., Binlinla G. and Obed S.A. (2013). Maternal deaths attributable to hypertensive disorders in a tertiary hospital in Ghana. Int J Gynaecol Obstet, 123(2): 110–113. pmid:23969337
  8. 8. Udainia A. and Jain M.L. (2001). Morphological study of placenta in pregnancy induced hypertension with its clinical significance. J Anat. Soc. India, 50(1): 24–27.
  9. 9. Eskild A. and Vatten L.J. (2010). Do pregnancies with PE have small placentas? A population study of pregnancies with & without growth restriction in the offspring. BJOG. 117: 1521–1526. pmid:20840528
  10. 10. Kurdukar M.D. and Deshpande N.M. (2007). Placenta in Pregnancy induced Hypertension. Indian J Pathol Mycrobiol. 50: 493–497.
  11. 11. Rosana C.R.M., Gilio D.B., Cavellani C.L., Paschoini M.C., Oliveira F.A., Peres L.C., et al. (2008). Placental morphometrical and histopathology changes in the different clinical presentations of Hypertensive Syndromes in Pregnancy. Arch Gynaecolobstr, 277(1): 201–206. pmid:17786461
  12. 12. Ferrazzani S., Luciano R., Garofalo S., D’Andrea V., De Carolis S., De Carolis, et al. (2011). Neonatal outcome in hypertensive disorders of pregnancy. Early Hum Dev, 87(6): 445–9. pmid:21497462
  13. 13. Martikainen A.M., Heinonen K.M. and Saarikoski S.V. (1989). The effect of hypertension in pregnancy on foetal and neonatal condition. Int J Gynaecol Obstet, 30(3): 213–20. pmid:2575045
  14. 14. NHBPEP, Working Group on High Blood Pressure in Pregnancy. (2000). Report of National High Blood Pressure Education Program, Working Group on High Blood Pressure in Pregnancy. American Journal Obstetrics and Gynaecology, 183: S1–S22.
  15. 15. Abaidoo C.S., Boateng K.A. and Warren M.A. (2008). Morphological variations of the “baby’s supply line”. Journal of Science and Technology, 28(2): 1–9.
  16. 16. Cunningham F.G., Leveno K.J. and Bloom S.L. (2005). Implementation, embryogenesis and placental development. Williams Obstetrics (22nd edition), McGraw-Hill, New York, USA.
  17. 17. Valsamakis G., Kanaka-Gantenbein C., Malamitsi-Puchner A. and Mastorakos G. (2006). Causes of intrauterine growth restriction and postnatal development of the metabolic syndrome. Annals of the New York Academy of Sciences, 1092: 138–147. pmid:17308140
  18. 18. Amiel-Tison C., Gosselin J. and Infante-Rivard C. (2002). Head growth and cranial assessment at neurological examination in infancy. Developmental Medicine and Child Neurology, 44: 643–8. pmid:12227620
  19. 19. ACOG. (2002). Diagnosis and management of preeclampsia and Eclampsia. American College of Obstetricians and Gynecologists, 99(1): 159–167.
  20. 20. Singh S., Ahmed E.B., Egondu S.C. and Ikechukwu N.E. (2014). Hypertensive disorders in pregnancy among pregnant women in a Nigerian Teaching Hospital. Niger Med J, 55(5): 384–388. pmid:25298602
  21. 21. Al-Ghamdi S.M., Al-Harbi A.S., Khalil A. and El-Yahyia A.R. (1999). Hypertensive Disorders of Pregnancy: Prevalence, classification and adverse outcomes in Northwestern Saudi Arabia. Ann Saudi Med, 19(6): 557–560. pmid:17277483
  22. 22. Ventura S.J., Martin J.A., Cortin S.G., Mathews T.J. and Park M.M. (2000). Births: final data for 1998, national vital statistics Reports, CDC, 48(3): 1–21.
  23. 23. Gaio D.S., Schmidt M.I., Duncan B.B., Nucci L.B., Matos M.C. and Branchtein L. (2001). Hypertensive disorder in pregnancy: frequency, and associated factors in a cohort of Brazilian women. Hypertension in pregnancy, 20: 269–281. pmid:12044335
  24. 24. Adu-Bonsaffoh K., Ntumy M.Y., Obed S.A., Seffah J.D. (2017). Prevalence of hypertensive disorders in pregnancy at Korle-bu teaching hospital in Ghana. J Gynecol Neonatal Biol, 3(1): 8–13.
  25. 25. Singh S., Ahmed E.B., Egondu S.C. and Ikechukwu N.E. (2014). Hypertensive disorders in pregnancy among pregnant women in a Nigerian Teaching Hospital. Niger Med J, 55(5): 384–388. pmid:25298602
  26. 26. Walle T.A. and Azagew A.W. (2017). Hypertensive disorders of pregnancy prevalence and associated factors among pregnant women attending antenatal care at Gondar town health Institutions, North West Ethiopia. Pregnancy Hypertension, 16: 79–84.
  27. 27. Anorlu R.I., Iwuala N.C. and Odum C.U. (2005). Risk factors for preeclampsia in Lagos, Nigeria. Aust N Z J Obstet Gynaecol, 45(4): 278–282. pmid:16029292
  28. 28. Sibai B.M. (1990b). Preeclampsia-eclampsia. Curr Prob Obstet Gynecol Fertil, 77: 514–519.
  29. 29. Ness R.B., Scholtland H.M., Flegal K.M. and Shofer F.S. (1994). Reproductive history and coronary heart disease risk in women. Epidemiol Rev, 16: 298–314. pmid:7713181
  30. 30. Silva L.M., Steegers E.A., Burdorf A., Ja ddoe V.W., Arends L.R., Hofman A., et al. (2008). No midpregnancy fall in diastolic blood pressure in women with a low educational level: the Generation R Study. Hypertension, 52(4): 645–51. pmid:18725583
  31. 31. Nama V., Antonios T.F., Onwude J. and Manyonda I.T. (2011). Mid-trimester blood pressure drop in normal pregnancy: myth or reality? J Hypertens, 29(4): 763–768.
  32. 32. Thompson M.L., Williams M.A. and Miller R.S. (2009). Modelling the association of blood pressure during pregnancy with gestational age and body mass index. Paediatr Perinat Epidemiol, 23(3): 254–63. pmid:19775387
  33. 33. Grindheim G., Estensen M., Langesaeter E., Rosseland L.A. and Toska K. (2012). Changes in blood pressure during healthy pregnancy: a longitudinal cohort study. J Hypertens, 30(2): 342–50. pmid:22179091
  34. 34. Cincotta R.B. and Brennecke S.P. (1998). Family history of preeclampsia as a predictor for preeclampsia in primigravidas. Int J Gynaecol Obstet, 60: 23–7. pmid:9506410
  35. 35. Fedrick J. and Adelstein P. (1978). Factor associated with low birth weight of infants delivered at rest. Br. J. Obstet. Gynaecol, 85: 1–7.
  36. 36. Cramer J.C. (1995). Racial and ethnic difference in birth weight: The role of income and financial assistance. Demography, 32: 231–247. pmid:7664962
  37. 37. Wolfe H.M., Zador I.E., Gross T.L., Martier S.S. and Sokol R.J. (1991). The clinical utility of maternal body mass index in pregnancy. Am J Obstet Gynecol, 164(5 Pt 1): 1306–1310. pmid:2035574
  38. 38. Sebire N.J., Jolly M., Harris J., Regan L. and Robinson S. (2001). Is maternal underweight really a risk factor for adverse pregnancy outcome? A population-based study in London. BJOG, 108(1): 61–66. pmid:11213006
  39. 39. Cnattingius S., Bergstrom R., Lipworth L. and Kramer M.S., (1998). Prepregnancy weight and the risk of adverse pregnancy outcomes. N Engl J Med, 338(3): 147–152. pmid:9428815
  40. 40. Udainia A., Bhagwat S.S. and Mehta C.D. (2004). Relation between placental surface area, infarction and foetal distress in pregnancy induced hypertension with its clinical relevance, Journal of Anatomical Society of India, 53(1): 27–30.
  41. 41. Majumdar S., Dasgupta H., Bhattacharya K. and Bhattacharya A. (2005). A Study of Placenta in Normal and Hypertensive Pregnancies. J Anat Soc India, 54(2): 1–9.
  42. 42. Navbir P. (2014). Placental morphology and its co-relation with foetal outcome in pregnancy induced hypertension. International Journal of Basic and Applied Medical Sciences, 2(3): 120–125.
  43. 43. Ashfaq M., Janjua M.Z. and Channa M.A. (2005). Effect of gestational diabetes and maternal hypertension on gross morphology of placenta. J Ayub Med Coll Abbottabad, 17(1): 44–47. pmid:15929527
  44. 44. Macpherson T. (1991). Fact and Fancy. Arch Pathol Lab Med, 115: 672–679. pmid:2064525
  45. 45. Das B., Dutta D., Chakraborthy S. and Nath P. (1996). Placental morphology in hypertensive disorders of pregnancy and its correlation with foetal outcome. J Obstet Gynecol India, 46(1): 40–46.
  46. 46. Masodkar A.R., Kalamkar L.R. and Patki P.S. (1985). Histopathology of placenta and its correlation with foetal outcome, J obstet Gynaecol India, 35: 294.
  47. 47. Salgado S.S. and Pathmeswaran A. (2008). Effects of placental infarctions on the foetal outcome in pregnancies complicated by hypertension. J Coll Physicians Surg Pak, 18(4): 213–216. pmid:18474153
  48. 48. Goswami P., Lata H., Memon S. and Khaskhelli L.B. (2011). Excessive placental calcification observed in PIH patients and its relation to foetal outcome. JLUMHS, 11: 143–8.
  49. 49. Harsh M., Sodhi S. and Mohan P.S. (1989). Foetal correlation with placental pathology in toxaemia of pregnancy. J Obstet Gynecol India, 39: 170–5.
  50. 50. Ezeigwe C.O., Okafor C.I., Eleje G.U., Udigwe G.O. and Anyiam D.C. (2018). Placental Peripartum Pathologies in Women with Preeclampsia and Eclampsia. Obstetrics and Gynecology, 8. pmid:30327674
  51. 51. Kotgirwar S., Mohd I., Gupta V. and Trivedi S. (2009). Morphology of placenta in pregnancy induced hypertension and its foetal outcome. Journal of Advance Researches in Biological Sciences, 1(2): 109–114.
  52. 52. Barker D.J.P., Thornburg K.L., Osmond C., Kanjantie E. and Eriksson J.G. (2010). The surface area of the placenta and hypertension in the offspring in later life. Int. J. Dev. Biol, 54: 525–530. pmid:19876839
  53. 53. Pradeep S., Londhe A. and Mane B. (2011). Morphometric study of placenta and its correlation in normal and hypertensive pregnancies. International Journal of Pharma and Bio Sciences, 2(4): 975–6299.
  54. 54. Abhilasha D., Sushma K.K., Kushal R.K. and Pushpa P. (2012). Study of effect of eclampsia and chronic hypertension on gross morphology of placenta. Int J Biol Med Res., 3(2):1771–1773.
  55. 55. Laurini R., Laurin J. and Marskar K. (1994). Placenta in Preeclamptic toxemia. Acta Obstet Gynecol Scand, 73: 529–34.
  56. 56. Little R.E., Zadorozhnaja T.D., Hulchiy O.P., Mendel N.A., Shkyryak-Nyzhnyk Z.A., Chyslovska N., et al. (2003). Placental weight and its ratio to birthweight in a Ukrainian city. Early Hum Dev, 71: 117–27. pmid:12663149
  57. 57. Kajantie E., Thornburg K.L., Eriksson J.G., Osmond C. and Barker D.J.P. (2010). In preeclampsia, the placenta grows slowly along its minor axis. Int J Dev Biol, 54: 469–473. pmid:19876819
  58. 58. Raghavendra A.Y., Veena P., Ramesh S.T. and Vinay K.K. (2013). Study of placental diameter and surface area in normal and hypertensive pregnancies. Anatomica Karnataka, 7(3): 18–22.
  59. 59. Devishankar K., Bhanu P.S., Kiran S., Ramakrishna B.A. and Shanthi V. (2012). Vasculo syncytial membrane in relation to syncytial knots complicates the placenta in preeclampsia: A histomorphometrical study. Anat Cell Biol, 45: 86–91. pmid:22822462
  60. 60. Ahmed M. and Daver R.G. (2013). Study of placental changes in pregnancy induced hypertension. Int J Reprod Contracept Obstet Gynecol, 2(4): 524–527.
  61. 61. Zia-ur-rehman M., Ullah H.M.F., Taj N., Malik Z.I. and Ullah E. (2013). Unfavourable effects of preeclampsia on the morphology of the placenta. Pak J Med Health Sci, 7(1): 207.
  62. 62. Gowda P. and Jayanthi K.S. (2014). Morphological and morphometrical study of placenta in normal and hypertensive pregnancies. NJCA, 3(1): 24–28.
  63. 63. Boyd P.A. and Scott A. (1985). Quantitative structural studies on human placentas associated with preeclampsia, essential hypertension and intrauterine growth retardation. Br J Obstet Gynecol, 92, 714–21. pmid:4016032
  64. 64. Teasdale F. (1987). “Histomorphometry of the human placentae in pre-eclampsia associated with severe intra-uterine growth retardation,” Placenta, 8(2): 119–128, 1987. pmid:3615372
  65. 65. Aherne W. and Dunnill M.S. (1966). Quantitative aspects of placental structure. J Pathol Bacteriol, 91: 123–39. pmid:5941387
  66. 66. Baergen RN. (2011). Pathology of the Umbilical Cord, in Manual of Pathology of the Human Placenta, Second edn. New York: Springer Science & Business Media; 2011.
  67. 67. Gilbert-Barness E., Drut R.M., Drut R., Grange D.K. and Opitz J.M. (1993). Developmental abnormalities resulting in short umbilical cord. Birth defects Orig, 29(1): 113–40. pmid:8280869
  68. 68. Vrabie S. C., Novac L., Manolea M. M., Dijmarescu L. A., Novac M., and Siminel M. A. (2018). Abnormalities of the Umbilical Cord. Congenital Anomalies—From the Embryo to the Neonate. IntechOpen 345–362.
  69. 69. Saha R. R., Farhat N., and Karmaker M. (2014). Study of Umbilical Cord in Pregnancy Induced Hypertension with and without Diabetes Mellitus. Bangladesh J. Anat. 2014; 12(1): 3–6.
  70. 70. Mohol F. M., Karim M., Afroze A., Haque J., and Khatun M., (2016). Insertion of Umbilical Cord on Placenta in Hypertensive Mother. Journal of National Institute of Neurosciences Bangladesh, 2(2): 89–93.
  71. 71. Kaur P., Kaushal S., Sharma A., and Singh K. (2014). To Study Relationship of Umblical Cord Insertion with Fetal Outcome in PIH and Normotensive Pregnancies. Int. J. Pure App. Biosci. 2 (6): 108–111.
  72. 72. Yadav S., Saxena U., Yadav R. and Gupta S. (1997). Hypertensive disorders of pregnancy and maternal and foetal outcome: A case controlled study. J Indian Med Asoc, 95: 548–51. pmid:9567600
  73. 73. Siromani S.M., Varahala A.M., Gopu S. and Chidugull S.K. (2015). Neonatal Outcome In Pregnancy Induced Hypertensive Mothers—A Tertiary Care Centre Experience. IOSR Journal of Dental and Medical Sciences, 14(11): 23–27.
  74. 74. Vats K and Paul M. (2016). Study of fetal outcome in hypertensive disorders of pregnancy in a tertiary care maternity hospital of Delhi. Int J Reprod Contracept Obstet Gynecol. 5(11):3773–3777.
  75. 75. Abdul H.B., Salma F.M. and Asmat K.A. (2012). Comparison of Placentae from Hypertension Associated Pregnancies and Normal Pregnancies. JLUMHS. 11(1).
  76. 76. Okoye H. C., Nwogoh B., and Odetunde O. I. (2017). Correlation of hematocrit and Apgar scores in newborns of women with hypertensive disorders in pregnancy. J Neonatal Perinatal Med., 10(4):387–392. pmid:29286929