<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2021.118093</article-id><article-id pub-id-type="publisher-id">OJOG-111268</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Study of the Role of Ethnicity in the Pathophysiology of Preeclampsia: A Prospective Observational Study in a Rural Hospital in India
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Indranil</surname><given-names>Banerjee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Archana</surname><given-names>Kumari</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gargi</surname><given-names>Mukherjee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Medical College, Kolkata, India</addr-line></aff><aff id="aff1"><addr-line>Basildon &amp;amp; Thurrock University Hospital, Basildon , UK</addr-line></aff><pub-date pub-type="epub"><day>30</day><month>07</month><year>2021</year></pub-date><volume>11</volume><issue>08</issue><fpage>978</fpage><lpage>1004</lpage><history><date date-type="received"><day>23,</day>	<month>February</month>	<year>2021</year></date><date date-type="rev-recd"><day>10,</day>	<month>August</month>	<year>2021</year>	</date><date date-type="accepted"><day>13,</day>	<month>August</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Hypertensive disorders (HD) of pregnancy are a leading cause of maternal and perinatal mortality and morbidity worldwide. Although several risk factors for hypertensive disorders of pregnancy have been firmly established, the risk attributable to specific race-ethnicities is less clear. The risk of preeclampsia-eclampsia may differ by maternal ethnicity 30 as also the course, severity 
  and
   prognosis. This study aimed to compare severe preeclampsia and eclampsia in tribal and nontribal women of 
  Jangalmahal
   area of West Bengal in terms of incidence, clinical, demographic picture, severity, course of 
  disease
  , response to treatment, complications 
  and
   delivery outcome including 
  foetal
   outcome and maternal outcome.
 
</p></abstract><kwd-group><kwd>Ethnicity</kwd><kwd> Pre Eclampsia</kwd><kwd> Tribal</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Hypertensive disorders (HD) of pregnancy constitute a perplexing and clinically challenging group of complications of pregnancy and are responsible for a substantial burden of illness. They are a leading cause of maternal and perinatal mortality and morbidity worldwide, but especially in developing countries [<xref ref-type="bibr" rid="scirp.111268-ref1">1</xref>].</p><p>Preeclampsia is a multisystem disorder of unknown aetiology characterized by development of hypertension with proteinuria after 20<sup>th</sup> week of gestation, in previously normotensive and non proteinuric pregnant women [<xref ref-type="bibr" rid="scirp.111268-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref3">3</xref>].</p><p>Preeclampsia when complicated with generalized tonic-clonic convulsions and/or coma is called Eclampsia [<xref ref-type="bibr" rid="scirp.111268-ref4">4</xref>].</p><p>Globally HD of pregnancy complicate approximately 5% - 10% of pregnancies [<xref ref-type="bibr" rid="scirp.111268-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref7">7</xref>]. The incidence of preeclampsia and the precursor of eclampsia, vary greatly worldwide. Preeclampsia complicates about 2% - 8% of all pregnancies [<xref ref-type="bibr" rid="scirp.111268-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref8">8</xref>].</p><p>WHO estimates the incidence of preeclampsia to be seven times higher in developing countries (2.8% of live births) than in developed countries (0.4%) which is due to poor health seeking behaviours and lack of availability of health care facilities and personnel [<xref ref-type="bibr" rid="scirp.111268-ref9">9</xref>].</p><p>Incidence of HD of pregnancy in India is found to be 11,266 out of 111,725 deliveries (10.08%) as observed through the data collected by the National Eclampsia Registry (NER) over 3 years (2011-2013) [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>]. Two thousand five hundred fifty-four of those 11,266 patients presented with eclampsia [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>]. The FOGSI-ICOG NER has brought forth some revealing trends. Eclampsia prevalence among registry patients is 1.9% [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>]. National sample surveys in the past have shown prevalence to be 1% - 5%. This is out of the 11,725 deliveries analyzed from the cases reported by 175 reporting centers. Seventeen percent of preeclampsia patients are actually in the adolescent age group reflecting the very early age at marriage in spite of several awareness programs and legal guidelines [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>]. 76.34% of the patients were between 21 and 30 years of age thus rendering a very young population morbid and at risk of mortality. It is also a disease of the first-time pregnant woman as 81% of the patients with preeclampsia are primigravida [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>].</p><p>Approximately 72,000 pregnant women die every year because of eclampsia and severe preeclampsia worldwide [<xref ref-type="bibr" rid="scirp.111268-ref10">10</xref>]. HD account for 16% of all maternal deaths in developed countries [<xref ref-type="bibr" rid="scirp.111268-ref11">11</xref>]. The risk that a woman in a developing country will die of preeclampsia or eclampsia is about 300 times that of a woman in a developed country [<xref ref-type="bibr" rid="scirp.111268-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref14">14</xref>].</p><p>Reliable statistics about women dying due to preeclampsia-eclampsia are difficult to obtain because of the poor quality of vital statistics registration systems and hospital records in many developing countries. In addition, a sizable number of deliveries take place at home, and thus there are no records at all for these births [<xref ref-type="bibr" rid="scirp.111268-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref18">18</xref>]. Therefore, data on women who die from preeclampsia-eclampsia are only available from a limited number of countries. Nevertheless, it is clear that the case fatality rates for preeclampsia-eclampsia vary greatly across countries, with the risk of death from preeclampsia-eclampsia being much higher in developing countries than in developed ones [<xref ref-type="bibr" rid="scirp.111268-ref19">19</xref>]. India is among those countries which have a very high MMR, i.e. 190 per 100,000 live births [<xref ref-type="bibr" rid="scirp.111268-ref20">20</xref>]. Hypertension accounts for 5% of maternal deaths in India [<xref ref-type="bibr" rid="scirp.111268-ref21">21</xref>].</p><p>HD is also associated with preterm birth, foetal growth restriction, perinatal death and long-term adult health problems in the offspring. Preeclampsia causes five fold increase in the perinatal mortality, with most of the deaths caused by iatrogenic prematurity [<xref ref-type="bibr" rid="scirp.111268-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref23">23</xref>]. In US, preeclampsia is responsible for 15% of premature births [<xref ref-type="bibr" rid="scirp.111268-ref24">24</xref>].</p><p>If the disorder occurs in early pregnancy, 53% of the infants are small for gestational age (SGA) [<xref ref-type="bibr" rid="scirp.111268-ref25">25</xref>]. Further, to be born SGA increases the risk of hypertension, diabetes and coronary heart disease as adults [<xref ref-type="bibr" rid="scirp.111268-ref26">26</xref>].</p><p>The risk of delivery of low birth weight (LBW) or growth-restricted babies in mothers with HD differs in different ethnic/racial groups [<xref ref-type="bibr" rid="scirp.111268-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref28">28</xref>].</p><p>However, the causes for preeclampsia-eclampsia remain unclear and thus preeclampsia-eclampsia has been called a “Disease of theories” [<xref ref-type="bibr" rid="scirp.111268-ref29">29</xref>]. Almost everyone (from an allergist to zoologist) had proposed a theory and almost anything on the earth (from watermelon season to a specific worm infestation) has been blamed [<xref ref-type="bibr" rid="scirp.111268-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref31">31</xref>]. Although the precise cause is unknown, the pathophysiologic processes underlying this disorder are described in two stages [<xref ref-type="bibr" rid="scirp.111268-ref32">32</xref>]. The first stage is characterized by reduced placental perfusion possibly related to abnormal placentation with impaired trophoblast invasion and inadequate remodeling of the uterine spiral arteries. The second stage refers to the maternal systemic manifestations with inflammatory, metabolic, and thrombotic responses converging to alter vascular function which can result in multi-organ damage [<xref ref-type="bibr" rid="scirp.111268-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref35">35</xref>].</p><p>Some risk factors for HD of pregnancy has been identified and these include nulliparity, older maternal age, multiple births, diabetes, chronic hypertension, obesity, previous h/o preeclampsia, family history of preeclampsia, a new partner and/or about 10 years since last pregnancy, renal disease, and the presence of antiphospholipid antibodies [<xref ref-type="bibr" rid="scirp.111268-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref36">36</xref>] - [<xref ref-type="bibr" rid="scirp.111268-ref43">43</xref>]. Studies have reported a 7% - 20% chance of recurrence of preeclampsia in a subsequent pregnancy [<xref ref-type="bibr" rid="scirp.111268-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref44">44</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref45">45</xref>].</p><p>Some other risk factors are still being investigated. Geographic, social, economic and racial differences are thought to be responsible for incidence rates up to 3 times higher in some populations [<xref ref-type="bibr" rid="scirp.111268-ref46">46</xref>].</p><p>Some studies have investigated racial and ethnic factors and identified some differences in severe preeclampsia and eclampsia in different population groups [<xref ref-type="bibr" rid="scirp.111268-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref47">47</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref48">48</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref49">49</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref50">50</xref>]. Among the major ethnic groups considered, East Asian women had the lowest risk of preeclampsia and Mexican women had the highest risk [<xref ref-type="bibr" rid="scirp.111268-ref47">47</xref>].</p><p>Caughey reported that the rates of preeclampsia were higher among African American women and lower among Latina and Asian women with all results being statistically significant as compared with white women [<xref ref-type="bibr" rid="scirp.111268-ref48">48</xref>]. Marcelo reported that immigrant women from the Caribbean, Sub-Saharan Africa and Hispanic America were at the highest risk of serious preeclampsia relative to immigrant women from industrialized nations [<xref ref-type="bibr" rid="scirp.111268-ref49">49</xref>]. In a study by Abubakar, among three tribal groups, the preeclamptic Fulani women are more likely to progress to eclampsia than the Hausa and Kanuri [<xref ref-type="bibr" rid="scirp.111268-ref18">18</xref>]. Black women were more likely to be diagnosed with preeclampsia than were White women [<xref ref-type="bibr" rid="scirp.111268-ref50">50</xref>]. The risk of preeclampsia-eclampsia may differ by maternal ethnicity [<xref ref-type="bibr" rid="scirp.111268-ref48">48</xref>] as also the course, severity and prognosis [<xref ref-type="bibr" rid="scirp.111268-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref52">52</xref>]. Such differences in severe preeclampsia and eclampsia in different ethnic population groups may also exist in India. But studies focussing on such aspects of preeclampsia and eclampsia in different population groups in India are scarce in literature. Ethnicity reflects many potential influences on health, including socioeconomic status, lifestyle (e.g. diet and physical activity), medical care utilization, and genetic background associated with geographic origin. Examining the relation of ethnicity with preeclampsia-eclampsia may provide important information that may highlight ethnic subgroups which need to be monitored more actively and could help guide screening and treatment, particularly in light of ethnic diversity of pregnancies [<xref ref-type="bibr" rid="scirp.111268-ref47">47</xref>].</p></sec><sec id="s2"><title>2. Aims and Objectives</title><p>The objectives of this study were to note whether any differences existed among tribal and nontribal women with severe preeclampsia and eclampsia in the Jangalmahal area of West Bengal due to different ethnicity in the following parameters:</p><p>&#183; Incidence.</p><p>&#183; Clinical and demographic picture.</p><p>&#183; Severity and course of disease.</p><p>&#183; Response to treatment and complications.</p><p>&#183; Delivery outcome including foetal and maternal outcomes.</p><p>Specific Objective:</p><p>To identify the ethnic/racial group at higher risk of severe preeclampsia and eclampsia among tribal and nontribal women.</p></sec><sec id="s3"><title>3. Materials and Methods</title><sec id="s3_1"><title>3.1. Study Area</title><p>The present study was conducted in The Department of Obstetrics &amp; Gynaecology, Midnapore Medical College &amp; Hospital, Paschim Midnapore, West Bengal. (The area concerned has got a huge tribal population).</p></sec><sec id="s3_2"><title>3.2. Study Period</title><p>The period of study was 1 year (1<sup>st</sup> May, 2014 to 30<sup>th</sup> April, 2015).</p></sec><sec id="s3_3"><title>3.3. Study Population and Sample Size</title><p>Two hundred consecutive mothers coming from Jangalmahal area and admitted to the Obstetrics &amp; Gynaecology Department, Midnapore Medical College &amp; Hospital, Paschim Midnapore with severe preeclampsia and eclampsia were included in the study.</p><p>The mothers were divided into two groups:</p><p>1) Tribal Group (T group)</p><p>2) Nontribal Group (NT group).</p></sec><sec id="s3_4"><title>3.4. Study Design</title><p>The study was a prospective observational comparative study.</p></sec><sec id="s3_5"><title>3.5. Criteria for Sample Selection</title><p>Inclusion criteria:</p><p>Mothers coming from Jangalmahal area of West Bengal and admitted to the Department of Obstetrics &amp; Gynaecology, Midnapore Medical College &amp; Hospital with severe preeclampsia and eclampsia were included in the study (BP &gt; 160 systolic and 110 diastolic along with UPCR &gt; 30 or Eclamptic fits).</p><p>Exclusion criteria:</p><p>&#183; Women with gestational ages of less than 20 weeks.</p><p>&#183; Pre-existing chronic hypertension/eesential hypertension.</p><p>&#183; Pre-existing diabetes.</p><p>&#183; Chronic renal disease (Q3).</p></sec><sec id="s3_6"><title>3.6. Parameters to Be Studied</title><p>The study was conducted to compare whether any differences exist in cases of severe preeclampsia and eclampsia among tribal and nontribal women of the Jangalmahal area of West Bengal in the following parameters:</p><p>1) Incidence, clinical and demographic picture, severity and course of disease.</p><p>2) Response to treatment and complications.</p><p>3) Delivery outcome including foetal outcome and maternal outcome.</p></sec><sec id="s3_7"><title>3.7. Study Tool</title><p>A detailed tool (case proforma) was developed and used to record data (observations) of each case as detailed in methods.</p><p>The data of individual patient was collected from the BHTs of patients, investigation reports, labour room records (Logbook), OT records and referral papers where applicable.</p></sec><sec id="s3_8"><title>3.8. Study Technique</title><p>The study was approved by the Ethics Committee of our institution. It was conducted in the Dept. of G &amp; O, M.M.C. &amp; H. Two hundred consecutive mothers coming from Jangalmahal area and admitted to the G &amp; O Department, M.M.C. &amp; H. with severe preeclampsia and eclampsia were enrolled in the study following the inclusion and exclusion criteria.</p><p>Pregnant women admitted in the labour room and meeting the inclusion criteria were selected after informed consent in the local language. The mothers included in the study were divided into two groups: Tribal (T) group &amp; Non tribal (NT) group.</p><p>Maternal ethnic ancestry was identified by self-report as recorded on the birth records and also the surnames which come under tribal groups were obtained from the District Magistrate’s office.</p><p>Severe preeclampsia was diagnosed [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>] if a preeclamptic mother had blood pressure ≥ 160/110 mmHg or proteinuria ≥ 3+ or any of the following features: Headache, vomiting, clouding (blurring) of vision/blindness, oliguria (passing less than 400 ml urine in 24 hrs)/anuria, upper abdominal pain (epigastric pain or pain in the right upper quadrant), pulmonary oedema, hyperreflexia, HELLP syndrome.</p><p>Eclampsia was diagnosed if there was convulsion and/or coma with features of preeclampsia [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>].</p></sec><sec id="s3_9"><title>3.9. Treatment Strategy</title><p>All the patients received standard management (which was being followed in the institution) as follows:</p><p>1) Antihypertensives: Inj. Labetalol (10 mg) i.v. were given to the patients with blood pressure &gt; 150/100 mmHg and then repeated if necessary with incremental doses of 20 mg, 40 mg and 80 mg at 10 mins interval [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>] titrating according to blood pressure. Our goal was to maintain blood pressure between 140/90 - 150/100 mmHg.</p><p>2) Anticonvulsant: Inj. Magnesium sulfate is the drug of choice for preventing and treating convulsions in severe preeclampsia and eclampsia [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref54">54</xref>]. It was given following Pritchard Regimen which is as follows [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref54">54</xref>].</p><p>&#183; LOADING DOSE: Magnesium sulfate 20% solution 4 gm i.v. over 5 mins followed immediately by 10 gm of 50% magnesium sulphate solution (5gm in each buttock) as deep i.m. injection with 1 ml of 2% lignocaine in the same syringe.</p><p>&#183; MAINTENENCEDOSE: 5 gm MgSO<sub>4</sub> (50% solution) plus 1 ml lignocaine 2% i.m. every 4 hrs into alternate buttocks continued till 24 hrs after delivery or the last convulsion whichever occurs last.</p><p>Each maintenance dose was administered after ensuring that:</p><p>- Urinary output was at least 30 ml/hr which is equivalent to 100 ml over 4 hours [<xref ref-type="bibr" rid="scirp.111268-ref53">53</xref>] (approx).</p><p>- Respiratory rate was at least 16/min.</p><p>- Patellar reflex was present.</p><p>3) Termination of pregnancy: Mode &amp; method of termination was decided as per merits of individual cases with the aim of prompt and safe delivery.</p><p>On admission, in each case the demographic profile of the mother (age, parity, socioeconomic status etc.), gestational age, foetal condition, maternal condition on admission, whether in labour or not, stage phase of labour (if in labour) and any complication were noted. The initial choice for mode of delivery was also noted.</p><p>Investigations included urine analysis for albumin, blood for urea, creatinine, uric acid, Liver Function Tests, Hb%, TC, DC, ESR &amp; platelet count and USG, CT scan &amp; MRI in selected cases. The results were noted.</p><p>Mothers were monitored for general conditions, progress of labour, complications if any, response to treatment (blood pressure &amp; fits control, dose requirement of antihypertensives &amp; anticonvulsants).</p><p>Delivery outcomes including mode of delivery, foetal &amp; maternal outcomes were recorded. All the informations/observations from each patient were recorded in the study tool (proforma).</p></sec><sec id="s3_10"><title>3.10. Plan for Analysis of Data</title><p>Data so collected was collated and analysed with appropriate statistical tests and methods.</p><p>Test of significance of difference was done by Student’s two-tail “t”-Test. P values less than 0.05 was considered as significant difference. Data were presented in tabular form and also represented by bar diagrams wherever needed. Data were expressed as Mean &#177; Standard error of mean (SEM). Softwares used: Microsoft excel, SPSS version 19; Origin Lab (Ver 8.0) and MedCalc (Ver 6.2).</p></sec><sec id="s3_11"><title>3.11. Results and Analysis</title><p>A total of consecutive 200 mothers, from Jangalmahal area, admitted to the Gynaecology &amp; Obstetrics Department of Midnapore Medical College &amp; Hospital with severe Preeclampsia and eclampsia were included in this study. Of these 200 mothers there were 65 mothers in Tribal (T) group and 135 mothers in Nontribal (NT) group. Of them 133 mothers had severe preeclampsia and 67 mothers had eclampsia. During the study period a total of 3768 (576 tribal and 3192 nontribal) women delivered in our institution. Thus, during the study period the overall incidence of severe preeclampsia and eclampsia in our institution were 3.53% and 1.78% respectively. Both severe preeclampsia and eclampsia were found to be significantly (p &lt; 0.001) more common in the T group than the NT group (7.29% vs. 2.85% and 3.99% vs. 1.38% respectively (<xref ref-type="table" rid="table1">Table 1</xref> &amp; <xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Both severe preeclampsia and eclampsia were found to be significantly (p &lt; 0.001) more common in the tribal group than the nontribal group (7.29% vs. 2.85% and 3.99% vs. 1.38%) respectively.</p><p>In both tribal and nontribal groups, majority of mothers with severe preeclampsia and eclampsia were under 25 years of age. In comparative analysis, the tribal mothers exhibited a significant (p &lt; 0.05) higher percentage for age group of ≤20 years and lower percentage for age group of 21 - 25 years than that of nontribal mothers. The difference was insignificant (p &gt; 0.05) for the age group 26 - 30 years. Frequency of suffering subjects in age groups of 31 - 35 years</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Incidence of severe preeclampsia and eclampsia in Tribal and Nontribal mothers</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Hypertensive disorder of pregnancy</th><th align="center" valign="middle" >T (n = 576) No. (%)</th><th align="center" valign="middle" >NT (n = 3192) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Severe preeclampsia</td><td align="center" valign="middle" >42 (7.29)</td><td align="center" valign="middle" >91 (2.85)</td></tr><tr><td align="center" valign="middle" >Eclampsia</td><td align="center" valign="middle" >23(3.99)</td><td align="center" valign="middle" >44(1.38)</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Age wise distribution of severe preeclampsia and eclampsia in Tribal and Nontribal group</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Age (Years)</th><th align="center" valign="middle" >Tribal (n = 65)</th><th align="center" valign="middle" >Nontribal (n = 135)</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >%</td></tr><tr><td align="center" valign="middle" >≤20 21 - 25 26 - 30 31 - 35 &gt;35</td><td align="center" valign="middle" >70.77 &#177; 2.38<sup>a</sup> 21.54 &#177; 1.32<sup>a</sup> 6.15 &#177; 1.19<sup>a</sup> 0 &#177; 0.00<sup>a</sup> 1.54 &#177; 0.11<sup>a</sup></td><td align="center" valign="middle" >64.44 &#177; 2.13<sup>b</sup> 25.93 &#177; 1.29<sup>b</sup> 8.15 &#177; 1.13<sup>a</sup> 1.48 &#177; 0.89<sup>b</sup> 0 &#177; 0.00<sup>b</sup></td></tr></tbody></table></table-wrap><p>(Data were expressed as Mean &#177; SEM in percentage value. Values of each row with different superscripts (a, b) differ from each other significantly (p &lt; 0.05)).</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Parity wise distribution of mothers in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parity</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Nullipara</td><td align="center" valign="middle" >56 (86.15)</td><td align="center" valign="middle" >108 (80)</td></tr><tr><td align="center" valign="middle" >Primipara</td><td align="center" valign="middle" >7 (10.77)</td><td align="center" valign="middle" >22 (16.30)</td></tr><tr><td align="center" valign="middle" >Multipara</td><td align="center" valign="middle" >2 (3.08)</td><td align="center" valign="middle" >5 (3.70)</td></tr></tbody></table></table-wrap><p>and &gt;35 years was negligible (<xref ref-type="table" rid="table2">Table 2</xref>, <xref ref-type="table" rid="table3">Table 3</xref>).</p><p>Parity distribution pattern showed that occurrence of Nulliparity was much higher than Primiparity and Multiparity in both groups. Comparative analysis showed that for variables “Nullipara” and “Primipara” significant (p &lt; 0.05) difference was found between T and NT groups. Significantly more mothers in tribal group (86.15%) were nulliparous than in nontribal group (80%) whereas primiparous mothers were significantly more common in nontribal group (16.30%) than tribal group (10.77%). For variable “multipara” there was no significant (p &gt; 0.05) difference between two groups (<xref ref-type="table" rid="table4">Table 4</xref>, <xref ref-type="fig" rid="fig2">Figure 2</xref> &amp; <xref ref-type="fig" rid="fig3">Figure 3</xref>).</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> State of consciousness of mothers in Tribal and Nontribal groups on the basis of Glasgow coma Scale (GCS)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >GCS on admission</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >&lt;8</td><td align="center" valign="middle" >7 (10.77)</td><td align="center" valign="middle" >5 (3.70)</td></tr><tr><td align="center" valign="middle" >8 - 12</td><td align="center" valign="middle" >10 (15.38)</td><td align="center" valign="middle" >23 (17.04)</td></tr><tr><td align="center" valign="middle" >13 - 15</td><td align="center" valign="middle" >48 (73.85)</td><td align="center" valign="middle" >107 (79.26)</td></tr></tbody></table></table-wrap><p>For class “&lt;8” and “13 - 15” tribal mothers showed significant (p &lt; 0.05) difference in intensity with nontribal mothers. For class “8 - 12” no significant difference (p &gt; 0.05) arrived. Unconsciousness (GCS &lt; 8) was more common in tribal group (10.77%) than in nontribal group (3.70%) and where as consciousness (GCS of 13 - 15) was more common in nontribal group (79.26%) than tribal group (73.85%).</p><p>Comparative analysis revealed that tribal mothers suffered from severe hypertension (≥160/110 mm of Hg) significantly (p &lt; 0.05) more commonly (76.92%) than nontribal mothers (69.60%) and significantly (p &lt; 0.05) more nontribal mothers (30.40%) had blood pressure &lt; 160/110 mm of Hg than tribal mothers (23.08%).</p><p>There was significant (p &lt; 0.05) difference found for all grades of proteinuria between T and NT group. Proteinuria in general was more common in tribal than nontribal mothers. Proteinuria was absent or trace in significantly (p &lt; 0.05) more number of nontribal mothers than tribal mothers whereas 1+ and 2+ proteinuria was significantly (p &lt; 0.05) more common in tribal than nontribal</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Comparison on the basis of blood pressure on admission between T and NT group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >BP on admission (mmHg)</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >&lt;160/110</td><td align="center" valign="middle" >15 (23.08)</td><td align="center" valign="middle" >41 (30.40)</td></tr><tr><td align="center" valign="middle" >≥160/110</td><td align="center" valign="middle" >50 (76.92)</td><td align="center" valign="middle" >94 (69.60)</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Urine for protein by dipstick method in Tribal and Nontribal group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Grades of proteinuria</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Negative</td><td align="center" valign="middle" >17 (26.15)</td><td align="center" valign="middle" >49 (36.3)</td></tr><tr><td align="center" valign="middle" >Trace</td><td align="center" valign="middle" >16 (24.6)</td><td align="center" valign="middle" >38 (28.15)</td></tr><tr><td align="center" valign="middle" >1+</td><td align="center" valign="middle" >22 (33.85)</td><td align="center" valign="middle" >28 (20.74)</td></tr><tr><td align="center" valign="middle" >2+</td><td align="center" valign="middle" >7 (10.77)</td><td align="center" valign="middle" >10 (7.4)</td></tr><tr><td align="center" valign="middle" >≥3+</td><td align="center" valign="middle" >3 (4.6)</td><td align="center" valign="middle" >10 (7.4)</td></tr></tbody></table></table-wrap><table-wrap id="table7" ><label><xref ref-type="table" rid="table7">Table 7</xref></label><caption><title> Comparison of severity of disease in Tribal and Nontribal group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Severity of disease</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Convulsion &gt; 4 times</td><td align="center" valign="middle" >23 (35.4)</td><td align="center" valign="middle" >79 (58.5)</td></tr><tr><td align="center" valign="middle" >Severe hypertension (≥160/110)</td><td align="center" valign="middle" >50 (76.9)</td><td align="center" valign="middle" >94 (69.6)</td></tr><tr><td align="center" valign="middle" >Proteinuria (≥3+)</td><td align="center" valign="middle" >3 (4.6)</td><td align="center" valign="middle" >10 (7.4)</td></tr></tbody></table></table-wrap><p>mothers. Severe proteinuria (≥3+), though significantly (p &lt; 0.05) more common in nontribals, was in general infrequent in both groups (Tables 5-7 and Figures 4-6).</p><p>Comparative analysis revealed that tribal mothers suffered from severe hypertension (≥160/110 mm of Hg) significantly (p &lt; 0.05) more commonly than NT group. Whereas nontribal mothers suffered significantly (p &lt; 0.05) more commonly from larger number of convulsions (&gt;4 times) when they developed eclampsia and severe proteinuria (≥3+) than tribal mothers.</p><p>Pregnant mothers with blood pressure &gt;150/100 mm of Hg (51 in tribal group and 98 in nontribal group) needed antihypertensive drug (Inj. Labetalol) therapy (Tables 8-9 and Figures 7-8).</p><table-wrap id="table8" ><label><xref ref-type="table" rid="table8">Table 8</xref></label><caption><title> Response to treatment with antihypertensive drugs in respect of time taken for BP to come below 150/100 mmHg (in mothers having BP &gt; 150/100 mmHg)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Time taken for BP control</th><th align="center" valign="middle" >T (51) No. (%)</th><th align="center" valign="middle" >NT (98) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >&lt;1/2 hr</td><td align="center" valign="middle" >10 (19.6)</td><td align="center" valign="middle" >23 (23.46)</td></tr><tr><td align="center" valign="middle" >1/2 hr - 1 hr</td><td align="center" valign="middle" >19 (37.25)</td><td align="center" valign="middle" >43 (43.9)</td></tr><tr><td align="center" valign="middle" >&gt;1 hr</td><td align="center" valign="middle" >22 (43.14)</td><td align="center" valign="middle" >32 (32.65)</td></tr></tbody></table></table-wrap><table-wrap id="table9" ><label><xref ref-type="table" rid="table9">Table 9</xref></label><caption><title> Response to anticonvulsant treatment: Recurrence/occurrence of convulsion in Tribal and Nontribal mothers after loading dose of MgSO<sub>4</sub></title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Convulsion after loading dose of MgSO<sub>4</sub></th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >1 (1.54)</td><td align="center" valign="middle" >2 (1.48)</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >64 (98.46)</td><td align="center" valign="middle" >133 (98.52)</td></tr></tbody></table></table-wrap><p>Mothers in both groups responded well to such treatment though significantly (&lt;0.01) more nontribal mothers responded earlier and to a smaller dose of anti-hypertensive drug than tribal mothers, and thus needed a smaller dose of anti-hypertensive drug, than tribal mothers for control of BP to the desired level of &lt;150/100 mmHg but not &lt;140/90 mmHg. Control of BP to the desired level required ≥1 hour of anti-hypertensive therapy (and thus larger doses) in significantly (&lt;0.01) more number of tribal mothers (43.14%) than nontribal mothers (32.65%).</p><p>Vast majority of mothers (98.46% of tribal mothers and 98.52% of nontribal mothers) in both the groups responded very well to anticonvulsant therapy with MgSO<sub>4</sub> and MgSO<sub>4</sub> was very effective in controlling convulsion in eclampsia and preventing it in case of severe preeclampsia in most mothers in both groups. Only a tiny fraction of mothers in both groups had convulsion after treatment was started with the loading dose of MgSO<sub>4</sub> and there was no significant difference (p &gt; 0.05) between the two groups.</p><p>Majority of mothers of both groups were already in labour at the time of admission. But comparative analysis revealed that the tribal mothers presented in labour significantly (p &lt; 0.05) more commonly than nontribal mothers, in both first stage (56.92% vs. 51.85%) and second stage (10.77% vs. 7.41%) of labour while antepartum (not in labour) mothers were significantly (p &lt; 0.05) more</p><table-wrap id="table10" ><label><xref ref-type="table" rid="table1">Table 1</xref>0</label><caption><title> Labour status on admission in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Status of labour</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Stage I</td><td align="center" valign="middle" >37 (56.92)</td><td align="center" valign="middle" >70 (51.85)</td></tr><tr><td align="center" valign="middle" >Stage II</td><td align="center" valign="middle" >7 (10.77)</td><td align="center" valign="middle" >10 (7.41)</td></tr><tr><td align="center" valign="middle" >Not in labour</td><td align="center" valign="middle" >18 (27.69)</td><td align="center" valign="middle" >49 (36.30)</td></tr><tr><td align="center" valign="middle" >Delivered</td><td align="center" valign="middle" >3 (4.62)</td><td align="center" valign="middle" >6 (4.44)</td></tr></tbody></table></table-wrap><p>common in nontribal group than tribal group (36.30% Vs 27.69%). Few mothers were admitted after delivery and the recorded intensities showed insignificant (p &gt; 0.05) difference between the selected two groups (<xref ref-type="table" rid="table1">Table 1</xref>0 and <xref ref-type="fig" rid="fig9">Figure 9</xref>).</p><p>Comparative analysis of different modes of delivery in tribal (n = 62) and nontribal (n = 129) mothers (admitted in ante partum and intra partum period) revealed that vaginal delivery (VD), both Normal VD and Assisted VD were significantly (p &lt; 0.05) more common in tribal group than nontribal group where as LSCS (Lower uterine Segment Caesarean Section) was significantly (p &lt; 0.05) more common in nontribal group than the tribal group.</p><p>Relatively few mothers presented in postpartum period and comparative analysis of modes of delivery in those mothers showed that LSCS was significantly more common (p &lt; 0.01) in nontribal mothers (66.66%) than tribal mothers (33.33%).</p><p>Majority of the mothers in both groups survived. Comparative analysis revealed that maternal mortality was significantly more common (p &lt; 0.05) in the</p><table-wrap-group id="11"><label><xref ref-type="table" rid="table1">Table 1</xref>1</label><caption><title> Comparison of mode of delivery in Antepartum and Intrapartum tribal and nontribal mothers</title></caption><table-wrap id="11_1"><caption><title> differ from each other significantly (p  0.05)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Mode of Delivery</th><th align="center" valign="middle" >Tribal (n = 62)</th><th align="center" valign="middle" >Nontribal (n = 129)</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >%</td></tr><tr><td align="center" valign="middle" >Normal VD</td><td align="center" valign="middle" >30.65 &#177; 1.81<sup>a</sup></td><td align="center" valign="middle" >20.93 &#177; 2.10<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Assisted VD</td><td align="center" valign="middle" >6.45 &#177; 1.06<sup>a</sup></td><td align="center" valign="middle" >3.10 &#177; 1.02<sup>b</sup></td></tr><tr><td align="center" valign="middle" >LSCS</td><td align="center" valign="middle" >62.90 &#177; 1.98<sup>a</sup></td><td align="center" valign="middle" >75.97 &#177; 2.48<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Undelivered</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td></tr></tbody></table></table-wrap></table-wrap-group><table-wrap id="table12" ><label><xref ref-type="table" rid="table1">Table 1</xref>2</label><caption><title> Mode of delivery in tribal and nontribal mothers admitted after delivery</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Mode of Delivery</th><th align="center" valign="middle" >Tribal (n = 3)</th><th align="center" valign="middle" >Nontribal (n = 6)</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >%</td></tr><tr><td align="center" valign="middle" >Normal VD</td><td align="center" valign="middle" >33.33 &#177; 2.19<sup>a</sup></td><td align="center" valign="middle" >33.33 &#177; 2.31<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Assisted VD</td><td align="center" valign="middle" >0 &#177; 0.00<sup>a</sup></td><td align="center" valign="middle" >33.33 &#177; 2.30<sup>b</sup></td></tr><tr><td align="center" valign="middle" >LSCS</td><td align="center" valign="middle" >66.66 &#177; 2.44<sup>a</sup></td><td align="center" valign="middle" >33.33 &#177; 2.31<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Undelivered</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td></tr></tbody></table></table-wrap><p>(Data were expressed as Mean &#177; SEM in percentage value. Comparative analysis performed by Student two tail t-test for means. Values of each row with different superscripts (a, b) differ from each other significantly (p &lt; 0.01)).</p><table-wrap id="table13" ><label><xref ref-type="table" rid="table1">Table 1</xref>3</label><caption><title> Maternal outcome in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Maternal Outcome</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Mortality</td><td align="center" valign="middle" >7 (10.77)</td><td align="center" valign="middle" >8 (5.92)</td></tr><tr><td align="center" valign="middle" >Survived</td><td align="center" valign="middle" >58 (89.23)</td><td align="center" valign="middle" >127 (94.07)</td></tr></tbody></table></table-wrap><table-wrap id="table14" ><label><xref ref-type="table" rid="table1">Table 1</xref>4</label><caption><title> Different complications suffered by tribal and nontribal mothers</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Maternal complication</th><th align="center" valign="middle" >Tribal</th><th align="center" valign="middle" >Nontribal</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >%</td></tr><tr><td align="center" valign="middle" >Pulmonary embolism</td><td align="center" valign="middle" >1.54 &#177; 0.19<sup>a</sup></td><td align="center" valign="middle" >2.96 &#177; 0.24<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Pulmonary Edema</td><td align="center" valign="middle" >1.54 &#177; 0.18<sup>a</sup></td><td align="center" valign="middle" >1.48 &#177; 0.33<sup>a</sup></td></tr><tr><td align="center" valign="middle" >CVA</td><td align="center" valign="middle" >6.15 &#177; 0.59<sup>a</sup></td><td align="center" valign="middle" >0.74 &#177; 0.16<sup>b</sup></td></tr><tr><td align="center" valign="middle" >RF</td><td align="center" valign="middle" >1.54 &#177; 0.17<sup>a</sup></td><td align="center" valign="middle" >0.74 &#177; 0.14<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Cerebral edema</td><td align="center" valign="middle" >1.54 &#177; 0.18<sup>a</sup></td><td align="center" valign="middle" >0.74 &#177; 0.13<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Hypovolemic shock</td><td align="center" valign="middle" >0 &#177; 0.00<sup>a</sup></td><td align="center" valign="middle" >0.74 &#177; 0.13<sup>b</sup></td></tr><tr><td align="center" valign="middle" >HELLP syndrome</td><td align="center" valign="middle" >1.54 &#177; 0.19<sup>a</sup></td><td align="center" valign="middle" >0 &#177; 0.00<sup>b</sup></td></tr></tbody></table></table-wrap><p>(Each row represents Mean &#177; SEM in percentage value. Values with same superscript (a) does not differ from each other significantly (p &gt; 0.05). Values of each row with different superscripts (a, b) differ from each other significantly (p &lt; 0.05)).</p><p>tribal group (10.77%) than the nontribal group (5.92%) (Tables 11-14 and <xref ref-type="fig" rid="fig1">Figure 1</xref>0).</p><p>Frequencies of pregnant mothers of both T and NT group suffered from different complications were compared statistically. Overall rate of serious complications was low. Final outcome showed that there was significant (p &lt; 0.05) difference in between these two groups for all the parameters except for ‘Pulmonary edema’ parameters (p &gt; 0.05). Tribal mothers suffered more commonly from cerebrovascular accidents (CVA) than nontribals who suffered more commonly from pulmonary embolism.</p><p>Comparative analysis revealed significant (p &lt; 0.01) difference between these groups. Tribal mothers needed admission to ICU significantly (p &lt; 0.01) more commonly (12.31%) than nontribal mothers (5.92%).</p><table-wrap id="table15" ><label><xref ref-type="table" rid="table1">Table 1</xref>5</label><caption><title> Need of ICU admission by tribal and nontribal mothers</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Needed ICU</td><td align="center" valign="middle" >8 (12.31%)</td><td align="center" valign="middle" >8 (5.92%)</td></tr></tbody></table></table-wrap><table-wrap id="table16" ><label><xref ref-type="table" rid="table1">Table 1</xref>6</label><caption><title> Hospital stay by survived mothers in Tribal and Nontribal group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Duration of hospital stay</th><th align="center" valign="middle" >T (n = 58) No. (%)</th><th align="center" valign="middle" >NT (n = 127) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >≤7 days</td><td align="center" valign="middle" >53 (91.38)</td><td align="center" valign="middle" >118 (92.9)</td></tr><tr><td align="center" valign="middle" >&gt;7 days</td><td align="center" valign="middle" >5 (8.62)</td><td align="center" valign="middle" >9 (7.09)</td></tr></tbody></table></table-wrap><table-wrap id="table17" ><label><xref ref-type="table" rid="table1">Table 1</xref>7</label><caption><title> Foetal outcome in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Foetal outcome</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Live birth</td><td align="center" valign="middle" >63 (96.92)</td><td align="center" valign="middle" >129 (95.60)</td></tr><tr><td align="center" valign="middle" >Stillbirth</td><td align="center" valign="middle" >2 (3.08)</td><td align="center" valign="middle" >6 (4.40)</td></tr></tbody></table></table-wrap><table-wrap id="table18" ><label><xref ref-type="table" rid="table1">Table 1</xref>8</label><caption><title> Birth asphyxia in newborn babies delivered in MMCH in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >T (n = 63) No. (%)</th><th align="center" valign="middle" >NT (n = 129) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >Asphyxiated new born baby</td><td align="center" valign="middle" >5 (7.90)</td><td align="center" valign="middle" >17 (13.18)</td></tr></tbody></table></table-wrap><p>Hospital stay for ≤ 7 days by survived tribal and nontribal mothers represented a higher frequency and their comparative analysis showed insignificant (p &gt; 0.05) difference in between them. Alongside comparative analysis in between frequencies of mothers with hospital stay for &gt;7 days duration also revealed insignificant (p &gt; 0.05) difference in between these two groups (Tables 15-18 and Figures 11-13).</p><p>Tribal and nontribal both the groups exhibited higher frequency of live births (96.92% and 95.60% respectively) in comparison to still birth babies with insignificant (p &gt; 0.05) difference in between these two study groups.</p><p>Comparative analysis showed a significant (p &lt; 0.001) higher percentage of asphyxiated foetal outcomes in nontribal study group (13.18%) than in tribal group (7.90%).</p><p>Neonatal death was rare. Need for admission to NICU was almost similar (insignificant, p &gt; 0.05) in the two groups, but there was a significant (p &lt; 0.05) higher percentage of preterm babies in nontribal group (17.04%) than tribal group (12.31%).</p><p>Significantly (p &lt; 0.001) greater percentage of new borns of tribal group (60%) were low birth weight (&lt;2.5 Kg) in comparison to new borns of the nontribal group (45.93%) (Tables 19-20 and Figures 14-15).</p><table-wrap-group id="19"><label><xref ref-type="table" rid="table1">Table 1</xref>9</label><caption><title> Foetal outcome: neonatal death, NICU admission and preterm birth in Tribal and Nontribal group</title></caption><table-wrap id="19_1"><caption><title> differ from each other significantly (p  0.05)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Complications of foetus</th><th align="center" valign="middle" >T (n = 65)</th><th align="center" valign="middle" >NT (n = 135)</th></tr></thead><tr><td align="center" valign="middle" >Neonatal Death</td><td align="center" valign="middle" >1.54 &#177; 0.68<sup>a</sup></td><td align="center" valign="middle" >0 &#177; 0.00<sup>b</sup></td></tr><tr><td align="center" valign="middle" >Needed NICU</td><td align="center" valign="middle" >23.08 &#177; 1.48<sup>a</sup></td><td align="center" valign="middle" >22.96 &#177; 1.89<sup>a</sup></td></tr><tr><td align="center" valign="middle" >Preterm</td><td align="center" valign="middle" >12.31 &#177; 1.86<sup>a</sup></td><td align="center" valign="middle" >17.04 &#177; 1.79<sup>b</sup></td></tr></tbody></table></table-wrap></table-wrap-group><table-wrap id="table20" ><label><xref ref-type="table" rid="table2">Table 2</xref>0</label><caption><title> Birth weight in Tribal and Nontribal groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Birth weight (kgs)</th><th align="center" valign="middle" >T (n = 65) No. (%)</th><th align="center" valign="middle" >NT (n = 135) No. (%)</th></tr></thead><tr><td align="center" valign="middle" >&lt;2.5 ≥2.5</td><td align="center" valign="middle" >39 (60) 26 (40)</td><td align="center" valign="middle" >62 (45.93) 73 (54.07)</td></tr></tbody></table></table-wrap></sec></sec><sec id="s4"><title>4. Discussion</title><p>In the presented study, there were 65 mothers in Tribal (T) group and 135 mothers in Nontribal (NT) group. Of them 133 mothers had severe preeclampsia and 67 mothers had eclampsia. Total number of deliveries conducted in this hospital was 3768 during the study period. Out of this tribal women were 576 and nontribal women were 3192. Thus, during the study period the overall incidence of severe preeclampsia and eclampsia in our institution were 3.53% and 1.78% respectively. The incidence of severe preeclampsia and eclampsia in tribal women were 7.29% and 3.99% respectively, and in nontribal women were 2.85% and 1.38% respectively. The incidence was found to be significantly (p &lt; 0.001) higher in T group than NT group. Other studies which have examined the association of maternal ethnicity and severe preeclampsia and eclampsia also found some ethnic groups at higher risk than other ethnic or racial groups. Myles Wolf et al. found Hispanic ethnicity to be independently associated with increased risk for preeclampsia and decreased risk for gestational hypertension [<xref ref-type="bibr" rid="scirp.111268-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref56">56</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref59">59</xref>]. Bryant AS et al. found Black women with hypertension in pregnancy in the absence of chronic hypertension more likely to be diagnosed with preeclampsia than were White women [<xref ref-type="bibr" rid="scirp.111268-ref50">50</xref>].</p><p>Advanced maternal age has been found to be an independent risk factor for preeclampsia, while in this study most of the mothers of both T and NT group were under 25 years of age, which is probably because we were dealing with women from rural area, where early marriage is more common. The incidence of severe preeclampsia and eclampsia was significantly (p &lt; 0.05) higher in tribal women of 20 yrs and below than NT group, whereas in 21 to 25 yrs of age group nontribal women were found to be more affected than tribal women. Myles Wolf et al. found that Hispanic women were younger than non-Hispanic and Caucasian groups [<xref ref-type="bibr" rid="scirp.111268-ref59">59</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref60">60</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref61">61</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref62">62</xref>]. Goodwin AA et al. reported that Caucasian women were older (27 vs. 24 yrs) than African American women [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>].</p><p>In our study, severe preeclampsia and eclampsia were more common in nulliparous and primiparous women of both groups but the incidence was significantly (p &lt; 0.05) higher in nulliparous tribal women (86.15%) than nontribals (80%), whereas primiparous mothers were significantly more common in nontribal group (16.30%) than tribal group (10.77%). Goodwin AA et al. found Caucasian women more likely nulliparous than African American and Hispanic women [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>]. Depending on ethnicity, the incidence of preeclampsia ranges from 3% to 7% in healthy nulliparas [<xref ref-type="bibr" rid="scirp.111268-ref36">36</xref>]. Gaurav Ghosh et al. reported that nulliparous Hispanic women and Asian/Pacific Islanders had an overall decreased risk compared to non-Hispanic whites [<xref ref-type="bibr" rid="scirp.111268-ref52">52</xref>]. A. K. Rao et al. found that among primiparous women, there is a disparity among ethnic groups as the risk in African American women is twice that of Caucasian women, and the risk is also very high in women of Indian and Pakistani origin [<xref ref-type="bibr" rid="scirp.111268-ref63">63</xref>] - [<xref ref-type="bibr" rid="scirp.111268-ref73">73</xref>].</p><p>In the presented study, T group demonstrated more severe hypertension than NT group. Goodwin AA et al. found that African Americans had more severe hypertension where as Hispanic women had less severe hypertension [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>].</p><p>In our study, Mothers in both groups responded well to treatment but control of blood pressure to the desired level required ≥1 hour of anti-hypertensive therapy (and thus larger doses) in significantly (&lt;0.01) more number of tribal mothers (43.14%) than nontribal mothers (32.65%). Tribal mothers were found to be less responsive to treatment than nontribal mothers, whereas nontribal mothers responded earlier and to a smaller dose of anti-hypertensive drug than tribal mothers, and thus needed a smaller dose of anti-hypertensive drug than tribal mothers. This finding is in agreement with what Goodwin AA et al. found among African American women as they needed more antihypertensive treatment intrapartum, postpartum and at discharge (p &lt; 0.03) than Hispanic women [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>].</p><p>No significant (p &gt; 0.05) difference in recurrence of convulsion after anticonvulsant treatment was found between the two groups. Goodwin AA et al. found no difference in severe proteinuria among Caucasian, African American and Hispanic women [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>] whereas in our study, proteinuria was significantly more common in T group, but severe proteinuria (≥3+), though uncommon in both groups, was more common in nontribals.</p><p>T group presented with poorer GCS score on admission than NT group. Nontribal women experienced more number of convulsions than T group.</p><p>Regarding the obstetrical condition on admission, most of the tribal and nontribal women had gone into labour, but it was found significantly more commonly in T group, while antepartum (not in labour) mothers were significantly (p &lt; 0.05) more common in nontribal group than tribal group (36.30% Vs 27.69%). In our study, tribal women found in stage I of labour were 56.9% and in stage II were 10.77%, which was significantly (p &lt; 0.05) higher than 51.85% and 7.4% respectively of nontribal women.</p><p>In our study, 30.65% of tribal women were delivered vaginally and 6.45% were delivered by assisted vaginal delivery (forceps delivery), which were significantly higher than nontribal women, 20.93% and 3.10% respectively. 75.97% of nontribal women were delivered by lower segment caesarean section (LSCS) than 62.9% tribal women. Myles Wolf et al. found that Hispanic women were less likely to deliver by Caesarean section than non-Hispanic Caucasian groups.</p><p>There were no cases of undelivered in our study. There was no significant difference found between T and NT group regarding modes of delivery in postpartum mothers.</p><p>In our study, regarding the maternal outcome, maternal mortality was significantly more common (p &lt; 0.05) in the tribal group (10.77%) than the nontribal group (5.92%). Maternal mortality was reported to be high among various tribal groups due to hypertensive disorders of pregnancy [<xref ref-type="bibr" rid="scirp.111268-ref74">74</xref>]. Black women with preeclampsia-eclampsia are more likely to die from these conditions than White women [<xref ref-type="bibr" rid="scirp.111268-ref75">75</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref76">76</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref77">77</xref>] [<xref ref-type="bibr" rid="scirp.111268-ref78">78</xref>].</p><p>The T group, in our study, found to be at higher risk of getting complicated with cerebrovascular accidents when they develop severe preeclampsia or eclampsia than NT group, whereas pulmonary embolism was found to be more common in nontribal women. Aparna Khan et al. found cerebral haemorrhage (40%) as the most common cause of death in their study. In Africa, 45.5% of hypertensive maternal death was due to cerebral complications. Goodwin AA et al. found that Caucasian women have more frequent HELLP syndrome [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>]. Tribal mothers needed admission to ICU significantly (p &lt; 0.01) more commonly (12.31%) than nontribal mothers (5.92%). There was no significant difference found between T and NT group for duration of hospital stay.</p><p>Regarding the foetal outcome in T and NT group, in our study, the incidence of live births and stillbirths were similar in both groups. The new born babies of nontribal mothers suffered significantly more commonly from birth asphyxia than new borns of T group (17% vs 5%). In two studies by Goodwin AA et al. [<xref ref-type="bibr" rid="scirp.111268-ref51">51</xref>] and Myles Wolf et al. [<xref ref-type="bibr" rid="scirp.111268-ref59">59</xref>], no difference in foetal death rates was found among different ethnic groups. There was one neonatal death recorded in T group in our study. The incidence of preterm births was found to be more in NT group than T group.</p><p>Our study is consistent with the other studies in respect of LBW babies. In our study, we found the incidence of LBW babies significantly (p &lt; 0.001) higher in T group (60%) than NT group (45.9%). Fang J et al. found that the population attributable risk of LBW in hypertensive mothers was highest among blacks and lowest among whites. They concluded that maternal hypertension is an important risk factor for LBW in New York City. Its impact, however, differed by race/ethnicity groups [<xref ref-type="bibr" rid="scirp.111268-ref72">72</xref>]. Odell CD et al. reported that differences in maternal risk factors and rates of LBW exist between Haitian and African-American women delivering infants in Massachusetts. While chronic hypertension and preeclampsia are strong risk factors for LBW for both Haitian and African-American women, “unknown factors” make these disorders much more potent for Haitian women [<xref ref-type="bibr" rid="scirp.111268-ref27">27</xref>]. Those unknown factors may be related to their race or ethnicity and this observation corroborates with our finding of higher incidence of LBW in ethnic tribals than nontribals.</p><p>In our study the admission to NICU was required in a small number of babies and the need for admission to NICU was found to be almost similar in both groups. This may be due to higher rate of delivery of asphyxiated infant and preterm babies in NT group which compensated the higher rate of SGA babies in T group.</p></sec><sec id="s5"><title>5. Conclusions</title><p>Hypertensive disorders of pregnancy remain an important maternal health problem in India. By this comparative study, we came to a conclusion that the tribal women are at higher risk of developing severe preeclampsia and eclampsia than nontribal women.</p><p>It is well established that extremes of age and nulliparity are strong risk factors for preeclampsia-eclampsia but these factors make the tribal ethnicity more prone to the disease.</p><p>Tribal women develop more severe hypertension and are less responsive to antihypertensive treatment than nontribal women.</p><p>Rate of caesarean section is high in both tribal and non tribal women with severe preeclampsia-eclampsia but comparatively higher among nontribal women.</p><p>The mortality and need of ICU care are more in tribal mothers than nontribal mothers when they develop severe preeclampsia-eclampsia.</p><p>Low birth weight neonates are more common in tribal women than nontribals whereas birth asphyxia and preterm births are more common in nontribal women.</p><p>These significant differences among the two groups suggest a strong role for ethnicity in the risk and pathogenesis of preeclampsia-eclampsia and it warrants further studies to understand it more clearly.</p><p>More awareness among both the tribal and non tribal group and routine antenatal checkup might improve the feto-maternal outcome in these groups of individuals (Q.7).</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Banerjee, I., Kumari, A. and Mukherjee, G. 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