<?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">OJPed</journal-id><journal-title-group><journal-title>Open Journal of Pediatrics</journal-title></journal-title-group><issn pub-type="epub">2160-8741</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojped.2018.82021</article-id><article-id pub-id-type="publisher-id">OJPed-85426</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>
 
 
  Prevalence of Hypoglycaemia in Newborn at Benue State University Teaching Hospital, Makurdi, Benue State, Nigeria
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Martha</surname><given-names>Omoo Ochoga</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>Michael</surname><given-names>Aondoaseer</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rose</surname><given-names>Okwunu Abah</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Onyilo</surname><given-names>Ogbu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Emeka</surname><given-names>Uba Ejeliogu</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>Geoffrey</surname><given-names>Ingyoroko Tolough</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Department of Epidemiology and Community Health, College of Health Sciences, Benue State University, Makurdi, Nigeria</addr-line></aff><aff id="aff1"><addr-line>Department of Paediatrics, Benue State University Teaching Hospital, Makurdi, Nigeria</addr-line></aff><aff id="aff2"><addr-line>Department of Pediatrics, University of Jos, Nigeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ochogamartha@gmail.com(MOO)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>17</day><month>04</month><year>2018</year></pub-date><volume>08</volume><issue>02</issue><fpage>189</fpage><lpage>198</lpage><history><date date-type="received"><day>14,</day>	<month>May</month>	<year>2018</year></date><date date-type="rev-recd"><day>18,</day>	<month>June</month>	<year>2018</year>	</date><date date-type="accepted"><day>21,</day>	<month>June</month>	<year>2018</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>
 
 
  Background:
   
  Neonatal hypoglycaemia is the most common metabolic abnormality in neonates and is associated with neurological damage and death when it occurs during the first few days of life.
   
  The main objective of this study was to determine the prevalence of hypoglycaemia in the newborn and the associated maternal/neonatal risk factors.
   
  <b>Setting and Methods:</b>
   
  This prospective descriptive study was conducted at the labour room and the Special Care Baby Unit of Benue State University Teaching Hospital, Makurdi, Benue State, Nigeria
  ,
   between July 2017-March 2018.
   
  <b>Results:</b>
   Of the 168 neonates, 140 (83.3%) were delivered in the hospital and 28 (16.7%) were delivered outside the hospital.
   
  Hypoglycaemia was found in 19 (11.0%) of the neonates. The mean (standard deviation) of gestational age was 37.8 (3.0) weeks. 91 (54.2%) were males and 77 (45.8%) were females
  .
   Male to female ratio is 1.2:1. A significantly higher proportion of 9 (32.1%) out born compared with 10 (7.1%) of inborn, 4 (44.4%) of birth &lt;
   
  1500
   
  g compared with 5 (22.7%) birth weight 1500
   
  g
   
  -
   
  2499
   
  g and 10 (7.3%) of birth weight 
  ≥
   2500 g 
  and 7 (22.6%) of babies with temperature 
  ≤
   
  36.5&#176;
  C
   compared with 7 (6.3%) of temperature 36.5&#176;
  C
   
  -
   
  37.5&#176;
  C
   and 5 (19.2%) of temperature 
  &gt; 
  37.5&#176;
  C
  , demonstrated hypoglycaemia respectively. Neonatal risk factors
  ,
   
  such as, 
  prematurity, low birth weight and respiratory distress syndrome
  ,
   were significantly associated with hypoglycaemia p-value of 0.02, 0.01 and 0.00 respectively.
   
  There were no statistically significant associations between maternal risk factors and hypoglycaemia. The common presenting symptoms were jitteriness
  ,
 
</p></abstract><kwd-group><kwd>Neonatal Hypoglycaemia</kwd><kwd> Prevalence</kwd><kwd> Risk Factors</kwd><kwd> Clinical Manifestations</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Neonatal hypoglycaemia is important because it is the most common metabolic abnormality in neonates and is associated with neurological damage and death when it occurs during the first few days of life [<xref ref-type="bibr" rid="scirp.85426-ref1">1</xref>] . It is defined either as whole blood glucose of less than 2.2 mmol/L or plasma glucose of less than or equal to 2.5 mmol/L [<xref ref-type="bibr" rid="scirp.85426-ref2">2</xref>] . Neonatal hypoglycaemia affects 5% to 15% of otherwise healthy babies [<xref ref-type="bibr" rid="scirp.85426-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref3">3</xref>] and is widespread in resource poor countries [<xref ref-type="bibr" rid="scirp.85426-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] . About 8% of large for gestational age infants and 15% of preterm infants and infants who have intrauterine growth retardation (IUGR) have been reported as having hypoglycaemia. The incidence in the entire population of high risk infants may be as high as 30% [<xref ref-type="bibr" rid="scirp.85426-ref6">6</xref>] . Prevalence of hypoglycaemia is increasing because of the increasing incidence of preterm birth [<xref ref-type="bibr" rid="scirp.85426-ref7">7</xref>] and maternal factors, such as diabetes [<xref ref-type="bibr" rid="scirp.85426-ref8">8</xref>] and obesity [<xref ref-type="bibr" rid="scirp.85426-ref9">9</xref>] , which can predispose babies to hypoglycaemia.</p><p>The symptomatic response of the neonate to low blood glucose is variable with non-specific clinical features including pallor, feeding difficulties, tachypnea, hypotonia, abnormal cry, jitteriness, apnea, coma and convulsions. Moderate asymptomatic hypoglycaemia should first be treated by adjusting the enteral feeding regimen. If this approach fails, intravenous therapy should be instituted when facilities are available. Studies have been done on neonatal hypoglycaemia in other parts of Nigeria [<xref ref-type="bibr" rid="scirp.85426-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] , but there has been no previous documentation on the prevalence of neonatal hypoglycaemia at Benue State University Teaching Hospital, Makurdi, Benue State. The present study was therefore undertaken to determine the prevalence of hypoglycaemia in the newborn, and the associated maternal/neonatal risk factors.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This prospective descriptive study was conducted at the labour room and the Special Care Baby Unit (SCBU) of the Benue State University Teaching Hospital (BSUTH), Makurdi, Benue State over a nine month period. All consecutive neonates delivered in the labour room and admitted into the SCBU within the first 24 hours of life were recruited into the study. The babies whose parents refused to give consent and those who have had intravenous infusion of fluid(s) were excluded from the study. A minimum sample size of 150.4 was arrived at using the formula [n = z<sup>2</sup>p (1 − p)/d<sup>2</sup>] [<xref ref-type="bibr" rid="scirp.85426-ref10">10</xref>] , based on the assumption of neonatal hypoglycaemia rate of 11.0% from a previous study [<xref ref-type="bibr" rid="scirp.85426-ref11">11</xref>] , and 5% degree of precision at 95% confidence interval. Considering attrition rate of 10%, the calculated sample size was adjusted to 168. Blood glucose was estimated on all the babies delivered in the labour room and those admitted into the SCBU after obtaining informed consent from the mother. Ethical clearance was obtained from the Ethical and Research Committee of the hospital. A research proforma was administered to every recruited patient. Neonates age, sex, place of birth, gestational age assessed according to the new Ballard scoring system, birth weight, temperature, maternal and neonatal risk factors for hypoglycaemia and the clinical manifestations of hypoglycaemia were recorded.</p><p>Random blood sugar level on each patient was estimated at birth or on admission, using standard laboratory methods. The first post natal glucose testing was performed within the first 24 hours of life. The blood glucose level of &lt;2.2 mmol/l was considered hypoglycaemic. Testing of neonatal glucose was performed using Accu-Check Active 07124112 glucometer. The glucometer strips were inserted into the meter and when the meter started blinking. Blood was applied to the test area on the strip. All babies with hypoglycaemic convulsions, were given a bolus of 4 ml/kg of 10% dextrose water, followed by continious glucose infusion of 4 to 6 mg/kg/min for full term infants and 6 to 8 mg/kg/min for premature infants. Other symptomatic infants were given intravenous 10% dextrose water 2 ml/kg bolus followed by the continious infusion of 10% dextrose water until the patient fully recovered. Data was analyzed using Statistical Package for the Social Sciences (SPSS) version 20. Descriptive statistics were generated for each study variable including frequencies and percentages for categorical variables, mean and standard deviation for continuous variables. Chi-square was used to test association between categories of the dimensions and socio-demographic, maternal risk factors, neonatal risk factors and signs of hypoglycaemia. Level of statistical significance was set at 5%.</p></sec><sec id="s3"><title>3. Results</title><p>Of the 168 neonates, 140 (83.3%) were delivered in the hospital and 28 (16.7%) were delivered outside the hospital. Hypoglycaemia was found in 19 (11.0%) of the neonates at the time of admission (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The mean (standard deviation) of gestational age was 37.8 (3.0) weeks with a proportion of 131 (78.0%) having greater or equal to thirty-seven weeks, 25 (14.9%) had gestational age thirty- three to thirty-six weeks, while 12 (7.1%) had less than or equal to thirty-two weeks. Of the 168 babies, 91 (54.2%) were males and 77 (45.8%) were females. Male to female ratio is 1.2:1. The median birth weight was 3200 g with a higher proportion of 137 (81.5%) who had birth weight ≥ 2500 g. The mean (SD) of temperature was 36.8˚C (1.01) with a higher proportion of 111 (66.1%) having normal temperature (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>As shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>, the prevalence of hypoglycaemia among neonates was 11%.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Baseline characteristics of babies with and without hypoglycaemia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristics</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percent</th></tr></thead><tr><td align="center" valign="middle" >Receiving status Inborn Outborn</td><td align="center" valign="middle" >140 28</td><td align="center" valign="middle" >83.3 16.7</td></tr><tr><td align="center" valign="middle" >Gestational age (in weeks) ≤32 33 - 36 ≥37 Mean 37.83 &#177; 2.98</td><td align="center" valign="middle" >12 25 131</td><td align="center" valign="middle" >7.1 14.9 78.0</td></tr><tr><td align="center" valign="middle" >Sex Male Female</td><td align="center" valign="middle" >91 77</td><td align="center" valign="middle" >54.2 45.8</td></tr><tr><td align="center" valign="middle" >Birth weight (in grams) &lt;1500 1500 - 2499 ≥2500 Median 3200</td><td align="center" valign="middle" >9 22 137</td><td align="center" valign="middle" >5.4 13.1 81.5</td></tr><tr><td align="center" valign="middle" >Temperature (˚C) ≤36.5 36.5 - 37.5 &gt;37.5 Mean 36.8 &#177; 1.01</td><td align="center" valign="middle" >31 111 26</td><td align="center" valign="middle" >18.5 66.0 15.5</td></tr></tbody></table></table-wrap><p>As shown in <xref ref-type="table" rid="table2">Table 2</xref>, a higher proportion of the out born newborns compared with the inborn newborns experienced hypoglycaemia and this was statistically significant (p = 0.000). There was no significant association between gestational age and hypoglycaemia. Hypoglycaemia was more among very low birth weight babies (44.4%) compared to the other birth weight groups and this was statistically significant (p = 0.002). Hypoglycaemia was recorded among newborns with temperature ≤ 36.5 and when compared to the other temperature group was statistically significant (p = 0.010).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Association of baseline characteristics and hypoglycaemia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle"  colspan="2"  ></th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th></tr></thead><tr><td align="center" valign="middle" >Variables</td><td align="center" valign="middle" >Babies with Hypoglycaemia (%)</td><td align="center" valign="middle" >Babies without Hypoglycaemia (%)</td><td align="center" valign="middle" >Test statistics</td><td align="center" valign="middle" >df</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle" >Receiving status Inborn Outborn</td><td align="center" valign="middle" >10 (7.1) 9 (32.1)</td><td align="center" valign="middle" >130 (92.9) 19 (67.9)</td><td align="center" valign="middle" >Continuity correction = 12.15</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Gestational age (in weeks) ≤32 33 - 36 ≥37</td><td align="center" valign="middle" >4 (33.3) 2 (8.0) 13 (9.9)</td><td align="center" valign="middle" >8 (66.7) 23 (92.0) 118 (90.1)</td><td align="center" valign="middle" >Fisher’s exact = 5.15</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.071</td></tr><tr><td align="center" valign="middle" >Sex Male Female</td><td align="center" valign="middle" >11 (12.1) 8 (10.4)</td><td align="center" valign="middle" >80 (87.9) 69 (89.6)</td><td align="center" valign="middle" >χ<sup>2</sup> = 0.12</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.729</td></tr><tr><td align="center" valign="middle" >Birth weight (in grams) &lt;1500 1500 - 2499 ≥2500</td><td align="center" valign="middle" >4 (44.4) 5 (22.7) 10 (7.3)</td><td align="center" valign="middle" >5 (55.6) 17 (77.3) 127 (92.7)</td><td align="center" valign="middle" >Fisher’s exact = 12.20</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.002</td></tr><tr><td align="center" valign="middle" >Temperature ≤36.5 36.5 - 37.5 &gt;37.5</td><td align="center" valign="middle" >7 (22.6) 7 (6.3) 5 (19.2)</td><td align="center" valign="middle" >24 (77.4) 104 (93.7) 21 (80.8)</td><td align="center" valign="middle" >Fisher’s exact = 8.31</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.010</td></tr></tbody></table></table-wrap><p><xref ref-type="table" rid="table3">Table 3</xref> shows that prematurity, low birth weight, small for gestational age, large for gestational age, jaundice, severe birth asphyxia, moderate birth asphyxia, respiratory distress, congenital heart disease and inadequate feeding were risk factors for hypoglycaemia in neonates. Hypoglycaemia was significantly more frequent among neonates with prematurity and respiratory distress and this was statistically significant with p &lt; 0.05.</p><p><xref ref-type="table" rid="table4">Table 4</xref> presents the association between maternal risk factors and hypoglycaemia. Maternal risk factors hypertension, diabetes, intrapartum administration of glucose and the use of beta blockers had no significant association with the development of hypoglycaemia amongst the neonates.</p><p><xref ref-type="table" rid="table5">Table 5</xref> shows the distribution of the clinical manifestations of hypoglycaemia among the newborns with and without hypoglycaemia. Hypoglycaemia was significantly associated with tachypnoea and seizure. Cyanosis, tachypnoea, apnoea, temperature instability, seizures and lethargy were identified in hypoglycaemic as well as non-hypoglycaemic newborns.</p></sec><sec id="s4"><title>4. Discussion</title><p>The prevalence of neonatal hypoglycaemia in the present study was 11.0 percent, much lower than the 28.3 percent reported from Port Harcourt by Frank-Briggs [<xref ref-type="bibr" rid="scirp.85426-ref4">4</xref>] and 32.7 percent by Dedeke et al. [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] . This is comparable to 9.5 percent reported by Njokanma and Fagbule [<xref ref-type="bibr" rid="scirp.85426-ref12">12</xref>] and 6.6 percent by Omene in Benin [<xref ref-type="bibr" rid="scirp.85426-ref13">13</xref>] . Our study showed that more males were affected than females and consistent with other studies [<xref ref-type="bibr" rid="scirp.85426-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref15">15</xref>] . However, being a male is not a risk factor for hypoglycaemia. In the present study, neonates with birth weight ≥ 2500 g at birth</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Association of neonatal risk factors and hypoglycaemia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Risk Factors</th><th align="center" valign="middle" >Babies with Hypoglycaemia N (%)</th><th align="center" valign="middle" >Babies without Hypoglycaemia N%)</th><th align="center" valign="middle" >Total N (%)</th><th align="center" valign="middle" >Test statistics</th><th align="center" valign="middle" >df</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >Prematurity Yes No</td><td align="center" valign="middle" >7 (25.9) 12 (8.5)</td><td align="center" valign="middle" >20 (74.1) 129 (91.5)</td><td align="center" valign="middle" >27 (16.1) 141 (83.9)</td><td align="center" valign="middle" >Continuity correction = 5.23</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.022</td></tr><tr><td align="center" valign="middle" >Low Birth Weight Yes No</td><td align="center" valign="middle" >7 (26.9) 12 (8.5)</td><td align="center" valign="middle" >19 (73.1) 130 (91.5)</td><td align="center" valign="middle" >26 (15.5) 142 (84.5)</td><td align="center" valign="middle" >Continuity correction = 5.75</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.017</td></tr><tr><td align="center" valign="middle" >Small for Gestational Age Yes No</td><td align="center" valign="middle" >2 (28.6) 17 (10.6)</td><td align="center" valign="middle" >5 (71.4) 144 (89.4)</td><td align="center" valign="middle" >7 (4.2) 161 (95.8)</td><td align="center" valign="middle" >Continuity correction = 0.75</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.388</td></tr><tr><td align="center" valign="middle" >Large for Gestational Age Yes No</td><td align="center" valign="middle" >2 (20.0) 17 (10.8)</td><td align="center" valign="middle" >8 (80.0) 141 (89.2)</td><td align="center" valign="middle" >10 (6.0) 158 (94.0)</td><td align="center" valign="middle" >Continuity correction = 0.14</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.704</td></tr><tr><td align="center" valign="middle" >Jaundice Yes No</td><td align="center" valign="middle" >1 (25.0) 18 (11.0)</td><td align="center" valign="middle" >3 (75.0) 146 (89.0)</td><td align="center" valign="middle" >4 (2.4) 164 (97.6)</td><td align="center" valign="middle" >Continuity correction = 0.01</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.939</td></tr><tr><td align="center" valign="middle" >Severe Birth Asphyxia Yes No</td><td align="center" valign="middle" >1 (14.3) 18 (11.2)</td><td align="center" valign="middle" >6 (85.7) 143 (88.8)</td><td align="center" valign="middle" >7 (4.2) 161 (95.8)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Moderate Birth Asphyxia Yes No</td><td align="center" valign="middle" >1 (33.3) 18 (10.9)</td><td align="center" valign="middle" >2 (66.7) 147 (89.1)</td><td align="center" valign="middle" >3 (1.8) 165 (98.2)</td><td align="center" valign="middle" >Continuity correction = 0.09</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.768</td></tr><tr><td align="center" valign="middle" >Respiratory distress Yes No</td><td align="center" valign="middle" >7 (41.2) 12 (7.9)</td><td align="center" valign="middle" >10 (58.8) 139 (92.1)</td><td align="center" valign="middle" >17 (10.1) 151 (89.9)</td><td align="center" valign="middle" >Continuity correction = 13.67</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >NNS Yes No</td><td align="center" valign="middle" >3 (20.0) 16 (10.5)</td><td align="center" valign="middle" >12 (80.0) 137 (89.5)</td><td align="center" valign="middle" >15 (8.9) 153 (91.1)</td><td align="center" valign="middle" >Continuity correction = 0.47</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.492</td></tr><tr><td align="center" valign="middle" >Congential Heart Disease Yes No</td><td align="center" valign="middle" >0 (0.0) 19 (11.4)</td><td align="center" valign="middle" >1 (100.0) 148 (88.6)</td><td align="center" valign="middle" >1 (0.6) 167 (99.4)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Inadequate feeding Yes No</td><td align="center" valign="middle" >4 (26.7) 15 (9.8)</td><td align="center" valign="middle" >11 (73.3) 138 (90.2)</td><td align="center" valign="middle" >15 (8.9) 153 (91.1)</td><td align="center" valign="middle" >Continuity correction = 2.37</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.123</td></tr></tbody></table></table-wrap><p>Note: 54.8% are without risk factors.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Association of maternal risk factors and blood glucose</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Babies with Hypoglycaemia N (%)</th><th align="center" valign="middle" >Babies without Hypoglycaemia N (%)</th><th align="center" valign="middle" >Total N (%)</th><th align="center" valign="middle" >Test statistics</th><th align="center" valign="middle" >df</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >Maternal Hypertension Yes No</td><td align="center" valign="middle" >2 (18.2) 17 (10.8)</td><td align="center" valign="middle" >9 (81.8) 140 (89.2)</td><td align="center" valign="middle" >11 (6.5) 157 (93.5)</td><td align="center" valign="middle" >Continuity correction = 0.55</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.801</td></tr><tr><td align="center" valign="middle" >Maternal Diabetes Yes No</td><td align="center" valign="middle" >0 (0.0) 19 (11.4)</td><td align="center" valign="middle" >1 (100.0) 148 (88.6)</td><td align="center" valign="middle" >1 (0.6) 167 (99.4)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Intrapartum Administration of Glucose</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes No</td><td align="center" valign="middle" >2 (13.3) 17 (11.1)</td><td align="center" valign="middle" >13 (86.7) 136 (88.9)</td><td align="center" valign="middle" >15 (8.9) 153 (91.1)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Beta Blockers Yes No</td><td align="center" valign="middle" >0 (0.0) 19 (11.5)</td><td align="center" valign="middle" >3 (100.0) 146 (88.5)</td><td align="center" valign="middle" >3 (1.8) 165 (98.2)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.704</td></tr></tbody></table></table-wrap><p>Note: 82.7% are without risk factors.</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Comparism of Clinical manifestations of hypoglycaemia among babies with and without hypoglycaemia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Clinical Manifestation</th><th align="center" valign="middle" >Babies with Hypoglycaemia N (%)</th><th align="center" valign="middle" >Babies without Hypoglycaemia N (%)</th><th align="center" valign="middle" >Total N (%)</th><th align="center" valign="middle" >Test statistics</th><th align="center" valign="middle" >df</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >Jitteriness Yes No</td><td align="center" valign="middle" >0 (0.0) 19 (11.5)</td><td align="center" valign="middle" >3 (100.0) 146 (88.5)</td><td align="center" valign="middle" >3 (1.8) 165 (98.2)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Cyanosis Yes No</td><td align="center" valign="middle" >1 (25.0) 18 (11.0)</td><td align="center" valign="middle" >3 (75.0) 146 (89.0)</td><td align="center" valign="middle" >3 (2.4) 164 (97.6)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.939</td></tr><tr><td align="center" valign="middle" >Tachypnoea Yes No</td><td align="center" valign="middle" >3 (42.9) 16 (9.9)</td><td align="center" valign="middle" >4 (57.1) 145 (90.1)</td><td align="center" valign="middle" >7 (4.2) 161 (95.8)</td><td align="center" valign="middle" >Continuity correction = 4.34</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.037</td></tr><tr><td align="center" valign="middle" >Hypotonia Yes No</td><td align="center" valign="middle" >0 (0.0) 19 (11.4)</td><td align="center" valign="middle" >1 (100.0) 148 (88.6)</td><td align="center" valign="middle" >1 (0.6) 167 (99.4)</td><td align="center" valign="middle" >Continuity correction = 0.00</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.000</td></tr><tr><td align="center" valign="middle" >Apnoea Yes No</td><td align="center" valign="middle" >2 (40.0) 17 (10.4)</td><td align="center" valign="middle" >3 (60.0) 146 (89.6)</td><td align="center" valign="middle" >5 (3.0) 163 (97.0)</td><td align="center" valign="middle" >Continuity correction = 1.80</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.180</td></tr><tr><td align="center" valign="middle" >Temperature instability Yes No</td><td align="center" valign="middle" >4 (22.2) 15 (10.0)</td><td align="center" valign="middle" >14 (77.8) 135 (90.0)</td><td align="center" valign="middle" >18 (10.7) 150 (89.3)</td><td align="center" valign="middle" >Continuity correction = 1.33</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.249</td></tr><tr><td align="center" valign="middle" >Seizure Yes No</td><td align="center" valign="middle" >4 (100.0) 15 (9.1)</td><td align="center" valign="middle" >0 (0.0) 149 (90.9)</td><td align="center" valign="middle" >4 (2.4) 164 (97.6)</td><td align="center" valign="middle" >Continuity correction = 23.71</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Lethargy Yes No</td><td align="center" valign="middle" >2 (40.0) 17 (10.4)</td><td align="center" valign="middle" >3 (60.0) 146 (89.6)</td><td align="center" valign="middle" >5 (3.0) 163 (97.0)</td><td align="center" valign="middle" >Continuity correction = 1.80</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.180</td></tr></tbody></table></table-wrap><p>were more than the other birth weight groups and this may have accounted for the lower prevalence of hypoglycaemia. The highest prevalence of hypoglycaemia was 44.4 percent among babies with very low birth weight (VLBW) and this was followed by 33.3 percent in very preterm babies and was statistically significant with p = 0.002. Our findings are consistent with that reported by other workers [<xref ref-type="bibr" rid="scirp.85426-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref17">17</xref>] but higher than that reported by Pildes and Pyati [<xref ref-type="bibr" rid="scirp.85426-ref18">18</xref>] .</p><p>In this study hypoglycaemia was found in a higher proportion amongst the outborn babies as compared to the inborn babies. This finding is comparable to that reported by Dedeke, Njokanma and Fagbule [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref12">12</xref>] . This could be as a result of delay in presentation of the outborn babies to the hospital and as a result of the babies being subjected to cold injury during transfer. The ideal method of transporting the babies is by use of transport incubators or proper wrappings. The lower prevalence rate among the inborn could be as a result of a high index of suspicion and better high risk neonate identification and interventions. Futher more since the patients were managed in the hospital, intrapartum conditions were better handled and that may reduce fetal distress and other related conditions that may predispose the babies to hypoglycaemia.</p><p>The maternal risk factors identified in the present study were maternal hypertension and intrapartum administration of glucose but were not statistically significant. Omene [<xref ref-type="bibr" rid="scirp.85426-ref13">13</xref>] also did not report any significant association with toxaemic mothers. This contrasts with the occurrence of hypoglycaemia in over half of infants of toxaemic mothers in other series [<xref ref-type="bibr" rid="scirp.85426-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref20">20</xref>] . Toxaemia of pregnancy among West Africans commonly take the acute form compared to the more chronic pattern observed among Europeans [<xref ref-type="bibr" rid="scirp.85426-ref21">21</xref>] . Hypoglycaemia is a common finding among infants of diabetic mothers [<xref ref-type="bibr" rid="scirp.85426-ref22">22</xref>] . This was not reported in our study. Dedeke [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] and Omene [<xref ref-type="bibr" rid="scirp.85426-ref13">13</xref>] did not observe hypoglycaemia among infants of diabetic mothers. The probable reason could have been as a result of proper management of diabetes in pregnancy.</p><p>Preterm babies have low glycogen stores and as a result are more predisposed to hypoglycaemia [<xref ref-type="bibr" rid="scirp.85426-ref23">23</xref>] . In this study 25.9 perecent neonates with hypoglycaemia were preterms. Prematurity was a significant risk factor for hypoglycaemia and similar to what was reported by Ayoub [<xref ref-type="bibr" rid="scirp.85426-ref14">14</xref>] and Dedeke [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] . Hypothermia was detected in 22.6 percent of the neonates and was a significant risk factor for hypoglycaemia, probabaly due to increased glucose utilization. This is at variance to the findings of Ayoub [<xref ref-type="bibr" rid="scirp.85426-ref14">14</xref>] where they attributed their own results to the small number of sample taken during the study. Other conditions found in the hypoglycaemic neonates were low birth weight 25.9 percent and respiratory distress 41.2 percent. These results compare with other studies [<xref ref-type="bibr" rid="scirp.85426-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.85426-ref15">15</xref>] .</p><p>In the present study the clinical manifestation of neonates with hypoglycaemia are similar to those reported in literature. Neonates manifested clinical features that are usually associated with hypoglycaemia [<xref ref-type="bibr" rid="scirp.85426-ref13">13</xref>] and this comprised cyanosis 25.0 percent, tachypnoea 42.9 percent, apnoea 40.0 percent, temperature instability 22.2 percent seizures 100.0 percent and lethargy 40.0 percent of the cases. Njokanma et al. reported similar findings [<xref ref-type="bibr" rid="scirp.85426-ref12">12</xref>] . There was no case of jitteriness observed in our study as compared to Omene in Benin reporting 20.0 percent [<xref ref-type="bibr" rid="scirp.85426-ref13">13</xref>] . The possible explanation for the observations could be that our neonates presented after onset of seizures, while the Benin patients presented earlier with jitteriness in the pre-convulsive stage. Dedeke however reported poor suck, cyanosis, convulsions and pallor as the commest manifestation of hypoglycaemia [<xref ref-type="bibr" rid="scirp.85426-ref5">5</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>The prevalence of hypoglycaemia was 11.0% in the present study. Gestational age, low birth weight and respiratory distress were risk factors documented for neonatal hypoglycaemia. The maternal risk factors associated with hypoglycaemia in the present study were not statistically significant. The clinical manifestations of neonatal hypoglycaemia in the present study were tachypnoea and seizures.</p></sec><sec id="s6"><title>Funding</title><p>The research was funded by the authors.</p></sec><sec id="s7"><title>Recommendations</title><p>Blood glucose estimation should be routine in the care of high-risk neonates. There is need to train and retrain health care workers on the prevention of neonatal hypoglycaemia and provision of suitable transfer medium for referred cases should be intensified.</p></sec><sec id="s8"><title>Authors’ Contributions</title><p>All the authors: for the proof reading of this article; Ochoga, MO and Michael, A: for initiation, protocol drafting, data collection, writing of report and article draft; Abah, RO: report writing; Ogbu, O and Ejeliogu, EU: report writing.</p></sec><sec id="s9"><title>Cite this paper</title><p>Ochoga, M.O., Aondoaseer, M., Abah, R.O., Ogbu, O., Ejeliogu, E.U. and Tolough, G.I. (2018) Prevalence of Hypoglycaemia in Newborn at Benue State University Teaching Hospital, Makurdi, Benue State, Nigeria. Open Journal of Pediatrics, 8, 189-198. https://doi.org/10.4236/ojped.2018.82021</p></sec></body><back><ref-list><title>References</title><ref id="scirp.85426-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Kerstjens, J.M., Bocca-Tjeertes, I.F., de Winter, A.F., Reijneveld, S.A. and Bos, A.F. (2012) Neonatal Morbidities and Developmental Delay in Moderately Preterm-Born Children. Pediatrics, 130, 265-272.  
https://doi.org/10.1542/peds.2012-0079</mixed-citation></ref><ref id="scirp.85426-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Cornblath, M., Hawdon, J.M., Williams, A.F., Green-Aynsley, A., Wad-Platt, M.P., Schwartz, R., et al. (2000) Controversies regarding Definition of Neonatal Hypoglycaemia: Suggested Operational Thresholds. Pediatrics, 105, 1141-1145.  
https://doi.org/10.1542/peds.105.5.1141</mixed-citation></ref><ref id="scirp.85426-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Hay, W.W., Raju, T., Higgins, R., Kalhan, S. and Devaskar, S. (2009) Knowledge Gaps and Research Needs for Understanding and Treating Neonatal Hypoglycaemia. Journal of Pediatrics, 155, 612-617. https://doi.org/10.1016/j.jpeds.2009.06.044</mixed-citation></ref><ref id="scirp.85426-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Frank-Briggs, A.I., Ojule, A.C. and Nkanginieme, K.E. (2008) Neonatal Hypoglycaemia: Prevalence and Clinical Manifestations in Porth Harcourt, Nigeria. Port Harcourt Medical Journal, 2, 166-170.</mixed-citation></ref><ref id="scirp.85426-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Dedeke, I.O.F., Okeniyi, J.A.O., Owa, J.A. and Oyedeji, G.A. (2011) Point-of-Admission Hypoglycaemia in a Nigerian Tertiary Hospital: Incidence, Risk Factors and Outcome. Nigerian Journal of Paediatrics, 38, 90-94. 
https://doi.org/10.4314/njp.v38i2.72252</mixed-citation></ref><ref id="scirp.85426-ref6"><label>6</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Williams</surname><given-names> A.F. </given-names></name>,<etal>et al</etal>. (<year>1997</year>)<article-title>Hypoglycaemia in Newborn: A Review</article-title><source> Bulletin of the World Health Organization</source><volume> 75</volume>,<fpage> 261</fpage>-<lpage>290</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.85426-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Blencowe, H., Cousens, S., Oestergaard, M.Z., Chou, D., Moller, A.B. and Narwal, R. (2012) National, Regional, and Worldwide Estimates of Preterm Birth Rates in the Year 2010 with Time Trends since 1990 for Selected Countries: A Systematic Analysis and Implications. The Lancet, 379, 2162-2172.  
https://doi.org/10.1016/S0140-6736(12)60820-4</mixed-citation></ref><ref id="scirp.85426-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Wild, S., Roglic, G., Green, A., Sicree, R. and King, H. (2004) Global Prevalence of Diabetes. Diabetes Care, 27, 1047-1053. https://doi.org/10.2337/diacare.27.5.1047</mixed-citation></ref><ref id="scirp.85426-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Doherty, D.A., Magann, E.F., Francis, J., Morrison, J.C. and Newnham, J.P. (2006) Pre-Pregnancy Body Mass Index and Pregnancy Outcomes. International Journal of Obstetrics and Gynecology, 95, 242-247. https://doi.org/10.1016/j.ijgo.2006.06.021</mixed-citation></ref><ref id="scirp.85426-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Taofeek, I. (2009) Research Methodology and Dissertation Writing for Health and Allied Health Professionals. 1st Edition, Cress Global Link Limited Publishers, Abuja, 70-75.</mixed-citation></ref><ref id="scirp.85426-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Pal, D., Manandhar, D., Rajbhandari, S., Land, J., Patel, N. and Costello, A. (2000) Neonatal Hypoglycaemia in Nepal 1. Prevalence and Risk Factors. Archives of Disease in Childhood, Fetal and Neonatal Edition, 82, 46-51.  
https://doi.org/10.1136/fn.82.1.F46</mixed-citation></ref><ref id="scirp.85426-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Njokanma, O.F. and Fagbule, D. (1994) Incidence, Aetiology and Manifestations of Neonatal Hypoglycaemia. Nigerian Journal of Paediatrics, 21, 26-31.</mixed-citation></ref><ref id="scirp.85426-ref13"><label>13</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Omene</surname><given-names> J.A. </given-names></name>,<etal>et al</etal>. (<year>1977</year>)<article-title>The Incidence of Neonatal Hypoglycaemia in Benin</article-title><source> Nigerian Journal of Paediatrics</source><volume> 4</volume>,<fpage> 19</fpage>-<lpage>23</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.85426-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Ayoub, N.I., Hanoudi, B.M. and Naif, M.H. (2013) Evaluation of Maternal and Neonatal Risk Factors for Neonatal Hypoglycaemia. Iraqi Journal of Community Medicine, 1, 13-18.</mixed-citation></ref><ref id="scirp.85426-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Bhand, S.A., Sheikh, F., Siyal, R.A., Nizamani, M.A. and Saeed, M. (2014) Neonatal Hypoglycaemia, Presenting Pattern and Risk Factors of Neonatal Hypoglycaemia. Professional Medical Journal, 21, 745-749.</mixed-citation></ref><ref id="scirp.85426-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Fluge, G. (1974) Clinical Aspects of Neonatal Hypoglycaemia. Acta Paediatrica Scandinavica, 63, 826-832. https://doi.org/10.1111/j.1651-2227.1974.tb04871.x</mixed-citation></ref><ref id="scirp.85426-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Lubchenco, L. and Bard, H. (1971) Incidence of Hypoglycaemia in Newborn Infants Classified by Birth Weight and Gestational Age. Pediatrics, 47, 831-838.</mixed-citation></ref><ref id="scirp.85426-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Pildes, R.S. and Pyati, S.P. (1986) Hypoglycaemia and Hyperglycaemia in Tiny Infants. Clinics in Perinatology, 13, 351-375.</mixed-citation></ref><ref id="scirp.85426-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Cornblath, M., Odell, G. and Levin, E.J. (1959) Symptomatic Neonatal Hypoglycaemia Associated with Toxaemia of Pregnancy. Journal of Pediatrics, 55, 545-562.  
https://doi.org/10.1016/S0022-3476(59)80239-0</mixed-citation></ref><ref id="scirp.85426-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Cornblath, M. and Reisner, S.A. (1965) Blood Glucose in the Neonate and Its Clinical Significance. The New England Journal of Medicine, 273, 378-381.  
https://doi.org/10.1056/NEJM196508122730707</mixed-citation></ref><ref id="scirp.85426-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Lawson, J.B. and Stewart, D.B. (1967) Obstertrics and Gynaecology in the Tropics and Developing Countries.1st Edition, Edward Arnold Ltd., London, 120-136.</mixed-citation></ref><ref id="scirp.85426-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Deorari, A.K., Kabra, S.K., Paul, V.K. and Singh, M. (1991) Perinatal Outcome of Infants Born to Diabetic Mothers. Indian Pediatrics, 28, 1271-1275.</mixed-citation></ref><ref id="scirp.85426-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Cornblath, M. and Schwartz, R. (2006) Hypoglycaemia in Neonate. Journal of Pediatric Endocrinology, 6, 113-129.</mixed-citation></ref></ref-list></back></article>