ORIGINAL  
Niger J Paed 2013; 40 (4): 384 –388  
Onyiriuka AN  
Awaebe PO  
Kouyaté M  
Hypoglycaemia at point of hospital  
admission of under-five children  
with acute diarrhoea: prevalence  
and risk factors  
DOI:http://dx.doi.org/10.4314/njp.v40i4,7  
Accepted: 18th April 2013  
Abstract Background: Hypogly-  
caemia is one of life-threatening  
immediate complications of acute  
diarrhoea among under-five chil-  
dren but its diagnosis may be  
overlooked because all the symp-  
toms may be mimicked by severe  
dehydration.  
Objective: To determine the  
prevalence of hypoglycaemia at  
the point of hospital admission of  
under-five children with acute  
diarrhoea and identify some of the  
risk factors.  
Methods: At the point of hospital  
admission, venous blood sample  
was collected into an appropriate  
sample bottle (fluoride-oxalate  
bottle) from 201 under-five chil-  
dren with acute diarrhoea for  
blood glucose determination. The  
blood samples were analysed  
using the glucose-oxidase method.  
One of the authors administered a  
questionnaire to each of the care-  
giver to obtain information on the  
socio-demographic characteristics  
and the clinical profile (e.g., pres-  
ence or absence of vomiting, du-  
ration of acute diarrhoea, time of  
last meal of the patients, and ad-  
ministration of ORS at home.  
Hypoglycaemia was defined as  
blood glucose value below 2.6  
mmol/L.  
admission, 7.7% (14 of 183; CI =  
3.7-11.7) under-five children with  
acute diarrhoea had hypoglycae-  
mia (blood glucose < 2.6 mmol/L)  
but dropped to 4.9% (CI=2.9-6.9)  
when a cutoff point of < 2.2 mmol/  
L was applied. The risk factors for  
hypoglycaemia were the presence  
of severe dehydration (p<0.001),  
hypernatraemia and acidosis  
(p<0.001). The prevalence of  
hypoglycaemia was 7 times higher  
in children whose time of last meal  
was 8 hours compared with their  
counterparts whose time of last  
meal was < 8 hours. Mortality rate  
was significantly higher in chil-  
dren with acute diarrhoea and hy-  
poglycaemia compared with their  
counterparts with normoglycaemia  
(p<0.01).  
(
)
Onyiriuka AN  
Department of Child Health,  
University of Benin Teaching Hospital,  
PMB 1111,  
Benin City, Nigeria.  
E-mail: alpndiony@yahoo.com  
didiruka@gmail.com  
Awaebe PO  
Medical Laboratory Unit,  
St Philomena Catholic Hospital,  
Benin City, Nigeria  
Kouyaté M  
Service de Pédiatrie,  
Unité d’endocrinologie pédiatrique  
Hôpital National de Donka,  
CHU de Conakry, Guinea.  
Conclusion: In acute diarrhea,  
hypoglycaemia is an important co-  
morbidity among children aged  
below 36 months and the signifi-  
cant associated risk factors for  
hypoglycaemia are severe dehy-  
dration,  
hypernatraemia and  
acidosis. Under-five children pre-  
senting with acute diarrhoea and  
hypoglycaemia at point of hospi-  
talization are at a significantly  
greater risk of death.  
Key words: Acute diarrhoea, hy-  
Results: At the point of hospital  
poglycaemia, hypernatraemia,  
Introduction  
been clearly established as the immediate life-  
threatening complications of acute diarrhoea, a  
Acute diarrhoea refers to diarrhoea of sudden onset  
non-dehydrating c4o-7mplication like hypoglycaemia is  
(
generally, ov1er hours rather than days), lasting for less  
equally important.  
Even in areas where oral rehydra-  
than 14 days. In developing countries, diarrhoeal dis-  
eases is a leading cause of morbidity and mortality  
among under-five children with an average of 3.3 epi-2  
sodes of diarrhoea being experienced per child per year.  
Acute diarrhoea is associat3ed with a high mortality rate  
among under-five children.  
tion therapy is being practised, mortality from acute  
8
diarrhoea still remains high, suggesting that other  
factors may be playing a role in the observed mortality  
rates. In Africa, there is limited data on hypoglycaemia  
as one of the clinical problems encounte9red in the man-  
agement of children with acute diarrhea. This scenario  
might be related to the fact that the symptoms of severe  
Although dehydration and electrolyte derangement have  
3
85  
dehydration and hypoglycaemia resemble each other,  
resulting in difficulty in -d6 ifferentiating between these  
tients. It has a fairly well equipped laboratory manned  
by qualified medical laboratory scientists and offers a 24  
-hour laboratory service.  
4
two clinical conditions . The co-existence of severe  
dehydration and hypoglycaemia in patients with acute  
4
,5,7  
diarrhorea has been shown to worsen prognosis ,  
At the point of admission, all children between the age  
of one and 59 months who presented with acute diar-  
rhoea were recruited into the study after explaining the  
relevant details of the study to their parents/caregivers  
and obtaining their consent subsequently. The study  
design was approved by the hospital authority. Follow-  
ing recruitment, pretreatment venous blood sample was  
obtained from each of the patients for blood glucose  
estimation. The blood sample was collected into the  
appropriate sample containers (dry fluoride-oxalate bot-  
tles) and forwarded immediately to the hospital labora-  
tory for processing. The blood glucose concentration  
was d1e4termined using glucose-oxidase reaction  
The urea and electrolyte profile of the pa-  
tients was also determined. Based on the serum sodium  
level, the type of dehydration was categorized as hypo-  
natraemic (serum sodium < 130 mmol/L); normonatrae-  
mia (serum sodium 130-150 mmol/L); and hypernatrae-  
mia (serum sodium > 150 mmol). Two medical labora-  
tory scientists (with over 20 years experience) processed  
the samples urgently at the request of the admitting  
physician and the average of the two plasma glucose  
values obtained was accepted. A blood film for malaria  
parasitaemia was performed. Inclusion criteria were age  
below 60 months, Nigerian, negative malaria parasitae-  
mia, absence of overt protein-energy malnutrition  
(kwashiorkor/marasmus), negative history of treatment  
with quinine and/or herbal concoctions. Subjects with a  
coexisting morbidity (e.g., malaria, pneumonia) that are  
known to cause hypoglycaemia were excluded. A struc-  
tured questionnaire was administered to the caregiver of  
each of the patients by one of the authors (ANO). Infor-  
mation obtained included socio-demographic character-  
istics such as age, gender, parents’ educational attain-  
ment and occupation. Data were also obtained on history  
of duration of diarrhoea, presence of vomiting or fever,  
time of last meal.  
implying that early detection and adequate treatment of  
the hypoglycaemia in such patients might improve out-  
come. Hypoglycaemia is a common clinical problem  
and it is associated with serious neurological sequelae  
when detection is delayed or treatment inadequate. Even  
though low blood glucose may often be transient, hypo-  
glycaemia itself is never phy0siological and should not be  
1
disregarded when detected. Some risk factors that have  
been identified include female gender, seizure, altered  
level of consciousness, vomiting, acidosis, d4u,7r,1a1tion of  
diarrhoea less than 72 hours, and bacteraemia.  
A review of the literature revealed that the prevalence of  
hypoglycaemia in4-6children with acute diarrhoea varied  
from 4.5-11.0%. This variability in prevalence rates  
have been obs4e,r6ved at different times, even within the  
same country . In a study in Calabar, Nigeria, 4.0% of  
under-five children presenting 7with acute diarrhoea were  
found to have hypoglycaemia. A study in a rural dis-  
trict hospital in Kenya, reported a prevalence of hypo-  
glycaemia as high as 23.3% among children2 with acute  
method.  
1
diarrhoea at the point of hospital admission. All previ-  
ous Nigerian studies on this subject were conducted in  
tertiary-healthcare hospitals and none in secondary-  
healthcare hospital, yet a significant number of children  
are cared for in secondary-healthcare facilities. Consid-  
ering that in developing countries, childhood diarrhoea  
7
itself is gro3ssly under-reported and its incidence under-  
1
estimated, the magnitude of the paucity of information  
on hypoglycaemia coexisting with diarrhoea becomes  
more obvious. At present, in Nigeria, the extent to  
which hypoglycaemia occur in children with diarrhoea is  
uncertain. We are not aware of any study in Benin City  
that has determined the prevalence of hypoglycaemia or  
examined its risk factors among under-five children with  
acute diarrhoea. The factors highlighted above prompted  
us to conduct the present study.  
The severity of dehydration was determined for each  
patient by physical examination. In the present study,  
hypoglycaemia was defined as blood glucose value be-  
low 2.6 mmol/L while hyperglycaemia was d0efined as  
The purpose of the present study was to determine the  
prevalence of hypoglycaemia at the point of hospital  
admission of under-five children with acute diarrhoea in  
Benin City and identify some of the risk factors. Hope-  
fully, such information would be useful to clinicians in  
developing appropriate protocol for management of chil-  
dren hospitalized for acute diarrhoea, thereby improving  
outcome.  
1
blood glucose value greater than 8.3 mmol/L. All the  
children found to have hypoglycaemia were treated with  
10% dextrose in water at 4ml/kg/hour. No treatment  
was given to the two children with hyperglycaemia. At-  
tention was equally paid to their fluid and electrolyte  
status with treatment as determined by the child’s clini-  
cal condition. The data was analyzed using the Com-  
puter Package for Epidemiologist (PEPI). Descriptive  
statistics such as frequencies, means, ratios, standard  
deviations, confidence intervals, percentages were used  
to describe all the variables. The Z-test was used in as-  
certaining the significance of differences between two  
proportions with the p-value set at <0.05.  
Patients and methods  
This descriptive cross-sectional study was conducted  
between January and December, 2010 at St Philomena  
Catholic Hospital (SPCH), Benin City, Nigeria. SPCH is  
a centrally located, easily accessible large secondary-  
healthcare institution that cares for all categories of pa-  
3
86  
Results  
Table 2: Prevalence of hypoglycaemia stratified by age and  
gender  
During the twelve-month study period, a total of 230  
under-five children were admitted for acute diarrhoea.  
Of this number, 37 (16.1%) had a positive malaria para-  
sitaemia and were excluded because malaria, itself, is an  
established cause of hypoglycaemia. Ten (4.3%) moth-  
ers declined to participate in the study, leaving 183 pa-  
tients whose data analysis is presented. The 183 patients  
consisted of 99(54.1%) males and 84(45.9%) females,  
giving a male-to-female ratio of 1.2:1. At the point of  
hospital admission, 7.7% (14 of 183; 95%CI 3.7-11.7)  
had hypogycaemia (blood glucose < 2.6 mmol/L),  
When a cutoff point of < 2.2 mmol/L was applied, the  
prevalence dropped to 4.9% (9 of 183); 95% CI = 2.9-  
Age (months) Subjects Hypogly Normogly  
Z-statistic  
(p-value)  
caemia  
No (%)  
caemia*  
No (%)  
No (%)  
a
<
12  
81(44.3) 7(8.6) 74(91.4) a vs b= 3.212 (p<0.01)  
63(34.4) 5(7.9) 57(91.9) b vs c=0.847 (p>0.05)  
39(21.3) 2(5.1) 36(92.3) a vs c=0.614 (p>0.05)  
183(100.0) 14(7.7) 165(90.2)  
b
c
12-35  
6-59  
Total  
3
Gender  
Male  
Female  
Total  
99(54.1) 8(8.1) 90(90.9) Odd Ratio 1.1  
84(45.9) 6(7.1) 77(91.7)  
183(100.0) 14(7.7) 167(91.3)  
*Two subjects had hyperglycaemia  
As depicted in Table2, 12(85.7%) of 14 children with  
hypoglycaemia were below 36 months of age. Only two  
6
.9). Two (1.1%) of 183 under-fives with acute diar-  
rhoea had hyperglycaemia. Comparing the age preva-  
lence of hypoglycaemia among children aged below 36  
months and their counterparts aged between 36-59  
months, it was 8.3% versus 5.1% respectively; Z-  
statistic = 0.761 p>0.05. The mean age of the subjects  
was 14.6±10.5 months (95% CI= 13.1-16.1). Vomiting  
accompanied diarrhoea in over half of the cases (Table  
(
1
14.3%) were aged 36 to 59 months. Nine (64.3%) of  
4 children with hypoglycaemia had acidosis. The dura-  
tion of diarrhoeal illness before presentation did not sig-  
nificantly influence the prevalence of hypoglycemia.  
Table 3 shows that the risk of hypoglycaemia was seven  
times higher when the time of last meal was 8 hours  
compared to when it is < 8 hours. Children with severe  
dehydration were at a significantly greater risk of hypo-  
glycaemia than their counterparts with a lower degree of  
dehydration (Table 4).  
1
). The mean electrolyte values are shown in Table 1.  
The distribution of type of dehydration (based on serum  
sodium concentration) among the study population was  
as follows: hyponatraemic dehydration 58.5% (107 of  
1
83), isonatraemic dehydration 36.6% (67 of 183) and  
hypernatraemic dehydration 4.9% (9 of 183). Seven  
77.8%) of 9 cases of hypernatraemia had acidosis and  
Table 3: Prevalence of hypoglycaemia according to time of last meal  
(
Time of  
last meal  
Subjects Hypoglycaemia Normoglycaemia* Odd Ratio  
hypoglycaemia.  
No (%)  
No(%)  
No(%)  
<
8 hours 118(64.5) 8(6.8)  
109(92.4)  
58(89.2)  
7.2  
8 hours 65(35.5)  
6(9.2)  
Table 1: Characteristics of the 183 children with acute  
diarrhoea.  
Total  
183(100.0) 14(7.7)  
167(91.3)  
Parameter  
Number  
%
*Two subjects had hyperglycaemia  
Duration of diarrhoea < 3 days*  
Duration of diarrhoea3 days  
Vomiting present  
Vomiting absence  
Fever present  
Fever absent  
Used ORS at home  
Did not use ORS at home  
101  
82  
96  
87  
85  
98  
100  
83  
Mean±SD (95% CI)  
130.2±7.4 (129.1-131.3)  
3.1±0.8 (3.0-3.2)  
98.4±8.5 (97.2-99.6)  
13.5±4.4 (12.9 -14.1)  
27.1±16.8 (24.7-29.5)  
55.2  
44.8  
52.5  
47.5  
46.4  
53.6  
54.6  
45.4  
Table 4: Prevalence of hypoglycaemia according to hydration  
status  
Hydration status  
Total  
Hypogly Normogly Z-statistic  
caemia caemia * (p-value)  
No (%)  
No (%)  
No (%)  
Mild dehydration  
46(25.1) 0(0.0) 45 (97.8)  
a
Moderate dehydration 118(64.5b) 5(4.2) 112(94.9) a vs b =3.723  
Severe dehydration 19(10.4) 9(47.4) 10(52.6) (0.001)  
Total 183(100.0) 14(7.7) 169(92.3)  
Mean serum sodium (mmol/L)  
Mean serum potassium (mmol/L)  
Mean serum chloride (mmol/L)  
Mean serum bicarbonate (mmol/L)  
Mean serum urea (mg/dl)  
*Two subjects had hyperglycaemia  
As shown in Table 5, the commonest type of dehydra-  
tion was hyponatraemic dehydration while hypernatrae-  
mic dehydration was the form of dehydration most com-  
monly associated with hypoglycaemia. A total of eight  
of 183 children died, representing a case fatality rate  
*Before presentation  
4
.4%. Five (62.5%) of the eight had hypoglyaemia.  
None of the two subjects with hyperglycaemia died.  
When mortality rate between the hypoglycaemic group  
was compared with the normoglycaemic group, it was  
3
5.7% (5/14) versus 1.8% (3/169); Z-statistic = 2.627  
p<0.01. Three of the five children with hypoglycaemia  
who died, also had hypernatraemia and acidosis. The  
remaining two hypoglycaemic children who died had a  
combination of hyponatraemia and acidosis. Of the  
3
87  
normoglycaemic children who died, two had severe hy-  
ponatraemia with acidosis and one had hypernatraemia  
with acidosis. In this series, it is of note that acidosis  
was a common factor among all the deaths.  
glycaemia whereas the substrates for gluconeogenesis  
were inappropriately low in them, leading to the conclu-  
sion that hypoglycaemia in such children was most  
likely due to impaired hepatic gluconeogenesis. The  
report of another study also linked hypoglycaemia asso-  
ciated diarrhoeal illnesses in children to glyco1g9en de-  
Table 5: Prevalence of hypoglycaemia according to type of  
dehydration  
pletion and impaired hepatic gluconeogenesis.  
The  
higher risk of hypoglycaemia observed in the present  
study among under-five children with diarrhoea in  
whom the time of last meal was 8 hours and above is in  
tandem with glycogen depletion as one of the pathoge-  
netic mechanisms of hypoglycaemia in diarrhoeal  
illnesses.  
Type of  
dehydration  
Subjects Hypogly Normogly  
caemia caemia *  
No (%) No (%) No (%)  
Z-statistic  
(p-value)  
a
Hyponatraemic 107(58.5) 5(4.7) 101(94.4) a vs b=0.582(p>0.05)  
b
67(36.6) 2 (3.0) 64(95.5) b vs c = 1.996 (p<0.05)  
c
Isonatraemic  
Hypernatraemic 9(4.9) 7 (77.8) 2(22.2) a vs c = 5.220 (p<0.001)  
Total 183(100.0) 14(7.7) 169(92.3)  
Hyperglycaemia was present in one out of every hun-  
dred patient in the present study. There was no mention  
of the occurrence of hyperglycaemia in the study in  
*Two subjects had hyperglycaemia  
7
Calabar, making it impossible to judge whether or not  
any of their subjects had hyperglycaemia. A2 study in  
1
Kenya has reported a similar observation. In that  
Discussion  
study, 12.9% of 96 children with hyperglycaemia had  
gastroenteritis as their diagnosis, representing a preva-  
lence of 3.7%. The prevalence of hyperglycaemia was  
higher in the Kenyan study than in the present one  
In the present study, the prevalence of hypoglycaemia at  
the point of hospital admission of under-five children  
presenting with acute diarrhoea was 7.7%. This was  
higher than the 4.0% and 4.5% r1e5ported from Calabar,  
despite the fact that they used a higher cut-off value of >  
1
0 mmol/L. The reason for this difference is not clear.  
7
Nigeria and Dhakar, Bangladesh respectively. On the  
In contrast to the Kenyan study, none of the two patients  
with hyperglycaemia died.  
other hand, the prevalence being reported here is lower  
than 11.0% reported from another study 4in Bangladesh  
among under-five diarrhoeal children. The higher  
prevalence rate observed in the present study compared  
to the previous study in Calabar may be explained by the  
differences in definition of hypoglycaemia used in the  
two studies. In the present study, a higher cut-off (<2.6  
mmol/L, based on the concept of operational threshold  
Data from the present study revealed that among under  
-
five children with acute diarrhoea, severe dehydration,  
hypernatraemia and acidosis were significant risk fac-  
tors for hypoglycaemia. This is not surpri7s,1i5ng as similar  
observation has been reported previously.  
The severe  
dehydration and acidosis may impair the function of  
various enzymes involved in gluconeogen1e5sis as well as  
interfere with the transport of substrates. However, in  
1
6
blood glucose values ) was used in defining hypogly-  
caemia whereas < 2.2 mmol/L was used as cut-off in the  
Calabar study, partly accounting for the higher preva-  
lence observed in the present study. The definition of  
hypoglycaem7 ia used in a study is known to influence its  
7
contrast, Ntia et al did not find any relationship be-  
tween the frequency of hypoglycaemia and serum elec-  
trolyte profile. Given the fact that they did not document  
in their results, the serum electrolyte profile of their pa-  
tients, it is possible they did not focus on electrolytes in  
relation to hypoglycaemia. However, in that report, they  
did state that five of the six children with hypoglycae-  
mia in their series had metabolic acidosis, supporting,  
albeit indirectly, the significant association between  
acidosis and frequency of hypoglycaemia observed in  
the present study.  
1
prevalence. This was amply demonstrated in the  
present study because when a cut-off of less than 2.2  
mmol/L was applied it resulted in a lower prevalence  
rate (4.9%). The explanation for the higher prevalence  
rate in the present study compared to the prevalence rate  
(
4.5%) observed in the study in Bangladesh may be due  
to differences in the age group of the study population.  
The present study involved o5nly under-five children  
1
whereas the Bangladesh study included children up to  
the age of 15 years. Studies have shown that the risk of  
hypoglycaemia is high1e8r in under-five children com-  
pared to older children.  
What is the clinical implication of these findings? Case  
management efforts in childhood diarrhoeal illnesses  
usually focus on correction of fluid and electrolyte  
derangement. Clinicians need, in addition, to consider  
the role of non-dehydrating complication like hypogly-  
caemia in causing death in children presenting with diar-  
rhoea. Thus, it might be beneficial for clinicians to  
consider the possibility of hypoglycaemia when devel-  
oping appropriate protocol for management of children  
hospitalized for acute diarrhoea, thereby reducing the  
already high mortality associated with childhood diar-  
rhoeal illnesses in developing countries. After treatment  
of shock, the use of dextrose-containing intravenous  
On the other hand, the lower prevalence rate (7.7%)  
observed in the present study compared with 11.0%  
found in the study by Huq et al may be explained by  
4
selection bias. In that study, they investigated only those  
children suspected to have hypoglycaemia. The mecha-  
nism by which diarrhoea predisposes to hypogly5caemia  
1
is poorly understood. However, Bennish et al, linked  
it to defective gluconeogenesis. In that study, they  
observed that the glucose counterregulatory hormones  
were appropriately elevated in the children with hypo-  
3
88  
solution in hospitalized children requiring parenteral  
fluid therapy is advocated, particularly where facilities  
for determination of blood glucose level is not available.  
All children presenting with diarrhoea and acidotic  
breathing should, in addition to correcting the acidosis,  
treated empirically for hypoglycaemia.  
and the significant associated risk factors are severe  
dehydration, hypernatraemia and acidosis. Routine  
assessment of blood glucose at the point of hospital ad-  
mission is advocated and where facility for determina-  
tion of blood glucose level is not available, treat empiri-  
cally for hypoglycaemia to improve outcome.  
Conflict of interest: None  
Funding: None  
Conclusion  
Hypoglycaemia is an important co-morbidity of acute  
diarrhoea among children below the age of 36 months  
References  
8
.
Rousmans C, Bennish ML,  
15. Bennish ML, Azad AK, Rahman  
O, Phillips RE. Hypoglycaemia  
during diarrhea in childhood:  
prevalence, pathophysiology and  
outcome. New Engl J Med 1990;  
322(19):1357-1363.  
16. Hay WW Jr, Raju TN, Higgins  
RD, Kalhan SC, Devaskar SU.  
Knowledge gaps and research  
needs for understanding and treat-  
ing neonatal hypoglycemia: work-  
shop report from Eunice Kennedy  
Shriver National Institute of Child  
Health and Human Development. J  
Pediatr 2009;155(5):612-617  
17. Williams AF. Hypoglycaemia in  
the newborn: a review. Bull World  
Health Organ 1997; 75(3): 261-  
290.  
18. Solomon T, Felix JM, Samuel M,  
Dengo GA, Saddanba RA,  
Schapira A, Phillips RE. Hypogly-  
caemia in paediatric admissions in  
Mozambique. Lancet 1994; 343:  
149-150.  
19. Butler T, Arnold M, Islam M. De-  
pletion of hepatic glycogen in the  
hypoglycaemia of fatal childhood  
diarrhoeal illnesses. Trans Royal  
Soc Trop Med Hyg 1989;83(6):839  
-843.  
1
.
Cutting WAM. Diarrhoeal dis-  
eases. In: Stanfield P, Brueton M,  
Chan M, Parkin M, Waterson T  
eds. Diseases of Children in the  
Subtropics and Tropics, 4 ed.  
London Arnold Publishers,  
Weizba T. Diagnosis and manage-  
ment of dysentery by community  
health workers. Lancet 1988;2:552  
-555.  
Lee LA, Dogore R, Redd SC,  
Dogore B, Metchock B, Diabate J,  
van Assendelft OW, DeCock K,  
Patrick E, Herrington J. Severe  
illness in African children with  
diarrhea: implications for case  
management strategies. Bull World  
Health Org 1995;73(6):779-785.  
th  
9
.
1
991:455-495.  
2
3
.
.
Patwari AK. Diarrhoeal diseases.  
In: Parthasarathy A ed. IAP Text-  
th  
book of Pediatrics 4 ed. Vol 1,  
New Delhi, Jaypee Brothers Medi-  
cal Publishers 2009:602-608.  
Synder JD, Merson MH. The mag-  
nitude of the global problem of  
acute diarrhoeal disease: a review  
of active surveillance data. Bull  
World Health Org 1982;60(4):605  
1
0. Ferry RJ Jr, Allen DB. Hypoglyce-  
mia. In: Kappy MS, Allen DB,  
Geffner ME. Pediatric Practice:  
Endocrinology. New York,  
McGraw Hill Companies Inc,  
-613.  
2
010:393-408.  
4
.
Huq S, Hassan MI, Malek MA,  
Faruque AS, Salam MA. Hypogly-  
caemia in under-five children with  
diarrhea. J Trop Paediatr  
1
1
1. Reid S, McQuillan S, Losek J.  
Hypoglycemia complicating dehy-  
dration due to acute gastroenteritis.  
Clin Pediatr (Phila) 2003;42  
2
007;53:197-201.  
(7):641-646.  
5
6
.
.
Reid SR, Losek JD. Hypoglycae-  
mia complicating dehydration in  
children with acute gastroenteritis.  
J Emerg Med 2005;29:141-145.  
Bennish ML, Azad AK, Rahman  
D, Philipe RE. Hypoglycaemia  
during diarrhea in childhood:  
Prevalence, pathophysiology and  
outcome. International Centre for  
Diarrhoeal Disease Research,  
Bangladesh, Dhaka. N Engl J Med  
2. Osier FHA, Berkley JA, Ross A,  
Sanderson F, Mohammed S, New-  
ton CRJC. Abnormal blood glu-  
cose concentrations on admission  
to a rural Kenyan district hospital:  
prevalence and outcome. Arch Dis  
Child 2003;88:621-625.  
3. Ogbonnaya O, Nebe A, Chigozie  
U, Ekperechi SA. Aetiology of  
acute infantile diarrhea and antibi-  
otic sensitivity profile. Inter J  
1
1
1
990;322:1357-1363.  
Third World Med 2008;5:153-159.  
4. Chesbrough M. District Labora-  
tory Practice in Tropical Countries  
7
.
Ntia HN, Anah MU, Udo JJ, Ewa  
AU, Onubi J. Prevalence of hypo-  
glycaemia in under-five children  
presenting with acute diarrhoea in  
University of Calabar Teaching  
Hospital, Calabar. Niger J Paedi-  
atr 2012;39(2):63-66.  
(Part 1). Cambridge, Cambridge  
University Press, 1998:340-348.