<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/css" href="https://imcjms.com/public/assets/rss.css" ?><rss version="2.0">
<channel>
    <title>IMC Journal of Medical Science</title>
    <link>https://imcjms.com/public</link>
    <description>Ibrahim Medical College Journal of Medical Science</description>

                        <item>
                <title><![CDATA[DIABETIC KETOACIDOSIS IN CHILDREN – AN EXPERIENCE IN A TERTIARY HOSPITAL]]></title>

                                    <author><![CDATA[Bedowra Zabeen]]></author>
                                    <author><![CDATA[Jebun Nahar]]></author>
                                    <author><![CDATA[Fauzia Mohsin]]></author>
                                    <author><![CDATA[Kishwar Azad]]></author>
                                    <author><![CDATA[Nazmun Nahar]]></author>
                
                <link data-url="https://imcjms.com/public/registration/journal_full_text/110">
    https://imcjms.com/public/registration/journal_full_text/110
</link>
                <pubDate>Sun, 09 Oct 2016 11:37:58 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[Ibrahim Med. Coll. J. 2008; 2(1): 17-20]]></comments>
                <description>Abstract
Ibrahim Med. Coll. J. 2008; 2(1): 17-20
Key
words: Ketosis, children,
diabetes, BIRDEM
Introduction
BIRDEM
is a tertiary level referral hospital. It is expected that childhood diabetics
who visit this hospital represent the population (childhood diabetics) of
Bangladesh as patients come to this hospital from almost all parts of the
country.In this study we have reviewed the experience
of a major paediatric diabetes care service over the last five years in respect
of admissions for DKA, its etiology and outcome.
Methods
Results
have been reported as mean ± SD. The detailed case records of the children were
analyzed by SPSS programme. A p value of less than .05 was considered to be
significant.
Results
&amp;nbsp;
&amp;nbsp;
&amp;nbsp;
&amp;nbsp;
The median duration of polyuria and/or polydipsia varied between
newly diagnosed and known diabetics (3.2 - 25d) (p&amp;lt;.001). Among other
symptoms, 57.8 % had vomiting and 35.7% had abdominal pain. All patients
presented with altered levels of consciousness and 35 (67.3%) were unconscious
of different grades.
Table-1: Glycaemic status in two groups

 
  
  Group I
  
  
  RBS
  
  
  24 ± 8.4
  
 
 
  
  13.8 ± 2.9
  
  
  &amp;nbsp;
Blood urea was higher in the newly diagnosed patients but was not
significant between the two groups (p&amp;lt;.738). Serum creatinine was higher in
group I than group II (p&amp;lt;.031). Cholesterol level was also higher in group I
than group II (p&amp;lt;.034). Mean pH was 7.18 ± 0.14 and HCO3&amp;nbsp;was 8.94 ± 6.6. There was no
statistical difference between two groups. Complications noted were acute renal
failure and cerebral edema. Three patients developed acute renal failure which
improved after peritoneal dialysis. There were four episodes of cerebral oedema
with two associated deaths.
Table-2: Cause of deaths in children with DKA

 
  
  Group I
  
  
  Septicaemia
  
  
  2
  
 
 
  
  1
  
  
  Cerebral oedema
  
  
  1
  
 
 
  
  2
  
  
  &amp;nbsp;
&amp;nbsp;
This
study provides a different picture regarding types of diabetes presenting with
DKA. One FCPD and three secondary types presented with DKA which is different
compared to the western world where mostly type 1 diabetic children present
with DKA9. The frequency of DKA at onset of diabetes
varies considerably from country to country. In our study, half of the patients
presented with ketoacidosis which is similar to different studies where 25% to
40% of children are newly diagnosed10,11. Amongst the
precipitating causes, infection was the commonest (50%) which is similar to a
study in Sudan where acute infections accounted for 38% of the episodes12. In our study those in the age range 10-14 years suffered from DKA
which was significant between the two groups and the mean age was 11.2 ± 4.4
years. The percentage of DKA cases in boys and girls is usually considered to
be the same11,13. In our study, girls faced an increased risk
of developing DKA at onset of diabetes mellitus. A study from Australia was
analogous in many ways: Bui et al.14&amp;nbsp;found a ratio of 1.3:1.0 in newly diagnosed
patients with DKA. Whilst newly diagnosed patients appeared to have a very
short duration (3.2 days) of polyuria and polydispia, the known diabetics had a
longer duration (25 days) in our study. Approximately 50% of the newly
diagnosed patients had experienced polyuria and/or polydipsia for more than 2 wks14.
The
outcome of treatment in the whole group was good in 46 (86.7%) patients who
recovered without complications. Five patients died, the causes of death being
septicaemia (n= 2), cerebral oedema (n-2) and pneumonia (n=1). There was no
significant difference in between the two groups regarding outcome (p&amp;lt;
.707). Sepsis and cerebral oedema have been reported as cause of death in DKA
patients in India22.
Conclusion
&amp;nbsp;
1.&amp;nbsp;&amp;nbsp; Scibilia J, Finegold D,
Dorman J, Becker D, Drash A. Why do children with diabetes die? Acta
Endocrinol 1986; Suppl 279: 326-333.
3.&amp;nbsp;&amp;nbsp; James R. Gavin III,
K.G.M.M Alberti et al. Report of the expert committee on the diagnosis
and classification of Diabetes mellitus. Diabetes Care 1999; 22(Sup1):
5-17.
5.&amp;nbsp;&amp;nbsp; Wolfsdorf J, Glaser N,
Sperling M.A. Diabetic ketoacidosis in infants, children and adolescents. Diabetes
Care 2006; 29(5): 1150-1159.
7.&amp;nbsp;&amp;nbsp; ISPAD Guidelines 2000,
Ed, PGF Swift, Publ, Med forum, Zeist, Netherlands.
9.&amp;nbsp;&amp;nbsp; Glaser, Nicole,
Kuppermann, Nathan. The evaluation and management of children with diabetic
ketoacidosis in the emergency department. Paediatr Emerg Care 2004; 20(7):
477-481.
11.Pinkney J, Bingley P,
Sawtell P. Presentation and progress of childhood diabetes mellitus: a
prospective population-based study. Diabetoogia 1994; 37: 70-74.
13.Sebastiani L, Guglielmi A.
The Eurodiab experience in Lazio. Ann Ig 1992; 4: 173-178.
15.Rosilio M, Cottton JB,
Wieliczko MC et al. Factors associated with glycaemic control. A cross-sectional
nationwide study in 2,579 French children with type 1 diabetes. Diabetes
Care 1998; 21: 1146-1153.
17.Mortensen HB, Robertson
KJ, Aanstoot HJ et al. Insulin management and metabolic control of type
1 diabetes mellitus in childhood and adolescence in 18 countries. Hvidore Study
Group on Childhood Diabetes. Diabet Med 1998: 15: 752-759.
19.Glaser N, Barnett P,
McCaslin I, et al.&amp;nbsp; Risk factors
for cerebral edema in children with diabetic ketoacidosis: the Pediatric
Emergency Medicine Collaborative Research Committee of the American Academy of
Pediatrics. N Eng J Med 2001; 344: 264 –269.
21.Edge JA, Hawkins MM,
Winter DL, Dunger DB. The risk and outcome of cerebral oedema developing during
diabetic ketoacidosis. Arch Dis Child 2001; 85: 16–22.</description>

            </item>
            
    <copyright>2026 Ibrahim Medical College. All rights reserved.</copyright>
</channel>
</rss>
