ORIGINAL  
Niger J Paed 2012; 39 (4):185 - 188  
Yousefi P  
Sadrnia S  
Rafiei M  
Prevalence of prolonged QTc-  
interval in electrocardiograms of  
1
-12 year-old seizure patients  
Aghapur L  
DOI:http://dx.doi.org/10.4314/njp.v39i4,7  
Accepted: 29th March 2012  
Abstract Background: Children  
with long QT intervals are prone to  
life-threatening ventricular arrhyth-  
mias which may lead to seizure and  
syncope and may be misdiagnosed  
as seizure.  
Objective: This study aimed to as-  
sess the frequency of long QT inter-  
vals in children with and without  
convulsion.  
Method: This study is case-control.  
ECG tracings were requested for all  
children aged between one to twelve  
years who were hospitalized due to  
convulsion with no underlying etiol-  
ogy and simultaneously for children  
of the same age and gender who  
were admitted due to other than  
seizure as case group. Consequently,  
QT intervals were measured and  
compared in the two groups.  
Results: If long QT interval was  
defined to be longer than 0.47 sec-  
ond, no significant difference was  
noted between two groups. On the  
other hand, if this interval was de-  
fined to be equal to or longer than  
0.46 second, long QT intervals are  
more frequent in convulsive chil-  
dren.  
Conclusions: In this study, long QT  
interval, defined as QT interval ³  
0.46 second, is found more fre-  
quently in children with seizure  
than non-convulsing ones. It is rec-  
ommended that children with his-  
tory of seizure without any identifi-  
able causes and that is unresponsive  
to anticonvulsive drugs should be  
investigated with ECG.  
(
)
Yousefi P  
Department of Paediatrics School of  
Medicine  
Sadrnia S  
Department of Internal Medicine  
Rafiei M  
Department of Biostatistics and  
Epidemiology  
Aghapur L  
Arak university of Medical Sciences  
Arak, Iran.  
Postal code: 3848176941  
Email: parayousefichaijan@yahoo.com  
Tel: +988614173502  
Fax: +988614173520  
Key words: Child, Diagnostic Er-  
rors, Long QT Syndrome, Seizure  
5, 6  
ministration of beta-blockers and ICD therapy  
Introduction  
Seizures can be caused by primary dysfunction of the  
central nervous system, or they can be secondary to  
metabolic disorders or systemic diseases. Differentiation  
of these cases is necessary, because, in addition to sei-  
zure control, the underlying disease should be treated.  
Prolonged QTc-interval syndrome is often diagnosed in  
children with recurrent episodes of syncope and frequent  
seizures, but in most of the cases, the patient's Electro-  
cardiogram (ECG) is considered normal, and the patient  
Early diagnosis and treatment of prolonged QTc-interval  
syndrome requires diagnostic accuracy and strong suspi-  
cion in order to save the children from sudden death  
7
, 8  
.
In this study, we conducted electrocardiograms on one  
to twelve year-old children with seizures in order to as-  
sess the frequency of long QT intervals in children with  
and without convulsions; in dealing with specific cases,  
we considered therapeutic interventions.  
1
is treated with a diagnosis of neurological problems .  
However, other disorders that mimic the manifestations  
of epilepsy are resistant to antiepileptic drugs2, and their  
treatment is so different from that of epilepsy .  
Method  
This syndrome often occurs following exercise, fright,  
or a sudden startle. Some attacks occur during sleep.  
Patients may initially experience seizures, presyncope,  
In this case-control study, we assessed 508 hospitalized  
children at Amirkabir Hospital in Arak, Iran, and di-  
vided them into two groups: 1) case (n=254) and control  
(n=254) groups. The case group included children with  
seizures of unknown etiology, and the control group  
included children who had no seizures and no history of  
seizures. The patients in both groups ranged in age from  
1
and palpitations . Diagnosis is based on electrocardio-  
graphic and clinical criteria. A corrected QT interval  
greater than 0.47 sec is highly indicative of prolonged  
QTc-interval syndrome, but QT intervals greater than  
3,4  
.44 sec is only suggestive . Treatment involves ad-  
0
1
86  
one to twelve years and were matched for age and sex.  
A questionnaire was completed for all patients upon  
admission, including information about the age and sex  
of the patient; family history of seizures, cardiac dis-  
eases, and sudden death; previous history of syncope;  
type of delivery; and child and maternal medications (if  
the child was breastfed). Then, a 12-lead electrocardio-  
gram (ECG) was recorded for each child. QT and RR  
intervals were measured in the patient's ECG (in the best  
lead), and QTc was calculated using Bazett's formula.  
The QT intervals were compared in both groups and  
evaluated on the basis of length. If we suspected a prob-  
lem based on the long corrected QT interval or questions  
in the questionnaire, the patient received a consultation  
with a cardiologist.  
Statistically, there was no significant difference between  
QTc interval stratified by sex between the two groups  
(p>0.05). When long QT interval was defined as greater  
than or equal to 0.46 sec, there also was no significant  
difference between QTc interval stratified by sex in both  
groups (p>0.05; Table 2).  
Table 2: Distribution frequencies of QTc levels in case  
and control groups if QTC0.46  
QTc Interval  
0.46  
0.44< QTc  
Interval <0.46  
QTc Inter-  
val<0.44  
Case  
66(13%)  
13(2.6%)  
27(5.3%)  
40(7.9%)  
175(34.4%)  
179(35.2%)  
354(69.7%)  
con-  
trol  
total  
48(9.4%)  
114(22.4%)  
Entry criteria included all children aged one to twelve  
years who were hospitalized with seizures without a  
specific cause, and for whom consent was given to par-  
ticipate in the study. Exclusion criteria included patients  
who were hospitalized due to secondary seizures (e.g.,  
hypocalcemia, meningitis, brain tumor) or if they were  
likely to have an underlying cause. Patients were also  
excluded in the case of underlying heart disease or lack  
of parental cooperation. Statistical analysis of the col-  
lected data was performed using SPSS software.  
In evaluating the QTc levels in the case group, 175 chil-  
dren (34.4%) had QTc levels less than or equal to 0.44  
sec, 64 children (12.6%) had QTc levels of 0.44–0.47  
sec, and 15 children (3%) had QTc levels greater than  
0.47 sec. In the control group, 178 children (35%) had  
QTc levels less than or equal to 0.44 sec, 71 children  
(
14%) had QTc levels of 0.44–0.47 sec, and five  
Ethical considerations  
children had QTc levels greater than 0.47 sec (Table 3).  
This study was approved by the ethics committee of  
Arak University of Medical Sciences. During the entire  
study period and in dealing with patients, the study  
group was committed to the principles of medical ethics  
set forth by the Ministry of Health and the Declaration  
of Helsinki.  
Table 3: Distribution frequencies of QTc levels in case  
and control groups if QTC>0.47  
QTc Inter-  
val >0.47  
0.44< QTc  
Interval <0.47  
QTc Interval<0.44  
Case  
15(3%)  
5(1%)  
64(12.6%)  
71(14%)  
175(34.4%)  
178(35%)  
Control  
Total  
20(3.9%)  
135(26.6%)  
353(69.5%)  
Results and discussion  
When prolonged QTc interval was defined as greater  
than 0.47 sec, 15 children (3%) in the case group and  
five children (1%) in the control group had a prolonged  
QTc interval. In this situation, there was no significant  
difference in frequency of prolonged QT interval  
between the two groups (p>0.05; Table 3). However,  
when prolonged QTc interval was considered to be  
greater than or equal to 0.46 sec, 66 children (13%) in  
the case group and 48 children (9.4%) in the control  
group had a prolonged QT interval, and there was a sta-  
tistically significant difference between the two groups  
In both groups of children in this study, 142 (55.9%)  
were male and 112 (44.1%) were female. The distribu-  
tion frequencies of QTc levels in males and females in  
both groups are shown in Table 1.  
Table 1: Distribution frequencies of QTc levels in males  
and females in both groups  
QTc Interval  
female male  
Total  
(
p<0.05; Table 2).  
Case  
QTc Interval <0.44 78  
101  
33  
179  
60  
0
val<0.47  
QTc Interval>0.47  
.44< QTc Inter-  
27  
7
Among all 508 children, only three had a QTc greater  
than or equal to 0.50 sec. In evaluating the history of  
syncope in both groups, there was no history of syncope  
in 251 (98.8%) children in the case group and none in  
8
15  
180  
67  
Control  
QTc Interval <0.44 79  
101  
35  
2
52 (99.2%) children in the control group. Syncope oc-  
0
val<0.47  
QTc Interval>0.47  
.44< QTc Inter-  
32  
1
curred in three (1.2%) children in the case group and  
two children (0.8%) in the control group; there was no  
significant difference in history of syncope between the  
two groups (p>0.05).  
4
5
1
87  
In evaluating family history of sudden death, there was a  
history of a father's sudden death and of a brother's sud-  
den death in the case group, and there was a family his-  
tory of sudden death of second-degree relatives in two  
children in the control group. There was no significant  
difference in family history of sudden death between the  
two groups (p>0.05).  
children with uncontrolled seizures or recurrent syncope.  
The difference could also be due to the fact that pro-  
longed QTc interval is defined by different values in  
various articles and references, and no constant value  
has been determined in this field. As such, when QTc is  
defined as greater than or equal to 0.46 sec in some ref-  
erences, the frequency of prolonged QTc in children  
with seizures is greater than in children who were re-  
ferred for reasons other than seizures. In this instance,  
the result would be consistent with the mentioned stud-  
ies.  
In our evaluation of the frequency of prolonged QTc  
interval in males and females in the two study groups,  
there was no significant association between sex and  
QTc levels (p>0.05). In our study, most of the children  
were male and in the age range of 12–48 months. When  
the frequency of prolonged QTc interval was defined as  
greater than 0.47 sec, it was equal in both sexes in the  
two groups. However, when prolonged QTc interval was  
defined as greater than or equal to 0.46 sec, the fre-  
quency of prolonged QTc interval was greater in the  
convulsive children than in the non-convulsive children.  
In addition, most of the children with a history of syn-  
cope or sudden death in family members had a QTc in-  
terval greater than or equal to 0.46 sec.  
In all of the listed studies, prolonged QTc syndrome was  
manifested by symptoms of seizures in children; these  
cases usually are under medical care for years because  
of episodes of seizures and syncope in childhood and  
adolescence. For this reason, diagnosis of this syndrome  
may be delayed, which may result in cardiac arrest or  
sudden death when the individual is older.  
In our study, there was a child in the case group with  
QTc=0.48 sec and two children in the control group with  
QTc=0.46 who had family histories of unexplained sud-  
den death in their families. The cause of those sudden  
death cases could have been due to this syndrome,  
which is consistent with previous studies.  
In the study that Moss and colleagues conducted on 328  
families, most children with long QTc who experienced  
9
syncope or cardiac arrest were female . In the study of  
Lukatti and colleagues in 1998, most of the cases were  
also female. However, clinical presenta10t.ions of this syn-  
drome had manifested earlier in males  
In a study conducted in the USA in 1993 on 287 patients  
under the age of 21 years who had been referred with  
syncope, seizures, and cardiac arrest and whose QTc  
intervals were greater than 0.44 sec, 9% of the patients  
presented with cardiac arrest, 26% with syncope, and  
Conclusions  
Because prolonged QTc syndrome can mimic symptoms  
of a seizure in children, and because these children  
might be treated with anticonvulsant drugs for years, it  
is recommended that follow ups and necessary meas-  
ures, such as requesting ECGs for any seizures that are  
unexplained or uncontrolled with antiepileptic drugs,  
should be taken. If this syndrome is suspected, the pa-  
tient should be referred to a cardiologist; if the syn-  
drome is confirmed, treatment should be initiated for the  
patient at the discretion of a specialist.  
11  
0% with seizures .  
1
In a study conducted in India in 2006 on a 10-year-old  
child with congenital deafness and a history of seizures  
and recurrent syncope, a QTc interval of 0.72 sec was  
observed after years of investigation. In evaluating the  
ECGs of the patient's mother and sister, their QTc inter-  
vals were 0.54 sec and 0.50 sec, respectively, and they  
also had asymptomatic prolonged QTc. This 10-year-old  
child had Jervell and Lange-Nielsen syndrome and had  
been wrongly treated with anticonvulsant drugs for  
Conflict of interest: None  
Funding: None  
1
2
.
years  
In a study performed in the USA in 2007 on a 15-year-  
old girl with an 11-year history of seizures, it became  
clear after realizing the ineffectiveness of anticonvulsant  
drugs and obtaining an ECG that she had a prolonged  
QTc interval, which shows that the syn13drome is easily  
Acknowledgements  
confused with seizures in young people  
.
We are grateful to the Research Council of Arak  
University of Medical Sciences for sponsoring this  
study.  
In our study, when prolonged QTc was defined as 0.47  
sec, there was no significant statistical difference in fre-  
quency of prolonged QTc interval between the two  
groups, which is not consistent with the mentioned stud-  
ies. The reason for this difference could be that all the  
mentioned studies were on people with prolonged QTc  
syndrome or were conducted on special cases, such as  
1
88  
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