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International Journal of Pediatric Otorhinolaryngology
journal homepage: www.elsevier.com/locate/ijporl
The effects of ondansetron versus dexamethasone on electrocardiographic
markers of ventricular repolarization in children undergoing cochlear
implant
Reza Safaeian
a
, Valiollah Hassani
a
, Alimohamad Asghari
b
, Masood Mohseni
a,*
, Haleh Ashraf
c
,
Zahra Sadat Koleini
a
a
Department of Anesthesiology, Iran University of Medical Sciences, Tehran, Iran
b
Skull Base Research Center, The Five Senses Health Research Institute, Iran University of Medical Sciences, Tehran, Iran
c
Cardiac Primary Prevention Research Center (CPPRC), Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran
ARTICLE INFO
Keywords:
Arrhythmia
QT interval
Ondansetron
Dexamethasone
Cochlear implant
Nausea
ABSTRACT
Introduction: Congenital hearing loss is associated with cardiac rhythm disturbances namely long Q-T syndrome.
This study was designed to investigate the effect of anti-emetic doses of ondansetron and dexamethasone on ECG
recordings in children undergoing cochlear implant surgery.
Methods: Sixty-three pediatric patients scheduled for elective cochlear implantation were enrolled in the study.
Two patients were excluded as their baseline ECG showed long QT syndrome. Anesthesia was induced with
fentanyl, propofol and atracurium and maintained with propofol. Dexamethasone 0.1 mg.kg
-1
or ondansetron
0.2 mg.kg
-1
was randomly administered for the participants approximately 30 min before the end of surgery.
ECG recording was performed 15 min after induction of anesthesia and 15 min after dexamethasone/ondan-
setron administration. RR interval, QRS duration, QT interval, and Tp-e interval were measured by a blinded
cardiologist.
Results: Ondansetron resulted in no significant changes in RR, JTc and QTc intervals; while prolongedTp-e in-
terval. Multivariable logistic regression analysis showed that use of ondansetron was an independent predictor of
QTc prolongation after adjustment for age, gender and baseline QTc (OR = 17.94, CI 95% 1.97–168.70,
p = 0.011). The incidence of postoperative retching/vomiting in ondansetron group was significantly lower
than dexamethasone group. (3.2% vs. 26.7%, p = 0.011).
Conclusion: The risk of arrhythmias with the use of ondansetron in otherwise healthy candidates of cochlear
implant is very low. However, the drug may induce significant changes in ECG parameters. The clinical sig-
nificance of these changes in patients with cardiac conduction abnormalities should be investigated in further
studies.
1. Introduction
Nowadays, many children are admitted for cochlear implant for
early onset inherited hearing loss [1]. One common complication of the
surgery is post-operative nausea and vomiting (PONV) due to manip-
ulation of the inner ear [1–3]. Common groups of antiemetic dugs in-
cluding dopamine receptor antagonists like droperidol, 5HT3R receptor
antagonists like ondansetron and corticosteroids such as dex-
amethasone may provoke the risk of QT prolongation [4,5]. Long QT
interval is partly because of delayed repolarization of the ventricles that
might lead to arrhythmias such as ventricular tachycardia and torsade
de point [6]. The frequency of long QT syndrome (LQTS) in children
among all patients with congenital deafness is thought to be less than 1
in 50,000. However, patients with congenital sensorineural hearing loss
including Jervell and Lange-Nielsen syndrome are already at increased
risk of sudden cardiac death, even being asymptomatic before [7]. This
necessitates ECG screening and a safe plan of anesthesia considering the
potential for arrhythmogenicity of medications.
New electrical markers, including the interval between the peak and
the end of the T wave (T p-e), stand out due to their ability to suggest
the presence of refractory transmural dispersion, with potential appli-
cation in the stratification of arrhythmogenic risk in different popula-
tions [8–12]. The JT interval is more effective for ventricle repolar-
ization as it has been described more specific for arrhythmia prognosis
https://doi.org/10.1016/j.ijporl.2020.109896
Received 26 September 2019; Received in revised form 6 January 2020; Accepted 18 January 2020
*
Corresponding author.
E-mail address: Masood.mohseni@gmail.com (M. Mohseni).
International Journal of Pediatric Otorhinolaryngology 132 (2020) 109896
Available online 22 January 2020
0165-5876/ © 2020 Elsevier B.V. All rights reserved.
T
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