Pediatric Transplantaton 2017; e12872; wileyonlinelibrary.com/journal/petr
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1 of 6
DOI: 10.1111/petr.12872
© 2017 John Wiley & Sons A/S.
Published by John Wiley & Sons Ltd
Accepted: 16 November 2016
DOI: 10.1111/petr.12872
ORIGINAL ARTICLE
Early and late neurological complicatons of liver
transplantaton in pediatric patents
Serdal Gungor
1
| Betul Kilic
1
| Mujgan Arslan
1
| M. Ayse Selimoglu
2
|
Hamza Karabiber
2
| Sezai Yilmaz
3
1
Department of Pediatric Neurology, Faculty
of Medicine, İnönü University, Malatya, Turkey
2
Department of Pediatric Gastroenterology,
Hepatology and Nutriton, Faculty of
Medicine, İnönü University, Malatya, Turkey
3
Department of Surgery, Faculty of
Medicine, İnönü University, Malatya, Turkey
Correspondence
Betul Kilic, MD, Department of Pediatric
Neurology, İnönü University Medical Faculty,
Malatya, Turkey.
Email: betulklc82@gmail.com
Abstract
NCs occur commonly afer solid organ transplantaton and afect 15%-30% of liver
transplant recipients. The aim of this retrospectve study was to evaluate the type and
incidence of neurologic events in pediatric patents following LT. Between May 2006
and June 2015, 242 patents (118 females, 124 males) requiring LT for diferent etolo-
gies at the İnönü University Liver Transplantaton Insttute were included. The inci-
dence, types, and risk factors of NCs that occurred following LT were evaluated
retrospectvely. Neurologic events occurred in 57 (23.5%) of the patents. Early NCs
were encephalopathy (12.4%), seizures (11.5%), and PRES (7%). Of 57 patents, fve
(8.7%) experienced NCs at least 1 month afer LT; these late NCs included tremor,
headaches, encephalopathy, ataxia, and neuropathy. The psychiatric symptoms afer
LT were noted in 42 patents (17.4%). The mortality rate afer LT in those with or with-
out neurological events was not signifcantly diferent (P=.73). There was a high inci-
dence of serious neurologic events afer LT. The major neurologic manifestaton in our
patents was encephalopathy followed by seizures.
KEYWORDS
childhood, liver transplantaton, neurological complicaton
1 | INTRODUCTION
LT is the only successful treatment modality for pediatric patents
with end-stage liver disease or acute liver failure. Advances in surgical
techniques, postoperatve management, and the appropriate use of
immunosuppressant agents have enhanced patent and graf survival
following pediatric LT.
1,2
NCs that can occur following LT in children are reported being more
severe and are associated with greater mortality compared with adults.
3,4
Various factors play a role in the pathogenesis of NCs following
LT including poorly functoning graf, electrolyte and metabolic de-
rangements, intracranial hemorrhage, cerebral infarcton, infecton,
or immunosuppressant toxicity.
5
Seizures are the most common NCs
afer LT.
3,6
Various other NCs reported afer LT are encephalopathy,
PRES, stroke, meningits, central pontne myelinolysis, cerebellar syn-
dromes, headache, neuropsychiatric manifestatons, cognitve decline,
sleep disturbances, tremors, and peripheral neuropathy.
3-10
Routne
preoperatve neurological evaluaton and close follow-up afer LT are
needed for detectng the earliest signs of complicatons and initatng
prompt and appropriate treatment or interventon.
3,4
We retrospectvely reviewed 242 consecutve pediatric LT cases
to assess the incidence, types, and risk factors of NCs that occurred
following LT.
2 | METHODS
The medical records of 242 children (age <18 years) who underwent
LT between May 2006 and June 2015 at Inönü University Liver
Abbreviatons: CNS, central nervous system; CT, computerized tomography; DDLT, de-
ceased donaton liver transplantaton; EEG, electroencephalography; EMG, electroneuromy-
ography; FLAIR, fuid-atenuated inversion recovery; GABA, gamma aminobutyric acid; IHS,
Internatonal Headache Society; LDLT, living-donor liver transplantaton; LT, liver transplan-
taton; MRI, magnetc resonance imaging; NCs, neurologic complicatons; NMDA, N-methyl
d-aspartate; PRES, posterior reversible leukoencephalopathy syndrome.