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Uti~ity ~An of Eectroencephalograms in Paediatrics iatrics Analysis of 66 Records I H M I Hussain, MRCp, A It Mazidah, MD, Neurology Unit, Paediatric Institute, Hospital Kuala Lumpur Discovered by Hans Berger at the beginning of this century electroencephalograms (EEG) have been widely used since the 90s, but are still limited to tertiary centres in most parts of the world, more so in the tropics. The actual indications for an EEG, apart from suspected epilepsy remain controversial especially with recent advances in neuroimaging. In November 99, a separate neurophysiology unit was established at the Paediatric Institute, and as of January 993, all EEGs in children under years referred to Kuala Lumpur Hospital were performed at the Institute. We present here an analysis of all the cases done in 993. A retrospective analysis was made of all EEGs recorded between January and 3 December 993 at the Paediatric Institute. The recordings were made on a SANEl Model la93 0 channel EEG machine. The International 00 system of electrode placement was used. All recordings included transverse and anterior posterior bipolar montages and a referential montage using the right auricular lead (A) as common 38 reference. Photic stimulation was used in all cases and hyperventilation in children who could cooperate. When sedation was required, syrup chloral hydrate was used in doses of 070mg/kg. Patient details namely age, sex, indication for EEG, clinical description of epileptic seizures and drug treatment were obtained from the EEG requisition card. All technical reports and conclusions for the EEGs were prepared by the first author, (HI HMI) and these were analysed in conjunction with the clinical data. The terminology used to describe EEG activity was that proposed by Binnie3 In patients with epilepsy, the seizures were classified according to the 98 Classification of the International League Against Epilepsy!. A total of 66 EEG records were analysed. The indications for an EEG are shown in Table. As expected the majority of requests (7.7%) were epilepsy related. The age distribution of these children is shown in Figure. The largest number of recordings was made in the first year of life. However, the remaining 8.3% of requests covered a wide spectrum of Med J Malaysia Vol No 3 Sepl 996

ELECTROENCEPHALOGRAMS IN PAEDIATRICS paediatric neurological disorders. The clinical classification of the 9 children with epilepsy is shown in Table n. Paucity of clinical details in the EEG requisition card did not allow a syndromic classification. Of the 337 with clinical generalised epilepsy, only 39 had generalised bilaterally synchronous spike wave discharges, 8 had secondary generalisation, 3 had continuous epileptic discharges suggesting status epilepticus, 0 had polyspike and wave discharges and 3 had multifocal epileptiform discharges, 6 had focal discharges, 7 had suspicious sharp activity and 83 were normal. Conversely although only children had partial seizure clinically, 89 epilepsy related records showed focal changes. Of the normal EEGs, 09 were for epilepsy, fortynine were newly diagnosed cases or suspected epilepsy, were children with epilepsy already on treatment and were children with epilepsy who had already been weaned off anticonvulsants. Among the non epileptic indications for an EEG, of the 7 EEGs done for encephalopathy were abnormal, but only 6 had lateralised abnormalities suggesting the possibility of Herpes simplex encephalitis. In all of these serology for herpes was subsequently reported as negative. All of the 37 records done for meningitis were in children whose acute illness had been complicated by fits. Thirtytwo of the records were abnormal; had multifocal epileptiform discharges, focal discharges and cases had focal slowing. Data on the number of these children who subsequently developed epilepsy is not available. 0.0.0.0. c 8. 3.7,.8 ~ ~ ~ ~ 9. 0.0 < mon,h 6 7 Y' 3 6 7 8 9 l{l Age Figo i: Age disrributioil @f patients with dil'lkal epilepsy The details of EEG findings in the other conditions listed in Table I are shown in Table Ill. The EEG is an important tool in assessing brain function, and together with advance in neuroimaging, has greatly improved our understanding of the nervous system. However, all tests have their limitations. The aim of this study was to analyse the usefulness and limitations of the EEG and draw guidelines for the optimal use of this investigative modality. As expected the majority of requests were epilepsy related but almost one third were for non epileptic conditions. Fifty per cent of EEG requests were in children under years of age reflecting the higher incidence of epilepsy in young children 3 Of the EEG done for epilepsy only.3% were normal, much lower than that predicted by some workers. This is lable I indk(lltiol"l for i:eg in 66 children C@!i/i! Noo P r(enf~ge Epilepsy 9 7.7% Encephalopathy 7.3% Post Meningitis 37.9% Mental Retardation 6.6% Regression of Development 8 3% Behaviour Disorder.% Acute Hemiplegia 0.6% Tumour 3 0.% Brain Death 0.8% Post Ischaemic Brain Damage 6.6% Birth Asphyxia 0.8% Neonatal Seizures 9 3.0% Intracranial Haemorrhage 9.%, Systemic Medical Illness 0.6% Total 66 00% Med J Malaysia Vol No 3 Sept 996 39

ORIGINAL ARTICLE T@ble Ii Types I\lf dinicc;i epilepsy seen Number I\lf Pt"!tientsi A) Partial Seizures Simple Partial Seizures 3 Complex Partial Seizures 7 Partial Seizures Secondarily Generalised B) Generali ed Seizures 337 Absence Seizures 3 Atypical Absence Seizures 3 Myoclonic Seizures 6 Clonic Seizures Tonic Seizures 7 TonicClonic Seizures 09 Atonic Seizures 37 Non Convulsive Status Per(en~ ge % 9.6% 0.%.9% 7% 7.8% 0.7% 3.6% 3.3% 6.7%.3% 8.7% 0.% 9 00% probably because almost all the EEGs done in children under are sleep recordings, and sleep is regarded as an activation procedure. The findings among patients with generalised epilepsy diagnosed clinically is interesting, as the majority, 6 out of abnormal records had focal changes, of which 8 had secondary bilateral synchrony documented on EEG. This may have therapeutic implications as traditionally, phenobarbitone and valproic acid have been used for primary generalised epilepsy while phenytoin and Carbamazepine are preferred for partial epilepsies with or without secondary generalisation. However, two recent studies. 6 have shown all these drugs to be equally effective in both types of epilepsy, although carbamazepine and valproic acid are preferred in children. Nonetheless this is an important clinical distinction as prognosis for control and risk of recurrence on withdrawal of treatment at.' significantly different in these two groups of patients 7 Fortynine children with newly diagnosed or suspected epilepsy had normal EEGs while a further 30 patients from the total of 9 had suspicious sharp activity Table III leoeog, filldkilgs in 66 records; altcordii'ijg to indicatll\lil Indicatil\ln N fg MY ME fd SSA SE EN EPILEPSY Encephalopathy Post meningilis Mental retardation MenIal regression Behavioural Acute hemiplegia Tumour Brain death Post ischaemic Birth asphyxa Neonata. seizures Intracranial H' age Systemic Illness 09 0 9 39 8 0 3 89 30 3 7 3 8 3 7 0 3 3 9 7 * 37 6# 6 8 * 3 6 9 9 Total 39 8 0 6 0 0 66 N: Normal, G: Generalised discharges, FG: Focal discharges with secondary generalisation, MY: Myoclonic, ME: Multifocal epileptiform discharges, FD: Focal discharge, SSA: Suspicious sharp activity, SE: Status epilepticus, EN: Encephalopathy, BD: Brain death, 0: Other. #: Delayed maturation, *: Focal slow. 30 Med J Malaysia Vol No 3 Sept 996

ELECTROENCEPHALOGRAMS IN PAEDIATRICS which is not a particularly useful finding, stressing the fact that the most important investigation in epilepsy is a good clinical history and an eyewitness account. On the other hand, the finding of multifocal epileptiform discharges and polyspike and wave discharges on EEG often have unfavourable implications that may not be apparent from the clinical history. This emphasises the poirit that epilepsy classification is an electroclinical one. Among the non epileptic requests it would appear that doing an EEG for mental retardation is not useful. The finding of delayed maturation of background activity does not affect manageme~t, nor does it help in the diagnostic workout. On the other hand, half of the patients with mental regression had significant findings, including one with non convulsive status epilepticus, which is a treatable cause of regression. Among the 8 who had multifocal discharges, had changes suggestive of an underlying poliodystrophy and others of a leukodystrophl. This information is particularly useful in centres like ours which do not have facilities to investigate lysosomal and peroxisomal disorders. The finding in meningitic and encephalopathic patients has been alluded to earlier and these requests were appropriate. Nine of patients with behavioural disorders had abnormalities on EEG, of whom had focal discharges, and were started on carbamazepine. We have, since, been very liberal in doing EEGs for such children. This contrasts with the EEG done for patients with hemiplegia and suspected tumours which did not help in their management. Two of the 3 patients with a suspected tumour had abnormalities on et scan, and neuroimaging should now replace EEG for this condition. All patients in the brain death group were infants who were clinically brain dead and an EEG is an added test for brain death in infants under year in our department. In the remaining groups shown in Table III, EEGs were done to help assess the extent of brain damage and to decide on the need for anticonvulsants. Of the children with systemic illness ( acute lymphoblastic leukaemia (ALL) with central nervous system involvement, systemic lupus erythematosus (LE) and with chorea, one of the patients with LE had a normal EEG whereas the child with ALL had diffuse slow activity suggestive of an encephalopathy. In conclusion, the EEG remains an important investigative tool in child neurology, not only in epilepsy but in a broad spectrum of disorders where EEG findings affect prognosis and may modify treatment. This is an important observation in an era where advances in neuroimaging may distract clinicians from the usefulness of neurophysiological testing, which is cheaper and more readily available in developing countries. Admow!edgemenis We would like to thank the Director General of Health, Malaysia for permission to publish this paper and Ms Elizabeth for typing assistance.. Commission on Classification and Terminology of the International League against Epilepsy: proposal for revised clinical and electroencephalographic classification of epileptic seizures. Epilepsia 98; : 890.. CO Binnie. Electroencephalography in Textbook of Epilepsy, Ed. Laidlaw, Ricken, Chadwick. th Edition. Churchill Livingstone, 993. 3. Cowan LO. Prevalence of Epilepsy in Childhood and Adolescence. Epilepsia 989;30() : 906.. Sundaram M, Hogan TP, Hiscook M. Factors affecting interictal spike discharges in adults with epilepsy. Electroencephalography and Clinical Neurophysiology 990 (7) : 3860. Med J Malaysia Vol No 3 Sepf 996 3

ORIGINAL ARTICLE. Verity CM, Hosking G, Easter DJ. A Multicentre Comparative Trial of Sodium Valproate and Carbamazepine in Paediatric Epilepsy. Dev Med Child Neurol 99;37 : 9708. 6. Heller AJ, Chesterman P, Elwes RDC et al. Phenobarbitone, Phenytoin, Carbamazepine or Sodium Valproate for newly diagnosed adult epilepsy: A randomised Comparative Monotl,erapy Trial. Journal of Neurology, Neurosurgery and Psychiatry 99;8 : 0. 7. Shinnar S, Beng AT, Moske SL et al. Discontinuing Antiepileptic Drugs in Children with Epilepsy: A Prospective Study. Ann Neurol 99;3 : 3. 8. Tharp BR. Neonatal and Paediatric Electroencephalograms in Electrodiagnosis in Clinical Neurology. Ed. Aminoff MJ. nd Edition Pg. 77. NY: Chur~hill Livingstone, 986. 3 Med J Malaysia Vol No 3 Sept 996