Status Epilepticus in Children: A Study of 54 Cases

Objectives: To review the clinical character, the management and outcome of status epilepticus in children. Methodology: We conducted a retrospective review of 54 cases treated between 1996 and 1997 at the Royal Alexandra Hospital for Children, Sydney, Australia. Among the variables collected for analysis in this study were age, sex, etiology of status epilepticus, median length of Paediatric Intensive Care Unit (PICU) stay and days of mechanical ventilation, and mortality of status epilepticus. Results: Of the patients with status epilepticus, 61% were male and 39% female, with an age range of 3 months to 15 years (mean 5.3 years). The etiology of status epilepticus is largely age related, with acute causes common in 1 - 3 year and 4 - 7 year ages, 44 cases (81.5%). The etiology of status epilepticus included febrile (35.18%), acute symptomatic (27.58%) and idiopathic (16.6%), total was 44 cases (81.4%). Median length of PICU stay and days of mechanical ventilation were 3.02 ± 1.6 days and 1.24 ± 0.5 days respectively. Mortality was 5.3%. (16.6%) and total was 44 (81.4%).


Introduction
Status epilepticus (SE) is one of the most common emergencies in paediatric neurology and is associated with a high mortality and morbidity, with an incidence of 20 per 100,000 children per year [1] [2]. It is more frequent in children than in adults and occurs in a variety of settings, especially in children with infections, and patients with previously established epilepsy, cerebral malformations, hypoxia, hypoglycaemia and head trauma. In many cases, SE can be the first unprovoked manifestation of a seizure disorder. Mortality rates associated with SE in children between 3 and 20 percent have been reported, with higher rates noted if a significant metabolic disturbance is present or a delay in termination [3] [4]. Although many studies have been devoted to the clinical, Electro Encephalography (EEG) and neuropathological features of SE, however, little is known on etiological and prognostic features of SE. This paper therefore presents the etiological, clinical characteristics, effect of treatment and prognosis in a large group of children with status epilepticus, with special attention been paid to their intensive care course and the presence of anticonvulsant drug toxicity.

Materials and Methods
The study was approved by the ethics committee of the Royal Alexandra Hospital for Children, Westmead, Sydney, Australia. The international classification of disease (ICD-9-CM) codes for seizures (780.3), SE (345.3) and convulsions (345.9) were used to classify patients (Dreifuss et al., 1981). Sixty two (62)  3) Acute symptomatic: SE occurring during an acute illness with known CNS involvement (eg: meningitis) 4) Remote symptomatic: SE without acute causes occurring in patients with a prior history of CNS insult known to be associated with increased risk of convulsions 5) Progressive neurological occurring during progressive neuropathy (eg: neurocutaneous diseases) Utilizing the advice definitions, 54 patients were selected, 47 patients had generalized convulsive status (grand mal), 2 patients had partial SE, 3 patients had non-convulsive SE and 2 patients had tonic status. All patients' diagnoses were confirmed by computarized tomography (CT), Magnetic Resonance Imaging (MRI), Electro Encephalography (EEG), cerebrospinal fluid findings and(or) culture, except 2 patients who suffered neurofibromatosis and neurocutaneous disease (Sturge-Weber syndrome) who were documented by biopsy. The 2 patients who died underwent autopsy. All patients received standard initial evaluation and therapy including physical examination, Creatine Phosphokinase (CPK), Serum Glutamic Oxaloacetic (SGOT), Complete Blood Count (CBC), phenytoin and phenobarbital serum levels, and other anticonvulsant levels as indicated.
Parameters established by the hospital's clinical laboratory were used as acriteria for identifying therapeutic and subtherapeutic drug ranges. The therapeutic range for phenytoin was 40 -89 umol/L, phenobarbital 60 -120 umol/L and carbamazepine 15 -40 umol/L. Status Epilepticus is a medical emergency requiring prompt therapy. In the hospital, the treatment protocol used for SE consisted of three steps, similar to what others recommend: 1) Benzodiazepine (BZD) and Phenytoin (PHT) to terminate and prevent seizure recurrence. Main BZD used were Diazepam (DZP) and Clonazepam (CZP). Diazepam's initial dose was 0.25 -0.4 mg/kg (max 10 mg), rate of <2 mg/min. The dose often needed to be repeated within 10 -15 minutes (Max 40 mg over 24 hours). Some patients received rectal administration at an initial dose of 0.5 mg/kg (max 20 mg). Rectal DZP is most useful in prehospital settings. Phenytoin: IV loading dose of 15 -20 mg/grate < 0.5 -1.0 mg/kg/min (<4 years old) or 25 mg/min (>4 years old). The combination of IV DZP and PHT stopped seizures in almost all the patients.
If this approach fails: 2) Phenobarbitone (PB) as the third drug is added, loading dose of 20 mg/kg (max 100 mg), rate < 100 mg/min.
3) General anaesthesia (GA) is utilized if SE continues > 60 minutes or the first and second line drugs fail. Short barbiturate anaesthesia: this is induced by a short-acting barbiturate-thiopentone sodium, administered by IV at 30 mg/kg over 1 hour, then 5 mg/hr as maintenance infusion, increased to 10 -20 mg/kg/h. The patients were admitted to the PICU, intubated and adapted to and placed on assisted ventilation, continuous EEG and cardiorespiratory monitoring. Arterial and intravenous lines were placed in all patients. Anaesthesia was F. Y. Jiao et al.
usually maintained at this rate for approximately 24 hours. If seizure discharges return as the general anaesthesia is slowly withdrawn, EEG should be re-converted to burst suppression or isoelectric tracing with GA during the following 24 hours.

Age and Sex
Fifty four (54) cases with SE were identified. Of these, there were 33 males and 21 females. 24 (44.4%) cases were less than 3 years of age and 20 (37.1%) cases between 4 to 7 years of age. Together, they represented 44 (81.5%) cases. The average age was 5.3 years, with an age range of 3 months to 15 years old (see Table 1).

Etiology of Status Epilepticus
Etiology of SE was idiopathic in 9 cases, febrile in 19 cases and acute symptomatic in 16 cases. The most common etiologies of SE were febrile, idiopathic and acute symptomatic ( Table 2).

Type of Seizure
Grand mal was the commonest type and was seen in 47 cases (87.3%). The remaining cases included partial SE with 2 cases, tonic status with 2 cases and non-convulsant SE with 3 cases. Previously diagnosed and treated epilepsy was present in 12 (22.22%) cases.
In 2 cases, PICU admission was not required for the management of Status Epilepticus. One child had febrile SE and the other had lissencephaly, clinically requiring the use of phenobarbitone. In all the other cases, phenobarbitone use was associated with mechanical ventilation.
In one case, irritability developed and was attributed to phenobarbitone. The child who expired with ALL also had phenobarbitone injection. Phenobarbitone levels were not known in either case.

Outcome
Status Epilepticus (SE) is a serious problem, since it is often associated with high mortality if it persists longer than 60 minutes. Therefore, this medical emergency requires prompt therapies including a proper airway ensured, oxygen admi-   There were 12 patients with pre-existing epilepsy and 7 patients had anticonvulsant drug withdrawal before the onset of status, so this may have played a role in inducing SE in a minority of patients [14].
Mortality rate in our study was 5.3%. Another report indicated a rate of 6 to The most common complications of SE included pneumonia (4%) and tonsillitis (5%) and intracranial hypertension (5%). The existence of more than one medical complication was related to worse outcome. The most severe complica-  [17]. Consequently, the importance of prompt treatment of medical complications during SE has been stressed. In our study, SE was categorized by etiology, where known. The classification included febrile, acute symptomatic, idiopathic, remote symptomatic and progressive neurological categories ( Table 2).
Most of the presentations of SE required PICU admission. Most of the Paediatrics Intensive Care Unit (PICU) admissions required mechanical ventilation probably reflecting good clinical judgement of the Emergency and PICU physicians in selecting admitted cases.
This study confirmed the findings of Maytal, et al. (1989) regarding mortality.
Status epilepticus itself is associated with low mortality. It is the concurrent pathological processes (Acute CNS injury or progressive encephalopathy) that mostly determine the cause of death [7] [9] [10] [17].
There was great concern for the emergency or PICU physicians regarding the oversubscribing of benzodiazepines or barbiturates in the acute resuscitative period, hence the necessity for PICU admission. The use of phenytoin has been encouraged. Most emergency centers will recommend the use of intravenous phenytoin when the seizure persists for more than 30 minutes. According to this study, around 50% of the cases employed phenytoin for seizure control. In 21% (6/29) of children receiving intravenous phenytoin, the need for intubation was avoided and in terms of budget, 5 PICU beds were saved. However, it could not be established whether the SE stopped spontaneously because of the direct effect of phenytoin. 13.8% (4/29) of children receiving intravenous phenytoin suffered from acute cerebellar toxicity. Except for 1 child with a level of 270 umol/l, there was no correlation of complications with the levels, nor the prior treatment with phenytoin. There were no other side effects seen in this study, although we did not follow any of these children up after discharge. With this relatively small study, it seems the use of phenytoin should be encouraged to prevent the need for assisted ventilation and its possible adverse effects.
Most of the phenobarbitone use was in the febrile or the idiopathic group. It prevented only 2 mechanical ventilations. This might reflect the sedative nature of the drug itself. Only 1 behavioral side effect was recorded.
We have demonstrated that intravenously administered diazepam and phenytoin remained the first-line therapy for SE [18]. Phenytoin combined with diazepam is effective and safe. Furthermore, there has been a lot of research on whether intravenous (IV) levetiracetam or IV phenytoin is the better second line treatment for the emergency management of CSE in children [13] [19] [20] [21], suggesting that IV levetiracetam is safer and more effective. More than half of the patients will response to the initial treatment. Refractory cases of SE may necessitate treatment with high-dose phenobarbital or inhalation of anaesthetic agents. Proper airway must be ensured, oxygen administered, blood pressure supported and intracranial pressure controlled in a timely manner.
One of the most recent major advances in management of seizure disorders is availability of methods for rapid determination of anticonvulsant blood levels.
Dosage schedule of anticonvulsant can now be adjusted to maintain serum drug levels within the therapeutic ranges. This provides a means of checking patient compliance and provides insights of drug metabolism of these compounds in individual patients. This is particularly important in young infants who may have variable absorption, when seizures are uncontrolled on therapy, drug toxicity is suspected or changes in drug treatment are planned. Diazepam is a good agent to arrest SE, but should not be used in combination with phenobarbital because of the risk of hypotension and respiratory depression, particularly in infants [13] [17] [21].
This study is limited by a small sample size of 54 persons, therefore, further study should be carried out on a larger sample size. Also, this study was conducted in a short term, hence further studies should be carried out in a long term > 1 year.
The study therefore reviewed the clinical character, the management and outcome of status epilepticus in children.