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Abstract Details

Acute seizure risk in encephalitis; analysis and modelling of 436 patients from two independent multi-centre cohorts
Infectious Disease
S38 - All Things HIV and ID (4:54 PM-5:06 PM)
008
Acute seizures in encephalitis are common, associated with worse outcome, and potentially amenable to treatment. However, it is unclear which patients are at greatest risk and therefore may benefit from primary anti-epileptic prophylaxis.

We aimed to determine the demographic, clinical and investigatory factors associated with seizures in encephalitis and develop a risk-stratification score.

We performed an analysis of 203 patients from 24 English hospitals (2005-2008) (Cohort 1). Outcome measures were seizures, inpatient seizures, and status epilepticus. A binary logistic regression risk model was converted to a clinical score and independently validated on 233 patients in the Enceph-UK study (2013-2016) (Cohort 2).

In Cohort 1, 121 (60%) patients had a seizure including 103 (51%) with witnessed inpatient seizures. Seizures were associated with fever (OR [95%CI] 2.21[1.13-4.34], p=0.019) and aetiology (p=0.003). Admission Glasgow coma scale (GCS) ≤8/15 was predictive of subsequent inpatient seizures (OR 5.55[2.10-14.64], p<0.001), including in those not presenting with seizures (OR 6.57[1.37-31.5], p=0.025). Status epilepticus occurred in 19 (9%) and was associated with fever (p=0.009).

A clinical score of seizure risk identified aetiology and admission GCS (AUROC = 0.775 [0.701-0.848]). The same model was validated in Cohort 2 (AUROC = 0.744 [0.677-0.811], p<0.001). Of patients with a low-risk score 14/57 (25%) had an inpatient seizure (reference group), of medium-risk 22/46 (48%; OR 2.82[1.22-6.49], p=0.015), of high-risk 23/31 (74%; 8.83[3.23-24.14], p<0.001) and of very high-risk 13/15 (87%;19.96[4.00-99.50], p<0.001). Although patients with seizures had a shorter pre-admission symptom duration (5[1-12] vs. 9[4-24] days, p=0.01), they had a worse outcome (Glasgow Outcome Scale<5 OR 1.81[1.01-3.23], p=0.04).

A small number of variables can effectively stratify acute seizure risk in patients with encephalitis. These findings can support the development of targeted interventions and aid clinical trial design.

Authors/Disclosures
Greta K. Wood, MBBS (University of Liverpool)
PRESENTER
Dr. Wood has nothing to disclose.
Mark A. Ellul, MD No disclosure on file
No disclosure on file
Ava M. Easton, PhD (The Encephalitis Society) Dr. Easton has received personal compensation for serving as an employee of Encephalitis Society. Dr. Easton has received publishing royalties from a publication relating to health care.
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
Angela Vincent, MBBS, MSc (John Radcliffe Hospital) Angela Vincent, MBBS,MSc has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Janssen. Angela Vincent, MBBS,MSc has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for UCB. Angela Vincent, MBBS,MSc has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Alexion. Angela Vincent, MBBS,MSc has received intellectual property interests from a discovery or technology relating to health care. Angela Vincent, MBBS,MSc has received intellectual property interests from a discovery or technology relating to health care.
Tom Solomon, MD (The University of Liverpool) No disclosure on file
No disclosure on file