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Abstract Details

Predictive Value of Consensus Criteria for the Early Detection of Pediatric Autoimmune Encephalitis
Child Neurology and Developmental Neurology
Child Neurology and Developmental Neurology Posters (7:00 AM-5:00 PM)
057
To determine the positive predictive value (PPV) and negative predictive value (NPV) of diagnostic consensus criteria for pediatric autoimmune encephalitis (AE) throughout the early disease process.

The diagnosis and treatment of AE is often delayed due to symptoms that overlap with other diagnoses including infectious encephalitis. Outcomes are best if treatment is started within the first month of symptom onset. Clinical criteria (Graus et al 2016) have been published to aid in earlier recognition of AE, and more recently, consensus criteria for pediatric AE (Cellucci et al 2020) were proposed. However, the predictive value of these criteria in the early stages of the disease have not yet been evaluated.

A retrospective chart review of patients presenting to Children’s Hospital Colorado with suspicion for encephalitis over the past 11 years was performed. Patients ≤ 18 years of age with a final diagnosis of antibody-positive or antibody-negative AE, or etiology-confirmed viral encephalitis were included in analysis. PPV and NPV were calculated for each set of clinical criteria for possible AE at multiple time points (1, 2, and 4 weeks after initial onset of neuropsych symptoms).

The data is still being processed, with 50 autoimmune and 15 infectious encephalitis cases expected.  Our hypothesis is that the pediatric consensus criteria will demonstrate improved PPV and NPV for detection of pediatric AE compared to prior criteria, and will assist in diagnosis at early time points.

The early initiation of immunotherapies in AE is important to improve clinical outcomes and decrease hospital stays. This requires a reliable method for the early diagnosis of AE.  Our data evaluating the accuracy of the 2020 consensus criteria for pediatric AE early in the disease process will help clinicians and researchers better understand the role of these criteria in clinical practice for children presenting with suspicion for encephalitis.

Authors/Disclosures
Tiffany Pointon, MD
PRESENTER
Dr. Pointon has nothing to disclose.
Ryan Kammeyer, MD (Childrens Hospital Colorado) The institution of Dr. Kammeyer has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Amgen. The institution of Dr. Kammeyer has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. Dr. Kammeyer has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Ogborn-Mihm Trial Lawyers. The institution of Dr. Kammeyer has received research support from Rocky Mountain Multiple Sclerosis Center.
No disclosure on file
Teri Schreiner, MD, MPH, FÂé¶¹´«Ã½Ó³»­ (University of Colorado/ Children's Hospital of Colorado) The institution of Dr. Schreiner has received personal compensation in the range of $500-$4,999 for serving as a Consultant for CDC. Dr. Schreiner has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. The institution of Dr. Schreiner has received research support from Roche Genentech.