Âé¶¹´«Ã½Ó³»­

Âé¶¹´«Ã½Ó³»­

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Longitudinal Changes in Driving Behavior Following Antibody-Mediated Encephalitis
Autoimmune Neurology
P11 - Poster Session 11 (8:00 AM-9:00 AM)
15-001
Evaluate naturalistic driving behaviors in patients recovering from antibody-mediated encephalitis (AME).

Safe driving requires integration of higher-order cognitive and motor functions. Impairment in these functions is common in patients diagnosed with AME, but may improve with appropriate treatment. The time course over which this improvement occurs and its association with driving behaviors are unknown.

Recovering AME patients were recruited from tertiary care clinics at Washington University (Saint Louis, MO). All patients met diagnostic criteria for AME associated with NMDAR (n=2) or LGI1 autoantibodies (n=3). Patients were >21 years-old, had ≥5 years of pre-illness on-road driving experience, and were cleared by their assessing physician to return to driving. Patients consented to installation of a commercial global positioning system data logger—termed the Driving Real World In-Vehicle Evaluation System (DRIVES)—into their private vehicle. Trip data and aggressive actions (e.g., hard braking, sudden acceleration, speeding) were continuously recorded each time the vehicle was driven by the designated driver. DRIVES data were compared between AME patients and a cohort of 2:1 sex-matched cognitively normal individuals enrolled within parallel studies.

Driving behaviors were measured in 5 AME patients (2 females, age range: 28-67 years) beginning with return to driving (median 1.8 months post-diagnosis; range, 0.4-3.8) and continuing for 14 months. When compared to cognitively normal individuals, AME patients were increasingly more likely to take trips ≥10 miles (0.22±0.1 vs. -0.09±0.06 trips per week; p=0.048) and to experience hard braking events (0.2±0.08 vs. -0.01±0.05 events per week; p=0.06) across the follow-up period. No accidents were self-reported by patients or captured by the DRIVES.

The DRIVES provided robust measures of in vivo driving behaviors in recovering AME patients. Longitudinal changes may reflect normalization of driving behaviors (e.g., taking longer trips into more congested areas), paralleling recovery in AME patients.
Authors/Disclosures
Gregory S. Day, MD, MSc, FÂé¶¹´«Ã½Ó³»­ (Mayo Clinic)
PRESENTER
Dr. Day has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Arialys Therapeutics. Dr. Day has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for DynaMed (EBSCO Health). Dr. Day has or had stock in ANI Pharmaceuticals. The institution of Dr. Day has received research support from National Institutes of Health / NIA. The institution of Dr. Day has received research support from National Institutes of Health / NINDS. The institution of Dr. Day has received research support from Amgen Pharmaceuticals. The institution of Dr. Day has received research support from AVID Radiopharmaceuticals. Dr. Day has received personal compensation in the range of $500-$4,999 for serving as a Presenter at Annual Meeting (CME) with Âé¶¹´«Ã½Ó³»­. Dr. Day has received personal compensation in the range of $500-$4,999 for serving as a Content Development (CME) with PeerView, Inc. Dr. Day has received personal compensation in the range of $5,000-$9,999 for serving as a Content Development (CME) with Continuing Âé¶¹´«Ã½Ó³»­, Inc. Dr. Day has received personal compensation in the range of $5,000-$9,999 for serving as a Content Development (CME) with Ionis Pharmaceuticals. Dr. Day has received personal compensation in the range of $500-$4,999 for serving as a Âé¶¹´«Ã½Ó³»­al Case Development + Presentation (video) with PeerDirect (P\S\L Group). Dr. Day has received personal compensation in the range of $500-$4,999 for serving as a Content Development / Presentation (non-CME) with MJH Life Sciences (NeurologyLive). Dr. Day has a non-compensated relationship as a Clinical Director with Anti-NMDA Receptor Encephalitis Foundation that is relevant to Âé¶¹´«Ã½Ó³»­ interests or activities.
Ganesh Babulal, PhD, OTD, MSCI, MOT (Washington University School of Medicine) Ganesh Babulal, PhD, OTD, MSCI, MOT has nothing to disclose.
No disclosure on file
No disclosure on file
Catherine M. Roe, PhD No disclosure on file