This is a retrospective series of 21-patient cohort, 16 acute patients, studied as on-going acute vestibular syndrome/ataxia cohort (two telemedicine), and 5 outpatients. All underwent neurological and neurophthalmologic examination and nystagmus recordings, they had at least one abnormal ancillary test; low serum pre-treatment thiamine, or abnormal head MRI.
Nine patients had horizontal (h) nystagmus (two types: vestibular and gaze holding nystagmus); thiamine replacement led to rapid nystagmus resolution, and prevented encephalopathy in all (including one, who had also upbeat nystagmus/truncal ataxia (UBN/TA), one patient has chronic UBN/TA for one year with improving WE at a slower pace. Six patients had conversion from UBN to permanent downbeat nystagmus/truncal ataxia (DBN/TA), and slower WE recovery; one patient had improved UBN/TA. Three outpatients with permanent DBN/TA had a previous history and labs compatible with thiamine deficiency. One patient did not have nystagmus. None of the study-cohort patients developed Korsakoff’s syndrome (KS).