Policies of administration and availability of EEG offered during nonbusine
ss hours vary widely among EEG laboratories. The authors surveyed medical d
irectors of accredited EEG laboratories (n = 84) to determine the ranges of
availability and clinical indications for approval of continuously availab
le emergent EEG (E-EEG). Of 46 respondents. 37 (80%) offered E-EEG. Two cen
ters recently lost funding for E-EEG. Availability was not associated with
the total number of EEGs performed annually. The mean estimated response ti
me from request to expert interpretation was 3 +/- 4 hours (range, 1-24 hou
rs). The five clinical indications for which most respondents approved E-EE
Gs were possible nonconvulsive status epilepticus (100%), treatment of stat
us epilepticus (84%). cerebral death exam (81%), diagnosis of convulsive st
atus epilepticus (79%), and diagnosis of coma or encephalopathy (70%). Resp
ondents disagreed widely when asked which clinical situations merited E-EEG
. with some approving all requests and others denying all except for noncon
vulsive status epilepticus. The wide range of current practice suggests tha
t research focused on outcomes of aggressive, EEG-aided patient evaluation
and treatment are needed to define better the costs and benefits of a conti
nuously available EEG service.