Single-photon emission tomography (SPET) brain imaging in epilepsy has beco
me an increasingly important noninvasive tool in localizing the epileptogen
ic site. Ictal SPET demonstrates the highest localization sensitivity as co
mpared with postictal and interictal SPET. While ictal SPET consistently re
veals hyperperfusion at the epileptogenic site, postictal SPET reveals eith
er hyper- or hypoperfusion depending on the timing of radiopharmaceutical i
njection. Much discussion in the literature exists about exactly when the t
ransition from hyper- to hypoperfusion occurs at the epileptogenic site in
postictal SPET The systematic examination of two clinical variables - time
of injection from seizure onset and offset - was useful in understanding po
stictal perfusion changes. Twenty-seven patients with medically refractory
epilepsy receiving postictal and interictal SPET scans were studied. Quanti
tative SPET difference imaging was used to evaluate perfusion changes in re
lationship to injection time. Perfusion changes were found to reflect the t
ime of injection in relation to seizure onset, but to be somewhat independe
nt of seizure offset. Thus, the majority of patients (8/12, 67%) receiving
postictal injections within 100 s after seizure onset demonstrated hyperper
fusion, while all patients (15/15, 100%) receiving postictal injections mor
e than 100 s after seizure onset showed hypoperfusion. The explanation of t
his phenomenon is unknown but the findings appear to parallel known changes
in cerebral lactate levels.