2002
DOI: 10.1053/seiz.2001.0601
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fMRI in patients implanted with a vagal nerve stimulator

Abstract: Our study in four patients shows fMRI can be performed safely in patients with an implanted vagal nerve stimulator. The successful use of fMRI during VNS offers potential advantages over PET imaging by allowing rapid image acquisition and the ability to repeatedly study patients over time. Our preliminary results differ from previous PET or SPECT studies in failing to detect changes in subcortical areas. This finding could be due to the smaller n in this study compared with the other studies.

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Cited by 60 publications
(35 citation statements)
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“…MRIs have been performed with the stimulator turned on to evaluate the impact of the stimulation. [88][89][90][91][92][93][94] In one study, the patient had a seizure on the table and diffusion weighted imaging demonstrated transient ischemia at the focus, which returned to normal at seizure completion. 95 …”
Section: Vns For Epilepsymentioning
confidence: 99%
“…MRIs have been performed with the stimulator turned on to evaluate the impact of the stimulation. [88][89][90][91][92][93][94] In one study, the patient had a seizure on the table and diffusion weighted imaging demonstrated transient ischemia at the focus, which returned to normal at seizure completion. 95 …”
Section: Vns For Epilepsymentioning
confidence: 99%
“…This has been confirmed electrophysiologically by showing increases in neuronal firing rates in those structures after acute VNS (Groves et al, 2005) or after long-term stimulation treatment in rats (Dorr and Debonnel, 2006). In humans in vivo, central effects of VNS, usually performed at about 30 Hz, have been studied mostly using electroencephalography (EEG) (Marrosu et al, 2005), positron emission tomography (PET) and single photon emission computer tomography (SPECT) (see (Chae et al, 2003) for a review) and functional magnetic resonance imaging (fMRI) (Bohning et al, 2001;Dietrich et al, 2008;Liu et al, 2003;Lomarev et al, 2002;Nahas et al, 2007;Narayanan et al, 2002;Sucholeiki et al, 2002). Despite a significant variability in reported findings, activations in the medulla/brainstem, limbic regions (insula, anterior cingulate cortex, hippocampus, amygdala, and hypothalamus), thalamus, cerebellum, and periaqueductal grey (PAG) were most commonly observed.…”
Section: Introductionmentioning
confidence: 99%
“…A recent SPECT study suggested that 4 weeks of active VNS therapy in depression is associated with decreased activity in hippocampus and amygdala and increased activity in left prefrontal cortex (Zobel et al, 2005). Researchers have also used functional MRI (fMRI) to investigate VNS in epilepsy (Narayanan et al, 2002;Sucholeiki et al, 2002;Liu et al, 2003) and depression (Maniker et al, 2000;Bohning et al, 2001;Lomarev et al, 2002;Mu et al, 2004). Initial studies of depressed participants showed the feasibility of performing VNS-synchronized fMRI studies and compared the location and amount of blood oxygenation level dependent (BOLD) signal change caused by acute VNS for 7 s with the period when the device was not firing (Bohning et al, 2001).…”
Section: Introductionmentioning
confidence: 99%