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376                                                  Lilach Bareket et al.


          risks of: infection (1%–2%) which could necessitate re-exploration and
          removal of the cranial bone flap or its replacement, hemorrhage requiring
          reoperation (1%), and possible injury to the sagittal or transverse venous
          sinuses which are at the edge of an occipital craniotomy exposing the visual
          cortex (Bjornsson et al., 2006). A craniotomy carries a small risk of infection
          (1%–2%) which could necessitate re-exploration and removal of the cranial
          bone flap or its replacement, and hemorrhage requiring reoperation (1%).
          There is a small risk of injury to the sagittal or transverse venous sinuses
          which are at the edge of an occipital craniotomy exposing the visual cortex.
          Local brain injury due to the insertion of the electrodes may cause micro-
          hemorrhage, local scarring, and loss of neurons. This would further impair
          the transmission of current into the brain (Bjornsson et al., 2006).
             Chronic focal stimulation of cerebral cortex may also cause development
          of epilepsy through a process called kindling, where this focal area of cortex
          becomes an independent generator of seizure activity (Goddard, 1967;
          Morimoto et al., 2004). The seizure activity may spread to other parts of
          the brain depending on the magnitude of electric currents passing through
          the cortex, the duration of the stimulation, and the individual’s threshold for
          seizure activation (Goddard, 1967; Morimoto et al., 2004). The potential for
          kindling of epileptic seizures may be increased if the patient has a history of
          epilepsy. The risk of seizures can be mitigated by low-stimulation currents
          (10s of μA range), limiting temperature rise, intermittent stimulation pat-
          terns rather than the same electrode firing constantly, and prophylactic anti-
          epileptic drugs (AEDs). These drugs, however, may also render the neurons
          less responsive (refractory) to the stimulation by the electrodes so a careful
          balance should be achieved (Bezard et al., 1999).




               4 ON AND LGN PROSTHESES
               Besides the great progress in restoration of visual sensation through
          retinal and cortical prostheses, electrical stimulation of the ON (Veraart
          et al., 2003; Sakaguchi et al., 2012) or the LGN (Panetsos et al., 2011;
          Pezaris and Eskandar, 2009) is also being investigated.
             The first to attempt a visual prosthesis based on stimulation of the ON
          were Veraart et al. (1998). The patient (blind due to RP) received a
          four-contact silicon cuff array implanted around the intracranial section of
          the ON. The four electrodes were located at 90-degree intervals, to enable
          stimulation to the entire visual field. Colored phosphenes were reproducibly
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