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Neurological Assessment and Monitoring 439

             have  been  developed  to  assist  nurses  when  caring  for   evaluating  cerebral  circulation  and  haemodynamics.
             patients with jugular bulb oximetry. 71              Pulses of ultrasound are directed using a handheld trans-
                                                                  ducer towards the vascular formations in the base of the
             Partial Brain Tissue Oxygenation Monitoring          skull.  Velocities  from  the  cerebral  arteries,  the  internal
             Changes  in  ICP  values  alone  do  not  accurately  depict   carotids,  the  basilar  and  the  vertebral  arteries  can  be
             poor cerebral blood flow or oxygenation deficits to brain   sampled  by  altering  transducer  location,  angle  and  the
             tissue.  Consequently  brain  tissue  hypoxaemia  is  often   instrument’s depth setting. The commonest windows in
             observed  during  the  first  24  hours  after  injury  despite   the cranium are located in the orbit (of the eye), and in
             controlled brain pressures. Monitoring partial pressure of   the  temporal  and  suboccipital  regions.  TCD  measures
             oxygen  in  brain  tissue  (PbtO 2 )  can  be  used  to  collect   systolic, diastolic and mean middle cerebral artery (MCA)
             more  accurate  and  timely  information  about  cerebral   flow velocities and a derived value, the pulsatility index
             oxygen  delivery  and  demand  than  ICP  allows.  A  tissue   (PI). Changes in the PI can be used to identify the thresh-
             oxygen  value  of  less  than  10 mmHg  for  more  than  10   old of autoregulation or cerebral perfusion pressure break
             minutes  carries  a  higher  risk  of  death.  Normal  brain   point  in  individual  patients.  In  subarachnoid  haemor-
             oxygen levels (PbtO 2  between 20 and 25 mmHg) emerge   rhage (SAH) and TBI this may be due to vasospasm, or
             as a critical determinant of outcome, with values below   impaired autoregulation or abnormal intracranial com-
             20 mmHg carrying a higher risk. 69                   pliance. TCD is a simple, portable and non-invasive tool,
                                                                  well suited to serial monitoring, that can be used at the
             Regardless of ICP, brain tissue oxygenation falls with a   bedside to detect relative changes in CBF in brain-injured
             decrease  in  cerebral  blood  flow  below  an  ischaemic   patients. 76
             threshold of 18 mL/100 g/min. ICP may respond to the
             changes but often several hours later when the damage   Continuous Electroencephalography
             can not be reversed. Alterations in cerebral metabolic rate   Electroencephalography (EEG) is the recording of electri-
             can  also  change  tissue  oxygen  levels.  Reducing  the   cal activity by sensors along the scalp produced by the
             patient’s energy consumption via reduced noise and/or   firing  of  neurons  within  the  brain.  Continuous  EEG
             distractions, and increasing their protein caloric intake to   (cEEG) has the advantage of being continuous, noninva-
             complement  their  increased  stress  state  can  improve   sive  and  carrying  the  potential  to  detect  alterations  in
             tissue oxygenation. 72                               brain physiology at a reversible stage, which may trigger
                                                                  treatment  before  permanent  brain  injury  occurs.  The
             Microdialysis                                        invention of digital EEG has made cEEG monitoring fea-
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             Cerebral microdialysis (using a catheter ideally placed in   sible for ICU patients.  Currently, the main applications
             the frontal lobe) is a tool for investigating the metabolic   of cEEG are diagnosing nonconvulsive status epilepticus,
             status  of  the  injured  brain  and  is  part  of  multimodal   monitoring and guiding the treatment of status epilepti-
             monitoring. The microdialysis probe is inserted into the   cus and detecting delayed cerebral ischaemia from vaso-
             cerebral tissue where substances in the extracellular fluid   spasm  in  subarachnoid  haemorrhage  patients.  Other
             surround the semipermeable membrane at the tip of the   applications may include monitoring of reperfusion after
             catheter. Following equilibration of the tissue metabolites   tissue plasminogen activator in acute stroke patients and
             with the perfusion fluid, the dialysate can be analysed for   detection of intracranial hypertension. Clinically unrec-
             concentrations of products of energy metabolism (glucose,   ognised electrographic seizures and periodic epileptiform
             lactate, pyruvate) as indicators of hypoxia and ischaemia.   discharges have been shown to be frequent and associ-
             In addition, interstitial glycerol can be determined, which   ated  with  poor  outcome  in  patients  with  severe  brain
             is a parameter of lipolysis and/or cell membrane damage.   injury from different aetiologies, including TBI, ischaemic
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             In  theory,  the  microdialysis  catheter  acts  like  a  blood   and haemorrhagic strokes and CNS infection.  The EEG
                     73
             capillary.  Thereby, it is proposed that microdialysis pro-  becomes substantially abnormal (suppressed) when cere-
             vides information regarding events that take place in the   bral blood flow declines to 20–30 mL/100 g/min. More
             tissue before any chemical events are reflected by changes   subtle abnormalities accompany lesser degrees of hypo-
                                                       74
             in systemic blood levels of indicator substances.  These   perfusion, including initial loss of beta activity, slowing
             molecules diffuse across the membrane part of the cath-  to the theta range, and then to the delta range. Irreversible
             eter  and  equilibrate  with  the  perfusion  fluid,  which  is   injury  to  brain  tissue  occurs  at  cerebral  flows  of  about
             pumped  through  the  probe  at  very  low  rates  of  flow.   10–12 mL/100 g/min. Thus, the EEG sensitivity to isch-
             Changes in the concentration of a substrate in the sur-  aemia allows its use in situations where cerebral perfu-
                                                                               79
             rounding milieu are reflected by subsequent changes in   sion is at risk.  To facilitate interpretation, digital EEG
                        75
             the dialysate.  Rather than inserting an instrument into   data can be transformed into power spectra by fast Fourier
             the tissue, microdialysate is extracted and later analysed   transformation. Changes over time in these quantitative
             in the laboratory or clinically at the patient’s bedside.  EEG  (qEEG)  parameters  can  trigger  remote  reading,
                                                                  focused neurological examination, imaging studies and
             NON-INVASIVE ASSESSMENT                              early treatment. Subtle EEG changes may be difficult to
             Transcranial Doppler                                 interpret in isolation, but may be better understood when
                                                                  interpreted in concert with other components of a mul-
             Transcranial Doppler (TCD) ultrasound has proven to be   timodality  monitoring  paradigm,  which  may  include
             a  safe,  reliable  and  relatively  inexpensive  technology     microdialysis, brain tissue oxygen and cerebral perfusion
             for  measuring  cerebrovascular  blood  velocities  and   pressure.
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