1IntroductionImbalances in oxidation-reduction potential (ORP), or redox status,o fh uman plasma are the result of an increasedp roduction of reactiveo xygen species (ROS)/reactive nitrogen species (RNS), ad ecrease in levels of endogenous non-enzymatic antioxidants,adecrease in antioxidante nzyme activity (such as superoxide dismutase (SOD),c atalase, and reduced nicotinamide adenined inucleotide( NADH) peroxidase), and/or ani nterference with mitochondrialo xidative phosphorylation [1,2].O xidative damage caused by an imbalance in redox status has been associated with the pathophysiology of acute clinicalc onditions including but not limited to traumatic brain injury (TBI), multiple trauma, sepsis,a nd stroke (Table 1) [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17].Reductive stress, whichc an result from an over-compensatory mechanism to oxidatives tress,m ay cause mitochondrial dysfunction and has deleterious effects on health [18][19][20].R OS generated by mitochondria can also result in both oxidative and reductive stress [18,19].T he criticalr ole of oxidative and reductive stress in disease is mainly due to damage to electron-rich biological targets such as lipids,p roteins,a nd DNA[ 1].C urrentm ethods for determiningr edox status therefore mainly utilize assays that allow assessment of damage caused to these individual biological targets.Unlike the assessment of as ingle biomarker of oxidative stress,a ssessing the ORP of ab iological sample provides ac omprehensive measureo fr edox status without lookingfor any particular molecule.ORP provides acomposite measurement of the balance between oxidants and antioxidants in as ample and thus does not rely on any single biomarker of redox stress.F urthermore,d etermining ORP does not require processing,p urification, or isolation of specific biomarkers,a nd reflects changes in redox status under conditions in which modificationso f individual targets are not detected. This important characteristic of measuring ORP makes it av ery valuable research tool readily applicable to ac linical lab setting. Despite the utility of measuring ORP over any single biomarker of redoxs tress,aplatform that allows for the fast Abstract:T he barriers to using plasma redoxp otential as am easure of oxidative stress in patients are the use of specialized equipment, necessity of sterilization between tests,a nd inconsistent electrodes urfaces and cell geometry.T hese problems are resolved using disposable test strips with built in electrochemicalc ells.M easuring the electrode potential at as mallc urrent yields as table value that is~50 mV higherf or isolated traumatic brain injury (ITBI) patients than for healthyi ndividuals.E ven with naturalv ariations within blood chemistry, this simple method may be clinically useful for assessing the degree of oxidative stress and injury severity in ITBI patients.