Semin Neurol 2017; 37(01): 019-024
DOI: 10.1055/s-0036-1597833
Review Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

The Brain after Cardiac Arrest

Jonathan Elmer
1   Department of Emergency Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania
2   Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania
,
Clifton W. Callaway
1   Department of Emergency Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania
› Author Affiliations
Further Information

Publication History

Publication Date:
01 February 2017 (online)

Abstract

Cardiac arrest is common and deadly. Most patients who are treated in the hospital after achieving return of spontaneous circulation still go on to die from the sequelae of anoxic brain injury. In this review, the authors provide an overview of the mechanisms and consequences of postarrest brain injury. Special attention is paid to potentially modifiable mechanisms of secondary brain injury including seizures, hyperpyrexia, cerebral hypoxia and hypoperfusion, oxidative injury, and the development of cerebral edema. Finally, the authors discuss the outcomes of cardiac arrest survivors with a focus on commonly observed patterns of injury as well as the scales used to measure patient outcome and their limitations.

 
  • References

  • 1 Mozaffarian D, Benjamin EJ, Go AS , et al; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics--2015 update: a report from the American Heart Association. Circulation 2015; 131 (4) e29-e322
  • 2 Lozano R, Naghavi M, Foreman K , et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012; 380 (9859): 2095-2128
  • 3 Nolan JP, Hazinski MF, Aickin R , et al. Part 1: Executive summary: 2015 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations. Resuscitation 2015; 95: e1-e31
  • 4 Kleinman ME, Brennan EE, Goldberger ZD , et al. Part 5: Adult Basic Life Support and Cardiopulmonary Resuscitation Quality: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2015; 132 (18, Suppl 2) S414-S435
  • 5 Callaway CW, Donnino MW, Fink EL , et al. Part 8: Post-cardiac arrest care: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2015; 132 (18, Suppl 2) S465-S482
  • 6 Conrad M, Angeli JP, Vandenabeele P, Stockwell BR. Regulated necrosis: disease relevance and therapeutic opportunities. Nat Rev Drug Discov 2016; 15 (5) 348-366
  • 7 Safar P, Behring W. Brain resuscitation after cardiac arrest. In: Layon AJ, Gabrielli A, Friedman WA, , eds. Textbook of neurointensive care. Philadelphia: Saunders; 2004: 457-498
  • 8 Greer DM. Mechanisms of injury in hypoxic-ischemic encephalopathy: implications to therapy. Semin Neurol 2006; 26 (4) 373-379
  • 9 Callaway CW, Ramos R, Logue ES, Betz AE, Wheeler M, Repine MJ. Brain-derived neurotrophic factor does not improve recovery after cardiac arrest in rats. Neurosci Lett 2008; 445 (1) 103-107
  • 10 Teschendorf P, Vogel P, Wippel A , et al. The effect of intracerebroventricular application of the caspase-3 inhibitor zDEVD-FMK on neurological outcome and neuronal cell death after global cerebral ischaemia due to cardiac arrest in rats. Resuscitation 2008; 78 (1) 85-91
  • 11 Derwall M, Timper A, Kottmann K, Rossaint R, Fries M. Neuroprotective effects of the inhalational anesthetics isoflurane and xenon after cardiac arrest in pigs. Crit Care Med 2008; 36 (11, Suppl) S492-S495
  • 12 Hicks SD, DeFranco DB, Callaway CW. Hypothermia during reperfusion after asphyxial cardiac arrest improves functional recovery and selectively alters stress-induced protein expression. J Cereb Blood Flow Metab 2000; 20 (3) 520-530
  • 13 Horn M, Schlote W. Delayed neuronal death and delayed neuronal recovery in the human brain following global ischemia. Acta Neuropathol 1992; 85 (1) 79-87
  • 14 Au AK, Chen Y, Du L , et al. Ischemia-induced autophagy contributes to neurodegeneration in cerebellar Purkinje cells in the developing rat brain and in primary cortical neurons in vitro. Biochim Biophys Acta 2015; 1852 (9) 1902-1911
  • 15 Metter RB, Rittenberger JC, Guyette FX, Callaway CW. Association between a quantitative CT scan measure of brain edema and outcome after cardiac arrest. Resuscitation 2011; 82 (9) 1180-1185
  • 16 Oku K, Kuboyama K, Safar P , et al. Cerebral and systemic arteriovenous oxygen monitoring after cardiac arrest. Inadequate cerebral oxygen delivery. Resuscitation 1994; 27 (2) 141-152
  • 17 Wolfson Jr SK, Safar P, Reich H , et al. Dynamic heterogeneity of cerebral hypoperfusion after prolonged cardiac arrest in dogs measured by the stable xenon/CT technique: a preliminary study. Resuscitation 1992; 23 (1) 1-20
  • 18 Nishizawa H, Kudoh I. Cerebral autoregulation is impaired in patients resuscitated after cardiac arrest. Acta Anaesthesiol Scand 1996; 40 (9) 1149-1153
  • 19 Sundgreen C, Larsen FS, Herzog TM, Knudsen GM, Boesgaard S, Aldershvile J. Autoregulation of cerebral blood flow in patients resuscitated from cardiac arrest. Stroke 2001; 32 (1) 128-132
  • 20 Schaafsma A, de Jong BM, Bams JL, Haaxma-Reiche H, Pruim J, Zijlstra JG. Cerebral perfusion and metabolism in resuscitated patients with severe post-hypoxic encephalopathy. J Neurol Sci 2003; 210 (1-2): 23-30
  • 21 Buunk G, van der Hoeven JG, Meinders AE. Cerebrovascular reactivity in comatose patients resuscitated from a cardiac arrest. Stroke 1997; 28 (8) 1569-1573
  • 22 Hickey RW, Kochanek PM, Ferimer H, Alexander HL, Garman RH, Graham SH. Induced hyperthermia exacerbates neurologic neuronal histologic damage after asphyxial cardiac arrest in rats. Crit Care Med 2003; 31 (2) 531-535
  • 23 Rittenberger JC, Popescu A, Brenner RP, Guyette FX, Callaway CW. Frequency and timing of nonconvulsive status epilepticus in comatose post-cardiac arrest subjects treated with hypothermia. Neurocrit Care 2012; 16 (1) 114-122
  • 24 Rossetti AO, Carrera E, Oddo M. Early EEG correlates of neuronal injury after brain anoxia. Neurology 2012; 78 (11) 796-802
  • 25 Youn CS, Callaway CW, Rittenberger JC ; Post Cardiac Arrest Service. Combination of initial neurologic examination and continuous EEG to predict survival after cardiac arrest. Resuscitation 2015; 94: 73-79
  • 26 Friberg H, Westhall E, Rosén I, Rundgren M, Nielsen N, Cronberg T. Clinical review: Continuous and simplified electroencephalography to monitor brain recovery after cardiac arrest. Crit Care 2013; 17 (4) 233
  • 27 Coppler PJ, Elmer J, Calderon L , et al; Post Cardiac Arrest Service. Validation of the Pittsburgh Cardiac Arrest Category illness severity score. Resuscitation 2015; 89: 86-92
  • 28 Ames III A, Wright RL, Kowada M, Thurston JM, Majno G. Cerebral ischemia. II. The no-reflow phenomenon. Am J Pathol 1968; 52 (2) 437-453
  • 29 Beylin ME, Perman SM, Abella BS , et al. Higher mean arterial pressure with or without vasoactive agents is associated with increased survival and better neurological outcomes in comatose survivors of cardiac arrest. Intensive Care Med 2013; 39 (11) 1981-1988
  • 30 Kilgannon JH, Roberts BW, Jones AE , et al. Arterial blood pressure and neurologic outcome after resuscitation from cardiac arrest*. Crit Care Med 2014; 42 (9) 2083-2091
  • 31 Schneider AG, Eastwood GM, Bellomo R , et al. Arterial carbon dioxide tension and outcome in patients admitted to the intensive care unit after cardiac arrest. Resuscitation 2013; 84 (7) 927-934
  • 32 Roberts BW, Kilgannon JH, Chansky ME, Mittal N, Wooden J, Trzeciak S. Association between postresuscitation partial pressure of arterial carbon dioxide and neurological outcome in patients with post-cardiac arrest syndrome. Circulation 2013; 127 (21) 2107-2113
  • 33 Carmona Suazo JA, Maas AI, van den Brink WA, van Santbrink H, Steyerberg EW, Avezaat CJ. CO2 reactivity and brain oxygen pressure monitoring in severe head injury. Crit Care Med 2000; 28 (9) 3268-3274
  • 34 Elmer J, Scutella M, Pullalarevu R , et al; Pittsburgh Post-Cardiac Arrest Service (PCAS). The association between hyperoxia and patient outcomes after cardiac arrest: analysis of a high-resolution database. Intensive Care Med 2015; 41 (1) 49-57
  • 35 Kilgannon JH, Jones AE, Shapiro NI , et al; Emergency Medicine Shock Research Network (EMShockNet) Investigators. Association between arterial hyperoxia following resuscitation from cardiac arrest and in-hospital mortality. JAMA 2010; 303 (21) 2165-2171
  • 36 Xiao F, Arnold TC, Zhang S , et al. Cerebral cortical aquaporin-4 expression in brain edema following cardiac arrest in rats. Acad Emerg Med 2004; 11 (10) 1001-1007
  • 37 Elmer J, Torres C, Aufderheide TP , et al; Resuscitation Outcomes Consortium. Association of early withdrawal of life-sustaining therapy for perceived neurological prognosis with mortality after cardiac arrest. Resuscitation 2016; 102: 127-135
  • 38 Cronberg T, Brizzi M, Liedholm LJ , et al. Neurological prognostication after cardiac arrest--recommendations from the Swedish Resuscitation Council. Resuscitation 2013; 84 (7) 867-872
  • 39 Wijdicks EF, Hijdra A, Young GB, Bassetti CL, Wiebe S ; Quality Standards Subcommittee of the American Academy of Neurology. Practice parameter: prediction of outcome in comatose survivors after cardiopulmonary resuscitation (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 2006; 67 (2) 203-210
  • 40 Sandroni C, Cariou A, Cavallaro F , et al. Prognostication in comatose survivors of cardiac arrest: an advisory statement from the European Resuscitation Council and the European Society of Intensive Care Medicine. Intensive Care Med 2014; 40 (12) 1816-1831
  • 41 Gold B, Puertas L, Davis SP , et al. Awakening after cardiac arrest and post resuscitation hypothermia: are we pulling the plug too early?. Resuscitation 2014; 85 (2) 211-214
  • 42 Larsson E, Lindvall O, Kokaia Z. Stereological assessment of vulnerability of immunocytochemically identified striatal and hippocampal neurons after global cerebral ischemia in rats. Brain Res 2001; 913 (2) 117-132
  • 43 Björklund E, Lindberg E, Rundgren M, Cronberg T, Friberg H, Englund E. Ischaemic brain damage after cardiac arrest and induced hypothermia--a systematic description of selective eosinophilic neuronal death. A neuropathologic study of 23 patients. Resuscitation 2014; 85 (4) 527-532
  • 44 Tiainen M, Poutiainen E, Oksanen T , et al. Functional outcome, cognition and quality of life after out-of-hospital cardiac arrest and therapeutic hypothermia: data from a randomized controlled trial. Scand J Trauma Resusc Emerg Med 2015; 23: 12
  • 45 Sabedra AR, Kristan J, Raina K , et al; Post Cardiac Arrest Service. Neurocognitive outcomes following successful resuscitation from cardiac arrest. Resuscitation 2015; 90: 67-72
  • 46 Harper SJ, Wilkes RG. Posthypoxic myoclonus (the Lance-Adams syndrome) in the intensive care unit. Anaesthesia 1991; 46 (3) 199-201
  • 47 Welsh JP, Yuen G, Placantonakis DG , et al. Why do Purkinje cells die so easily after global brain ischemia? Aldolase C, EAAT4, and the cerebellar contribution to posthypoxic myoclonus. Adv Neurol 2002; 89: 331-359
  • 48 Venkatesan A, Frucht S. Movement disorders after resuscitation from cardiac arrest. Neurol Clin 2006; 24 (1) 123-132
  • 49 Sieber FE, Palmon SC, Traystman RJ, Martin LJ. Global incomplete cerebral ischemia produces predominantly cortical neuronal injury. Stroke 1995; 26 (11) 2091-2095 , discussion 2096
  • 50 Lilja G, Nielsen N, Friberg H , et al. Cognitive function in survivors of out-of-hospital cardiac arrest after target temperature management at 33°C versus 36°C. Circulation 2015; 131 (15) 1340-1349
  • 51 Hopkins RO, Weaver LK, Collingridge D, Parkinson RB, Chan KJ, Orme Jr JF. Two-year cognitive, emotional, and quality-of-life outcomes in acute respiratory distress syndrome. Am J Respir Crit Care Med 2005; 171 (4) 340-347
  • 52 Moulaert VR, van Heugten CM, Winkens B , et al. Early neurologically-focused follow-up after cardiac arrest improves quality of life at one year: A randomised controlled trial. Int J Cardiol 2015; 193: 8-16
  • 53 Takahashi K, Sasanuma N, Itani Y , et al. Impact of early interventions by a cardiac rehabilitation team on the social rehabilitation of patients resuscitated from cardiogenic out-of-hospital cardiopulmonary arrest. Intern Med 2015; 54 (2) 133-139
  • 54 WHO Towards a common language for function, disability, and health. International Classification of Functioning, Disability and Health (ICF). Geneva, Switzerland: World Health Organization; 2002
  • 55 Rittenberger JC, Raina K, Holm MB, Kim YJ, Callaway CW. Association between Cerebral Performance Category, Modified Rankin Scale, and discharge disposition after cardiac arrest. Resuscitation 2011; 82 (8) 1036-1040
  • 56 Raina KD, Callaway C, Rittenberger JC, Holm MB. Neurological and functional status following cardiac arrest: method and tool utility. Resuscitation 2008; 79 (2) 249-256
  • 57 Raina KD, Rittenberger JC, Holm MB, Callaway CW. Functional outcomes: one year after a cardiac arrest. BioMed Res Int 2015; 2015: 283608
  • 58 Moulaert VR, Verbunt JA, van Heugten CM, Wade DT. Cognitive impairments in survivors of out-of-hospital cardiac arrest: a systematic review. Resuscitation 2009; 80 (3) 297-305
  • 59 Cronberg T, Lilja G, Horn J , et al; TTM Trial Investigators. Neurologic function and health-related quality of life in patients following targeted temperature management at 33°C vs 36°C after out-of-hospital cardiac arrest: a randomized clinical trial. JAMA Neurol 2015; 72 (6) 634-641
  • 60 Phelps R, Dumas F, Maynard C, Silver J, Rea T. Cerebral Performance Category and long-term prognosis following out-of-hospital cardiac arrest. Crit Care Med 2013; 41 (5) 1252-1257