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Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model
by
Sekhon, Mypinder S.
, Griesdale, Donald E.
, Ainslie, Philip N.
in
Adenosine triphosphate
/ Anemia
/ Apoptosis
/ Brain
/ Brain - metabolism
/ Carbon dioxide
/ Cardiac arrest
/ Cardiac arrhythmia
/ Cardiopulmonary resuscitation
/ Cerebral edema
/ Cerebral oxygen delivery
/ Cerebrovascular Circulation - physiology
/ Complications and side effects
/ CPR
/ Critical care
/ Critical Care Medicine
/ Edema
/ Emergency Medicine
/ Health aspects
/ Heart Arrest - complications
/ Heart attacks
/ Humans
/ Hyperthermia, Induced - mortality
/ Hyperthermia, Induced - standards
/ Hypothermia
/ Hypoxemia
/ Hypoxia, Brain - etiology
/ Hypoxia, Brain - mortality
/ Hypoxia, Brain - physiopathology
/ Hypoxic ischemic brain injury
/ Injuries
/ Intensive
/ Ischemia
/ Medicine
/ Medicine & Public Health
/ Mortality
/ Reperfusion Injury - complications
/ Reperfusion Injury - etiology
/ Reperfusion Injury - physiopathology
/ Review
/ Risk factors
/ Rodents
/ Targeted temperature management
2017
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Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model
by
Sekhon, Mypinder S.
, Griesdale, Donald E.
, Ainslie, Philip N.
in
Adenosine triphosphate
/ Anemia
/ Apoptosis
/ Brain
/ Brain - metabolism
/ Carbon dioxide
/ Cardiac arrest
/ Cardiac arrhythmia
/ Cardiopulmonary resuscitation
/ Cerebral edema
/ Cerebral oxygen delivery
/ Cerebrovascular Circulation - physiology
/ Complications and side effects
/ CPR
/ Critical care
/ Critical Care Medicine
/ Edema
/ Emergency Medicine
/ Health aspects
/ Heart Arrest - complications
/ Heart attacks
/ Humans
/ Hyperthermia, Induced - mortality
/ Hyperthermia, Induced - standards
/ Hypothermia
/ Hypoxemia
/ Hypoxia, Brain - etiology
/ Hypoxia, Brain - mortality
/ Hypoxia, Brain - physiopathology
/ Hypoxic ischemic brain injury
/ Injuries
/ Intensive
/ Ischemia
/ Medicine
/ Medicine & Public Health
/ Mortality
/ Reperfusion Injury - complications
/ Reperfusion Injury - etiology
/ Reperfusion Injury - physiopathology
/ Review
/ Risk factors
/ Rodents
/ Targeted temperature management
2017
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Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model
by
Sekhon, Mypinder S.
, Griesdale, Donald E.
, Ainslie, Philip N.
in
Adenosine triphosphate
/ Anemia
/ Apoptosis
/ Brain
/ Brain - metabolism
/ Carbon dioxide
/ Cardiac arrest
/ Cardiac arrhythmia
/ Cardiopulmonary resuscitation
/ Cerebral edema
/ Cerebral oxygen delivery
/ Cerebrovascular Circulation - physiology
/ Complications and side effects
/ CPR
/ Critical care
/ Critical Care Medicine
/ Edema
/ Emergency Medicine
/ Health aspects
/ Heart Arrest - complications
/ Heart attacks
/ Humans
/ Hyperthermia, Induced - mortality
/ Hyperthermia, Induced - standards
/ Hypothermia
/ Hypoxemia
/ Hypoxia, Brain - etiology
/ Hypoxia, Brain - mortality
/ Hypoxia, Brain - physiopathology
/ Hypoxic ischemic brain injury
/ Injuries
/ Intensive
/ Ischemia
/ Medicine
/ Medicine & Public Health
/ Mortality
/ Reperfusion Injury - complications
/ Reperfusion Injury - etiology
/ Reperfusion Injury - physiopathology
/ Review
/ Risk factors
/ Rodents
/ Targeted temperature management
2017
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Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model
Journal Article
Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model
2017
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Overview
Hypoxic ischemic brain injury (HIBI) after cardiac arrest (CA) is a leading cause of mortality and long-term neurologic disability in survivors. The pathophysiology of HIBI encompasses a heterogeneous cascade that culminates in secondary brain injury and neuronal cell death. This begins with primary injury to the brain caused by the immediate cessation of cerebral blood flow following CA. Thereafter, the secondary injury of HIBI takes place in the hours and days following the initial CA and reperfusion. Among factors that may be implicated in this secondary injury include reperfusion injury, microcirculatory dysfunction, impaired cerebral autoregulation, hypoxemia, hyperoxia, hyperthermia, fluctuations in arterial carbon dioxide, and concomitant anemia.
Clarifying the underlying pathophysiology of HIBI is imperative and has been the focus of considerable research to identify therapeutic targets. Most notably, targeted temperature management has been studied rigorously in preventing secondary injury after HIBI and is associated with improved outcome compared with hyperthermia. Recent advances point to important roles of anemia, carbon dioxide perturbations, hypoxemia, hyperoxia, and cerebral edema as contributing to secondary injury after HIBI and adverse outcomes. Furthermore, breakthroughs in the individualization of perfusion targets for patients with HIBI using cerebral autoregulation monitoring represent an attractive area of future work with therapeutic implications.
We provide an in-depth review of the pathophysiology of HIBI to critically evaluate current approaches for the early treatment of HIBI secondary to CA. Potential therapeutic targets and future research directions are summarized.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Anemia
/ Brain
/ Cardiopulmonary resuscitation
/ Cerebrovascular Circulation - physiology
/ Complications and side effects
/ CPR
/ Edema
/ Heart Arrest - complications
/ Humans
/ Hyperthermia, Induced - mortality
/ Hyperthermia, Induced - standards
/ Hypoxia, Brain - physiopathology
/ Hypoxic ischemic brain injury
/ Injuries
/ Ischemia
/ Medicine
/ Reperfusion Injury - complications
/ Reperfusion Injury - etiology
/ Reperfusion Injury - physiopathology
/ Review
/ Rodents
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