Improving Outcomes After Post-Cardiac Arrest Brain Injury: A Scientific Statement From the International Liaison Committee on Resuscitation

被引:5
作者
Perkins, Gavin D.
Neumar, Robert
Hsu, Cindy H.
Hirsch, Karen G.
Aneman, Anders
Becker, Lance B.
Couper, Keith
Callaway, Clifton W.
Hoedemaekers, Cornelia W. E.
Lim, Shir Lynn
Meurer, William
Olasveengen, Theresa
Sekhon, Mypinder S.
Skrifvars, Markus
Soar, Jasmeet
Tsai, Min-Shan
Yengamma, Bhuma
Nolan, Jerry P.
机构
关键词
AHA Scientific Statements; acute brain injuries; cardiopulmonary resuscitation; post-cardiac arrest syndrome; rehabilitation; resuscitation; CARDIOVASCULAR CARE SCIENCE; TARGETED TEMPERATURE MANAGEMENT; CEREBRAL-BLOOD-FLOW; MILD THERAPEUTIC HYPOTHERMIA; CARDIOPULMONARY-RESUSCITATION; COMATOSE SURVIVORS; ANIMAL-MODELS; SPREADING DEPOLARIZATION; INHALED XENON; NO-REFLOW;
D O I
10.1016/j.resuscitation.2024.110196
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
This scientific statement presents a conceptual framework for the pathophysiology of post-cardiac arrest brain injury, explores reasons for previous failure to translate preclinical data to clinical practice, and outlines potential paths forward. Post-cardiac arrest brain injury is characterized by 4 distinct but overlapping phases: ischemic depolarization, reperfusion repolarization, dysregulation, and recovery and repair. Previous research has been challenging because of the limitations of laboratory models; heterogeneity in the patient populations enrolled; overoptimistic estimation of treatment effects leading to suboptimal sample sizes; timing and route of intervention delivery; limited or absent evidence that the intervention has engaged the mechanistic target; and heterogeneity in postresuscitation care, prognostication, and withdrawal of life-sustaining treatments. Future trials must tailor their interventions to the subset of patients most likely to benefit and deliver this intervention at the appropriate time, through the appropriate route, and at the appropriate dose. The complexity of post-cardiac arrest brain injury suggests that monotherapies are unlikely to be as successful as multimodal neuroprotective therapies. Biomarkers should be developed to identify patients with the targeted mechanism of injury, to quantify its severity, and to measure the response to therapy. Studies need to be adequately powered to detect effect sizes that are realistic and meaningful to patients, their families, and clinicians. Study designs should be optimized to accelerate the evaluation of the most promising interventions. Multidisciplinary and international collaboration will be essential to realize the goal of developing effective therapies for post-cardiac arrest brain injury.
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页数:23
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共 147 条
[21]   Mechanistic role of calpains in postischemic neurodegeneration [J].
Bevers, Matthew B. ;
Neumar, Robert W. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2008, 28 (04) :655-673
[22]   Ischaemic brain damage after cardiac arrest and induced hypothermia-a systematic description of selective eosinophilic neuronal death. A neuropathologic study of 23 patients [J].
Bjorklund, Erik ;
Lindberg, Eva ;
Rundgren, Malin ;
Cronberg, Tobias ;
Friberg, Hans ;
Englund, Elisabet .
RESUSCITATION, 2014, 85 (04) :527-532
[23]   A Core Outcome Set for Critical Care Ventilation Trials [J].
Blackwood, Bronagh ;
Ringrow, Suzanne ;
Clarke, Mike ;
Marshall, John C. ;
Connolly, Bronwen ;
Rose, Louise ;
McAuley, Daniel F. .
CRITICAL CARE MEDICINE, 2019, 47 (10) :1324-1331
[24]   THIOPENTAL AMELIORATION OF BRAIN-DAMAGE AFTER GLOBAL ISCHEMIA IN MONKEYS [J].
BLEYAERT, AL ;
MICKELL, JJ ;
SAFAR, P ;
RAO, GR ;
MOOSSY, J ;
STEZOSKI, SW ;
NEMOTO, EM .
ANESTHESIOLOGY, 1978, 49 (06) :390-398
[25]   Use of a novel smartphone-based application tool for enrolment and randomisation in pre-hospital clinical trials [J].
Bloom, Jason E. ;
Partovi, Andi ;
Bernard, Stephen ;
Okyere, Daniel ;
Heritier, Stephane ;
Mahony, Emily ;
Eliakundu, Amminadab L. ;
Dawson, Luke P. ;
Voskoboinik, Aleksandr ;
Anderson, David ;
Ball, Jocasta ;
Chan, William ;
Kaye, David M. ;
Nehme, Ziad ;
Stub, Dion .
RESUSCITATION, 2023, 187
[26]   Molecular mechanisms and consequences of mitochondrial permeability transition [J].
Bonora, Massimo ;
Giorgi, Carlotta ;
Pinton, Paolo .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2022, 23 (04) :266-285
[27]   The cerebral 'no-reflow' phenomenon after cardiac arrest in rats - Influence of low-flow reperfusion [J].
Bottiger, BW ;
Krumnikl, JJ ;
Gass, P ;
Schmitz, B ;
Motsch, J ;
Martin, E .
RESUSCITATION, 1997, 34 (01) :79-87
[28]   CARTILAGE FUCOPROTEINS WITH SITES FOR CROSS-LINKING BY TRANSGLUTAMINASE [J].
BOWNESS, JM .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1987, 65 (04) :280-285
[29]   Oxygen titration after resuscitation from out-of-hospital cardiac arrest: A multi-centre, randomised controlled pilot study (the EXACT pilot trial) [J].
Bray, Janet E. ;
Hein, Cindy ;
Smith, Karen ;
Stephenson, Michael ;
Grantham, Hugh ;
Finn, Judith ;
Stub, Dion ;
Cameron, Peter ;
Bernard, Stephen .
RESUSCITATION, 2018, 128 :211-215
[30]   Acute respiratory distress syndrome subphenotypes and differential response to simvastatin: secondary analysis of a randomised controlled trial [J].
Calfee, Carolyn S. ;
Delucchi, Kevin L. ;
Sinha, Pratik ;
Matthay, Michael A. ;
Hackett, Jonathan ;
Shankar-Hari, Manu ;
McDowell, Cliona ;
Laffey, John G. ;
O'Kane, Cecilia M. ;
McAuley, Daniel F. .
LANCET RESPIRATORY MEDICINE, 2018, 6 (09) :691-698