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Cómo MorimosCómo Morimos
Bryan E. Bledsoe, DO, FACEP
The George Washington University Medical Center
Bryan E. Bledsoe, DO, FACEP
The George Washington University Medical Center
How We DieHow We Die
Bryan E. Bledsoe, DO, FACEP
The George Washington University Medical Center
Bryan E. Bledsoe, DO, FACEP
The George Washington University Medical Center
How We DieHow We Die
Life is pleasant. Death is peaceful. It is the transition that is troublesome.
Isaac Asimov
Life is pleasant. Death is peaceful. It is the transition that is troublesome.
Isaac Asimov
How We DieHow We Die
Estimated 500,000 deaths each year attributable to cardiac arrest.
Estimated 500,000 deaths each year attributable to cardiac arrest.
How We DieHow We Die
Regardless, the resuscitation rate remains < 5% and has changed little in the last 40 years.
Regardless, the resuscitation rate remains < 5% and has changed little in the last 40 years.
History of ResuscitationHistory of Resuscitation
1740—The Paris Academy of Sciences officially recommended mouth-to-mouth resuscitation for drowning victims.
1767—The Society for the Recovery of Drowned Persons became the first organized effort to deal with sudden and unexpected death.
1740—The Paris Academy of Sciences officially recommended mouth-to-mouth resuscitation for drowning victims.
1767—The Society for the Recovery of Drowned Persons became the first organized effort to deal with sudden and unexpected death.
History of ResuscitationHistory of Resuscitation
1891—Dr. Friedrich Maass performed the first equivocally documented chest compression in humans.
1891—Dr. Friedrich Maass performed the first equivocally documented chest compression in humans.
History of ResuscitationHistory of Resuscitation1903—Dr. George Crile reported the first successful use of external chest compressions in human resuscitation.1904—The first American case of closed-chest cardiac massage was performed by Dr. George Crile.
1903—Dr. George Crile reported the first successful use of external chest compressions in human resuscitation.1904—The first American case of closed-chest cardiac massage was performed by Dr. George Crile.
History of ResuscitationHistory of Resuscitation
1947—Claude Beck developed first defibrillator and first human saved with defibrillation.
1947—Claude Beck developed first defibrillator and first human saved with defibrillation.
History of ResuscitationHistory of Resuscitation
1954—James Elam was the first to prove that expired air was sufficient to maintain adequate oxygenation.
1954—James Elam was the first to prove that expired air was sufficient to maintain adequate oxygenation.
History of ResuscitationHistory of Resuscitation
1956—Peter Safar and James Elam invented mouth-to-mouth resuscitation.
1956—Peter Safar and James Elam invented mouth-to-mouth resuscitation.
History of ResuscitationHistory of Resuscitation
1957—The United States military adopted the mouth-to-mouth resuscitation method to revive unresponsive victims.
1957—The United States military adopted the mouth-to-mouth resuscitation method to revive unresponsive victims.
History of ResuscitationHistory of Resuscitation1960—CPR was developed. The American Heart Association started a program to acquaint physicians with closed-chest cardiac resuscitation and became the forerunner of CPR training for the general public.
1960—CPR was developed. The American Heart Association started a program to acquaint physicians with closed-chest cardiac resuscitation and became the forerunner of CPR training for the general public.
History of ResuscitationHistory of Resuscitation
1963—Cardiologist Leonard Scherlis started the American Heart Association's CPR Committee, and the same year, the American Heart Association formally endorsed CPR.
1963—Cardiologist Leonard Scherlis started the American Heart Association's CPR Committee, and the same year, the American Heart Association formally endorsed CPR.
History of ResuscitationHistory of Resuscitation1965—J. Frank Pantridge converted an ambulance into a mobile coronary care unit with a portable defibrillator and recorded ten pre-hospital resuscitations.
50% long-term survival rate.
1965—J. Frank Pantridge converted an ambulance into a mobile coronary care unit with a portable defibrillator and recorded ten pre-hospital resuscitations.
50% long-term survival rate.
History of ResuscitationHistory of Resuscitation
1966—The National Research Council of the National Academy of Sciences convened an ad hoc conference on cardiopulmonary resuscitation to establish standardized training and performance standards for CPR.
1966—The National Research Council of the National Academy of Sciences convened an ad hoc conference on cardiopulmonary resuscitation to establish standardized training and performance standards for CPR.
History of ResuscitationHistory of Resuscitation
1972—Leonard Cobb held the world's first mass citizen training in CPR in Seattle, Washington called Medic 2. He helped train over 100,000 people the first two years of the programs.
1972—Leonard Cobb held the world's first mass citizen training in CPR in Seattle, Washington called Medic 2. He helped train over 100,000 people the first two years of the programs.
History of ResuscitationHistory of Resuscitation
1979—The first automated external defibrillators (AEDs) became available, further extending the concept of pre-hospital care.
1979—The first automated external defibrillators (AEDs) became available, further extending the concept of pre-hospital care.
History of ResuscitationHistory of Resuscitation
1981—A program to provide telephone instructions in CPR began in King County, Washington. Dispatcher-assisted CPR is now standard care for dispatcher centers throughout the United States.
1981—A program to provide telephone instructions in CPR began in King County, Washington. Dispatcher-assisted CPR is now standard care for dispatcher centers throughout the United States.
How We DieHow We Die
We now know a great deal more about the pathophysiology of sudden death—especially ventricular fibrillation.
We now know a great deal more about the pathophysiology of sudden death—especially ventricular fibrillation.
How We DieHow We Die
Three Phase Model:Electrical Phase
Circulatory Phase
Metabolic Phase
Three Phase Model:Electrical Phase
Circulatory Phase
Metabolic Phase
Phases of Cardiac ArrestPhases of Cardiac Arrest
Electrical Phase 0 - 4 minutes
Circulatory Phase 4 - 10 minutes
Metabolic Phase > 10 minutes
Electrical Phase 0 - 4 minutes
Circulatory Phase 4 - 10 minutes
Metabolic Phase > 10 minutes
Electrical PhaseElectrical Phase
Adequate oxygen content in myocardium.
Adequate energy substrates (ATP).
Near-normal pH.
No myocardial ischemia.
No myocardial infarction.
Adequate oxygen content in myocardium.
Adequate energy substrates (ATP).
Near-normal pH.
No myocardial ischemia.
No myocardial infarction.
Electrical PhaseElectrical Phase
Early defibrillation a Class I recommendation.
Survival rates approach 50%.
Early defibrillation a Class I recommendation.
Survival rates approach 50%.
Electrical PhaseElectrical Phase
Most effective treatment during electrical phase is rapid defibrillation.
Most effective treatment during electrical phase is rapid defibrillation.
Circulatory PhaseCirculatory Phase
Inadequate oxygen content in myocardium.
Inadequate energy substrates (ATP).
Acidosis.
Possible myocardial ischemia.
No myocardial infarction.
Inadequate oxygen content in myocardium.
Inadequate energy substrates (ATP).
Acidosis.
Possible myocardial ischemia.
No myocardial infarction.
Circulatory PhaseCirculatory Phase
DEFIBRILLATION IN THE GLOBALLY ISCHEMIC HEART MAY BE DETRIMENTAL!
DEFIBRILLATION IN THE GLOBALLY ISCHEMIC HEART MAY BE DETRIMENTAL!
Circulatory PhaseCirculatory Phase
Chest compressions and tissue oxygen delivery take precedence over defibrillation.
Initial therapy should be chest compressions and ventilations followed by defibrillation.
Defibrillation usually delayed by 1-3 minutes.
Chest compressions and tissue oxygen delivery take precedence over defibrillation.
Initial therapy should be chest compressions and ventilations followed by defibrillation.
Defibrillation usually delayed by 1-3 minutes.
Circulatory PhaseCirculatory Phase
Animals allowed to fibrillate for 1,3,5, or 9 minutes prior to defibrillation.
Immediate defibrillation optimal when performed in 3 minutes or less.
Animals allowed to fibrillate for 1,3,5, or 9 minutes prior to defibrillation.
Immediate defibrillation optimal when performed in 3 minutes or less.
Circulatory PhaseCirculatory Phase
CPR + epinephrine resulted in better survival when performed after 5-9 minutes.
> 5 minutes of cardiac arrest, immediate defibrillation resulted in 30% successful defibrillation and 0% ROSC.
1 minute of CPR + epinephrine before defibrillation resulted in 70% conversion rate and 40% ROSC.
Yakaitis et al. Crit Care Med. 1980;8:157-163
CPR + epinephrine resulted in better survival when performed after 5-9 minutes.
> 5 minutes of cardiac arrest, immediate defibrillation resulted in 30% successful defibrillation and 0% ROSC.
1 minute of CPR + epinephrine before defibrillation resulted in 70% conversion rate and 40% ROSC.
Yakaitis et al. Crit Care Med. 1980;8:157-163
Circulatory PhaseCirculatory Phase
In animals with 7.5 minutes of untreated v-fib, 5 minutes of CPR + epinephrine was compared to immediate defibrillation.
Significant improvement (64% vs. 21% survival) when compared to immediate defibrillation.
Niemann et al. Resusc. 1992;85:281-287
In animals with 7.5 minutes of untreated v-fib, 5 minutes of CPR + epinephrine was compared to immediate defibrillation.
Significant improvement (64% vs. 21% survival) when compared to immediate defibrillation.
Niemann et al. Resusc. 1992;85:281-287
Circulatory PhaseCirculatory Phase
In animals, 8 minutes of untreated v-fib treated with immediate defibrillation or CPR + drug cocktail (epinephrine, lidocaine, bretylium, propranolol) then defibrillation.
77% versus 22% ROSC for the drug cocktail group.
Menegazzi et al. Ann Emerg Med 1993;22:235-239
In animals, 8 minutes of untreated v-fib treated with immediate defibrillation or CPR + drug cocktail (epinephrine, lidocaine, bretylium, propranolol) then defibrillation.
77% versus 22% ROSC for the drug cocktail group.
Menegazzi et al. Ann Emerg Med 1993;22:235-239
Circulatory PhaseCirculatory Phase
Seattle:Standard immediate defibrillation: 24% survival
90 seconds CPR then defibrillation: 30% survival
Subgroup analysis:Immediate defibrillation superior to 90 seconds CPR for first 3 minutes only.
Cobb et al. JAMA 1999;281:1182-1188
Seattle:Standard immediate defibrillation: 24% survival
90 seconds CPR then defibrillation: 30% survival
Subgroup analysis:Immediate defibrillation superior to 90 seconds CPR for first 3 minutes only.
Cobb et al. JAMA 1999;281:1182-1188
Circulatory PhaseCirculatory Phase
Oslo:> 5 minutes after collapse, if CPR performed for 3 minutes prior to defibrillation.
Survival to hospital discharge 22% vs. 4%
1 year survival 20% vs. 4%Wik et al. Circ. 2002;106 (Suppl 2):A1823
Oslo:> 5 minutes after collapse, if CPR performed for 3 minutes prior to defibrillation.
Survival to hospital discharge 22% vs. 4%
1 year survival 20% vs. 4%Wik et al. Circ. 2002;106 (Suppl 2):A1823
The Metabolic PhaseThe Metabolic Phase
Effectiveness of both immediate defibrillation and CPR + defibrillation decrease rapidly.
Survival rates poor.
Effectiveness of both immediate defibrillation and CPR + defibrillation decrease rapidly.
Survival rates poor.
The Metabolic PhaseThe Metabolic Phase
Tissue injury from global ischemic events and reperfusion cause circulating metabolic factors that cause injury in excess of local ischemia.
Tissue injury from global ischemic events and reperfusion cause circulating metabolic factors that cause injury in excess of local ischemia.
The Metabolic PhaseThe Metabolic Phase
Gut mucosa begins to malfunction secondary to ischemia.
Translocation of gram-negative bacteria cause endotoxin and cytokine release.
Both suppress myocardial function after defibrillation.
Gut mucosa begins to malfunction secondary to ischemia.
Translocation of gram-negative bacteria cause endotoxin and cytokine release.
Both suppress myocardial function after defibrillation.
The Metabolic PhaseThe Metabolic Phase
Reperfusion in this phase can contribute to cell death and diminished organ function independent of the adverse effects of ischemia.
Key to survival during this phase appears to be control of injurious factors during reperfusion.
Reperfusion in this phase can contribute to cell death and diminished organ function independent of the adverse effects of ischemia.
Key to survival during this phase appears to be control of injurious factors during reperfusion.
The Metabolic PhaseThe Metabolic Phase
Induced-hypothermia may be the answer for patients in the metabolic phase.
Induced-hypothermia may be the answer for patients in the metabolic phase.
The Metabolic PhaseThe Metabolic Phase
Induced-hypothermia (34-32˚ C) have shown an improvement in neurologically-intact survival after out-of-hospital cardiac arrest.
Patients cooled late in cardiac arrest:49% survival compared with 26%
55% good neurological outcomeHypothermia Study Group NEJM 2002;346:549-556
Induced-hypothermia (34-32˚ C) have shown an improvement in neurologically-intact survival after out-of-hospital cardiac arrest.
Patients cooled late in cardiac arrest:49% survival compared with 26%
55% good neurological outcomeHypothermia Study Group NEJM 2002;346:549-556
The Metabolic PhaseThe Metabolic Phase
Possible beneficial technologies:Correcting calcium-entry
Correcting sodium alterations
Preventing inflammation
Possible beneficial technologies:Correcting calcium-entry
Correcting sodium alterations
Preventing inflammation
The Metabolic PhaseThe Metabolic Phase
The Metabolic PhaseThe Metabolic Phase
Metabolic-focused treatmentCardiopulmonary bypass
Administration of metabolic therapies (similar to what is used in cardiac bypass procedures):
Amino acid-enriched solution with:Buffer
Low calcium
Increased potassium
High-dextrose
Metabolic-focused treatmentCardiopulmonary bypass
Administration of metabolic therapies (similar to what is used in cardiac bypass procedures):
Amino acid-enriched solution with:Buffer
Low calcium
Increased potassium
High-dextrose
The Metabolic PhaseThe Metabolic Phase
Whereas epinephrine may be beneficial during the circulatory phase, it may be detrimental during the metabolic phase.
Epinephrine:Increases gut ischemia
May lead to sepsis
Whereas epinephrine may be beneficial during the circulatory phase, it may be detrimental during the metabolic phase.
Epinephrine:Increases gut ischemia
May lead to sepsis
So What Does This All Mean?So What Does This All Mean?
This concept based on ventricular fibrillation.
May be similar for trauma and hypoxia induced cardiac arrest.
This concept based on ventricular fibrillation.
May be similar for trauma and hypoxia induced cardiac arrest.
So What Does This All Mean?So What Does This All Mean?
So What Does This All Mean?So What Does This All Mean?
So What Does This All Mean?So What Does This All Mean?
Vilke et al. The three-phase model of cardiac arrest as applied to ventricular fibrillation is a large, urban emergency medical services system. Resuscitation. 2005;84:341-346
Vilke et al. The three-phase model of cardiac arrest as applied to ventricular fibrillation is a large, urban emergency medical services system. Resuscitation. 2005;84:341-346
What Does This All Mean?What Does This All Mean?
EMS arrival < 4 minutes after collapse EMS arrival < 4 minutes after collapse
Immediate defibrillationImmediate defibrillationBystander CPR not as important during this phase.
What Does This All Mean?What Does This All Mean?
EMS arrival less than >4 but <10 minutes after collapse EMS arrival less than >4 but <10 minutes after collapse
CPR + defibrillationCPR + defibrillationBystander CPR VERY important during this phase.
What Does This All Mean?What Does This All Mean?
EMS arrival > 10 minutes after collapse EMS arrival > 10 minutes after collapse
??
> 10 Minute Down Time> 10 Minute Down Time
Induced-HypothermiaInduced-Hypothermia
Dandenong Hospital, Melbourne, VIC
30 mL/kg cold (4˚- 8˚ C) lactated Ringer’s administered in ED after out-of-hospital resuscitation by paramedics.
Dandenong Hospital, Melbourne, VIC
30 mL/kg cold (4˚- 8˚ C) lactated Ringer’s administered in ED after out-of-hospital resuscitation by paramedics.
Induced-HypothermiaInduced-Hypothermia
Patients: n=22
Age: 70 (55-75)
Cause of Arrest:Cardiac=21
TCA OD=1
Rhythm:V-fib=14
Asystole=4
PEA=4
Patients: n=22
Age: 70 (55-75)
Cause of Arrest:Cardiac=21
TCA OD=1
Rhythm:V-fib=14
Asystole=4
PEA=4
EMS Call: 2 minutes
Response: 8 minutes
EMS arrival to ROSC: 16 minutes
Collapse to ROSC: 26 minutes
ROSC to infusion:73 minutes
EMS Call: 2 minutes
Response: 8 minutes
EMS arrival to ROSC: 16 minutes
Collapse to ROSC: 26 minutes
ROSC to infusion:73 minutes
Induced-HypothermiaInduced-Hypothermia
Induced-HypothermiaInduced-Hypothermia
Survival (initial rhythm):
V-fib: 8/14 (80%)
Not v-fib: 2/8 (25%)Bernard et al. Resusc. 2003;56:9-13
Survival (initial rhythm):
V-fib: 8/14 (80%)
Not v-fib: 2/8 (25%)Bernard et al. Resusc. 2003;56:9-13
What about ventilations?What about ventilations?
Lay public can not or will not do mouth-to-mouth in many cases.
Adequate oxygen stores initially.
Patient may gasp for a minute.
May take away from effective chest compressions.
Lay public can not or will not do mouth-to-mouth in many cases.
Adequate oxygen stores initially.
Patient may gasp for a minute.
May take away from effective chest compressions.
2005 AHA Recommendations2005 AHA Recommendations
Chain of SurvivalChain of Survival
SummarySummary
Try and know the phase your patient is in.
Most EMS responses will arrive in the circulatory phase and 1-3 minutes of chest compressions are essential.
Many new therapies coming down the line.
Try and know the phase your patient is in.
Most EMS responses will arrive in the circulatory phase and 1-3 minutes of chest compressions are essential.
Many new therapies coming down the line.
Major ReferenceMajor Reference
Weisfeldt ML and Becker LB. Resuscitation After Cardiac Arrest: A 3-Phase Time-Sensitive Model. Journal of the American Medical Association. 2002;288(23):3035-3038
Weisfeldt ML and Becker LB. Resuscitation After Cardiac Arrest: A 3-Phase Time-Sensitive Model. Journal of the American Medical Association. 2002;288(23):3035-3038
SummarySummary
Questions?
This presentation available at: http://www.bryanbledsoe.com
Questions?
This presentation available at: http://www.bryanbledsoe.com