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Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation
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Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

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Page 1: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Course Objectives

CPR: Ongoing Challenges. New Solutions.October 2007

© 2007 ZOLL Medical Corporation

Page 2: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

This program was made possible by an educational grant from

ZOLL Medical Corporation.

Page 3: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Faculty & Planning Committee Disclosures

Benjamin S. Abella, MD, MPhil1. Paid honorarium for participation in this program. Has also

received honoraria for other educational activities (article, speaking

engagement) performed on behalf of the sponsoring organization.2. No product that is not labeled for the use under

discussion was discussed.3. No preliminary research data was disclosed.

Joseph P. Ornato, MD, FACP, FACC, FACEP1. Paid honorarium for participation in this program. Serves as a member of the Scientific Advisory Board of the sponsoring organization.2. No product that is not labeled for the use under discussion

was discussed.3. No preliminary research data was disclosed.

Page 4: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Target Audience

• Physicians

• Nurses

• Paramedics

• EMTs

• Resuscitation Researchers

Page 5: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Objectives• Upon completion of this program,

the viewer will be able to:– Discuss the effects of chest compression on

Coronary Perfusion (CPP) and Return of Spontaneous Circulation (ROSC)

– List at least three changes in the 2005 AHA Guidelines that relate to CPR performance

– Discuss the outcome of at least one clinical study and one pre-hospital study on the effects of survival with load-distributing band CPR

– Discuss the rationale for implementing CPR prior to defibrillation in cases with extended down time

Page 6: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Key Terms and Abbreviations• AHA American Heart Association• A-CPR AutoPulse CPR• C-CPR Conventional CPR• CPP Coronary Perfusion Pressure• Deploy To implement and position

for readiness• DowntimeNumber of minutes from onset

of sudden cardiac arrest to initiation of

resuscitation efforts

Page 7: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Key Terms and Abbreviations• Duty cycle The time is takes to

complete one cycle• ECC Emergency Cardiovascular

Care• LDB Load-distributing band• ROSC Return of Spontaneous

Circulation• SCA Sudden Cardiac Arrest• VF Ventricular Fibrillation

Page 8: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Circulation is Critical for Survival

• Provides oxygen to preserve vital organ function

• Converts non-shockable rhythms (asystole, PEA) to shockable ones (VF, VT)– More than half of all arrests involve non-

shockable rhythms

Page 9: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Presenting Rhythms in SCARecent studies show that VF or VT

is the initial rhythm less than 50% of the time

Peberdy MA et al. Resuscitation. 2003;58:297-308.Kaye W et al. JAMA. 2002:39(5),Suppl A.Cobb L et al. JAMA. 2002;288(23):3008-3013.

25%

41%

75%59%

0%

20%

40%

60%

80%

100%

120%

Hospital EMS

% o

f C

ard

iac

Arr

es

ts

VF/VT PEA/Asystole

Page 10: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Why are they non-shockable more than half the time?– EMS

• Long response times

– Hospital• Some drugs (e.g., calcium channel blockers and beta

blockers) significantly shorten the time in which a person is in VF

Presenting Rhythms in SCA

Page 11: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Right Atrial Pressure

(RAP)

Aortic Pressure

(AP)

Coronary Perfusion Pressure

CPP = AP minus RAPCPP = AP minus RAP

Page 12: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Coronary Perfusion and ROSC

A well perfused myocardium is more likely to experience return of spontaneous circulation (ROSC)

Page 13: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPP and ROSC (Paradis et al.)

46%

0%

79%

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

<15 15-25 >25

CPP (mm Hg)

% o

f p

ati

en

ts w

/ RO

SC

Paradis NA et al. JAMA. 1990;263:1106-1113.

Victims with CPP < 15 mmHg do not achieve ROSCWith conventional CPR, the overall mean CPP = 12.5

Page 14: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AHA Guidelines 2005: CPR

“Simply put: …push hard, push fast, allow full chest recoil, minimize interruptions in

compressions…”

Circulation. 2005;112:IV-206.

Page 15: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AHA Guidelines 2005: CPR

• High quality, consistent and uninterrupted chest compressions

• Push hard, push fast• Compression to ventilation ratio: 30:2• Rate: 100 manual compressions per

minute• Depth: 1½ - 2 inches / 4 - 5 centimeters• Duty cycle: 50% - 50%• Ventilation: 8 -10 breaths per minute

Page 16: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges

• Poor quality– Inconsistent rate, depth, duty cycle

• Harmful interruptions– Required due to clinician fatigue, patient

transport

• Inadequate cerebral and coronary perfusion

• Ineffective defibrillation support

Page 17: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Quality (Abella et al.)

Abella BS et al. JAMA. 2005;293:305-310.

• “…quality of multiple parameters of CPR was inconsistent and often did not meet published guideline recommendations….”

Parameter (1st 5 minutes)

Criteria% of Time Incorrect

Rate too slow < 90/min

28.1%

Depth too shallow < 1.5 in 37.4%

Ventilation rate too high > 20/min

60.9%

Page 18: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Quality (Abella et al.)

60.9%

37.4%

28.1%

0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

Par

amet

er (

1st

5 m

inu

tes)

% of Time Incorrect

Rate too slow

Depth too shallow

Ventilation rate too high

Abella BS et al. JAMA. 2005;293:305-310.

Page 19: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Quality (Wik et al.)

“…chest compressions were not delivered half of the time, and most compressions were too shallow…”

52%48%

Wik L et al. JAMA. 2005;23 299-304.

FlowNo Flow

Page 20: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Quality

• CPR feedback to rescuers can help improve CPR quality– Elkadi et al.

• Pre-hospital Emergency Care. 2005;8:81-82.

– Handley et al.• Resuscitation. 2003;57:57-62.

Page 21: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Aufderheide TP et al. Circulation. 2004;109:1960-1965.

Mean ventilation rate: 30/minute ± 3.2

first group: 37/minute ± 4 after retraining: 22/minute ± 3

16 seconds

v v v v v v v v v v

CPR Challenges: HyperventilationHyperventilation induces hypotension

Page 22: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Future of CPR Quality Study

International consortium for data collection

Oslo, Norway Vienna, Austria London, UK

Stockholm, Sweden Chicago, USA

Phase I: Collect baseline data on CPR qualityPhase II: Implement feedback system to monitor and improve

CPR performance

Page 23: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Interruptions

77% decrease in ROSC when pre-shock time increased from </= 9.7 seconds to </= 22.5 seconds

Edelson et al. Circulation. 2005;112(17)II-1099

87%

20%

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

100%

</= 9.7 sec </= 22.5 sec

RO

SC

Edelson DP, Abella BS et al. Circulation. 2005;112(17):II-1099.

(Edelson,Abella et al.)

Page 24: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Interruptions (Kern et al.)

“…Any technique that minimizes lengthy interruptions of chestcompressions during the first 10 to 15 minutes of basic life

supportshould be given serious consideration in future efforts to

improveoutcome results from cardiac arrest….”

38%

62%

Kern KB et al. Circulation. 2002;105:645-649.

Flow

No Flow

Page 25: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Berg et al, 2001

Blo

od

pre

ssu

reCPR Challenges: Interruptions (Berg et al.)

Time

Berg RA et al. Resuscitation. 2001;104:2465-2470.

Interrupting chest compressions for rescue breathing canadversely affect hemodynamics during CPR for VF

Chest compressions

Page 26: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Perfusion (Kern)

Manual CPR provides minimal blood flow to the heart and brain

30% - 40% of normal flow10% - 20% of normal flow

Kern KB Bailliere’s Clinical Anaesthesiology. 2000;14(3):591-609.

Page 27: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPR Challenges: Defibrillation Support

After ~4 minutes of VF, the myocardium is nearly depleted of ATP*, a vital energy source needed for successful defibrillation

*Adenosine triphosphate (ATP), which breaks down into adenosine diphosphate (ADP).

Page 28: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Effective compressions help restore ATP,increasing the likelihood of successful defibrillation

CPR Challenges: Defibrillation Support

Page 29: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Defibrillation is most effective during the first few minutes after cardiac arrest

Engdahl J et al. Resuscitation. 2002;52(3):235-245.Guidelines for CPR and ECC. Circulation. 2000;102(suppl I):I-23.

Defibrillation most effective Circulation

enhances outcome

CPR Challenges: Defibrillation Support

Page 30: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

“LDB*-CPR may be considered for use by properly trained personnel as an

adjunct to CPR for patients with cardiac arrest in the out-of-hospital or in-hospital setting (Class IIb).”

AHA Guidelines 2005: LDB CPR

*Load-distributing band.

Circulation. 2005;112:IV-59.

Page 31: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse® LDB CPR

Page 32: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse LDB CPR• What is the AutoPulse?

– The world’s only load-distributing band chest compression device

• What does the AutoPulse do?– Compressions that humans can’t

possibly do

• What does the AutoPulse do for the SCA patient?– Moves more blood, more

effectively, to the heart and brain– Offers the promise of better

outcomes

Page 33: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Summary of LDB CPR Benefits

• Improved blood flow

• Functions as an “additional person”

• Fast, easy and intuitive to start-up and use

• Clinician safety

Page 34: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Improved Blood flow

• To the brain• To the coronary arteries • Consistent, uninterrupted

compressions• Thoracic and cardiac compression

Page 35: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Dual Function

Compresses onlythe heart

Compresses theentire chest

Cardiac Pump Thoracic Pump

Compresses onlythe heart

Compresses muchof the chest

Compressesmainly the heart

Compresses theentire chest

Page 36: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Functions as an “Additional Person”

• Clinicians are free to perform other critical tasks

• Eliminates clinician fatigue

Page 37: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Extremely simple user interface

• Automatically “sizes the patient,” calculating…– Size– Shape– Compliance/resistance

• Helps to “organize” or “calm” the code situation

Fast, Easy and Intuitive

Page 38: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Clinician Safety

• No risk of being injured while attempting to do manual compressions during chaotic codes and/or patient transport

Page 39: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

30:2 or Continuous Modes

• Change without stopping operation• Default settings administrator-configurable

Page 40: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Battery Operated

• Minimum 30 minutes of continuous compressions

• Maximum 4¼ hours recharge time

Page 41: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Easily Transportable

Transporter for HospitalsCarry Case for EMS

Page 42: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Halperin et al. @ Johns Hopkins• 20 16-kg pigs induced with VF for one minute• Treated with conventional CPR (“The Thumper”) or

the AutoPulse• Two arms of study

– “BLS” scenario – no epinephrine– “ALS” scenario – with epinephrine

• Regional flow measured with neutron-activated microspheres

Animal Hemodynamics Study (Halperin et al.)

Page 43: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse produced pre-arrest levels ofblood flow to the heart and brain

(ACLS protocol – with epinephrine)

Animal Hemodynamics Study (Halperin et al.)

29% 31%

127% 129%

0%

20%

40%

60%

80%

100%

120%

140%

Heart (Myocardium*) Brain (Cerebrum**)

% o

f P

re-a

rres

t B

loo

d F

low

Conventional CPR AutoPulse

Halperin HR et al. JACC. 2004;44(11):2214-20.

*p<0.02**p<0.003

Page 44: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Ikeno et al. @ Stanford• Objective was to evaluate the ability of

AutoPulse’s improved hemodynamics to affect survival

• Used a clinically relevant cardiac arrest model:– 8 min down – 4 min BLS – 4 min ALS

• End-points were ROSC, 24-hour survival and neurologic status at 24-hours

• CPR treatment was randomized to AutoPulse or conventional CPR (“The Thumper”)

Animal Survival Study (Ikeno et al.)

Page 45: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• 73% of subjects supported with the AutoPulse returned to normal blood flow and survived - 88% of the survivors were neurologically normal

• 0% of the subjects supported with only conventional CPR survived

Ikeno F et al. Resuscitation. 2006;68:109-118.

0

73%

0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

100%

% S

urv

ival

Conventional CPR AutoPulse

Animal Survival Study (Ikeno et al.)

0%

*p<0.01

Page 46: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Timerman et al. in Sao Paolo, Brazil• 16 terminally ill subjects who experienced in-hospital

cardiac arrest• Study initiated after at least 10 minutes of failed ACLS

support• AutoPulse and manual compressions were alternated for

90 seconds each• Catheters were placed in the thoracic aorta and right

atrium to measure CPP and peak aortic pressure• Average time between arrest and the start of

experiment was 30 (+/-5) minutes

Human Hemodynamics Study (Timerman et al.)

Page 47: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse-generated Coronary Perfusion Pressure (CPP)was 33% better than manual CPR

Human Hemodynamics Study (Timerman et al.)

Timerman S et al. Resuscitation. 2004;61:273-280.

15

20

0

5

10

15

20

25C

oro

na

ry P

erf

us

ion

Pre

ss

ure

(C

PP

) m

mH

g

Manual CPR AutoPulse

*p=0.015

Page 48: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

CPP drops quickly when AutoPulse

compressions stop

Manual CPR

CPP returns after several AutoPulse

compressions

AutoPulse AutoPulse

Human Hemodynamics Study Example

Timerman S et al. Resuscitation. 2004;61:273-280.

Page 49: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Casner et al. in San Francisco, CA• Compared the rate of delivery of 162 patients in

ROSC sustained to the ED– 93 patients treated with manual CPR– 69 patients treated with the AutoPulse

• Increased sustained ROSC rate was most pronounced when the initial presenting rhythm was asystole or PEA

Human Short-term Survival Study (Casner et al.)

Page 50: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse improved the rate of delivery of patients in ROSC sustained to the ED by 35%

Human Short-term Survival Study (Casner et al.)

Casner M et al. Prehospital Emergency Care. 2005;9(1):61-67.

*p=0.003

29%

39%

0%

10%

20%

30%

40%

RO

SC

to

ED

Ra

te

Manual CPR AutoPulse

Page 51: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Swanson et al. in Volusia County, FL• Compared the rate of delivery of 523 patients in

ROSC sustained to the ED– 405 patients treated with manual CPR– 118 patients treated with the AutoPulse

• Increased sustained ROSC rate was most pronounced when the initial presenting rhythm was asystole or PEA

Human Short-term Survival Study (Swanson et al.)

Page 52: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse improved the rate of delivery of patients in ROSC sustained to the ED by 53%

Human Short-term Survival Study (Swanson et al.)

Swanson M et al. Circulation. 2005;112(17):II-106.

*p=0.02

19%

29%

0%

10%

20%

30%R

OS

C t

o E

D R

ate

Manual CPR AutoPulse

Page 53: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Conducted by Ornato et al. in Richmond, VA• Compared survival rates in 783 patients

– 499 patients treated with manual CPR– 284 patients treated with the AutoPulse

• 235% improvement in survival to discharge• 88% improvement in survival to hospital admission• 71% improvement in field ROSC

(Ong, Ornatoet al.)

Human Long-term Survival Study

Page 54: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

AutoPulse improved survival to hospital discharge by 235%

(Ong, Ornatoet al.)

Ong ME, Ornato J et al. JAMA. 2006;295(22):2629-2637.

2.9%

9.7%

0%

5%

10%%

Su

rviv

al

Manual CPR AutoPulse

*p=0.0001

Human Long-term Survival Study

Page 55: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

• Clinical evidence support AutoPulse benefits– Animal study (Halperin et al.) shows blood

pressure equivalent to pre-arrest levels– Animal study (Ikeno et al.) shows blood pressure

equivalent to normal and neurologically intact survival

– Human study (Timerman et al.) shows improved blood pressure

– 2 human studies (Swanson et al. and Casner et al.) show improved short-term survival

– Human study (Ong, Ornato et al.) shows improved short and long-term survival

Research Synopsis

Page 56: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Disclosure Policy

It is the policy of Saint Louis University School of Medicine to insure balance,independence, objectivity and scientific rigor in its continuing medical education program. Faculty and planning committee participating in the planning and presentation of these activities are required to disclose to the audiences prior to the activity the following:

– Existence of any significant financial or other relationship with the manufacturer of any commercial product or provider of any commercial service discussed.

– Their intention to discuss a product that is not labeled for the use under discussion.

– Their intention to discuss preliminary research data.

Saint Louis University has reviewed this activity’s disclosures and resolved all identified conflicts of interest, if applicable.

Page 57: Course Objectives CPR: Ongoing Challenges. New Solutions. October 2007 © 2007 ZOLL Medical Corporation.

Validation of Content Statement

Saint Louis University School of Medicine follows the policy of the Accreditation Council for Continuing Medical Education (ACCME) regarding validation of clinical content for CME activities, which requires accredited sponsors to insure that: – All recommendations involving clinical medicine are based on

evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients.

– All scientific research referred to, reported or used in CME in support or justification of a patient care recommendation conforms to the generally accepted standards of experimental design, data collection and analysis.