Resuscitation Outcomes Consortium: Overview and Update

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Transcription:

Resuscitation Outcomes Consortium: Overview and Update RESUSCITATION OUTCOMES CONSORTIUM OPALS PRG Annual Meeting Ottawa 2006

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED 4Others The Future

1. Mandate and Overview Cardiac arrest and severe traumatic injury common problems in North America Mortality high: 4 90-95% for cardiac arrest 4 60% for severe trauma Much progress in managing acute MI and HF patients due to basic and clinical trial research funded by NHLBI and CIHR Historically only modest amount of funding for basic research on cardiac arrest and severe traumatic injury

1. Mandate and Overview The ROC Consortium the first large-scale effort to conduct clinical trials in cardiac arrest and severe traumatic injury Focuses on very early delivery of interventions by Emergency Medical Services (EMS) teams in the field, when optimal potential for benefit

1. Mandate and Overview In the first two years, ROC investigators have: Launched a large out-of-hospital cardiac arrest and trauma registry (Epistry) Started enrolling trauma patients in clinical trial of hypertonic IV fluid (HSD Trial) Rolled out a plan to monitor CPR Process in all out-of-hospital cardiac arrests Prepared to launch a factorial cardiac arrest trial (ROC PRIMED) that will evaluate: 4 ITD valve - small CPR adjunct 4 Strategy of delayed defibrillation

1. Mandate and Overview Expected enrollment: 4 10,000 major trauma cases/year in Epistry 4 17,500 cardiac arrests/year in Epistry 4 5,848 patients in HSD Trial 4 15,000 patients in ROC PRIMED Trial

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners 4Funding 4Sites 4 Data Collection Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED

RESUSCITATION OUTCOMES CONSORTIUM National Heart, Lung and Blood Institute Canadian Institutes of Health Research U.S. Department of Defense National Defence Canada

ROC 10 Clinical Sites

2. Partners: Sites and PIs Alabama Resuscitation Center: Jeff Kerby, MD Dallas, TX: Ahamed Idris, MD Iowa City, IA: Richard Kerber, MD Milwaukee, WI: Tom Aufderheide, MD Pittsburgh, PA: Clif Calloway, MD Portland, OR: Jerris Hedges, MD Ottawa, ON / Vancouver, BC: Ian Stiell, MD Jim Christenson, MD, Co-PI San Diego, CA: Dan Davis, MD Seattle / King County, WA: Peter Kudenchuk, MD Toronto, ON: Art Slutsky, MD Laurie Morrison, MD and Paul Dorian, MD, Co-PIs

2. Partners: How Big are We? 268 EMS and fire agencies 35,000 square miles 24 million people 3,500 EMS vehicles 30,000 EMS personnel 100 IRB s 289 hospitals

2. Partners: Data Coordinating Center (DCC) U of Washington Clinical Trials Center: Scott Emerson, MD, PhD - PI Graham Nichol, MD - Co-PI Eileen Bulger, MD - Co-PI Judy Powell, BSN - Project Director Art Kerr, MBA - Project Manager Berit Bardarson, RN - Consultant, Trauma Lois Von Ottingham, RN Consultant, Cardiac Gena Sears, RN Consultant, Epistry

2. Partners: Study Chairs and NIH Project Officer Myron L. Weisfeldt, MD -Study Chair 4 Johns Hopkins Medical Institutions 4 Baltimore, MD Joseph P. Ornato, MD - Co-Chair-Cardiac 4 Virginia Commonwealth University Health 4 Richmond, VA David Hoyt, MD - Co-Chair-Trauma 4 University of California 4 San Diego, CA George Sopko, MD Project Officer 4 NHLBI

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED 4Others The Future

3. Project Updates: ROC Epistry A prospective, population-based, epidemiologic data registry of patients seen by EMS providers: Life-threatening trauma Cardiac arrest

3. Project Updates: ROC Epistry Primary aims: A comprehensive ongoing data infrastructure to facilitate ROC clinical trials Define the incidence and outcome of major trauma and out-of-hospital cardiac arrest Describe the relationships between resuscitation performance and EMS structure Evaluate relationships between outcome and patient, EMS, regional, and temporal factors

3. Project Updates: - ROC Epistry Will become world s largest traumatic injury and cardiac resuscitation data sets: 4 10,000/year major trauma 4 17,500/year cardiac arrest Opportunity to develop and assure quality of data collection and communication systems among EMS systems, sites, and DCC Will facilitate subsequent clinical trials where timely acquisition of quality data is essential

3. Project Updates: ROC Epistry Launched in December 2005 EMS providers are becoming familiar with rigorous data gathering and quality control ROC DCC staff conducted field visits to all sites to review sample cases Employs both web-based or batch upload data entry Comprehensive operations manual with detailed definitions of all variables

Epistry Update October 23 2006 15,135 cases enrolled overall 4 58% of estimated annual enrollment 4 One site has just received IRB approval 3,825 trauma cases 4 59% completed 4 median time to completion 66 days 11,310 cardiac arrest cases 4 62% completed 4 median time to completion 55 days

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial in Trauma 4CPR Process 4ROC PRIMED 4Others The Future

3. Project Updates: HSD Trial in Trauma Hypertonic Saline Dextran Trial - hemorrhagic shock and severe traumatic brain injury (TBI) Data suggest potential benefits from pre-hospital resuscitation with hypertonic fluids Potential to improve outcome via: 4 Improved tissue perfusion 4 Reduced cerebral swelling in TBI 4 Modulation of inflammatory response

3. Project Updates: HSD Trial in Trauma The primary aims are to determine if pre-hospital hypertonic fluid resuscitation: Reduces mortality after hemorrhagic shock Improves neurologic outcome after severe TBI Reduces the rates of inflammatory organ injury (ARDS and MODS) after hemorrhagic shock Requires dextran as a component to impact outcome

3. Project Updates: HSD Trial in Trauma Randomized double-blind trials to evaluate same intervention in 2 patient cohorts: 4 Severe TBI 4 Hemorrhagic shock Compares field IV administration of 250 ml: 1. 7.5% saline alone 2. 7.5% saline / 6% Dextran-70 3. 0.9% saline Primary outcomes: 4 Neurologic outcome at 6 months - TBI cohort 4 28-day survival - shock cohort

3. Project Updates: HSD Trial in Trauma Sample size 5,848: 4 2,122 in TBI cohort 4 3,726 in shock cohort Timeline: 4 24 months for TBI 4 42 months for shock Importance: 4 Definitively define the role of these therapies in the early resuscitation of trauma 4 Potential to change the standard for resuscitation that has not changed in 30 years

HSD Trial in Trauma Status October 26 th 1 st site commenced enrollment June 2006 5 of the 10 ROC sites had started All sites expected to have IRB approval by Jan 2007 140 cases enrolled

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED 4Others The Future

3. Project Updates: CPR Process Monitoring Rationale: Recent studies have demonstrated that CPR is often not performed according to guidelines Greater rate of chest compressions associated with higher rate of ROSC Observation of deleterious hyperventilation in recent study confirms importance of monitoring CPR process

3. Project Updates: CPR Process Monitoring Evolving Technologies offer the ability to monitor CPR process through AEDs: Chest impedance to monitor chest compression rate and ventilation rate Chest acceleration to monitor chest compression rate, depth, release, and duty cycle Audio recording to monitor audible events

3. Project Updates: CPR Process Monitoring Measurement of CPR Process: Rate of chest compressions Rate of ventilation CPR flow fraction 4 proportion of pulseless resuscitation time with chest compressions First five minutes

3. Project Updates: CPR Process Monitoring Devices ALS: 4 LP-12 Medtronic ERS Inc 4 MRX Philips Inc and Laerdal Inc 4 M- and E-Series Zoll Inc BLS: 4 LifePak 500 Medtronic ERS Inc 4 Heartstart & MRX Philips Inc and Laerdal 4 AED Pro BLS Zoll Inc

3. Project Updates: CPR Process Monitoring Performance Standards Parameter Target Min-Max Ventilation / min 10-12 6-16 Chest Compression / min 100 80-120 CPR Flow Fraction 0.85 0.5 -

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED for Cardiac Arrest 4Others

3. Project Updates: ROC PRIMED for Cardiac Arrest A Factorial Design of An Active Impedance Threshold Valve versus Sham Valve and Analyze Later versus Analyze Early Incorporates 2 interventions to improve hemodynamics during CPR: 1. Impedance threshold device (ITD) 2. Chest compressions before rhythm analysis

3. Project Updates: ROC PRIMED for Cardiac Arrest 1. Impedance Threshold Device (ITD) Enhances venous return and cardiac output by increasing negative intrathoracic pressure during decompression phase of CPR Promising results in preliminary clinical trial [Aufderheide] Randomize real valve vs. sham valve ResQPod Advanced Circulatory Systems

Impedance Threshold Device Bag Valve Mask Set-up Endotracheal Tube Set-up

3. Project Updates: ROC PRIMED for Cardiac Arrest 2. Analyze Later Vs. Analyze Early Defibrillation may be more effective if CPR is given prior to shock for patients in circulatory phase of VF (prime the pump) Electrical Phase Circulatory Phase Metabolic Phase 0 2 4 6 8 10 12 14 16 18 20 Arrest Time (min)

2. Analyse Later vs. Analyse Early Cluster Randomization; EMS & Fire Compressor Other Provider(s) Compressor Other Provider(s) 30-60 sec Apply AED and turn on Apply ITD 30-60 sec 50+ compressions Apply AED and turn on Apply ITD 300 compressions Analyze/shock 3 min Analyze/shock ACLS ACLS Analyse Later Analyse Early

3. Project Updates: ROC PRIMED for Cardiac Arrest Primary outcome: survival to hospital discharge with Modified Rankin Score <3 Sample size and timeline: 15,000 patients over 16-18 months Approvals: ROC Protocol Review Committee, ROC DSMB, Health Canada, and FDA IRB reviews underway Detailed training package and data entry screens developed Expected launch: early 2007

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED 4 Other Projects The Future

3. Project Updates: Other Projects Ancillary studies will test physiological or mechanistic hypotheses or refine methodology: 1. In HSD Trial, will evaluate the effect of interventions on inflammatory response 2. In ROC PRIMED, will test real-time auditory and visual feedback on the performance of CPR 3. In ROC PRIMED, will evaluate the optimal assessment tool for functional status of survivors of cardiac arrest

3. Project Updates: Other Projects 4. In Epistry, expanded data collection to refine triage criteria of patients to trauma centers 5. In Epistry, determine associations between ventilation rate and outcome in cardiac arrest and trauma 6. In HSD and ROC PRIMED, will collect data on time and effort required to perform community consultation and notification required to obtain waiver/exception from informed consent for emergency research

Resuscitation Outcomes Consortium: Overview Mandate and Overview Partners Project Updates: 4Epistry 4HSD Trial 4CPR Process 4ROC PRIMED 4 Other Projects The Future

4. Future Projects In Cardiac Arrest: The value of ECG waveform analysis to indicate shock or no shock The value of immediate CPR performance feedback Early hypothermia A number of pharmacologic agents including beta blockers, erythropoietin, and female hormones

4. Future Projects In Traumatic Injury: The value of controlled ventilation Female sex hormones Other solutions as suggested by the current HSD Trial Anti-oxidant agents with a broad safety profile

RESUSCITATION OUTCOMES CONSORTIUM

Resuscitation Outcomes Consortium Ian Stiell MD MSc FRCPC Professor and Chair Dept of Emergency Medicine University of Ottawa