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Peel/Halton 2010 CME Sheldon Cheskes, MD CCFP(EM) FCFP Medical Director Sunnybrook – Osler Centre for Prehospital Care Li Ka Shing Knowledge Institute,

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Presentation on theme: "Peel/Halton 2010 CME Sheldon Cheskes, MD CCFP(EM) FCFP Medical Director Sunnybrook – Osler Centre for Prehospital Care Li Ka Shing Knowledge Institute,"— Presentation transcript:

1 Peel/Halton 2010 CME Sheldon Cheskes, MD CCFP(EM) FCFP Medical Director Sunnybrook – Osler Centre for Prehospital Care Li Ka Shing Knowledge Institute, St. Michael’s Hospital Co Principal Investigator, Resuscitation Outcomes Consortium, Toronto Regional Rescuenet

2 Resuscitation Outcomes Consortium (ROC) What Studies Are Coming Down The Pike?

3 Previous Trials  ROC Epistry: Cardiac Arrest Data Base  ROC PRIMED: Early Vs Late Analysis and use of ITD  ROC HS: Hypertonic Saline in TBI and Hypovolemic Shock

4 EMS Providers Views  Enjoy taking part in randomized controlled trials  “Lots of work”  “Pain in the @@#%”  Challenges of randomization, documentation, and CPR process capture

5 Overwhelming View  Despite findings of previous ROC RCT  “Thirst for a positive trial”

6 What's Next For ROC EMS Agencies Cardiac Trials  ROC CCC  ROC Amiodarone Trauma Trials  ROC Lactate  ROC Hypotensive Resuscitation

7 Upcoming Trial Overview  Science  Methodology  EMS Challenges

8 ROC CCC Trial of Continuous Compressions vs Standard CPR in patient’s with out- of-hospital cardiac arrest

9 ROC CCC Science  Greater coronary perfusion pressure associated with greater ROSC in animal and human studies  Interruptions in chest compression reduce CPP  Observational studies suggest at least as effective as standard CPR  Observational trials instituted multiple changes? Impact of CCC

10 ROC CCC Science  Insertion of advanced airway associated with interruption in CPR  CCF (hands on time) increased in sites using CCC model  Increased CCF associated with increased survival from VF/VT

11 ROC CCC Methodology EMS arrival at patient (>18, non –traumatic cardiac arrest, lack of exclusion criteria) with randomization to: Control group  3 cycles of 2 minutes of standard (30:2) CPR  analysis after each 2 minute CPR cycle  standard site ventilatory treatment

12 ROC CCC Methodology Randomization Group:  3 cycles of 2 minutes of CPR using continuous compressions with no stops for ventilation  Analysis after each 2 minute CPR cycle

13 ROC CCC Methodology Ventilation Strategy In Randomization Group:  Sites will choose between two ventilation strategies Positive pressure ventilation  10 ventilations/minute via BVM with no CPR interruptions for ventilations Passive ventilation  Oral airway with oxygen via non re- breather at 15 l/min

14 ROC CCC Methodology Both Groups:  IV or IO with epinephrine or vasopressin given within 5 minutes of ALS arrival  After advanced airway inserted ventilation rate at 10/minute compression rate at 100/minute (current standard) until ROSC or termination of resuscitation

15 ROC CCC EMS Challenges  Maximize CPR process files***  Randomization: cluster and frequency of cross over  ALS medics not intubating for first five minutes  Supraglottic airways: advanced or not?  Bagging while doing compressions in unprotected airway

16 ROC Amiodarone Amiodarone (pm101), lidocaine or neither for out-of-hospital cardiac arrest due to ventricular fibrillation or tachycardia

17 ROC Amiodarone Science  Little evidence that anti-arrythmics have any impact on survival from OHCA  Given lack of evidence question is not just which anti-arrythmic should be used but should any be used?  Since no evidence of improvement in survival to discharge inclusion of placebo arm is required

18 ROC Amiodarone Science  Three staged model of cardiac arrest  Antiarrythmics necessary to correct electrical abnormalities  Previous trials of antiarrythmics delayed administration until well into metabolic phase  Optimal approach would be administration during electrical or circulatory phase

19 ROC Amiodarone Science  ALIVE: amiodarone recipients more likely to survive to hospital  ARREST: similar results to ALIVE  Neither trial designed or powered to evaluate survival to discharge  Occurred in era of “poor CPR” (stacked shocks, shock pauses of greater length, pulse checks)  Late amiodarone! (given 21-25 after call received, given 10 minutes after IV established)

20 ROC Amiodarone Science Amiodarone the drug  Amio insoluble in water, polysorbate 80 used as diluent  Makes amio difficult to deliver, drawn up from glass ampules then diluted before use  Tends to foam due to diluent  Incompatible with solutions other then D5W  Diluent (as opposed to drug) causes hypotension and phlebitis

21 ROC Amiodarone Science Captisol-enabled amiodarone (pm101)  New FDA approved formulation using diluent (captisol)  Diluent clear, hemo and electro inert  Compatible with solutions other then D5W  does not absorb in plastic  pre filled syringe  IV push immediately after IV established

22 ROC Amiodarone Methodology  Confirmed non traumatic cardiac arrest  BLS CPR, analysis, shock and IV/IO established  After 1st shock**, CPR established, vasopressor flush, study drug x 2 flush while ongoing CPR  2nd analysis if shockable> shock, CPR, advanced airway, vasopressor  3rd analysis if shockable> shock, CPR, study drug x1

23 ROC Amiodarone Methodology Study Drug Kit Contents

24 ROC Amiodarone Methodology Rationale for lack of Rescue arm for persistent VF/VT  Further open label doses may risk toxicity  Require un-blinding in field (difficult)  Neither study drug class 1 recommendation  No preclusion to other treatments (EPI, MAG, B Blocker, etc)  Cross-over makes analysis more difficult

25 ROC Amiodarone EMS Challenges  Timing of Amiodarone delivery (voice, defib, guess!)  Tracking study kits, (remember ITDs!)  Randomization  Focus on early administration (new approach to delivery)  Local REB > will they allow a placebo arm?

26 ROC Lactate Prehospital lactate for the identification of shock in trauma

27 ROC Lactate Science  Recent prospective out-of-hospital research suggest HR and hypotension poor predictors of need for intervention in trauma  Hypotension late finding  Delayed identification of hypo-perfusion results in delayed definitive care

28 ROC Lactate Science  Lactate biomarker of organ oxygen supply/demand mismatch  Elevated in sepsis, MI, trauma  Historically only measured in hospital  Now available point of care (POC) testing of lactate level in prehospital care  To date lactate testing predicts severity of hemorrhage, mortality and need for ICU admission

29 ROC Lactate Science  Can POC testing be used as a triage tool?  Can we predict patients who will need resuscitative care that would not have been predicted otherwise?

30 ROC Lactate Methodology Prospective observational study to identify patients suffering from hypo-perfusion secondary to trauma  Included patients meet local TT guidelines:  BP < 100,  Transported to level 1 or 2 trauma center  Died in field or en route  Exclusions >isolated penetrating head injury

31 ROC Lactate Methodology  Patient identified, IV established, 50 micro liter (drop of blood) applied to POC lactate meter (similar to glucometer)  EMS blinded to result until reach ER  No change in EMS treatment based on POC testing  Second lactate to be drawn in ER

32 ROC Lactate Methodology ROC Lactate Meter

33 ROC Lactate EMS Challenges  Pure ALS trial  Need for trauma center transport  Accurate documentation of lactate time of draw  Will medics un-blind and alter treatment?  POC calibration  POC tracking  Blood sample after IV as opposed to before

34 ROC Hypotensive Resuscitation Field trial of hypotensive resuscitation vs. Standard resuscitation in patients with hemorrhagic shock after trauma-a pilot study

35 ROC Hypotensive Resuscitation Science  Traditional treatment of trauma patients> aggressive fluid resuscitation to restore circulating volume, SBP  Increasing animal and human studies showing detrimental effects of massive fluid resus prior to hemorrhage control  Associated with cardiac dysfunction, abdominal compartment syndrome, ARDS, hypothermia and coagulopathy

36 ROC Hypotensive Resuscitation Science  Three RCTS, two observational studies suggest harm of aggressive fluid resuscitation as opposed to no prehospital fluids until hospital arrival  No study shows clear superiority of aggressive fluid resus vs hypotensive resuscitation yet aggressive fluid resus cornerstone of ATLS and PTLS teaching  RCT required to better answer the question

37 ROC Hypotensive Resuscitation Methodology  Patient with shock after trauma randomized to either standard or hypotensive Resusc arm  Inclusion: blunt or penetrating trauma, age> 15 or 50 kg, SBP 8  Exclusions (many)> fluid started by non ROC agency, ongoing CPR

38 ROC Hypotensive Resuscitation Methodology  Complete randomization (as opposed to a priori)  Participating agencies carry pre randomized, sealed, numbered containers  Patient randomized and entered once container opened  Containers with 1000 cc or 250 cc iv normal saline bags  EMS will not know randomization until container opened

39 ROC Hypotensive Resuscitation Methodology Tote bag to hold two Hypotensive Resusc fluid boxes Two cardboard boxes per tote will disguise/blind different size of IV fluid bags

40 ROC Hypotensive Resuscitation Methodology Once container opened if 1000 cc bag randomized to control arm:  IV fluid given as rapidly as possible until ER arrival  If prehospital volume of 2 liters reached fluid stopped if SBP >110

41 ROC Hypotensive Resuscitation Methodology If container opened and 250 cc bag randomized to experimental group:  IV hung and if radial pulse or SBP > 70 TKVO fluids  no radial pulse or SBP < 70 begin 250 cc infusion until radial pulse returns or SBP 70  EMS agencies given option of using radial pulse or SBP as means of BP monitoring

42 ROC Hypotensive Resuscitation Methodology  ALS trial  Significant in-hospital component  Bong  Canister technique  Hypotensive resuscitation in severe head injury?  Tracking of treatment canisters

43 Other Studies At Various Levels  ROC Hypothermia (PreHospital Hypothermia)  ROC RESUCE (Estrogen Use In Trauma)

44 EMS Challenges For All ROC Trials  Competing non ROC research  Training and training cycles  REB approvals  Multiple studies…which one do we choose?  SMC requirements for continued participation  Paramedic research burnout  Long down time between recent HS and PRIMED

45 Questions?


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