1 / 29

CPR 2000

CPR 2000. Dr. THANAPONG HONGPROMYATI. Adult Cardiac Arrest. BLS algorithm if appropriate. Precordial thumb if appropriate. Attach defibrillator/monitor. Assess rhythm. 1. 2. Figure 1. ILCOR Universal/International ACLS Algorithm. Assess rhythm. 3. 4. Check pulse+/-. VF/VT.

ravi
Download Presentation

CPR 2000

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. CPR 2000 Dr. THANAPONG HONGPROMYATI

  2. Adult Cardiac Arrest BLS algorithm if appropriate Precordial thumb if appropriate Attach defibrillator/monitor Assess rhythm 1 2 Figure 1. ILCOR Universal/International ACLS Algorithm.

  3. Assess rhythm 3 4 Check pulse+/- VF/VT Non-VF/VT During CPR 5,6 Attempt defibrillation *3 as necessary 3 • Check electrode/paddle position and contact • Attempt to place, confirm, secure airway • Attempt and verify IV access • Patients with VF/VT refractory to initial shocks: - Epinephrine 1 mg IV, every 3-5 min or - Vasopressin 40 U IV, single dose, 1 time only • Patients with non-VF/VT rhythm: - Epinephrine 1 mg IV, every 3-5 min • Consider: buffers, antiarrhythmics, pacing • Search for and correct reversible cause CPR up to 3 min CPR for 1 min Figure 1. ILCOR Universal/International ACLS Algorithm.

  4. Consider causes that are potentially reversible • Hypovolemia • Hypoxia • Hydrogen ion-acidosis • Hyper-/Hypokalemia • Hypothermia • “Tablet” (drug OD,accidents) • Temponade, cardiac • Tension pneumothorax • Thrombosis, coronary (ACS) • Thrombosis, pulmonary (embolism) 7 Figure 1. ILCOR Universal/International ACLS Algorithm.

  5. Person collapses • Possible cardiac arrest • Assess responsiveness Unresponsive Begin Primary ABCD Survey (Begin BLS Algorithm) 1 • Activate emergency response system • Call for defibrillator • A Assess breathing (open airway, look, listen, and feel) No Breathing • B Give 2 slow breaths • C Assess pulse, if no pulse • CStart chest compressions • D Attach monitor/defibrillator when available 1 No pulse Figure 2. Comprehensive ECC Algorithm.

  6. No pulse • CPR continues • Assess rhythm Attempt defibrillation (Up to 3 shock if VF persists) Non-VF/VT (asystole or PEA) 2 3 Secondary ABCD Survey 4,5 • Airway: attempt to place airway device • Breathing: confirm and secure airway device, ventilation, oxygenation • Circulation: gain intravenous access; give adrenergic agent; consider antiarrhythmics, buffer agents, pacing CPR up to 3 min CPR for 1 min Non-VF/VT patients: - Epinephrine 1 mg IV, repeat every 3-5 min VF/VT patients: - Vasopressin 40 U IV, single dose, 1 time only or - Epinephrine 1 mg IV, repeat every 3-5 min • Differential Diagnosis: search for and treat reversible cause Figure 2. Comprehensive ECC Algorithm.

  7. Primary ABCD Survey Focus: basic CPR and defibrillation • Check responsiveness • Activate emergency response system • Call for defibrillator Rhythm after first 3 shocks? 1 A Airway:open the airway B Breathing: provide positive-pressure ventilations C Circulation: give chest compressions D Defibrillation: assess for and shock VF/pulesless VT, up to 3 times (200J,200-300J,360J, or equivalent biphasic) if necessary Figure 3. Ventricular Fibrillation/Pulseless VT Algorithm.

  8. Secondary ABCD Survey A Airway: Place airway device as soon as possible • B Breathing: • Confirm airway device placement by exam plus confirmation device. • Secure airway device; purpose-made tube holders preferred. • Confirm effective oxygenation and ventilation. Focus: more advanced assessments and treatments • C Circulation: • Establish IV access. • Identify rhythm; monitor. • Administer drugs appropriate for rhythm and condition. D Differential Diagnosis: Search for and treat identified reversible causes. Persistent or recurrent VF/VT 2 Figure 3. Ventricular Fibrillation/Pulseless VT Algorithm.

  9. Resume attempts to defibrillate 5 Epinephrine 1 mg IV push, repeat every 3 to 5 minutes or Vasopressin 40 U IV, single dose, 1 time only 3 Resume attempts to defibrillate 1*360J (or equivalent biphasic) within 30 to 60 sec. Consider antiarrhythmics: amiodarone (IIb), lidocaine (Indeterminate), magnesium (IIb if hypomagnesemic state), procainamide (IIb for intermittent/recurrent VF/VT). Consider buffers. 4 Figure 3. Ventricular Fibrillation/Pulseless VT Algorithm.

  10. Antiarrhythmics & Buffer • Amiodarone(class IIb) 300 mg IV push (cardiac arrest dose) If VF/pulseless VT recurs, consider administration of a second dose of 150 mg IV. Max cumulative dose 2.2 g over 24 hr. • Lidocaine (class Indeterminate) 1.0 - 1.5 mg/kg IV push. Consider repeat in 3 to 5 min to a max cumulative dose of 3 mg/kg. • Magnesiumsulfate 1 to 2 g IV in polymorphic VT (torsades de pointes) and suspected hypomagnesemic state. • Procainamide 30 mg/min in refractory VF (Max total dose: 17 mg/kg) is acceptable but not recommended • Sodiumbicarbonate 1 mEq/kg IV is indicated for several conditions known to provoke sudden cardiac arrest.

  11. PULSELESS ELECTRICAL ACTIVITY (PEA = Rhythm on monitor, without detectable pules) Primary ABCD Survey Focus: basic CPR and defibrillation • Check responsiveness • Activate emergency response system • Call for defibrillator A Airway:open the airway B Breathing: provide positive-pressure ventilations C Circulation: give chest compressions D Defibrillation: assess for and shock VF/pulesless VT Figure 4. Pulseless Electrical Activity Algorithm.

  12. A Airway: Place airway device as soon as possible Secondary ABCD Survey • B Breathing: • Confirm airway device placement by exam plus confirmation device. • Secure airway device; purpose-made tube holders preferred. • Confirm effective oxygenation and ventilation. Focus: more advanced assessments and treatments • C Circulation: • Establish IV access. • Identify rhythm; monitor. • Administer drugs appropriate for rhythm and condition. • Assess for occult blood flow (“pseudo-EMT”) D Differential Diagnosis: Search for and treat identified reversible causes. EMD=electro-mechanical dissociation Figure 4. Pulseless Electrical Activity Algorithm.

  13. Review for most frequent causes 1 • Hypovolemia • Hypoxia • Hydrogen ion-acidosis • Hyper-/Hypokalemia • Hypothermia • “Tablet” (drug OD,accidents) • Temponade, cardiac • Tension pneumothorax • Thrombosis, coronary (ACS) • Thrombosis, pulmonary (embolism) Epinephrine 1 mg IV push, repeat every 3 to 5 minutes 2 Atropine 1 mg IV (if PEA rate is slow), repeat every 3-5 minutes as need, to a total dose of 0.04 mg/kg 3 Figure 4. Pulseless Electrical Activity Algorithm.

  14. Primary ABCD Survey Focus: basic CPR and defibrillation • Check responsiveness • Activate emergency response system A Airway:open the airway • Call for defibrillator B Breathing: provide positive-pressure ventilations C Circulation: give chest compressions Confirm true asystole D Defibrillation: assess for VF/pulesless VT; shock if indicate Asystole 1 Rapid scene survey: any evidence personnel should not attempt resuscitation? Figure 5. Asystole: The Silent Heart Algorithm.

  15. A Airway: Place airway device as soon as possible Secondary ABCD Survey • B Breathing: • Confirm airway device placement by exam plus confirmation device. • Secure airway device; purpose-made tube holders preferred. • Confirm effective oxygenation and ventilation. Focus: more advanced assessments and treatments • C Circulation: • Confirm true asystole • Establish IV access. • Identify rhythm; monitor. • Administer drugs appropriate for rhythm and condition. D Differential Diagnosis: Search for and treat identified reversible causes. 2,3 Figure 5. Asystole: The Silent Heart Algorithm.

  16. Transcutaneous pacing If considered, perform immediately 4 Epinephrine 1 mg IV push, repeat every 3 to 5 minutes 5 Atropine 1 mg IV, repeat every 3 to 5 minutes up to a total of 0.04 mg/kg 6 Asystole persists Withhold or cease resuscitation efforts? 7,8,9 • Consider quality of resuscitation? • Atypical clinical features present? • Support for cease-efforts protocols in place? Figure 5. Asystole: The Silent Heart Algorithm.

  17. 2 7 • Confirm true asystole- Check lead and cable connection- Monitor power on?- Monitor gain up ?- Verify asystole in another lead • Review the quality of the resuscitation attempt- Was there an adequate trial of BLS? of ACLS? Has the team done the following:- Achieved tracheal intubation?- Performed effective ventilation?- Shocked VF if present?- Obtained IV access?- Given epinephrine IV? Atropine IV?- Ruled out or corrected reversible causes?- Continuously documented asystole >5 to 10 min after all of the above have been accomplished? • Reviewed for atypical clinical features?- Not a victim of drowning or hypothermia?- No reversible therapeutic or illicit drug overdose? 8

  18. Bradycardia • Slow (absolute bradycardia = rate<60bpm • Relatively slow (rate less than expected relative to underlying condition or cause) Primary ABCD Survey • Assess ABCs • Secure airway noninvasively • Ensure monitor/defibrillator is available Secondary ABCD Survey • Assess secondary ABCs (invasive airway management needed?) • Oxygen-IV access-monitor-fluids • Vital sign, pulse oximeter, monitor BP • Obtain and review 12 lead ECG • obtain and review portable Chest x-ray • Problem-focused history • Problem-focused physical examination • Consider cause (differential diagnoses) Figure 6. Bradycardia Algorithm.

  19. Serious sign or symptom? Due to the bradycardia? 1,2 Yes No • Intervention sequence • Atropine 0.5-1.0 mg • Transcutaneous pacing if available • Dopamine 5-20 ug/kg per min • Epinephrine 2-10 ug/min 3,4,5 Type II second-degree AV block or Third-degree AV block? 6 No Yes • Prepare for transvenous pacer • If symptoms develop, use transcutaneous pacemaker until transvenous pacer placed 7 Observe Figure 6. Bradycardia Algorithm.

  20. 1 2 • If the patient has serious sign or symptoms, make sure they are related to the slow rate. • Clinical manifestations include- Symptoms (chest pain, shortness of breath, decrease level of consciousness)- Signs (low blood pressure, shock, pulmonary congestion, CHF) • If the patient is symptomatic, do not delay transcutaneous pacing while awaiting IV access or for atropine to take effect • Denervated transplanted hearts will not response to atropine. Go at once pacing, catecholamine infusion, or both. • Never treat the combination of third-degree heart block and ventricular escape beats with lidocaine (or any agent that suppresses ventricular escape rhythms) 3 4 6

  21. Evaluate patient • Is patient stable or unstable? • Are there serious signs or symptoms? • Are signs and symptoms due to tachycardia? Stable Unstable • Unstable patient: serious signs or symptoms • Establish rapid heart rate as cause of signs and symptoms • Rate related signs and symptoms occur at many rates, seldom < 150 bpm • Stable patient: no serious signs and symptoms • Initial assessment identified 1 of 4 type of tachycardia • Atrial fibrillation/flutter • Narrow-complex tachycardia • Stable wide-complex tachycardia: unknown type • Stable monomorphic VT and/or polymorphic VT • Prepare for immediate cardioversion (see algorithm) Figure 7. The Tachycardia Overview Algorithm.

  22. 1. Atrial fibrillation Atrial flutter Evaluation focus, 4 clinical features: 1. Patient clinical unstable? 2. Cardiac function impaired? 3. WPW present? 4. Duration<48 or >48 hours? Treatment focus: clinical evaluation 1. Treat unstable patient urgently 2. Control the rate 3. Convert the rhythm 4. Provide anticoagulation Treatment of atrial fibrillation/atrial flutter (See following table) Figure 7. The Tachycardia Overview Algorithm.

  23. 2. Narrow-complex tachycardia • Attempt to establish a specific diagnosis • 12 lead ECG • Clinical information • Vagal maneuvers • Adenosine • Diagnosis effort yield • Ectopic atrial tachycardia • Multifocal atrial tachycardia • Paroxysmal supraventricular tachycardia Treatment of SVT (see narrow-complex tachycardia algorithm) Figure 7. The Tachycardia Overview Algorithm.

  24. 3. Stable wide-complex tachycardia: unknown type 4. Stable monomorphic VT and/or polymorphic VT • Attempt to establish a specific diagnosis • 12-lead ECG • Esophageal lead • Clinical information Treatment of stable monomorphic and polymorphic VT (see stable VT: monomorphic and polymorphic algorithm) Confirmed SVT Confirmed stable VT Wide-complex tachycardia of unknown type Treatment of SVT (see narrow- complex tachycardia algorithm) Preserved cardiac function Ejection fraction < 40% Clinical CHF Dc cardioversion or Amiodarone Dc cardioversion or Procainamide or Amiodarone Figure 7. The Tachycardia Overview Algorithm.

  25. Control of Rate and Rhythm (Continued From Tachycardia Overview) • AF/flutter with • Normal heart • Impair heart • WPW 2. Control Rhythm 1. Control Rate Duration<48Hrs Duration>48Hrs or Unknown • Consider • DC cardioversion Note: If AF>48 hours’ duration, use agents to convert rhythm with extreme caution in patients not receiving adequate anticoagulation because of possible embolic complications. • NODC cardioversion! • Note: Conversion of AF to NSR with drugs or shock may cause embolization of atrial thrombi unless patient has adequate anticoagulation. • Use antiarrhythmic agents with extreme caution if AF>48 hours’ duration (see note below). or • Use only 1 of the Class IIa following agents (see note below): • Amiodarone • Ibutilide • Flecainide • Propafenone • Procainamide • For additional drugs that are Class IIb recommendation, see Guidelines or ACLS text Normal cardiac function • Use only 1 of the following agents (see note below): • Calcium channel blockers(ClassI) • B-Blockers(ClassI) • For additional drugs that are ClassIIb recommendations, see Guideline or ACLS text • Delayed cardioversion Anticoagulation * 3 weeks at proper levels • Cardioversion, then • Anticoagulation * 4 weeks more or Early cardioversion • Begin IV heparin at once • TEE to exclude atrial clot. then • Cardioversion within 24 h. then • Anticoagulation * 4 more weeks Note:If AF>48hours’ duration, use agents to convert rhythm with extreme caution in patients not receiving adequate anti coagulation because of possible embolic complications. • Consider • DC cardioversion or • Amiodarone (ClassIIb) Impaired heart (EF<40% or CHF) • Anticoagulation as described above, following by • DC cardioversion • Use only 1 of the following agents: • Digoxin (ClassIIb) • Diltiazem (ClassIIb) • Amiodarone(ClassIIb)

  26. Control of Rate and Rhythm (Continued From Tachycardia Overview) • AF/flutter with • Normal heart • Impair heart • WPW 1. Control Rate 2. Control Rhythm Heart Function Preserved Impaired Heart EF<40% or CHF Duration<48Hrs Duration>48Hrs or Unknown Note: If AF>48 hours’ duration, use agents to convert rhythm with extreme caution in patients not receiving adequate anticoagulation because of possible embolic complications. Note: If AF>48 hours’ duration, use agents to convert rhythm with extreme caution in patients not receiving adequate anticoagulation because of possible embolic complications. • Consider • DC cardioversion or • Primary anti- arrhythmic agents Use only 1 of the following agents (see note below**): • Anticoagulation as described above, following by • DC cardioversion WPW • DC cardioversion or • Primary anti- arrhythmic agents Use only 1 of the following agents (see note below): • DC cardioversion or • Amiodarone (ClassIIb) • Amiodarone (ClassIIb) • Flecainide (ClassIIb) • Procainamide (ClassIIb) • Propafenone (ClassIIb) • Sotalol (ClassIIb) • Amiodarone (ClassIIb) • Flecainide (ClassIIb) • Procainamide (ClassIIb) • Propafenone (ClassIIb) • Sotalol (ClassIIb) • Class III (can be harmful) • Adenosine • B-Blockers • Calcium blockers • Digoxin • Class III (can be harmful) • Adenosine • B-Blockers • Calcium blockers • Digoxin

  27. Narrow-Complex Supraventricular Tachycardia, Stable • No DC Cardioversion • Amiodarone • B-Blocker • Ca2+ channel blocker • Attempt therapeutic diagnosis maneuver • Vagal stimulation • Adenosine Preserved EF<40%, CHF • No DC cardioversion • Amiodarone Junctional tachycardia • Priority order: • Ca2+ Channel blocker • B-Blocker • Digoxin • DC cardioversion • Consider procainamide, amiodarone, sotalol Preserved Paroxysmal supraventricular tachycardia • Priority order: • No DC cardioversion • Amiodarone • Diltiazem EF<40%, CHF • No DC cardioversion • Ca2+ channel blocker • B-Blocker • Amiodarone Preserved Ectopic or multifocal atrial tachycardia EF<40%, CHF • No DC cardioversion • Amiodarone • Diltiazem Figure 8. Narrow-Complex Supraventicular Tachycardia Algorithm.

  28. Stable Ventricular Tachycardia Monomorphic or Polymorphic? • Monomorphic VT • Is cardiac function impaired? • Polymorphic VT • Is QT baseline interval prolonged? Note! May go directly to cardioversion Prolong baseline QT interval (suggests torsades) Normal baseline QT interval Normal function Poor ejection fraction • Medications: any one • Procainamide • SotalolOther acceptable • Amiodarone • Lidocaine • Long baseline QT interval • Correct abnormal electrolytesMedications: any one • Magnesium • Overdrive pacing • Isoproterenol • Phenytoin • Lidocaine • Normal baseline QT interval • Treat ischemia • Correct electrolytesMedications: any one • B-Blocker or • Lidocaine or • Amiodarone or • Procainamide or • Sotalol • Amiodarone • 150 mg IV bolus over 10 min. orLidocaine • 0.5 to 0.75 mg/kg IV push. Then use • Synchronized cardioversion Figure 9. Stable Ventricular Tachycardia (Monomorphic or Polymorphic) Algorithm.

  29. Synchronized cardioversion • ventricular tachycardia • Paroxysmal supraventriculartachycardia • Atrial fibrillation • Atrial flutter 100J, 200J 300J, 360J monophasic energy dose (or clinical equivalent biphasic energy dose) Tachycardia with serious signs and symptoms related to the tachycardia If ventricular rate is > 150 bpm, prepare for immediate cardioversion. May give brief trial of medications based on specific arrhythmias. Immediate cardioversion is generally not need if heart rate is <= 150 bpm. • Have available at bedside • oxygen saturation monitor • IV line • Intubation equipment Premedicate whenever possible Figure 10. Synchronized Cardioversion Algorithm.

More Related