Surgery Lab 4: Anesthetic Emergencies and Cardiopulmonary Resuscitation


CPR vs. CPCR and Species Differences

  • Definitions and Core Terminology:

    • Cardiopulmonary Resuscitation (CPR): A foundational emergency procedure utilized across human and veterinary medicine designed to address and treat cardiopulmonary arrest (CPA).

    • Cardiopulmonary Cerebral Resuscitation (CPCR): An expanded clinical designation emphasizing that resuscitation must accomplish more than restoring cardiac activity; the fundamental preservation and restoration of cerebral perfusion and brain function are paramount.

  • Comparative Resuscitation: Humans vs. Animals:

    • Resuscitation protocols, procedural physical interventions, and pharmacologic algorithms employed in veterinary species are frequently extrapolated directly from human emergency medicine standards.

    • Fundamental physiological, pathological, and prognostic variations distinguish animal resuscitation from human protocols across four key domains:

    • Etiology of CPA: The primary pathological events triggering cardiopulmonary arrest differ markedly between human patients and veterinary species.

    • Response to Physical Resuscitation: Animals display differing physical biomechanics and physiological responses to external chest compressions and manual ventilatory techniques.

    • Response to Resuscitative Pharmacology: Emergency cardiovascular and neurovascular drugs yield divergent metabolic and hemodynamic outcomes in veterinary species.

    • Prognosis for Functional Survival: Veterinary clinical populations exhibit divergent survival statistics and reduced rates of return to normal baseline neurologic and systemic function compared to humans.

  • Unique Veterinary Arrest Complications:

    • Resuscitated veterinary patients experience a high incidence of secondary rearrest following initial return of spontaneous circulation (ROSC).

    • Severe post-arrest complications frequently prompt humane euthanasia decisions in veterinary clinical practice.

    • Veterinary patients exhibit minimal responsiveness to electrical defibrillation compared to human arrest patients due to differing underlying etiologies of CPA.

Resuscitation Prognosis and Ethical Considerations

  • Comparative Survival Metrics:

    • Human Patients:

    • Initial successful resuscitation rate: up to 40–60%40\text{--}60\%

    • Final survival to hospital discharge: approximately 17%17\%

    • Canine Patients:

    • Initial successful resuscitation rate: 13%13\%

    • Final survival to hospital discharge: 4.1%4.1\%

    • Feline Patients:

    • Initial successful resuscitation rate: 15.6%15.6\%

    • Final survival to hospital discharge: 9.6%9.6\%

  • Ethical Resuscitation Deliberations:

    • Clinical appropriateness must be evaluated before or during resuscitation based on individual patient circumstances.

    • Resuscitative interventions prompt significant ethical scrutiny regarding whether to perform CPR on terminally ill patients.

    • Resuscitative viability must consider whether interventions will result in intractable, ongoing quality-of-life deficits.

Tiers of Resuscitative Intervention: BLS vs. ALS

  • Basic Life Support (BLS):

    • Constitutes the foundational baseline of resuscitation, encompassing:

    • Airway management

    • Breathing and ventilatory support

    • Circulatory support via chest compressions

    • Basic emergency drug delivery

    • Standard capability across virtually all veterinary clinical practices and hospital settings.

  • Advanced Life Support (ALS):

    • Encompasses all components of Basic Life Support combined with advanced critical interventions:

    • Advanced cardiovascular pharmacology

    • Continuous electrocardiographic (ECG) monitoring

    • Electrical defibrillation when indicated by underlying rhythm analysis

    • Internal cardiac massage (internal chest compressions), performed selectively under specific anatomical indications

    • Typically established in dedicated critical care facilities and emergency centers, though many general practices retain the capacity to deliver substantial ALS components.

  • The CABD Algorithmic Sequence:

    • Clinical assessment and intervention follow a prioritized progression:

    • C — Circulation: Assessed and addressed first.

    • A — Airway: Cleared and secured.

    • B — Breathing: Ventilatory support initiated.

    • D — Drugs: Pharmacological support administered.

Circulation (C): Assessment, Positioning, and Compression Mechanics

  • Primary Circulatory Assessment:

    • Rapid assessment of circulatory function precedes all other interventions via:

    • Auscultation of cardiac fields

    • Palpation of central and peripheral pulses

    • Inspection of mucous membrane (MM) color

    • Assessment of capillary refill time (CRT)

    • Critical Safety Rule: Never initiate or deliver chest compressions when the heart is actively beating.

  • Patient Positioning for Compressions:

    • Primary Recumbency: Right lateral recumbency.

    • Alternative Recumbency: Dorsal recumbency.

    • Anatomical Target: Intercostal spaces 5 through 6 (5th–6th5^{\text{th}}\text{--}6^{\text{th}} intercostal space).

  • Hand Placement Mechanics by Patient Size:

    • Small Patients (Felines and Small Canines):

    • Direct the fingers underneath the ventral chest wall.

    • Position the thumb along the dorsal aspect of the chest.

    • Deliver chest compressions by directly squeezing the thorax between the thumb and opposing fingers.

    • Medium-Sized Patients:

    • Place one hand flat underneath the chest for stabilization.

    • Position the heel of the opposing hand directly over the cardiac field on the upper thoracic wall to deliver downward compressions.

    • Large Patients:

    • Place a firm bolster (such as a book or sandbag) beneath the dependent thorax to prevent dissipation of force.

    • Interlock the fingers of both hands directly over the widest portion of the chest.

    • Maintain locked, rigid arms at the elbows.

    • Pivot and rock from the hips, utilizing upper body mass rather than arm musculature to execute compressions.

  • Compression Rate, Depth, and Physiological Goals:

    • Compression Frequency: Baseline delivery is 100 compressions/minute100\,\text{compressions/minute} (equivalent to approximately 2 compressions/second2\,\text{compressions/second}).

    • Smaller patients require faster compression rates.

    • Larger patients require comparatively slower compression rates.

    • Displacement Depth: Depress the thoracic cage by approximately 13\frac{1}{3} of its total width.

    • Physiological Objectives of Compressions:

    • Induce rapid shifts in intrathoracic pressure.

    • Maximize systemic venous return to the right atrium.

    • Optimize forward stroke volume and cardiac output.

  • Operational Priorities and Simultaneous Techniques:

    • Chest compressions represent the single most vital component of CPCR.

    • Passive air movement into and out of the pulmonary parenchyma occurs naturally alongside chest displacement.

    • Solo Rescuer Management: Concentrate exclusively on uninterrupted chest compressions; do not stop compressions to provide breaths.

    • Multi-Rescuer Management: Deliver simultaneous ventilations concurrently with ongoing chest compressions.

    • Interposed Abdominal Compressions: Compressing the abdomen alternately with thoracic compressions augments venous return returning from the caudal circulation.

Assessing Compression Efficacy and Resuscitation Monitoring

  • Physical Palpation Monitoring:

    • Lingual Pulse: Direct palpation of the lingual artery to verify perfusion to cranial structures.

    • Digital Pulse: Palpation of distal extremities to evaluate terminal peripheral microvascular flow.

    • Femoral Pulse: Rapidly palpated at the onset of CPR to confirm whether chest compressions are generating forward hemodynamic flow.

    • Expected Physical Finding: Rescuers must palpate a distinct peripheral pulse synchronized with each external compression cycle.

  • Instrument-Based Hemodynamic Monitoring:

    • Doppler Flowmetry:

    • Position the crystal probe directly over the cornea/eyeball or beneath the tongue over the lingual artery.

    • Effective compressions produce an audible, rhythmic systolic flow signal.

    • Pulse Oximetry (SpO2\text{SpO}_2):

    • Clip the sensor probe to the lingual mucosa.

    • Hemodynamically effective compressions correlate with measurable upward trajectories in oxygen saturation (SpO2\text{SpO}_2).

    • Capnography (PaCO2\text{PaCO}_2 / End-Tidal CO2\text{CO}_2):

    • Real-time pulmonary blood flow and functional cardiac output correlate with gas exchange.

    • Successful compressions generate progressive increases in partial pressure of carbon dioxide (PaCO2\text{PaCO}_2).

Timing Cycles, Corrective Actions, and Internal Cardiac Compressions

  • Compression Timing Cycles:

    • Maintain uninterrupted compressions for uninterrupted cycles of approximately 3 minutes3\,\text{minutes}.

    • Pause briefly at the completion of each 3-minute3\text{-minute} cycle to check for persistent spontaneous cardiac pulses.

    • If a spontaneous pulse is absent, immediately resume external compressions.

    • Immediate Cessation Criteria: Terminate compressions instantly if the patient exhibits:

    • Purposeful consciousness or voluntary movement

    • Independent, spontaneous breathing efforts

    • Palpable pulse or auscultated heartbeat independent of external compressions

  • Troubleshooting Ineffective Compressions:

    • When compressions fail to yield palpable pulses, Doppler signals, or rising capnography values, systematically alter:

    • Patient recumbency and thoracic angle

    • Exact positioning of hands over the thoracic wall

    • Force and physical depth of compressions

    • Rescuer fatigue (rotate the person delivering compressions)

    • Consideration of internal compressions

  • Internal Cardiac Compressions (Open-Chest CPR):

    • Generally avoided in routine resuscitation due to a severe decline in long-term functional recovery for patients who already carry a grave prognosis.

    • Specific anatomical and clinical indications where open-chest compressions may be considered:

    • Patients exceeding 20 kg20\,\text{kg} in body mass

    • Severe pneumothorax

    • Pleural effusion

    • Pericardial effusion or cardiac tamponade

    • Penetrating thoracic trauma

    • Severe thoracic wall trauma or flail chest

    • Hemoperitoneum

    • Diaphragmatic hernia

Airway (A): Assessment, Clearing, and Securing Techniques

  • Airway Evaluation and Decontamination:

    • The initial priority requires inspecting the oral cavity and pharynx to ensure complete patency.

    • Clear all foreign objects, mucosal fluids, and vomitus using mechanical scoop-and-drain techniques.

  • Comparative Modalities of Airway Access:

    • Mouth-to-Snout Ventilation:

    • Most accessible baseline technique for acute trauma in field settings (e.g., structure fires, vehicular trauma/Hit-by-Car [HBC]).

    • Primary drawbacks involve personal safety, hygiene, and operator reluctance when managing unfamiliar animals.

    • Face Mask Delivery:

    • Readily applicable non-invasive bridge, but fails to isolate or deliver gas volume directly into the lower respiratory tract.

    • Endotracheal (ET) Intubation:

    • The gold standard for securing the airway in veterinary resuscitation.

    • Requires a cuffed endotracheal tube.

    • Critical technical check: Confirm placement within the tracheal lumen, which can prove technically challenging in entirely apneic patients.

    • Emergency Tracheostomy:

    • Indicated when oral mass lesions, physical obstructions, or foreign bodies preclude oral intubation.

    • Surgical procedure performed by the veterinarian (DVM) requiring extensive post-procedural nursing and airway management.

    • Transtracheal Catheterization:

    • Less invasive surgical alternative to formal tracheostomy.

    • Facilitates the administration of high fractions of oxygen, though volumetric flow remains limited by narrow catheter luminal diameters.

Breathing (B): Oxygenation, Ventilation Parameters, and Acupuncture Stimulation

  • Ventilatory Support Parameters:

    • Resuscitative gas source: Provide 100% O2100\%\,\text{O}_2.

    • Target rate: Administer 1 breath every 6 seconds1\,\text{breath every } 6\,\text{seconds}, establishing a baseline frequency of approximately 10 breaths/minute10\,\text{breaths/minute}.

    • Delivered tidal volume (VT\text{V}_T): Maintain delivery within 10–15 mL/kg10\text{--}15\,\text{mL/kg}.

    • Peak Inspiratory Pressure Limits: Prevent pulmonary barotrauma and overinflation:

    • Canine Limit: Do not exceed 20 cmH2O20\,\text{cmH}_2\text{O}

    • Feline Limit: Do not exceed 15 cmH2O15\,\text{cmH}_2\text{O}

  • Equipment Setup and Safety Checks:

    • Ambu Bags: Self-filling resuscitation bags deliver ambient air unless plumbed directly to an oxygen tank or anesthetic circuit to provide 100% O2100\%\,\text{O}_2.

    • Anesthetic Machine Setup:

    • When using an anesthetic circuit for manual ventilation, the rebreathing bag empties and refills progressively; an Ambu bag attached to oxygen can resolve filling delays.

    • Vaporizer: Confirm the anesthetic vaporizer is completely turned OFF to avoid delivering inhalant to an unstable patient.

    • Carbon Dioxide Absorbent: Ensure the soda lime canister is chemically active and not exhausted.

  • Acupuncture Respiratory Stimulation (GV 26):

    • Equipment: 25-gauge25\text{-gauge} hypodermic needle.

    • Anatomical Site: Nasal philtrum midline, positioned midway between the ventral margin of the nares and the margin of the upper lip.

    • Application: Advance the needle directly until making firm contact with underlying premaxillary bone; rotate and twist the needle continuously.

    • Intended Outcomes: Triggers sympathetic reflex pathways stimulating intrinsic pulmonary respiration and chronotropic/inotropic cardiac drive.

  • Discontinuation Criteria for Ventilatory Support:

    • Do not terminate ventilation simply because a spontaneous heartbeat or pulse returns.

    • Continue manual ventilations until mucosal color remains fully pink and regular spontaneous breathing resumes.

    • Gradually step down to intermittent manual bagging throughout post-arrest recovery.

Drugs (D): Administration Routes and Anatomical Prioritization

  • Institutional Preparedness:

    • Dosing protocols in emergency medicine evolve continually; reference current veterinary emergency formularies.

    • Post pre-calculated emergency dosage charts in critical procedural zones throughout the hospital.

  • Administration Routes in Descending Order of Priority:

    • 1. Intravenous (IV) — Central Vein (Preferred Route):

    • Provides rapid delivery directly into core central circulation.

    • Cannulation of the external jugular vein utilizing large-bore vascular catheters.

    • 2. Intratracheal (IT):

    • Utilized when vascular access is not established.

    • Dosing Adjustment: Double (2×2\times) standard IV dosages to account for incomplete pulmonary absorption.

    • Dilution: Dilute the calculated drug volume with 3–5 mL3\text{--}5\,\text{mL} of sterile saline.

    • Administration: Deliver the solution deep into the lower bronchial tree through the ET tube using a red rubber feeding tube or urinary catheter.

    • 3. Intravenous (IV) — Peripheral Vein:

    • Common access point during anesthesia, though transit times to the central circulation are delayed compared to central routes.

    • Placing an additional peripheral catheter assists with rapid fluid resuscitation.

    • 4. Intraosseous (IO):

    • Rapid non-collapsible vascular access indicated for neonates, pediatric patients, avian patients, and exotic species.

    • Anatomical entry sites: Trochanteric fossa of the femur, proximal greater tubercle of the humerus, tibial crest.

    • 5. Intralingual:

    • Sublingual injection into the lingual vascular bed provides rapid uptake near cerebral venous drainage.

    • 6. Intracardiac (Contraindicated):

    • Not recommended due to severe clinical risks: pulmonary parenchymal laceration, direct myocardial laceration, coronary vessel disruption, and refractory tension pneumothorax.

Emergency Pharmacology: Core Resuscitative Agents and Vasopressors

  • Vasopressin:

    • Physiology: Endogenous non-adrenergic peptide (antidiuretic hormone) produced in the hypothalamus and stored/secreted by the posterior pituitary; regulates systemic free water reabsorption.

    • Resuscitative Profile:

    • Induces peripheral arterial vasoconstriction independent of adrenergic receptors, making it effective during severe metabolic acidemia.

    • Preserves cerebral tissue oxygenation, restores coronary perfusion pressure, improves initial ROSC rates, and supports post-arrest neurologic recovery.

    • Human clinical trials demonstrate survival rates equivalent to epinephrine.

    • Clinical Indications: Asystole, pulseless electrical activity (PEA), ventricular tachycardia.

    • Dosage Regimen:

    • Bolus dose: 0.4–0.8 U/kg0.4\text{--}0.8\,\text{U/kg}

    • Constant Rate Infusion (CRI): 0.01–0.04 U/kg/min0.01\text{--}0.04\,\text{U/kg/min}

  • Epinephrine:

    • Physiology: Mixed α\alpha- and β\beta-adrenergic receptor agonist stimulating sympathetic cardiovascular pathways.

    • Hemodynamic Effects: α1\alpha_1-mediated peripheral vasoconstriction routes cardiac output to core coronary and cerebral beds within seconds of administration.

    • Administration Interval: Administer repeat doses every 3–5 minutes3\text{--}5\,\text{minutes}.

    • Dosage Protocol: Protocols feature low-dose or high-dose options; start at the low-dose tier, reserving high-dose escalations for refractory arrest.

  • Dopamine:

    • Physiology: Inotropic catecholamine that increases myocardial contractile force and chronotropic speed.

    • Clinical Utility: Acts as an active cardiac stimulant indicated for hemodynamic failure when the heart maintains intrinsic electrical rhythm.

    • Administration: Requires continuous administration through a controlled, slow intravenous infusion.

Secondary Pharmacologic Agents, Buffers, and Reversals

  • Atropine:

    • Anticholinergic (parasympatholytic) that blocks muscarinic receptors to resolve severe bradycardia.

    • Onset of clinical action occurs over several minutes.

    • Alternative Agent: Glycopyrrolate, which carries a lower risk of precipitating post-administration tachyarrhythmias.

  • Lidocaine NEAT:

    • Formulated strictly as lidocaine hydrochloride without epinephrine additive.

    • Epinephrine must not be co-administered in this setting to avoid unnecessary myocardial stimulation.

    • Administered as an antiarrhythmic to suppress ventricular tachycardia and prevent ventricular fibrillation (VF).

    • Increases the electrical threshold required to achieve successful defibrillation.

  • Doxapram:

    • Analeptic central respiratory stimulant.

    • Increases myocardial oxygen consumption (MVO2\text{MVO}_2), which may worsen ischemic myocardial injury.

    • Clinical availability in veterinary medicine is currently limited within Canada.

  • Corticosteroids:

    • Clinical Status: No longer indicated for routine CPR; prospective controlled studies fail to show survival benefit.

    • Historical Indications: Membrane stabilization, lactic acid clearance, and attenuation of endotoxic shock.

    • Major Risk: Induces rapid peripheral vascular collapse and hypotension if administered without concurrent intravenous volume expansion.

    • Formulations Historically Encountered: Prednisolone sodium succinate, dexamethasone.

  • Sodium Bicarbonate:

    • Alkalinizing agent indicated for pre-existing metabolic acidosis and hyperkalemia.

    • Clinical guidelines advise confirming metabolic acid-base status on blood gas analysis prior to administration.

    • Alternatively, avoid empiric use until arrest durations surpass 10 minutes10\,\text{minutes}, when severe intracellular and extracellular acidosis has developed.

  • Calcium Gluconate:

    • Not indicated for routine cardiopulmonary arrest.

    • Reserved for arrest precipitated by severe documented hypocalcemia, life-threatening hyperkalemia, or calcium channel blocker toxicosis.

Fluid Therapy Protocols in Cardiopulmonary Arrest

  • Traditional Shock Fluid Rates:

    • Historical full-shock fluid resuscitation guidelines:

    • Canines: Up to 90 mL/kg/h90\,\text{mL/kg/h} for the initial hour maximum

    • Felines: Up to 45 mL/kg/h45\,\text{mL/kg/h} for the initial hour maximum

    • Complications associated with traditional rates include:

    • Rapid dilution of clotting factors and red blood cell mass (hemodilution)

    • Systemic fluid overload and pulmonary edema

    • Escalation of intracranial pressure (ICP)

  • Updated Shock Fluid Resuscitation Rates:

    • Resuscitation protocols utilize fractional aliquots, administering 14\frac{1}{4} of the traditional shock rate over a 15-minute15\text{-minute} window, followed by formal patient re-evaluation:

    • Canines: Administer 22 mL/kg/h22\,\text{mL/kg/h}, delivered in 15-minute15\text{-minute} bolus increments as clinically indicated

    • Felines: Administer 11 mL/kg/h11\,\text{mL/kg/h}, delivered in 15-minute15\text{-minute} bolus increments as clinically indicated

  • Fluid Types and Prescriptions:

    • First-Line Fluids: Balanced isotonic crystalloids.

    • Adjunctive Solutions: Synthetic colloids or hypertonic saline (7–7.5% NaCl7\text{--}7.5\%\,\text{NaCl}) depending on intravascular volume needs.

    • Dextrose Contraindication: Avoid dextrose infusions during CPR unless hypoglycemia is confirmed via glucometry.

    • Oxygen Carriers: Consider hemoglobin-based oxygen carriers (Oxyglobin) when available.

Defibrillation: Indications, Mechanics, and Energy Delivery

  • Etiological Variations in Defibrillation:

    • Electrical defibrillation serves as an immediate first-line intervention in human CPR, where ventricular fibrillation (VF) represents the most common arrest rhythm.

    • In veterinary medicine, VF occurs infrequently in dogs and is rare in cats; as a result, routine defibrillation is less commonly indicated.

    • Automated External Defibrillators (AEDs) algorithmically analyze cardiac rhythms to identify shockable waveforms and deliver titrated shocks.

  • Defibrillation Technique and Clinical Precautions:

    • Position the patient in dorsal recumbency or lateral recumbency.

    • Shave thoracic hair coats over electrode contact zones when time permits.

    • Apply generous quantities of conductive electrode gel to the paddle interfaces.

    • Critical Safety Warning: Never use alcohol during defibrillation due to electrical arcing and fire risk.

  • Defibrillation Energy Dosing:

    • External Paddles:

    • Initial external shock energy dose: Deliver 3–5 J/kg3\text{--}5\,\text{J/kg}

    • Refractory rhythms: Increase the energy dose by 50%50\%

    • Internal Paddles:

    • Indicated during open-chest CPR with direct epicardial paddle placement

    • Internal energy dose: Deliver 0.5–1 J/kg0.5\text{--}1\,\text{J/kg}