Cardiac I Flashcards
Preop eval of cardiac patient
- Cardiac:
- Severity of disease/hemodynamic status
- Degree of impairment of contractility
- Development of compensatory mechanisms
- Exercise tolerance
- Hx of CHF, or MI-ST segment changes
- Angina
- Dysrhythmias
- Compensatory increase in sympathetic nervous outflow, ie Hr, anxiety, diaphoresis
- Hx of previous surgery
- Pulmonary
- COPD
- Renal
- PVD-especially carotid disease
- Diabetes
- Obesity
Laboratory data for cardiac patients?
- CBC
- Electrolytes
- Cardiac Enzymes
- Serum Creatinine
- Coagulation profile
- Type and Cross
Must have PRBCs available
Lab data for MI?
Peak A, early release of myoglobin or CK-MB isoforms after AMI
Peak B, cardiac troponin after AMI
Peak C, CK-MB after AMI
Peak D, cardiac troponin after unstable angina.
- The most recently described and preferred biomarker for myocardial damage is cardiac troponin. (gold standard)
- Absolute myocardial tissue specificity
- High sensitivity
- Thereby reflecting even microscopic zones of myocardial necrosis.
- will see peak even after only angina
Apex-
- CKMB
- initial elevation 3-12 hours
- peak 24 hours
- return to baseline 2-3 days
- Troponin I
- Initial 3-12 hours
- Peak 24 hours
- return 5-10 days
- Troponin T
- initial 3-12 hours
- peak 12-48 hours
- returnto baseline 5-14 days

Other cardiac testing you may want to evaluate before cardiac surgery?
- Catheterization data
- LVEDP
- EF
- CI
- Echocardiography data
- EF
- Wall motion abnormalities
- Chest X-Ray
- Cardiomegaly
- Pulmonary vascular congestion, edema, effusion
- Angiography
- EKG
- Ischemia/infarct
What cardiac drugs should be continued DOS?
The following should be continued until the operative day:
- *Antiarrhythmics
- •Amiodarone-special concern (1/2life 30d)
- *Ca+ Channel blockers
- *Β blockers
- *Nitrates
Premedication/anxiolysis prior to cardiac surgery?
Explain operative course and postop to the patient
Premedication
Narcotics
Anxiolytics
Antibiotics
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Monitors used for cardiac surgery?
- Pulse Ox
- TEE
- EKG
- Leads V5 & II
- Temperature
- ABP
- Usually radial, sometimes femoral
- CVP
- Mandatory for infusion of drugs
- PA Catheter
- Pts with severe LV dysfunction
- Pts with profound pulmonary HTN
TEE use in cardiac?
- Intermittent pulses with a frequency of 2.5-7.5 MHz.
- Can determine:
- Preload
- Hypotension
- CO
- LV Filling Pressures
- LV contractility
- LV afterload
- Ischemia, emboli, valvular pathology
- Assessment of surgical repairs
Cardiac OR setup?
- Usual airway equipment/machine check
- Pacemaker
- Drips
- Vary b/w institutions
- Most commonly:
- NTG/NTP
- Epinephrine/Norepinephrine
- Phenylephrine/Ephedrine
- Dopamine/Dobutamine as needed
- Antiarrhythmics (esmolol, lidocaine, mag, amiodarone)
- Heparin-and coag. monitoring capability
- Emergency drugs
- PRBC available in OR
Anesthetic agents for cardiac?
- Opiods
- Fentanyl 50-100mg/Kg
- Sufentanil 10-20mg/Kg
- Inhalation Agents
- Forane
- N2O
- Induction Drugs
- Etomidate
- Benzodiazepines
- NM Blockers
- Pavulon
- ED95 dose Vecuronium
Preinduction period for cardiac surgery?
- Evaluate need/effectiveness of premed
- Preoxygenation
- Monitor placement
- Large-bore Ivs
- Invasive monitors
- •In some institutions preinduction vs post
- •In severe disease –> preinduction
Goals of induction and intubation of cardiac patient?
- Smooth induction
- Avoid cough, larygospasm, truncal rigidity
- Avoid hypo- or hyper- tension
- Deep plane of anesthesia
- Short duration laryngoscopy
- Tape tube, eyes
- Pad pressure points
- Check monitors in this busy period
Considerations for pre-incision period of cardiac surgery?
- Hypotension
- Lack of stimulation
- Systemic pressure support
- Risks involved with vasoconstrictors
- Recall rare at this point, unless severe hypotension occurs in the face of purely opiod technique
Considerations for incision to bypass period
-
Intense surgical stimuli → STERNOTOMY
- Hypertension
- Deepen the anesthetic
- Narcotics (PAINFUL)
- Vasoactive agents
- NTG/NTP
-
Sternotomy
-
Drop lungs
- Disconnect circuit from ETT/vent (lungs will deflate)
-
Drop lungs
- Hypertension
-
Heart Handling by surgeon
-
Communication is of the utmost importance
- Arrythmias/HoTN common
- Bleeding can be significant
- Identifying and localizing ischemia
- Arterial and Saphenous veins are harvested
-
Communication is of the utmost importance
Considerations around the administration of heparin prior to initiation of bypass?
MOA of heparin? Dose? Peak?
Anti-coagulate the pt with Heparin
-
MOA:
- Binds to antithrombin 3 (AT3) and potentiates its natural anticoagulant properties
- Dose: 200-300units/kg
-
Peak: 2 mins
- 3 min → Check activated clotting time (ACT)
- Normal ACT = < 130 seconds (70-110 average)
-
Heparinized ACT = 350-500 seconds acceptable (> 400-450)
- *Safe to go on bypass
- Administered through CVP or directly into RA
- 3 min → Check activated clotting time (ACT)
Considerations:
-
SVR & BP can ↓ by 10-20%
- D/t blood viscosity reduction
- While blousing → monitor for HoTN and tx
- D/t blood viscosity reduction
- ACT checked after 3-5mins
- (Should be > 300-400 sec)
What are some special cirucmstance that would interfere with heparinization?
Special circumstances that interfere with heparinization- Examples: ACT may not increase
- Antithrombin III deficiency
- Long term heparin therapy
- Excessive hemodilution
- min fluids → interferes w/ heparinization
- Heparin-induced thrombocytopenia
- Antibody mediated response
- NTG long term
- Heparin resistance?
-
Alternatives to increase ACT:
- FFP
- Thrombate III
- Scenario: Appropriate heparin dose admin and ACT doesn’t increase appropriately → admin thombate III or FFP, then wait, then give additional dose of heparin and check ACT
- NEVER go on pump unless appropriate ACT
What cannulations are performed to initiate CPB
Bypass:
- Aorta (Arterial side) → brings O2 rich blood to systemic circulation
- RA (venous side) → brings O2 blood back from systemic circulation
Cannulation
-
1st→ Aortic cannulation (Arterial side): must DROP BP!! (esp if calcified)
- Can cause aortic rupture!
- Ex: SBP 90-100
- Cannulated 1st bc perfusionist can rapidly admin fluids through arterial line in case BP drops
- 2nd → RA cannula (venous side):
- BP might drop &/or arrhythmias can occur while placing
- 3rd → Cannulation of the coronary sinus for retrograde cardioplegia to arrest heart
- Anatomy: Coronary sinus is where coronary vessels empty into to get reperfused
-
Retrograde cardioplegia- providing poor RV myocardial perfusion, stopping the heart
- Cannulation → similar effects as RA (severe ↓ BP)
- Tx: Fluids by perfusionists, vasoactive agents
- Cannulation → similar effects as RA (severe ↓ BP)
-
*Medicate pt w/ extra Midaz and Fentanyl right before going on bypass
- Priming fluid of bypass machine increases Vd → diluting anesthetic agents
- INCREASE RECALL RISK
- Priming fluid of bypass machine increases Vd → diluting anesthetic agents
What are some considerations when initiating bypass?
- Pt placed on bypass, adequate perfusion flow and pressure, pt cooling starts (arterial side)
- Cease ventilation (dc circuit)
- IV fluids shut off
- Volatile anesthetic turned off
- Make sure perfusionist has instituted anesthetic
- Pull back Swan catheter – tends to float in further
- Give NMB to prevent shivering, along with fentanyl/versed
What do the clamps create during CPB?
Clamp separates two sections.
- Aortic cannulation allows blood to go to systemic circulation
- Cardioplegia solution- contains high K+ & cold
- Clamp prevents cold/K+ soln going to arterial side since right next to each other

Purpose of cardioplegia solution? Contents?
Heart stops
- Cold- 4°C
- Reduces metabolism of heart (protection)
- V-fib occurs at 25-30°C
- Contains K+ (high dose)
- Depolarization of heart
What happens with the intiation of bypas?
Significant drop in BP
-
Causes:
-
Hemodilution → ↓ viscosity
- From priming fluids (perfusionist)
- Rapid dilution of catecholamines
-
Rapid cooling
- for brain, heart, liver
- Aortic cross-clamp-to prevent systemic extravasation of antegrade cardioplegic solution
-
Hemodilution → ↓ viscosity
What is the pump primed with?
Primed with 2000 cc of crystalloids (rich in…)
- Heparin
- Mannitol
- NaHCO3-
- Albumin
- Corticosteroids
- Antifibrinolytics (aminocaproic acid/Amicar) to protect blood vessels
What hemodynamic changes occur with the initiation of bypass?
- Once the heart has been arrested (heart goes into fibrillation d/t cardioplegia soln)
- Revascularization/valve replacement is instituted
- Flow is no longer pulsatile (no BP, just flow from bypass machine)
- only have MAP
-
Flow rate (BP is one number, reflective of flow)
- Flow rate usually 50-60 ml/kg (bypass lecture 2.4L/min/m2
-
BP maintained at 50-60 mmHg
- Considerations;
- Lower BP (flow)
- beneficial for hematology
- (saving blood cells and preventing blood cell breakdown)
- Possibly issues perfusing brain/kidneys during non-pulsatile flow
- beneficial for hematology
- Higher BP (flow)
- beneficial for stroke pts/carotid dz (need extra cerebral perfusion) or kidneys
- Lower BP (flow)
- Considerations;
-
CVP is 0mmHg
- if higher → may have kink
What are some hematological effects of CPB?
- Effects both extrinsic and intrinsic coagulation pathways
- Factor XII conversion to Factor XIIa on various surfaces of CPB circuit
- Directly impairs platelet function
- Rapid adhesion and conformational alteration of plasma proteins
- i.e., von Willebrand factor (vWF) and fibrinogen (Fib)
- Platelet aggregation, and detachment due to shear forces
- Rapid adhesion and conformational alteration of plasma proteins
- Monocyte and endothelial activation with TF and tissue/vessel injury
- Tissue (vessel) injury → Extrinsic pathway → release of TF → causes both initiation of intrinsic pathway and common pathway
- Intrinsic pathway (via IX)
- Common pathway (via X)
- Understand adhesion and damage to cell from pt being on bypass

How do we provide prophylaxis for bleeding?
- Prophylactic use of antifibrinolytic drugs before CPB
- reduces bleeding and transfusion
- Drugs include:
- Synthetic lysine analogues
- ε-aminocaproic acid (EACA) – Amicar
- Transexamic acid (TXA)
- Serine protease inhibitor = Aprotinin
- Taken off the market dt significant tissue organ damage
- Being researched again in Canada
- Amicar bolus and infusion PRE pump to reduce bleeding and need for transfusion
- Synthetic lysine analogues
What are some CNS risks while on pump? People at risk?
Risks:
- Embolization
- Hypoperfusion
- Bypass machine at low pressures/flow
- Inflammation from pulsatile to flow BP
Influencing Factors/predisposition: (people at risk)
- Aortic atheromatous plaque (atherosclerosis in aorta)
- Cerebrovascular disease
- Altered cerebral autoregulation (elderly)
- HoTN
- Intracardiac debris
- Plagues
- Air
- Cerebral venous obstruction on bypass
- Cardiopulmonary bypass circuit surface and damaged blood cells
- Reinfusion of unprocessed shed blood (cell saver)
- Cerebral hyperthermia (rewarmed too quickly)
- Hypoxia (serial ABGs)
How can we provide cerebral protection while on bypass?
- Emboli are biggest culprits
-
PROTECTION:
- Hypothermia → decrease CMRO2
- Barbiturate therapy?
- Used to give TPL/Methohexital decrease BF to brain
- CCBs
- increase perfusion to brain
- Blood gas management
- Draw from aline
- Adequate BP (run machine at good flows)
- blood cell damage vs. CPP? Individualized
- (look at risk list above and those prob need higher pressures)
- blood cell damage vs. CPP? Individualized
- Cerebral oximetry
Fluid managmeent considerations while on bypass?
-
Minimize crystalloids – hemodilutes pt
- 1-1.5 L acceptable for crystalloids
- Replace blood w/:
- Colloids
- Cell saver
- PRBCs
Rewarming considerations?
- Begins at different times: (Surgeon can ask for rewarming of pt)
- Begins prior to aortic cross-clamp removal (or)
- 2. Begins with the last distal anastomosis in angioplasty procedure (or)
- 3. Begins when all the valve sutures are in and knots are being tied down
-
Considerations:
-
1° C per 3-5 mins (slowly)
- Usually takes ~ 30-40 mins
- Turn on heating blanket
- Temp gradient bt arterial and venous blood should remain < 5-10°C
- if gradient higher → higher risk of air emboli
- Amnestic and NMB agents should be given (recall)
- SVR drops d/t vasodilation
- Monitor pressure*
- Phenylephrine can be given to perfusionist since they have more direct access
-
1° C per 3-5 mins (slowly)
What must occur prior to the discontinuation of bypass?
- Pt must be warmed
- Surgical field should be _dry (_no bleeding)
-
Lab values checked
- Admin Ca & Mag to decrease effects of cardioplegic soln (high K)
-
Pulmonary compliance evaluated
- Begin ventilating lungs slowly (attach circuit)
- Manually bag pt to see compliance → watch lungs
- Then switch to ventilator
- Begin ventilating lungs slowly (attach circuit)
- Regulate cardiac rhythm by pacing, defibrillating or pharmacologically
- Ca, Mg
- Transfuse pt with pump volume (~50-100cc by perfusionist)
- Look at:
- PA Diastolic pressure
- TEE*
- Actual heart over drapes (floppy?)
- VS
- Look at:
Pneumonic to help remember preparation to wean from bypass?
- “CVP”
- Cells- PRBCs
- Vaporizers- turn on gas since perfusionist turns off theirs
- Volume expanders- for HoTN
- Predictors:
- Based off preop assessment
- Arrythmias beforehand?
- Based off preop assessment
- Potassium/Mag/Calcium balance
- Protamine- AFTER everything else looks good (last thing)

Considerations during discontinuation of bypass?
- Use the ratio of systemic BP to pulm BP
-
EXAMPLES:
-
If pulm pressure ↑, but BP ↓ = ventricular failure (inotropic agent)
- PA pressure high → diastolic fx not working properly and BP low → SV or stroke pressure poor → ventricle not fx properly
- Tx: Inotropic agent→ increase force of contraction
- PA pressure high → diastolic fx not working properly and BP low → SV or stroke pressure poor → ventricle not fx properly
-
If CO is low, but BP is adequate = SVR high (overly vasoconstricted)
- BP good but heart cant pump against heavy constriction
- Tx: vasodilation
- BP good but heart cant pump against heavy constriction
-
If BP is low:
- Inotropes
- volume (cell saver, PRBC, whole blood)
-
If pulm pressure ↑, but BP ↓ = ventricular failure (inotropic agent)
- Diagnose THEN treat
- Look at BP and PA pressures
- Once the pt is stable, bypass is completely d/c’d
How do we support ventricular function during bypass weaning?
Assess function
LV support =
- Inotropes
- PRBC
- Preload
- afterload
RV support = (need to ↓ pulm vasoconstriction)
- Nitric oxide-based vasodilators
- β2 agonists
- prostaglandin E1
-
RV failing unrelated to pulm vasoconstriction:
- cyclic adenosine monophosphate-specific phosphodiesterase inhibitors
- (Phosphodiesterase inhibitors are a class of medications that promote blood vessel dilation (vasodilation) and smooth muscle relaxation in certain parts of the body, such as the heart, lungs, and genitals)
- cyclic adenosine monophosphate-specific phosphodiesterase inhibitors
- If not working:
- IABP (intra-arterial balloon pump)
- Ventricular Assist Devices
-
RV failing unrelated to pulm vasoconstriction:
“Steps” for bypass weaning?
Step 1:
HR < 70 (conduction block)
- Pace
- Atropine
- Isopril
HR > 100
- Balance Mg/K
- Cardiovert
- Amiodarone
Preload optimization →
High Preload:
- stop filling
- head up tilt (reduce blood coming back to heart)
- diuretics
MAP > 90
- vasodilators (NTG, NPS)
Once all criteria met → then can successfully come off bypass and remove arterial cannula and TE
THEN give protamine. (ACT come back to normal)
Step 2: (if not able to wean)
- Ventricular failure
- Tx: inotropes, blood back from pump, inhaled NO, etc
- If successful, ok to come off arterial cannula and TEE→ then give protamine and ACT check
If not successful → balloon pump or VAD to leave

Parameters used to determine treatment for TEE?
Example:
- BP and VFP high
- CO low
- Dx: high vasoconstriction (or)
- Low contractility
- Tx: Inotrope or vasodilation
Example:
- BP down
- Filling pressures down
- SV up
- Dx: DECREASE SVR
- Tx: Vasoconstrictor

What is protamine? Dosage?
- Derived from salmon sperm
- Pts w/ vasectomies (develop AB against sperm) → Allergic Rx to protamine
-
Dose:
- 2-4 mg/kg
-
1-1.3 mg per 100units of Heparin given
- Administration considerations:
- SLOWLY push (over 5-10 min)
- *Massive vasodilation/drop in BP*
- CVP line (draw back and ensure good line)
- Check ACT and give more accordingly
- ~ < 100
- SLOWLY push (over 5-10 min)
- Administration considerations:
Considerations for anaphylaxis with protamine?
-
Anaphylaxis can occur: Admin w/ premedication or alternatives to heparin
- Pts with previous exposure
- Pts with vasectomy
- Pts on NPH (Neutral Protamine Hagedorn) (prior exposure technically)
- Can cause vasodilation, give slowly over >5mins.
- Pts with documented adverse events related to protamine → do not rechallenge with protamine
- Pharmacologic alternatives to protamine:
- Do not reverse heparin
- Non–heparin-based CPB
- Performing off-pump coronary artery bypass (OPCAB) with an alternative to heparin
- Surgeon dependent (variable)
-
Non-protamine heparin reversal drugs: (if heparin used)
- PF4
-
Heparinase
- MOA: deactivates heparin (not technically reversing it)
- Simply waiting for heparin’s effects to dissipate
Post bypass and postop considerations after cardiac surgery?
Post Bypass
- Transfusion
- Coagulation
- Stability of VS
- Drop in BP with chest closure *
- Maintain inotropes, NTG, NTP, etc.
- Continue vigilant watch
Post op
- Travel to ICU/CCU with monitors & + O2
- Bring backs
- 4-10%
- usually d/t bleeding → less common now w/ TEE
- Cardiac tamponade
- 4-10%
- Post op pain control
- Sternotomy very painful!
- Ex: Fentanyl drip, morphine, dilaudid, etc
- Sternotomy very painful!
Considerations around minimally invasive cardiac surgery?
- Numerous approaches
- Techniques vary amongst sites and surgeons
-
Good practice:
-
↓ HR and ↑ preload
- Surgeon handling heart → good way to maintain BP
- Avoid and tx arrhythmias
- Handing might cause arrythmias
- Adjust ventilator settings
- Ex: small TV, higher RR, add PEEP
- Heparin available in case pt has to go on bypass
- Reversal of heparin depends on the institution
-
↓ HR and ↑ preload