Cardiac/Bypass 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
Monitors used for cardiac surgery?
- Pulse Ox
- TEE
- EKG
- Leads V5(ischemia) & II (arrhythmia)
- 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
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 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 on Factor Xa and thrombin
-
Dose: 200-300units/kg (300-400 unin/kg from bypass lecture)
- Admin via central line or by surgeon directly into R atrium
- Dose is facility dependent
- Ex: 70 kg pt → 28,000 units (or round up to 30,000 units)
- Once the chest and pericardium are open and surgeon is happy with exposure, they will ask the anesthesia provider to give heparin via IV or will give it directly into the right atrium
-
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
- Inconvenient (must thaw and want to avoid blood product during CV sx)
- 1 unit of ATIII per mL of FFP
- ~ Adult: usually 2 units of 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
- FFP
From bypass lecture:
Look for ATIII level from preop labs
- Sometimes ACT will not reach the goal of 480 seconds with the loading heparin dose alone, when this happens the first step is for the perfusionist to provide the anesthesia provider with a second, smaller dose of heparin in hopes of getting closer to goal ACT
- Increasing heparin dose w/ increasing body wt is only effective to some degree bc the heparin is mainly distributed in plasma.
- Once the additional heparin reaches > 600 units/kg and the pt is still < 300 seconds → pt is “heparin resistant”
-
Heparin does need anti-thrombin 3 as a co-factor to work
- so even additional heparin will not provide enough anti-coagulation because of an anti-thrombin 3 deficiency.
- This can be inherited or acquired r/t prior heparin exposure.
- Why it’s helpful to get pre-op ATIII level so a poor response to heparin can be anticipated and prepared for.
- In cases when you have ATIII deficiency → Administer:
- recombinant anti-thrombin (thrombate) or
- FFP (contains ATIII)
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
- Arterial cannula size
- Too small → limit flow due to increased resistance and then jetting of blood (high pressure) – this can potentially cause an aortic dissection, biggest risk of cannulation
-
Too large → cause vessel damage
- Need balance
- Adult Cannula Size: 22 - 24 French aortic canula
- Once the arterial canula is in place, the perfusionist will check the arterial line pressure is reading as this is a reflection of the [aortic] root pressure
- excessively high = sign of aortic dissection.
- Perfusionist will check for pulsatility so some fluctuation up and down in the pressure on the A-line, and can give a test transfusion of a small amount of volume to ensure the pressure doesn’t jump up.
- The surgeon wants the pressure on the LOWER side for canulation to avoid additional bleeding during this period.
- The pt will lose blood during cannulation, but this is only temporary.
- Hypotension should be treated with VASOPRESSORS not volume.
- 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 needs to occur (by anesthesia) 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 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 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