Cardiac Intra-op Mgmt (pt 2/2) Flashcards

1
Q

List the basic sequence during CPB

A

-Go on bypass
-Cool patient
-Cross clamp aorta
-Arrest heart with cardioplegia
-Do operation
-Warm patient
-Unclamp aorta
-Pacing wires
-Prepare for weaning
-Come off bypass

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2
Q

Why do they cross clamp the aorta?

A

-Don’t want cardioplegia solution going throughout the body
-Clamp proximal to cannula
-MAP will drop briefly
-Surgeon will say “flows down” to perfusion

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3
Q

How do you arrest the heart?

A

-Cardioplegia infused antegrade through the coronaries or retrograde through the coronary sinus to arrest the heart.
-Myocardial blood supply is interrupted by placement of aortic XC: must arrest myocardium (with cardioplegia)
-Antegrade technique achieved by administering cardioplegia solution directly into the aortic root between the aortic valve and XC
-Interval between placement of XC and administration of cardioplegia kept to a minimum to prevent any warm ischemia
-Solution usually high in potassium, which arrests heart in diastole
-Retrograde administration occurs through the coronary sinus
-Can be placed under TEE guidance

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4
Q

Which bypass grafts are done first?

A

-Distal SVGs placed on most severely diseased coronaries first, to facilitate administration of additional cardioplegia via vein graft to distal stenosis
-IMA often constructed last because of its fragility and shorter length.

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5
Q

When does rewarming begin?

A

Rewarming typically begins when final distal anastomosis is begun.
-Brain warms faster than body (may need additional anesthetic)
-High risk for recall with rewarming!
-Vasodilators facilitate rewarming by improving distribution of blood and permitting higher pump flow rates
-Avoid shivering with adequate anesthesia and muscle relaxation
-Additional Heparin may be required as metabolic rate normalizes
-Rewarming should be complete (37 C) by the end of the procedure.
-May need to defib the heart once it’s warm.

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6
Q

How do you determine the rate of rewarming?

A

-Rate of rewarming depends on max safe temp gradient between water temp in the heat exchanger and the blood.
-Must be <10 C. Some use max of 6-8 C
-Higher gradient = inc risk of microbubbles

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7
Q

Why do you need to de-air the heart?

A

Air may collect in the pulmonary veins, LA, or LV which will be aspirated through aortic root vent (Antegrade Cardioplegia Line) prior to XC release.
-Temporarily raising the CVP and inflating the lungs will fill LV and permit easier surgical aspiration of intracavity air
-Residual air detected using TEE

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8
Q

How do you unclamp the aorta?

A

-Aorta may be unclamped, then an aortic side clamp placed to allow for proximal anastomosis while cardioplegia washed out of heart
-Partial occlusion clamp allows blood flow to these proximal grafts.
-Proximals may be completed with aortic clamp in place in order to reduce instrumentation of aorta

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9
Q

What are the “C”s in the checklist for termination of CPB?

A

1) Core (Bladder) Temperature >36 (Ideally 36.5). Nasopharyngeal shouldn’t exceed 37.5
2) Conduction – 80-100 bpm
-Sinus Rhythm > Atrial Pacing > AV Pacing > Ventricular Pacing
-Patients with AS/Hypertensive heart disease, atrial kick can contribute up to 40% of SV
3) Calcium - >1.0
-Often treated by perfusionist
4) Cardiac Output:
-Normal? Are ventricles actually getting blood out?
5) Cells – Hgb >7.5 (patient will be getting blood back from the pump and the 2 units you pulled off earlier)
6) Coagulation – FFP/Platelets/Cryo

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10
Q

What are the “V”s in the checklist for termination of CPB?

A

1) Ventilation – Re-expand with big breaths
-May be requested by surgeon prior to removal of cross clamp to assist with de-airing heart (open procedures)
-FiO2 100%
2) Vaporizer on – anesthesia is your responsibility again when the pump is off
3) Volume Expanders – Crystalloid and Albumin
-Crystalloid is preferred; albumin is expensive & has not shown long-term benefit
4) Visualization – Look at the heart to assess function
-Look over the drape!
-Assess ventricular & valvular function, intracardiac air with TEE

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11
Q

What are the “P”s in the checklist for termination of CPB?

A

1) Predictors – First attempt at weaning is always the best
-Low EF, Renal Disease, Female, Elderly, Prolonged (>2 hr) CPB Time
-Check all the boxes – if you’re not ready to come off, tell the surgeon to wait!
-Are they making urine? VS normal?
2) Pressure – Arterial and PAP must be adequate
-Arterial diastolic pressure must be adequate to provide perfusion
-Pulmonary artery pressure must Not be high, due to risk of RV failure
3) Pacer – Pacemaker must be functional and capturing
4) Pressors – Inotrope, Vasopressor & Vasodilator
-In line and infusing – most cases will require inotropic support (Epi 2-4mcg/min)
5) Potassium: <6.0
-Insulin administration to rapidly reduce potassium may be required
6) Protamine
-Dose provided by perfusionist based on heparin activity
-Premature protamine administration is Catastrophic

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12
Q

Describe the steps of termination of CPB.

A

1) Perfusionist decreases venous drainage to “fill the heart”
2) Heart “fills” and begins to eject
-Look for pulsatile waveforms on ABP & PAP
3) Assessment of ventricular & valvular function with eyes & TEE
4) Reduction of arterial inflow by perfusionist
-“What are you flowing?” “4 Liters” “Come down to 2 liters”
5) Progressive reduction of arterial flow by perfusionist to 0 - “Off Bypass”
6) Volume administration from CPB Pump
7) Protamine Administration

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13
Q

What is the most complicated, tenuous time of cardiac surgery?

A

Progressive reduction of arterial flow by perfusionist to 0 - “Off Bypass”
-Continuous assessment of preload, contractility, rhythm and ABP/PAP
-THIS IS THE MOST COMPLICATED, TENUOUS TIME OF CARDIAC SURGERY
-LV & RV Contractility must remain adequate – Epinephrine boluses may be needed to get heart going.
-Diastolic perfusion pressure must remain adequate - Vasopressor infusion
-Hypertension must be avoided to prevent stress on suture lines (AVOID HTN due to risk of blowing graft). SBP 100-120 is good.
-Volume status must be carefully monitored to prevent RV distension and subsequent failure

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14
Q

How does volume administration from the CPB pump happen?

A

-Surgeon will remove the venous cannula & close the hole in the right atrium
-Arrhythmias and hypotension are common
-Blood in Venous Cannula will be returned to CPB Reservoir
-Residual volume in the CPB Reservoir will be administered through the aortic cannula
-“How much you got left?” “I’ve got 500” ”Give me 100”
-Good Ventricular function + Volume = Increase in blood pressure due to increase in CO
-If BP does not increase with volume administration, you are probably at the flat portion of the Frank-Starling Curve – More volume will not improve your situation!
-Maintain vigilance – Assess BiVentricular Function, maintain normotension, avoid RV overload

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15
Q

Describe how you should administer Protamine?

A

Protamine = basic; Heparin = acidic; Acid/Base reaction = Neutralization

-Test Dose – Administer 1-2ml then wait 30-60 seconds
-Rapid administration can cause hypotension, anaphylaxis, or anaphylactoid rxn.
-Announce to room when protamine administration is Halfway
-Once protamine is about halfway infused, can start pulling Aortic Cannula
-Draw ACT (& ABG) 3 minutes after full dose given
-You can never go too slowly with Protamine – But you can definitely go too fast
-Everyone gets hypotension

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16
Q

Describe anaphylaxis reaction to Protamine.

A

Hypotension, bronchospasm etc.
Happens very quickly. Don’t give more Protamine.

17
Q

Describe anaphylactoid reaction to Protamine.

A

Hypotension, 3x elevation in PA Pressures, RV Failure
Can tx with Benadryl or steroids

18
Q

What is the dosing of Heparin for CPB?

A

-Initial dose prior to CPB is 300 units/kg
-Dosed based on baseline ACT - will be determined by Perfusion
-Heparin distributes primarily into the plasma compartment; seldom reason for initial dose >35-40k regardless of weight
-CPB priming solution should contain heparin at ~the same concentration as that of the patient’s blood at onset of CPB
-Dosing for off-pump is controversial
-Draw ACT 3 minutes after administration
-Need ACT > 450 to cannulate.

19
Q

What is the MOA of Heparin?

A

Binds to ATIII, which potentiates the action of ATIII more than 1000-fold, thereby inhibiting thrombin and factor Xa, as well as IXa, XIa, and XIIa.
-Inhibition of thrombin requires simultaneous binding of heparin to both ATIII and thrombin, whereas inhibition of factor Xa requires only that heparin binds to ATIII
-Thrombin inhibition therefore requires a longer saccharide chain, and shorter chains can selectively inhibit Xa

20
Q

How does Protamine neutralize Heparin?

A

-Strongly cationic protamine combines with strongly anionic heparin to produce stable complex devoid of anticoagulant activity
-Combine in proportion to weight: 1 mg protamine neutralizes 1 mg (~100 units) heparin
-Dose of protamine required should match amount of heparin remaining in patient’s blood circulation at time of neutralization

21
Q

What is the dose of Protamine?

A

-Dose provided by perfusion based on heparin activity.
-Most often, 25-50 mg protamine will complete neutralization
-Draw ACT & ABG 3 minutes after full dose is given

22
Q

Describe administration of Protamine.

A

-Go slow - hypotension
-Continuous infusion rather than hand-operated technique highly recommended by the text
-Injected dose of protamine cannot neutralize heparin bound to plasma proteins or within endothelial cells
-Release of heparin from these stored areas after initial protamine administration may result in reappearance of heparin anticoagulant effect (heparin rebound)
-Post-protamine ACT should return to <10% above patient’s baseline

23
Q

When is Amicar used?

A

Better to use it prophylactically: give at beginning of case before going on pump.
-Reduce bleeding
-Decrease need for blood transfusion during CPB

Benefits of Amicar and TXA have been demonstrated in multiple meta-analyses to reduce bleeding in cardiac surgery when used prophylactically rather than as rescue agents

24
Q

What is the MOA of Amicar?

A

-Amicar & TXA act as lysine analogs and bind to lysine-binding sites of plasmin and plasminogen
-Form reversible complex with plasmin which then inhibits fibrinolysis (natural breakdown of clots)
-Fibrin degradation products inhibit platelet function thus plasmin inhibition may protect platelets

25
Q

What is the goal of off-pump CABG?

A

To avoid the risks and complications associated with CPB (SIRS, Hemodilution) and Aortic Cross clamping (debris embolization)

25
Q

Why is ATIII important?

A

-AT3 is needed to bind Heparin.
-If deficiency is present, can replace ATIII, or administer FFP.
-AT III can be provided in the form of FFP, liquid plasma, and AT III concentrates

26
Q

What is the monitoring for OP CABG?

A

Monitoring, preop mgmt very similar to standard CABG
-CPP is maintained by keeping a HIGH map during distals (MAP 90-100)

27
Q

What is unique about volume administration and OP CABG?

A

-Require increased volume administration
-No hemodilution from bypass prime
-Use fluid as treatment for hemodynamic changes

28
Q

What is unique about temperature during OPCABG?

A

Not corrected on pump… so ACTIVE WARMING throughout case is necessary

29
Q

What about heparinization with OPCABG?

A

-Partial (>300) or Full (>400/450) depends on the surgeon. Still monitor Q30
-In case of urgent bypass needed

30
Q

T/F: You always give Amicar with OPCABG.

A

False; Antifibrinolytics not routinely used bc blood is not exposed to bypass pump

31
Q

What is different about management of the patient during OP CABG?

A

-Heart is lifted to provide exposure and stabilizers are used- lead to increased hemodynamic and ischemic issues
-CPP is maintained by keeping a HIGH map during distals (MAP 90-100)
-Blood loss is hidden due to CO2 “Blower” facilitating visualization

Apex is verticalized:
-Chambers compressed, vessel torsion
-Watch for ischemic changes on ECG and TEE
-Treat with VOLUME, PRESSORS, and STEEP T-berg