Cardiac I Flashcards

1
Q

Preop eval of cardiac patient

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Laboratory data for cardiac patients?

A
  • CBC
  • Electrolytes
  • Cardiac Enzymes
  • Serum Creatinine
  • Coagulation profile
  • Type and Cross

Must have PRBCs available

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Lab data for MI?

A

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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Other cardiac testing you may want to evaluate before cardiac surgery?

A
  • Catheterization data
    • LVEDP
    • EF
    • CI
  • Echocardiography data
    • EF
    • Wall motion abnormalities
  • Chest X-Ray
    • Cardiomegaly
    • Pulmonary vascular congestion, edema, effusion
  • Angiography
  • EKG
    • Ischemia/infarct
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What cardiac drugs should be continued DOS?

A

The following should be continued until the operative day:

  • *Antiarrhythmics
    • •Amiodarone-special concern (1/2life 30d)
  • *Ca+ Channel blockers
  • *Β blockers
  • *Nitrates
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Premedication/anxiolysis prior to cardiac surgery?

A

Explain operative course and postop to the patient

Premedication

Narcotics

Anxiolytics

Antibiotics

n

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Monitors used for cardiac surgery?

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

TEE use in cardiac?

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Cardiac OR setup?

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Anesthetic agents for cardiac?

A
  • Opiods
    • Fentanyl 50-100mg/Kg
    • Sufentanil 10-20mg/Kg
  • Inhalation Agents
    • Forane
    • N2O
  • Induction Drugs
    • Etomidate
    • Benzodiazepines
    • NM Blockers
      • Pavulon
      • ED95 dose Vecuronium
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Preinduction period for cardiac surgery?

A
  • Evaluate need/effectiveness of premed
  • Preoxygenation
  • Monitor placement
  • Large-bore Ivs
  • Invasive monitors
    • •In some institutions preinduction vs post
    • •In severe disease –> preinduction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Goals of induction and intubation of cardiac patient?

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Considerations for pre-incision period of cardiac surgery?

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Considerations for incision to bypass period

A
  • 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)
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Considerations around the administration of heparin prior to initiation of bypass?

MOA of heparin? Dose? Peak?

A

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

Considerations:

  • SVR & BP can ↓ by 10-20%
    • D/t blood viscosity reduction
      • While blousing → monitor for HoTN and tx
  • ACT checked after 3-5mins
    • (Should be > 300-400 sec)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are some special cirucmstance that would interfere with heparinization?

A

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
17
Q

What cannulations are performed to initiate CPB

A

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
  • 2ndRA cannula (venous side):
    • BP might drop &/or arrhythmias can occur while placing
  • 3rdCannulation 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
  • *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
18
Q

What are some considerations when initiating bypass?

A
  • Pt placed on bypass, adequate perfusion flow and pressure, pt cooling starts (arterial side)
    1. Cease ventilation (dc circuit)
    2. IV fluids shut off
    3. Volatile anesthetic turned off
    4. Make sure perfusionist has instituted anesthetic
    5. Pull back Swan catheter – tends to float in further
    6. Give NMB to prevent shivering, along with fentanyl/versed
19
Q

What do the clamps create during CPB?

A

Clamp separates two sections.

  1. Aortic cannulation allows blood to go to systemic circulation
  2. Cardioplegia solution- contains high K+ & cold
  • Clamp prevents cold/K+ soln going to arterial side since right next to each other
20
Q

Purpose of cardioplegia solution? Contents?

A

Heart stops

  • Cold- 4°C
    • Reduces metabolism of heart (protection)
    • V-fib occurs at 25-30°C
  • Contains K+ (high dose)
    • Depolarization of heart
21
Q

What happens with the intiation of bypas?

A

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
22
Q

What is the pump primed with?

A

Primed with 2000 cc of crystalloids (rich in…)

  • Heparin
  • Mannitol
  • NaHCO3-
  • Albumin
  • Corticosteroids
  • Antifibrinolytics (aminocaproic acid/Amicar) to protect blood vessels
23
Q

What hemodynamic changes occur with the initiation of bypass?

A
  • 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
        • Higher BP (flow)
          • beneficial for stroke pts/carotid dz (need extra cerebral perfusion) or kidneys
    • CVP is 0mmHg
      • if higher → may have kink
24
Q

What are some hematological effects of CPB?

A
  • 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
  • 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
25
Q

How do we provide prophylaxis for bleeding?

A
  • 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
26
Q

What are some CNS risks while on pump? People at risk?

A

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)
27
Q

How can we provide cerebral protection while on bypass?

A
  • 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)
    • Cerebral oximetry
28
Q

Fluid managmeent considerations while on bypass?

A
  • Minimize crystalloids – hemodilutes pt
    • 1-1.5 L acceptable for crystalloids
  • Replace blood w/:
    • Colloids
    • Cell saver
    • PRBCs
29
Q

Rewarming considerations?

A
  • Begins at different times: (Surgeon can ask for rewarming of pt)
      1. 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
30
Q

What must occur prior to the discontinuation of bypass?

A
  • 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
  • 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
31
Q

Pneumonic to help remember preparation to wean from bypass?

A
  • “CVP”
    • Cells- PRBCs
    • Vaporizers- turn on gas since perfusionist turns off theirs
    • Volume expanders- for HoTN
    • Predictors:
      • Based off preop assessment
        • Arrythmias beforehand?
    • Potassium/Mag/Calcium balance
    • Protamine- AFTER everything else looks good (last thing)
32
Q

Considerations during discontinuation of bypass?

A
  • 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
    • If CO is low, but BP is adequate = SVR high (overly vasoconstricted)
      • BP good but heart cant pump against heavy constriction
        • Tx: vasodilation
    • If BP is low:
      • Inotropes
      • volume (cell saver, PRBC, whole blood)
  • Diagnose THEN treat
    • Look at BP and PA pressures
  • Once the pt is stable, bypass is completely d/c’d
33
Q

How do we support ventricular function during bypass weaning?

A

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)
    • If not working:
      • IABP (intra-arterial balloon pump)
      • Ventricular Assist Devices
34
Q

“Steps” for bypass weaning?

A

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

35
Q

Parameters used to determine treatment for TEE?

A

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
36
Q

What is protamine? Dosage?

A
  • 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
37
Q

Considerations for anaphylaxis with protamine?

A
  • 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
38
Q

Post bypass and postop considerations after cardiac surgery?

A

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
  • Post op pain control
    • Sternotomy very painful!
      • Ex: Fentanyl drip, morphine, dilaudid, etc
39
Q

Considerations around minimally invasive cardiac surgery?

A
  • 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