test 1 part 4 Flashcards

1
Q

What we want in pediatrics for cardioplegia:

A
  • Small prime
  • Good heat exchange
  • Air handling capabilities
  • A versatile system
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2
Q

Cardioplegia circuits may include:

A
  • Blood shunt
  • Crystalloid component
  • Blood component
  • Heat exchanger
  • Bubble trap
  • Air detector
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3
Q

CSC 14 heat exchanger

A
  • has a stopcock on the bottom
    - used for priming
    - while priming, stopcock pointing up and the fluid can go straight through the bottom and the prime will go up through the filter and purge back into the reservoir
    - when you go on bypass, you flip the stopcock down and the fluid will go up through the filter and back down which allows the air to be removed
  • priming volume of 30 cc
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4
Q

Aortic root cardioplegia cannula selection by weight in Kg

A
  • DLP 18 gauge = 0-7 kg

- DLP 16 gauge = 7-20 kg

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5
Q

Retrograde CPG delivery

A

Retrograde cardioplegia is given into the coronary sinus. A balloon is inflated or self inflated and provides two functions:
 Prevents backflow
 Holds cannula in place
- Flow should be titrated to maintain a coronary sinus pressure of 30-40 mmHg.
- only delivers to the left side of the heart and not the right

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6
Q

High K+/Low K+ ANTEGRADE DELIVERY

A

Initial dose: 30 mL/kg

Maintenance doses: 15 mL/kg every 15-30 minutes

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7
Q

Custodiol ANTEGRADE DELIVERY

A

Initial dose: 30-50 mL/kg (up to 2 L)
Maintenance dose: 10 mL/kg every 2 hours
- Deliver at LINE pressure ~125 mmHg until arrest, then drop to line pressure of ~80 – 90 mmHg

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8
Q

Del Nido ANTEGRADE DELIVERY

A

Initial dose: 20 mL/kg (up to 1 L)

  • 10 mls/kg maintenance
  • delivery at 90-180 mls/min
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9
Q

MECHANISM OF POTASSIUM ARREST

A
  • stops phase 3
  • prevents repolarization
  • extracellular
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10
Q

CUSTODIOL SOLUTION (BRETSCHNEIDER, HTK)

A
  • Intracellular solution
  • Low Na arrest
  • hyperpolarizing of myocytes and plasma membrane
  • Histidine: buffer- against acidosis during XC
  • Tryptophan: stabilizes cell membrane
  • Ketoglutarate: improves ATP production during reperfusion
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11
Q

TEMPERATURE AND CARDIOPLEGIA

A

Cold (<10°C) cardioplegia most common

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12
Q

Magnesium addition

A
  • The addition of magnesium may provide a protective effect on the hypoxic-ischemic immature heart.
  • This effect probably due to the antiarrhythmic effect of magnesium, inhibited entry of calcium into the myocytes, and decreased uptake of sodium by myocytes during ischemia.
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13
Q

MODIFIED ULTRAFILTRATION (MUF)

A

Utilization of a hemoconcentrator at a specific point post CPB

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14
Q

What’s really happening at the hemoconcentrator level while MUFing

A

A. Raising Hct
B. Extravascular fluid crosses ( rapid, large increase in COP) (noncellular or non protein volume)
C. Removes inflammatory mediators
D. C-Reactive Proteins cross
E. Protein reactive cytokines cross
F. Complement activation factors cross (C3a, sC56-9, C3 bound)
G. Pulmonary effects > Systemic effects with IL-6, IL-8, and TNF

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15
Q

MUF overview

A
  • After CPB
  • blood removed from patient by aortic cannula and goes through hemoconcentrator and fed back into patients right atrium
    • Suction is applied to the filter port of the hemoconcentrator, resulting in an ultrafiltration rate of 20 to 30 mL per minute
    • Ultrafiltration is carried out with the end point being either time (10–20 minutes) or the achievement of a hematocrit value of approximately 40-50.
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16
Q

Blood flow through the hemoconcentrator approximately

A

20mL/kg/min max

17
Q

Beneficial effects of MUF:

A

 total body water is reduced as a direct result of removing the ultrafiltrate.
 Reduced edema
 Reduced hospital stay
 Reduced ventilation times
 Reduced incidence of pleural and pericardial effusions.

18
Q

Arguments against MUF:

A

 Possible air embolism
 Remember that air would be entering
venous side
 Circuit complexity and cost
 Prolonged exposure to foreign surface
 “Patient can be concentrated before coming of CPB”

19
Q

CLINICAL STUDIES HAVE DEMONSTRATED THAT MUF IS ASSOCIATED WITH

A
  • Increased ventricular systolic function;
  • Improved cerebral blood flow (CBF), cerebral metabolic activity, cerebral oxygen delivery
  • Pulmonary function, decreased postoperative ventilation
  • Decreased postoperative bleeding, chest-tube drainage, pleural effusions
  • They equal short hospital stays
20
Q

MUF circuit

A

DRAW IT