test 1 part 3 Flashcards

1
Q

3 major differences between pediatrics and adults

A

Anatomic differences
Metabolic differences
Physiologic differences

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

Anatomic Differences Structural and Functional

A

Myocytes and myofibrils increase in size as they mature
The number of mitochondria increases as the oxygen requirements of the heart rises.
The amount of sarcoplasmic reticulum and its ability to sequester calcium similarly increase in early development.
Activity of Na+/K+ adenosine triphosphatase (ATPase) increases with maturation, and affects the sodium-calcium exchange. (big effect on bringing the cell back to its resting membrane potential)
Ca++ handling in immature myocardium ↑’s intracellular Ca ++ concentrations post ischemia/reperfusion.
Activates energy-consuming processes -> decreased levels of adenosine triphosphatase (ATPase) -> lack of energy sources for cardiac function
Contributes to dysfunction observed after CPB

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

Metabolic Differences

A

 Increased myocardial oxygen demands
 associated with a switch from anaerobic metabolism after birth to a more aerobic metabolism.
the increased ability of the immature myocardium to rely on anaerobic glycolysis, it can withstand ischemic injury better than an adult myocardium can.
 In the mature (3-12 mo) heart, long-chain fatty acids are the primary substrates (increased mitochondria needed)

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

Physiologic differences

A

Premature infants prone to:
 HYPOCALCEMIA, hypoxia, infection, stress, diabetes
Effects of hemodilution is enhanced in neonates
decreased plasma proteins, coagulation factors, and Hgb
 Infants/neonates have high oxygen-consumption rates
require flow rates as high as 200 mL/kg/min at normal temperature (kg based flow rates)

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

Most important difference between adults and kids

A
  • Presence of Intra-cardiac and extra-cardiac shunts and the reactive pulmonary vasculature are unique anatomic and physiologic findings in patients with congenital cardiac disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Glucose control difference between adults and kids

A
  • Adult: Control high blood sugar
    CPB => stress response => hyperglycemia
    Studies link hyperglycemia with adverse outcomes
  • Peds: Control low blood sugar
    Hypoglycemia is due to decreased glycogen stores and reduced hepatic gluconeogenesis
    more common on pediatric CPB is hypoglycemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Hematologic Effects difference between adults and kids

A

Adult:
 Inflammatory response upon surgery/CPB
Pediatric:
Exaggerated response to surgery/CPB (because their immune response isn’t built up yet)

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

The events that trigger stress:

A

Ischemia
Hypothermia
Anesthesia
Surgery

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

Stress Response: CPB causes hormone release and also releases: (adults and kids)

A
Catecholamines
Cortisol 
ACTH
TSH
Endorphins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Cardiac Effects difference between adults and kids

A
  • Adult
    Less ischemia tolerance (because of their aerobic metabolism)
    May/may not be preconditioned to ischemia
    More tolerant of overfilling (myocardium more mature)
  • Pediatrics
    Tolerate ischemia
    Higher lactates seen (cost of tolerating ischemia)
    Prone to stretch injury (overfilling)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

CNS Effects difference between adults and kids

A
- Adult
        More neurological injuries
        Multifaceted etiology
        Stem from disease processes
- Pediatrics
        Neuro problems rare with routine CPB
        Increased with DHCA (?25%)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Pulmonary difference between adults and kids

A
- Adult
        Lungs fully developed
        LESS REACTIVE VASCULATURE
        May have preexisting disease
- Pediatrics
        Lungs not fully developed
        MORE REACTIVE VASCULATURE
        Usually without existing disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Renal difference between adults and kids

A
  • Adults
    The normal urine output for adults can be 0.5 to 1 ml/min, regardless of weight. That translates to 60 ml/hr.
  • Peds
    For children, the expected urine output is closer to 1ml/kg/hour of urine
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Hypothermia in Children: What can you expect?

A

Due to the complex congenital heart repairs you will see that children are often brought to colder temperatures more frequently than adults
Different temperature monitoring sites in pediatrics (not a lot of bladder, see a lot of rectal)
Smaller children cool more rapidly than adults
DHCA is more often utilized

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

Hypothermia temperatures

A
Warm => 36-37°C
 Mild Hypothermia => 32-35°C
 Moderate Hypothermia => 28-31°C
Deep Hypothermia => 18-27°C
Profound Hypothermia => < 18°C
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Q10 principle

A
  • Relates the increase or decrease in reaction rates or metabolic processes to a temperature change of 10 degrees C
  • Oxygen consumption is a
    reaction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Reduction in metabolic rates (2ND Principle)

A

• Every 7°C drop in temperature will result in a 50% decrease in oxygen consumption

18
Q

Pediatric Monitoring of Temperature during Hypothermia locations:

A
I. Core (central)
         Bladder (not on small children)
         Nasopharyngeal
         Tympanic
         Esophageal
         Venous
         Rectal
II. Shell (peripheral)
         Skin
19
Q

Protective effects of hypothermia

A
  • Excitatory neurotransmitter release is reduced with hypothermia
  • Hypothermia helps to protect organs against injury caused by the compromised substrate supply to tissues resulting from reduced flow.
  • This protection occurs because of a reduced metabolic rate and decreased oxygen consumption.
20
Q

”Safe” Circ Arrest Times

A

37 - 32⁰ C (mild) = < 10 mins
31 –28⁰ C (moderate) = 10-20 mins
27 - 18⁰ C (deep) = 20-45 mins
< 18 ⁰ C (Profound) (rare) = 45-60 mins

21
Q

Negative effects of hypothermia

A

Cerebral blood flow loses autoregulation at extreme temperatures (20 degrees C) which makes blood flow highly dependent on extracorporeal perfusion.
this uncoupling of autoregulation is a serious issue and is the basis for the Alpha stat/pH stat debate

22
Q

DHCA (deep hypothermic circ arrest): overview

A

DHCA provides excellent surgical exposure by eliminating the need for several cannulas in the surgical field and by providing a motionless and bloodless field.
Cooling is started before CPB by simply cooling room.
CPB is started and cooling begins for at least 20-30 minutes. After adequate cooling is achieved, the circulation is arrested. The desired duration of DHCA is limited to the shortest time possible.
After circulation is resumed, the final repairs are done on warming

23
Q

Arterial Cannulation spots

A

 Ascending aorta
 Innominate (first branch off of aorta)
 Femoral

24
Q

venous cannulation sites

A

 Usually a single venous (RA)
 The heart is not opened until circulatory arrest
 If Bicaval
 Usually if intracardiac repairs are necessary
 Heart can be opened before circulatory arrest, while cooling

25
The good of DHCA
Allows exposure Reduces metabolic rate and molecular movement Allows cessation of circulation
26
The bad of DHCA
``` Neurologic injury & morbidity Brain is at the most risk >60 min arrest is detrimental >40 min increases risk MUST monitor temp gradients closely ```
27
Temp gradient from art to venous
NOT > 8°C
28
Hypothermic Low Flow vs Cardiopulmonary Bypass (HLFB)
• Trials to compare the 2 methods (DHCA vs. HLFB) have demonstrated lowered rates of neural dysfunction in patients undergoing HLFB.
29
Hypothermic Intermittent Low Flow Cardiopulmonary Bypass (ILFB)
 using DHCA with INTERMITTENT LOW FLOW BYPASS (ILFB) for 1-2 minutes every 15-20 minutes
30
Antegrade Cerebral Perfusion
- Perfusing the head vessels in an antegrade fashion to perfuse the brain during DHCA - Via head vessels/shunt - pressure of 40-50 mm Hg in the right radial artery. - Higher flows of 30-40 mL/kg/min are recommended for neonates.
31
Retrograde Cerebral Perfusion
- Perfusing the head vessels in a retrograde fashion to perfuse the brain during DHCA - Via SVC - The concept of RCP originated as the treatment of massive air embolism during CPB. Pressure in the superior vena cava is maintained at 15-20 mm Hg otherwise cerebral edema - cerebral edema formation when pressure exceeds 25 mmHg  the amount of perfusate that provides cerebral nutrition is low, corresponding to only about 5% of total retrograde flow Most of this flow is drained from the SVC into the inferior vena cava given the rich network of collaterals between the veins.
32
Antegrade Cerebral Perfusion drawbacks
dissection of the arterial wall air atheromatous plaque embolization malposition of the cannula overcrowding of the operative field with cannulas ACP can be given continuously or intermittently
33
Ph Stat
pH-stat pH management is temperature-corrected. (at the patient's temperature) pH stat leads to higher pCO2 (respiratory acidosis), and increased cerebral blood flow.
34
Ph stat - GOOD
Improved neurologic outcome, shorter EEG recovery times, and reduced number of postop seizures. Decreased pulmonary collateral circulation flow during CPB Increased cortical oxygen saturation before arrest Decreased cortical oxygen metabolic rates during arrest Increased brain-cooling rates CBF during reperfusion increases by using a pH stat management strategy.
35
Ph stat -BAD
 increased CBF can increase embolic events, high CBF during reperfusion, and reperfusion injury, cerebral edema Acid load induced by pH-stat strategy may impair enzymatic function and metabolic recovery. Lose autoregulation - perfusion pressure then rules
36
Alpha-Stat
 Blood samples warmed to room temperature have a pH of 7.4 and a PCO2 of 40 mmHg. These conditions allow the alpha imidazole group of the histidine moiety on blood/cellular proteins to maintain a constant buffering capacity, which enhances enzyme function and metabolic activity. - READ ABG’s AT 37°C
37
Alpha- stat: The Good
• Cerebral Blood Flow (CBF) autoregulation is maintained, which allows for metabolism and blood flow coupling. CBF can be adjusted depending on the patient's cerebral metabolic activity and oxygen needs. • Normal enzyme function  Most studies of this approach have been performed in adults.
38
Alpha–stat: bad
* Vasoconstriction | * Poor (slows down) Cooling, which potentiates problems at the cellular level
39
The Compromise Combination for acid base management:
That is, initial cooling is accomplished with the pH stat method, which is then switched to alpha-stat method to normalize the pH in the brain before ischemic arrest is induced (some do it on the last gas before arrest)
40
Three cerebral oximeters Food and Drug Administration approved in the United States for use in the infant population
INVOS NONIN EQUANOX FORE-SIGHT