Utstein - animal studies and lab reporting Flashcards

1
Q

Define baseline conditions

A

The physiological conditions attained before induction of cardiac arrest, usually in an anesthetized, intubated, ventilated, and instru- mented animal.

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2
Q

Define induction of CA

A

The method and time of induction of a hemody- namic condition of no blood flow is essential infor- mation and should be depicted graphically on a time line.

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3
Q

Define standard chest compressions

A

External closed chest compressions applied to an area of the chest approxi- mately the size of the heel of an adult’s hand (15 to 25 cm*). The frequency of compressions is usually 60 to 100 per min, with a 50% duty cycle and a downward compression force sufficient to produce 3.8 to 5 cm (1.5 to 2 in) of chest displacement in a large animal.

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4
Q

Define CA

A

In the clinical setting, cardiac arrest is defined as the ‘cessation of cardiac mechanical activity…. It is a clinical diagnosis, confirmed by unresponsiveness, the absence of a detectable pulse and apnoea.

Most laboratory studies produce cardiac arrest by electrically inducing ventricular fibrillation, which can be confirmed by electrocardiography. Blood flow stops quickly, and this can be identified by the sudden loss of arterial pulsations on intravascular pressure monitors and by a systolic aortic blood pressure of < 25 mm Hg

With cardiac arrest secondary to asphyxia or exsanguination, the gradual decline in blood pressure is not usually accompanied by a sudden change in cardiac rhythm or ECG pattern. Regardlessof which technique is used to induce cardiac arrest, it should be defined precisely enough to allow reproduction by other investi- gators

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5
Q

Define ventilation

A

Any movement of gas in and out of the lungs.

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6
Q

Define alveolar ventilation

A

The amount of inspired gas available for gas exchange (minute ventilation minus dead-space ventilation).

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7
Q

Define compression phase

A

Measurements obtained when applied force decreasesthe thoracic votume (analogous to the systolic phase in a beating heart).

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8
Q

Define release phase

A

Measurements made during the CPR cycle when little or no pressure is being applied to the thorax. allowing it to recoil.

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9
Q

Define active decompression

A

When an outward force is ap- plied to the external chest during the release phase.

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10
Q

Define coronary perfusion pressure

A

The simultaneous difference between the aortic and right atria1 (or central venous) pressures during diastole

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11
Q

Define ROSC

A

Maintenance of a systolic aortic blood pressure of at least 60 mm Hg for at least 10 consecutive minutes.

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12
Q

Define survival

A

Existence beyond return of spontaneous circulation and the immediate postarrest period - at least 24 hours.

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13
Q

Define non-intervention interval

A

The interval of un- treated cardiac arrest without chest compression.

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14
Q

What are the methods of inducing CA?

A
  • Exsanguination
  • Hypoxia
  • Asphyxia
  • IV wire
  • Fibrillatory shock
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15
Q

How do you assess cerebral outcome in animal studies?

A

Cerebral outcome should be measured in terms of brain morphology (with such tools as the histopatho- logic damage score) and function (with such tools as the overall performance and neurological damage scores).

Electroencephalogram patterns of early postarrest recovery in animals are quite consistent but do not correlate well with functional and morphological out- come score

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