Test 2- GENERAL ANESTHESIA Flashcards

1
Q

Balanced anesthesia

A

refers to the achievement of a combination of unconsciousness, analgesia and muscle relaxation. Although all three of these factors may be achievable by using a single drug, it often requires high doses and will have undesirable side effects. Using a combination of different drugs whose actions complement each other generally allows each drug to be used at lower dose which reduces negative effects.

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2
Q

anesthetic plan or anesthetic protocol

A

he selection of a variety of drugs to be used at different stages of anesthesia and recovery is referred to as the anesthetic plan or anesthetic protocol.

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3
Q

‘dose sparing

A

Using one drug to reduce the required dose of another is called ‘dose sparing’.

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4
Q

The anesthetic protocol typically consists of the following:

A
  • Drugs for premedication (at this point you usually want sedation and analgesia).
  • Drugs for induction of anesthesia, to take the patient from just being sedated to being fully
    anesthetized, usually this is when endotracheal intubation will happen (injectable or inhalant
    anesthetic protocols can be used).
  • Drugs for maintenance of anesthesia (usually an inhalant with oxygen, but can be injectable).
    o Additional drugs may be needed for muscle relaxation, further analgesia, prophylactic therapy (antibiotics).
    o If inhalant anesthetics are not used it is termed ‘Total Intravenous Anesthesia (TIVA)’. - Drugs for recovery
    o Additional drugs may be needed to ‘smooth’ the process of waking up from general anesthesia), to provide additional analgesia and sometimes will include prophylactic therapy (antibiotics).
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5
Q

Induction of anesthesia goes through several stages:

A

I. Analgesia
II. Excitement phase (we try to minimize this with our drug selection).
III. Surgical anesthesia
a. Light plane – very light anesthesia, the patient may respond to painful stimulation.
b. Medium plane – deeper anesthesia than a light plane, patient will not respond to
mild stimuli but something very painful may cause a response.
c. Deep plane – even very strong stimuli (e.g. pain) will not cause a response.
IV. Medullary paralysis (severe inhibition of the medulla oblongata resulting in loss of autonomic functions of the respiratory and vasomotor centers). You don’t want to be at this stage, get the patient to a lower stage of anesthesia ASAP or else you may end up at the next stage….
V. Death (obviously we don’t want this to happen).

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6
Q

When it comes time to induce anesthesia (at which point your patient is either awake or sedated to varying degrees)

A

When it comes time to induce anesthesia (at which point your patient is either awake or sedated to varying degrees)

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7
Q

Induction can be achieved with

A

Induction can be achieved with inhalant anesthetics alone but that is generally less preferable (see that section of the notes).

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8
Q

The pros of injectable anesthetic drugs are:

A
  • They cause an extremely rapid onset of anesthesia, and this allows you to get control of the
    airway very quickly by intubating the patient (and controlling the airway and thus oxygenation
    of your patient is of the highest importance).
  • With some injectable drugs IM injection is possible which may be useful in cases where
    placement of a catheter ahead of time is not feasible (like a feral cat).
  • They require minimal equipment (compared to inhalational anesthetics)
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9
Q

However there are cons as well:

A
  • These are often controlled substances that require close monitoring, have paperwork associated
    with them and serve as a potential attractant for theft or substance abuse.
  • You may have minimal control over when your patient awakes (which is why these are often used just for induction and then the more rapid inhalant drugs are used for maintenance,
    allowing the injectable drug to be metabolized before you need to wake the patient up).
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10
Q

Central nervous system:

A

o Since our goal is to make the animal sleep just enough (and not too much) this is
monitored constantly and the plane of anesthesia assessed to make sure the patient is
not ‘too light’ and at risk for waking up or ‘too deep’ and at risk of death.
o Additionally we may be concerned about the intracranial pressure (ICP). For some patients this will not be a major concern, but if a patient has a neurologic disease or injury then increases to intracranial pressure could be very detrimental and so it is
useful to know if your drugs will reduce or increase ICP.

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11
Q

Cardiovascular:

A

o Blood pressure (usually with a doppler or other blood pressure monitor).
o Heart rate and pulse rate (these are normally the same but can differ when there is a
problem).

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12
Q

Respiratory:

A
o Breathing rate and depth.
o Oxygen (by way of a ‘pulse ox’ monitor that clips to an ear or lip and measures the percentage of oxygenation in the blood) and Carbon dioxide (by way of a capnograph which attaches to the endotracheal tube and measures the end-tidal (end of breathing cycle) CO2 levels).
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13
Q

Skeletal system (degree of muscle relaxation):

A

o For most surgeries it is necessary to have skeletal muscle relaxation, it also helps for
intubation of the patient and expressing their bladder (in advance of abdominal
surgery).
o In other situations you may not want too much skeletal relaxation, eye surgery is a great
example of this (because as the periocular muscles relax the eye will ‘roll down’ and
make work on the cornea difficult).

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14
Q

Other systems:

A
o Renal system: We are mostly concerned about whether and how much our drugs may cause risk of renal injury or a decrease in glomerular filtration (GFR).
o Reproductive system: Most important if anesthetizing pregnant animals (effects on uterus and fetus).
o Miscellaneous: Unique effects of clinical importance for any given drug or class of drugs.
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15
Q

The pros of inhalant anesthetic drugs are:

A
  • You have control of the airway and ventilation

- You have close control over drug uptake and elimination

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16
Q

The cons of inhalant anesthesia are:

A
  • Specialized (expensive) equipment needed

- Equipment can fail (need monitoring and expertise)

17
Q

The dosage for inhalant anesthetic drugs

A

The dosage for inhalant anesthetic drugs is usually expressed as a concentration (in volume %) of the whole gas mixture (inhalant drug plus the oxygen that is carrying it).

18
Q

Most inhalant anesthetics are

A

Most inhalant anesthetics are vapors (the exception is Nitrous Oxide which is a gas). A vapor refers to the gaseous state of a substance that at ambient temperature and pressure is a liquid. Thus the inhalant anesthetics are supplied as bottles of liquid and in order to use them as a ‘gas’ a specialized vaporizer is needed.

19
Q

vaporizer

A

The vaporizer will hold the liquid anesthetic agent at a specific pressure and allow precise levels of gas (oxygen) to flow across the liquid, thus picking up the evaporated drug (vapor) to deliver to the patient. Because the vapor pressure for different drugs varies, the vaporizer has to be matched to the specific drug.

20
Q

Blood/Gas solubility coefficient

A

The Blood/Gas solubility coefficient is the most clinically relevant measure of solubility. This is important to us because it is a direct reflection of the speed of induction and recovery, as well as how fast responses to changes in dose of the anesthetic agent will be.

21
Q

The more soluble the anesthetic agent (higher blood/gas coefficient) the

A

The more soluble the anesthetic agent (higher blood/gas coefficient) the longer it will take to reach equilibrium (e.g. slower induction, recovery, and response to changes in dose).

22
Q

The more insoluble the agent (lower blood/gas coefficient)

A

The more insoluble the agent (lower blood/gas coefficient) the faster it will reach equilibrium.

23
Q

MAC

A

A term that we use frequently with inhalant anesthetics is the MAC (Minimum Alveolar Concentration). This is the equilibrium concentration of an anesthetic in the alveolus that is required to prevent movement and response to pain in 50% of individuals (so similar to an anesthetic ED50). MAC will vary between different drugs, and between different species for the same drug.

24
Q

Absorption

A

The pharmacokinetics of inhalant anesthetics is very different than most drugs because it occurs primarily via the lungs.
Absorption happens completely through the lungs at the level of the alveolus. In order to be absorbed the gas (oxygen + anesthetic) needs to reach the alveoli, then it must diffuse across the alveolus into the capillaries. Normally this is a very efficient process, so we can generally assume that the concentration in the alveoli is going to be equal to the concentration in the bloodstream.

25
Q

Distribution

A

Distribution is generally good for anesthetic agents, they are all lipid soluble which is necessary to cross the blood-brain barrier.

  • We expect to have an initial induction phase where higher rates of inhalant are needed until the tissue reservoirs have ‘filled’ and equilibrium is reached. After those initial few minutes the rate of inhalant delivery (i.e. vaporizer setting) can be turned down and much lower ongoing dose is needed to maintain blood and tissue (brain) levels, this is considered the maintenance phase.
  • Just as they cross the blood-brain barrier, inhalant anesthetics will also cross the placenta.
26
Q

Metabolism

A

Metabolism is variable between different anesthetic agents, with the most common current agents undergoing almost no metabolism (see details under the specific drugs below).

27
Q

Excretion

A

Excretion is primarily via the lungs.