Intravenous Anesthetics Flashcards

1
Q

What does repetitive administration of barbiturates result in?

A

It saturates the peripheral compartments, minimizing redistribution and making the duration of action more dependent on elimination. This is known as context sensitivity.

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2
Q

How do barbiturates affect cerebral blood flow?

A

Barbiturates constrict the cerebral vasculature, leading to a decrease in cerebral blood flow, cerebral blood volume, and intracranial pressure.

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3
Q

What is a respiratory risk associated with benzodiazepine induction?

A

Even small intravenous doses of diazepam and midazolam can result in respiratory arrest.

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4
Q

How does ketamine differ from other anesthetic agents in terms of cardiovascular effects?

A

Ketamine increases arterial blood pressure, heart rate, and cardiac output, particularly after rapid bolus injections.

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5
Q

What effect does etomidate have on hormone synthesis?

A

Induction doses of etomidate transiently inhibit enzymes involved in cortisol and aldosterone synthesis.

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6
Q

What precaution must be taken when handling propofol?

A

Propofol formulations can support bacterial growth, so sterile technique must be followed, and it should be administered within 6 hours of opening the ampule.

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7
Q

What are the primary mechanisms of action of barbiturates?

A

Barbiturates depress the reticular activating system in the brainstem and potentiate the action of GABA by increasing the duration of chloride ion channel openings.

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8
Q

What determines the hypnotic potency and anticonvulsant activity of barbiturates?

A

Substitution at carbon C5 determines potency, with long-branched chains conveying more potency and phenyl groups contributing to anticonvulsant activity.

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9
Q

What is the effect of replacing oxygen at C2 with a sulfur atom in barbiturates?

A

It increases lipid solubility, leading to greater potency, more rapid onset, and shorter duration of action, as seen in thiopental and thiamylal.

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10
Q

How does the distribution of thiopental affect its duration of action?

A

The duration of action is determined by redistribution to peripheral compartments, which lowers plasma and brain concentration within 20-30 minutes.

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11
Q

How does the pharmacokinetic profile of methohexital differ from thiopental?

A

Methohexital is cleared more rapidly by the liver than thiopental, leading to faster recovery of psychomotor function after a sleep dose.

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12
Q

How does barbiturate biotransformation occur?

A

Barbiturates are principally biotransformed via hepatic oxidation to inactive water-soluble metabolites.

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13
Q

What are the cardiovascular effects of barbiturates?

A

Barbiturates cause a decrease in blood pressure and an increase in heart rate, with hemodynamic responses varying based on the rate of administration and other factors.

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14
Q

What respiratory effects do barbiturates have?

A

Barbiturates depress the medullary ventilatory center, leading to decreased ventilatory response to hypercapnia and hypoxia, and often cause apnea after induction.

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15
Q

How do barbiturates affect cerebral oxygen consumption?

A

Barbiturates decrease cerebral oxygen consumption by up to 50%, without negatively impacting cerebral blood flow.

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16
Q

What is the effect of barbiturates on renal function?

A

Barbiturates reduce renal blood flow and glomerular filtration rate in proportion to the fall in blood pressure.

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17
Q

What is the immunological effect of sulfur-containing thiobarbiturates?

A

Sulfur-containing thiobarbiturates can evoke mast cell histamine release in vitro, which may affect asthmatic or atopic patients.

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18
Q

How do benzodiazepines increase chloride ion channel openings?

A

Benzodiazepines bind to a different site on the GABA-A receptor, increasing the frequency of chloride ion channel openings.

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19
Q

What effect does midazolam’s imidazole ring have on its solubility?

A

The imidazole ring of midazolam increases its water solubility at low pH, facilitating its absorption.

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20
Q

What is the effect of diazepam and lorazepam on cardiovascular function?

A

They display minimal cardiovascular depressant effects, but can decrease arterial blood pressure, cardiac output, and peripheral vascular resistance slightly.

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21
Q

How do benzodiazepines affect the ventilatory response to CO2?

A

Benzodiazepines depress the ventilatory response to CO2, with a risk of respiratory arrest if administered intravenously or in combination with other depressants.

22
Q

How do benzodiazepines affect cerebral blood flow and intracranial pressure?

A

Benzodiazepines reduce cerebral oxygen consumption, cerebral blood flow, and intracranial pressure, but not to the extent of barbiturates.

23
Q

What is the clinical effect of benzodiazepines on muscle relaxation?

A

Benzodiazepines have mild muscle-relaxing properties, mediated at the spinal cord level, not at the neuromuscular junction.

24
Q

What drug interactions should be considered with benzodiazepines?

A

Cimetidine, erythromycin, and heparin can alter the metabolism of benzodiazepines, leading to prolonged effects. They also potentiate the effects of other CNS depressants.

25
Q

How do benzodiazepines interact with opioids?

A

The combination of opioids and benzodiazepines significantly reduces arterial blood pressure and peripheral vascular resistance.

26
Q

What is the effect of benzodiazepines on the minimum alveolar concentration (MAC) of volatile anesthetics?

A

Benzodiazepines reduce the MAC of volatile anesthetics by as much as 30%.

27
Q

What is the primary mechanism of action of ketamine?

A

Ketamine is an NMDA receptor antagonist, which inhibits excitatory neurotransmitter effects in selected areas of the brain and causes dissociation between the thalamus and limbic cortex.

28
Q

What kind of anesthesia does ketamine produce?

A

Ketamine produces dissociative anesthesia, where the patient may appear conscious but is unable to process or respond to sensory input.

29
Q

What structural similarity does ketamine share with phencyclidine?

A

Ketamine is a structural analogue of phencyclidine, retaining many of its psychotomimetic effects.

30
Q

How does ketamine affect the cardiovascular system?

A

Ketamine increases arterial blood pressure, heart rate, and cardiac output due to central sympathetic stimulation and inhibition of norepinephrine reuptake.

31
Q

What is the effect of ketamine on the respiratory system?

A

Ketamine minimally affects ventilatory drive but can cause apnea with rapid intravenous bolus or when combined with opioids. It is also a potent bronchodilator.

32
Q

What is ketamine’s effect on cerebral circulation?

A

Ketamine increases cerebral blood flow, oxygen consumption, and intracranial pressure, though when combined with a benzodiazepine, it may not increase intracranial pressure.

33
Q

How is ketamine metabolized?

A

Ketamine is biotransformed in the liver to several metabolites, including norketamine, which retains anesthetic activity.

34
Q

How does ketamine affect patients with coronary artery disease or uncontrolled hypertension?

A

Large bolus injections of ketamine should be administered cautiously in these patients due to the risk of increased myocardial work and blood pressure.

35
Q

What are the psychotomimetic effects of ketamine?

A

Ketamine can cause hallucinogenic effects, though they are often minimized in clinical practice with the use of sedatives like midazolam.

36
Q

What are the major side effects of ketamine at subanesthetic doses?

A

At subanesthetic doses, ketamine can cause hallucinogenic effects, though these are usually avoided with premedication.

37
Q

What interactions does ketamine have with other anesthetic agents?

A

Ketamine has a synergistic interaction with volatile anesthetics and an additive effect with propofol, benzodiazepines, and other GABA-receptor agents.

38
Q

What effect does ketamine have on sympathetic stimulation?

A

Ketamine’s central sympathetic stimulation increases heart rate, blood pressure, and cardiac output.

39
Q

How does ketamine affect airway reflexes?

A

Ketamine tends to preserve upper airway reflexes but may cause partial airway obstruction, especially in patients at risk for aspiration pneumonia.

40
Q

What is the effect of ketamine on cerebral oxygen consumption and blood flow?

A

Ketamine increases both cerebral oxygen consumption and cerebral blood flow, although this may not be detrimental when combined with controlled ventilation.

41
Q

What is the cardiovascular effect of large doses of ketamine?

A

Large doses of ketamine can unmask direct myocardial depressant effects, especially in cases of sympathetic blockade or exhaustion of catecholamine stores.

42
Q

What is the role of the S(+) stereoisomer of ketamine?

A

The S(+) stereoisomer has greater potency and a stronger affinity for NMDA receptors, offering increased anesthetic potency and decreased psychotomimetic side effects.

43
Q

What is the pharmacokinetics of ketamine in terms of absorption?

A

Ketamine can be administered orally, nasally, rectally, subcutaneously, and epidurally, but is commonly given intravenously or intramuscularly for rapid onset.

44
Q

How does ketamine distribute in the body?

A

Ketamine is highly lipid-soluble and undergoes rapid brain uptake and redistribution, with a distribution half-life of 10–15 minutes.

45
Q

What is the excretion route of ketamine’s metabolites?

A

End products of ketamine biotransformation are primarily excreted in the urine.

46
Q

What are the effects of ketamine on ventilation?

A

Ketamine typically does not significantly affect ventilatory drive, but rapid bolus administration or combination with opioids may result in apnea.

47
Q

How does ketamine interact with α-adrenergic and β-adrenergic antagonists?

A

These antagonists unmask ketamine’s direct myocardial depressant effects, which are usually outweighed by its sympathetic stimulation.

48
Q

What is the use of ketamine for deep sedation in clinical practice?

A

Ketamine is often combined with other agents like propofol or midazolam for deep conscious sedation during procedures like nerve blocks and endoscopy.

49
Q

What is the role of ketamine in trauma or hypovolemia?

A

Ketamine is useful in trauma or hypovolemic patients due to its ability to maintain sympathetic stimulation and increase blood pressure, heart rate, and cardiac output.

50
Q

What are the major side effects associated with ketamine use?

A

The major side effects of ketamine include increased intracranial pressure, psychotomimetic effects, and possible airway obstruction in some patients.