GENERAL ANAESTHESIA Flashcards

1
Q

Nitrous oxide and diethyl ether

NO synthesized by _______ in 1776

_________ wrote that the ________ of diethyl ether is NO-like

Except for ____________ to produce highs at ether frolics

A

Priestley; Michael Faraday

inhalation; carnival inhalation

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2
Q

Anaesthesia before 1846

(Common or Uncommon?) before 1846

(Many or Few?) operations were carried out

Mortality was (frequent or rare?)

A

Uncommon; Few

Frequent

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3
Q

Anaesthesia before 1846

•______________ for open fracture

•Drainage of an abscess

•Drugs like _______,________, and ______ derivatives

A

Amputation of a limb

alcohol, harshish and opium

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4
Q

Anaesthesia before 1846

Physical methods for the production of analgesia.

•_______
•Unconsciousness induced by __________ or —————-
•Restraint by _______

A

ice pack

a blow on the head or strangulation

force

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5
Q

GOALS OF ANAESTHESIA:

  1. To create a/an (reversible or irreversible?) condition of comfort
  2. _________

3._____________ in a patient before, during and after performance of a procedure that would otherwise be painful; frightening, or hazardous.

A

reversible

quiescence

physiological stability

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6
Q

General anaesthesia

The hallmark of General anaesthesia is _______________________ which equals __________

A

LOSS OF CONSCIOUSNESS

GOING TO SLEEP

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7
Q

General anaesthesia

QUALITIES OF GA:
List 5!!!!!

A

Hypnosis, Amnesia, Analgesia, inhibition of autonomic reflexes, Muscle Relaxation

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8
Q

General anaesthesia

Pre & Intra (_______,________, and ________) and Post operative periods
.

A

Induction, Maintenance and emergence

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9
Q

General anaesthesia

INTRAOPERATIVE PERIOD

•Hemodynamic effect- _____ease in systemic arterial blood pressure.

The causes include direct vaso_______, myocardial ________, a blunting of __________ , and a generalized _____ease in central sympathetic tone.

•The ____tensive response is enhanced by underlying volume ________ or preexisting ______________.

A

decr; dilation; depression

baroreceptor control; decr

hypo; depletion

myocardial dysfunction

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10
Q

Patients
To reduce complications;

  1. Minimizing the _________ effects of anesthetic agents and techniques.
  2. Sustaining ____________ during surgical procedures that may involve major blood loss, tissue ischemia, reperfusion of ischemic tissue, fluid shifts, exposure to a cold environment, and impaired coagulation.
  3. Improving ______________ by choosing techniques that block or treat components of the ______________, which may lead to short- or long-term sequelae
A

potentially deleterious

physiologic homeostasis

postoperative outcomes

surgical stress response

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11
Q

Anesthetic drugs and techniques have profound effects on human physiology. Hence, a focused review of all major organ systems should be completed prior to surgery.

T/F

A

T

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12
Q

Preoperative Evaluation
Goals of the preoperative evaluation is to ensure that ___________________

A

the patient is in the best (or optimal) condition.

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13
Q

Preoperative Evaluation

Patients with unstable symptoms should _________ for optimization prior to elective surgery.

A

be postponed

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14
Q

Steps of the preoperative visit :

_________ Identification
______________
___________ Preparation
Plan of _______________

A

Problem

Risk Assessment

Preoperative

Anesthetic Technique

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15
Q

Problem Identification through :

●__________
●________ examination
●__________ investigation

A

History

Physical

laboratory

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16
Q

Patients with an abnormal airway (including Class __________ airway) should be considered at higher risk “.

A

III or IV

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17
Q

Preoperative Preparation

•Anesthetic indications:
-Anxiolysis, sedation and amnesia. e.g. ________
-Analgesia e.g ______
-Drying of airway secretions e.g _______,______,_____

-Reduction of anesthetic requirements ,Facilitation of smooth induction

-Patients at risk for GE reflux : ________,________,__________

A

benzodiazepine

narcotics

atropine,glycopyrrolate,scopolamine

ranitidine ,metoclopramide , sodium citrate

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18
Q

Preoperative Preparation : Surgical indications

-Antibiotic prophylaxis for infective endocarditis.
-Prophylaxis against DVT for high risk patients : ________ or ________ intermittent calf compression, or warfarin.

A

low-dose heparin or aspirin

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19
Q

Preoperative Preparation

Co-existing Disease indications:

Some medications should be continued on the day of surgery e,g _____,__________.

Others are stopped e.g _________ and _________

Steroids within the last six months may require __________

A

B blockers, thyroxine

oral hypoglycemics and antidepressants

supplemental steroids

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20
Q

Preoperative medications

Anti_________,

_______ are controversial as well as _____/_______ (drug interaction)

Pre- and postoperative administration of ________(_____) = significant decrease in myocardial ischeamia and mortality

A

hypertensives

Diuretics; metformin/ MAO inhibitors

β-receptor antagonist (atenolol)

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21
Q

Preoperative medications

Anticholinergic- employed for their _____ and membrane _____ effect

Anti-acidity- (npo-no per os)- decreasing the volume of gastric contents reduces ____,______,________

Sedative-hypnotics/ anxiolytics + opioids- reduces _______________ release

Opioids - pain

A

vagolytic; drying

regurgitation, prokinetic agents, cimetidine

catecholamine release

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22
Q

Finally, we plan our anesthetic technique :

1._______ or ______ anesthesia
2. _______ anesthesia
3. ________________ with _______________

A

Local or Regional

General

Combined regional with general anesthesia.

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23
Q

Finally, we plan our anesthetic technique :
1.Local or Regional anesthesia with ‘______‘ monitoring with or without _______.

  1. General anesthesia; with or without _______. _______ or _______ ——— is used.
  2. Combined regional with general anesthesia.
A

standby; sedation

intubation; Spontaneous or controlled ventilation

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24
Q

Molecular Mechanisms of General Anesthetics

Most intravenous general anesthetics act predominantly through _______ receptors

A

GABAA

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25
Q

Molecular Mechanisms of General Anesthetics

some interactions with other ligand-gated ion channels such as ______ receptors and ___-pore ____ channels and ——- channels gated by the (inhibitory or excitatory ?) receptors

A

NMDA

Two; K+ ; Chloride

Inhibitory; GABAA

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26
Q

Molecular Mechanisms of General Anesthetics

At clinical concentrations, general anesthetics increase the ________ of the GABAA receptor to GABA

A

sensitivity

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27
Q

Molecular Mechanisms of General Anesthetics

______ -gated Cl− channels (_____ receptors) may play a role in mediating inhibition by anesthetics

_____________ anesthetics enhance the capacity of glycine to activate glycine receptors,

A

Glycine; glycine

Inhalational

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28
Q

Molecular Mechanisms of General Anesthetics

Subanesthetic concentrations of the inhalational anesthetics inhibit ______ classes of ________________ receptors

A

some classes of neuronal nicotinic ACh

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29
Q

_______,________, and ———— potentiate glycine-activated currents

A

Propofol, neurosteroids, and barbiturates

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30
Q

______,_______,_________, and _______ inhibit NMDA receptor

A

Ketamine, nitrous oxide, cyclopropane, and xenon

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31
Q

_________ inhalational anesthetics activate some members of a class of K+ channels known as ___-pore domain channels

A

Halogenated

two

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32
Q

Cellular Mechanisms of Anesthesia

General anesthetics produce two important physiologic effects at the cellular level:

Inhalational anesthetics can ____________ neurons.

Both inhalational and intravenous anesthetics have substantial effects on __________ and much smaller effects on _______________ or __________

A

hyperpolarize

synaptic transmission

action potential generation or propagation.

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33
Q

Cellular Mechanisms of Anesthesia

Neuronal hyperpolarization may affect ________ activity and —————————————

A

pacemaker

pattern-generating circuits.

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34
Q

Cellular Mechanisms of Anesthesia

Their predominant actions are at the ———-, where they have profound and relatively specific effects on the ____________ to released neurotransmitter

A

synapse

postsynaptic response

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35
Q

General Anaesthesia (GA)

A variety of drugs are given to the patient that have different effects with the overall aim of ensuring ____,_______, and _______

A

unconsciousness, amnesia and analgesia.

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36
Q

Stages Of General Anesthesia

Stage I: _______,________ consciousness

Stage II: _______ stage, delirium, ___________ movement, ______ breathing. Goal is to ______________________________________

Stage III: ________ anesthesia; return of ___________

Stage IV: ————-; essentially an _______ and represents _____. This is the stage between _______ and ________ due to ____________.

A

Disorientation, altered

Excitatory; uncontrolled; irregular; move through this stage as rapidly as possible.

Surgical; regular respiration

Too deep; overdose ; anesthetic crisis

respiratory arrest and death ; circulatory collapse.

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37
Q

Stages Of General Anesthesia

Stage III: Surgical anesthesia; return of regular respiration.

Plane 1: “______” anesthesia

Plane 2: Loss of _____ reflex, _______ respiration .

Plane 3:______ anesthesia. _____ breathing, ______ ventilation needed.

Plane 4: ________ respiration only, _______ ventilation is required. _________ impairment.

A

light

blink; regular

Deep; Shallow; assisted

Diaphragmatic; assisted; Cardiovascular

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38
Q

Stages Of General Anesthesia

Level of anesthesia for painful surgeries is ????

A

Stage 3 plane 3

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39
Q

Earliest stage in which Surgical procedures can be performed is??

A

Stage 3 plane 2

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40
Q

Anesthetics divide into 2 classes

_______ Anesthetics

___________ Anesthetics

A

Inhalation

Intravenous

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41
Q

Inhalation Anesthetics

______ or ———-

Usually ___________

A

Gasses or Vapors

Halogenated

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42
Q

Intravenous Anesthetics

Given by _______
Anesthetics or ______ agents

A

Injections

induction

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43
Q

Inhalation Anesthetics

_________
_____________

A

Nitrous oxide
Halogenated anaes

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44
Q

Halogenated Anaes

List 4

A

Isoflurane
Halothane
Sevoflurane
Enflurane

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45
Q

Mechanism of Action of Inhalation Anesthetics

Interaction with ______ receptors

Volatile A – increase ______ and ________

A

protein

GABA and Glycine

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46
Q

MAC(__________________________)

A measure of _______________________

A

minimum alveolar concentration

potency of inhaled anesthetics

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47
Q

MAC is the concentration necessary to __________________________

A

prevent responding in 50% of population.

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48
Q

Pharmacokinetics of Inhaled Anesthetics

Amount that reaches the brain
Indicated by ______ ratio (lipid solubility)

Solubility of gas into blood
The (lower or higher?) the blood:gas ratio, the more anesthetics will arrive at the brain

A

oil:gas

Lower

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49
Q

General Actions of Inhaled Anesthetics

Respiration
–___________ respiration and response to CO2

Kidney
–_________ of renal blood flow and urine output

Muscle
– High enough concentrations will _____ skeletal muscle

A

Depressed

Depression

relax

50
Q

General Actions of Inhaled Anesthetics

Cardiovascular System

– Generalized ______ in arterial pressure and peripheral vascular resistance.

– _______ maintains CO and coronary function better than other agents

A

reduction

Isoflurane

51
Q

General Actions of Inhaled Anesthetics

Central Nervous System
– ____eased cerebral blood flow and _____eased cerebral metabolism

A

Incr

decr

52
Q

Nitrous Oxide
• widely used
• Potent __________
• Produce a ____ anesthesia

• Used as ______ to ___________

A

analgesic

light

adjunct

supplement other inhalationals

53
Q

Nitrous Oxide depress the respiration/vasomotor center

T/F

A

F

Do not depress the respiration/vasomotor center

54
Q

Halothane

flammable or non-flammable

____% metabolism by P450

(induction or inhibition?) of hepatic microsomal enzymes

A

non-flammable

20

induction

55
Q

Halothane

Myocardial ———— (SA node)

___________ of myocardium to catecholamines - arrhythmia

A

depressant

sensitization

56
Q

Halothane

Transient ______ damage
Liver _______ In repeated exposure Immuno____________

A

hepatic

necrosis

sensititation

57
Q

Malignant Hyperthermia

Malignant hyperthermia (MH) is a pharmacogenetic ________ state of ________ induced in susceptible individuals by ____________ and/or _____________ (and maybe by stress or exercise).

A

hypermetabolic

skeletal muscle

inhalational anesthetics

succinylcholine

58
Q

Malignant Hyperthermia

Genetic susceptibility- ____ channel defect (_________) or _______(_______ receptor)

Excess ______ ion leads to excessive ——————————

A

Ca+

CACNA1S

RYR1 ; ryanodine

calcium

ATP breakdown/depletion

59
Q

Malignant Hyperthermia

Signs: ——-cardia, _____pnea, metabolic _______, ____thermia, muscle _______, _______, arrhythmia

A

tachy; tachy; acidosis

Hyper ; rigidity

Sweating

60
Q

Malignant Hyperthermia May be fatal

T/F

A

T

61
Q

Malignant Hyperthermia

Treated with ___________

A

dantrolene

62
Q

Inhaled Anesthetics: Enflurane

(Slow or Rapid?) , (smooth or difficult?) __________________________

2-10% metabolized in liver

A

Rapid ; smooth

induction and maintenance

63
Q

_________ is Introduced as replacement for halothane

A

Enflurane

64
Q

Isoflurane

(Slow or Rapid?) , (smooth or difficult?) _____ and __________

very little metabolism (0.2%)

A

Smooth ; rapid

induction and recovery

65
Q

Isoflurane

Few reports of hepatotoxicity or renotoxicity

A

F

no reports of hepatotoxicity or renotoxicity

66
Q

________ is the most widely employed halogenated Inhalational anaesthetic

A

Isoflurane

67
Q

Intravenous Induction Agents

Commonly used IV induction agents:

List 3

A

Propofol
Thiopental sodium
Ketamine

68
Q

Intravenous Anesthetics

Most exert their actions by potentiating __________ receptor

A

GABAA

69
Q

Intravenous Anesthetics

GABAergic actions may be similar to those of ______ anesthetics, but act at different ______

A

volatile

sites on receptor

70
Q

Organ effect of Intravenous Anesthetics

Most ____ease cerebral metabolism

Most ____ease intracranial pressure

Most cause respiratory _________

May cause _____ after induction of anesthesia

A

decr; decr

depression

apnea

71
Q

Cardiovascular Effects of Intravenous Anesthetics

Barbiturates, benzodiazepines and propofol cause cardiovascular ________.

A

depression

72
Q

Thiopental sodium

(Slow or rapid?) onset (_____)

(short or long?) -acting

A

Rapid

20 sec

Short

73
Q

Thiopental sodium

Effect terminated not by _________ but by _________

repeated administration or prolonged infusion approaches _________ at _________ sites

Build-up in adipose tissue = _______ emergence from anesthesia

A

metabolism; redistribution

equilibrium

redistribution

very long

74
Q

Thiopental sodium

Side effects

_____tension
_________
_____ obstruction

A

Hypo

apnoea

airway

75
Q

Propofol

(Short or Long?) -acting agent used for the ________ and _______of GA and sedation

Onset within __________ of injection

A

Short

induction

maintenance

one minute

76
Q

Propofol

It is highly _______ in vivo and is metabolised by conjugation in the liver

A

Protein bound

77
Q

Propofol

Side-effect

_____ on injection

______tension

transient ______ following induction

A

pain

hypo

apnoea

78
Q

Ketamine

_______ Receptor Antagonist

A

NMDA

79
Q

Ketamine

usually (stimulate or depress?) the circulatory system

A

usually stimulate rather than depress the circulatory system

80
Q

Ketamine

Function
_________
_________ anesthesia

_______ appearance, eyes ____, reflexes are _______, ________ but ________ movement

A

Analgesic

dissociative

Cataleptic; intact

purposeless but coordinated

81
Q

Ketamine

(Stimulates or Depresses?) sympathetic nervous system

Psychomimetic – “________ reactions”

——- dreaming _______ (___________) experience

mis________, mis_________, illusions

may be associated with euphoria, excitement, confusion, fear

A

Stimulates; emergence

vivid; extracorporeal; floating “out-of-body”

perceptions; interpretations

82
Q

General anesthesia

__________

____________

A

Induction

Maintenance

83
Q

For induction

Which has faster onset?

Inhalation or intravenous anaesthetic

A

Intravenous

84
Q

For induction

(Inhalation or intravenous anaesthetic ?) avoids the excitatory phase of anaesthesia

A

Intravenous

85
Q

For induction

_______ is used where IV access is difficult

A

Inhalational

86
Q

For induction

_______ anaesthetic is used based on patient preference (children)

A

Inhalational

87
Q

Maintenance

In order to ______ anaesthesia for the required duration

______ to a carefully controlled mixture of _____,__________, and a________ anaesthetic agent

transferred to the patient’s _____ via the ——- and the _______, and the patient remains unconscious

A

prolong

breathe

oxygen, nitrous oxide, and a volatile

brain; lungs; bloodstream

88
Q

For maintenance

________ agents are supplemented by _______ anaesthetics, such as _________ ( usually _______ or _______)

A

Inhaled

intravenous

opioids; fentanyl or morphine

89
Q

What is Balanced Anesthesia?
Use specific drugs for each component

  1. Sensory
    _____,______,________ for analgesia
  2. Cognitive
    •Produce _______, and preferably ______. •inhaled agent
    •IV hypnotic
  3. Motor
    _____________
A

N20, opioids, ketamine

amnesia; unconsciousness

Muscle relaxants

90
Q

Simple Combinations
____________
____________

____________
____________
Relaxant of choice

A

Morphine
Propofol
N2O
Sevoflurane
Relaxant of choice

91
Q

Simple Combinations
__________

__________

__________

_________

Relaxant of choice

A

Fentanyl
Thiopental sodium
N2O
Halothane
Relaxant of choice

92
Q

There are three broad types of Anesthesia

-______ anesthesia
– _____ anesthesia
– _____ anesthesia

A

General anesthesia
– Local anesthesia
– Regional anesthesia

93
Q

PROCESS of an anesthesia

•_________
•Induction
– Transition of ________________ to __________

•Maintenance
– Maintenance of the _______________________

•________ & control of ______.

A

Premedication

an awake patient to an anaesthetized one.

desired depth of anaesthesia

Reversal; pain

94
Q

The depth of anesthesia has been divided into four major stages
They includes
– Stage I: _________
– Stage II: _________
– Stage III: _________ anesthesia
– Stage IV: ________________

A

Stage I: Analgesia
– Stage II: Excitement
– Stage III: Surgical anesthesia
– Stage IV: Medullary paralysis

95
Q

STAGE I/ ANALGESIA:

•From inhalation to _________
•Loss of _____ sensation occurs
•This results from interference with _________ in the ______________
•The patient is initially _______ and _______
•Then _______ and a reduced __________ occur as Stage II is approached.

A

loss of consciousness.

pain

sensory transmission ; spinothalamic tract.

conscious and conversational.

amnesia ; awareness of pain

96
Q

Strage 2/ excitement
•From loss of consciousness to the beginning of __________.
•The patient experiences _________
•Possibly displays _____,_______ behaviour.
•_____ease in blood pressure.
•____ease in respiratory rate and jerky breathing
•____eased muscle tone
•______eased ocular movement

A

loss of consciousness ; regular respiration.

delirium; violent, combative

Increase; Increase; Increased ; Increased

97
Q

STAGE III/ SURGICAL ANAESTHESIA

•From onset of __________ to cessation of ____________
•______ respiration and ________ of the skeletal muscles occur in this stage.
•Eye reflexes ____ease progressively
•Eye movements finally ____ and the pupil is ______.

A

regular respiration ; spontaneous breathing
Regular ; relaxation

decrease; cease; fixed.

98
Q

Surgery may proceed stage ___

A

3(surgical anaesthesia)

99
Q

STAGE IV/ MEDULLARY PARALYSIS

•_______ of breathing to __________ and _______
•Severe ______ of the _______ and ________ centres occur during this stage.
•______ can rapidly ensue unless measures are taken to maintain ________ and ___________

A

STAGE IV/ MEDULLARY PARALYSIS
Cessation ; failure of circulation and death.

depression ; respiratory and vasomotor centres

Death ; circulation and respiration.

100
Q

MECHANISM OF ACTION

Bind and Stimulate GABA receptor
–______,_________, and ________

Bind and Block Nicotinic Cholinergic receptors – ———- ________

Bind and Block NMDA receptors – ________ and __________

Bind and Activate K+ channels – ______

A

Barbiturate, Benzodiazepines and Propofol.

Volatile Hydrocarbons

Ketamine and Nitrous oxide,

Others

101
Q

MECHANISM OF ACTION

Bind and Stimulate ______ receptor
– Barbiturate, Benzodiazepines and Propofol.

Bind and Block ________ receptors – Volatile Hydrocarbons

Bind and Block ______ receptors – Ketamine and Nitrous oxide,

Bind and Activate _____channels – Others

A

GABA

Nicotinic Cholinergic

NMDA

K+

102
Q

PROPERTIES of the ideal anesthesia

Pro- PATIENT

Pleasant
Non ———-
Not associated with ______ and _______

(Slow or Fast?) induction and recovery

No _____________

A

irritating

nausea and vomiting

Fast

after effects

103
Q

PROPERTIES of the ideal anesthesia

Pro- SURGEON

Adequate ________
Adequate _______
_______ relaxation
Non ______ and non ______

A

analgesia

immobility

Muscle

flammable; explosive

104
Q

PROPERTIES of the ideal anesthesia

Pro- ANAESTHETIST

•Administration easy, controllable and versatile
•(Narrow or Wide?) margin of safety
•no _______
•No ________ on the major organs
•_____ – needing _____ concentrations
•Does not affect _______
•(Gradual or Rapid?) adjustment in depth of anesthesia
•Cheap, stable and easily stored
•Not react with ________ or ________

A

fall in BP

adverse effect

Potent ; low

oxygenation

Rapid

rubber tubing or soda lime

105
Q

PRE-ANESTHETIC AGENT

List 7

A

Anticholinergic
Antiemetics
Antihistamines
Barbiturates
Benzodiazepine
Muscle relaxant
Opioid

106
Q

PRE-ANAESTHETIC MEDICATION
It is the use of drugs _______ to make it _________________ .

A

prior to anesthesia

more safe and pleasant

107
Q

PRE-ANAESTHETIC MEDICATION

To relieve ________ - benzodiazepines.

To prevent __________- antihistaminics.

To prevent _________ -antiemetics.

To provide __________ - opioids.

To prevent ______-protonpumpinhibitor

To prevent ______________- atropine.

A

anxiety

allergic reactions

nausea and vomiting

analgesia; acidity

bradycardia and secretion

108
Q

PRE-ANAESTHETIC MEDICATION

To relieve anxiety - ________.

To prevent allergic reactions-_____.

To prevent nausea and vomiting-_______.

To provide analgesia- ________.

To prevent acidity-_________——

To prevent bradycardia and secretion- _________.

A

benzodiazepines

antihistaminics.

antiemetics.

opioids.

protonpumpinhibitor

atropine.

109
Q

CLASSIFICATION of general Anesthesia

INTRAVENOUS

Slow Acting:
– __________

–______ analgesia Eg _______

–________ anesthesia Eg ________

A

Benzodiazepines

Opioid; fentanyl

Dissociative; ketamine

110
Q

CLASSIFICATION of general Anesthesia

INTRAVENOUS

Fast Acting:
– _________

–___________

– _________

A

Barbiturates

Propofol

Etomidate

111
Q

NITROUS OXIDE Also called LAUGHING GAS

Relatively (Cheap or Expensive?)

_______ and ______ gas

(Low or High?) potency anaesthetic

(Good or Bad?) analgesic

(Minimal or Maximal?) muscle relaxation
(Low or High?) blood solubility

(Slow or Fast?) onset and recovery
(Low or High?) MAC

A

Cheap

Colourless and odourless

Low ; Good

Minimal ;Low

Fast ; High

112
Q

HALOGENATED HYDROCARBON

All contain ——-

________ is the most widely used volatile anaesthetic

A

fluorine

Isoflurane

113
Q

HALOGENATED HYDROCARBON

Decrease in Solubility – _________> _________> _________ > _________ > _________ > _________

Decrease in Potency – _________> _________ > _________ > _________ > _________ > _________

Increase in MAC – _________> _________ > _________ > _________ > _________ > _________

A

Methoxyflurane> Halothane>Enflurane > Isoflurane > Sevoflurane > Desflurane

Methoxyflurane> Halothane > Isoflurane > Enflurane > Sevoflurane > Desflurane

Methoxyflurane> Halothane > Isoflurane > Enflurane > Sevoflurane > Desflurane

114
Q

HALOGENATED HYDROCARBON
Adverse effect

– Specific

Isoflurane
–______ Phenomenon

Sevoflurane
–_________ ————

Desflurane
–___________
– ———-

A

Steal

Malignant Hyperthermia

Bronchospasm

Cough

115
Q

INHALATIONAL ETHER

Highly _____ liquid
Highly _________ and _________
Highly _________ and _________

Very _________
Also a called a _________ _________ AGENT

(Mildly or Highly?) soluble in blood

(Slow or Fast?) and Prolonged induction

(Slow or Fast?) recovery

A

volatile

Inflammable and explosive

Irritant and Pungent
Potent

COMPLETE ANAESTHETIC AGENT
Highly
Slow ;Slow

116
Q

Ether

No longer in used in developed countries because of _____________
Used in developing countries because it is ____________________

A

its unpleasant and inflammable nature

relatively safe and cheap

117
Q

Propofol

Used for __________________
(Slow or Rapid?) induction and recovery

(Short or Long?) lasting

Patient becomes unconscious in _____-_____

A

both induction and maintenance

Rapid ; Short

15-45s

118
Q

Propofol is irritant to the airway

T/F

A

F

Not irritant to the airway

119
Q

KETAMINE

Is a _______ derivative, Hence a _________
Effect is describes as ———ANAESTHESIA

(Slow or Fast?) induction and recovery

Site of action – ______ and _______ regions

A

phencyclidine; Hallucinogen

DISSOCIATIVE

Slow

cortical and subcortical

120
Q

THIOPENTAL

Is a ______
Commonly used for _______

Has (low or high?) lipid solubility

(Slow or Rapid?) action and (short or long?) duration

(Slowly or Rapidly?) metabolized

____ analgesic effect

A

Barbiturate; Induction

High; Rapid

Short

Slowly ; No

121
Q

ETOMIDATE

Similar to _____ but (more or less?) quickly metabolised

(More or Less?) risk of cardiovascular depression

May cause _________ during induction

Possible risk of _________ suppression

A

thiopental; more

Less

involuntary movements

adrenocortical