General anesthesia Definition of anesthesia It is a reversable - - PowerPoint PPT Presentation

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General anesthesia Definition of anesthesia It is a reversable - - PowerPoint PPT Presentation

General anesthesia Definition of anesthesia It is a reversable blocking of pain feeling in whole body or in a part of it using pharmacology or other methods Anesthesia- division Local- regional anesthesia, patient is conscious or


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SLIDE 1

General anesthesia

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SLIDE 2

Definition of anesthesia

  • It is a reversable blocking of pain feeling in

whole body or in a part of it using pharmacology or other methods

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SLIDE 3

Anesthesia- division

  • Local- regional anesthesia, patient is

conscious or sedated

  • General- anesthesia interact with whole

body, function of central nervous system is depressed:

– Intravenous – Inhalation (volatile) – Combined, balanced

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SLIDE 4

TIVA

Total Intra Venous Anaesthesia

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SLIDE 5

VIMA

Volatile Induction and Maintain Anaesthesia

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SLIDE 6

Parts of general anesthesia

  • Hypnosis- pharmacological sleep,

reversable lack of consciousness

  • Analgesia-pain management
  • Areflexio-lack of reflexes
  • Relaxatio musculorum- muscle relaxation,

pharmacological reversable neuromuscular blockade

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SLIDE 7

Parts of general anesthesia must be in balance

Hypnosis (anesthesia) Analgesia Lack of reflexes (muscle relaxation)

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SLIDE 8
  • General anesthesia

features

Lack Lack of

  • f reflexes

reflexes

3

Lack Lack of

  • f consciousness

consciousness

1 1

Pain Pain management management

2 2

Neuromuscular Neuromuscular blockade blockade

4 4

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SLIDE 9

Stages of general anesthesia

  • Stadium analgesiae (analgesia and

sedation stage)

  • Stadium excitationis (excitation stage)
  • Stadium anaesthesiae chirurgicae

(anesthesia for surgery)

  • Stadium paralysis respirationis

(intoxication, respiratory arrest)

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SLIDE 10
  • I. Analgesia stage
  • Patient consciouss
  • Spontaneus respiration
  • Reflexes present
  • Possible small surgery procedures like

dressing change in burns

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SLIDE 11
  • II. Excitation stage
  • Possible uncontrolled movements,

vomitings

  • Increase in respiratory rate
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SLIDE 12
  • III. Anesthesia for surgery
  • It begins with lack of lid reflex
  • 4 substages
  • Airway opening necessary
  • Possible surgery except for abdominal
  • pening if no relaxants are used
  • Possible endotracheal intubation
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SLIDE 13
  • IV. intoxication, overdosing
  • Respiratory arrest
  • If anesthesia not discontinued possible

cardiac arrest

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SLIDE 14

Estimation Estimation of

  • f the

the risk risk of

  • f anesthesia

anesthesia ( (American American Society Society of

  • f Anesthesiologists

Anesthesiologists scale scale) )

  • ASA 1

ASA 1: : healthy healthy patient patient. .

  • ASA 2

ASA 2: : patient patient with with stable stable, , treated treated illness illness like like arterial arterial hypertension hypertension, , diabetes diabetes melitus melitus, , asthma asthma bronchiale bronchiale, ,

  • besity
  • besity
  • ASA

3 ASA 3: : patient patient with with systemic systemic illness illness decreasing decreasing suffitiency suffitiency like like heart heart ilness ilness, , late late infarct infarct

  • ASA 4

ASA 4: : patient patient with with serious serious illness illness influencing influencing his his state state like like renal renal insuficiency insuficiency, , unstable unstable hypertension hypertension, , circulatory circulatory insuficiency insuficiency

  • ASA 5

ASA 5: : patient patient in in life life treatening treatening illness illness

  • ASA 6

ASA 6: : brain brain death death-

  • potential

potential organ donor

  • rgan donor
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SLIDE 15

Premedication Premedication

Main Main reasons reasons for for premedication premedication: :

  • Anxiolysis

Anxiolysis-

  • lack

lack of

  • f threat

threat

  • Sedation

Sedation – – calming calming down down

  • Amnesia

Amnesia – – lack lack of

  • f memories

memories of

  • f

perioperative perioperative period period

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SLIDE 16
  • Methods of general anesthesia

OPEN SEMIOPEN SEMICLOSED CLOSED

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SLIDE 17
  • METHODS OF GENERAL ANESTHESIA

OPEN- old SEMIOPEN – used mostly in pediatric anesthesia SEMICLOSED- most common CLOSED- modern anesthesia

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SLIDE 18
  • Methods of general anesthesia

CIRCLE SYSTEM CIRCLE SYSTEM *HIGH HIGH-

  • FLOW

FLOW FRESH GAS FLOW  3 l/min. *LOW LOW-

  • FLOW

FLOW FGF ok. 1l/min. *MINIMAL MINIMAL-

  • FLOW

FLOW FGF ok. 0,5 l/min.

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SLIDE 19

Stages of general anesthesia

  • Introduction to anesthesia (induction)
  • Maintaining of anesthesia (conduction)
  • Recovery from anesthesia
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SLIDE 20

Anesthesia agents

1. Inhalation anesthetics (volatile anesthetics)

  • gases : N2O, xenon
  • Fluids (vaporisers)

2. Intravenous anesthetics

  • Barbiturans : thiopental
  • Others : propofol, etomidat

3. Pain killers

  • Opioids: fentanyl, sufentanil, alfentanil, remifentanil, morphine
  • Non Steroid Anti Inflamatory Drugs: ketonal, paracetamol

4. Relaxants

  • Depolarising : succinilcholine
  • Non depolarising : atracurium, cisatracurium, vecuronium, rocuronium

5. adiuvants

  • benzodiazepins: midasolam, diazepam
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SLIDE 21

Volatile vs intravenous anesthesia

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SLIDE 22

Mechanism of action of inhaled anesthetics

  • Reaction depends on concentration. This depends
  • n alveolar (first compartment), blood and brain

(central compartment) concentration , (third compartment- other tissue like muscles, fat- accumulation effect):

– Minute ventilation – Lung blood perfusion – Solubility in tissues

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SLIDE 23

MAC-minimal alveolar concentration

  • Concentration in which 50% of anesthetised

patients do not react on skin incision

  • Corelation with solubility in fat tissue
  • The lower MAC is the higher strenght of

action is

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SLIDE 24

Inhalation agents

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SLIDE 25

Division of inhalation agents

1. Gases:

  • N2O – old, weak, used as adiuvant
  • Xenon – lately introduced

2. Vapors (fluids):

  • Halothan
  • Enfluran
  • Isofluran
  • Sevofluran
  • Desfluran
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SLIDE 26

Features of ideal volatile anesthetic

  • Not disturbing smell
  • Fast acting, titrable
  • Low solubility in blood- fast transport to brain
  • Stable when stored, not reacting with other

chemicals

  • Non- flamable, non- explosive
  • Low methabolism in body, fast elimination, no

accumulative effect

  • No depressing effect on circulatory and respiratory

systems

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SLIDE 27

Nitrous oxide, laughing gas

  • Old
  • Weak
  • Used as adiuvant
  • Will be removed form medical use up to

2010- destroyes ozone lawyer

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SLIDE 28

Halothan

  • Used for many years with good effect
  • First non-flamable volatile fluid anesthetic
  • MAC high
  • Depression of circulatory system
  • May destroy liver
  • Now-a-days used only in pediatric

anesthesia

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SLIDE 29

Isofluran

  • Disturbing smell
  • May interact with heart contractivity
  • Increases relaxation of muscles
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SLIDE 30

Sevofluran

  • Not disturbing smell- may be used for VIMA
  • Low solubility in blood- fast acting
  • Does not disturbs airway
  • May depress circulatory system
  • Methabolised to Compound A- may be renal toxic

(but not confirmed in humans)

  • May be used in one-day surgery
  • Modern, and more and more widely used volatile

anesthetic

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SLIDE 31

Desfluran

  • Very disturbing smell- can not be used for

VIMA

  • Is not methabolised
  • Very fast acting
  • May be used for one-day surgery
  • Expensive, difficult to store (boiling temp.

about 20 C)

  • Modern and widelly used
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SLIDE 32

Intravenous anesthesia

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SLIDE 33

Target Controlled Infusion

TCI

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SLIDE 34
  • TCI is an infusion system which allows the

anaesthetist to select the target blood concentration required for a particular effect … … and then to control depth of anaesthesia by adjusting the requested target concentration

Defining TCI

When applied to anaesthesia

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SLIDE 35

What is TCI?

  • Instead of setting ml/h or a dose rate (mg/kg/h),

the pump can be programmed to target a required blood concentration.

  • Effect site concentration targeting is now

included for certain pharmacokinetic models.

  • The pump will automatically calculate how

much is needed as induction and maintenance to maintain that concentration.

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SLIDE 36

Intravenous anesthetics

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SLIDE 37

Thiopental

  • Old, one of the first used intravenous

anesthetics

  • Depressing effect on circulatory system
  • May be used in patients with ASA 1
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SLIDE 38

Ketamine

  • Only intravenous anesthetic which has good analgesia

effect

  • Does not depress circulatory nor respiratory function
  • Used in children, and in emergency and diseaster medicine
  • Gives night mare dreams in adult patients
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SLIDE 39

Etomidat

  • Has no depressing effect on circulatory

system- may be used in patients with circulatory insufficiency

  • May give musle contractions
  • Depressing effect on epirenals function
  • Can not be given in repeated bolus nor

continuous infusion

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SLIDE 40

Propofol

  • Very good anesthetic for induction and

maintaince of anesthesia with no accumulation effect

  • Titrable
  • May be used in short procedures – titrated

do not effect circulatory and respiratory system in important manner

  • Good for sedation, brain protecting effect
  • May be used in TCI
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SLIDE 41

Pain killers

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SLIDE 42

Opioids

  • fentanyl, alfentanil, sufentanil, remifentanil
  • May be used for induction and maintain of

anesthesia in repeated bolus or continuous infusion technique

  • Sedative effect
  • In high doses may be used alone for so called
  • pioid anesthesia- formerly used in

cardioanesthesia- very stable circulatory effect

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SLIDE 43

Compications of use

  • Respiratory depression !!!!
  • Muscle rigidity in high doses
  • Post-Operative Nausea and Vomitings
  • Accumulation effect after prolonged

administration (except for remifentanil)

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SLIDE 44

Remifentanil – modern opioid analgesic

  • T1/2 3-5 min !!
  • Methabolised by non-specific tissue

esterases- methabolism is not altered by renal or liver function

  • No accumulation effect after prolonged

infusion !!

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SLIDE 45

NSAID

  • Used as adiuvants in short, not very painful

procedures

  • Used for „preemptive analgesia” –

reduction of consumption of opioids by blocking COX

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SLIDE 46

Benzodiazepines

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SLIDE 47

Benzodiazepiny

  • Used in anesthesia:

– Diazepam – Midazolam

  • Used as adiuvants for premedication
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SLIDE 48

Muscle relaxants

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SLIDE 49

Division of relaxants depending

  • n mechanism of action

1.nondepolarising- combine with receptor for Ach like antagonists- they are fake mediators – do not cause muscle contractation but block access to receptors for Ach 2.depolarising- they combine with receptors for Ach and cause contractation of muscle but they stay connected with receptor blocking access to it for

  • Ach. They act like agonists.
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SLIDE 50

Nondepolarising agents

  • d-tubocurine – oldest deliverate of curarine
  • alcuronium
  • pancuronium – cheap and still used
  • pipercuronium
  • vercuronium
  • atracurium
  • cisatracurium
  • mivacurium
  • rocuronium
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SLIDE 51

Division of nondepolarising relaxants due to Chemical structure:

Miwakurium (Mivacron)

Cisatrakurium (Nimbex) Atrakurium (Trakurium)

Pankuronium (Pavulon) Pipekuronium (Arduan) Rapakuronium (Raplon) Rokuronium (Esmeron) Wekuronium (Norcuron)

Benzylizochinolons: Aminosteroids:

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SLIDE 52

Division of nondepolarising relaxants due to time of action:

  • Short acting < 3 min: still searching
  • Midle time <60 min: mivacurium,

atracurium, cisatracurium, rocuronium, vecuronium

  • Long acting > 60 min: pancuronium,

pipecuronium

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SLIDE 53

Atracurium

  • Elimination non-enzymatic, independent of

renal and liver function, Hoffman elimination- hydrolisis

  • Releases histamine
  • Acts about 30 min
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SLIDE 54

Cisatracurium

  • One of stereoisomers of atracurium,
  • Do not release histamine
  • Acts about 60 min
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SLIDE 55

Mivacurium

  • Releases histamine
  • Acts about 15-20 min – used for short

procedures

  • Methabolised by plasma esterases
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SLIDE 56

Rocuronium

  • Fast acting- time to 100% supresion 60 sec.
  • Do not release histamine
  • Acts about 60 min
  • Is methabolised in liver- disfunction of liver

may alter elimination

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SLIDE 57

Reverse of neuromuscular blockade

  • Neostigmine, piridostigmine- blockers of

acetylocholinesterase

  • Must be given toghether with atropine to

avoid bradycardia caused by activation of perisympatic system

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SLIDE 58

Depolarising agents

Only one: chlorsuccinilocholine

  • It is methabolised by pseudocholinesterase
  • Causes many complications, has many

contraindications

  • Indications:

Rapid sequence induction: full stomach, suspected difficult intubation because it acts very fast < 30 seconds and short < 3 min

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SLIDE 59

Monitoring during general anesthesia

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SLIDE 60

Obligatory

  • Clinical observation
  • Circulatory system function: ECG, blood

pressure - Non-Invasive-Blood Pressure

  • Respiratory function: SpO2 (pulsoxymetry),

EtCO2

  • Neuromuscular function- ie accelerometry

TOF Guard

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SLIDE 61

Additional- advanced

  • Invasive Blood Pressure
  • Haemodynamic monitoring ie Doppler

transesophageal probe

  • EEG monitoring for deepness of anesthesia

ie BIS (Bispectral Index), AEP - Auditory Evoced Potentials, Entropy

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SLIDE 62

Complications of general anesthesia

  • Respiratory: residual relaxants/opioids

action

  • Circulatory
  • Neurological: residual anesthetics/opioids

action

  • Post-Operative Nausea and Vomitings
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SLIDE 63

Mortality connected with anesthesia

  • 0,05

0,05 -

  • 4/10000 GA

4/10000 GA

  • 2

2 -

  • 16 %

16 % of

  • f surgical

surgical patients patients

  • 80 %

80 % is is caused caused by by human human mistake mistake

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SLIDE 64

Major causes of deaths

  • Airway

Airway obstruction

  • bstruction
  • Difficult

Difficult and and unefficient unefficient intubation intubation

  • Insufficient

Insufficient ventillation ventillation

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SLIDE 65

Other causes of mortality and morbidity

  • Anoxia

Anoxia

  • Haemodynamic

Haemodynamic instability instability

  • Aspiration

Aspiration

  • Toxity

Toxity of

  • f drugs

drugs – – mostly mostly inhalation inhalation agents agents

  • Anaphylaxia

Anaphylaxia and and drug drug interations interations

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SLIDE 66

Airway management and artificial ventillation

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SLIDE 67

AIRWAY MANAGEMENT AIRWAY MANAGEMENT

Respiratory Distress vs. Respiratory Failure Respiratory Distress vs. Respiratory Failure

Distress Distress

  • Increased work of breathing

Increased work of breathing

  • Relative

Relative hypoxia/ hypoxia/hypercapnea hypercapnea

  • Compensating

Compensating Failure Failure

  • Increased work of breathing

Increased work of breathing

  • Profound

Profound hypoxia/ hypoxia/hypercapnea hypercapnea

  • Decompensating

Decompensating

It’s a constant reassessment process…

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SLIDE 68

Contraindications for face mask and bag ventillation

  • Hernia hiatus aesophagus
  • gastric reflux
  • injury of face or neck
  • brochial-esophagaeal connection
  • injury of trachea cartiladges
  • full stomach patient, vomitings
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SLIDE 69

Indications for ET (endotracheal intubation)

  • Airway obstruction
  • Cardio Pulmonary Resuscitation
  • Artificial ventilation
  • Anesthesia
  • Brain injury, facial injury, facial burn,

airway burn

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SLIDE 70

Complications of ET

  • Injuries:
  • theeth injury, mouth injury
  • laryngs rupture
  • aspiration
  • bleeding
  • oesophagus intubation
  • one bronchus intubation
  • Reactions: vomitings, coughing, apnea,

laryngospasm, bradycardia, hypertension

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SLIDE 71

Alternative airway management

  • Laryngeal mask- for short, not major
  • perations ecxept for head and neck surgery
  • for elective surgery- patient must be

prepared for anesthesia