The autonomic nervous system and its implications in

dranugiri 9,508 views 78 slides Jan 18, 2015
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The Autonomic The Autonomic
Nervous System And Nervous System And
Its Implications In Its Implications In
AnaesthesiaAnaesthesia
Guided byGuided by : :
Dr. Bakshi Dr. Bakshi
MadamMadam
Presented by :Presented by :
Dr. Neha SoaresDr. Neha Soares
Dated : 26Dated : 26
thth
July 2007 July 2007

IntroductionIntroduction
Anatomy Anatomy
Physiology Physiology
Drugs acting on ANSDrugs acting on ANS
Tests for autonomic integrityTests for autonomic integrity
Anaesthesia and ANS Anaesthesia and ANS a) Generala) General
b) Regionalb) Regional
Autonomic reflexes during anaesthesia and Autonomic reflexes during anaesthesia and
surgerysurgery
ANS ANS dysfunctiondysfunction
Anaesthesia in patients with ANS dysfunctionAnaesthesia in patients with ANS dysfunction
ANS in intensive careANS in intensive care
ANS and chronic painANS and chronic pain

INTRODUCTIONINTRODUCTION
Anesthesiologists manipulate the physiology and Anesthesiologists manipulate the physiology and
pharmacology of the autonomic nervous system.pharmacology of the autonomic nervous system.

ANATOMYANATOMY
Comprises Comprises all afferent fibresall afferent fibres from the CNS from the CNS
except those supplying skeletal muscles.except those supplying skeletal muscles.
Includes :Includes :
1) 1) sympatheticsympathetic nervous system nervous system
2) 2) parasympatheticparasympathetic nervous system nervous system
3) 3) entericenteric nervous system nervous system

Sympathetic Nervous SystemSympathetic Nervous System
Originates from the Originates from the Thoraco-lumbarThoraco-lumbar spinal spinal
cord (T1 to L2/L3)cord (T1 to L2/L3)
Composed of 2 neurons:Composed of 2 neurons:
a) a) prepre-ganglionic-ganglionic
b) b) postpost-ganglionic-ganglionic

PairedPaired sympathetic chains having sympathetic chains having 22 paired ganglia22 paired ganglia

Unpaired Unpaired prevertebral ganglia in the abdomen and prevertebral ganglia in the abdomen and
pelvispelvis
Celiac Celiac
Superior mesenteric Superior mesenteric
Inferior mesentericInferior mesenteric
Aortico renalAortico renal

terminal/collateral gangliaterminal/collateral ganglia

Terminal or collateral gangliaTerminal or collateral ganglia
Small and few in numberSmall and few in number
Present Present near targetnear target organ organ
Eg. Nerves supplying adrenal medulla Eg. Nerves supplying adrenal medulla
and other chromaffin tissueand other chromaffin tissue
Comprise Comprise preganglionicpreganglionic fibres itself that fibres itself that
pass to target tissue without synapsingpass to target tissue without synapsing

PARASYMPATHETIC NERVOUS PARASYMPATHETIC NERVOUS
SYSTEMSYSTEM
75% from 75% from vagusvagus
Arises from Arises from III, VII, IX, X cranialIII, VII, IX, X cranial nerves, nerves,
S2-3S2-3 and occasionally S1and4 and occasionally S1and4
Occur proximal to or within the innervated Occur proximal to or within the innervated
organorgan
Hence, Hence, pre-ganglionic fibres very longpre-ganglionic fibres very long
PNS more targetedPNS more targeted

Preganglionic fibres Preganglionic fibres
arise fromarise from
CENTRALCENTRAL
Edinger WestpalEdinger Westpal nucleus – nucleus –
# oculomotor nerve# oculomotor nerve
#synapses in ciliary ganglia#synapses in ciliary ganglia
#Innervates smooth muscles #Innervates smooth muscles
of iris and ciliary musclesof iris and ciliary muscles
Medulla OblongataMedulla Oblongata – –
#Facial nerve #Facial nerve
#Glossopharyngeal nerve #Glossopharyngeal nerve
#Vagus nerve #Vagus nerve
PERIPHERALPERIPHERAL
Sacral segments/ Pelvic nervesSacral segments/ Pelvic nerves

ENTERIC NERVOUS SYSTEMENTERIC NERVOUS SYSTEM
Found Found within the wallswithin the walls
of the GIT, pancreas of the GIT, pancreas
and gall-bladderand gall-bladder
High degree of High degree of
autonomyautonomy
Peristalsis and Peristalsis and
digestion persists even digestion persists even
if sphincter function if sphincter function
impaired following impaired following
SAB/transections.SAB/transections.
Submucous(Submucous(Meissner’s Meissner’s
plexus)plexus)
Myenteric(Myenteric(Auerbach’s Auerbach’s
plexus) plexus)

PHYSIOLOGYPHYSIOLOGY
Either Either sympathetic or parasympathetic systemsympathetic or parasympathetic system
dominatesdominates a particular organ function, hence a particular organ function, hence
providing the resting toneproviding the resting tone
Few organs have only sympathetic innervation – Few organs have only sympathetic innervation –
blood vessels, spleen, piloerector muscles, blood vessels, spleen, piloerector muscles,
adrenal medulla, uterusadrenal medulla, uterus
Some organs have only parasympathetic Some organs have only parasympathetic
innervation – stomach, pancreasinnervation – stomach, pancreas
Sympathetic deals with FIGHT OR FLIGHTSympathetic deals with FIGHT OR FLIGHT
Parasympathetic deals with discrete adjustments Parasympathetic deals with discrete adjustments
in relaxed homeostasisin relaxed homeostasis

Target organTarget organSNSSNS ReceptorReceptorPNSPNS
1.1.Hair follicle Hair follicle
smooth musclesmooth muscle
2.2.Iris –radial msIris –radial ms
3.3.Iris- circular msIris- circular ms
4.4.Ciliary msCiliary ms
5.5.Glands – nasal Glands – nasal
parotid,lacrimalparotid,lacrimal
submandibularsubmandibular
gastric,pancraeticgastric,pancraetic
ContractionContraction
PiloerectionPiloerection
MydriasisMydriasis
None None
Slight Slight
MydriasisMydriasis
Slight Slight
increaseincrease
Alpha1Alpha1
Alpha 1Alpha 1
Beta Beta
Alpha 1Alpha 1
NoneNone
None None
Miosis Miosis
Accomoda-Accomoda-
tiontion
CopiousCopious
IncreaseIncrease
Action of SNS and PNS on various organsAction of SNS and PNS on various organs

Target organTarget organSNSSNS ReceptorReceptorPNSPNS
6. Sweat gland6. Sweat gland
7. Apocrine gland7. Apocrine gland
8. Heart 8. Heart
-Rate-Rate
-Force of contractn-Force of contractn
-Coronaries -Coronaries
CopiousCopious
IncreaseIncrease
Thick Thick
odoriferousodoriferous
Increase Increase
Increase Increase
DilatedDilated
Constricted Constricted
Alpha 1Alpha 1
Beta 1 Beta 1
Beta 1Beta 1
Beta 2Beta 2
Alpha Alpha
Sweating of Sweating of
PalmsPalms
NoneNone
DecreaseDecrease
Decrease Decrease
xcept atriaxcept atria

Target organTarget organSNSSNS ReceptorReceptorPNSPNS
9. Lungs 9. Lungs
-Bronchi -Bronchi
-Blood vessels-Blood vessels
10. Gut lumen10. Gut lumen
Sphincter Sphincter
11.Pancreas 11.Pancreas
12.Liver 12.Liver
13.Gall bladder13.Gall bladder
14.Kidney 14.Kidney
Dilation Dilation
Constricted Constricted
Decreased Decreased
Increased Increased
Decreased Decreased
Glucose Glucose
releasedreleased
Relaxed Relaxed
Output and Output and
renin lessrenin less
Beta 2 Beta 2
Alpha2Alpha2
Alpha2Alpha2
Alpha2 Alpha2
Alpha1Alpha1
Beta1 Beta1
ConstrictnConstrictn
DilationDilation
IncreasedIncreased
peristalsisperistalsis
RelaxedRelaxed

Target organTarget organSNSSNS ReceptorReceptorPNSPNS
15.Bladder 15.Bladder
- Detrusor- Detrusor
-TrigoneTrigone
16. Ureter16. Ureter
17. uterus, vas 17. uterus, vas
deferens,deferens,
prostrateprostrate
18.Arterioles 18.Arterioles
-viscera,skin-viscera,skin
-muscle-muscle
RelaxedRelaxed
ContractedContracted
ContractedContracted
ContractedContracted
ConstrictedConstricted
ConstrictedConstricted
DilatedDilated
BetaBeta
Alpha1Alpha1
Alpha1Alpha1
Alpha1Alpha1
AlphaAlpha
beta2beta2

Target organTarget organSNSSNS ReceptorReceptorPNSPNS
19.Veins 19.Veins
20.Blood20.Blood
21.Basal metab21.Basal metab
22.Adrenal medulla22.Adrenal medulla
secretionsecretion
23. Mental activity23. Mental activity
24.Fat cell24.Fat cell
ConstrictedConstricted
Coag,lipid, Coag,lipid,
glucose ^glucose ^
100% rise100% rise
IncreasedIncreased
IncreasedIncreased
LipolysisLipolysis
Alpha2Alpha2

Dominance at specific siteDominance at specific site
Parasympathetic :Parasympathetic :
Ciliary muscleCiliary muscle
IrisIris
Salivary glandsSalivary glands
SA nodeSA node
GITGIT
UterusUterus
Urinary bladderUrinary bladder
Sympathetic :Sympathetic :
Arterioles Arterioles
Veins Veins
Sweat glandsSweat glands
Spleen Spleen

ANS of HeartANS of Heart

NeurotransmittersNeurotransmitters
Acetylcholine Acetylcholine – Secreted by – Secreted by
**all preganglionic fibresall preganglionic fibres
*Postganglionic parasympathetic *Postganglionic parasympathetic
fibres\postganglionic sympathetic fibres fibres\postganglionic sympathetic fibres
of sweat gland,piloerctor muscle and of sweat gland,piloerctor muscle and
blood vesselsblood vessels
Norepinephrine Norepinephrine – Secreted by all – Secreted by all
postganglionic sympatheticpostganglionic sympathetic fibres fibres

Acetylcholine receptors are of 2 types:Acetylcholine receptors are of 2 types:
- - MuscarinicMuscarinic: action similar to that : action similar to that
produced by produced by parasympatheticparasympathetic system system
- - NicotinicNicotinic: action on : action on skeletal andskeletal and
ganglionicganglionic synapses only synapses only
Adrenergic receptors are of 2 tyes:Adrenergic receptors are of 2 tyes:
- - AlphaAlpha: alpha1(smooth muscle : alpha1(smooth muscle
vasoconstriction)vasoconstriction)
alpha2 (presynapses)alpha2 (presynapses)
- - BetaBeta: beta1 (cardiac tissue): beta1 (cardiac tissue)
beta2 (smooth muscle relaxation in beta2 (smooth muscle relaxation in
some some organs)organs)

Action of Important Drugs on ANSAction of Important Drugs on ANS
Site of actionSite of action
1.Sympathetic 1.Sympathetic
and and
parasympatheticparasympathetic
gangliaganglia
2.Endings of post2.Endings of post
ganglionic nonganglionic non
adrenergicadrenergic
NeuronsNeurons
Agonist Agonist
1.Stimulate post-1.Stimulate post-
ganglionganglion- nicotin- nicotin
2.2.InhibitACh’trsInhibitACh’trse-e-
PhysostigminePhysostigmine
NeostigmineNeostigmine
Parathion Parathion
Release NARelease NA
-TyramineTyramine
-EphedrineEphedrine
-Amphetamine Amphetamine
Antagonist Antagonist
HexamethoniumHexamethonium
MecamylamineMecamylamine
TrimethaphanTrimethaphan
High conc.Ach,High conc.Ach,
AnticholinestrsesAnticholinestrses
Curare Curare
Block NA synthBlock NA synth
-metyrosine-metyrosine
Stop NA storageStop NA storage
-reserpine,guane-reserpine,guane
thidinethidine

Site of actionSite of action
3.Alpha receptors3.Alpha receptors
Agonist Agonist
Stimulate alpha1Stimulate alpha1
-methoxamine-methoxamine
-phenylephrine-phenylephrine
Stimulate alpha2Stimulate alpha2
-clonidine-clonidine
Antagonist Antagonist
Stop NA Stop NA
breakdownbreakdown
-MA inhibitors-MA inhibitors
False False
transmitterstransmitters
-methydopa-methydopa
-phenoxybenza-phenoxybenza
minemine
-phentolamine-phentolamine
-prazocin-alpha1-prazocin-alpha1
-yohimbin-alpha2-yohimbin-alpha2

Site of actionSite of action
4.Beta receptors4.Beta receptors
5.Domaninergic5.Domaninergic
receptorsreceptors
Agonist Agonist
-isoproterenol-isoproterenol
-dobutamine-dobutamine
-salbutamol-salbutamol
(beta2)(beta2)
DA1 – dopamineDA1 – dopamine
DA2 DA2
-bromocriptine-bromocriptine
Antagonist Antagonist
-propanolol-propanolol
-metoprolol-metoprolol
-esmolol-esmolol
-Butoxamine-Butoxamine
(beta2)(beta2)
DA1 – DA1 –
metoclopramidemetoclopramide
DA2-haloperidolDA2-haloperidol

TESTS FOR AUTONOMIC TESTS FOR AUTONOMIC
INTEGRITYINTEGRITY
Autonomic functions can be evaluated by:Autonomic functions can be evaluated by:
HistoryHistory
Non-invasive testsNon-invasive tests
Invasive testsInvasive tests

History History
CVSCVS (postural/orthostatic hypotension) (postural/orthostatic hypotension)
Fainting episodesFainting episodes
DizzinessDizziness
HeadacheHeadache
Diminution of visionDiminution of vision
Genitourinary Genitourinary
ImpotencyImpotency
Incontinence of urineIncontinence of urine
Retention of urineRetention of urine
Frequency in urinationFrequency in urination
GlandsGlands
Decreased salivation with difficulty in eatingDecreased salivation with difficulty in eating
Decreased lacrimation causing eye irritationDecreased lacrimation causing eye irritation
Impaired sweating causing temperature elevationImpaired sweating causing temperature elevation

CNS CNS (affection of fibres supplying iris)(affection of fibres supplying iris)
Night-blindnessNight-blindness
Chronic diseasesChronic diseases
Diabetes mellitusDiabetes mellitus
Chronic renal failureChronic renal failure
HypertensionHypertension
Family historyFamily history
Personal historyPersonal history
Chronic alcoholismChronic alcoholism
Drugs like Antihypertensive antidepressants, Drugs like Antihypertensive antidepressants,
tranquilizers , diureticstranquilizers , diuretics

Non – invasive testsNon – invasive tests
Tests for cardiac vagal functionTests for cardiac vagal function
Respiratory sinus arrhythmiaRespiratory sinus arrhythmia
Vasalva ratio(Phase IV/II)Vasalva ratio(Phase IV/II)
Bradycardia during Bradycardia during
phenylephrine challengephenylephrine challenge
Absence of tachycardia with Absence of tachycardia with
atropineatropine
Tests for sympathetic functionTests for sympathetic function
I) CARDIACI) CARDIAC
Tachycardia during standing or Tachycardia during standing or
head-up tilthead-up tilt
Tachycardia during vasalva Tachycardia during vasalva
strain(PhaseII)strain(PhaseII)
II) PERIPHERALII) PERIPHERAL
Blood pressure overshoot Blood pressure overshoot
after vasalva releaseafter vasalva release
BP increase with cold BP increase with cold
pressure testpressure test
Diastolic BP rise with Diastolic BP rise with
isometric handgripisometric handgrip
Systolic and diastolic BP Systolic and diastolic BP
response to upright response to upright
positionposition

Respiratory sinus arrhythmiaRespiratory sinus arrhythmia
Tests Tests parasympathetic parasympathetic functionfunction
Determines the max. to min. heart rate variation in Determines the max. to min. heart rate variation in
forceful breathingforceful breathing
Patient in sitting or lying down positionPatient in sitting or lying down position
6 breaths/min.(5secs inspiration,5secs expiration)6 breaths/min.(5secs inspiration,5secs expiration)
Record mx. and min. HR and RR intervalRecord mx. and min. HR and RR interval
Av. variation should be >10 beats/minAv. variation should be >10 beats/min
E : I ratio = longest RR interval in expiration/shortest RR E : I ratio = longest RR interval in expiration/shortest RR
interval in inspirationinterval in inspiration
In <40yrs age, In <40yrs age, E:I<1.2 is abnormalE:I<1.2 is abnormal

Postural stress: Supine to standingPostural stress: Supine to standing
Tests the Tests the sympatheticsympathetic function function
Commonly performed bed-side testCommonly performed bed-side test
Note HR and BP in supine position after Note HR and BP in supine position after
10mins rest10mins rest
Note changes in HR and BP after assuming Note changes in HR and BP after assuming
standing posture unaided after 50 secsstanding posture unaided after 50 secs
Drop of systolic BP >20mm of Hg and/or Drop of systolic BP >20mm of Hg and/or
diastolic BP >10 mm of Hg is abnormaldiastolic BP >10 mm of Hg is abnormal
Absence of tachycardia when standing is Absence of tachycardia when standing is
abnormal (Marrey’s Law of baro receptor abnormal (Marrey’s Law of baro receptor
stimulation)stimulation)

Cold Pressure testCold Pressure test
Tests the Tests the peripheral sympatheticperipheral sympathetic
vasoconstrictorsvasoconstrictors
Record BP 1min after immersing hand in Record BP 1min after immersing hand in
ice cold waterice cold water
Both systolic and diastolic BP should Both systolic and diastolic BP should
increase by 10mm of Hgincrease by 10mm of Hg

Isometric Hand grip ExerciseIsometric Hand grip Exercise
Tests the Tests the efferent sympatheticefferent sympathetic function function
Sustained isometric contraction at 30% of Sustained isometric contraction at 30% of
patients max. strength should increase BP by patients max. strength should increase BP by
10-15mm of Hg10-15mm of Hg

Vasalva ManouverVasalva Manouver
Tests both Tests both sympathetic and parasympatheticsympathetic and parasympathetic function function
Subject sits quietly or lies supine, blows into a mouth-Subject sits quietly or lies supine, blows into a mouth-
piece with an open glottis, holds airway pressure of piece with an open glottis, holds airway pressure of
40mm of Hg for 15secs(PhaseII40mm of Hg for 15secs(PhaseII) and then releases the ) and then releases the
pressurepressure

HR increasesHR increases 10to15secs after initiating blowing(PhaseII) and 10to15secs after initiating blowing(PhaseII) and
before release of pressurebefore release of pressure
This implies that the This implies that the sympathetic response is intactsympathetic response is intact
On release of strain(PhaseIV), preload and cardiac output On release of strain(PhaseIV), preload and cardiac output
restored, restored, BP overshootBP overshoot….this implies that the peripheral ….this implies that the peripheral
sympathetic vasoconstriction is intactsympathetic vasoconstriction is intact
Baroreceptors stimulated, reflex Baroreceptors stimulated, reflex bradycardiabradycardia…this implies that the …this implies that the
parasympathetic system is intactparasympathetic system is intact

To test cardiac vagal function a ratio has been devisedTo test cardiac vagal function a ratio has been devised
Vasalva ratio = longest RR interval[max HR] in Phase IV(x)/Vasalva ratio = longest RR interval[max HR] in Phase IV(x)/
shortest RR interval[min HR] in Phase II(y)shortest RR interval[min HR] in Phase II(y)
Vasalva ratio <1.2 is abnormalVasalva ratio <1.2 is abnormal

EPINEPHRINE TESTEPINEPHRINE TEST – –
3 drops in eye at I min. interval 3 times3 drops in eye at I min. interval 3 times
Check pupil sixe at 15, 30 and 45 minsCheck pupil sixe at 15, 30 and 45 mins
Normal pupil = no effectNormal pupil = no effect
Sympathetically denervated pupil = dilationSympathetically denervated pupil = dilation
COCAINE TESTCOCAINE TEST – –
Method same as aboveMethod same as above
Normal pupil = dilationNormal pupil = dilation
Sympathetic denervated pupil = no change in sizeSympathetic denervated pupil = no change in size
HISTAMINE TESTHISTAMINE TEST – –
0.05ml of 1:1000 histamine injected intracutaneously0.05ml of 1:1000 histamine injected intracutaneously
Normal response – triple response with 1cm whealNormal response – triple response with 1cm wheal
Familial dysautonomia and peripheral neuropathy – Familial dysautonomia and peripheral neuropathy –
absent whealabsent wheal

EPHEDRINE TESTEPHEDRINE TEST – –
Give 25mg imGive 25mg im
Normal subjects = HR increasesNormal subjects = HR increases
Sympathetic denervation = no change in HRSympathetic denervation = no change in HR
ATROPINE TESTATROPINE TEST – –
Give 0.8mg imGive 0.8mg im
Normal subjects = HR increases by 20 Normal subjects = HR increases by 20
beats/minbeats/min
Sympathetic denervation = no changeSympathetic denervation = no change
NEOSTIGMINE TESTNEOSTIGMINE TEST – –
Give 1mg imGive 1mg im
Normal subjects = HR decreasesNormal subjects = HR decreases
Parasympathetically denervated = no changeParasympathetically denervated = no change

Power Spectral Analysis of HR Power Spectral Analysis of HR
variabilityvariability
Slower periodic oscillations in heart, can be decomposed Slower periodic oscillations in heart, can be decomposed
into a series of sine waves with diff. amplitudes and into a series of sine waves with diff. amplitudes and
frequenciesfrequencies

This frequency domain reveals a This frequency domain reveals a consistant peakconsistant peak/ power at the breathing / power at the breathing
frequency frequency 0.2 to 0.3Hz0.2 to 0.3Hz… this implies … this implies intact parasympatheticintact parasympathetic innervaton of innervaton of
SA nodeSA node
There is another peak at low frequencies There is another peak at low frequencies 0.05 to 0.150.05 to 0.15 Hz…due to changing Hz…due to changing
cardiac cardiac sympatheticsympathetic activity activity
This low frequency component is augmented by increased sympathetic This low frequency component is augmented by increased sympathetic
drive eg.head up tilt, mental arithmatics and is reduced in quadriplegics due drive eg.head up tilt, mental arithmatics and is reduced in quadriplegics due
to interrupted sympathetic pathways.to interrupted sympathetic pathways.

INVASIVE TESTSINVASIVE TESTS
Done to locate Done to locate precise siteprecise site of pathology of pathology
Done for Done for researchresearch purpose purpose
Intraneural recordingIntraneural recording of post-ganglionic of post-ganglionic
sympathetic activitysympathetic activity
Eliciting Eliciting axon reflexaxon reflex by intradermal injection of by intradermal injection of
acetyl-cholineacetyl-choline
Response of ANS to infusion of Response of ANS to infusion of pressor drugspressor drugs : :
injection or epinephrine(1 : 1000) in conjunctival sacinjection or epinephrine(1 : 1000) in conjunctival sac
Cocaine (4 to 10%) topical applicationCocaine (4 to 10%) topical application
Ephedrine testEphedrine test
Atropine testAtropine test
Neostigmine testNeostigmine test

OTHER TESTSOTHER TESTS
Measurement of skin Measurement of skin temperaturetemperature
Tests for Tests for sudomotorsudomotor function function
Weight of sweatWeight of sweat
Galvanic skin resistance testGalvanic skin resistance test
Tests for Tests for lacrimal lacrimal functionfunction
Tests for Tests for bladder and GITbladder and GIT dysfunction dysfunction
LaboratoryLaboratory tests tests
Measure plasma levels of catecholamines and other vasoactive Measure plasma levels of catecholamines and other vasoactive
hormones like renin, angiotensin and vasopressinhormones like renin, angiotensin and vasopressin
Measurement of forearm blood flow with plethysmographyMeasurement of forearm blood flow with plethysmography
Cerebral EEG blood flow studiesCerebral EEG blood flow studies
SELECTION OF TESTSSELECTION OF TESTS : :
To assess ANS involvement, 5 simple non-invasive tests are To assess ANS involvement, 5 simple non-invasive tests are
sufficientsufficient
To assess definitive abnormality, 2 or more specific tests are To assess definitive abnormality, 2 or more specific tests are
recommendedrecommended

ANAESTHESIA AND AUTONOMIC ANAESTHESIA AND AUTONOMIC
NERVOUS SYSTEMNERVOUS SYSTEM
GENERAL ANAESTHESIAGENERAL ANAESTHESIA
Pre medicationPre medication : :
Agents used to decrease secretions like Agents used to decrease secretions like
atropine,glycopyrolate are atropine,glycopyrolate are anti cholinergicsanti cholinergics
Antiemetic metoclopramide is a Antiemetic metoclopramide is a dopaminergicdopaminergic
anti emeticanti emetic
Opiods cause respiratory depression by Opiods cause respiratory depression by
inhibiting Ach release from CNSinhibiting Ach release from CNS
Morphine releases histamine, venous pooling, Morphine releases histamine, venous pooling,
reduced peripheral vascular resistancereduced peripheral vascular resistance

Pentazocine increases plasma catecholaminesPentazocine increases plasma catecholamines
Fentanyl causes vagal bradycardia during intubationFentanyl causes vagal bradycardia during intubation
Beta antagonistsBeta antagonists reduce stress response during intubation reduce stress response during intubation
Alpha2 agonist, Alpha2 agonist, clonidine,clonidine, reduces dose of induction agent and reduces dose of induction agent and
stress response duringstress response during
Induction agents –
All induction agents except ketamine reduce sympathetic
activity
Arterial pressure drops
Baroreceptor mediated tachycardia may/may not occur
Ketamine stimulates the sympathetic system
Etomidate is a potent inhibitor of adrenergic
steroidogenesis

Inhalational AgentsInhalational Agents – –
Halothane, enflurane, isoflurane reduce pre-ganglionic Halothane, enflurane, isoflurane reduce pre-ganglionic
sympathetic activity and hence decrease plasma sympathetic activity and hence decrease plasma
catecholaminescatecholamines
Cyclopropane and diethyl ether increase sympathetic Cyclopropane and diethyl ether increase sympathetic
activity by central action and by action on vasomotor activity by central action and by action on vasomotor
neurons in spinal cordneurons in spinal cord
Muscle RelaxantsMuscle Relaxants – –
Pancuronium releases adrenaline and raises HR and BPPancuronium releases adrenaline and raises HR and BP
Autonomic changes like decreasing Autonomic changes like decreasing
arterial BP,HR and plasma arterial BP,HR and plasma
catecholamines and cortisol indicate catecholamines and cortisol indicate
increasing depth of anaesthesiaincreasing depth of anaesthesia

SPINAL ANAESTHESIASPINAL ANAESTHESIA
Causes sympathetic blockade, hypotension and Causes sympathetic blockade, hypotension and
bradycardia depending on the level of blockadebradycardia depending on the level of blockade

• In low SAB sacral parasympathetic and lumbar plus In low SAB sacral parasympathetic and lumbar plus
lower thoracic sympathetics are blocked, lower thoracic sympathetics are blocked, uninhibited vagal uninhibited vagal
parasympathetics acting on splanchnic bed and visceraparasympathetics acting on splanchnic bed and viscera
In high SAB, In high SAB, all sympathetics are blockedall sympathetics are blocked, vagal , vagal
parasympathetics to thoracic and abdominal viscera parasympathetics to thoracic and abdominal viscera
become over active and cause severe bradycardia and become over active and cause severe bradycardia and
even asystoleeven asystole
In In saddle blocksaddle block sacral parasympathetic is blocked, sacral parasympathetic is blocked,
thoracolumbar sympathetic is intact…causing minimal thoracolumbar sympathetic is intact…causing minimal
physiologic disturbancephysiologic disturbance

Features of Autonomic Imbalance after Features of Autonomic Imbalance after
Spinal AnaesthesiaSpinal Anaesthesia
CVSCVS
HypotensionHypotension
BradycardiaBradycardia
GITGIT
Increased peristalsisIncreased peristalsis
Intestines usually activeIntestines usually active
RSRS
In high SAB(upper 5 or 6 thoracic sympathetic)In high SAB(upper 5 or 6 thoracic sympathetic)
Some bronchial spasm due to increased vagal activitySome bronchial spasm due to increased vagal activity
EPIDURAL ANAESTHESIAEPIDURAL ANAESTHESIA
Less hypotensionLess hypotension
SegmentalSegmental type of anaesthesia is possible type of anaesthesia is possible
Onset of action is slowerOnset of action is slower
Hence compensatory mechanisms initiated well in advanceHence compensatory mechanisms initiated well in advance

Autonomic reflexes during Autonomic reflexes during
Anaesthesia and SurgeryAnaesthesia and Surgery
Oculocardiac reflexOculocardiac reflex : :
Pressure over eyeballs or traction of external Pressure over eyeballs or traction of external
ocular musclesocular muscles
Causes bradycardia, asystole, cardiac Causes bradycardia, asystole, cardiac
dysrhytthmia, ventricular fibrillationdysrhytthmia, ventricular fibrillation
Light plane on anaesthesia, hypoxia, Light plane on anaesthesia, hypoxia,
hypercarbia aggravate this reflexhypercarbia aggravate this reflex
Prophylaxis with anticholinergics..still a Prophylaxis with anticholinergics..still a
controversycontroversy

Abdominal reflexAbdominal reflex : :
Due to stimulation of ANS by traction or Due to stimulation of ANS by traction or
pressure during surgeries within the abdominal pressure during surgeries within the abdominal
cavitycavity
Circulatory effect – bradycardia, hypotentionCirculatory effect – bradycardia, hypotention
Respiratory effect – apnea, tachypnea, Respiratory effect – apnea, tachypnea,
laryngospasmlaryngospasm
These are :These are :
•Peritoneal and mesentericPeritoneal and mesenteric reflex reflex
•Coeliac plexusCoeliac plexus reflex – traction of stomach,gall reflex – traction of stomach,gall
bladder, hilum of liver or retraction of duodenumbladder, hilum of liver or retraction of duodenum
•Brewer LuckhardtBrewer Luckhardt reflex/ Diaphragmatic traction reflex/ Diaphragmatic traction
reflex reflex
•Reflexes associated with pelvic nerveReflexes associated with pelvic nerve

Recto – laryngeal reflexRecto – laryngeal reflex : :
Caused by dilation of anal sphincter under GACaused by dilation of anal sphincter under GA
Afferent is via pelvic and sacral nerve to Afferent is via pelvic and sacral nerve to vagalvagal motor motor
nucleusnucleus
Efferent is via Efferent is via recurrent laryngealrecurrent laryngeal nerve nerve
Causes laryngeal spasm and apneaCauses laryngeal spasm and apnea
Recto – cardiac reflexRecto – cardiac reflex : :
Anal sphincter dilation causes bradycardia, hypotensionAnal sphincter dilation causes bradycardia, hypotension
Preventions :Preventions :
These autonomic reflexes can be prevented by adequate These autonomic reflexes can be prevented by adequate
depth of anaesthesiadepth of anaesthesia
Atropine prophylaxis maybe givenAtropine prophylaxis maybe given
Ask surgeon to avoid manipulations, proceed gently and Ask surgeon to avoid manipulations, proceed gently and
slowlyslowly

ANS DYSFUNCTIONANS DYSFUNCTION
PRIMARY –PRIMARY –
Idiopathic orthostatic hypotensionIdiopathic orthostatic hypotension
Shy Dragger syndromeShy Dragger syndrome
FAMILIAL –
Riley Day syndrome
Leesch Neehan syndrome
•Genetic disorder of purine metabolism in
males
•Sympathetic response to stress is
enhanced
Gill Familia dysautonomia

SECONDARY TO SYSTEMIC SECONDARY TO SYSTEMIC
DISORDERSDISORDERS
AgeingAgeing
Diabetes MellitusDiabetes Mellitus
Chronic alcoholismChronic alcoholism
Chronic renal failureChronic renal failure
Neurological diseasesNeurological diseases
Tabes dorsalisTabes dorsalis
SyringomyeliaSyringomyelia
amyloidosisamyloidosis
Chagas diseaseChagas disease
Hypertension Hypertension
TetanusTetanus
PheochromocytomaPheochromocytoma
Spinal cord injurySpinal cord injury
Guillian Barre Guillian Barre
syndromesyndrome
Carcinomatosis Carcinomatosis

AGINGAGING
20% of people over 65yrs have 20% of people over 65yrs have postural hypotensionpostural hypotension
Symptoms – dizziness, faintness, loss of consciousnessSymptoms – dizziness, faintness, loss of consciousness
Selective/ Selective/ early parasympatheticearly parasympathetic involvement involvement
Delayed/ slow sympathetic involvementDelayed/ slow sympathetic involvement
Blunting of – Vasalva maneuverBlunting of – Vasalva maneuver
Respiratory cycleRespiratory cycle
HR changes to changes in BPHR changes to changes in BP
Resting and exercise induced NE responseResting and exercise induced NE response

ALCOHOLISMALCOHOLISM
Acute, chronic or alcohol withdrawal causes orthostatic Acute, chronic or alcohol withdrawal causes orthostatic
intoleranceintolerance
Poor nutrition impairs SNSPoor nutrition impairs SNS
Baroreceptors less sensitiveBaroreceptors less sensitive
Vasalva ratio and cardiac acceleration following iv Vasalva ratio and cardiac acceleration following iv
atropine is diminished in presence of neurological atropine is diminished in presence of neurological
impairmentimpairment

TETANUSTETANUS
Sympatho adrenal Sympatho adrenal
hyperactivity is the hyperactivity is the
chief cause of deathchief cause of death
Direct effect of Direct effect of
tetanus toxin on SNS tetanus toxin on SNS
causes rise in plasma causes rise in plasma
catecholaminescatecholamines

PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA
Catecholamine secreting tumourCatecholamine secreting tumour
Hypertension, hypermetabolism, hyperglycemiaHypertension, hypermetabolism, hyperglycemia
Preop alpha blockers are given toPreop alpha blockers are given to
Restore blood volumeRestore blood volume
Assess end organ damageAssess end organ damage
Treat cardiac arrhythmiasTreat cardiac arrhythmias

GUILLIAN BARRE GUILLIAN BARRE
SYNDROMESYNDROME
•ANS involvement ANS involvement
secondary to secondary to axonal axonal
degenerationdegeneration
•Variable BP, facial Variable BP, facial
flushing, urinary flushing, urinary
retention, tachy – retention, tachy –
brady arrhythmiasbrady arrhythmias
•Neuropathic lesions in Neuropathic lesions in
afferent limb of afferent limb of
baroreceptor may lead baroreceptor may lead
to to SIADH, SIADH,
hyponatremiahyponatremia

Neuronal degenerationNeuronal degeneration
Metabolically related neuronal Metabolically related neuronal
dysfunctiondysfunction
Afferent, central and efferent Afferent, central and efferent
pathways involvedpathways involved
Vagal neuropathyVagal neuropathy occurs before occurs before
systemic neuropathysystemic neuropathy
Symptomatic postural Symptomatic postural
hypotension implies poor hypotension implies poor
prognosisprognosis
Esophageal gastric hypomotility, Esophageal gastric hypomotility,
bradycardia, silent myocardial bradycardia, silent myocardial
infarcts, impaired ventilatory infarcts, impaired ventilatory
control, unexplained cardio control, unexplained cardio
respiratory arrests may occurrespiratory arrests may occur

AUTONOMIC CHANGES IN SPINAL AUTONOMIC CHANGES IN SPINAL
CORD TRANSECTIONCORD TRANSECTION
Affects motor, sensory and ANS depending on level of transectionAffects motor, sensory and ANS depending on level of transection
Acute effects/ Acute effects/ Spinal ShockSpinal Shock : :
Flaccid paralysisFlaccid paralysis
Total absence of sensationTotal absence of sensation
Loss of temperature regulationLoss of temperature regulation
Loss of spinal reflexes below level of injuryLoss of spinal reflexes below level of injury
Decreased systolic BPDecreased systolic BP
BradycardiaBradycardia
Abnormal ECG, ST-T changes, VPCsAbnormal ECG, ST-T changes, VPCs

Management of Anaesthesia :Management of Anaesthesia :
•AirwayAirway management management
•Avoidance of Avoidance of hypovolemiahypovolemia
Anaesthesia is given so that pt. tolerates Anaesthesia is given so that pt. tolerates
tubetube
Muscle relaxant is used as neededMuscle relaxant is used as needed

ANAESTHESIA IN PATIENTS WITH ANS ANAESTHESIA IN PATIENTS WITH ANS
DYSFUNCTIONDYSFUNCTION
UnderstandUnderstand the impact the impact
Reduced ANS activity on CVS Reduced ANS activity on CVS
responses to change inresponses to change in
obody positionbody position
opositive airway pressure positive airway pressure
oacute blood loss acute blood loss
oeffects due to negative effects due to negative
inotropic anaesthetic agentsinotropic anaesthetic agents
Posture Posture – shift patient to OT – shift patient to OT
and induce in supine positionand induce in supine position
Preloading Preloading should be done should be done
properlyproperly
Pre medicationPre medication – –
Atropine may fail to produce Atropine may fail to produce
tachycardiatachycardia
Ranitidine and metoclopramideRanitidine and metoclopramide
to avoid regurg and aspirationto avoid regurg and aspiration
Narcotics and other respiratory Narcotics and other respiratory
depressants are avoideddepressants are avoided
MonitoringMonitoring – –
Pulse oxPulse ox
Continuous arterial BPContinuous arterial BP
ECGECG
CVPCVP
TemperatureTemperature
Urine outputUrine output

GENERAL ANAESTHESIAGENERAL ANAESTHESIA
InductionInduction – –
Thiopentone given slowly with proper iv fluid Thiopentone given slowly with proper iv fluid
replacementreplacement
Diazepam and fentanyl may also be usedDiazepam and fentanyl may also be used
Ketamine produces accentuated BP responseKetamine produces accentuated BP response
Rapid sequence intubationRapid sequence intubation as patients have as patients have
gastro-paresisgastro-paresis
Maintenance on spontaneous breathing with Maintenance on spontaneous breathing with
N2O and O2, with N2O and O2, with minimal halothaneminimal halothane
If needed, cardio stable muscle relaxants like If needed, cardio stable muscle relaxants like
Vec should be usedVec should be used

IPPV produces exaggerated reduction in IPPV produces exaggerated reduction in
BPBP
Blood loss should be replaced promptly as Blood loss should be replaced promptly as
compensatory tachycardia is absentcompensatory tachycardia is absent
Volatile anaesthetics produce excessive Volatile anaesthetics produce excessive
myocardial depression and hypotension myocardial depression and hypotension
Maintain fluid balanceMaintain fluid balance
Avoid hypothermiaAvoid hypothermia (pts may become (pts may become
poikilothermic due to sympathetic poikilothermic due to sympathetic
dysfunction)dysfunction)
Vasopressors should be used with cautionVasopressors should be used with caution

REGIONAL ANAESTHESIAREGIONAL ANAESTHESIA
Risk of hypotension with SAB and Risk of hypotension with SAB and
epiduralsepidurals
Post spinal urinary retention may occurPost spinal urinary retention may occur
Pre opPre op presence of presence of impotenceimpotence must be must be
brought to notice to avoid brought to notice to avoid medico legalmedico legal
implicationsimplications

ANS IN INTENSIVE CAREANS IN INTENSIVE CARE
Mechanical IPPVMechanical IPPV causes increased intra thoracic causes increased intra thoracic
pressure, decreased cardiac filling and hence, pressure, decreased cardiac filling and hence,
decreased cardiac outputdecreased cardiac output
All reflex mechanisms fail hence cardiac output falls All reflex mechanisms fail hence cardiac output falls
drasticallydrastically
Suction careSuction care

ANS IN CHRONIC PAINANS IN CHRONIC PAIN

LUMBAR SYMPATHETIC BLOCKLUMBAR SYMPATHETIC BLOCK
Used to alleviate the Used to alleviate the rest pain of chronic PVDrest pain of chronic PVD
Preganglionic sympathetics are from lower Preganglionic sympathetics are from lower
thoracic chain and pre ganglionic somatic fibres thoracic chain and pre ganglionic somatic fibres
are from 1are from 1
stst
and 2 and 2
ndnd
lumbar nerves lumbar nerves
Post ganglionic fibres are vasoconstrictor to Post ganglionic fibres are vasoconstrictor to
arterioles, pilomotor and sudomotor to skinarterioles, pilomotor and sudomotor to skin
Hence, its block causes absence of sweating Hence, its block causes absence of sweating
and warm dry skinand warm dry skin

COELIAC PLEXUS BLOCKCOELIAC PLEXUS BLOCK
Used for intractable pain caused by Used for intractable pain caused by
cancer of pancreas, stomach, gall bladder cancer of pancreas, stomach, gall bladder
and liverand liver
SUPERIOR HYPOGASTRIC PLEXUS SUPERIOR HYPOGASTRIC PLEXUS
BLOCKBLOCK
Relates pain from pelvic organsRelates pain from pelvic organs
Used in cancer pain due to Used in cancer pain due to
cervical,prostate,testicular cancers and in cervical,prostate,testicular cancers and in
radiation injuryradiation injury

COMPLEX REGIONAL PAIN SYNDROMECOMPLEX REGIONAL PAIN SYNDROME
Consequence of limb trauma with or Consequence of limb trauma with or
without obvious nerve lesionswithout obvious nerve lesions
Characterised by motor, sensory and ANS Characterised by motor, sensory and ANS
symptomssymptoms
ANS features include abnormal skin blood ANS features include abnormal skin blood
flow, temperature and sweatingflow, temperature and sweating
PHANTOM LIMBPHANTOM LIMB
Ectopic discharge of Ectopic discharge of epinephrine from a stump neuromaepinephrine from a stump neuroma is is
an important peripheral mechanisman important peripheral mechanism
Sympathetic block, sympathectomies or beta blockers Sympathetic block, sympathectomies or beta blockers
increase blood flow and reduce intensity of burning painincrease blood flow and reduce intensity of burning pain
Decreased blood flow causes phantom limb painDecreased blood flow causes phantom limb pain

CONCLUSIONCONCLUSION
ANS plays a very dominant role in maintaining ANS plays a very dominant role in maintaining
haemodynamic stabilityhaemodynamic stability
Influences the outcome after anaesthesia and surgeryInfluences the outcome after anaesthesia and surgery

THANK THANK
YOU…YOU…
THANK THANK
YOU…YOU…
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