THERMOREGULATION
Physiology & Monitoring
BY- Dr. Abhinav Shreeram
DNB Trainee
Dept. of Anaesthesiology
INTRODUCTION
• Humans are homeothermic.
• Any deviation ----> derraned metabolic function-----> Death
• Normal Body Temp ≈370 C
• Decrese of core temp 1-20 C will lead to:
:Raised incidence of cardiac mrbidity
:3 times more chance of wound infection
:Increased surgical blood loss
:20% increased chance of blood transfusion.
:Prolonged post anaesthesia recovery
NORMAL THERMOREGULATION
• +/- Feedback system.
• Multiple signal from nearly every
tissue.
• Processing in 3 phases:
1) Afferent thermal sensing.
2) Central regulation.
3) Efferent response.
AFFERENT INPUT
• Thermal sensing receptors all over the body.
• 80% by skin & 20% by others (spinal cord, thoracic tissue,
abdominal tissue etc.)
• Different for cold & warm.
:Cutaneous warm receptor
:TRP Receptor
• Pathways :
:C fibres : Warm + Pain
:Aδ fibres : cold
• Ascending lateral Spinothalamic Tract mainly but overlaps.
CENTRAL CONTROL
• 10 by Hypothalamus : Acts as Integrated Circuit.
• Preprocessed : In spinal cord & other brain areas.
• So in High spinal transection : Intact Thermoregulation.
• Few terms:
1.Gain of thermoregulation.
2.Threshold temp.
3.Inter threshold Range.
4.Maximum Intensity.
• Gain : Slope of response Intensity Vs Core temp.
• Threshold: Temp at which the regulatory response occur.
• Inter Threshold Range: Core temp not triggering response.
Tight control in humans.
• Maximum intensity: Mximum achievable response.
• Determinants of threshold : Not well understood but mediated
by : NE, Dopamine, 5HT, Ach, PGE1 & Neuropeptides.
• Threshold follows cicardian rythm.
• Alteration of threshold temp :
food intake, infection, hypothyroidism, hyperthyroidism,
Anaesthetic drugs, Alcohol, Thermal adaption.
• Central regulation intact in infants even premature ones.
• Sweating and vasocontriction both more in females.
EFFERENT RSPONSE
• Increased metabolic heat production.
• Alteration of Environmental Loss (Vasoconstriction/dilation)
• All response has own gain, threhold & Maximum.
• For hypothermia vasocontrion is 1st response: Energy efficient.
• 2nd is Increased production : Active process.
• Behavioural regulation : Most important effector.
1. VASOCONSTRICTION
• Cutaneous response.
• Most effective autonomic response.
• Controlled by a adrenergic symp. nerves.
• Numerous in palm & digits.
• Capillaries and AV shunts.
2. METABOLIC HEAT
• Increases whole body oxygen consumption.
• No mechanical work involved.
• Infants have two times more efficiency.
• Not that much effective in adults.
• Occurs in skeletal muscle & brown fat.
• Mediated by NE release.
• Through uncoupling protein.
• Increases only core temp.
3. SUSTAINED SHIVERING
• Augments metabolic heat production.
• Increases the O2 consumption by 50-100%
• Not so effective than exercise (500%
increased O2 consumption)
• ≤250 Hz rapid, unsyncronised, not
centrally controlled.
• Superimposed by waxing and waning (4-8
times), Centrally controlled.
• Less muscle mass, NM diseases & Muscle
relaxants reduces shivering.
4. SWEATING
• Only mechanism for raised body
temperature.
• Mediated by post ganglionic cholinergic
nerves.
• Active process.
• Inhibited by nerve block & atropin
administration.
• Normal : 1L/H, Athletes: 2L/H.
• 0.58 Kcal/g energy lost in evaporated sweat.
• With sweating vasodilation too occur.
• During extreme heat stress blood flow from
cutaneous vessels : 7.5L/min.
REGULATION DURING GENERAL ANAESTHESIA
• No behavioral regulation : Paralysed, uncouncious.
• Impared autonomic thermal control.
• Warm response increases.
• Cold response dcreases too much.
• So hypothermia is more common.
• Gain: Normal.
• Interthreshold range : 2-40 C (N=0.20 C)
• Maximum intensity : Normal.
RESPONSE THRESHOLD IN GA
• Drugs which increases the sweating threshold & decreses the
shivering & vasoconstriction threshold:
Propofol
Alfentanyl
Dexmed
Isoflurane
Desflurane
Sevoflurane
Halothane
N2O+ Fentanyl Combination
Clonidine
• No change in gain & Max intensity
HYPOTHERMIA DURING GA
• Most common thermoregulation defect.
• Due to combination of Anaesthetic drugs & Low OT temp.
• Heat loss in OT: by radiation, conduction, convection, evaporation
& perioperative.
• If still air then less loss.
• Heat lost by evaporation is least.
• Infants tends to loose more heat because of thin skin.
• Respiratory heat loss is almost nil.
PATTERN OF HEAT LOSS
• Initial rapid decrease in core
temp.
• Almost 0.5 to 1.50 C during 1st 4
hours.
• Volatiles leads to heat loss by
direct peripheral vasodilation.
• Core temp is generally 3-40 C
more than the peripheral ones.
REGULATION IN NEURAXIAL ANAESTHESIA
• Always impared.
• Intra -op decrease in core temp.
• Not perceived conciously.
• Triggers shivering.
• Paradox : Hypothermia but not feeling cold.
• Decreas in VC & Shivering threshold above the level of block.
• Alteration in central control.
• No perception of cold below the level of block.
• Epidural block even decreases the gain and maximum intensity.
• Sedatives & analgesics used with block and advanced age will
agment the impairment.
• Decrese in core temp may not trigger response because it depends
mainly on skin temp.
Regional Block
Relative warm perception of skin temp
Shivering & VC threshold decrese
Neglecting monitoring
Decrease in Core temp
Hypothermia
• Heat loss after regional anaesthesia almost same as during GA.
• 0.5 to 1 C decrease in temp. shortly after induction.
• Core temp. does not plateau like GA.
• So decresing temp will lead to hypothermia.
• VC in leg is directly prevented by block.
• With combined RA + GA 1C more dip in response trigger.
• Shivering in RA is common occuring due to core hypothermia.
• Temp of injected LA doesn't affect.
MILD INTRA-OP HYPOTHERMIA
BENEFITS
• Protection against cerebral ischemia & hypoxia.
• Far better protection than high dose isoflurane or barbiturate
coma.
• Can be used in asphaxiated neonates.
• Under research : role in raised ICT, CVA, SAH, AMI.
• Can be used in post cardiac arrest patients.
ADVERSE EFFECTS:
• Impairement of coagulation by platelet function defect.
• May be directly imparing the enzymes of coagulation.
• Increases tranfusion requirement.
• 1 C decrease in temp increases chance of complication by 20%.
• Decrease in drug metabolism. So will raise the plasma conc of all
the anaesthetics.
• if Core temp goes below 20 C we do not require any anaesthesia.
• MAC decrese by 5% with dip of every 1 C.
• Delayed wound healing.
• Worst experience of patients life.
POST ANAETHESIA SHIVERING
• Almost 40% incidence.
• But now is decreasing.
• Increses O2 consumption by 100%.
• Poorly corelated with MI.
• IOP & ICT increases.
• Wound pain also increases.
• Happens more in young age.
• Possible etiology:
1.Uninhibited spinal reflex.
2.Pain.
3.Decreased symp activity.
4.Pyrogen release.
5.Adrenal suppresion.
6.Respiratory alkalosis.
7.Intra- Op hypothermia.
• Characterised by tonic and phasic pattern.
• Tonic : Waxing & Waning (4/8 cycles per min).
• Phasic: Bursting pattern (5-7 Hz)
• Clonic pattern if seen will always be pathologic.
• Treatment:
: Skin surface warming : Augments Core temp.
: Cutaneus warmer machine.
: Drugs:
1. Meperidine
2. Clonidine (75ug iv)
3. Ketanserin(10mg iv)
4. Tramadol(50mg iv)
5. Physostigmine(0.04 mg/kg iv)
6. Nefopam(0.15mg/kg)
7. Dexmed
8. MgSO4 (30mg/kg iv)
• No specific drug mechanism.
• Clonidin & dexmed acts centrally.
• Alfentanyl is u receptor agonist.
• Meperidine is best which reduces the shivering and VC
threshold by almost half keeping gain & max intensity
normal.
PERIOPERATIVE THERMAL MANIPULATIONS
1. Increasing Vasomotor Tone:
: Reaching plateau early.
: Transfers heat from periphery to core.
2. Prevention of redistribution hypothermia:
: prewarming the periphery.
3. Airway heating and humidification:
: More effective in infants & children.
: Actively heating the airway much better.
4. I.V. Fluids:
: Not effective to treat but good for prevention
: Can't greatly exceeds body temp.
: 1U refridgerated blood/ 1L of crystalloids at room
temp will decrease the body temp by 0.25 C.
: Fluid warmers are used in prolonged Surgeries.
5.CUTANEOUS WARMING
• Room temp 23 C for adults & 26 C for infants is ideal but not
practical.
• Passive insulators to be used : Cotton blankets, surgical drapes,
plastic sheatings, reflective composits(space blanket)
• Warming the blanket is of not that much use.
• Prevention is better & more effective.
• Depends on surface area.
• Common false perception that heat loss from head is more.
• Wrong to only cover the head & leave the arm.
• Active warming advised for prolonged surgeries.
• Circulating water matress & forced air is commonly used.
• No or very little heat loss from the back.
• If No cutaneous heat loss the metabolic heat will raise the
body temp by 1C/hour.
MILD THERAPEUTIC HYPOTHERMIA
• Target temp: 32 to 34 C but have to reach very quickly.
• Generaly useful in neuro surgeries.
• Immersion of patient in cold water will be ideal but its not practical.
• Refrigerated IVF : reduction by 0.5C/L but fluid restriction in neuro
Sx.
• Forced air cooling : Slow (2.5 Hrs)
• Energy exchange pads.
• Best is endovascular cooling : heat exchanging servo catheters in
IVC. Decreases temp by 4C/hour.
• Body has to tolerate that hypothermia.
• So we will augment it with drugs.
• Buspiron+ Mepiridine : Synergisticaly reduces shivering
threshold to 34 C.
• Ondansetron + Doxapram + MgSO4 can be used but its not
that effective.
SEVERE DELIBERATE HYPOTHERMIA
• Used in cardiac surgeries mostly.
• Earlier 28C was used for bypass surgeries but it shows no benefit.
• Can be lethal.
• Procedure at normothermia or 33C shows much better prognosis.
• But its still a routine for causing intentional circulatory arrest.
MONITORING GUIDELINES
• Core body temp should be measured in most patients given general
anaesthesia for more than 30 mins.
• Temp should also be measured during regional anaesthesia when
changes in body temp are intended, anticipated or suspected.
• Unless hypothermia is specifically indicated (for protection against
ischemia), efforts sould be made to maintain intraoperative core
temp higher than 36C.
TEMP MONITORING SITES
• Core temp measuring sites :
:Pulmonary artery
:Distal esophagus
:Tympanic Membrane
:Nasopharynx.
• Can be estimated with
reasonable accuracy using oral,
axillary, rectal & bladder temp.
THANK YOU!

Perioperative Thermoregulation

  • 1.
    THERMOREGULATION Physiology & Monitoring BY-Dr. Abhinav Shreeram DNB Trainee Dept. of Anaesthesiology
  • 2.
    INTRODUCTION • Humans arehomeothermic. • Any deviation ----> derraned metabolic function-----> Death • Normal Body Temp ≈370 C • Decrese of core temp 1-20 C will lead to: :Raised incidence of cardiac mrbidity :3 times more chance of wound infection :Increased surgical blood loss :20% increased chance of blood transfusion. :Prolonged post anaesthesia recovery
  • 3.
    NORMAL THERMOREGULATION • +/-Feedback system. • Multiple signal from nearly every tissue. • Processing in 3 phases: 1) Afferent thermal sensing. 2) Central regulation. 3) Efferent response.
  • 4.
    AFFERENT INPUT • Thermalsensing receptors all over the body. • 80% by skin & 20% by others (spinal cord, thoracic tissue, abdominal tissue etc.) • Different for cold & warm. :Cutaneous warm receptor :TRP Receptor • Pathways : :C fibres : Warm + Pain :Aδ fibres : cold • Ascending lateral Spinothalamic Tract mainly but overlaps.
  • 5.
    CENTRAL CONTROL • 10by Hypothalamus : Acts as Integrated Circuit. • Preprocessed : In spinal cord & other brain areas. • So in High spinal transection : Intact Thermoregulation. • Few terms: 1.Gain of thermoregulation. 2.Threshold temp. 3.Inter threshold Range. 4.Maximum Intensity.
  • 6.
    • Gain :Slope of response Intensity Vs Core temp. • Threshold: Temp at which the regulatory response occur. • Inter Threshold Range: Core temp not triggering response. Tight control in humans. • Maximum intensity: Mximum achievable response.
  • 7.
    • Determinants ofthreshold : Not well understood but mediated by : NE, Dopamine, 5HT, Ach, PGE1 & Neuropeptides. • Threshold follows cicardian rythm. • Alteration of threshold temp : food intake, infection, hypothyroidism, hyperthyroidism, Anaesthetic drugs, Alcohol, Thermal adaption. • Central regulation intact in infants even premature ones. • Sweating and vasocontriction both more in females.
  • 8.
    EFFERENT RSPONSE • Increasedmetabolic heat production. • Alteration of Environmental Loss (Vasoconstriction/dilation) • All response has own gain, threhold & Maximum. • For hypothermia vasocontrion is 1st response: Energy efficient. • 2nd is Increased production : Active process. • Behavioural regulation : Most important effector.
  • 9.
    1. VASOCONSTRICTION • Cutaneousresponse. • Most effective autonomic response. • Controlled by a adrenergic symp. nerves. • Numerous in palm & digits. • Capillaries and AV shunts.
  • 10.
    2. METABOLIC HEAT •Increases whole body oxygen consumption. • No mechanical work involved. • Infants have two times more efficiency. • Not that much effective in adults. • Occurs in skeletal muscle & brown fat. • Mediated by NE release. • Through uncoupling protein. • Increases only core temp.
  • 11.
    3. SUSTAINED SHIVERING •Augments metabolic heat production. • Increases the O2 consumption by 50-100% • Not so effective than exercise (500% increased O2 consumption) • ≤250 Hz rapid, unsyncronised, not centrally controlled. • Superimposed by waxing and waning (4-8 times), Centrally controlled. • Less muscle mass, NM diseases & Muscle relaxants reduces shivering.
  • 12.
    4. SWEATING • Onlymechanism for raised body temperature. • Mediated by post ganglionic cholinergic nerves. • Active process. • Inhibited by nerve block & atropin administration. • Normal : 1L/H, Athletes: 2L/H. • 0.58 Kcal/g energy lost in evaporated sweat. • With sweating vasodilation too occur. • During extreme heat stress blood flow from cutaneous vessels : 7.5L/min.
  • 13.
    REGULATION DURING GENERALANAESTHESIA • No behavioral regulation : Paralysed, uncouncious. • Impared autonomic thermal control. • Warm response increases. • Cold response dcreases too much. • So hypothermia is more common. • Gain: Normal. • Interthreshold range : 2-40 C (N=0.20 C) • Maximum intensity : Normal.
  • 14.
    RESPONSE THRESHOLD INGA • Drugs which increases the sweating threshold & decreses the shivering & vasoconstriction threshold: Propofol Alfentanyl Dexmed Isoflurane Desflurane Sevoflurane Halothane N2O+ Fentanyl Combination Clonidine • No change in gain & Max intensity
  • 15.
    HYPOTHERMIA DURING GA •Most common thermoregulation defect. • Due to combination of Anaesthetic drugs & Low OT temp. • Heat loss in OT: by radiation, conduction, convection, evaporation & perioperative. • If still air then less loss. • Heat lost by evaporation is least. • Infants tends to loose more heat because of thin skin. • Respiratory heat loss is almost nil.
  • 16.
    PATTERN OF HEATLOSS • Initial rapid decrease in core temp. • Almost 0.5 to 1.50 C during 1st 4 hours. • Volatiles leads to heat loss by direct peripheral vasodilation. • Core temp is generally 3-40 C more than the peripheral ones.
  • 18.
    REGULATION IN NEURAXIALANAESTHESIA • Always impared. • Intra -op decrease in core temp. • Not perceived conciously. • Triggers shivering. • Paradox : Hypothermia but not feeling cold. • Decreas in VC & Shivering threshold above the level of block. • Alteration in central control. • No perception of cold below the level of block.
  • 19.
    • Epidural blockeven decreases the gain and maximum intensity. • Sedatives & analgesics used with block and advanced age will agment the impairment. • Decrese in core temp may not trigger response because it depends mainly on skin temp.
  • 20.
    Regional Block Relative warmperception of skin temp Shivering & VC threshold decrese Neglecting monitoring Decrease in Core temp Hypothermia
  • 21.
    • Heat lossafter regional anaesthesia almost same as during GA. • 0.5 to 1 C decrease in temp. shortly after induction. • Core temp. does not plateau like GA. • So decresing temp will lead to hypothermia. • VC in leg is directly prevented by block. • With combined RA + GA 1C more dip in response trigger. • Shivering in RA is common occuring due to core hypothermia. • Temp of injected LA doesn't affect.
  • 22.
    MILD INTRA-OP HYPOTHERMIA BENEFITS •Protection against cerebral ischemia & hypoxia. • Far better protection than high dose isoflurane or barbiturate coma. • Can be used in asphaxiated neonates. • Under research : role in raised ICT, CVA, SAH, AMI. • Can be used in post cardiac arrest patients.
  • 23.
    ADVERSE EFFECTS: • Impairementof coagulation by platelet function defect. • May be directly imparing the enzymes of coagulation. • Increases tranfusion requirement. • 1 C decrease in temp increases chance of complication by 20%. • Decrease in drug metabolism. So will raise the plasma conc of all the anaesthetics. • if Core temp goes below 20 C we do not require any anaesthesia. • MAC decrese by 5% with dip of every 1 C. • Delayed wound healing. • Worst experience of patients life.
  • 24.
    POST ANAETHESIA SHIVERING •Almost 40% incidence. • But now is decreasing. • Increses O2 consumption by 100%. • Poorly corelated with MI. • IOP & ICT increases. • Wound pain also increases. • Happens more in young age.
  • 25.
    • Possible etiology: 1.Uninhibitedspinal reflex. 2.Pain. 3.Decreased symp activity. 4.Pyrogen release. 5.Adrenal suppresion. 6.Respiratory alkalosis. 7.Intra- Op hypothermia. • Characterised by tonic and phasic pattern. • Tonic : Waxing & Waning (4/8 cycles per min). • Phasic: Bursting pattern (5-7 Hz) • Clonic pattern if seen will always be pathologic.
  • 26.
    • Treatment: : Skinsurface warming : Augments Core temp. : Cutaneus warmer machine. : Drugs: 1. Meperidine 2. Clonidine (75ug iv) 3. Ketanserin(10mg iv) 4. Tramadol(50mg iv) 5. Physostigmine(0.04 mg/kg iv) 6. Nefopam(0.15mg/kg) 7. Dexmed 8. MgSO4 (30mg/kg iv)
  • 27.
    • No specificdrug mechanism. • Clonidin & dexmed acts centrally. • Alfentanyl is u receptor agonist. • Meperidine is best which reduces the shivering and VC threshold by almost half keeping gain & max intensity normal.
  • 28.
    PERIOPERATIVE THERMAL MANIPULATIONS 1.Increasing Vasomotor Tone: : Reaching plateau early. : Transfers heat from periphery to core. 2. Prevention of redistribution hypothermia: : prewarming the periphery. 3. Airway heating and humidification: : More effective in infants & children. : Actively heating the airway much better.
  • 29.
    4. I.V. Fluids: :Not effective to treat but good for prevention : Can't greatly exceeds body temp. : 1U refridgerated blood/ 1L of crystalloids at room temp will decrease the body temp by 0.25 C. : Fluid warmers are used in prolonged Surgeries.
  • 30.
    5.CUTANEOUS WARMING • Roomtemp 23 C for adults & 26 C for infants is ideal but not practical. • Passive insulators to be used : Cotton blankets, surgical drapes, plastic sheatings, reflective composits(space blanket) • Warming the blanket is of not that much use. • Prevention is better & more effective. • Depends on surface area. • Common false perception that heat loss from head is more.
  • 31.
    • Wrong toonly cover the head & leave the arm. • Active warming advised for prolonged surgeries. • Circulating water matress & forced air is commonly used. • No or very little heat loss from the back. • If No cutaneous heat loss the metabolic heat will raise the body temp by 1C/hour.
  • 32.
    MILD THERAPEUTIC HYPOTHERMIA •Target temp: 32 to 34 C but have to reach very quickly. • Generaly useful in neuro surgeries. • Immersion of patient in cold water will be ideal but its not practical. • Refrigerated IVF : reduction by 0.5C/L but fluid restriction in neuro Sx. • Forced air cooling : Slow (2.5 Hrs) • Energy exchange pads. • Best is endovascular cooling : heat exchanging servo catheters in IVC. Decreases temp by 4C/hour.
  • 33.
    • Body hasto tolerate that hypothermia. • So we will augment it with drugs. • Buspiron+ Mepiridine : Synergisticaly reduces shivering threshold to 34 C. • Ondansetron + Doxapram + MgSO4 can be used but its not that effective.
  • 34.
    SEVERE DELIBERATE HYPOTHERMIA •Used in cardiac surgeries mostly. • Earlier 28C was used for bypass surgeries but it shows no benefit. • Can be lethal. • Procedure at normothermia or 33C shows much better prognosis. • But its still a routine for causing intentional circulatory arrest.
  • 35.
    MONITORING GUIDELINES • Corebody temp should be measured in most patients given general anaesthesia for more than 30 mins. • Temp should also be measured during regional anaesthesia when changes in body temp are intended, anticipated or suspected. • Unless hypothermia is specifically indicated (for protection against ischemia), efforts sould be made to maintain intraoperative core temp higher than 36C.
  • 36.
    TEMP MONITORING SITES •Core temp measuring sites : :Pulmonary artery :Distal esophagus :Tympanic Membrane :Nasopharynx. • Can be estimated with reasonable accuracy using oral, axillary, rectal & bladder temp.
  • 37.