2018A11 Describe the respiratory response to hypoxaemia in both the awake and the anaesthetized patient.



·         Intro and importance

·         Hyperventilation: sensor, integrator, effector

·         Hypoxic pulmonary vasoconstriction

·         Sympathetic outflow


Intro: hypoxaemia


·   PaO2 < 60mmHg


·   Increased alveolar ventilation -> ↑PaO2

·   Hypoxic pulmonary vasoconstriction

o Improved V/Q matching -> ↑PaO2

o ↑PVR

·   ↑SNS output -> ↑cardiac output -> DO2

Effect of anaesthesia on responses

·   Suppression of all responses

·   Dose-dependent effects

High risk if:

·   Alone (e.g. post-op ward at night)

·   CO2-insensate (e.g. severe COPD, OSA, OHS)

·   Sensitive to resp depression (e.g. elderly, neonate)

·   Respiratory depressant drugs (e.g. morphine)

·   Sedated (e.g. midazolam)

·   Synergistic respiratory depressant drugs (e.g. benzo+ opioid)


Alveolar hyperventilation:




·   Peripheral chemoreceptors

o Carotid bodies (CNIX Hering’s nerve)

o Aortic bodies (CNX)

·   Type 1 glomus cell: responsive to ↓pO2, ↓pCO2, (↓pH carotids only)

·   Type 2 sustentacular cell: support

·   Blood flow 2000mL/min/100g -> supply by dissolved O2 only


·   ↓ PaO2 -> closure of K+ channel -> depolarisation -> ↑afferent to resp centre

·   Response is minimal until PaO2 <100mmHg, profound <50mmHg

·   Response is rapid, <1 second

Effect of anaesthesia

·   Volatiles:

o ↓Chemoreceptor afferents is the most important resp effect

o 1 MAC: ablated response

o 0.1 MAC: significant depression of response

o Hence need for O2 supplementation post-op for safety



·   Propofol:

o ↓Chemoreceptor afferents

o Less potent than volatiles




·   Respiratory centre, medulla

·   Multiple cell types: dorsal inspiratory, ventral expiratory, pre-Botzinger pacemakers

·   Afferents via nucleus tractus solitarius

·   Efferents via nucleus ambiguus and dorsal motor nucleus of CNX


·   ↑Stimulation -> ↑amplitude and frequency of neuronal output to effectors

·   ↓PaO2 is synergistic with ↑PaCO2 and ↓pH

Effect of anaesthesia

·   Suppression:

o General anaesthesia (↑GABA/glycine activity)

o Opioids (μ receptor agonist in resp centre – most important opioid effect)

o Neuraxial: ↓input to reticular activating system -> ↓conscious state, ↓resp centre output

·   Stimulation:

o Pain -> ↑input to reticular activating system -> ↑resp centre output




·   Primary inspiratory: diaphragm, external intercostals, pharyngeal dilators

·   Accessory inspiratory: e.g. sternocleidomastoid

·   Expiratory: e.g. internal intercostals, abdominals (normally inactive)


·   ↑Respiratory centre output -> ↑RR, VT -> ↑VA -> ↑PaO2

·   Completion of negative feedback loop

Effect of anaesthesia

·   Volatile:

o Skeletal muscle relaxation (inhibit nAChR)

o Inhibit a-motor neuron (↑GABA/↑glycine)

o Affects intercostals > diaphragm

·   Propofol:

o As for volatiles

o But less potent: ↓glycine activity, ↓spinal cord effect

·   Benzodiazepines:

o Skeletal muscle relaxation

·   Neuraxial:

o Inhibit α-motor neuron (intercostals)

o No effect on diaphragm unless C-spine level

·   Paralysis:

o No effector response

·   Position:

o Supine, Trendelenburg -> ↑work of breathing -> impaired effector

·   Apparatus dead space (tubing distal to Y piece):

o ↓VA for a given MV


Hypoxic pulmonary vasoconstriction:


·   Match ventilation with perfusion, ↑PaO2


·   Vasoconstriction 1 / (PAO20.6 x PvO20.4)

Biphasic response

·   Phase 1: onset immediate, plateau 5 mins

o ? Inhibition of K+ channel

o ? ↓mitochondrial ROS

o ? ↓ATP:ADP

·   Phase 2: onset 40 minutes, plateau 2 hours

o ? ↑↓COX, LOX production

o ? ↑hypoxia-inducible transcription

Effect of anaesthesia

·   Volatile:

o Inhibit L-Ca2+ channel, ↑NO release, ↓medulla SNS output

o Generalised vasodilatation including pulmonary

·   Propofol:

o Similar mechanisms

o Less potent, preferred in one lung ventilation


Sympathetic response:


·   ↓PaO2 <50mmHg -> CNS acidosis


·   ↑SNS output

·   ↑HR, ↑contractility, venoconstriction -> ↑preload

·   ↑Cardiac output -> ↑O2 delivery

·   No change to PaO2

Effect of anaesthesia

·   Volatiles, propofol:

o ↓SNS output from medulla (↑GABA, glycine activity)

o Inhibit L-Ca2+ on heart, blood vessels

o ↑Nitric oxide release

o Dose-dependent suppression of baroreceptor response (propofol > volatiles)

·   Opioids, benzodiazepines:

o ↓SNS output

·   Neuraxial:

o ↓SNS output below block upper limit


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