DNB Final Exam — Paper 1, Post Diploma (FAT 2025)
Complete Model Answers
Q1. Oxygen Cascade and Dissociation Curve
Oxygen Cascade
The oxygen cascade describes the stepwise fall in PO₂ from atmospheric air to mitochondria:
| Location | PO₂ (mmHg) |
|---|
| Dry atmospheric air | 159 |
| Humidified tracheal air | 149 |
| Alveolar gas (PAO₂) | ~100 |
| Arterial blood (PaO₂) | ~95 |
| Capillary/tissue | 40 |
| Mitochondria | 1–5 |
Alveolar gas equation: PAO₂ = FiO₂(PB − PH₂O) − PaCO₂/RQ
- At sea level: PAO₂ = 0.21 × (760 − 47) − 40/0.8 ≈ 100 mmHg
- A–a gradient: normally <15 mmHg (increases with V/Q mismatch, shunt, diffusion defect)
Oxyhaemoglobin Dissociation Curve (ODC)
- Sigmoid shape due to cooperative binding (T→R state transition of Hb)
- P50 = 26.5 mmHg (normal); at this PO₂, Hb is 50% saturated
Factors causing RIGHT SHIFT (↑P50, ↓Hb affinity, promotes O₂ delivery to tissues):
- ↑CO₂ (Bohr effect), ↑H⁺ (↓pH), ↑Temperature, ↑2,3-DPG, Stored blood (initially ↑2,3-DPG depleted)
Factors causing LEFT SHIFT (↑Hb affinity, impairs O₂ delivery):
- ↓CO₂, ↓H⁺ (↑pH), ↓Temperature, ↓2,3-DPG, Fetal Hb (HbF), CO poisoning, MetHb
Clinical relevance in anaesthesia:
- Hypothermia during CPB shifts curve left — O₂ delivery maintained by ↑CO
- Stored blood: 2,3-DPG depleted after 1 week → left shift → impaired tissue O₂ delivery
- Massive transfusion → transient left shift
Q2. Desflurane and Remifentanil
Desflurane
| Property | Value |
|---|
| MAC (adults) | 6–7% |
| Blood:gas partition coefficient | 0.45 (lowest among volatiles → fastest wash-in/out) |
| Oil:gas partition coefficient | 18.7 |
| SVP at 20°C | 669 mmHg (near room temp → special heated pressurized vaporizer required) |
| Metabolism | <0.02% (safest with respect to hepatotoxicity) |
Advantages:
- Fastest emergence and recovery (ideal in day care, obese patients, neuroanaesthesia)
- Minimal metabolism → no organ toxicity
- Low solubility → rapid titration
Disadvantages:
- Airway irritant — causes coughing, laryngospasm, bronchospasm (avoid for inhalational induction)
- ↑SVR, ↑HR on rapid increases in concentration (sympathetic stimulation)
- ↑Cerebral blood flow and ICP (at >1 MAC) — use with caution in neurosurgery
- Reacts with dry CO₂ absorbent → CO production
- GWP (global warming potential) = 2540 (environmental concern; being phased out in UK/Europe)
- Requires a unique, electrically heated vaporizer (Tec 6)
Remifentanil
| Property | Value |
|---|
| Class | Ultra-short acting μ-opioid agonist |
| Structure | Ester linkage in side chain |
| Metabolism | Plasma & tissue esterases (organ independent) |
| Elimination half-life | 3–5 minutes |
| Context-sensitive half-time | ~3–4 min (independent of infusion duration) |
| Potency | ~100x morphine |
Advantages:
- Predictable, rapid offset regardless of infusion duration — ideal for TIVA/TCI
- Organ-independent metabolism → safe in hepatic/renal failure
- Blunts intubation response (1–1.5 mcg/kg bolus)
- Infusion: 0.05–2 mcg/kg/min
Disadvantages:
- No residual analgesia after stopping → must provide multi-modal analgesia pre-emptively
- Opioid-induced hyperalgesia (OIH) with prolonged high-dose infusion
- Bradycardia and hypotension
- Muscle rigidity at high bolus doses
- Susceptible to context-dependent hypoventilation
- Not suitable as sole agent — must be combined with hypnotic
Use in TIVA: Remifentanil (TCI Minto model, target 3–8 ng/mL) + Propofol (TCI Marsh/Schnider model)
Q3. Capnography and Neuromonitoring
Capnography
Phases of normal capnogram:
- Phase I: Inspiratory baseline (EtCO₂ = 0; dead space gas)
- Phase II: Expiratory upstroke (mixing of dead space and alveolar gas)
- Phase III: Alveolar plateau (EtCO₂ peaks ~35–45 mmHg)
- Phase 0: Inspiratory downstroke
Normal EtCO₂: 35–45 mmHg; normally 2–5 mmHg less than PaCO₂
Clinical uses:
- Confirmation of ETT placement (most reliable method)
- Monitoring ventilation adequacy
- Detecting oesophageal intubation (flat trace)
- Detecting air embolism (sudden ↓ EtCO₂)
- Detecting endobronchial intubation
- ROSC during CPR (sudden ↑ EtCO₂ >40 mmHg)
- Monitoring metabolic rate (↑ in MH, thyroid storm)
- Guide to diagnosis: shark-fin pattern = bronchospasm; plateau disappears = sampling error
Neuromonitoring (Intraoperative Neurophysiological Monitoring – IONM)
| Modality | What it monitors | Alert criteria |
|---|
| EEG | Cortical activity, depth of anaesthesia | Burst suppression, ↓ amplitude/frequency |
| BIS (Bispectral Index) | Depth of anaesthesia (40–60 = surgical plane) | <40 (deep), >60 (light) |
| SSEP (Somatosensory EP) | Posterior column/sensory pathways | ↓50% amplitude or ↑10ms latency |
| MEP (Motor EP) | Corticospinal tract (motor) | ↓>50% amplitude |
| BAEP (Brainstem Auditory EP) | Auditory pathway/posterior fossa | Wave V loss |
| EMG | Cranial nerve/nerve root integrity | Free-run or evoked |
| TCD | Cerebral blood flow velocity | Emboli detection in cardiac surgery |
Anaesthesia considerations for IONM:
- Volatile agents suppress SSEP/MEP in dose-dependent manner (avoid >0.5 MAC)
- TIVA preferred for MEP monitoring (Propofol + Remifentanil)
- Neuromuscular blockade abolishes MEP (avoid if MEP monitoring)
- Nitrous oxide suppresses MEPs
- Maintain MAP >80 mmHg, normothermia, normocapnia
Q4. Shockable and Non-Shockable Rhythms; Management of Pulseless Rhythm
Shockable Rhythms
- Ventricular Fibrillation (VF)
- Pulseless Ventricular Tachycardia (pVT)
Non-Shockable Rhythms
- Pulseless Electrical Activity (PEA)
- Asystole
Management of Pulseless Rhythm (Adult ALS Algorithm 2021)
Immediate:
- Call for help, start CPR (30:2 ratio), attach defibrillator
- High-quality CPR: Rate 100–120/min, depth 5–6 cm, full chest recoil, minimize interruptions
IF SHOCKABLE (VF/pVT):
- Deliver 1 shock (200 J biphasic, or 360 J monophasic)
- Immediately resume CPR × 2 minutes
- After 2 min → reassess rhythm
- If VF/pVT persists → 2nd shock → CPR 2 min
- After 3rd shock: Adrenaline 1 mg IV + Amiodarone 300 mg IV
- Subsequent adrenaline every 3–5 min (alternate cycles)
- After 5th shock: Amiodarone 150 mg additional dose (if VT/VF refractory)
IF NON-SHOCKABLE (PEA/Asystole):
- Continue CPR 30:2
- Adrenaline 1 mg IV immediately (as soon as IV access obtained)
- Adrenaline every 3–5 min
- Treat reversible causes (4H + 4T)
4Hs: Hypoxia, Hypovolaemia, Hypo/Hyperkalaemia, Hypothermia
4Ts: Tension pneumothorax, Tamponade, Thrombosis (PE/MI), Toxins
Drug doses:
- Adrenaline: 1 mg IV/IO every 3–5 min
- Amiodarone: 300 mg IV bolus (shockable, after 3rd shock), then 150 mg after 5th shock
- If no amiodarone: Lignocaine 100 mg IV (1–1.5 mg/kg)
Post-ROSC care: TTM (32–36°C × 24h), PCI, avoid hyperoxia, blood glucose 6–10 mmol/L
Q5. Fascia Iliaca Block
Anatomy:
- Target: Femoral nerve, Lateral femoral cutaneous nerve (LFCN), and partially obturator nerve
- Fascia iliaca = fibrous sheet over the iliopsoas muscle
- LA is deposited deep to the fascia iliaca, lateral to the femoral vessels
Indications:
- Hip fracture (fractured neck of femur) — excellent for perioperative analgesia
- Total hip arthroplasty (THA), Total knee arthroplasty (TKA)
- Femoral shaft fractures, ORIF procedures
- As alternative to femoral nerve block or 3-in-1 block
Approaches:
- Landmark-based (Dalens' method): 1 cm below junction of lateral 1/3 and medial 2/3 of inguinal ligament; loss of resistance at 2 fascia pops (fascia lata + fascia iliaca)
- Infrainguinal US-guided: Femoral vessels identified; LA deposited between fascia iliaca and iliopsoas lateral to femoral nerve
- Suprainguinal US-guided: Above inguinal ligament; better spread toward obturator nerve; preferred for hip surgery (PENG block alternative)
Volume: 30–40 mL (0.25–0.375% ropivacaine or 0.25% bupivacaine)
Nerves blocked:
- Femoral nerve (L2-L4) — reliably
- LFCN (L2-L3) — reliably
- Obturator nerve (L2-L4) — variably (better with suprainguinal approach)
Advantages over femoral nerve block:
- Covers larger area, single injection for 3 nerves
- Less risk of femoral nerve injury (not targeting nerve directly)
Complications:
- LA systemic toxicity (LAST) — use max recommended dose
- Femoral vessel puncture
- Intravascular injection
- Quadriceps weakness/fall risk (femoral block effect)
- Hematoma
Q6. Methods to Reduce ICP and Maintain Cerebral Perfusion Pressure
Normal Values
- ICP: <15 mmHg (normal 5–15 mmHg)
- CPP = MAP − ICP (target CPP ≥60–70 mmHg in TBI)
Methods to Reduce ICP
1. Head Positioning:
- Head-up 30° (reduces venous congestion)
- Head midline (prevents jugular venous obstruction)
2. Ventilation (most rapidly effective):
- Hyperventilation: ↓PaCO₂ → cerebral vasoconstriction → ↓CBF → ↓ICP
- Target PaCO₂ 35 mmHg (mild hyperventilation); avoid <30 mmHg (ischemia risk)
- Avoid hypoxia (maintain SpO₂ >94%)
3. Osmotherapy:
- Mannitol 20%: 0.25–1 g/kg IV over 20–30 min; osmotic diuresis; onset 20–40 min; avoid if serum osmolality >320 mOsm/L
- Hypertonic saline (3% NaCl): Equal or superior to mannitol; preferred in hypovolaemia/haemodynamic instability; Na+ target 145–160 mEq/L
4. Sedation and Anaesthesia:
- Propofol infusion: ↓CMRO₂, ↓CBF, ↓ICP; allows burst suppression at high doses
- Midazolam/fentanyl for ICU sedation
- Barbiturates (thiopentone): Reduce CMRO₂ 50–55%; second-line for refractory ICP
- Avoid ketamine (historically; now used cautiously as it may not raise ICP if normocapnia maintained)
5. CSF Drainage:
- Ventriculostomy (EVD): Direct ICP measurement + drainage — most effective
- Lumbar drain: Only when basal cisterns are patent
6. Steroids:
- Dexamethasone: Effective for vasogenic oedema (tumour, abscess) — NOT recommended in TBI (CRASH trial showed ↑ mortality)
7. Neuromuscular blockade:
- Prevents rises in ICP from coughing, Valsalva, patient–ventilator dyssynchrony
8. Temperature Management:
- Avoid hyperthermia (fever raises CMRO₂ and ICP)
- Mild hypothermia (32–35°C) can reduce ICP — limited evidence for outcomes in TBI
9. Surgery:
- Decompressive craniectomy (refractory ICP >25 mmHg)
- Evacuation of haematoma/mass lesion
Anaesthetic drugs affecting ICP:
- ↓ ICP: Propofol, barbiturates, benzodiazepines, opioids (if normocapnia), etomidate, lignocaine
- ↑ ICP (avoid): Ketamine (relative), volatile agents >1 MAC, N₂O, succinylcholine (transient)
- ↑ CPP: Vasopressors (noradrenaline, phenylephrine) to raise MAP
Q7. Anaesthesia Management: 80-year-old Diabetic and Hypertensive for Unilateral TKR
Preoperative Assessment
Comorbidity optimization:
- Diabetes: HbA1c ideally <8.5%; check renal function (metformin — stop 48h before if eGFR <60); check for autonomic neuropathy, gastroparesis
- Hypertension: Optimise BP <160/100 pre-op; continue antihypertensives on morning of surgery (except ACEI/ARB — omit on day of surgery to avoid intraoperative hypotension); ECG for LVH, rhythm
- Cardiac evaluation: Functional capacity (METs); echocardiogram if poor functional capacity; consider stress testing if significant cardiac risk
- Airway: Assess for DM-related atlantoaxial/cervical stiffness, limited mouth opening
- Investigations: CBC, RFT, LFT, electrolytes, ECG, CXR, blood glucose, HbA1c, coagulation if neuraxial planned
Anaesthetic Options
Regional anaesthesia is preferred for elderly TKR (avoids GA risks, superior analgesia, reduced DVT, no airway manipulation):
A. Spinal Anaesthesia (Gold standard for TKR)
- Hyperbaric bupivacaine 0.5% (2–3 mL) ± fentanyl 25 mcg or morphine 100 mcg
- Advantages: Avoids GA, excellent block, reduced blood loss, reduced DVT, early mobilisation
- Caution: Hypotension more pronounced in hypertensive/elderly → pre-load with crystalloid, have vasopressor ready (phenylephrine/ephedrine)
- Block level: T12–L1 sufficient for TKR
B. Combined Spinal-Epidural (CSE)
- Allows extending block duration
- Useful if surgery expected >2.5 hrs
C. General Anaesthesia (if neuraxial contraindicated)
- Anticoagulation, patient refusal, severe spinal stenosis
- Use LMA if possible; TIVA preferable in elderly
- Avoid long-acting opioids; use multimodal analgesia
Perioperative Considerations
Glucose management:
- Target glucose 6–10 mmol/L intraoperatively
- Monitor glucose every 1–2 hours
- Variable rate insulin infusion (VRII) if glucose poorly controlled
- Avoid hypoglycaemia (worse than mild hyperglycaemia)
Blood pressure management:
- Maintain MAP within 20% of baseline
- Spinal-induced hypotension: treat with fluids + vasopressors
- Avoid intraoperative hypertension (LA use in surgical field, tourniquet inflation)
DVT prophylaxis:
- Mechanical: Pneumatic compression devices, TED stockings
- Pharmacological: LMWH (enoxaparin) — timing based on anaesthetic technique
Analgesia (multimodal):
- Femoral nerve block / Adductor canal block (ACB): Preferred — preserves quadriceps strength (important for rehab); ACB: 15–20 mL 0.5% ropivacaine
- Fascia iliaca block as alternative
- Periarticular infiltration by surgeon (ropivacaine + ketorolac + epinephrine)
- Paracetamol 1g IV/oral QID (safe in elderly)
- NSAIDs cautiously (impaired renal function in elderly/diabetic)
- Avoid systemic opioids (confusion, urinary retention in elderly)
Tourniquet considerations:
- Standard inflation pressure 250–300 mmHg (100 mmHg above systolic in hypertensive)
- Tourniquet time <90 min; pain from tourniquet (ischaemic pain) under spinal after ~45 min
Positioning: Supine with knee flexed; padding pressure points (diabetic neuropathy risk)
Postoperative:
- Continue antihypertensives and insulin regimen
- Early mobilisation Day 1
- Blood glucose monitoring 4-hourly for 24h post-op
- Restart metformin when eating and renal function confirmed normal
Q8. Equipment Used in OLV — Describe DLT, Indications, and Complications
Equipment for One-Lung Ventilation (OLV)
1. Double-Lumen Tube (DLT) — most commonly used
2. Bronchial Blockers — used via single-lumen tube
- Cohen Flexitip BB, Arndt BB, Fuji Uniblocker, EZ-Blocker, Larndt, Lernaite (SLT)
3. Univent Tube — single-lumen tube with built-in bronchial blocker channel
4. Single-Lumen Tube — advanced into main bronchus (emergency)
Double-Lumen Tube (DLT)
Structure:
- Two lumens: tracheal lumen + bronchial lumen
- Two cuffs: tracheal cuff (white/clear) + bronchial cuff (blue/coloured)
- Bronchial lumen: 15 mm shorter, enters left or right main bronchus
- 4-connector (blue = bronchial, clear = tracheal)
Sizes: 28F, 32F, 35F, 37F, 39F, 41F
- Females: 35–37F; Males: 39–41F
Types:
- Left DLT: Bronchial limb enters left main bronchus — preferred in most cases (longer left main bronchus = wider safety margin)
- Right DLT: Has Murphy eye (ventilation hole) for right upper lobe; used when left bronchus is involved (left pneumonectomy, left bronchial surgery, left main stem tumour/stricture)
Confirmation of position: Fibreoptic bronchoscopy (gold standard) — should visualize carina + blue cuff just below left main bronchus takeoff
Indications for OLV/DLT
Absolute (Lung isolation mandatory):
- Prevent contamination of healthy lung: pulmonary abscess, massive haemoptysis, empyema (pus), bronchopleural fistula
- Differential lung ventilation (different PEEP each lung)
- Unilateral bronchopulmonary lavage (pulmonary alveolar proteinosis)
Relative (Surgical exposure):
- Pulmonary resection (pneumonectomy, lobectomy, segmentectomy)
- Oesophagectomy (thoracoscopic or open)
- Thoracic aortic surgery (VATS, descending aorta)
- Anterior thoracic spine surgery
- VATS procedures
- Minimally invasive cardiac surgery
Complications of DLT
Intraoperative:
- Malposition — most common
- Too deep: enters wrong bronchus → collapse of both lungs
- Too shallow: both lungs ventilated, no isolation
- Right DLT: Murphy eye may obstruct RUL → RUL collapse
- Hypoxia during OLV: V/Q mismatch, ↑ shunt (non-ventilated lung)
- Airway trauma: Tracheobronchial rupture (overinflation of bronchial cuff — inflate with minimum volume to seal)
- Tooth/airway damage during insertion (large tube)
- Obstruction: Secretions, blood
Postoperative:
- Sore throat, hoarseness
- Bronchial rupture (rare) — more risk with right DLT
Troubleshooting OLV hypoxia (FLAP-i):
- FiO₂ → increase to 1.0
- Lung recruitment of dependent (ventilated) lung
- Apply PEEP to dependent lung (5–10 cmH₂O)
- PEEP/CPAP to non-dependent (collapsed) lung
- inform surgeon to allow intermittent re-expansion
Q9. Difficult Airway Algorithm and Blocks Used in Awake Fibreoptic Intubation
Difficult Airway Algorithm (ASA/DAS 2022 approach)
Anticipated Difficult Airway: Awake Intubation is the default
ASA Algorithm steps (unanticipated difficult intubation):
- Preoxygenation (mandatory — 3 min tidal breathing or 8 vital capacity breaths with FiO₂ = 1.0)
- Direct laryngoscopy × 2 attempts → if failed → declare difficult intubation
- Facemask ventilation (maintain oxygenation)
- Plan B: Video laryngoscope, different blade, stylet/bougie
- Plan C: Supraglottic airway (SGA: LMA/iGel)
- Plan D (CICO — Cannot Intubate, Cannot Oxygenate):
- Front-of-neck airway (FONA): Surgical cricothyrotomy (scalpel-finger-bougie technique) — preferred in emergency
- Needle cricothyrotomy (temporizing measure)
DAS Guidelines key principles:
- Limit intubation attempts (maximum 3 + 1 by expert)
- Call for help early
- Avoid multiple blind attempts
- Maintain oxygenation at every step
- "If in doubt, don't" — wake up, abandon if non-emergent
Awake Fibreoptic Intubation (AFOI)
Indications:
- Predicted difficult airway (Mallampati III/IV, short neck, limited neck extension, OSA)
- Cervical spine instability (trauma, RA, ankylosing spondylitis)
- Previous failed intubation
- TMJ ankylosis, pharyngeal mass
- Obese with multiple predictors
Drugs for AFOI:
Premedication:
- Antisialogogue: Glycopyrrolate 0.2–0.3 mg IM/IV (30 min before) — dries secretions, improves visibility
- Anxiolytic: Midazolam 1–2 mg IV
Sedation (to maintain cooperation):
- Dexmedetomidine 1 mcg/kg over 10 min, then 0.2–0.7 mcg/kg/hr — preferred (sedation without respiratory depression, cooperative patient)
- Remifentanil TCI (target 1–2 ng/mL) — co-sedation
- Fentanyl 25–50 mcg aliquots
- Avoid heavy sedation (defeats the purpose of AFOI)
Regional Blocks for AFOI
1. Nasal route — topicalisation:
- Co-phenylcaine spray (lignocaine + oxymetazoline) or cocaine 4% (nasal decongestant + anaesthetic)
- Nasal airway lubricated with lignocaine gel
2. Airway blocks:
a) Superior Laryngeal Nerve (SLN) Block (internal branch):
- Anaesthetises the laryngeal mucosa above vocal cords (epiglottis, aryepiglottic folds, arytenoids)
- Technique: Lateral approach — identify thyrohyoid membrane, inject 2 mL 2% lignocaine beneath each cornu of the hyoid bone, just lateral to midline
- Target nerve: Internal branch of SLN
b) Transtracheal (Transcricoid) Block:
- Anaesthetises the mucosa below the vocal cords (trachea)
- Technique: 22G needle through cricothyroid membrane in midline, confirm air aspiration, inject 2–4 mL 4% lignocaine at end-expiration → immediate cough distributes LA
- Provides anaesthesia from cords to carina
c) Glossopharyngeal Nerve Block:
- Anaesthetises the oropharynx, posterior tongue, tonsillar pillars
- Technique: Peritonsillar injection at posterior palatoglossal arch (tonsillar pillar) with 2 mL 1% lignocaine; risk of carotid artery puncture
- Alternative: Anterior tonsillar pillar approach
d) Topical pharyngeal anaesthesia:
- 10% lignocaine spray to oropharynx and tongue
- Nebulised 4% lignocaine (preferred — no block needed, safe): 4 mL via nebuliser over 20 min — covers from nose to trachea
3. "All-in-one" approach (most common):
- Nebulised lignocaine 4% (4 mL)
- Topical 10% lignocaine spray to posterior pharynx
- Transtracheal block 4% lignocaine
- ± SLN block
Maximum safe dose of lignocaine for topical airway anaesthesia: 9 mg/kg (topical absorption is lower than IV; most use ≤8 mg/kg)
Q10. Malignant Hyperthermia and Compartment Syndrome
(Note: The question paper lists these together — answered separately as they are two distinct conditions linked by the MH notes in the image)
A. Malignant Hyperthermia (MH)
Definition: Pharmacogenetic disorder of skeletal muscle Ca²⁺ regulation triggered by volatile anaesthetics and succinylcholine → uncontrolled release of Ca²⁺ from sarcoplasmic reticulum → sustained muscle contraction and hypermetabolism.
Genetics: Autosomal dominant; RyR1 gene mutation (ryanodine receptor type 1) most common; also CACNA1S. Penetrance variable.
Triggers:
- All volatile agents (halothane, sevoflurane, isoflurane, desflurane)
- Succinylcholine
- (Stress, exercise — for exercise-induced MH variants)
Safe agents (can use in MH-susceptible):
- Propofol, midazolam, ketamine, opioids, all NMBDs except succinylcholine, local anaesthetics, N₂O (safe)
Clinical Features (Mnemonic: TEMP rise + CO₂ + Rigidity):
Early signs:
- Masseter muscle rigidity (esp. after succinylcholine)
- ↑ EtCO₂ (earliest and most sensitive sign — CO₂ production soars)
- Tachycardia, tachypnoea
- Generalised muscle rigidity
- Hyperthermia (temperature rise 1–2°C every 5 min → can reach >42°C)
- Metabolic + respiratory acidosis
Late signs:
- Hyperthermia (prominent)
- Rhabdomyolysis → dark urine (myoglobinuria)
- ↑CPK (>20,000 IU/L)
- Hyperkalaemia (cardiac arrhythmias → VF)
- Acute renal failure
- DIC
- Cardiac arrhythmias
Management (MHAUS Protocol):
Immediate actions:
- Call for help — dedicated MH team
- Stop all triggering agents (volatile agent off, stop succinylcholine)
- Flush anaesthesia machine — high O₂ flow (≥10 L/min) × 10 min; change circuit + soda lime
- Maintain surgery if life-threatening; otherwise conclude and wake up
- Dantrolene — definitive treatment
- Initial dose: 2.5 mg/kg IV (rapid bolus)
- Repeat 1 mg/kg boluses every 5 min until symptoms controlled
- Total dose: up to 10 mg/kg (or more if needed)
- Mechanism: Blocks ryanodine receptor (RyR1), preventing Ca²⁺ release from SR
- Preparation: Each vial = 20 mg dantrolene + 3g mannitol in 60 mL sterile water (difficult to reconstitute — need multiple personnel)
- Dantrolene nanosuspension (Ryanodex): 250 mg/vial — reconstitutes rapidly in 5 mL
Specific treatments:
- Cooling: Ice packs to axilla/groin/head, IV cold saline (10 mL/kg × 3 boluses), cooling blanket; stop cooling at 38.5°C
- Treat hyperkalaemia: Calcium gluconate IV, insulin + dextrose, NaHCO₃ (if metabolic acidosis)
- Treat acidosis: Sodium bicarbonate (if pH <7.2)
- Arrhythmias: If VT/VF — cardiovert; do NOT use calcium channel blockers (CCB) with dantrolene (risk of hyperkalemia + cardiac arrest)
- Urine output: Maintain >1 mL/kg/hr with IV fluids; Furosemide if needed (prevent renal failure from myoglobinuria)
- Catheterise: Urine output monitoring essential
Monitoring:
- ABG, electrolytes, CK, coagulation (DIC screen), urine myoglobin
- Core temperature (oesophageal/rectal/bladder)
- ECG continuous
Postoperative:
- ICU monitoring for 24–48 hrs
- Dantrolene 1 mg/kg IV 4-hourly for 24h (to prevent recurrence)
- Genetic counselling + RYR1 mutation testing for patient and family
- Caffeine-halothane contracture test (CHCT) for susceptibility testing
- MHAUS hotline: 1-800-MH-HYPER
B. Compartment Syndrome (as relevant in TKR/tourniquet context)
Definition: Condition where pressure within a closed muscle compartment rises to a level that compromises perfusion, leading to ischaemia.
Critical pressure: Compartment pressure > 30 mmHg (or within 30 mmHg of diastolic BP = delta pressure <30 mmHg) → fasciotomy indicated
Causes in orthopaedic anaesthesia:
- Prolonged tourniquet use (>90 min), tourniquet pressure too high
- Tight cast/bandage post-surgery
- Reperfusion injury post-tourniquet
- Trauma, fractures
Signs (5Ps): Pain (disproportionate, especially on passive stretch), Pressure (tense compartment), Paraesthesia, Pallor, Pulselessness (late)
Treatment: Emergency fasciotomy — release ALL compartments; do NOT elevate limb above heart level; IV fluids, maintain MAP
Sources: Miller's Anesthesia 10e, Barash Clinical Anesthesia 9e, Morgan & Mikhail Clinical Anesthesiology 7e, Katzung Pharmacology 16e, MHAUS Guidelines 2020, ALS Guidelines 2021, DAS Guidelines 2015/2022, ASA Difficult Airway Algorithm 2022