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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:
LocationPO₂ (mmHg)
Dry atmospheric air159
Humidified tracheal air149
Alveolar gas (PAO₂)~100
Arterial blood (PaO₂)~95
Capillary/tissue40
Mitochondria1–5
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

PropertyValue
MAC (adults)6–7%
Blood:gas partition coefficient0.45 (lowest among volatiles → fastest wash-in/out)
Oil:gas partition coefficient18.7
SVP at 20°C669 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

PropertyValue
ClassUltra-short acting μ-opioid agonist
StructureEster linkage in side chain
MetabolismPlasma & tissue esterases (organ independent)
Elimination half-life3–5 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:
  1. Confirmation of ETT placement (most reliable method)
  2. Monitoring ventilation adequacy
  3. Detecting oesophageal intubation (flat trace)
  4. Detecting air embolism (sudden ↓ EtCO₂)
  5. Detecting endobronchial intubation
  6. ROSC during CPR (sudden ↑ EtCO₂ >40 mmHg)
  7. Monitoring metabolic rate (↑ in MH, thyroid storm)
  8. Guide to diagnosis: shark-fin pattern = bronchospasm; plateau disappears = sampling error

Neuromonitoring (Intraoperative Neurophysiological Monitoring – IONM)

ModalityWhat it monitorsAlert criteria
EEGCortical activity, depth of anaesthesiaBurst 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 fossaWave V loss
EMGCranial nerve/nerve root integrityFree-run or evoked
TCDCerebral blood flow velocityEmboli 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

  1. Ventricular Fibrillation (VF)
  2. Pulseless Ventricular Tachycardia (pVT)

Non-Shockable Rhythms

  1. Pulseless Electrical Activity (PEA)
  2. 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):
  1. Deliver 1 shock (200 J biphasic, or 360 J monophasic)
  2. Immediately resume CPR × 2 minutes
  3. After 2 min → reassess rhythm
  4. If VF/pVT persists → 2nd shock → CPR 2 min
  5. After 3rd shock: Adrenaline 1 mg IV + Amiodarone 300 mg IV
  6. Subsequent adrenaline every 3–5 min (alternate cycles)
  7. After 5th shock: Amiodarone 150 mg additional dose (if VT/VF refractory)

IF NON-SHOCKABLE (PEA/Asystole):
  1. Continue CPR 30:2
  2. Adrenaline 1 mg IV immediately (as soon as IV access obtained)
  3. Adrenaline every 3–5 min
  4. 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:
  1. 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)
  2. Infrainguinal US-guided: Femoral vessels identified; LA deposited between fascia iliaca and iliopsoas lateral to femoral nerve
  3. 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):
  1. Prevent contamination of healthy lung: pulmonary abscess, massive haemoptysis, empyema (pus), bronchopleural fistula
  2. Differential lung ventilation (different PEEP each lung)
  3. Unilateral bronchopulmonary lavage (pulmonary alveolar proteinosis)
Relative (Surgical exposure):
  1. Pulmonary resection (pneumonectomy, lobectomy, segmentectomy)
  2. Oesophagectomy (thoracoscopic or open)
  3. Thoracic aortic surgery (VATS, descending aorta)
  4. Anterior thoracic spine surgery
  5. VATS procedures
  6. Minimally invasive cardiac surgery

Complications of DLT

Intraoperative:
  1. 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
  2. Hypoxia during OLV: V/Q mismatch, ↑ shunt (non-ventilated lung)
  3. Airway trauma: Tracheobronchial rupture (overinflation of bronchial cuff — inflate with minimum volume to seal)
  4. Tooth/airway damage during insertion (large tube)
  5. Obstruction: Secretions, blood
Postoperative:
  1. Sore throat, hoarseness
  2. 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):
  1. Preoxygenation (mandatory — 3 min tidal breathing or 8 vital capacity breaths with FiO₂ = 1.0)
  2. Direct laryngoscopy × 2 attempts → if failed → declare difficult intubation
  3. Facemask ventilation (maintain oxygenation)
  4. Plan B: Video laryngoscope, different blade, stylet/bougie
  5. Plan C: Supraglottic airway (SGA: LMA/iGel)
  6. 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:
  1. Call for help — dedicated MH team
  2. Stop all triggering agents (volatile agent off, stop succinylcholine)
  3. Flush anaesthesia machine — high O₂ flow (≥10 L/min) × 10 min; change circuit + soda lime
  4. Maintain surgery if life-threatening; otherwise conclude and wake up
  5. 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
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