PART 1: Mitral Stenosis (MS) in Pregnancy Posted for Emergency LSCS - Anaesthetic Considerations and Management
Pathophysiology Relevant to Anaesthesia
Mitral stenosis (most commonly rheumatic) obstructs left ventricular inflow. Left atrial pressure must rise to maintain cardiac output. Key haemodynamic vulnerabilities:
- Heart rate (HR) is the most critical variable - tachycardia reduces diastolic filling time, escalates LA pressure, and precipitates pulmonary oedema
- Preload dependence - the stenotic valve requires maintained preload to generate adequate forward flow; however, fluid overload raises LA pressure
- Pulmonary hypertension - secondary to chronic LA hypertension; manipulation of PVR determines right heart stability
- Fixed cardiac output - the patient cannot increase CO in response to the haemodynamic demands of pregnancy, labour, and surgery
- Atrial fibrillation - loss of atrial kick and fast ventricular rate causes dramatic haemodynamic deterioration
Pregnancy aggravates MS via: 40-50% increase in blood volume, 25-30% rise in HR, 40-50% increase in cardiac output - all peaking at 28-32 weeks and during labour/delivery.
WHO risk classification: Severe symptomatic MS = Class IV (pregnancy contraindicated)
Preoperative Assessment (Emergency - Time-Compressed)
History and symptoms:
- NYHA class, exercise tolerance
- Symptoms: dyspnoea, orthopnoea, haemoptysis, palpitations
- Onset/duration of any AF
- Current medications (digoxin, beta-blockers, diuretics, anticoagulants)
Investigations (as available urgently):
- ECG - look for AF, P-mitrale (bifid P in sinus rhythm), RVH, right axis deviation
- Echocardiogram - mitral valve area (MVA) defines severity:
- Mild MS: MVA >1.5 cm²
- Moderate MS: MVA 1.0-1.5 cm²
- Severe MS: MVA <1.0 cm²
- Also assess: LA size, PAP, pulmonary pressures, LV function, TR
- CXR - cardiomegaly, pulmonary oedema, Kerley B lines
- ABG if hypoxic
- Full blood count, coagulation profile (if on anticoagulants), renal function
- SpO2
Functional assessment: CARPREG score, mWHO classification
Haemodynamic Goals for Anaesthesia in MS
| Parameter | Goal | Rationale |
|---|
| Heart rate | Slow - 60-80 bpm | Most important; tachycardia is catastrophic |
| Rhythm | Sinus rhythm | AF with fast rate = acute decompensation |
| Preload | Maintain (avoid hypovolaemia and overload) | Stenotic valve needs preload; but overload raises LA pressure |
| Afterload (SVR) | Maintain or slightly increase | Avoid vasodilation; hypotension compromises coronary and uterine blood flow |
| Contractility | Maintain | LV function usually preserved in pure MS |
| PVR | Minimise | Avoid hypoxia, hypercarbia, acidosis, pain, hypothermia |
| Aortocaval compression | Avoid | Left lateral tilt 15° mandatory |
Mnemonic: SRPAL - Slow rate, Sinus rhythm, Preload maintain, Afterload maintain, Limit PVR rise
Multidisciplinary Team Preparation
- Anaesthesiologist (senior/consultant), obstetrician, cardiologist on standby
- Neonatologist for baby
- ICU/HDU bed arranged for postoperative care
- IABP/ECMO team on standby in severe cases with PHT
- Blood bank alert
Monitoring (Invasive Monitoring is Essential)
Mandatory:
- Intra-arterial line (A-line) - beat-to-beat BP, beat-to-beat arterial waveform, ABG access
- Central venous catheter - CVP monitoring, vasopressor/inotrope infusion
- SpO2, ETCO2, ECG (5-lead), temperature
- Continuous urine output (Foley catheter)
- Fetal heart rate monitoring until delivery
Consider in severe MS/PHT:
- Pulmonary artery catheter (rarely used now) - PCWP monitoring
- Transoesophageal echocardiography (TOE/TEE) if available - most valuable real-time haemodynamic monitor
Choice of Anaesthetic Technique
Option 1: Epidural Anaesthesia (PREFERRED for emergency LSCS in stable/moderate MS)
Advantages:
- Slow, titrated onset - gradual sympathectomy, avoids sudden vasodilation
- Allows incremental dosing to maintain haemodynamic stability
- Avoids airway manipulation and intubation stress (which causes tachycardia)
- Better postoperative analgesia - prevents pain-induced tachycardia
- Epidural catheter can be used for labour analgesia if patient was in labour
Technique:
- Position: left lateral decubitus (15° tilt after sitting for epidural) - avoid supine hypotension
- Level: L2-L3 interspace
- Test dose: 3 ml of 2% lignocaine + adrenaline (1:200,000)
- Incremental doses: 0.5% bupivacaine in 5 ml aliquots to achieve T4-T6 level
- Slow titration is the key - target level T4 (allows handling of uterus without pain)
- Supplement with epidural fentanyl (50-100 mcg) for analgesia and to reduce bupivacaine dose
- Manage hypotension with small doses of phenylephrine (vasopressor of choice - does not increase HR) or noradrenaline; avoid ephedrine (causes tachycardia)
- IV crystalloid judiciously - avoid fluid bolus loading (worsens MS)
Phenylephrine infusion - 25-50 mcg/min prophylactically to prevent post-spinal/post-epidural hypotension
Option 2: Combined Spinal-Epidural (CSE) - Cautious Use
- Preferred if time is critical and epidural titration is slow
- Use low-dose spinal: 1.5-2 ml of 0.5% heavy bupivacaine (7.5-10 mg) + fentanyl 15-25 mcg intrathecally
- Establish epidural catheter simultaneously for supplementation
- Risk: even low-dose spinal can cause abrupt vasodilation in severe MS - have vasopressors ready
Option 3: General Anaesthesia (for truly emergent situations, failed regional, or severe PHT)
Indications for GA:
- Patient refusal of regional
- Coagulopathy (anticoagulants - not reversed)
- True emergency (category 1 LSCS - <30 min decision-to-delivery)
- Failed regional block
- Severe pulmonary hypertension with haemodynamic instability
GA Goals:
- Blunt intubation response (tachycardia from laryngoscopy is dangerous)
- Avoid all tachycardia-inducing drugs
Induction sequence (Modified RSI):
- Preoxygenation: 100% O2 for 3-5 min (SpO2 >94% mandatory, FRC reduced in pregnancy)
- Antacid prophylaxis: sodium citrate 30 ml PO + IV ranitidine/metoclopramide
- Pre-induction beta-blockade: esmolol 0.5-1 mg/kg IV (short-acting, controls intubation tachycardia; monitor fetal HR after delivery), or metoprolol 1-2 mg IV
- Fentanyl 2-3 mcg/kg IV (2-3 min before induction) - blunts laryngoscopy response
- Induction agent: Etomidate 0.2-0.3 mg/kg (haemodynamic stability) - preferred. Ketamine and thiopentone are alternatives but ketamine increases HR (AVOID in MS); thiopentone can cause vasodilation
- Muscle relaxant: Rocuronium 1 mg/kg (RSI dose) - succinylcholine 1.5 mg/kg acceptable (use with caution - increases HR with repeated doses)
- Sellick's cricoid pressure during RSI
- Laryngoscopy - rapid and smooth; topical lignocaine 4% spray or IV lignocaine 1.5 mg/kg 3 min before intubation to blunt response
- Intubate with 7-7.5 mm cuffed ETT
Maintenance:
- O2:N2O (50:50) or O2:air - avoid high N2O (fetal concerns, debated)
- Isoflurane/sevoflurane at low MAC (0.5-1 MAC) - reduce in pregnancy (MAC reduced 25-30%)
- IV fentanyl infusion for analgesia
- Atracurium for neuromuscular blockade (non-depolarising)
- Avoid halothane (sensitises to arrhythmias)
- Control ventilation: maintain normocarbia (EtCO2 32-35 mmHg) - hypercarbia increases PVR
Post-delivery management (after cord clamping):
- Oxytocin: give as SLOW infusion (10 units in 500 ml NS over 4-8 hours) - avoid bolus; oxytocin bolus causes profound vasodilation, hypotension, reflex tachycardia - can be catastrophic in MS
- Ergometrine/Syntometrine: CONTRAINDICATED in MS (causes severe hypertension and pulmonary oedema)
- Carboprost (prostaglandin F2α): use with caution - can cause pulmonary vasoconstriction
- Misoprostol: safer alternative uterotonic in MS
Drugs to AVOID in MS
| Drug | Reason to Avoid |
|---|
| Atropine | Causes tachycardia |
| Ketamine | Increases HR and SVR |
| Pancuronium | Causes tachycardia |
| Ephedrine | Beta-agonist, increases HR |
| Ergometrine/Syntometrine | Severe vasoconstriction, pulmonary oedema |
| Glycopyrrolate (routine dose) | Tachycardia |
| Meperidine/pethidine | Increases HR |
| Halothane | Arrhythmogenic |
Special Situations
If Patient is in AF at Presentation:
- Rate control is priority: IV digoxin (slow), or IV metoprolol 1-5 mg (titrated)
- Esmolol infusion (50-300 mcg/kg/min) for acute control
- DC cardioversion if haemodynamically unstable AF in emergency (50-100 J synchronised)
- Anticoagulation if AF >48 hours (risk of embolism)
If Pulmonary Oedema is Present:
- IV furosemide 40 mg
- Sit patient upright, oxygen
- Controlled ventilation if severe
- Proceed to emergency LSCS once stabilised or if fetal distress mandates immediate delivery
If Severe PHT (PAP >50% systemic or >50 mmHg):
- Very high-risk - maternal mortality up to 50%
- Consider inhaled NO (20 ppm) - reduces PVR without systemic vasodilation
- Sildenafil pre-loaded if time permits
- Vasopressors: phenylephrine preferred, noradrenaline second
- Avoid RV afterload increase (hypercarbia, hypoxia, acidosis)
Postoperative Management
- ICU/HDU mandatory - haemodynamic instability peaks in puerperium (autotransfusion effect)
- Continue arterial line monitoring for 24-48 hours
- Analgesic plan: epidural catheter left in situ for continued analgesia (prevents tachycardia from pain); IV paracetamol + IV opioids as needed
- Continue beta-blocker therapy
- Anticoagulation: restart when surgically safe
- Monitor for: pulmonary oedema, arrhythmia, cardiac failure, DVT/PE
- Fluid balance strictly negative postoperatively
- DVT prophylaxis
PART 2: Non-Obstetric Surgery in the Pregnant Patient - Anaesthetic Considerations and Management
Epidemiology
- Approximately 1-2% of pregnant women require non-obstetric surgery during pregnancy
- Most common indications: acute appendicitis, cholecystitis, ovarian cysts, trauma, adnexal masses, cardiac surgery
- Emergency surgery cannot be deferred - should proceed regardless of trimester
Physiological Changes of Pregnancy Relevant to Anaesthesia
Respiratory System
| Change | Anaesthetic Implication |
|---|
| Decreased FRC (by 20-30%) | Rapid desaturation during apnoea |
| Increased oxygen consumption (20-30%) | Apnoea tolerance reduced - desaturation in <90 sec |
| Mucosal oedema, capillary engorgement of airway | Difficult intubation, use smaller ETT (7.0 mm) |
| Progesterone raises respiratory drive, hyperventilation | Reduced PaCO2 (32 mmHg normal); target EtCO2 32-35 |
| Reduced MAC (25-30%) | Less inhalational agent required |
Cardiovascular
| Change | Implication |
|---|
| 40-50% increase in blood volume | Dilutional anaemia; altered drug volumes |
| HR increases 15-20% | Baseline tachycardia |
| CO increases 40-50% | Altered pharmacokinetics |
| SVR decreases | Lower BP (mid-pregnancy physiological hypotension) |
| Aortocaval compression (from 20 weeks) | Left lateral tilt mandatory; supine position reduces CO by 25% |
Gastrointestinal
- Reduced LES tone, raised intra-abdominal pressure = increased aspiration risk
- Aspiration precautions from 16-18 weeks (many practitioners from first trimester or whenever uterus becomes intra-abdominal)
- Delayed gastric emptying during active labour (NOT in non-labouring pregnant patients - gastric emptying is normal)
Haematological
- Hypercoagulable state - increased risk DVT/PE
- Reduced plasma cholinesterase (affects suxamethonium - duration prolonged)
- Physiological anaemia (dilutional)
Renal
- Increased GFR - faster clearance of renally excreted drugs
- Physiological glycosuria
Timing of Surgery
| Urgency | Approach |
|---|
| Elective | Defer until postpartum |
| Semi-elective | Best in 2nd trimester - organogenesis complete (fetal safety), uterus not yet causing significant compression, lowest risk of preterm labour |
| Emergency | Proceed regardless of trimester - never deny necessary surgery |
First trimester concern: organogenesis (day 15 - day 56); teratogen exposure risk highest
Third trimester concern: premature labour, difficult airway, aortocaval compression
Teratogenicity of Anaesthetic Drugs
| Drug | Safety |
|---|
| Thiopentone | Safe (category B) |
| Propofol | Widely used, considered safe; limited human data |
| Etomidate | Limited data; adrenal suppression concern |
| Ketamine | Avoid high doses; increases uterine tone in first trimester |
| Benzodiazepines | Avoid in 1st trimester - cleft palate association (controversial); safe otherwise |
| Opioids | Cross placenta - neonatal respiratory depression; use with care near delivery |
| Suxamethonium | Safe; dose may need adjustment (reduced pseudocholinesterase) |
| Rocuronium | Safe - large molecule, limited placental transfer |
| Isoflurane/sevoflurane | Generally safe; reduce MAC by 25-30% |
| Nitrous oxide | Avoid in 1st trimester (inhibits methionine synthase, theoretically teratogenic); short use in 2nd/3rd trimester acceptable |
| Local anaesthetics | Safe; reduced dose required (enhanced neural sensitivity, altered epidural space) |
| Neostigmine | Use with care - can increase uterine activity |
Fetal Considerations
Goals:
- Avoid teratogens (especially 1st trimester)
- Maintain uteroplacental perfusion
- Prevent preterm labour
- Avoid fetal asphyxia
Uterine blood flow is NOT autoregulated - entirely dependent on maternal perfusion pressure (MAP). Hypotension directly reduces uterine perfusion.
- Maintain maternal MAP >65-80 mmHg (or within 20% of baseline)
- Treat hypotension immediately with phenylephrine (vasoconstrictor of choice in pregnancy - preserves uteroplacental blood flow without increasing HR); noradrenaline also acceptable
- Avoid ephedrine as first-line (increases fetal acidosis compared to phenylephrine - COMET trial)
- Avoid hyperventilation (PaCO2 <25 mmHg causes uterine vasoconstriction and fetal hypoxia)
- Avoid hypoventilation (PaCO2 >45 mmHg causes fetal respiratory acidosis)
- Target maternal PaCO2: 32-35 mmHg (normal in pregnancy)
Anaesthetic Technique
Regional vs General Anaesthesia
Regional anaesthesia is preferred when feasible:
- Minimises fetal drug exposure
- Maintains maternal airway reflexes
- Reduces aspiration risk
- Provides postoperative analgesia
- Better outcome data in obstetric population
Considerations with neuraxial:
- Increased sensitivity to local anaesthetics (25-30% dose reduction)
- Increased risk of hypotension - treat aggressively with phenylephrine
- Lipid rescue should be available at all times (increased toxicity risk)
General anaesthesia - when required:
- Rapid sequence induction from 16-18 weeks (or earlier by many guidelines)
- Preoxygenation: 3-5 min 100% O2 (or 4 vital capacity breaths) - essential given reduced FRC
- Cricoid pressure (Sellick's manoeuvre) - until ETT confirmed
- Use smaller ETT (6.5-7.0 mm) - mucosal oedema
- Antacid prophylaxis: sodium citrate 30 ml, ranitidine 150 mg oral or 50 mg IV, metoclopramide 10 mg IV (30-60 min before)
- Induction agent: propofol/thiopentone - standard doses; propofol infusion (TIVA) or volatile maintenance both acceptable
- Neuromuscular monitoring essential (altered pharmacokinetics)
- Reverse with sugammadex (rocuronium) or neostigmine - note neostigmine can stimulate uterus; use glycopyrrolate (not atropine) as anticholinergic
Airway Management in Pregnant Patient
| Risk | Management |
|---|
| Mallampati class increases with gestation | Detailed airway assessment; senior anaesthetist |
| Oedematous mucosa | Smaller ETT (6.5-7.0), gentle laryngoscopy |
| Rapid desaturation | Maximise preoxygenation; high-flow nasal oxygen during apnoea |
| Cannot intubate/cannot oxygenate | Must have plan: video-laryngoscope, LMA, surgical airway |
| Failed intubation rate in obstetric patients | 1:250-300 vs 1:2000 in general surgical population |
Airway plan: Have video laryngoscope (C-MAC/D-blade, King Vision) available. Failed intubation protocol must be in place. "In cannot intubate-cannot oxygenate" - proceed to surgical airway without delay.
Positioning
- Left lateral tilt (15°) from 16-18 weeks (or when uterus palpable above umbilicus)
- Prevents aortocaval compression by gravid uterus
- Use a wedge under right hip or tilt the operating table
Monitoring
| Monitor | Mandatory | Notes |
|---|
| ASA standard monitors (ECG, SpO2, NIBP/IBP, EtCO2, temperature) | Yes | |
| Fetal heart rate (Doppler/CTG) | Yes - before and after surgery | Continuous intraoperative monitoring if viable gestation and trained personnel available |
| Uterine contraction monitoring | Yes - post-surgery | For preterm labour detection |
Preterm labour monitoring: All patients of viable gestational age (>23-24 weeks) should have FHR and contraction monitoring before, during (if possible), and after surgery.
Specific Drug Considerations
Tocolytics:
- Do NOT use prophylactically
- Use only if evidence of preterm labour develops intraoperatively or postoperatively
- Indomethacin (1st/2nd trimester), nifedipine, or atosiban (2nd/3rd trimester)
- Volatile agents (isoflurane, sevoflurane) have uterine relaxing properties - slightly protective
Antibiotics:
- Cephalosporins, penicillins - safe in pregnancy
- Tetracyclines, quinolones - avoid
- Metronidazole - 2nd and 3rd trimester only for most indications
Anticoagulation:
- Low molecular weight heparin (LMWH) for DVT prophylaxis - safe
- Avoid warfarin (teratogenic in 1st trimester; crosses placenta)
Laparoscopic Surgery in Pregnancy - Special Considerations
- Safe in all trimesters - evidence supports safety
- Position: reverse Trendelenburg to displace uterus; use left tilt
- Pneumoperitoneum pressure: keep ≤15 mmHg (lower if possible - 10-12 mmHg preferred)
- CO2 insufflation causes: hypercapnia (absorbed CO2), fetal respiratory acidosis if maternal ventilation not adjusted
- Increase minute ventilation to maintain EtCO2 32-35 mmHg
- Open Hasson technique preferred for trocar insertion (avoids uterine injury)
- FHR monitoring before and after procedure
Postoperative Care
- Fetal monitoring: CTG for minimum 2 hours postoperatively (longer if surgery was prolonged or complicated)
- Uterine activity monitoring for 24 hours
- Multimodal analgesia: paracetamol + regional techniques preferred; opioids as needed (with caution near term)
- NSAIDs: Avoid after 28-32 weeks (risk: premature closure of ductus arteriosus)
- DVT prophylaxis: early mobilisation, compression stockings, LMWH
- Monitor for preterm labour symptoms
Key Points Summary Table
| Mitral Stenosis for Emergency LSCS | Non-Obstetric Surgery in Pregnancy |
|---|
| Primary concern | Tachycardia precipitating pulmonary oedema | Teratogenicity, uteroplacental perfusion, preterm labour |
| Preferred technique | Epidural (titrated, slow) | Regional if feasible; GA when required (RSI) |
| Critical drug avoidance | Atropine, ketamine, ephedrine, ergometrine | Nitrous oxide (1st trimester), NSAIDs >28 wks, benzodiazepines (1st trimester) |
| Vasopressor of choice | Phenylephrine (maintains SVR without raising HR) | Phenylephrine |
| Uterotonic of choice | Oxytocin slow infusion ONLY | N/A |
| Monitoring | A-line, CVP, TEE essential | FHR monitoring, EtCO2, CTG before and after |
| Postoperative setting | ICU/HDU | Labour ward HDU; CTG for 2+ hours |
| Most feared complication | Pulmonary oedema, AF with fast rate, RV failure | Fetal distress, preterm labour, maternal aspiration |
References
- Creasy & Resnik's Maternal-Fetal Medicine (Mitral Stenosis in Pregnancy section)
- Misra MK et al. "Mitral stenosis and pregnancy: Current concepts in anaesthetic practice." Indian J Anaesth (PMC2991654)
- Lal AK et al. "Anesthetic Management of Cesarean Sections in Parturients with Valvular Heart Disease." Can J Anaesth 2025 (PMC12103142)
- "Anesthetic Management of the Pregnant Patient Undergoing Non-Obstetric Surgery." J Med Life 2025 (PMC12028341)
- Braunwald's Heart Disease, 12e
- WFSA Update in Anaesthesia - Anaesthesia for non-obstetric surgery during pregnancy (PMC9947972)
- ACOG Practice Bulletin on non-obstetric surgery in pregnancy