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MS GENERAL SURGERY - EXAM ANSWERS
Nutrition | Fluid, Electrolytes & Acid-Base | Shock
SECTION A: NUTRITION IN SURGICAL PATIENTS
Q21. Calculate the composition of 3:1 TPN formula required for a 70kg man with an enterocutaneous fistula. How do you monitor a patient receiving TPN? (2023)
DEFINITION
TPN = delivery of all nutritional requirements intravenously when enteral route is not possible/insufficient. In a 3:1 bag: glucose : amino acids : lipid = 3:1 ratio of non-protein energy : protein energy, all in a single 3-litre bag.
CALCULATION FOR 70 kg MAN (ECF = hypermetabolic state)
Energy requirement:
- Stressed patient (ECF, sepsis risk) = 30-35 kcal/kg/day
- = 30 × 70 = 2100 kcal/day (use 2100-2500 kcal)
Macronutrient breakdown:
| Component | Requirement | Amount |
|---|
| Protein (N) | 0.25 g N/kg/day = 1.5 g protein/kg/day | 105 g protein (~16.8 g N) |
| Carbohydrate | 50-60% of non-protein calories | 200-300 g glucose |
| Fat | 30-50% of non-protein calories | 50-100 g lipid/day |
| Fluid | 30-35 mL/kg/day | 2100 mL (adjust for fistula output) |
Electrolytes (daily):
- Na: 0.9-1.2 mmol/kg = 70-84 mmol
- K: 1 mmol/kg = 70 mmol
- Phosphate: 20-30 mmol (essential - prevents hypophosphataemia)
- Ca: 5 mmol; Mg: 1 mmol
Vitamins: Folic acid 15 mg 1-2×/week; Vitamin B12 monthly; water-soluble vitamins daily; fat-soluble vitamins A, D, E, K added
ECF-specific extra: Add fistula output volume + replace Na, K, HCO3 lost in fistula fluid (small bowel fistula = high Na/K/bicarb losses)
MONITORING TPN PATIENT
Clinical:
- Daily weight, fluid balance, vitals
- Catheter site inspection daily (line sepsis in up to 15%)
- Look for signs of refeeding syndrome: arrhythmia, oedema, weakness
Biochemical (Frequency):
| Parameter | Frequency |
|---|
| Blood glucose | 4-6 hourly initially |
| Urea, creatinine, electrolytes (Na, K, Mg, PO4, Ca) | Daily |
| LFTs, albumin | Twice weekly |
| FBC, coagulation | Weekly |
| Zn, Cu, Se, ferritin, B12, folate, Vit D | If TPN >28 days; then every 3 months in long-term |
Line care:
- Strict aseptic technique; paired blood cultures if fever
- CXR post-insertion: tip at inferior third SVC or atrioventricular junction
- No femoral lines for PN
Q22. Discuss nutritional augmentation in surgical patients (NRS-2002) (2020)
DEFINITION
Nutritional augmentation = active intervention to meet/exceed estimated nutritional requirements in malnourished or at-risk surgical patients, going beyond mere maintenance.
NUTRITIONAL RISK SCREENING - NRS 2002
A validated tool to identify patients needing nutritional support:
- Score ≥3 = patient is at nutritional risk → start nutritional support
- Components: impaired nutritional status score + disease severity score + age adjustment (+1 if >70 years)
NRS-2002 Scoring:
| Nutritional Status | Disease Severity |
|---|
| 0 = normal | 0 = normal |
| 1 = mild (wt loss >5% in 3 mo, or food intake <50-75%) | 1 = mild (hip fracture, chronic disease) |
| 2 = moderate (wt loss >5% in 2 mo, BMI 18.5-20.5 + impaired intake) | 2 = moderate (major abdominal surgery, stroke, pneumonia) |
| 3 = severe (BMI <18.5 + impaired intake, wt loss >5% in 1 mo) | 3 = severe (ICU patient, head injury, bone marrow transplant) |
ASSESSMENT - ABCD
- Anthropometry: BMI, MUAC, TSF, MAMC, % weight change
- Biochemistry: albumin, CRP, WBC, Hb, electrolytes, phosphate
- Clinical: symptoms (nausea, dysphagia, diarrhoea), comorbidities
- Dietary: food diary, calorie intake vs calculated requirements
INDICATORS FOR SUPPORT
- BMI <18.5 + wt loss >10% in 3-6 months
- OR BMI <20 + wt loss >5% in 3-6 months
ROUTES OF AUGMENTATION (Enteral preferred over Parenteral)
- Oral supplements (ONS) - 200 kcal/200 mL carton, 2 g N per carton
- Nasogastric/nasojejunal tube feeding - 10-20 mL/h → 75 mL/h
- Gastrostomy/jejunostomy (surgical or PEG/PEJ)
- Supplemental/Total Parenteral Nutrition - when enteral not possible
Enhanced Recovery After Surgery (ERAS): Pre-op carbohydrate drinks up to 2 hours before surgery to reduce insulin resistance; early post-op feeding within 24 hours
Q23. Discuss the role of nutrition and its methods in surgical patients / Indications and techniques of supplementing nutrition in surgical patients (2017/2019)
WHY NUTRITION MATTERS IN SURGERY
- Metabolic response to surgery causes insulin resistance, catabolism, negative nitrogen balance
- Counter-regulatory hormones (adrenaline, cortisol, glucagon, GH) increase energy requirements up to 40 kcal/kg/day in severe stress
- Malnutrition → impaired wound healing, infection, prolonged stay, increased mortality
CALCULATING REQUIREMENTS
- Energy: 25-35 kcal/kg ideal body weight/day
- Protein: 0.15 g N/kg/day (normal) → 0.25 g N/kg/day (ill patient) = 1.5 g protein/kg/day
- Carbohydrate: 45-65% total calories; glucose minimum 100-200 g/day
- Fat: 30-50% calories; 100-200 g/week long chain triglycerides
METHODS (Enteral > Parenteral - always preferred)
A. Enteral Nutrition:
Preserves gut mucosal barrier, maintains immunity, prevents gut atrophy, lower infection rates, better wound healing
| Route | Indication |
|---|
| Oral supplements (ONS) | Mild-moderate malnutrition, able to swallow |
| Nasogastric tube | Short-term (<4 weeks), unable to eat |
| Nasojejunal tube | Gastroparesis, post-op delayed gastric emptying |
| PEG (Percutaneous Endoscopic Gastrostomy) | Long-term (>4 weeks) enteral feeding |
| Jejunostomy | Post-esophagectomy/gastrectomy, gastric dysfunction |
Starting rate: 10-20 mL/h, titrate up to 75 mL/h to avoid refeeding syndrome
B. Parenteral Nutrition (PN):
- Supplemental PN: enteral feeding inadequate
- TPN: enteral route impossible (short bowel syndrome, ECF, ileus, obstruction)
- Via PICC (weeks-months) or CVC (subclavian/IJV, tip at SVC/atrial junction)
- 3-litre bag: lipid emulsion + amino acids + glucose + electrolytes + vitamins + trace elements
- Energy ratio: 150-250 kcal per g of protein N; 30-50% energy from fat
C. ERAS Protocol:
- Pre-op CHO loading (carbohydrate drinks 2 hr pre-op)
- Minimise fasting; early post-op oral/enteral feeding
- Minimally invasive surgery where possible
MONITORING (see Q21)
Q24. Indications and contraindications of PN; monitoring; complications; catheter issues; Home PN (2011/2013)
INDICATIONS FOR PN
- Short bowel syndrome (massive intestinal resection, <200 cm small bowel)
- Intestinal fistulation (enterocutaneous fistula - high output)
- Severe gut failure/ileus
- Acute severe pancreatitis (if enteral not tolerated)
- Bowel obstruction, radiation enteritis
- Severe inflammatory bowel disease unresponsive to treatment
- Pre-op optimization in severely malnourished patients when surgery needs to be delayed
- Post-major GI surgery when enteral route unavailable
Supplemental PN: when enteral intake < 60% requirements for > 7-10 days
CONTRAINDICATIONS
- Functional gut available (relative - enteral always preferred)
- Short expected duration (<7 days)
- Haemodynamic instability (correct first)
- No vascular access possible
MONITORING (See Q21)
COMPLICATIONS
A. Insertion Complications:
- Pneumothorax (0.5-1%, most common with subclavian approach)
- Line misplacement (confirm on CXR - tip at inferior 1/3 SVC/AV junction)
- Arterial puncture, haemothorax, air embolism
B. Line Complications:
- Line sepsis (most important - up to 15% of patients; → septicaemia, fungal infections causing uveitis and endocarditis)
- Management: paired blood cultures (line + peripheral), stop line use, remove if cultures positive, antibiotics
- Line thrombosis: SVC occlusion, PE → anticoagulate
C. Metabolic Complications:
- Refeeding syndrome (hypophosphataemia, K, Mg, Ca shifts - arrhythmia, respiratory failure, death)
- Hyperglycaemia (use variable insulin infusion)
- Hypoglycaemia (when PN interrupted without adjusting insulin)
- Liver dysfunction/fatty liver (>25% long-term) → IFALD (intestinal failure-associated liver disease)
- Metabolic bone disease
- Vitamin deficiencies (B12, fat-soluble A,D,E,K)
CATHETER ISSUES IN PN
- PICC (basilic > cephalic/brachial vein): weeks to months; preferred long-term
- CVC (subclavian/IJV): check CXR post-insertion; AVOID femoral lines (infection risk)
- Tunnelled catheters / implanted ports (Hickman, Port-a-cath): for Home PN
- Occlusion treated with urokinase/tPA instillation
- Infection: antibiotic lock therapy or line removal
HOME PARENTERAL NUTRITION (HPN)
- Indication: long-term intestinal failure (short bowel, chronic motility disorder, radiation enteritis)
- Via tunnelled central venous catheter or implanted port
- Overnight infusion (12-16 hr/day) to allow daytime freedom
- Patient and carer training essential
- Regular monitoring: micronutrients (Zn, Cu, Se, ferritin, B12, Vit D) - every 3 months
- Complications: IFALD, metabolic bone disease, sepsis
- Multidisciplinary team: surgeon, dietitian, nurse, pharmacist
Q25. Immunonutrition in surgical patients (2014)
DEFINITION
Immunonutrition = addition of specific pharmaconutrients to enteral/parenteral feeds to modulate the immune response, reduce inflammation and improve surgical outcomes.
KEY IMMUNONUTRIENTS
| Nutrient | Mechanism | Benefit |
|---|
| Glutamine | Fuel for enterocytes and lymphocytes; maintains gut barrier; antioxidant (GSH synthesis) | Reduced infections, gut permeability, length of stay |
| Arginine | Substrate for NO synthesis; T-cell proliferation; wound healing | Improved immune function, N balance |
| Omega-3 fatty acids (EPA/DHA) | Anti-inflammatory (replace AA-derived prostaglandins); modulate macrophage cytokine production | Reduced systemic inflammation, organ failure |
| Nucleotides | Necessary for rapidly dividing immune cells | Enhanced T-cell response |
| Selenium, Zinc, Vitamins C & E | Antioxidants; reduce oxidative stress | Reduced infection, better wound healing |
INDICATIONS
- Major elective GI surgery (upper GI especially)
- Critically ill surgical patients (ICU)
- Severe trauma and burns
- Patients at high nutritional risk (NRS-2002 ≥3)
EVIDENCE (Bailey & Love 28e)
- ESPEN guidelines support pre-op immunonutrition for 5-7 days before major GI surgery
- Combination feeds (arginine + omega-3 + nucleotides) most evidence
- Reduces: infectious complications, anastomotic leak rate, length of stay
- Glutamine supplementation in PN associated with reduced infections in ICU patients
REFEEDING SYNDROME (bonus scoring point)
- Monitor phosphate, K, Mg, Ca when starting feeds in malnourished patients
- Start at 10 kcal/kg/day max; supplement thiamine (vitamin B1) before feeds
Q26. Percutaneous Endoscopic Gastrostomy (PEG) (2010)
DEFINITION
PEG = endoscopically guided placement of a feeding tube through the anterior abdominal wall directly into the stomach, under local anaesthesia ± sedation.
INDICATIONS
- Long-term enteral feeding (>4 weeks) when oral intake inadequate
- Neurological dysphagia (stroke, MND, head injury, Parkinson's, dementia)
- Head and neck cancers (post-radiation, post-surgery)
- Oesophageal obstruction (malignancy)
- Cystic fibrosis, failure to thrive
- Chronic respiratory failure requiring nocturnal feeding
CONTRAINDICATIONS
- Absolute: inability to perform upper GI endoscopy, inability to transilluminate anterior abdominal wall, previous total gastrectomy
- Relative: ascites, peritoneal dialysis, coagulopathy, obesity, gastric varices, previous abdominal surgery
TECHNIQUE (Pull/Push/Introducer Methods)
Pull technique (Ponsky-Gauderer - most common):
- Patient supine; IV sedation/LA
- Upper GI endoscopy; stomach insufflated; transilluminate anterior abdominal wall
- Skin incision + needle cannula puncture into stomach under endoscopic vision
- Guidewire passed through cannula into stomach; grasped by endoscope
- Wire pulled out through mouth
- PEG tube attached to wire; pulled back down oesophagus and through abdominal wall
- Internal bumper secures tube against gastric wall; external disk/clamp secures at skin
Push (Sacks-Vine) and Introducer (Russell) are alternatives.
POST-PROCEDURE
- CXR/X-ray at 4 hours if any concern
- Feed commenced within 4-6 hours
- Tube site cleaned daily; inspect for buried bumper, cellulitis, leakage
COMPLICATIONS
| Early | Late |
|---|
| Bleeding, perforation | Tube blockage, displacement |
| Aspiration during procedure | Buried bumper syndrome |
| Peritonitis (rare) | Peristomal infection/leakage |
| Tumour seeding (in H&N ca) | Granulation tissue |
REPLACEMENT/REMOVAL
- PEG can be removed when no longer needed (endoscopically or traction if balloon type)
- Replaced by balloon gastrostomy button after tract established (4-6 weeks)
SECTION B: FLUID, ELECTROLYTES & ACID-BASE BALANCE
Q27. Describe ABG, metabolic alkalosis, metabolic acidosis - causes, management, complications/significance (2020)
NORMAL ABG VALUES
| Parameter | Normal Range |
|---|
| pH | 7.35-7.45 |
| PaCO2 | 35-45 mmHg |
| PaO2 | 75-100 mmHg |
| HCO3- | 22-26 mmol/L |
| Base Excess (BE) | -2 to +2 |
| SpO2 | 95-100% |
STEP-BY-STEP ABG INTERPRETATION
- pH → acidaemia (<7.35) or alkalaemia (>7.45)?
- Primary disorder: ↓pH + ↑CO2 = resp. acidosis; ↓pH + ↓HCO3 = met. acidosis
- Compensation: appropriate?
- Anion gap = Na - (Cl + HCO3) [Normal: 8-12 mEq/L]
- Delta-delta (if AG elevated): rule out mixed disorders
METABOLIC ACIDOSIS
Definition: pH <7.35 + HCO3 <22 mmol/L + compensatory ↓PCO2 (Winter's formula: expected PCO2 = 1.5×HCO3 + 8 ±2)
Causes - ANION GAP ELEVATED (MUDPILES):
- M - Methanol; U - Uraemia; D - DKA; P - Propylene glycol; I - Isoniazid/Iron; L - Lactic acidosis; E - Ethylene glycol; S - Salicylates
Causes - NORMAL ANION GAP (HARDUPS/FUSED):
- Diarrhoea, fistulae (small bowel), RTA, Acetazolamide, Addison's, NH4Cl, Saline excess (hyperchloraemic)
Surgical significance:
- Shock (lactic acidosis - most common surgical cause; lactate >2 mmol/L = tissue hypoperfusion)
- ECF/fistula (HCO3 loss)
- Sepsis, post-op ARF
Management:
- Treat underlying cause (most important)
- Fluid resuscitation in shock/lactic acidosis
- NaHCO3 only if pH <7.1 (controversial; risk CO2 paradox)
- Dialysis for uraemic acidosis
- Target lactate clearance >10%/hr in ICU
Complications: arrhythmia, reduced cardiac contractility, impaired coagulation, hyperkalemia, cerebral oedema
METABOLIC ALKALOSIS
Definition: pH >7.45 + HCO3 >26 mmol/L + compensatory ↑PCO2
Causes (Chloride-Responsive vs. Chloride-Resistant):
| Chloride-Responsive (UCl <20 mEq/L) | Chloride-Resistant (UCl >20 mEq/L) |
|---|
| Vomiting (HCl loss) | Hyperaldosteronism (primary/secondary) |
| NGT aspiration | Cushing's syndrome |
| Diuretics (K and Cl loss) | Severe K+ depletion |
| Post-hypercapnia | Bartter's/Gitelman's syndrome |
Surgical significance: Pyloric stenosis (classic) - hypochloraemic, hypokalaemic metabolic alkalosis (paradoxical aciduria)
Management:
- Chloride-responsive: IV 0.9% saline + KCl replacement; stop NGT aspiration
- Pyloric stenosis: resuscitate with 0.9% saline + KCl; surgery (pyloroplasty) ONLY after biochemical correction
- Chloride-resistant: treat underlying cause (aldosterone antagonists)
Complications: tetany (↓ionised Ca), arrhythmia, reduced O2 delivery (Bohr effect), hypoventilation
Q28. Clinical features and management of hypokalemia (2020)
DEFINITION
Serum K+ <3.5 mmol/L
SEVERITY
- Mild: 3.0-3.5 mEq/L; Moderate: 2.5-3.0; Severe: <2.5
CAUSES
| Category | Examples |
|---|
| Inadequate intake | Starvation, TPN without K |
| GI losses | Vomiting, diarrhoea, NGT suction, fistulae, ileostomy, laxative abuse |
| Renal losses | Diuretics (loop/thiazide), hyperaldosteronism, renal tubular acidosis, Mg deficiency |
| Redistribution | Insulin, beta-agonists, alkalosis, re-feeding |
| Surgical causes | NGT aspiration, bowel prep, EC fistula, post-op (stress response + aldosterone) |
CLINICAL FEATURES (Severity-dependent)
Neuromuscular:
- Muscle weakness (proximal > distal), fatigue, cramps
- Hypo/areflexia in severe cases
- Respiratory muscle weakness → respiratory failure (K <2.5)
- Paralytic ileus (smooth muscle)
Cardiac (most dangerous):
- ECG: flattened/inverted T waves, U waves (hallmark), ST depression, prolonged QU interval
- Arrhythmias: PVCs, AF, VT, VF (especially with digoxin)
- Cardiac arrest in severe (<2.0)
Renal:
- Nephrogenic DI (polyuria, polydipsia)
- Metabolic alkalosis (H+ moves into cells as K+ moves out)
MANAGEMENT
General: 30 mL/kg/day maintenance fluid; K requirement = 1 mmol/kg/day
Oral replacement (preferred if mild-moderate, tolerating orally):
- KCl slow-release tablets; 40-80 mmol/day; divided doses
IV replacement (moderate-severe, symptomatic, or nil by mouth):
- Rate: max 20 mmol/hr peripherally; up to 40 mmol/hr centrally (with continuous ECG monitoring)
- Concentration: max 40 mmol/L peripherally; higher only via CVC
- Never give IV K+ as bolus - risk of cardiac arrest
- Replace Mg2+ simultaneously (hypomagnesaemia perpetuates hypokalaemia)
Specific:
- Stop offending drugs (diuretics)
- Treat underlying cause
- In refractory hypokalaemia: check and correct hypomagnesaemia first
Monitor: Serum K+, Mg2+, ECG throughout replacement
Q29. Clinical approach to hyponatremia; post-operative hyponatremia; etiology and management (2019)
DEFINITION
Serum Na+ <135 mmol/L
CLASSIFICATION
| Type | Plasma Osmolality | ECF Volume | Cause |
|---|
| Hypo-osmolar hyponatremia | <275 mOsm/kg | Hypovolaemic | GI losses, burns, diuretics |
| | Euvolaemic | SIADH, hypothyroidism, Addison's |
| | Hypervolaemic | Heart failure, cirrhosis, nephrotic syndrome |
| Iso-osmolar | 275-295 | - | Pseudohyponatremia (lipids, protein) |
| Hyperosmolar | >295 | - | Hyperglycaemia, mannitol |
CLINICAL FEATURES (based on severity)
- Mild (Na 130-135): anorexia, nausea, malaise
- Moderate (Na 125-130): headache, lethargy, confusion
- Severe (Na <125): seizures, coma, cerebral oedema → death
- Rate of fall more important than absolute level
POST-OPERATIVE HYPONATREMIA
Mechanism:
- Stress response → ADH (vasopressin) surge → free water retention
- Administration of hypotonic IV fluids (5% dextrose, 0.45% saline) intraoperatively/post-op
- NGT losses replaced with hypotonic solutions
- Pain, nausea → non-osmotic ADH release
High-risk groups: Women, elderly, children, neurological patients, thiazide use
Prevention: Use isotonic fluids (0.9% saline, Hartmann's) post-op; avoid hypotonic solutions; restrict free water; careful fluid balance
MANAGEMENT
Key principle: Correct no faster than 8-10 mmol/L per 24 hours (risk of osmotic demyelination syndrome - ODS/central pontine myelinolysis if corrected too fast, especially in chronic hyponatremia)
| Type | Treatment |
|---|
| Hypovolaemic | 0.9% saline; replace volume |
| SIADH/Euvolaemic | Fluid restriction (500-1000 mL/day); treat cause; in severe: hypertonic saline (3%) with close monitoring |
| Hypervolaemic | Fluid restriction + diuretics; treat cause (heart failure, cirrhosis) |
| Symptomatic (seizures/coma) | Hypertonic saline 3% (100-150 mL bolus); max raise 1-2 mmol/L/hr until symptoms resolve |
Formula (Adrogue-Madias): Na correction = (infusate Na - serum Na) / (TBW + 1)
Q30. Flow-guided fluid therapy; colloids as resuscitation fluids (2017)
FLOW-GUIDED / GOAL-DIRECTED FLUID THERAPY (GDFT)
Definition: Titrating IV fluid therapy to specific haemodynamic end-points (cardiac output, stroke volume, DO2) rather than fixed volumes.
Rationale:
- Both fluid under-resuscitation (AKI, gut ischaemia) and over-resuscitation (pulmonary oedema, anastomotic leak, ileus) are harmful
- Standard monitoring (HR, BP, urine output) poor predictors of fluid responsiveness
Parameters used:
| Parameter | Method |
|---|
| Stroke Volume (SV) / Stroke Volume Variation (SVV) | Oesophageal Doppler; arterial waveform analysis (LiDCO, PiCCO, FloTrac) |
| Pulse Pressure Variation (PPV) | Arterial line; PPV >13% suggests fluid responsiveness in ventilated patients |
| Cardiac Index (CI) | Target >2.5 L/min/m² |
| Mixed venous O2 saturation (SvO2) | PA catheter or ScvO2 via CVC |
| Fluid challenge response | Passive leg raise + SV response |
Evidence (Bailey & Love 28e): GDFT using oesophageal Doppler in major abdominal surgery reduces:
- Post-operative complications
- Anastomotic leak rate
- Length of hospital stay
- Time to return of gut function
Algorithm: Give 200-250 mL fluid bolus → reassess SV → if SV increases >10%, patient is fluid-responsive → repeat; if no response → stop fluids
COLLOIDS AS RESUSCITATION FLUIDS
Types:
| Colloid | Composition | Properties |
|---|
| Gelofusine / Volplex | 4% succinylated gelatin | MW 30,000 Da; volume expansion ~80% |
| Voluven | 6% hydroxyethyl starch (HES) | MW 130,000 Da |
| Human albumin solution (HAS) | 4-5% or 20-25% | Natural; MW 69,000 Da |
Theoretical advantage: Stay longer in intravascular space than crystalloids (oncotic pressure)
Evidence - BALANCE AGAINST COLLOIDS:
- SAFE trial: Albumin = saline in general ICU (except TBI where albumin worse)
- CHEST trial: HES 6% increased risk of AKI and renal replacement therapy vs. saline
- HES banned/restricted in many countries due to nephrotoxicity and coagulopathy
- Gelatins: no proven benefit over crystalloids; risk of anaphylaxis
Current recommendations (Bailey & Love 28e):
- No benefit for albumin outside specific indications (ascites replacement, liver failure, SBP prophylaxis)
- Balanced crystalloids (Hartmann's/Plasmalyte) preferred over NS for resuscitation
- Best fluid for haemorrhage = blood
- Avoid HES in ICU/surgical patients
Q31. Recent strategy for assessment and monitoring of IV fluids and electrolytes in peri-operative period (2021)
BACKGROUND
Traditional approach (vital signs + urine output) is insufficient - occult hypoperfusion (metabolic acidosis despite normal vitals) increases mortality if persisting >12 hours.
MODERN MONITORING STRATEGY
A. Clinical Assessment:
- Pulse, BP, capillary refill time, JVP
- Urine output (target: >0.5 mL/kg/hr)
- Fluid balance charts (ins + outs including drains, fistulae, NG losses)
- Weight (daily - 1 kg ≈ 1 L fluid)
B. Haemodynamic Monitoring:
| Tool | Use |
|---|
| Arterial line | Continuous BP; pulse pressure variation (PPV); fluid responsiveness |
| CVP | Trend monitoring (not absolute values); target 8-12 cmH2O |
| Oesophageal Doppler | SV-guided fluid therapy; real-time cardiac output |
| PiCCO / LiDCO / FloTrac | Minimally invasive CO monitoring; SVV |
| Pulmonary Artery Catheter | Rarely used; wedge pressure; mixed SvO2 |
| Point-of-care echo (TTE/TOE) | IVC collapsibility (>50% = hypovolaemic); LV filling assessment |
C. Biochemical Monitoring:
- Serum electrolytes (Na, K, Mg, Ca, PO4): daily or more frequently post-major surgery
- Lactate: marker of tissue perfusion; target <2 mmol/L; clearance >10%/hr
- ABG: acid-base status, BE, HCO3
- Urine Na: low (<20 mEq/L) = hypovolaemia; high = SIADH or AKI
- Serum osmolality
D. NICE Guidance (UK) - Post-op fluid prescribing:
- Use the "5 Rs" framework: Resuscitation, Routine maintenance, Replacement, Redistribution, Reassessment
- Isotonic fluids for maintenance; avoid excessive 0.9% saline (hyperchloraemic acidosis)
- Target: 25-30 mL/kg/day water; 1 mmol/kg/day Na, K, Cl; 50-100 g/day glucose
Q32. Peri-operative fluid management (2013)
PRINCIPLES
Fluid therapy aims to:
- Maintain intravascular volume
- Preserve organ perfusion
- Correct electrolyte/acid-base disturbances
- Avoid fluid overload (pulmonary oedema, gut oedema → ileus, anastomotic leak)
DAILY MAINTENANCE (70 kg adult)
- Water: ~2.5 L/day (30-35 mL/kg); urine 1.5 L + insensible 0.9 L + faeces 0.1 L
- Na: 70-84 mmol/day (0.9-1.2 mmol/kg)
- K: 70 mmol/day (1 mmol/kg)
- Glucose: 50-100 g/day (prevents catabolism, ketosis)
IV FLUIDS - COMPOSITION TABLE (Bailey & Love 28e, Table 25.2)
| Fluid | Na | Cl | K | HCO3 | Glucose | Osmolality |
|---|
| Plasma | 135-145 | 95-105 | 3.5-5.3 | 24-32 | 3.5-5.5 | 275-295 |
| 0.9% Saline | 154 | 154 | 0 | 0 | 0 | 308 |
| Hartmann's (RL) | 131 | 111 | 5 | 29 | 0 | 273 |
| 5% Dextrose | 0 | 0 | 0 | 0 | 227.8 | 278 |
Ringers Lactate composition: Na 131, K 5, Ca 2, Cl 111, Lactate 29 mmol/L
PHASES OF PERIOPERATIVE FLUID MANAGEMENT
Pre-operative:
- NBM minimum time (2hr clear fluids, 6hr solids) - ERAS
- Pre-op CHO drinks (carbohydrate loading)
- Correct existing deficits
Intra-operative:
- Anaesthetic vasodilation → relative hypovolaemia → balanced crystalloids to maintain MAP
- Replace surgical blood loss (blood after 1-1.5L loss; FFP:RBC:platelet = 1:1:1 in massive haemorrhage)
- Avoid fluid excess (Goal-Directed Fluid Therapy preferred)
- Hartmann's/Plasmalyte preferred over 0.9% saline (less hyperchloraemic acidosis)
Post-operative:
- IV maintenance until oral fluids tolerated
- Replace ongoing losses (drains, NG, stoma, fistula)
- Switch to oral route ASAP (ERAS)
- Target urine output >0.5 mL/kg/hr; monitor electrolytes daily
Q33. Concept of zero fluid balance in perioperative fluid management (2016)
DEFINITION
Zero fluid balance = a strategy targeting net fluid balance of zero over the perioperative period - i.e., fluid input equals fluid output, preventing both fluid deficit and fluid accumulation.
RATIONALE / EVIDENCE
- Surgical patients traditionally received 3-5 L excess fluid perioperatively
- Each litre of excess fluid → systemic oedema, gut oedema, ileus, impaired wound healing
- Wet tissue = poor outcomes: anastomotic leak, pulmonary oedema, AKI, prolonged ITU stay
- Zero/near-zero or slightly positive fluid balance (< +500 mL) in major GI surgery = better outcomes
PHYSIOLOGICAL BASIS
- Capillary Starling equilibrium disrupted in surgical stress (endothelial glycocalyx damage)
- Excess crystalloid distributes to interstitium (3:1 ratio for crystalloids)
- Oedematous bowel → delayed gastric emptying, poor anastomotic healing, infection
- Sodium and water retention post-op due to ADH, aldosterone, cortisol
HOW TO ACHIEVE ZERO FLUID BALANCE
- Preoperative: ERAS protocol (CHO drinks, minimal fasting, avoid traditional bowel prep)
- Intraoperative: GDFT (oesophageal Doppler/SV-guided); replace blood loss with blood; restrict crystalloids to <2 L
- Postoperative: Switch to oral ASAP; restrict IV fluids after adequate volume established; target UO 0.5-1 mL/kg/hr (avoid chasing urine output with excessive fluids)
- Daily review: Weight + fluid balance chart; aim cumulative balance near zero by Day 3-5
LIMITATIONS
- Not applicable in haemorrhagic shock or large bowel losses
- Requires meticulous measurement
- Intra-operative insensible losses are difficult to quantify
Q34. Post-operative IV fluid protocol after major GI surgery and composition of Ringer's Lactate (2021)
POST-OP IV FLUID PROTOCOL - MAJOR GI SURGERY
Phase 1: Immediate post-op (0-6 hours)
- Continue intraoperative haemodynamic support
- Target: MAP >65 mmHg, UO >0.5 mL/kg/hr, lactate trending down
- Use vasopressors (noradrenaline) to treat vasodilation rather than excess fluids
- Fluid challenge (250 mL over 10-15 min) only if evidence of hypovolaemia
Phase 2: Day 0-1 post-op
- IV maintenance only: 25-30 mL/kg/day balanced crystalloid (Hartmann's preferred)
- Add K+ 40 mmol per litre bag
- Replace documented losses: NG aspirate (0.9% saline + KCl), stoma output, drains
- Avoid 5% dextrose alone (hyponatraemia risk)
- Avoid large-volume 0.9% saline (hyperchloraemic acidosis)
Phase 3: Day 1-3 post-op
- Daily electrolytes: correct Na, K, Mg as needed
- Monitor for post-op hyponatraemia (ADH surge)
- Aim to reduce IV fluids as oral intake resumes
- ERAS: Encourage oral fluids from Day 1; free clear fluids if tolerated
Phase 4: Transition
- Stop IV fluids when oral intake >1500 mL/day
- Ensure adequate analgesia and anti-emetics to facilitate early oral intake
STOP rule (Avoid harm):
- Do NOT give >500 mL IV bolus without reassessment
- Do NOT prescribe unlimited "keep vein open" orders
- Do NOT give hypotonic fluids (0.45% saline, 5% dextrose) as routine maintenance
COMPOSITION OF RINGER'S LACTATE (Hartmann's Solution)
(Bailey & Love Table 25.2)
| Electrolyte | Concentration |
|---|
| Sodium (Na+) | 131 mmol/L |
| Chloride (Cl-) | 111 mmol/L |
| Potassium (K+) | 5 mmol/L |
| Calcium (Ca2+) | 2 mmol/L |
| Lactate (HCO3- precursor) | 29 mmol/L |
| pH | 5.0-7.0 |
| Osmolality | 273 mOsm/L |
Why Hartmann's > 0.9% saline for major surgery:
- More physiological electrolyte profile (mirrors plasma better)
- Lower Cl- load → less hyperchloraemic metabolic acidosis
- Lactate converted to HCO3- by liver (mild alkalinising effect)
- Preferred fluid in major GI, hepatobiliary and vascular surgery
SECTION C: SHOCK AND HAEMORRHAGE
Q35. Classify shock, discuss pathophysiology, management of shock (endotoxic/septic) (Year Q)
DEFINITION
Shock = a systemic state of low tissue perfusion inadequate for normal cellular respiration, leading to switch from aerobic to anaerobic metabolism and, if uncorrected, cell death. (Bailey & Love 28e, p.32)
CLASSIFICATION (Bailey & Love - Mechanism-Based)
- Haemorrhagic/Hypovolaemic - reduced circulating volume (haemorrhage, vomiting, diarrhoea, third-spacing)
- Cardiogenic - pump failure (MI, dysrhythmias, cardiomyopathy, valve disease, myocardial contusion)
- Obstructive - mechanical obstruction of cardiac filling (tamponade, tension PTX, massive PE, air embolism)
- Distributive - vasodilatation + maldistribution (Septic/endotoxic, anaphylactic, neurogenic)
- Endocrine - adrenal insufficiency, thyroid crisis
PATHOPHYSIOLOGY OF SEPTIC/ENDOTOXIC SHOCK
Trigger: Gram-negative bacteria → LPS (endotoxin) → monocyte/macrophage activation → cytokine storm (TNF-α, IL-1, IL-6, IL-8)
Cellular level:
- Tissue hypoperfusion → aerobic → anaerobic metabolism → lactic acid → metabolic acidosis
- Glucose depletion → Na/K pump failure → lysosomal autodigestion → cell lysis → hyperkalaemia
Microvascular:
- Hypoxia + acidosis → complement activation → leukocyte priming → oxygen free radicals + cytokines → endothelial injury → capillary leak → tissue oedema → worsens cellular hypoxia
Cardiovascular (Distributive pattern):
- Vasodilation (iNOS-mediated NO overproduction) → ↓SVR → ↓afterload → initially ↑CO (warm, bounding pulses, warm peripheries)
- Later: myocardial depression (TNF-α, IL-1) → ↓CO; relative hypovolaemia from capillary leak
Compensatory responses (ALL types):
- Baroreceptor → ↑sympathetic → tachycardia, vasoconstriction (except distributive)
- ↑RR → respiratory alkalosis (compensates metabolic acidosis)
- RAA axis + ADH → Na/H2O retention, ↓urine output
STAGES OF SHOCK
| Stage | BP | HR | UO | Consciousness |
|---|
| Compensated (mild) | Normal | ↑ | Normal | Mild anxiety |
| Moderate | ↓mild | ↑↑ | <0.5 mL/kg/hr | Drowsy, confused |
| Severe | ↓↓ | ↑↑↑ | Anuric | Unconscious |
Loss of >30-40% circulating volume → BP falls; >15% = within compensatory mechanisms
MANAGEMENT OF SEPTIC/ENDOTOXIC SHOCK (Surviving Sepsis Bundle)
Immediate (1 hour bundle):
- A-B-C: Airway, O2 (target SpO2 >94%), intubation if GCS <8
- 2 large-bore IV cannulae (14-16G antecubital)
- Blood cultures (2 sets, peripheral + central) BEFORE antibiotics
- Broad-spectrum antibiotics within 1 hour of recognition (e.g. Pip-Taz + Metronidazole; or Meropenem if severe/resistant)
- IV fluid resuscitation: 30 mL/kg balanced crystalloid (Hartmann's) within 3 hours if hypotension/lactate >4
- Vasopressors if MAP <65 mmHg despite adequate fluids: Noradrenaline (first-line), target MAP ≥65 mmHg
- Lactate measurement - if >2 mmol/L = sepsis-induced tissue hypoperfusion
After stabilisation (6-hour bundle):
- ICU admission; arterial line + CVC
- Source control: Identify and drain/debride/remove infective focus (laparotomy, percutaneous drain)
- Vasopressor: Noradrenaline 0.01-3 mcg/kg/min; add vasopressin if refractory
- Corticosteroids if vasopressor-refractory septic shock: Hydrocortisone 200 mg/day IV
- Glucose control (target 6-10 mmol/L)
- DVT prophylaxis, stress ulcer prophylaxis
- Target: UO >0.5 mL/kg/hr; lactate clearance; MAP ≥65; ScvO2 ≥70%
Monitoring:
- Hourly UO, continuous ECG, pulse oximetry
- ABG (lactate, pH, BE) 2-4 hourly
- CVP (8-12 cmH2O); ScvO2 via CVC
- Regular electrolytes, FBC, CRP, procalcitonin
Q36. Role of vasoactive drugs in shock (2023)
CLASSIFICATION OF VASOACTIVE DRUGS
A. Vasopressors (increase SVR - treat vasodilatory/distributive shock):
| Drug | Receptor | Mechanism | Dose | Use |
|---|
| Noradrenaline (1st line) | α1 > β1 | ↑SVR; mild ↑HR & CO | 0.01-3 mcg/kg/min IV | Septic shock (first choice) |
| Vasopressin | V1 (AVPR1) | Smooth muscle vasoconstriction; potentiates catecholamines | 0.03-0.04 units/min | Add-on to noradrenaline; refractory shock |
| Phenylephrine | α1 | Pure vasoconstrictor; ↑SVR, ↓CO | 0.5-5 mcg/kg/min | Vasodilatory shock with tachycardia; spinal shock |
B. Inotropes (increase cardiac contractility - treat cardiogenic shock):
| Drug | Receptor | Mechanism | Dose | Use |
|---|
| Dobutamine (1st line cardiogenic) | β1 > β2 | ↑CO, ↓SVR, ↑HR | 2.5-20 mcg/kg/min | Cardiogenic shock, low CO states |
| Adrenaline (Epinephrine) | α1, β1, β2 | ↑HR, ↑CO, ↑SVR | 0.01-1 mcg/kg/min | Anaphylaxis (IM 0.5 mg), cardiac arrest, refractory cardiogenic/septic shock |
| Milrinone (PDE-3 inhibitor) | PDE-3 | ↑cAMP → ↑CO; vasodilation (inodilator) | 0.375-0.75 mcg/kg/min | Post-cardiac surgery low output; beta-blocker toxicity |
| Levosimendan | Calcium sensitiser | ↑myocardial contractility without ↑O2 demand | 0.1-0.2 mcg/kg/min | Acute decompensated heart failure |
C. Combination Vasopressor + Inotrope (for mixed shock):
| Drug | Dose-dependent Action |
|---|
| Dopamine | Low (1-5 mcg/kg/min): renal/mesenteric vasodilation (D1) [controversial benefit]; Medium (5-10): β1 → ↑CO; High (>10): α1 → ↑SVR. NOT recommended as first-line in septic shock (↑arrhythmia vs. noradrenaline) |
| Adrenaline | Combines inotrope + vasopressor; use in anaphylaxis and refractory shock |
D. Vasodilators (in hypertensive crisis / cardiogenic shock with high afterload):
| Drug | Mechanism | Use |
|---|
| GTN (Nitroglycerin) | ↑NO → venodilation | Acute pulmonary oedema, high SVR cardiogenic shock |
| Sodium nitroprusside | ↑NO → mixed arterio-venodilation | Hypertensive emergency; high afterload in cardiogenic shock |
SPECIFIC PROTOCOLS BY SHOCK TYPE
| Shock Type | First-line Vasoactive | Second-line |
|---|
| Septic/Distributive | Noradrenaline | + Vasopressin; + Hydrocortisone |
| Cardiogenic | Dobutamine | + Noradrenaline if hypotension |
| Anaphylactic | Adrenaline IM (0.5 mg) | + Antihistamines + steroids |
| Neurogenic (spinal) | Noradrenaline / Phenylephrine | Atropine if bradycardia |
| Haemorrhagic | Volume + blood products first; vasopressors only as bridge | Noradrenaline |
MONITORING EFFICACY
- MAP ≥65 mmHg (target)
- UO >0.5 mL/kg/hr
- Lactate clearance
- ScvO2 ≥70%
- Skin perfusion improvement (capillary refill <2 sec)
- Wean vasopressors when MAP stable without escalating doses
QUICK EXAM SCORING TIPS
| Question | Key Scoring Points | Time Allocation |
|---|
| Q21 | Calculation table, monitoring frequency table | 15 min |
| Q22 | NRS-2002 scoring, ABCD assessment, routes | 15 min |
| Q23 | Metabolic response, enteral > parenteral, routes table | 15 min |
| Q24 | Indications, 3 complication categories, Home PN | 15 min |
| Q25 | 4 immunonutrients + mechanisms, ESPEN evidence | 15 min |
| Q26 | Indications, pull technique steps, complications table | 15 min |
| Q27 | Normal values, MUDPILES, Chloride-responsive table | 15 min |
| Q28 | ECG changes (U waves), IV rate limits, Mg co-replace | 15 min |
| Q29 | Classify by osmolality+volume, post-op mechanism, 8-10 mmol/24hr rule | 15 min |
| Q30 | GDFT algorithm, colloids evidence (SAFE, CHEST trials) | 15 min |
| Q31 | 5 monitoring tools, NICE 5Rs, lactate target | 15 min |
| Q32 | 4 phases, RL composition table, Hartmann's vs saline | 15 min |
| Q33 | Zero balance concept, ERAS phases, limitations | 15 min |
| Q34 | 4-phase protocol, RL composition table | 15 min |
| Q35 | Classification (5 types), sepsis bundle (1hr + 6hr), stages table | 15 min |
| Q36 | Drug classification table, receptors, doses, shock-type protocol | 15 min |
*All answers sourced from Bailey & Love's Short Practice of Surgery, 28th Edition (ISBN: 9780367548117)*All 16 questions answered. Here's a summary of what's covered:
What You Got
16 complete exam answers directly from Bailey & Love's 28th Edition, structured for 15-minute exam writing:
Section A - Nutrition (Q21-Q26)
- Q21 - TPN 3:1 formula calculation (with the actual numbers for 70 kg) + monitoring schedule
- Q22 - NRS-2002 scoring tool explained + nutritional augmentation methods
- Q23 - Metabolic response to surgery, all routes of nutritional support (enteral > parenteral hierarchy)
- Q24 - Full PN indications/contraindications, 3-category complications, catheter issues, Home PN (HPN)
- Q25 - 4 key immunonutrients (glutamine, arginine, omega-3, nucleotides) with mechanisms + ESPEN evidence
- Q26 - PEG - indications, step-by-step pull technique, complications table, replacement
Section B - Fluid, Electrolytes & Acid-Base (Q27-Q34)
- Q27 - ABG normal values, MUDPILES for high-AG acidosis, chloride-responsive vs. resistant alkalosis table
- Q28 - Hypokalemia: U waves on ECG, IV K+ rate limits (20 mmol/hr peripheral, 40 central), Mg co-replacement
- Q29 - Hyponatremia by osmolality+volume classification, post-op mechanism, 8-10 mmol/24hr correction rule
- Q30 - GDFT algorithm, SAFE/CHEST trial evidence against colloids
- Q31 - 5-tier monitoring strategy, NICE 5Rs, lactate targets
- Q32 - Perioperative 4-phase fluid management + RL vs. NS comparison table
- Q33 - Zero fluid balance concept, ERAS integration, physiological basis
- Q34 - Post-major GI surgery 4-phase IV fluid protocol + Hartmann's exact composition table
Section C - Shock (Q35-Q36)
- Q35 - 5-type classification, full septic shock pathophysiology, surviving sepsis 1-hour and 6-hour bundles, stages table
- Q36 - Full drug classification table with receptors, doses, and shock-type-specific protocols