Skip to main content
OrthoVellum
Knowledge Hub

Study

  • Topics
  • MCQs
  • ISAWE
  • Operative Surgery
  • Flashcards

Company

  • About Us
  • Editorial Policy
  • Contact
  • FAQ
  • Blog

Legal

  • Terms of Service
  • Privacy Policy
  • Cookie Policy
  • Medical Disclaimer
  • Copyright & DMCA
  • Refund Policy

Support

  • Help Center
  • Accessibility
  • Report an Issue
OrthoVellum

© 2026 OrthoVellum. For educational purposes only.

Not affiliated with the Royal Australasian College of Surgeons.

Blood Management Strategies in Orthopaedic Surgery

Back to Topics
Contents
0%

Blood Management Strategies in Orthopaedic Surgery

Comprehensive exam-ready guide to perioperative blood management - preoperative optimization, tranexamic acid, cell salvage, transfusion thresholds, and massive transfusion protocols

complete
Updated: 2025-12-25
High Yield Overview

BLOOD MANAGEMENT STRATEGIES

Optimize Preop | Minimize Blood Loss | Transfuse Appropriately

30-50%Reduction in transfusion with TXA
Hb less than 70 g/LRestrictive transfusion threshold
4-6 weeksIron therapy before elective surgery
1:1:1RBC:FFP:Platelets in massive transfusion

PATIENT BLOOD MANAGEMENT PILLARS

Pillar 1: Optimize
PatternPreoperative anemia detection and treatment (iron, EPO)
TreatmentScreen Hb, ferritin; treat 4-6 weeks preop
Pillar 2: Minimize
PatternReduce surgical blood loss (TXA, cell salvage, technique)
TreatmentTXA 15-20 mg/kg IV; cell salvage for expected loss greater than 500 mL
Pillar 3: Manage
PatternAppropriate transfusion thresholds and massive transfusion protocols
TreatmentRestrictive threshold Hb less than 70 g/L; balanced MTP 1:1:1

Critical Must-Knows

  • Preoperative anemia (Hb less than 130 g/L men, less than 120 g/L women) increases transfusion risk 3-4 fold
  • Tranexamic acid (TXA) 15-20 mg/kg IV reduces transfusion by 30-50% without increasing VTE
  • Restrictive transfusion threshold (Hb less than 70 g/L) is safe and reduces complications vs liberal (less than 100 g/L)
  • Cell salvage contraindicated in malignancy, infection, bowel contamination
  • Massive transfusion protocol: 1:1:1 ratio RBC:FFP:Platelets to prevent dilutional coagulopathy

Examiner's Pearls

  • "
    CRASH-2 trial: TXA within 3h of trauma reduces mortality (not just blood loss)
  • "
    Iron therapy takes 4-6 weeks - plan elective surgery timing accordingly
  • "
    Jehovah's Witness patients: multi-modal approach (EPO, TXA, cell salvage, accept lower Hb)
  • "
    Hypotensive anesthesia (MAP 50-60 mmHg) reduces blood loss but requires experienced anesthetist

Clinical Imaging

Perioperative Blood Management

Labeled blood bag containing packed red blood cells for transfusion
Click to expand
Labeled blood bag demonstrating critical safety information for transfusion medicine. This packed red blood cell unit (AS-5 with adenine-saline solution) shows the essential labelling elements: blood type (B Rh POSITIVE) prominently displayed, collection date, unit number, and expiration date fields, 'VOLUNTEER DONOR' source indication, 'Rx Only' prescription requirement, and 'PROPERLY IDENTIFY INTENDED RECIPIENT' safety instruction. Understanding blood product labelling is fundamental to safe transfusion practice - before administration, two staff members must verify patient identity against the blood bag label to prevent ABO incompatibility reactions.Credit: BruceBlaus (Blausen Medical) via Wikimedia - CC BY 3.0

Critical Exam Concepts

Preoperative Anemia is Modifiable

Screen ALL elective patients. Hb less than 130 g/L (men) or less than 120 g/L (women) = anemia. Treat with oral iron 4-6 weeks preop or IV iron if time limited. EPO if renal failure or severe anemia.

TXA is Evidence-Based Standard

Give TXA to ALL major ortho cases unless contraindicated. Loading dose 15-20 mg/kg IV at induction, maintenance 1-2 mg/kg/h. CRASH-2 showed mortality benefit in trauma.

Restrictive Threshold is Safe

Transfuse at Hb less than 70 g/L (asymptomatic stable patients). Higher threshold (less than 80 g/L) if cardiovascular disease or symptomatic. Liberal transfusion increases complications.

Jehovah's Witness Management

Multi-modal approach: EPO preop, TXA, cell salvage (if acceptable), meticulous hemostasis, hypotensive anesthesia, accept Hb 60-70 g/L. Document consent clearly.

Blood Management Strategy Quick Reference

StrategyTimingEvidence/EffectKey Considerations
Oral iron therapy4-6 weeks preopIncreases Hb by 10-20 g/LNeed time - not effective if less than 2 weeks
IV iron (ferric carboxymaltose)1-2 weeks preopRapid Hb increase 10-30 g/LMore expensive, use if time limited
Erythropoietin (EPO)3-4 weeks preopIncreases Hb 20-40 g/L with ironExpensive, renal failure or severe anemia
Tranexamic acid (TXA)At induction and intraop30-50% reduction in transfusionSafe, no VTE increase, give to all major cases
Cell salvageIntraoperativeReduces allogeneic transfusion 30-40%Contraindicated: malignancy, infection, bowel
Hypotensive anesthesiaIntraoperativeReduces blood loss 20-30%MAP 50-60 mmHg, requires experienced anesthetist
Mnemonic

OPTPatient Blood Management Pillars

O
Optimize
Optimize hemoglobin preoperatively (screen, iron, EPO)
P
Protect
Protect blood volume intraoperatively (TXA, cell salvage, technique)
T
Transfuse appropriately
Transfuse based on restrictive thresholds (Hb less than 70 g/L)

Memory Hook:OPT for optimal blood management - optimize preop, protect intraop, transfuse appropriately!

Mnemonic

CRASHTranexamic Acid Indications

C
Cardiac surgery
Reduces transfusion in CABG, valve replacement
R
Revision arthroplasty
Higher blood loss - TXA highly effective
A
Arthroplasty primary
THA, TKA standard - reduces transfusion 30-50%
S
Spine surgery
Multi-level fusion, deformity correction
H
Hip fracture
CRASH-2 trial showed mortality benefit in trauma

Memory Hook:Think of CRASH-2 trial - TXA saves lives in trauma and reduces transfusion in elective ortho!

Mnemonic

MIBCell Salvage Contraindications

M
Malignancy
Risk of tumor cell dissemination (absolute contraindication)
I
Infection
Risk of sepsis from reinfusing contaminated blood
B
Bowel contamination
GI content contamination (pelvic fractures with bowel injury)

Memory Hook:MIB are absolute contraindications - Malignancy, Infection, Bowel contamination - do NOT salvage!

Mnemonic

RATIOMassive Transfusion Protocol Components

R
RBC
Red blood cells - 1 unit
A
All components equal
Equal ratio prevents dilutional coagulopathy
T
Thawed FFP
Fresh frozen plasma - 1 unit
I
Immediate platelets
Platelet concentrate - 1 unit
O
O negative if unknown
Use O neg RBC if type unknown, switch when available

Memory Hook:Remember RATIO 1:1:1 for massive transfusion - RBC:FFP:Platelets in equal amounts!

Overview and Clinical Significance

Patient Blood Management Paradigm Shift

The Patient Blood Management (PBM) approach has replaced the old "type and cross" reactive model. PBM is proactive: detect and treat anemia BEFORE surgery, minimize blood loss DURING surgery, and transfuse appropriately AFTER surgery. This reduces transfusion rates by 30-50% and improves outcomes.

Why Blood Management Matters

  • Preoperative anemia present in 30-40% elective ortho patients
  • Anemia increases transfusion risk 3-4 fold
  • Allogeneic transfusion increases infection, LOS, mortality
  • Blood is scarce resource - donor shortages worldwide
  • Cost - 1 unit RBC costs $500-1000 AUD including administration

Three Pillars of Patient Blood Management

  1. Optimize hematopoiesis - detect and treat preop anemia
  2. Minimize blood loss - surgical technique, TXA, cell salvage
  3. Harness physiologic reserve - restrictive transfusion thresholds

WHO and NHMRC endorsed approach

Transfusion Risks

Allogeneic blood transfusion is NOT benign. Risks include acute hemolytic reaction (1:40,000), transfusion-related acute lung injury (TRALI 1:10,000), infection transmission (very low with modern screening), immunosuppression, and increased surgical site infection.

Pathophysiology

Physiology of Hemostasis

Coagulation Cascade:

  • Intrinsic pathway: Contact activation (XII → XI → IX → VIII → X)
  • Extrinsic pathway: Tissue factor exposure (VII → X) - primary initiator in surgical bleeding
  • Common pathway: X → V → thrombin → fibrinogen → fibrin clot
  • Fibrinolysis: Plasminogen → plasmin → fibrin degradation (target of TXA)

Physiological Response to Blood Loss:

Blood LossHemodynamic ChangesSymptoms
Class I (up to 15%)MinimalNone - compensated
Class II (15-30%)Tachycardia, narrow pulse pressureAnxiety, delayed capillary refill
Class III (30-40%)Tachycardia, hypotension, tachypneaConfusion, decreased urine output
Class IV (greater than 40%)Severe hypotension, absent pulsesLethargy, anuria, impending death

Oxygen Delivery Physiology

Oxygen Delivery Equation: DO₂ = CO × CaO₂ = CO × (1.34 × Hb × SaO₂ + 0.003 × PaO₂)

Key Concepts:

  • Hemoglobin is the primary oxygen carrier (1.34 mL Oâ‚‚/g Hb)
  • Normal DOâ‚‚: 900-1100 mL/min; VOâ‚‚: 200-250 mL/min
  • Critical DOâ‚‚: ~300 mL/min - below this, anaerobic metabolism ensues
  • Compensatory mechanisms: increased cardiac output, oxygen extraction ratio
  • Young healthy patients tolerate Hb 70 g/L due to compensation; elderly/cardiac patients less so

Impact of Anemia on Surgical Outcomes

Preoperative Anemia Effects:

  • Increased 30-day mortality (OR 1.4-2.9 depending on severity)
  • Increased postoperative complications (infections, AKI, cardiac events)
  • Increased length of stay and readmission rates
  • Often triggers transfusion, which compounds risks

Perioperative Coagulopathy:

  • Hypothermia impairs enzyme function in coagulation cascade
  • Acidosis reduces clotting factor activity (pH 7.2 = 50% activity)
  • Hemodilution from crystalloid/colloid resuscitation
  • Consumption coagulopathy in massive hemorrhage
  • Lethal triad: Hypothermia + acidosis + coagulopathy

Pillar 1: Preoperative Optimization

Preoperative Anemia Screening

WHO Definition of Anemia:

  • Men: Hb less than 130 g/L
  • Women: Hb less than 120 g/L
  • Pregnancy: Hb less than 110 g/L

Screen ALL Elective Patients

Australian NHMRC guidelines recommend screening hemoglobin and ferritin for ALL patients undergoing elective surgery with expected moderate-high blood loss (greater than 500 mL). This includes most major orthopaedic procedures.

TestInterpretationAction
Hb less than 130/120 g/LAnemia presentInvestigate cause, treat 4-6 weeks preop
Ferritin less than 30 mcg/LIron deficiency anemiaOral iron 200 mg elemental iron daily
Ferritin 30-100 mcg/LFunctional iron deficiencyConsider IV iron if time limited
MCV less than 80 fLMicrocytic anemiaIron deficiency vs thalassemia - check ferritin
MCV greater than 100 fLMacrocytic anemiaB12/folate deficiency - supplement

Anemia Workup in Orthopaedics

Most common causes in elective ortho patients: (1) iron deficiency (chronic blood loss, poor intake), (2) anemia of chronic disease (inflammatory arthritis), (3) renal impairment (hip OA patients often elderly with CKD). Check FBC, ferritin, CRP, creatinine as minimum.

This completes the screening protocol overview.

Iron Supplementation

Oral vs IV Iron

RouteDoseTimelineHb IncreaseIndications
Oral iron200 mg elemental iron daily4-6 weeks10-20 g/LTime available, mild anemia, tolerated
IV iron (FCM)1000 mg single dose1-2 weeks10-30 g/LTime limited (less than 4 weeks), intolerance, severe anemia
Iron + EPOOral/IV iron PLUS EPO3-4 weeks20-40 g/LSevere anemia, renal failure, Jehovah's Witness

Oral Iron Formulations:

  • Ferrous sulfate 325 mg (65 mg elemental iron) TDS
  • Ferrous gluconate 300 mg (36 mg elemental iron) TDS
  • Ferrous fumarate 200 mg (66 mg elemental iron) TDS
  • Target: 150-200 mg elemental iron per day

IV Iron Options (PBS Listed):

  • Ferric carboxymaltose (Ferinject) - 1000 mg single dose (most common)
  • Iron polymaltose (Ferrosig) - 500 mg doses
  • Iron sucrose (Venofer) - 200 mg doses

IV Iron Advantages

IV iron (especially ferric carboxymaltose) is superior when surgery is less than 4 weeks away. Single 1000 mg dose can increase Hb by 10-30 g/L within 2 weeks. Side effects are minimal (less than 1% anaphylaxis). Oral iron takes 4-6 weeks and has 30-40% GI intolerance.

Iron Without Inflammation

Iron therapy only works if inflammation is controlled. CRP greater than 5 mg/L reduces iron absorption and utilization. Treat inflammatory arthritis (RA) with DMARDs before expecting iron response. Consider EPO if refractory.

This completes the iron therapy section.

Erythropoietin (EPO) Therapy

Indications for EPO:

  • Chronic kidney disease with anemia (CrCl less than 30 mL/min)
  • Severe anemia (Hb less than 100 g/L) with surgery in less than 4 weeks
  • Anemia of chronic disease refractory to iron
  • Jehovah's Witness patients refusing transfusion

EPO Dosing Protocol:

  • Epoetin alfa (Eprex): 40,000 units SC weekly x 3-4 weeks
  • OR Darbepoetin (Aranesp): 150 mcg SC weekly x 3-4 weeks
  • MUST give with iron (oral or IV) - EPO is ineffective without iron
ScenarioEPO ProtocolExpected Hb Increase
CKD Stage 4-5 anemia40,000 units weekly x 4 weeks + IV iron20-30 g/L
Severe preop anemia40,000 units weekly x 3 weeks + IV iron20-40 g/L
Jehovah's WitnessHigh-dose EPO + IV iron + TXA + cell salvageMaximize Hb preop, accept lower postop

EPO Cost and PBS Restrictions

EPO is expensive ($300-500 per dose). PBS restriction: approved for CKD, cancer chemotherapy, specific conditions. For elective ortho anemia, often self-funded or hospital-funded. Reserve for patients where benefit justifies cost (severe anemia, Jehovah's Witness, time limited).

EPO Side Effects:

  • Hypertension (10-20% - monitor BP)
  • Thrombosis risk (theoretical - no proven increase in ortho setting)
  • Headache, flu-like symptoms
  • Pure red cell aplasia (very rare, with long-term use)

This completes the EPO therapy overview.

Timing of Preoperative Optimization

Screening bloods - FBC, ferritin, CRP, creatinine at pre-admission clinic

Oral iron therapy - if anemia detected and time available (200 mg elemental iron daily)

IV iron - if time limited or oral intolerance (ferric carboxymaltose 1000 mg single dose)

EPO therapy - if severe anemia, CKD, or Jehovah's Witness (40,000 units weekly x 3-4)

Recheck Hb - confirm response to therapy, plan intraop and postop management

Delay Surgery if Severely Anemic

If Hb less than 100 g/L at final preop check, consider delaying elective surgery by 2-4 weeks to optimize further. Anemic patients have 3-4x higher transfusion risk and worse outcomes. Exception: urgent surgery (trauma, tumor) where delay is not possible.

This completes the timing section.

Pillar 2: Minimize Intraoperative Blood Loss

Tranexamic Acid (TXA) - Evidence and Protocols

TXA Mechanism of Action

TXA is a lysine analogue that competitively inhibits plasminogen activation, preventing fibrinolysis. It stabilizes formed clot by blocking plasmin from degrading fibrin. Effect lasts 3-4 hours. Does NOT increase clot formation (not pro-thrombotic), just prevents clot breakdown.

TXA Dosing Regimens:

ProcedureLoading DoseMaintenanceTiming
Primary THA/TKA15-20 mg/kg IVOptional 1-2 mg/kg/h infusionAt induction before tourniquet
Revision THA/TKA20 mg/kg IV2 mg/kg/h for 3-6 hoursAt induction, continue postop
Spine surgery10-15 mg/kg IV1 mg/kg/h for durationAt incision, throughout case
Trauma (CRASH-2)1 g IV bolus1 g IV over 8 hoursWithin 3 hours of injury (critical)
Topical (intra-articular)1-3 g in 50-100 mL salineLeave in joint 5 min before closureAt closure before drain placement

CRASH-2 Trial Changed Practice

The CRASH-2 trial (20,211 trauma patients) showed TXA within 3 hours of injury reduced all-cause mortality from 16% to 14.5% (NNT=67). Given between 3-8 hours, NO benefit. After 8 hours, HARM (increased mortality). Time is critical in trauma.

TXA Contraindications:

  • Active thromboembolic disease (DVT, PE, MI, stroke less than 3 months)
  • History of seizures (TXA crosses BBB, rare seizure risk at high doses)
  • Known allergy to TXA
  • Renal impairment (reduce dose if CrCl less than 30 - risk of accumulation)

TXA Safety Profile

Multiple meta-analyses (over 100 RCTs) show TXA does NOT increase VTE, MI, or stroke rates in orthopaedic surgery. It is safe and effective. The theoretical thrombosis risk is not seen in practice. Give TXA to ALL major ortho cases unless contraindicated.

This completes the tranexamic acid section.

Intraoperative Cell Salvage

Cell Salvage Mechanism

Cell salvage collects shed blood from surgical field, washes RBCs to remove debris and clotting factors, and reinfuses autologous RBCs (Hct 50-60%). Typically reduces allogeneic transfusion by 30-40% in procedures with expected blood loss greater than 500-1000 mL.

Indications for Cell Salvage:

  • Expected blood loss greater than 500-1000 mL (threshold varies)
  • Revision THA/TKA (high blood loss expected)
  • Spine deformity correction, multi-level fusion
  • Pelvic and acetabular fracture ORIF
  • Jehovah's Witness patients (acceptable if continuous circuit)
  • Rare blood type or multiple antibodies (difficult crossmatch)

Cell Salvage Contraindications

ContraindicationReasonAbsolute or Relative
MalignancyRisk of tumor cell disseminationABSOLUTE
Infection/sepsisRisk of reinfusing bacteriaABSOLUTE
Bowel contaminationGI content contaminationABSOLUTE
Sickle cell diseaseReinfused cells may sickleRelative
Antibiotic-impregnated cementTheoretical antibiotic reinfusionRelative (use leukocyte filter)

Jehovah's Witness Acceptability

Many (but not all) Jehovah's Witness patients accept cell salvage if the circuit is continuous (blood never leaves patient's circulation). Discuss preoperatively and document. Some accept, some refuse. Also discuss EPO, TXA, and acceptable minimum Hb threshold.

Cell Salvage Process:

  1. Collection - suction shed blood into reservoir with anticoagulant (heparin)
  2. Washing - centrifuge separates RBCs, washes with saline to remove debris
  3. Concentration - produces RBC concentrate (Hct 50-60%)
  4. Reinfusion - filtered autologous RBCs reinfused via IV

Limitations:

  • Only salvages RBCs (no clotting factors or platelets)
  • Requires minimum 500 mL blood loss to be cost-effective
  • Equipment and technician cost ($500-1000 per case)
  • Does NOT reduce allogeneic transfusion if blood loss is minimal

This completes the cell salvage section.

Surgical Technique and Hypotensive Anesthesia

Surgical Factors Affecting Blood Loss:

FactorLow Blood LossHigh Blood Loss
Surgical approachMinimally invasive, muscle-sparingExtensile, muscle-cutting approaches
Operative timeEfficient surgery under 2 hoursProlonged surgery greater than 3 hours
Tourniquet useTourniquet in limb surgeryNo tourniquet (higher blood loss)
HemostasisMeticulous bipolar cauteryPoor hemostasis, uncontrolled ooze
Revision surgeryPrimary arthroplastyRevision with bone loss, scarring

Hypotensive Anesthesia:

  • Controlled reduction in MAP to 50-60 mmHg during surgery
  • Reduces surgical field bleeding and total blood loss by 20-30%
  • Requires experienced anesthetist - risk of cerebral/cardiac ischemia
  • Contraindications: severe CAD, cerebrovascular disease, hypertension
  • Used in spine surgery, revision arthroplasty

Tourniquet and Blood Loss

Tourniquet in TKA reduces intraoperative blood loss but may INCREASE total blood loss (including postop drain output). Meta-analyses show no difference in transfusion rates with or without tourniquet. Use tourniquet for surgical field visibility, not primarily for blood conservation.

Other Intraoperative Strategies:

  • Drain use - controversial. May increase total blood loss. Modern practice: avoid drains or remove early (less than 24h)
  • Fibrin sealants - expensive, minimal benefit over TXA
  • Topical hemostatic agents - bone wax, gelatin sponges, thrombin - useful for bone bleeding
  • Bipolar electrocautery - superior to monopolar for hemostasis with less tissue damage

This completes the surgical technique section.

Preoperative Autologous Blood Donation (PABD)

PABD is Largely Abandoned

Preoperative autologous blood donation (donating your own blood 2-4 weeks before surgery for reinfusion) has been largely abandoned in modern practice. Meta-analyses show PABD does NOT reduce allogeneic transfusion and may INCREASE overall transfusion due to preoperative anemia from donation.

Why PABD Fell Out of Favor:

  • Donating blood preoperatively makes patient anemic (Hb drops 10-20 g/L)
  • Anemic patient more likely to need transfusion (including their autologous unit PLUS allogeneic)
  • 50% of donated autologous units are discarded (wasted resource)
  • Bacterial contamination risk with storage
  • Cost of storage and processing
  • Patient Blood Management (iron, EPO, TXA) is superior

Current Role of PABD:

  • Rare blood types with difficult crossmatch (consider but cell salvage preferred)
  • Patients with multiple RBC antibodies
  • Jehovah's Witness patients who refuse allogeneic but accept autologous (rare)

Exam Answer on PABD

If asked about PABD in exam: "Preoperative autologous donation has limited role in modern practice. It can cause preoperative anemia and does not reduce overall transfusion. Current best practice is Patient Blood Management with preoperative optimization (iron, EPO), intraoperative strategies (TXA, cell salvage), and restrictive transfusion thresholds."

This completes the autologous donation section.

Pillar 3: Appropriate Transfusion Management

📊 Management Algorithm
Management algorithm for Blood Management Strategies
Click to expand
Management algorithm for Blood Management StrategiesCredit: OrthoVellum

Restrictive vs Liberal Transfusion Thresholds

Paradigm Shift to Restrictive Strategy

The TRICC trial (1999) and multiple subsequent trials showed restrictive transfusion (Hb less than 70 g/L) is as safe as liberal (Hb less than 100 g/L) and reduces transfusion-related complications. This changed practice worldwide. Liberal transfusion does NOT improve outcomes and increases infection and mortality.

Transfusion Thresholds by Patient Population

Patient TypeTransfusion ThresholdEvidence
Healthy, asymptomaticHb less than 70 g/LTRICC, FOCUS trials - safe, reduces transfusion
Cardiovascular diseaseHb less than 80 g/LSubset analysis suggests higher threshold safer
Acute coronary syndromeHb less than 80 g/L or symptomsMINT trial - restrictive non-inferior
Symptomatic anemiaSymptoms (dyspnea, tachycardia, angina)Transfuse for symptoms regardless of Hb
Active bleedingTransfuse to maintain Hb greater than 70-80 g/LReplace ongoing losses

Symptoms Trump Numbers

Transfusion triggers are GUIDELINES, not absolutes. Symptoms of anemia (dyspnea, tachycardia, chest pain, confusion) are indication for transfusion regardless of Hb. Patient with Hb 75 g/L who is asymptomatic does NOT need transfusion. Patient with Hb 85 g/L with angina DOES need transfusion.

Signs/Symptoms Suggesting Need for Transfusion:

  • Tachycardia (HR greater than 100 at rest) not explained by pain/anxiety
  • Dyspnea or increased work of breathing
  • Chest pain or ECG changes (ischemia)
  • Postural hypotension or dizziness
  • Confusion or altered mental state
  • Oliguria (less than 0.5 mL/kg/h)

This completes the transfusion threshold section.

Massive Transfusion Protocols

Definition of Massive Transfusion:

  • Loss of 1 blood volume (approximately 70 mL/kg or 5 liters in 70 kg adult) in 24 hours
  • OR transfusion of greater than 4 units RBC in 1 hour
  • OR ongoing transfusion of greater than 1 unit RBC per hour

1:1:1 Balanced Ratio

Massive transfusion should use 1:1:1 ratio of RBC:FFP:Platelets to prevent dilutional coagulopathy. Old practice of "RBC first, then FFP when INR rises" leads to coagulopathy and death. Give balanced products from the start in massive hemorrhage.

Massive Transfusion Protocol Components:

ComponentRatioRationale
RBC1 unitRestore oxygen-carrying capacity
FFP (Fresh Frozen Plasma)1 unitReplace clotting factors (II, V, VII, IX, X, XI)
Platelets1 unit (pool of 5 or apheresis)Maintain platelet count greater than 50-75
Cryoprecipitate1 unit per 10 kg if fibrinogen less than 1.5Replace fibrinogen
Tranexamic acid1 g IV bolus, then 1 g over 8hPrevent hyperfibrinolysis

MTP Activation Criteria:

  • Systolic BP less than 90 mmHg despite 2L crystalloid
  • HR greater than 120 persistently
  • Clinical suspicion of major hemorrhage (pelvic fracture, multiple long bone fractures, hemothorax)
  • Anticipated transfusion of greater than 4 units RBC in next hour

MTP activated - call blood bank, mobilize team, start massive transfusion pack 1

Pack 1 arrives - 4 RBC, 4 FFP, 1 platelet pool. Start transfusing 1:1:1 ratio.

Lab results - check Hb, platelets, INR, fibrinogen, calcium. Adjust ratios based on results.

Continue MTP - repeat packs, recheck labs every 30-60 min, stop when bleeding controlled.

Lethal Triad in Massive Transfusion

Monitor for the lethal triad: (1) Hypothermia (use blood warmers, warm fluids, Bair Hugger), (2) Acidosis (give bicarb if pH less than 7.2), (3) Coagulopathy (give FFP, platelets, maintain 1:1:1 ratio). This triad is associated with high mortality.

This completes the massive transfusion section.

Blood Product Characteristics

Blood Products Overview

ProductContentsVolumeIndications
Packed RBCRBCs, Hct 55-60%250-350 mLIncrease oxygen-carrying capacity (1 unit increases Hb 10 g/L)
Fresh Frozen Plasma (FFP)All clotting factors200-250 mLCoagulopathy, massive transfusion (1:1:1 ratio)
PlateletsPooled 5 donors or apheresis200-300 mLThrombocytopenia less than 50 or bleeding despite normal count
CryoprecipitateFibrinogen, Factor VIII, vWF, Factor XIII50 mL per unitHypofibrinogenemia (less than 1.5 g/L), massive transfusion
Prothrombin Complex Concentrate (PCC)Factors II, VII, IX, X (concentrated)20-50 mLWarfarin reversal (rapid), factor deficiencies

Expected Increments per Unit:

  • 1 unit RBC � Hb increase 10 g/L, Hct increase 3%
  • 1 unit FFP � fibrinogen increase 0.25 g/L, modest correction of INR
  • 1 unit platelets (pool) � platelet count increase 30-50 x 10^9/L
  • 1 unit cryoprecipitate � fibrinogen increase 0.5 g/L

Type-Specific vs Crossmatched Blood

  • O negative universal donor - use if type unknown in emergency (greater than 95% compatibility)
  • Type-specific - ABO/Rh matched, available in 10-15 min (99% compatible)
  • Crossmatched - fully matched, takes 45-60 min (greater than 99.9% compatible)

In massive hemorrhage, start with O neg, switch to type-specific when available.

This completes the blood products section.

Transfusion Complications

Transfusion Reactions by Timing

ComplicationTimingIncidenceFeatures
Acute hemolytic reactionMinutes to hours1:40,000ABO incompatibility - fever, hypotension, DIC, renal failure
Febrile non-hemolyticDuring/within 4h1:100Fever, chills (cytokine release) - benign, give paracetamol
Allergic/urticariaDuring transfusion1:100Rash, itching - antihistamines, usually benign
AnaphylaxisMinutes1:50,000Bronchospasm, hypotension, angioedema - stop transfusion, IM adrenaline
TRALIWithin 6 hours1:10,000Acute respiratory distress, bilateral infiltrates, hypoxia
TACODuring/within 6h1:100Volume overload - dyspnea, hypertension, pulmonary edema
Delayed hemolytic3-10 days1:1,000Alloantibodies - jaundice, anemia, positive DAT
Infection transmissionVariableVery rareHIV less than 1:1,000,000, HCV less than 1:1,000,000 with modern screening

Stop Transfusion if Acute Reaction

If patient develops fever, hypotension, dyspnea, or rash during transfusion: (1) STOP transfusion immediately, (2) maintain IV access with saline, (3) notify blood bank and clinician, (4) send unit and patient bloods for investigation, (5) check clerical error (common cause).

TRALI vs TACO

Both present with dyspnea during/after transfusion. Distinguish by:

  • TRALI (inflammatory) - hypotension, fever, normal/low CVP, bilateral infiltrates, hypoxia out of proportion to volume
  • TACO (volume overload) - hypertension, elevated JVP, pulmonary edema, responds to diuretics

TRALI management: supportive (ventilation if needed). TACO management: diuretics, slow transfusions.

This completes the transfusion complications section.

Jehovah's Witness Patient Management

Jehovah's Witness Beliefs

Jehovah's Witness patients refuse allogeneic blood transfusion (RBC, FFP, platelets) based on religious beliefs. However, acceptance of other strategies varies individually: many accept cell salvage (if continuous circuit), EPO, TXA, albumin. Must discuss and document individual preferences preoperatively. Do NOT assume all refuse all products.

Usually Acceptable

  • Erythropoietin (EPO) preoperatively
  • Tranexamic acid (TXA)
  • Cell salvage (if continuous circuit)
  • Crystalloid and colloid (albumin often accepted)
  • Hypotensive anesthesia
  • Iron supplementation (oral or IV)
  • Accepting lower Hb (60-70 g/L) postoperatively

Usually Refused

  • Allogeneic RBC transfusion
  • Fresh frozen plasma (FFP)
  • Platelet transfusion
  • Cryoprecipitate
  • Whole blood
  • Some refuse cell salvage if circuit is not continuous
  • Some refuse albumin or factor concentrates

Multi-Modal Blood Management Strategy:

Preoperative optimization - screen Hb, start EPO 40,000 units weekly x 4 + IV iron 1000 mg. Goal: Hb greater than 140 g/L preop.

Document preferences - which products acceptable (cell salvage, EPO, TXA, albumin?). Document in chart and consent. Discuss acceptable minimum Hb (usually 60-70 g/L).

Minimize blood loss - meticulous hemostasis, TXA (20 mg/kg load + infusion), cell salvage, hypotensive anesthesia, consider staged procedures if bilateral.

Accept lower Hb - most Jehovah's Witness patients tolerate Hb 60-70 g/L. Continue EPO postop if needed, supplemental oxygen, mobilize early, recheck Hb daily.

Informed Consent and Documentation

Obtain informed consent documenting patient refuses transfusion even if life-threatening. Have patient sign specific Jehovah's Witness refusal form. Document discussion of risks (including death) if severe blood loss occurs. Consider having witness to consent. Respect patient autonomy.

When to Refuse Surgery

If Jehovah's Witness patient presents for high blood loss procedure (revision THA, spine tumor resection) with preop Hb less than 100 g/L and refuses transfusion, consider: (1) delay surgery to optimize with EPO + iron (if elective), (2) frank discussion of mortality risk, (3) may need to refuse surgery if risk unacceptable. Document decision-making thoroughly.

Australian Guidelines and Context

NHMRC Patient Blood Management Guidelines

The National Blood Authority (NBA) Patient Blood Management Guidelines (2012) are Australian standard. They recommend: (1) preoperative anemia screening and treatment for all elective surgery, (2) use of TXA and cell salvage, (3) restrictive transfusion thresholds (Hb less than 70 g/L). These are exam-relevant and frequently cited.

Australian Guidelines and Resources:

  • NBA PBM Guidelines (Module 2: Perioperative) - comprehensive evidence-based recommendations
  • eTG (Therapeutic Guidelines: Antibiotic) - includes perioperative bleeding management
  • ANZCA (Australian and New Zealand College of Anaesthetists) - transfusion and blood management position statements
  • ANZSBT (Aust NZ Society Blood Transfusion) - transfusion practice guidelines

PBS (Pharmaceutical Benefits Scheme) Coverage:

  • IV iron (ferric carboxymaltose) - PBS listed for iron deficiency anemia (authority required for elective surgery indication)
  • EPO (erythropoietin) - PBS listed for CKD, chemotherapy-induced anemia (NOT for elective surgery - hospital or patient funded)
  • Tranexamic acid - PBS listed, inexpensive (less than $10 per dose)

Australian Blood Product Costs (Approximate)

ProductCost per Unit (AUD)Total Cost Including Administration
1 unit RBC$300-400$500-800 (with testing, administration, monitoring)
1 unit FFP$150-200$300-400
1 unit platelets$400-600$600-900
Cell salvage setup$500-1000$500-1000 per case (equipment + technician)
IV iron 1000 mg$300-400$400-500 (hospital outpatient)
EPO 40,000 units$300-500$1200-2000 for 4 doses (not PBS for elective ortho)

Australian Blood Supply

Australia has excellent blood safety but relies on voluntary donors. Red Cell shortage alerts occur periodically. This drives Patient Blood Management approach - conserve blood, transfuse appropriately, minimize waste. O negative is always in short supply (universal donor, only 9% of population).

Key Evidence and Trials

CRASH-2 Trial (2010)

Level I
Key Findings:
  • TXA reduced mortality from 16% to 14.5% (RR 0.91)
  • Must be given within 3 hours of injury
  • No increase in vascular occlusive events
  • Dosing: 1g bolus then 1g over 8 hours
Clinical Implication: This evidence guides current practice.

TRICC Trial (1999)

Level I
Key Findings:
  • Restrictive threshold 70 g/L vs liberal 100 g/L
  • 30-day mortality similar (18.7% vs 23.3%)
  • Restrictive strategy reduces transfusion requirements
  • Liberal transfusion may cause harm (TACO, infection)
Clinical Implication: This evidence guides current practice.

FOCUS Trial (2011)

Level I
Key Findings:
  • Hip fracture patients: restrictive 80 g/L vs liberal 100 g/L
  • No difference in mortality or walking ability at 60 days
  • Restrictive strategy safe even in elderly with comorbidities
  • Orthopaedic-specific evidence for restrictive transfusion
Clinical Implication: This evidence guides current practice.

TXA Meta-Analysis in Orthopaedic Surgery

Level I
Key Findings:
  • 60 RCTs, 5000+ patients in THA/TKA
  • TXA reduced transfusion by 30-50% (RR 0.62)
  • Blood loss reduced by 300-500 mL
  • No increase in DVT, PE, MI, or stroke
Clinical Implication: This evidence guides current practice.

NHMRC Patient Blood Management Guidelines (2012)

Guideline
Key Findings:
  • 3 pillars: optimize, minimize blood loss, manage anemia
  • Preoperative anemia screening and treatment essential
  • TXA and cell salvage recommended
  • PBM programs reduce transfusion by 30-50%
Clinical Implication: This evidence guides current practice.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOModerate

Scenario 1: Preoperative Anemia in Elective TKA

EXAMINER

"A 72-year-old woman is listed for elective TKA in 6 weeks. Preoperative Hb is 105 g/L, ferritin 18 mcg/L, CrCl 55 mL/min. How would you manage her preoperatively?"

EXCEPTIONAL ANSWER
This patient has iron deficiency anemia (Hb 105 g/L, ferritin 18 mcg/L) which increases her transfusion risk 3-4 fold. I would take a systematic approach: **Assessment:** - Confirm diagnosis: repeat FBC, ferritin, check for source of iron loss (GI workup if not obvious) - CrCl 55 is mild renal impairment - iron will still work **Treatment Plan (6 weeks available):** - **First-line:** Oral iron 200 mg elemental iron daily for 4-6 weeks - **Alternative:** IV iron (ferric carboxymaltose 1000 mg single dose) if GI intolerance or time limited - Goal: Hb greater than 120 g/L by surgery **Recheck at 2-4 weeks** - ensure response. If inadequate, add IV iron or consider EPO if severe. **Intraoperative** - use TXA 15 mg/kg, consider cell salvage if patient preferences **Postoperative** - restrictive transfusion threshold Hb less than 70 g/L This approach optimizes her preoperatively, reducing transfusion risk and improving outcomes.
KEY POINTS TO SCORE
Recognize anemia (Hb less than 120 g/L in women) as modifiable risk factor
Iron deficiency diagnosed by ferritin less than 30 mcg/L
Oral iron takes 4-6 weeks - she has time
Recheck Hb to ensure response before surgery
Multi-modal approach includes TXA and restrictive transfusion
COMMON TRAPS
✗Proceeding with surgery without treating anemia - increases transfusion risk
✗Not checking for source of iron deficiency - may have occult GI bleeding
✗Using EPO as first-line - expensive and not needed with mild anemia and time available
✗Not rechecking Hb before surgery - patient may not respond to oral iron
LIKELY FOLLOW-UPS
"What if surgery is in 2 weeks instead of 6 weeks?"
"What if ferritin is 100 mcg/L (not iron deficiency)?"
"What if CrCl is 25 mL/min (Stage 4 CKD)?"
"What preoperative Hb would you accept for elective TKA?"
"What is your transfusion threshold postoperatively?"
VIVA SCENARIOStandard

Scenario 2: Massive Hemorrhage During Revision THA

EXAMINER

"You are performing revision THA for aseptic loosening. During acetabular component removal, the patient develops massive hemorrhage from pelvic vessels. BP drops to 70/40, HR 130. Anesthetist estimates 2L blood loss in 10 minutes. How do you manage this?"

EXCEPTIONAL ANSWER
This is a life-threatening hemorrhage requiring immediate systematic management: **Immediate Actions (Damage Control):** 1. **Call for help** - senior surgeon, vascular surgeon, activate massive transfusion protocol 2. **Compress bleeding** - pack pelvis with lap sponges, direct pressure on vessel 3. **Resuscitation** - 2 large bore IVs, rapid infuser, activate MTP **Massive Transfusion Protocol:** - Call blood bank - activate MTP, request Pack 1 (4 RBC, 4 FFP, 1 platelet pool) - **1:1:1 ratio** - balanced transfusion prevents dilutional coagulopathy - Give **TXA 1g IV bolus**, then 1g over 8 hours (CRASH-2 protocol) - Warm patient (Bair Hugger, warm fluids) - prevent lethal triad **Definitive Hemostasis:** - If vessel identified - direct suture ligation or vascular clamp - If diffuse pelvic bleeding - continue packing, consider angio-embolization postop - May need to abort procedure - pack, close, stabilize, return later **Monitor:** Hb, INR, fibrinogen, platelets every 30-60 min. Adjust transfusion based on labs. **Transfer to ICU** postoperatively for ongoing resuscitation and monitoring.
KEY POINTS TO SCORE
Activate MTP early - do not wait for Hb results
1:1:1 ratio RBC:FFP:Platelets prevents coagulopathy
TXA within 3 hours of bleeding (CRASH-2 protocol)
Damage control - pack, compress, resuscitate
Monitor for lethal triad (hypothermia, acidosis, coagulopathy)
COMMON TRAPS
✗Giving only RBCs initially - leads to dilutional coagulopathy (lethal)
✗Not calling for help early - this needs vascular surgeon and senior support
✗Continuing with revision - need to abort, pack, stabilize, return later if unstable
✗Forgetting TXA - proven mortality benefit in trauma hemorrhage
LIKELY FOLLOW-UPS
"What is the 1:1:1 ratio and why is it important?"
"What is the lethal triad in massive transfusion?"
"When would you activate massive transfusion protocol?"
"What if blood bank says Pack 1 will take 20 minutes?"
"How do you prevent hypothermia intraoperatively?"
VIVA SCENARIOStandard

Scenario 3: Jehovah's Witness Patient for Bilateral TKA

EXAMINER

"A 68-year-old Jehovah's Witness patient presents for bilateral TKA. Preoperative Hb is 118 g/L. She refuses all blood products. How would you counsel and manage this patient?"

EXCEPTIONAL ANSWER
This requires careful counseling, multi-modal blood management, and clear documentation: **Preoperative Counseling:** - **Discuss beliefs** - confirm which products are acceptable (EPO, TXA, cell salvage, iron?) - Many accept: EPO, TXA, cell salvage (if continuous circuit), iron - Most refuse: RBC, FFP, platelets, cryoprecipitate - **Document preferences clearly** - have patient sign Jehovah's Witness refusal form - **Discuss risks** - bilateral TKA has high blood loss, risk of severe anemia or death if hemorrhage - **Consider staging** - offer sequential unilateral TKA instead of bilateral (lower blood loss per procedure) **Multi-Modal Blood Management:** 1. **Preoperative optimization** - EPO 40,000 units weekly x 4 weeks + IV iron 1000mg. Goal Hb greater than 130 g/L 2. **Intraoperative:** - TXA 20 mg/kg load + 2 mg/kg/h infusion - Cell salvage (if acceptable to patient) - Meticulous hemostasis - Hypotensive anesthesia (MAP 50-60 mmHg) if patient suitable 3. **Postoperative:** - Continue EPO weekly - Accept lower Hb (60-70 g/L) - patient must understand and consent - Supplemental oxygen, early mobilization - Recheck Hb daily **Document:** Informed consent that patient refuses transfusion even if life-threatening. Have witness to consent. If patient unwilling to stage and Hb optimization inadequate, may need to decline surgery due to unacceptable risk.
KEY POINTS TO SCORE
Individual variation - must discuss and document acceptable products
Multi-modal approach: EPO, TXA, cell salvage, accept lower Hb
Clear documentation and consent - patient accepts risk of death
Consider staging bilateral procedures to reduce per-procedure blood loss
May need to decline surgery if risk unacceptable
COMMON TRAPS
✗Assuming all Jehovah's Witness patients refuse all products - beliefs vary, must discuss individually
✗Not optimizing preoperatively - EPO + iron can significantly raise Hb
✗Not documenting consent clearly - medicolegal risk if complication occurs
✗Proceeding with bilateral TKA in patient with Hb 100 g/L who refuses transfusion - very high risk
LIKELY FOLLOW-UPS
"What if she refuses EPO and cell salvage as well?"
"What is the lowest Hb you would accept postoperatively?"
"Would you perform bilateral TKA or insist on staging?"
"What if she develops postoperative hemorrhage with Hb 65 g/L?"
"How do you document Jehovah's Witness refusal medicolegally?"

MCQ Practice Points

Exam Pearl

Q: What is the evidence-based transfusion threshold for hemodynamically stable patients following major orthopaedic surgery?

A: Hb 70 g/L (7 g/dL) for most patients. The FOCUS, TRACS, and TRICC trials demonstrated no benefit of liberal (100 g/L) over restrictive (70-80 g/L) transfusion thresholds. Exceptions requiring higher thresholds (80-100 g/L): acute coronary syndrome, symptomatic anaemia, ongoing significant bleeding. Single unit transfusion is appropriate unless ongoing hemorrhage.

Exam Pearl

Q: What dose of tranexamic acid (TXA) is recommended for total joint arthroplasty and what is its mechanism?

A: 1-2g IV given preoperatively (10-15mg/kg), with optional repeat dose at wound closure. TXA is an antifibrinolytic that competitively inhibits plasminogen activation, preventing clot breakdown. Reduces blood loss by 30-50% and transfusion risk by 50%. Contraindicated in active thromboembolic disease. NOT contraindicated in patients with DVT/PE history with adequate thromboprophylaxis.

Exam Pearl

Q: What are the key elements of a Patient Blood Management (PBM) program in orthopaedic surgery?

A: Three pillars: (1) Optimize red cell mass preoperatively - treat iron deficiency (IV iron if Hb under 130), EPO in selected cases. (2) Minimize blood loss - surgical technique, TXA, controlled hypotension, cell salvage. (3) Optimize physiological tolerance - restrictive transfusion thresholds, multimodal analgesia, early mobilization. The Australian National Blood Authority has specific PBM guidelines for surgery.

Exam Pearl

Q: When is intraoperative cell salvage indicated in orthopaedic surgery?

A: Expected blood loss greater than 1000-1500mL (or anticipated need for greater than 2 units allogeneic blood). Common indications: revision arthroplasty, major spine surgery, pelvic/acetabular trauma, bilateral TKA. Cell salvage reinfuses the patient's own washed red cells. Contraindicated in malignancy (relative) and infection (absolute). Processing removes activated clotting factors.

Exam Pearl

Q: What is the recommended management of anticoagulation in a patient on warfarin requiring urgent hip fracture surgery?

A: Reverse with IV Vitamin K 5-10mg + Prothrombinex-VF (25-50 IU/kg) for INR greater than 1.5. Surgery can proceed once INR under 1.5. Fresh frozen plasma (FFP) is second-line if Prothrombinex unavailable. Do NOT delay surgery more than 48 hours waiting for INR to normalize with vitamin K alone. Bridging with LMWH is NOT recommended for most hip fracture patients.

BLOOD MANAGEMENT STRATEGIES - EXAM CHEAT SHEET

High-Yield Exam Summary

Three Pillars of Patient Blood Management

  • •**Pillar 1: Optimize** - Detect and treat preop anemia (iron, EPO)
  • •**Pillar 2: Minimize** - Reduce intraop blood loss (TXA, cell salvage, technique)
  • •**Pillar 3: Manage** - Appropriate transfusion (restrictive threshold Hb less than 70 g/L)

Preoperative Anemia Management

  • •**Screen:** Hb less than 130 g/L (men), less than 120 g/L (women) = anemia. Check ferritin, CRP, creatinine
  • •**Oral iron:** 200 mg elemental iron daily x 4-6 weeks (increases Hb 10-20 g/L)
  • •**IV iron:** Ferric carboxymaltose 1000 mg single dose (increases Hb 10-30 g/L in 1-2 weeks) - use if time limited
  • •**EPO:** 40,000 units SC weekly x 3-4 weeks + iron (increases Hb 20-40 g/L) - CKD, severe anemia, Jehovah's Witness
  • •**Recheck Hb** 1 week preop to confirm response

Tranexamic Acid (TXA)

  • •**Mechanism:** Inhibits plasminogen activation, prevents fibrinolysis, stabilizes clot
  • •**Dosing:** 15-20 mg/kg IV load at induction, optional 1-2 mg/kg/h maintenance
  • •**Evidence:** 30-50% reduction in transfusion, NO increase in VTE/MI/stroke
  • •**CRASH-2:** 1g bolus + 1g over 8h in trauma - reduces mortality if given within 3h
  • •**Use:** All major ortho cases (THA, TKA, spine, trauma) unless contraindicated

Cell Salvage

  • •**Indications:** Expected blood loss greater than 500-1000 mL (revision THA/TKA, spine, pelvis)
  • •**Mechanism:** Collects shed blood, washes RBCs, reinfuses autologous Hct 50-60%
  • •**Contraindications (MIB):** Malignancy, Infection, Bowel contamination (all absolute)
  • •**Effect:** 30-40% reduction in allogeneic transfusion
  • •**Jehovah's Witness:** Many accept if continuous circuit

Transfusion Thresholds

  • •**Restrictive:** Hb less than 70 g/L (asymptomatic stable patients) - SAFE and reduces complications
  • •**Liberal:** Hb less than 100 g/L (old practice) - NO benefit, increases complications
  • •**Cardiovascular disease:** Threshold Hb less than 80 g/L (slightly higher)
  • •**Symptomatic anemia:** Transfuse for symptoms (dyspnea, tachycardia, angina) regardless of Hb
  • •**Evidence:** TRICC, FOCUS trials - restrictive is as safe as liberal with less transfusions

Massive Transfusion Protocol

  • •**Definition:** Loss of 1 blood volume in 24h OR greater than 4 units in 1h
  • •**1:1:1 ratio:** RBC:FFP:Platelets in equal amounts - prevents dilutional coagulopathy
  • •**TXA:** 1g IV bolus, then 1g over 8h (CRASH-2 protocol - within 3h of injury)
  • •**Lethal triad:** Hypothermia, Acidosis, Coagulopathy - monitor and correct
  • •**Lab monitoring:** Hb, INR, fibrinogen, platelets every 30-60 min

Jehovah's Witness Management

  • •**Discuss:** Individual beliefs vary - many accept EPO, TXA, cell salvage (continuous circuit)
  • •**Document:** Signed refusal form, documented risks including death, witness to consent
  • •**Optimize:** EPO 40,000 units weekly x 4 + IV iron 1000 mg. Goal Hb greater than 130 g/L preop
  • •**Minimize:** TXA, cell salvage, meticulous hemostasis, hypotensive anesthesia, consider staging bilateral procedures
  • •**Accept:** Lower Hb postop (60-70 g/L). Supplemental O2, early mobilization

Key Trials and Evidence

  • •**CRASH-2 (2010):** TXA in trauma reduces mortality (16.0% to 14.5%) if given within 3h. After 8h, harmful.
  • •**TRICC (1999):** Restrictive (Hb less than 70) vs liberal (less than 100) - restrictive safe, reduces transfusions
  • •**FOCUS (2011):** Hip fracture patients - restrictive (Hb less than 80) safe even in elderly with comorbidities
  • •**Cochrane TXA (2015):** 60 RCTs ortho - TXA reduces transfusion 30-50%, NO VTE increase
  • •**NHMRC PBM Guidelines (2012):** Australian standard - optimize, minimize, manage transfusion appropriately

Australian Context

  • •**NBA PBM Guidelines:** Module 2 Perioperative - screen anemia, TXA, cell salvage, restrictive transfusion
  • •**PBS:** IV iron (FCM) listed with authority. EPO NOT listed for elective ortho (hospital/patient funded)
  • •**Blood costs:** 1 unit RBC $500-800 AUD including administration, testing, monitoring
  • •**Donor supply:** Voluntary donors, periodic shortages (esp O neg) - drives PBM approach
Quick Stats
Reading Time129 min
Related Topics

Deep Vein Thrombosis - Diagnosis and Treatment

Delirium Prevention in Orthopaedic Surgery

Enhanced Recovery After Surgery (ERAS) Protocols

Multimodal Analgesia