What is a massive transfusion protocol (MTP)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 14, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

What is a Massive Transfusion Protocol?

A massive transfusion protocol (MTP) is a standardized, pre-established institutional algorithm that enables rapid delivery of blood products in fixed ratios (typically 1:1:1 of red blood cells:fresh frozen plasma:platelets) to patients experiencing life-threatening hemorrhage, activated immediately when massive bleeding is anticipated or confirmed. 1, 2

Core Definition and Activation

Hospitals must have an MTP in place that includes clinical, laboratory, and logistic responses. 1 The protocol is typically activated when:

  • 1-1.5 blood volumes may need to be infused acutely or within a 24-hour period 1
  • The traditional definition involves transfusion of ≥10 units of packed red blood cells within 24 hours, though this occurs in less than 2% of civilian trauma patients 1, 3
  • The nature of injury alerts clinicians to probable massive hemorrhage before formal thresholds are met 1

A critical pitfall: Delaying MTP activation increases mortality—activate immediately when massive hemorrhage is declared or anticipated, rather than waiting for laboratory confirmation. 2, 4

Organizational Structure

The MTP requires designated team roles: 1

  • Team leader (usually the most senior physician) who declares the massive hemorrhage situation and coordinates management
  • Communications lead whose sole role is liaising with laboratories and other departments
  • Dedicated personnel to transport blood samples and products between laboratory and clinical areas
  • IV access specialist to secure large-bore (8-Fr central) or intraosseous access

Blood Product Delivery Strategy

The cornerstone of modern MTPs is early administration of blood products in balanced ratios, specifically 1:1:1 of RBC:FFP:platelets, based on military experience showing improved survival. 1, 2, 5

Key transfusion principles:

  • Begin early FFP administration at 10-15 ml/kg to prevent dilutional coagulopathy before it develops 1, 2, 4
  • Maintain platelet count ≥75 × 10⁹/L throughout resuscitation 2, 4
  • Use warmed blood products—start with O-negative blood if needed immediately, then transition to group-specific or cross-matched blood 2, 4
  • For established coagulopathy (fibrinogen <1 g/L or PT/APTT >1.5× normal), administer >15 ml/kg of FFP 2, 4

The evidence base evolved significantly: Seven retrospective studies showed better outcomes with high FFP:RBC ratios (approaching 1:1), with casualties receiving 1:4 ratios having three-fold higher mortality than those receiving 2:3 ratios. 1 This military data, though retrospective and involving young males with penetrating injuries, fundamentally changed civilian practice. 1

Critical Protocol Components

MTPs must address both clinical management and logistics to deliver blood products rapidly to the patient while organizing definitive hemorrhage control (surgical or radiological). 1

Essential elements include:

  • Immediate control of obvious bleeding through direct pressure, tourniquets, or hemostatic dressings 2, 4
  • High FiO₂ administration and securing large-bore IV access 2, 4
  • Baseline laboratory tests (FBC, PT, aPTT, Clauss fibrinogen, cross-match) 2, 4
  • Active warming of patient and all transfused fluids to prevent hypothermia 2, 4
  • Consideration of cell salvage autotransfusion when appropriate 2, 4

Coagulopathy Management

Target fibrinogen levels >1 g/L using fibrinogen concentrate or cryoprecipitate, as fibrinogen <1 g/L represents established hemostatic failure and predicts microvascular bleeding. 2, 4

The most effective rapid fibrinogen replacement is achieved with fibrinogen concentrate or cryoprecipitate. 2, 4

Common Pitfalls

Several critical errors undermine MTP effectiveness:

  • Do not wait for laboratory results before administering blood products in obvious massive hemorrhage—this increases mortality 2, 4
  • Do not administer excessive crystalloid, as this causes dilutional coagulopathy and worsens outcomes; transition to blood products early 4, 6
  • Do not use hemoglobin level as the sole trigger for transfusion, as this fails to account for the dynamic nature of hemorrhagic shock 4, 6

Post-Resuscitation Care

Once bleeding is controlled, aggressively normalize blood pressure, acid-base status, and temperature, then admit to critical care for ongoing monitoring. 2, 4

Initiate standard venous thromboprophylaxis as soon as hemostasis is secured, as patients rapidly develop a prothrombotic state following massive hemorrhage. 1, 2, 4

Effectiveness and Outcomes

MTPs are effective in decreasing mortality, with better outcomes when blood products are readily available in the trauma bay upon patient arrival. 5 However, massive transfusion carries significant mortality (approximately 15% for trauma patients, up to 40-53% overall), which increases with the number of products transfused. 7, 8, 3

The strongest predictors of mortality include the number of PRBC transfusions at 4 and 24 hours, age, mechanism of injury, and initial Glasgow Coma Scale. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Massive Bleeding

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Massive Blood Transfusion Reaction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Massive transfusion protocol in adult trauma population.

The American journal of emergency medicine, 2020

Guideline

Protocol for Transfusing Blood in Hemorrhagic Shock

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Massive transfusion: an overview of the main characteristics and potential risks associated with substances used for correction of a coagulopathy.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, 2012

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.