How many units of Fresh Frozen Plasma (FFP) should be transfused for a prolonged Activated Partial Thromboplastin Time (APTT)?

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FFP Dosing for Prolonged APTT

For a prolonged APTT with active bleeding, transfuse 4 units of FFP initially (approximately 10-15 ml/kg), which provides roughly 1000 ml for an average 70 kg adult. 1, 2

Clinical Context Determines FFP Administration

The decision to transfuse FFP for prolonged APTT depends critically on whether the patient is actively bleeding:

Active Bleeding with Prolonged APTT

  • Initial dose: 4 units of FFP (approximately 1000 ml or 15 ml/kg) 1, 2
  • This dose is necessary to achieve the minimum 30% concentration of plasma factors required for hemostasis 2, 3
  • Each FFP unit contains approximately 250-300 ml 2
  • Maintain 1:1 ratio of RBC:FFP if massive transfusion is ongoing until coagulation results are available 1

No Active Bleeding

  • Do not transfuse FFP solely to correct laboratory values 1, 4
  • FFP transfusion in non-bleeding patients with mild-moderate coagulation abnormalities does not prevent bleeding and increases transfusion-related complications 2, 4
  • Studies demonstrate that FFP fails to correct PT in 99% of patients with mild coagulation abnormalities 5

Specific Clinical Scenarios

Obstetric Hemorrhage

  • Withhold FFP until 4 units of RBC have been transfused, unless early coagulopathy is diagnosed on coagulation testing 1
  • APTT prolongation is uncommon in postpartum hemorrhage, affecting only 1% of hemorrhages at 1000 ml and typically occurring after >4000 ml blood loss 1
  • After 4 units RBC with ongoing bleeding: give 4 units FFP and maintain 1:1 ratio until coagulation results available 1

Major Trauma

  • Replacement of coagulation factors during major hemorrhage is a primary indication for FFP 1, 3
  • APTT >2 times normal with microvascular bleeding warrants FFP transfusion 1, 3

Disseminated Intravascular Coagulation (DIC)

  • FFP indicated for acute DIC with bleeding 1, 3
  • PT and APTT prolongation beyond that expected by dilution, with thrombocytopenia and fibrinogen <1.0 g/L, suggests DIC 1
  • Administer FFP sooner rather than later in sufficient dosage to avoid progression 1

Critical Dosing Thresholds

APTT must be >1.5 times normal (or >2 times normal per some guidelines) with active bleeding to justify FFP transfusion 1:

  • PT >1.5 times mean normal value correlates with increased risk of clinical coagulopathy 1
  • INR >1.5 with active bleeding is an indication 1, 3
  • Doses below 10 ml/kg are unlikely to achieve the 30% factor concentration threshold needed for hemostasis 2

Important Caveats

Prioritize Fibrinogen Replacement

  • Hypofibrinogenaemia is the most common factor deficiency, occurring before APTT prolongation 1
  • If fibrinogen <1.5 g/L (or <2 g/L in obstetrics), prioritize cryoprecipitate over FFP 1
  • Four units of FFP contain only approximately 2 g of fibrinogen, whereas two pools of cryoprecipitate (10 units) contain at least 4 g 1

Recheck Coagulation Parameters

  • Repeat coagulation tests after FFP transfusion to determine need for additional doses 2
  • Laboratory turnaround time may necessitate requesting components before results are available in rapid bleeding 1

Avoid Common Pitfalls

  • Do not use FFP for volume replacement - this is not an indication 1, 4
  • Do not transfuse prophylactically in non-bleeding patients with isolated APTT prolongation 1, 4
  • In liver disease patients without bleeding, FFP does not correct PT and exposes patients to unnecessary risks including TRALI and circulatory overload 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Plasma Fresco Congelado: Uso y Administración

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Plasma Fresco Congelado: Indicaciones y Uso Adecuado

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Coagulopathy in Acute-on-Chronic Liver Failure

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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.

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