Fresh Frozen Plasma (FFP) Transfusion Indications
FFP transfusion is indicated primarily for major hemorrhage with documented or presumed coagulopathy, with an initial dose of 10-15 ml/kg, and should be administered early in massive bleeding rather than waiting for laboratory confirmation. 1
Definitive Indications for FFP Transfusion
Major Hemorrhage and Coagulopathy
- Administer FFP in massive bleeding (>10 units RBC in 24 hours or >6 units in 6 hours) using high-ratio transfusion strategies of at least 1:2 FFP:RBC, ideally approaching 1:1 in trauma patients. 1
- FFP is indicated when PT >1.5 times normal, INR >2.0, or APTT >2 times normal in the presence of active microvascular bleeding. 1, 2
- In trauma with massive hemorrhage, maintain a 1:1:1 ratio of RBC:FFP:platelets until coagulation results become available. 3
- The standard therapeutic dose is 10-15 ml/kg (approximately 3-4 units or 750-1000 ml for a 70 kg adult). 1, 2
Critical pitfall: Doses below 10 ml/kg are unlikely to achieve the 30% factor concentration threshold needed for hemostasis and should be avoided. 2
Disseminated Intravascular Coagulation (DIC)
- FFP is indicated for acute DIC with evidence of active bleeding or high bleeding risk (e.g., planned surgery or invasive procedures). 1, 4
Warfarin Reversal
- FFP is indicated for urgent reversal of warfarin anticoagulation in the presence of active bleeding only when prothrombin complex concentrate (PCC) is not available. 1, 4
- When PCC is unavailable, use 5-8 ml/kg FFP for warfarin reversal (lower dose than for general coagulopathy). 2
Important caveat: PCC should be strongly preferred over FFP for warfarin reversal when available, as it provides faster and more complete reversal with lower volume. 4
Thrombotic Microangiopathies
- FFP is indicated as replacement fluid for therapeutic plasma exchange in thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS). 1, 5
Hereditary Angioedema
- FFP contains C1-esterase inhibitor and is indicated for hereditary angioedema when specific therapies are unavailable. 1, 2
Conditional Indications (Use with Caution)
Specific Coagulation Factor Deficiencies
- FFP may be used for single coagulation factor deficiencies when specific factor concentrates are not available. 4, 5
Massive Transfusion Protocol
- After transfusion of one blood volume (approximately 70 ml/kg) with ongoing bleeding, administer FFP empirically when coagulation tests are unavailable. 3, 6
- In obstetric hemorrhage, withhold FFP until 4 units of RBC have been transfused unless early coagulopathy is documented, then maintain 1:1 ratio. 2
Absolute Contraindications and Inappropriate Uses
Do NOT Use FFP For:
- Prophylactic correction of abnormal coagulation tests (PT, APTT) prior to low-risk invasive procedures in critically ill, hemodynamically stable patients. 1
- Mild-to-moderate coagulation abnormalities (INR ≤1.5) in non-bleeding patients—this practice does not prevent bleeding and unnecessarily exposes patients to transfusion risks. 2, 7, 8
- Volume replacement or hypovolemia—use crystalloids or colloids instead. 1, 5
- Nutritional support, protein replacement, or albumin augmentation. 5
- Correction of coagulopathy in cirrhotic patients without active bleeding, as FFP can significantly increase portal pressure. 2
- Isolated thrombocytopenia without coagulopathy. 3
Critical evidence: A prospective audit demonstrated that FFP transfusion for mild coagulation abnormalities (INR 1.1-1.85) normalized PT-INR in only 0.8% of patients and failed to correct PT in 99% of patients. 8
Practical Administration Guidelines
Preparation and Timing
- FFP can be thawed using dry oven (10 minutes), microwave (2-3 minutes), or water bath (20 minutes). 2
- Once thawed, FFP must be used within 30 minutes if removed from refrigeration, or within 24 hours if stored at 4°C. 2
- Alert the blood bank immediately in anticipated massive hemorrhage to minimize delays—early FFP administration reduces mortality. 3
Infusion Rate
- In acute bleeding situations, infuse FFP as rapidly as clinically tolerated, prioritizing rapid correction of coagulopathy over adherence to a specific infusion rate. 2
Blood Type Compatibility
- FFP must be ABO-compatible with the patient's red blood cells; use AB plasma if blood type is unknown. 2, 4
Important Limitations and Alternatives
FFP Limitations
- FFP has relatively low fibrinogen content (four units contain only approximately 2 g fibrinogen), making it inefficient for isolated fibrinogen replacement. 1, 3
- Large volumes are required to correct established coagulopathy, which may be difficult to achieve rapidly. 3
- Abnormal standard coagulation tests (PT, APTT) are poor predictors of bleeding in critically ill, hemodynamically stable patients and do not reflect true hemostatic status in advanced liver disease. 1
Preferred Alternatives
- For hypofibrinogenemia (<1.0-1.5 g/L): Use cryoprecipitate or fibrinogen concentrate instead of FFP, as these are more effective and efficient. 1, 3
- For warfarin reversal in emergency situations: Use prothrombin complex concentrate (PCC) preferentially over FFP. 4
- For congenital coagulation factor deficiencies: Use specific factor concentrates when available. 5
Serious Risks and Monitoring
Major Complications
- Transfusion-related acute lung injury (TRALI)—the most serious complication, with FFP and platelets being the most frequently implicated products. 1, 3
- Transfusion-associated circulatory overload (TACO). 1, 3
- ABO incompatibility reactions. 1
- Transmission of infectious diseases (including prion diseases). 1
- Allergic reactions. 1
- Citrate toxicity with massive transfusion leading to hypocalcemia/hypomagnesemia. 2