What are the indications for administering cryoprecipitate (cryoprecipitated antihemophilic factor)?

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Indications for Cryoprecipitate Administration

Cryoprecipitate is indicated when fibrinogen concentration is less than 80-100 mg/dL in the presence of excessive bleeding, for patients with congenital fibrinogen deficiencies, and as an adjunct in massively transfused patients when fibrinogen concentrations cannot be measured in a timely fashion. 1

Primary Indications

  • When fibrinogen concentration is less than 80-100 mg/dL in the presence of excessive bleeding 1
  • For patients with congenital fibrinogen deficiencies (consultation with the patient's hematologist is recommended whenever possible) 1
  • As an adjunct in massively transfused patients when fibrinogen concentrations cannot be measured in a timely fashion 1
  • When a test of fibrinogen activity indicates fibrinolysis 1

Specific Clinical Scenarios

  • Hypofibrinogenemia due to major hemorrhage and massive transfusion, particularly in:
    • Major trauma 1
    • Obstetric hemorrhage (maintain fibrinogen >2 g/L) 1
    • Cardiac surgical bleeding 1
  • Combined liver and renal failure with bleeding 1
  • Bleeding associated with thrombolytic therapy 1
  • Disseminated intravascular coagulation (DIC) with fibrinogen <1.0 g/L 1
  • Advanced liver disease, to maintain fibrinogen level >1.0 g/L 1

Von Willebrand Disease Management

  • For bleeding patients with von Willebrand disease types 1 and 2A: Use only if there is no response to or availability of desmopressin or VWF/FVIII concentrate 1
  • For bleeding patients with von Willebrand disease types 2B, 2M, 2N, and 3: Use if specific VWF/FVIII concentrate is not available 1

Important Considerations and Limitations

  • Transfusion of cryoprecipitate is rarely indicated if fibrinogen concentration is greater than 150 mg/dL in nonpregnant patients 1
  • During major hemorrhage, fibrinogen should be maintained >1.5 g/L, except in active obstetric hemorrhage where >2 g/L fibrinogen should be maintained 1
  • Cryoprecipitate contains factor VIII, von Willebrand factor, fibrinogen, factor XIII, and fibronectin 2, 3, 4
  • The effectiveness of cryoprecipitate in achieving therapeutic levels of factor X may be limited, and specific factor concentrates are preferred when available 1

Administration Guidelines

  • Adult dose is typically two pools; transfuse using a standard blood giving set with a 170-200 μm filter 1
  • Each single unit contains approximately 400-450 mg of fibrinogen, and pools of five units contain at least 2 g 1
  • Once thawed for administration, cryoprecipitate can be kept at ambient temperature for 4 hours and should not be refrigerated again 1

Historical Context and Evolution of Use

  • Originally developed for treatment of hemophilia A (factor VIII deficiency), but now rarely used for this purpose due to availability of more purified factor concentrates 2, 5, 6
  • In some European countries, cryoprecipitate has been withdrawn from use due to safety concerns, including transmission of blood-borne pathogens 5
  • Current use focuses primarily on fibrinogen replacement in acquired hypofibrinogenemia with bleeding 5, 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

A protocol for the preparation of cryoprecipitate and cryodepleted plasma.

Methods in molecular biology (Clifton, N.J.), 2011

Research

Cryoprecipitate therapy.

British journal of anaesthesia, 2014

Research

Cryoprecipitate: an outmoded treatment?

Transfusion medicine (Oxford, England), 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.

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