What is the administration protocol for cryoprecipitate (Cryoprecipitated Antihemophilic Factor)?

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Last updated: May 14, 2025View editorial policy

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From the Guidelines

Cryoprecipitate should be administered intravenously through a standard blood giving set with a 170- to 200-µm filter, with the adult dose being two pools, as recommended by the most recent guidelines 1. The administration of cryoprecipitate involves several key steps to ensure safe and effective use.

  • The product should be thawed and then administered within a specific timeframe, with some guidelines suggesting it can be kept at ambient temperature for 4 hours after thawing 1.
  • The typical adult dose is two pools, which is equivalent to a significant amount of fibrinogen, approximately 2 g or more, depending on the specific product and pooling 1.
  • Infusion rates may vary based on the clinical situation, but the use of a standard blood giving set with an appropriate filter is crucial to prevent complications.
  • Before administration, it is essential to verify patient identification and consider ABO compatibility, although cryoprecipitate is generally considered ABO-compatible.
  • Monitoring for signs of transfusion reactions, such as fever, chills, or respiratory distress, is also critical during and after the infusion.
  • The use of cryoprecipitate is supported by recent guidelines for managing major bleeding and coagulopathy, particularly in cases of hypofibrinogenemia, where an initial supplementation of 3–4 g of fibrinogen is recommended, which can be achieved with cryoprecipitate or fibrinogen concentrate 1.

From the Research

Administration of Cryoprecipitate

  • Cryoprecipitate is a pooled product that comes with a spectrum of other coagulation factors which may further enhance or even disturb hemostasis 2
  • The administration of cryoprecipitate is often used to treat perioperative bleeding, but its use has been questioned in favor of virus-inactivated fibrinogen concentrate 3
  • Cryoprecipitate is commonly used in the operating room and intensive care units, and its use is often audited to evaluate the appropriateness of its usage 4

Comparison with Fibrinogen Concentrate

  • Fibrinogen concentrate is a pathogen-inactivated, pooled product that offers a highly purified single factor concentrate, and its use has been compared to cryoprecipitate in several studies 2, 5
  • A randomized clinical trial found that fibrinogen concentrate is noninferior to cryoprecipitate with regard to the number of blood components transfused in a 24-hour period post-bypass in patients undergoing cardiac surgery 5
  • Another study found that fibrinogen supplementation in the form of fibrinogen concentrate is associated with improved outcomes and reduced transfusion requirements compared to cryoprecipitate in traumatic hemorrhagic patients 6

Usage Guidelines

  • The use of cryoprecipitate should be guided by the patient's clinical condition, laboratory values, and the presence of bleeding or coagulopathy 4
  • The administration of cryoprecipitate should be carefully considered, taking into account the potential risks and benefits, as well as the availability of alternative treatments such as fibrinogen concentrate 3

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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