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Heparin concentration in cell salvage during heparinization: a pilot study
Takahiro Tamura1,2, Jonathan H Waters2, Kimitosi Nishiwaki1
1Department of Anesthesiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya Journal of Medical Science
|November 2, 2020
Summary
Cell salvage effectively reduces allogeneic blood transfusions in cardiovascular surgery. This study found salvaged blood contains minimal heparin, not enough to impact clotting times.
Area of Science:
- Cardiovascular Surgery
- Anesthesiology
- Transfusion Medicine
Background:
- Cell salvage is a common practice to minimize allogeneic blood transfusions during cardiovascular surgery.
- Concerns exist regarding potential heparin contamination in salvaged blood, which could affect patient anticoagulation.
- Heparin is crucial for maintaining anticoagulation during cardiopulmonary bypass, with target activated clotting times exceeding 400 seconds.
Purpose of the Study:
- To investigate the presence and quantity of heparin in salvaged blood during cardiovascular surgery.
- To determine if heparin levels in salvaged blood are sufficient to clinically influence activated clotting time.
Main Methods:
- A prospective, observational pilot study involving 12 patients undergoing cardiovascular surgery (May-October 2018).
- Collection of blood samples during heparinization and salvaged blood samples from three different cell salvage systems after protamine administration.
- Measurement of heparin concentration in all collected samples.
Main Results:
- Heparin concentrations in salvaged blood from two devices were below the limit of quantification (0.10 IU/mL).
- One device showed a mean measurable heparin concentration of 0.15 IU/mL in salvaged blood.
- No significant levels of heparin were detected that would clinically impact activated clotting time.
Conclusions:
- Salvaged blood during cardiovascular surgery, using the evaluated systems, does not contain clinically significant amounts of heparin.
- The practice of cell salvage is unlikely to interfere with anticoagulation management in these patients.
- Further studies with larger sample sizes may be warranted to confirm these findings across various devices and patient populations.

