Plasma transfusion is commonly performed for the correction of abnormal coagulation screening tests. The goal of this investigation was to assess the relationship between the dose of plasma administered and changes in coagulation test results in a large and diverse cohort of patients with varying levels of coagulation abnormalities and comorbid disease and in a variety of clinical settings.
In this single-center historical cohort study, all plasma transfusion episodes in adult patients with abnormal coagulation screening tests were extracted between 2011 and 2015. The primary outcome was the proportion of patients attaining normal posttransfusion international normalized ratio (INR ≤ 1.1) with secondary outcomes including the proportion of patients attaining partial normalization of INR (INR ≤ 1.5) or at least 50% normalization in pretransfusion values with respect to an INR of 1.1.
In total, 6779 unique patients received plasma with a median (quartiles) pretransfusion INR of 1.9 (1.6–2.5) and a median transfusion volume of 2 (2–3) units. The majority (85%) of transfusions occurred perioperatively, with 20% of transfusions administered prophylactically before a procedure. The median decrease in INR was 0.4 (0.2–0.8). Complete INR normalization was obtained in 12%. Reductions in INR were modest with pretransfusion INR values <3. Patients receiving ≥3 units of plasma were more likely to achieve at least 50% normalization in INR than those receiving ≤2 units (68% vs 60%; P < .001).
Changes in INR after plasma transfusion were modest at typically used clinical doses, particularly in those with less severely deranged baseline coagulation screening tests. Further studies are necessary to assess the relationships between plasma-mediated changes in INR and clinical outcomes.
From the *Division of Critical Care Medicine, Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota
†Periprocedural Outcomes, Information and Transfusion Study Group, Mayo Clinic, Rochester, Minnesota
‡Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota
§Department of Anesthesiology and Perioperative Medicine, Anesthesia Clinical Research Unit, Mayo Clinic, Rochester, Minnesota
‖Patient Blood Management, Mayo Clinic, Rochester, Minnesota
¶Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Published ahead of print March 27, 2018.
Accepted for publication February 5, 2018.
Funding: This study was supported by grants from the Mayo Clinic Department of Anesthesiology and Perioperative Medicine and the Critical Care Integrated Multidisciplinary Practice, Rochester, MN. In addition, this study was supported by a National Institutes of Health R01 grant (HL121232) to D.J.K.
The authors declare no conflicts of interest.
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Address correspondence to Matthew A. Warner, MD, Division of Critical Care Medicine, Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 1st St SW, Rochester, MN 55905. Address e-mail to firstname.lastname@example.org.