Evidence map›Paper›PMID 42561704›Full record

ArticleHematology, transfusion and cell therapy2026

In vitro compatibility of whole blood with commonly used medications in the pediatric trauma setting.

Summer Byerley, David Nash, Pamela D Reiter

Abstract read
In one paragraph

Article in Hematology, transfusion and cell therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Summer ByerleyDepartment of Pharmacy, Children's Hospital Colorado, 4090 Briargate Parkway Colorado Springs, Aurora, CO, 80920, USA.
David NashDepartment of Pharmacy, Children's Hospital Colorado, 4090 Briargate Parkway Colorado Springs, Aurora, CO, 80920, USA.
Pamela D ReiterDepartment of Pharmacy, Children's Hospital Colorado, 4090 Briargate Parkway Colorado Springs, Aurora, CO, 80920, USA. Electronic address: pam.reiter@childrenscolorado.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCurrent guidelines do not endorse co-infusion of blood with medication due to concerns for hemolysis and/or clotting. However, concomitant delivery may be required in emergency situations with limited intravenous access. The purpose of this study was to explore the physical compatibility of nine medications used in pediatric emergencies with leukoreduced group O whole blood.

methodsBlood was manually mixed with study medication and centrifuged at 6500 RPMs for three minutes. A mixture of normal saline and whole blood served as the control. The supernatant was tested for hemolysis using lactate dehydrogenase activity. Each sample was inspected for coalescence or separation. Two separate experiments were performed to demonstrate reproducibility. Compatibility was defined as the absence of gross clot formation/separation provided that lactate dehydrogenase concentrations remained below control values and increased by no more than10% from baseline.

resultsLactate dehydrogenase activity was measured at two intervals: 15 to 30min and 30 to 60min post-mixing. Cefazolin, epinephrine, succinylcholine, and tranexamic acid in combination with whole blood yielded lactate dehydrogenase concentrations that were stable and below the control values - thus, these were considered compatible at 30-60min. Etomidate and rocuronium could not be analyzed due to either mechanical interference or high analyte concentrations and were considered incompatible. Norepinephrine, calcium chloride, and sodium bicarbonate were considered incompatible as they exceeded the 10% threshold, exhibited lactate dehydrogenase values above control, or showed evidence of separation.

conclusionCo-infusion of select medications with whole blood may be considered in the setting of limited intravenous access.

Indexed as

CompatibilityMedicationWhole blood

Identifiers

PMID42561704
PMCPMC13464203

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.