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Updated: Jan 24, 2026

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
Published on: January 12, 2018
Effect of incubation with crystalloid solutions or medications on packed red blood cells
Domagoj Mladinov1, Kristine Yarnoff2, Enika Nagababu1
1Department of Anesthesiology, University of Alabama, Birmingham, Alabama.
Insights
Co-incubating packed red blood cells (PRBCs) with isotonic crystalloids or catecholamines for five minutes does not harm PRBCs. However, co-incubation with 5% dextrose in water (D5W) or Propofol may increase hemolysis.
Area of Science:
- Transfusion Medicine
- Hematology
- Critical Care Medicine
Background:
- Current American Association of Blood Banks (AABB) guidelines recommend dedicated intravenous (IV) catheters for packed red blood cell (PRBC) administration.
- Limited literature supports this recommendation, despite the risks associated with obtaining additional IV access, including pain, cost, and infection.
- This study investigates the impact of co-incubating PRBCs with common crystalloids and medications on key red blood cell parameters.
Purpose of the Study:
- To evaluate the effect of co-incubating PRBCs with various crystalloids and medications on PRBC hemolysis, membrane deformability, and aggregation.
- To assess the impact of co-incubation on medication concentration within the PRBC mixture.
- To provide evidence-based data to inform transfusion practices regarding IV catheter use for PRBC administration.
Main Methods:
- Packed red blood cells (PRBCs) were co-incubated for 5 minutes with plasma, normal saline (NS), 5% dextrose in water (D5W), Plasmalyte, epinephrine, norepinephrine, dopamine, or Propofol.
- Assessed parameters included hemolysis (free hemoglobin, serum potassium), membrane deformability (elongation index), aggregation (smear, critical shear stress), and drug concentration using LCMS-MS.
- Statistical significance was determined using Wilcoxon-paired comparisons or Wilcoxon/Kruskall Wallis with post-hoc Dunn's test.
Main Results:
- Co-incubation with D5W significantly increased hemolysis (elevated free hemoglobin and potassium) compared to plasma.
- Membrane deformability showed a trend towards lower values with D5W and higher values with Propofol.
- PRBC aggregation was significantly reduced with NS, D5W, and Plasmalyte, and trended lower with epinephrine, norepinephrine, and dopamine.
- Medication concentrations were intermediate between predicted values based on plasma-only or full distribution.
Conclusions:
- Short-term (5 minutes) co-incubation of PRBCs with isotonic crystalloids or catecholamines does not adversely affect hemolysis, membrane deformability, or aggregation.
- 5% dextrose in water (D5W) co-incubation appears to increase PRBC hemolysis.
- Propofol co-incubation may also promote hemolysis, warranting further investigation.
Background:
American Association of Blood Banks (AABB) guidelines suggest that packed red blood cells (PRBCs) be administered through a dedicated intravenous (IV) catheter. Literature supporting this broad-scope declaration are scarce. Obtaining additional IV access is painful, costly, and an infectious risk. We evaluated the effect of co-incubating PRBCs with crystalloids and medications on PRBC hemolysis, membrane deformability, and aggregation, as well as medication concentration.
Methods:
PRBCs were co-incubated 5 minutes with plasma, normal saline (NS), 5% dextrose in water (D5W), Plasmalyte, epinephrine (epi), norepinephrine (norepi), dopamine (dopa), or Propofol (prop). Samples were then assessed for hemolysis (free hemoglobin, serum potassium), membrane deformability (elongation index [EI]), aggregation (smear, critical shear stress [mPa]) and drug concentration (High Performance Liquid Chromatography/Tandem Mass Spectrometry [LCMS-MS]). Significance (p ≤ 0.05) was determined by Wilcoxon-paired comparisons or Wilcoxon/Kruskall Willis with post-hoc Dunn's test.
Results:
Compared to co-incubation with plasma: 1) co-incubation resulted in significantly increased hemolysis only when D5W as used (free hemoglobin, increased potassium); 2) EI trended lower when co-incubated with D5W and trended toward higher when co-incubated with prop; 3) aggregation was significantly lower when PRBCs co-incubated with NS, D5W, or Plasmalyte, and trended lower when co-incubated with epi, norepi, or dopa. Medication concentrations were between those predicted by distribution only in plasma and distribution through the entire intra- and extracellular space.
Conclusion:
Our data suggest that 5 minutes of PRBC incubation with isotonic crystalloids or catecholamines does not deleteriously alter PRBC hemolysis, membrane deformability, or aggregation. Co-incubation with D5W likely increases hemolysis. Propofol may promote hemolysis.
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