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Anesth Analg 1979; 58:274-278
© 1979 International Anesthesia Research Society
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Massive Blood Replacement

Correlation of Ionized Calcium, Citrate, and Hydrogen Ion Concentration

Roberta C. Kahn, MD*, Dennis Jascott, MD{dagger}, Graziano C. Carlon, MD{ddagger}, Olga Schweizer, MD§, William S. Howland, MD||, and Paul L. Goldiner, MD

*Clinical Assistant Attending, Department of Anesthesiology/ Intensive Care Unit. {dagger}Associate Attending Anesthesiologist. {dagger}Co-Director, Intensive Care Unit. §Chief of Service, Recovery Room. ||Vice President for Clinical Affairs and Chainnan, Department of Anesthesiology. ¶Associate Chairman, Department of Anesthesiology. Department of Anesthesia, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021.

Abstract

Fifty-three patients were studied intraoperatively during massive transfusion of CPD-preserved blood and fresh frozen plasma (FFP). Baseline concentrations of total calcium (Ca), ionized calcium (Ca2+), albumin, total protein, and hydrogen ion concentration [H+] were measured prior to transfusion, at intervals during transfusion of 2500 ml of blood, and at the end of transfusion. Systemic arterial pressure (BPI, central venous pressure (CVP) and/or pulmonary artery wedge pressure (PAW), and corrected Q-T intervals on electrocardiographic tracings were measured at the time blood samples were obtained.

Ca2+ decreased from 2.07 ± 0.03 mEq/L at baseline to 1.52 ± 0.05 mEq/L (p < 0.01) during transfusion at peak rates of 33 ± 3.2 ml/kg/hr. Following completion of transfusion, Ca2+ was significantly higher than at peak rates of transfusion, but still below baseline. Serum citrate levels rose from a baseline value of 1.87 ± 0.17 mg/dl to 6.30 ± 0.49 mg/dl (p < 0.01) at peak rate of transfusion and fell to 4.76 ± 0.48 immediately upon completion of transfusion (p < 0.011. The changes in Ca2+ and serum citrate levels showed a strong statistical correlation with each other. [H+] increased, but not significantly, at peak rates of infusion; after completion of transfusion, [H+] was significantly lower than during peak rates of transfusion. Ca levels were 4.10 ± 0.05 mEq/L at baseline, 3.90 ± 0.05 mEq/L at peak rates of infusion, and 3.89 ± 0.06 mEq/L after transfusion was completed. Albumin levels at the same sampling intervals were 3.60 ± 0.07, 3.71 ± 0.06, 3.87 ± 0.07 g/dl, respectively. Total protein levels were 5.95 ± 0.07, 5.67 ± 0.07, and 5.88 ± 0.09 g/dl, respectively.

Corrected Q-T intervals were significantly prolonged at peak rates of transfusion and upon completion of transfusion. Correlation between changes in Ca2+ and corrected Q-T intervals was statistically significant. However, hemodynamic variables remained stable throughout the period of observation.

Massive transfusions depressed Ca2+ due to administration of citrate, but this was only transient. Ca2+ rapidly returned to normal levels as citrate was redistributed and metabolized. The changes in Ca2+ were without hemodynamic significance. Clinically significant metabolic acidosis due to transfusion was not observed. We conclude, therefore, that as long as circulating volume is maintaines, as determined by measurement of CVP or PAW, calcium salts need to be administered during blood replacement, either empirically on the basis of rate or volume or transfusion, or on the basis of changes in samples indicate the development of metabolic acidosis.

Key Words: TRANSFUSION, Stored blood




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Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 1979 by the International Anesthesia Research Society.