Autor: |
Giosa L; Department of Critical Care Medicine, Guy's and St. Thomas' National Health Service Foundation Trust, London, United Kingdom.; Centre for Human and Applied Physiological Sciences, King's College London, London, United Kingdom., Zadek F; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy., Busana M; Department of Anesthesiology, University Medical Center Göttingen, Göttingen, Germany., De Simone G; Department of Sciences, Roma Tre University, Rome, Italy., Brusatori S; Department of pathophysiology and Transplantation, University of Milan, Milan, Italy., Krbec M; Department of Anesthesia and Intensive Care Medicine, The Third Faculty of Medicine, Charles University and FNKV University Hospital, Prague, Czechia., Duska F; Department of Anesthesia and Intensive Care Medicine, The Third Faculty of Medicine, Charles University and FNKV University Hospital, Prague, Czechia., Brambilla P; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy., Zanella A; Department of pathophysiology and Transplantation, University of Milan, Milan, Italy., Di Masi A; Department of Sciences, Roma Tre University, Rome, Italy., Caironi P; Department of Anesthesia and Critical Care, AOU S. Luigi Gonzaga, Turin, Italy.; Department of Oncology, University of Turin, Turin, Italy., Perez E; Department of biomedical and neuromotor sciences, Headquarter of Human physiology, University of Bologna, Bologna, Italy., Gattinoni L; Department of Anesthesiology, University Medical Center Göttingen, Göttingen, Germany., Langer T; Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.; Department of Anesthesia and Intensive Care Medicine, Niguarda Ca' Granda, Milan, Italy. |
Abstrakt: |
It is commonly assumed that changes in plasma strong ion difference (SID) result in equal changes in whole blood base excess (BE). However, at varying pH, albumin ionic-binding and transerythrocyte shifts alter the SID of plasma without affecting that of whole blood (SID wb ), i.e., the BE. We hypothesize that, during acidosis, 1 ) an expected plasma SID (SID exp ) reflecting electrolytes redistribution can be predicted from albumin and hemoglobin's charges, and 2 ) only deviations in SID from SID exp reflect changes in SID wb , and therefore, BE. We equilibrated whole blood of 18 healthy subjects (albumin = 4.8 ± 0.2 g/dL, hemoglobin = 14.2 ± 0.9 g/dL), 18 septic patients with hypoalbuminemia and anemia (albumin = 3.1 ± 0.5 g/dL, hemoglobin = 10.4 ± 0.8 g/dL), and 10 healthy subjects after in vitro-induced isolated anemia (albumin = 5.0 ± 0.2 g/dL, hemoglobin = 7.0 ± 0.9 g/dL) with varying CO 2 concentrations (2-20%). Plasma SID increased by 12.7 ± 2.1, 9.3 ± 1.7, and 7.8 ± 1.6 mEq/L, respectively ( P < 0.01) and its agreement (bias[limits of agreement]) with SID exp was strong: 0.5[-1.9; 2.8], 0.9[-0.9; 2.6], and 0.3[-1.4; 2.1] mEq/L, respectively. Separately, we added 7.5 or 15 mEq/L of lactic or hydrochloric acid to whole blood of 10 healthy subjects obtaining BE of -6.6 ± 1.7, -13.4 ± 2.2, -6.8 ± 1.8, and -13.6 ± 2.1 mEq/L, respectively. The agreement between ΔBE and ΔSID was weak (2.6[-1.1; 6.3] mEq/L), worsening with varying CO 2 (2-20%): 6.3[-2.7; 15.2] mEq/L. Conversely, ΔSID wb (the deviation of SID from SID exp ) agreed strongly with ΔBE at both constant and varying CO 2 : -0.1[-2.0; 1.7], and -0.5[-2.4; 1.5] mEq/L, respectively. We conclude that BE reflects only changes in plasma SID that are not expected from electrolytes redistribution, the latter being predictable from albumin and hemoglobin's charges. NEW & NOTEWORTHY This paper challenges the assumed equivalence between changes in plasma strong ion difference (SID) and whole blood base excess (BE) during in vitro acidosis. We highlight that redistribution of strong ions, in the form of albumin ionic-binding and transerythrocyte shifts, alters SID without affecting BE. We demonstrate that these expected SID alterations are predictable from albumin and hemoglobin's charges, or from the noncarbonic whole blood buffer value, allowing a better interpretation of SID and BE during in vitro acidosis. |