Correspondence  |   February 2000
Avoiding Iatrogenic Hyperchloremic Acidosis—Call for a New Crystalloid Fluid
Author Notes
  • Rebecca Terry White Distinguished Chair
  • Department of Anesthesiology
  • Professor and Chief
  • Section on Pulmonary Medicine and Critical Care
  • The University of Texas Medical Branch
  • Galveston, Texas 77555-0591
Article Information
Correspondence   |   February 2000
Avoiding Iatrogenic Hyperchloremic Acidosis—Call for a New Crystalloid Fluid
Anesthesiology 2 2000, Vol.92, 625. doi:
Anesthesiology 2 2000, Vol.92, 625. doi:
In Reply:—
We appreciate the comments of Drummond 1 and Story et al.  2 Both letters address issues that clarify the report by Scheingraber et al.  3 
First, Drummond 1 appropriately calls additional attention to the important study by his colleagues at the Royal Infirmary in Edinburgh. 4 Both McFarlane and Lee 4 and Scheingraber et al.  3 conducted randomized clinical trials comparing 0.9% saline balanced salt solutions. The two studies differ in that McFarlane and Lee 4 enrolled patients undergoing “major hepatobiliary or pancreatic surgery” averaging approximately 3.5 h in duration, whereas Scheingraber et al.  3 enrolled patients undergoing “lower abdominal gynecologic surgery” averaging approximately 2.25 h. Despite the somewhat shorter duration of surgery, the gynecologic patients randomized to the saline group received a slightly greater total volume 3 (71 ± 14 ml/kg during the first 120 min of infusion) than the patients receiving saline in the study by McFarlane et al.  4 (14.6 ± 41 ml · kg−1· h−1during an interval of 219 ± 77 min). As a consequence, the increase in plasma chloride and the decrease in plasma bicarbonate were greater in the gynecologic patients. Together, the reports suggest that hyperchloremic acidosis is a dose-dependent consequence of saline administration. Whether this acid–base abnormality is in fact harmful remains unclear, although we 5 were unable to cite any compelling evidence of adverse effects. We are skeptical that differences in outcome, if any, related to the choice of saline or balanced salt solution would justify the cost of a randomized clinical trial.
However, one noteworthy characteristic of Plasmalyte 148, the balanced salt solution used by McFarlane and Lee, 4 is that the sodium concentration is 140 mEq/l. Consequently, in contrast to lactated Ringer’s solution, infusion of substantial volumes does not decrease serum sodium and serum osmolality, and does not raise the same theoretical concerns about increases in brain water. 5 
We agree with Story et al.  2 that the Stewart approach 6,7 offers interesting insights into acid–base chemistry; however, we disagree that the relative merits of the Stewart approach versus  the conventional Henderson-Hasselbalch approach constitute a “central issue.” Regardless of its attractive biochemical features, the Stewart approach has not yet become popular for routine clinical use, perhaps because it is less simple to quantify at the bedside and because it prompts no important differences in treatment.
Drummond GB: Article supports findings of previous comparison. ANESTHESIOLOGY 2000; 92:625Drummond, GB
Story DA, Liskaser F, Bellomo R: Saline infusion, acidosis and the Stewart approach. ANESTHESIOLOGY 2000; 92:624Story, DA Liskaser, F Bellomo, R
Scheingraber S, Rehm M, Sehmisch C, Finsterer U: Rapid saline infusion produces hyperchloremic acidosis in patients undergoing gynecologic surgery. ANESTHESIOLOGY 1999; 90:1265–70Scheingraber, S Rehm, M Sehmisch, C Finsterer, U
McFarlane C, Lee A: A comparison of Plasmalyte 148 and 0.9% saline for intra-operative fluid replacement. Anaesthesia 1994; 49:779–81McFarlane, C Lee, A
Prough DS, Bidani A: Hyperchloremic metabolic acidosis is a predictable consequence of intraoperative infusion of 0.9% saline. ANESTHESIOLOGY 1999; 90:1247–9Prough, DS Bidani, A
Stewart PA: Modern quantitative acid–base chemistry. Can J Physiol Pharmacol 1983; 61:1444–61Stewart, PA
Fencl V, Leith DE: Stewart’s quantitative acid–base chemistry: Applications in biology and medicine. Respir Physiol 1993; 91:1–16Fencl, V Leith, DE