In this issue of Revista Brasileira de Terapia Intensiva, Masevicius et al.( 11. Masevicius FD, Vazquez AR, Enrico C, Dubin A. Urinary strong-ion difference is a major determinant of the changes in plasma chloride concentration in postoperative patients. Rev Bras Ter Intensiva. 2013;25(3):197-204. ) reported on the behavior of the plasma chloride concentration ([Cl-]plasma) of 148 consecutive postoperative patients in the first 24 hours after their intensive care unit (ICU) admission. The authors' major finding was that, at the end of the first day in the ICU, the [Cl-]plasmawas primarily dependent upon the [Cl-]plasma on ICU admission and on the urinary strong ion difference ([SID]urine), also called the urinary anion gap. There were 3 patient groups: (1) increased, (2) decreased or (3) unaltered [Cl-]plasma during the 24 hours period. The increased [Cl-]plasma group had the lower [Cl-]plasma on ICU admission and the higher strong ion gap (SIG), i.e., the higher concentration of unmeasured anions. The opposite was observed in this same group after 24 hours: the higher [Cl-]plasma and the lower SIG. The volume of infused fluids and the SID of these fluids (only crystalloids) on the first ICU day were similar between groups, which led the authors to conclude that the fluids received during this period were not responsible for the distinct between-group [Cl-]plasma behaviors.
These results must be carefully interpreted. First, it is intuitive that the
[Cl-]plasma on ICU admission is a determinant of the
[Cl-]plasma after 24 hours because the latter greatly depends
on the former (which was different between groups) and the amount of [Cl-]
received during this 24 hours period (which was similar between groups). Normal saline,
which has a high [Cl-] content (154mEq/L, well above the initial
[Cl-]plasma in the 3 groups), was the primary fluid used;
therefore, a decreased or even an unchanged [Cl-]plasma would not
be expected. On the contrary, an increase in the [Cl-]plasma would
be expected in all groups, particularly in the group with the lower initial
[Cl-]plasma. At this point, the [SID]urine and the
total urine volume play crucial roles. Because the kidneys are the major organs
responsible for the SID regulation in plasma, it is expected that both the urine volume
and [SID]urine are determinants of the final
[Cl-]plasma. Diuresis volume in the 24 hours period was similar
between groups, which directed our attention to the [SID]urine. The urine is
the main fluid by which we excrete [Cl-]. Urinary [Cl-] excretion
is of paramount relevance in acid-base equilibrium because it is usually the anion that
follows ammonium (NH4
+) excretion, the main form of acid excretion by the organism. In the
Masevicius et al. study,(
11. Masevicius FD, Vazquez AR, Enrico C, Dubin A. Urinary strong-ion
difference is a major determinant of the changes in plasma chloride concentration in
postoperative patients. Rev Bras Ter Intensiva. 2013;25(3):197-204.
)
the increased [Cl-]plasma group had the higher [SID]urine,
suggesting less capacity to excrete [Cl-] and manage saline-induced
hyperchloremia. This finding could be an indirect sign of renal
impairment,(
22. Masevicius FD, Tuhay G, Pein MC, Ventrice E, Dubin A. Alterations in
urinary strong ion difference in critically ill patients with metabolic acidosis: a
prospective observational study. Crit Care Resusc.
2010;12(4):248-54.
3. Maciel AT, Park M, Macedo E. Urinary electrolyte monitoring in
critically ill patients: a preliminary observational study. Rev Bras Ter Intensiva.
2012;24(3):236-45.
-
44. Moviat M, Terpstra AM, van der Hoeven JG, Pickkers P. Impaired renal
function is associated with greater urinary strong ion differences in critically ill
patients with metabolic acidosis. J Crit Care. 2012;27(3):255-60.
) although in the present study, few
patients met an AKIN(
55. Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG,
Levin A; Acute Kidney Injury Network. Acute Kidney Injury Network: report of an
initiative to improve outcomes in acute kidney injury. Crit Care.
2007;11(2):R31.
)
stage 1 criterion for acute kidney injury (AKI), and the incidence of AKI was similar
between groups.
Another between-group difference was the SIG value upon ICU admission. It is difficult to explain the reasons why SIG had distinct values based solely on the information provided by the authors. In addition, in terms of prognosis and therapeutic management of critically ill patients, the SIG utility remains to be determined. The opposite behaviors of [Cl-] and unmeasured anions (one increases, the other decreases and vice-versa) may be a physiological phenomenon, which has been suggested as an explanation for hypochloremia in untreated diabetic ketoacidosis( 66. Funk GC, Zauner C, Bauer E, Oschatz E, Schneeweiss B. Compensatory hypochloraemic alkalosis in diabetic ketoacidosis. Diabetologia. 2003;46(6):871-3. ) or for an increased SIG in the presence of hypoalbuminemia.( 77. Gómez JL, Gunnerson KJ, Song M, Li J, Kellum JA. Effects of hypercapnia on BP in hypoalbuminemic and Nagase analbuminemic rats. Chest. 2007;131(5):1295-300. ) However, it may just be a mathematical coupling because until now, the SIG has been a calculated variable and not a directly measured variable. The fact that the increased [Cl-]plasma group had the higher SIG upon admission may also influence our interpretation of [SID]urine in the present study. In the presence of a predominantly SIG acidosis, it is possible that unmeasured anions, not [Cl-], follow urinary NH4 + excretion, which results in less [Cl-] excretion and higher [SID]urine values.
In conclusion, this important paper by Masevicius et al.( 11. Masevicius FD, Vazquez AR, Enrico C, Dubin A. Urinary strong-ion difference is a major determinant of the changes in plasma chloride concentration in postoperative patients. Rev Bras Ter Intensiva. 2013;25(3):197-204. ) brings some uncertainty about how to interpret the data: [SID]urine determines the changes in plasma [Cl-] or initial [Cl-] and SIG determine [SID]urine? Anyway, one certainty this study brings: we must evaluate the electrolyte composition of urine for a full understanding of the acid-base equilibrium, and intensivists should perform this evaluation daily. The relevance of urine in the ICU extends well beyond its volume and flow.
REFERÊNCIAS
-
1Masevicius FD, Vazquez AR, Enrico C, Dubin A. Urinary strong-ion difference is a major determinant of the changes in plasma chloride concentration in postoperative patients. Rev Bras Ter Intensiva. 2013;25(3):197-204.
-
2Masevicius FD, Tuhay G, Pein MC, Ventrice E, Dubin A. Alterations in urinary strong ion difference in critically ill patients with metabolic acidosis: a prospective observational study. Crit Care Resusc. 2010;12(4):248-54.
-
3Maciel AT, Park M, Macedo E. Urinary electrolyte monitoring in critically ill patients: a preliminary observational study. Rev Bras Ter Intensiva. 2012;24(3):236-45.
-
4Moviat M, Terpstra AM, van der Hoeven JG, Pickkers P. Impaired renal function is associated with greater urinary strong ion differences in critically ill patients with metabolic acidosis. J Crit Care. 2012;27(3):255-60.
-
5Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, Levin A; Acute Kidney Injury Network. Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury. Crit Care. 2007;11(2):R31.
-
6Funk GC, Zauner C, Bauer E, Oschatz E, Schneeweiss B. Compensatory hypochloraemic alkalosis in diabetic ketoacidosis. Diabetologia. 2003;46(6):871-3.
-
7Gómez JL, Gunnerson KJ, Song M, Li J, Kellum JA. Effects of hypercapnia on BP in hypoalbuminemic and Nagase analbuminemic rats. Chest. 2007;131(5):1295-300.
Publication Dates
-
Publication in this collection
Jul-Sep 2013