Prediction of mortality with unmeasured anions in critically ill patients on mechanical ventilation
Abstract
Background/Aim. Acid-base disorders are common within critically ill patients. Physicochemical approach described by Stewart and modified by Figge gives precise quantification method of metabolic acidosis and insight into its main mechanisms, as well as influence of unmeasured anion on metabolic acidosis. The aims of this study were to determine whether the conventional acid-base variables are connected with survival rate of critically ill patients at Intensive care unit; whether strong ion difference/strong ion gap (SID/SIG) is a better predictor of mortality rate comparing to conventional acid-base variables; to determine all significant predictable parameters for the 28-day mortality rate at intensive care units. Methods. This retrospective observational analytic study included 142 adult patients requiring mechanical ventilation, survivors (n = 68) and nonsurvivors (n = 74). Apparent strong ion difference (SIDapp), effective strong ion difference (SIDeff) and SIG values were calculated with the Stewart-Figge’s quantitative biophysical method. Descriptive and analytical statistical methods were used in the study [t-test, Mann-Whitney U test, χ2-test, binary logistic regression, Reciever operating characteristic (ROC) curves, calibration]. Results. Age, Na+, acute physiology and chronic health evaluation (APACHE II), Cl-, albumin, SIG, SID app, SIDeff, and aninon gap (AG) were statistically significant predictors. AG represented a model with imprecise calibration, i.e. a model with little predictive power. APACHE II had p-value more than 0.05 if it was near it, and therefore it could be considered potentially unreliable for outcome prediction. SIDeff and SIG represented models with well-defined calibration. ROC analysis results showed that APACHE II, Cl-, albumin, SIDeff, SIG i AG had the largest area bellow the curve. By creation of logistic models with calibration methods, we found that outcome depends on SIG and APACHE II score. Conclusion. Based on our data, unmeasured anions provide prediction of mortality of critically ill patients on mechanical ventilation, unlike the traditional acid-base variables which are not accurate predictors of the 28-day mortality rate.
References
Gunnerson KJ, Srisawat N, Kellum JA. Is there a difference be-tween strong ion gap in healthy volunteers and intensive care unit patients. J Crit Care 2010; 25(3): 520−4.
Astrup P, Jorgensen K, Andersen OS, Engel K. The acid-base meta-bolism. A new approach. Lancet 1960; 14: 1035−9.
Kalezić N, Ugrinović Đ. Acido-base balance and disorders. In: Kalezić N, Ugrinović Đ, editors. Anesthesia and intensive care of surgical patients. Kragujevac: Faculty of Medicine; 2010. p. 155-183
Maciel AT, Park M. Differences in acid-base behavior between intensive care unit survivors and nonsurvivors using both a physicochemical and a standard base excess approach: a pros-pective, observational study. J Crit Care 2009; 24(4): 477−83.
Balasubramanyan N, Havens PL, Hoffman GM. Unmeasured anions identified by the Fencl-Stewart method predict mortali-ty better than base excess, anion gap, and lactate in patients in the pediatric intensive care unit. Crit Care Med 1999; 27(8): 1577−81.
Chawla LS, Shih S, Davison D, Junker C, Seneff MG. Anion gap, anion gap corrected for albumin, base deficit and unmeasured anions in critically ill patients: implications on the assessment of metabolic acidosis and the diagnosis of hyperlactatemia. BMC Emerg Med 2008; 8: 18.
Juneja D, Singh O, Dang R. Admission hyperlactatemia: causes, incidence, and impact on outcome of patients admitted in a general medical intensive care unit. J Crit Care 2011; 26(39: 316−20.
Moviat M, Terpstra AM, Ruitenbeek W, Kluijtmans LA, Pickkers P, van der Hoeven JG. Contribution of various metabolites to the "unmeasured" anions in critically ill patients with metabolic acidosis. Crit Care Med 2008; 36(3): 752−8.
Stewart PA. Modern quantitative acid-base chemistry. Can J Physiol Pharmacol 1983; 61(12): 1444−61.
Figge J, Rossing TH, Fencl V. The role of serum proteins in acid-base equilibria. J Lab Clin Med 1991; 117(6): 453−67.
Kellum JA. Closing the gap on unmeasured anions. Crit Care 2003; 7(3): 219−20.
Lopes AD, Maciel AT, Park M. Evolutive physicochemical cha-racterization of diabetic ketoacidosis in adult patients admitted to the intensive care unit. J Crit Care 2011; 26(3): 303−10.
Lloyd P, Freebairn R. Using quantitative acid-base analysis in the ICU. Crit Care Resusc 2006; 8(1): 19−30.
Rocktaeschel J, Morimatsu H, Uchino S, Bellomo R. Unmeasured anions in critically ill patients: can they predict mortality. Crit Care Med 2003; 31(8): 2131−6.
Hosmer D, Lemeshow S. Applied logistic regression. New York: Wiley; 2000.
Cusack RJ, Rhodes A, Lochhead P, Jordan B, Perry S, Ball JA, et al. The strong ion gap does not have prognostic value in critically ill patients in a mixed medical/surgical adult ICU. Intensive Care Med 2002; 28(7): 864−9.
Fidkowski C, Helstrom J. Diagnosing metabolic acidosis in the critically ill: bridging the anion gap, Stewart, and base excess methods. Can J Anaesth 2009; 56(3): 247−56.
Boniatti MM, Cardoso PR, Castilho RK, Vieira SR. Acid-base dis18, orders evaluation in critically ill patients: we can improve our diagnostic ability. Intensive Care Med 2009; 35(8): 1377−82.
Kaplan LJ, Kellum JA. Initial pH, base deficit, lactate, anion gap, strong ion difference, and strong ion gap predict outcome from major vascular injury. Crit Care Med 2004; 32(5): 1120−4.
Antonini B, Piva S, Paltenghi M, Candiani A, Latronico N. The early phase of critical illness is a progressive acidic state due to unmeasured anions. Eur J Anaesthesiol 2008; 25(7): 566−71.
Fencl V, Jabor A, Kazda A, Figge J. Diagnosis of metabolic acid-base disturbances in critically ill patients. Am J Respir Crit Care Med 2000; 162(6): 2246−51.
