Comparative Quantitative Acid Base Analysis in Coronary Artery Bypass, Severe Sepsis, and Diabetic Ketoacidosis

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Edward M. Omron MD, MPH
Pulmonary, Critical Care Medicine
Morgan Hill, CA 95037

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Comparative Quantitative Acid Base Analysis in Coronary Artery Bypass, Severe Sepsis, and Diabetic Ketoacidosis

  1. 1. Journal of Intensive Care Medicine http://jic.sagepub.com Comparative Quantitative Acid-Base Analysis in Coronary Artery Bypass, Severe Sepsis, and Diabetic Ketoacidosis Edward M. Omron J Intensive Care Med 2005; 20; 269 DOI: 10.1177/0885066605279955 The online version of this article can be found at: http://jic.sagepub.com/cgi/content/abstract/20/6/269 Published by: http://www.sagepublications.com Additional services and information for Journal of Intensive Care Medicine can be found at: Email Alerts: http://jic.sagepub.com/cgi/alerts Subscriptions: http://jic.sagepub.com/subscriptions Reprints: http://www.sagepub.com/journalsReprints.nav Permissions: http://www.sagepub.com/journalsPermissions.nav Citations http://jic.sagepub.com/cgi/content/refs/20/6/269 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009
  2. 2. REVIEW OF A LARGE CLINICAL SERIES Comparative Quantitative Acid-Base Analysis in Coronary Artery Bypass, Severe Sepsis, and Diabetic Ketoacidosis Edward M. Omron, MD, MPH, FCCP altered in multiple disease states. Separation of the The main objective of this study was to assess the rela- metabolic versus the respiratory components has tionship of standard base excess (SBE) to delta strong ion difference effective ( SIDe) in critical illness. Critical ill- been attempted using derived parameters such ness is characterized by variable plasma nonvolatile weak as [HCO3–], anion gap, confidence intervals, and acid components ( A–), and SBE becomes discordant with base excess derivatives [1]. All of these approaches SIDe. The author hypothesized that both acid-base mod- assume a normal plasma nonvolatile weak acid els are equivalent when SBE and SIDe are corrected for buffer content (albumin and inorganic phosphate). A–. A retrospective chart review was performed to assess this hypothesis by looking at changes in SBE, SIDe, and This assumption originates from the first clinical A– in 30 coronary artery bypass graft surgery patients, studies of metabolic acid-base status [2–5]. It is now 30 severe sepsis patients, and 15 diabetic ketoacidosis realized that the main plasma weak-acid buffers are patients. SBE equals the sum of the SIDe and A–. The albumin and inorganic phosphate and that major SBE quantifies the magnitude of the metabolic acid-base surgery and acute illness result in large fluctuations derangement, the SIDe quantifies the plasma strong cat- ion/anion imbalance, and the A– quantifies the magnitude of albumin concentration [6,7]. of the hypoalbuminemic alkalosis. The partitioning of SBE Both standard base excess (SBE) and physico- into physicochemical components can facilitate analyses chemical analysis are quantitative measures of of complex acid-base disorders in critical illness. metabolic acid-base status. Physicochemical analy- sis introduces strong ion difference effective (SIDe) Key words: acidosis, alkalosis, anion gap, buffers, hypoalbu- as a measure of plasma cation/anion imbalance and minemia incorporates the variable plasma nonvolatile weak acid buffer content ( A–) [8–12]. In contrast, SBE measurement assumes a normal plasma nonvolatile Accurate assessment of metabolic acid-base status weak acid buffer content [5]. At normal plasma is of critical importance in the intensive care unit. weak acid buffer concentrations (albumin, phos- Hydrogen ion concentration and PaCO2 form the phate), a change in SBE must always be accom- traditional front line of investigation during initial panied by an equal change in SIDe ( SIDe), and assessment and are the key physiologic parameters thus both parameters are equivalent quantitative measures of metabolic acid-base status in this spe- From the Division of Pulmonary Medicine, National Naval cial circumstance [6,13]. Critical illness, however, is Medical Center, Bethesda, MD. characterized by variable plasma nonvolatile weak Received Oct 13, 2004, and in revised form Mar 30, 2005. acid components ( A–), and thus a change in SBE Accepted for publication Jun 9, 2005. no longer correlates with a change in SIDe, and Address correspondence to Edward M. Omron, MD, MPH, Pulmonary and Critical Care Specialists, P.C., 39650 Orchard Hill which parameter is the better measure of acid-base Place, Suite 100, Novi, MI 48375-5331, or e-mail: edwardom- derangements is the focus of debate [6,13–15]. ron@hotmail.com. Physicochemical analysis allows direct calculation The opinion or assertions contained herein are the private of A–, and the author hypothesized that equiva- views of the author and are not construed as official or as reflecting the views of the Department of the Navy, Army or lence between both acid-base models would again the Department of Defense. be restored if SBE and SIDe were corrected for I gratefully acknowledge the kind assistance of Kevin M. A–. Restoration of equivalence between both acid- O’Neil, MD; Thomas M. Fitzpatrick, MD, PhD; Russell C. base models at variable plasma nonvolatile weak Gilbert, MD; and Rodney M. Omron, MD, MPH, for insightful discussions in the preparation of this manuscript. acid concentrations would prove useful by allowing Omron EM. Comparative quantitative acid-base analysis in SBE to be partitioned into physicochemical com- coronary artery bypass, severe sepsis, and diabetic ketoacido- ponents and thus facilitate analyses of metabolic sis. J Intensive Care Med. 2005;20:269-278. acid-base disorders. To assess the hypothesis that DOI: 10.1177/0885066605279955 SBE equals the algebraic sum of SIDe and A– at Copyright © 2005 Sage Publications Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009 269
  3. 3. Omron variable plasma nonvolatile weak acid buffer con- [Mg2+], and [Ca2+] in mEq/L—can be found in the centrations, the author performed a retrospective appendix. chart review looking at changes in SBE, SIDe, Descriptive statistics and formula calculations and A– in three critically ill groups: pre- and post- were performed using Microsoft Excel 97 Data coronary artery bypass graft (CABG) surgery, severe Analysis Package (Microsoft, Redmond, Wa). Statis- sepsis, and diabetic ketoacidosis (DKA) patients on tical analysis consisted of the two-tailed Student’s admission and during recovery. t test for equal and unequal variances for direct comparisons between study variables and linear regression. Statistical significance was achieved if Materials and Methods the two-tailed P value was <.05. Logistic regression analysis was performed using JMP release 5.1 (SAS The medical records of 30 consecutive nonemer- Institute, Cary, NC). Paired data were analyzed gent CABG surgery, 30 severe sepsis, and 15 DKA graphically by Bland-Altman analysis [19]. In this patients who presented to Walter Reed Army analysis, the mean difference between the paired Medical Center surgical and medical intensive care measurements is plotted against the average of the units were reviewed. CABG patients had labora- two values to visually display bias and precision. tory values drawn immediately before surgery and Data are expressed as the mean 95% confidence then again after presentation to the surgical inten- interval (CI). The Department of Clinical Investigation at Walter sive care unit per cardiothoracic surgery protocol. Reed Army Medical Center approved this study. Severe sepsis and DKA patients had laboratory values drawn on presentation to the intensive care unit. Severe sepsis was established by published criteria [16,17]. The diagnosis of DKA was based on Review of Models the classic criteria of positive serum acetone and urinary ketones, hyperglycemia, and an anion gap Standard Base Excess. The base excess (BE) of metabolic acidosis. whole blood equals the quantity of strong acid or Patient data, including age, admission diagnosis, base (mmol/L or mEq/L) needed to restore plasma sex, and laboratory values, were collected by retro- pH to 7.4 at a PaCO2 equilibrated to 40 mm Hg at a spective chart review. Laboratory samples were col- temperature of 37°C. A positive value indicates an lected from an indwelling arterial line and handled excess of base, whereas a negative value indicates according to standardized hospital protocols. Labo- an excess of fixed acid. ratory values recorded include [Na+], [K+], [Mg2+], The normal buffer base of blood is the sum of [Ca2+], [Cl–], creatinine, lactate, albumin, inorganic the buffer anions of the blood and plasma ([HCO3–], phosphate, serum acetone, pH, PaCO2, and urinaly- hemoglobin, and total protein) at a pH of 7.4 and sis to assess for ketonuria. Samples were analyzed PaCO2 of 40 mm Hg, at a hemoglobin concentration by clinical staff at the hospital central laboratory of 15 g/dL and fixed total protein = 7.2 g/dL. The by the Vitros Chemistry System (Ortho-clinical buffer base (BB) of blood is normally 48 mEq/L, diagnostics, Johnson and Johnson, Rochester, NY) and changes in the BB quantify the metabolic com- and the Rapilab 865 Blood Gas Analyzer System ponent of an acid-base disorder. The buffer base (Bayer, Tarrytown, NY). The Vitros chemistry will vary with changing hemoglobin concentration system uses both direct and indirect ion-selective and is related to the BE (in vitro or whole blood) methodologies for measurement. Cardiorespiratory, as follows: BE = BB (measured) – 48 [4,5,20]. In laboratory, and neurologic data were extracted this model, a constant plasma nonvolatile weak to determine the Acute Physiology and Chronic acid buffer total (albumin, inorganic phosphate) Health Evaluation (APACHE II) [18] score in the is assumed. In vitro, BE remains constant as PaCO2 severe sepsis group. is varied. In vivo, however, this linear relationship Equations used for calculation of derived param- is not preserved [21,22]. Acute changes in PaCO2 eters—strong ion difference effective (SIDe), delta induce a redistribution of strong ions not only strong ion difference effective ( SIDe), strong ion within the blood but also throughout the extracel- difference apparent (SIDa), strong ion gap (SIG), lular fluid compartment as compensation, indepen- standard base excess (SBE), actual bicarbonate dent of renal mechanisms, skewing the base excess [HCO3–]HH, plasma nonvolatile weak acid buffer nomogram. Empirical observations in the 1960s content (A–), plasma nonvolatile weak acid buf- revealed that this buffering effect in vivo could be fer deficit ( A–), anion gap (ANG), adjusted ANG, corrected for if the blood sample is diluted three- 270 Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009
  4. 4. Comparative Quantitative Acid-Base Analysis fold with plasma or by setting the hemoglobin anions or cations are collectively termed the strong equal to 5 g/dL. This modified in vitro base excess ion gap (SIG) and are codeterminants of the strong was designated as standard base excess (SBE) or ion difference. The strong ion gap is calculated as BE extracellular fluid and is conventionally calcu- SIG = SIDa – SIDe and quantitatively reflects the lated as Equation 5 in the appendix [23]. SBE is a unmeasured acid component of a metabolic acid- quantitative estimate of the magnitude of a meta- base disorder [12]. The SIG is normally <6 mEq/L. It bolic acid-base derangement in vivo with respect to is independent of changes in [albumin–] or pH. The the extracellular fluid compartment. anion gap (ANG) is akin to the SIG and is calcu- lated from Equation 9 in the appendix [25]. Unlike Physicochemical Analysis. In the physicochemical the SIG, the value of the ANG includes the negative analysis model, there are 3 independent determi- charge component of the albumin moiety and is nants of hydrogen and bicarbonate ion concen- profoundly affected by albumin and hydrogen ion tration within the plasma compartment in vivo: concentration [26]. An adjusted ANG is calculated PaCO2, the SID, and total concentration of plasma according to equation 10 in the appendix, which nonvolatile weak acid buffers [24]. The SID consists corrects for hypoalbuminemia [27]. of 2 components, the strong ion difference effective The total concentration of plasma nonvolatile and apparent. The strong ion difference effective weak acid buffers is composed of [albumin–] and (SIDe) is the net electrical charge difference of the inorganic phosphate ([PI]) and consists of the plasma strong cations minus the strong anions and disassociated (A–) and undisassociated (HA) com- is in charge balance with the plasma buffer base. ponents. Normal baseline in plasma is set to [albu- Strong electrolytes are completely dissociated and min–] = 4.4 g/dL, and [PI] = 3.6 mg/dL. The focus of chemically nonreacting. The plasma buffer base this analysis is on the disassociated component, A–, consists of both the volatile ([HCO3–]) and non- which reflects the net charge (mEq/L) of both albu- volatile (albumin and inorganic phosphate) weak min and inorganic phosphate and is derived from acid buffers within the plasma compartment. This Equation 7 in the appendix [12]. The nonvolatile differs from the SBE buffer base in several respects: weak acid buffer deficit ( A–) reflects alterations Hemoglobin is not considered a plasma buffer in the concentrations of albumin and phosphate and is not included in the calculation, the analysis from normal baseline, consequent to surgery or is limited to the plasma compartment versus the acute illness, and is derived from equation 8 in the extracellular fluid compartment, and the equations appendix. Note that A– is expressed as a positive are not empirical but are derived from the laws of quantity because a decrement in plasma nonvola- electrical neutrality, conservation of mass, and dis- tile weak acid content is equal to a gain in base. sociation equilibria. Deviation from the normal SIDe value of 39 mEq/ L reflects the magnitude of the strong cation/anion imbalance and metabolic acid-base derangement Results in vivo in the plasma compartment. SIDe is calcu- lated from Equation 1 in the appendix [12]. In the In the 30 CABG patients (Table 1), mean values base excess format for direct comparison of SBE ( 95% CI) were age = 63 4 years, and time with SIDe, the delta strong ion difference effective between pre- and postsurgery measurements = 338 is calculated as SIDe = SIDe (measured) – 39. A 20 minutes. In presurgery CABG patients, the SBE positive value indicates an excess of base or plasma was equivalent to the algebraic sum of the SIDe strong cations, whereas a negative value indicates and A–. The difference between SIDe (–0.1 an excess of fixed acid or plasma strong anions. 0.08 mEq/L) and SBE (0.8 0.6 mEq/L) approached The strong ion difference apparent (SIDa) is the statistical significance (P = .06), and the plasma net electrical charge difference between the com- nonvolatile weak acid buffer content was mildly monly measured strong cations minus the strong reduced ( A– = 1.0 0.5 mEq/L). The change in anions in the plasma. The SIDa differs from SIDe in SBE presurgery (0.8 0.6 mEq/L) and postsurgery that unmeasured anions or cations are not included (–1.0 0.5 mEq/L) was statistically significant (P < in the calculation. The normal value for SIDa varies .001) but did not suggest the presence of a signifi- from 42 to 44 mEq/L and is derived from equation cant metabolic acid-base disorder. 3 in the appendix [12]. In contrast, the changes in SIDe and A– presur- In critical illness, unmeasured anions or cations gery (–0.1 0.8 mEq/L, 1.0 0.5 mEq/L) and post- may appear (eg, ketone acids, anions of renal surgery (–7.4 0.8 mEq/L, 6.4 0.5 mEq/L) were failure, cationic paraproteins, etc). These strong statistically significant (P < .001), which did suggest Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009 271
  5. 5. Omron Table 1. Demographic and Clinical Laboratory Characteristics of the Study Groups Coronary Artery Severe DKA Bypass Graft Surgery (n = 30) Sepsis (n = 15) (n = 10) (n = 11) Characteristic Presurgery Postsurgery (n = 30) Admission 12 Hours Resolution Age (years) 63 4 61 4 34 11 Sex, M/F 21/9 17/13 6/9 Laboratory data pH 7.43 0.02 7.41 0.03 7.35 0.03 7.15 0.11 7.26 0.08 7.37 0.04 PaCO2 (mm Hg) 38.5 1.1 37.9 3.1 32.5 2.4 19.4 5.0 25.7 8.6 33.0 3.7 [HCO3–]HH (mmol/L) 24.7 0.6 23.1 0.5 17.8 1.5 8.3 3.4 12.3 5.5 18.9 3.1 SIDe (mEq/L) –0.1 0.8 –7.4 0.8 –10.9 1.8 –17.9 3.4 –17.0 6.0 –10.1 3.0 SBE (mEq/L) 0.8 0.6 –1.0 0.5 –6.8 1.7 –18.6 4.5 –13.2 6.0 –5.5 3.3 SIDa (mEq/L) 43.8 0.7 33.4 0.7 37.5 2.3 43.1 3.9 32.8 4.6 35.0 3.0 SIDe (mEq/L) 38.9 0.8 31.6 0.8 28.1 1.8 21.1 3.4 22.0 6.0 28.9 3.1 Anion gap 16 1 9 1 18 2 31 5 17 3 12 2 Adjusted anion gap 17 1 14 1 22 2 32 3 20 2 16 2 SIG (mEq/L) 4.9 0.9 1.8 0.5 9.4 1.3 22.1 3.7 10.8 2.3 6.0 1.8 Lactate (mEq/L) 0.8 0.1 1.9 0.4 2.4 0.8 NA NA NA Sodium (mEq/L) 143 1 136 1 138 2 140 4 142 6 142 4 Potassium (mEq/L) 4.1 0.2 3.7 0.1 4.2 0.3 4.3 0.4 3.5 0.4 3.7 0.2 Magnesium (mEq/L) 1.6 0.1 1.9 0.1 1.8 0.3 1.5 0.2 1.8 0.3 1.7 0.3 Calcium (mEq/L) 2.3 0.1 2.0 0.1 2.1 0.1 2.3 0.1 2.1 0.2 2.1 0.1 Chloride (mEq/L) 106 1 108 1 106 3 105 4 116 6 114 6 Albumin (g/dL) 4.0 0.2 2.4 0.2 2.8 0.3 4.2 0.5 3.2 0.3 3.1 0.4 Phosphorus (mg/dL) 3.7 0.2 2.4 0.2 4.2 0.6 4.3 1.0 2.0 0.7 2.1 0.4 A– (mEq/L) 13.6 0.5 8.1 0.4 10 0.7 12.7 1.4 9.4 1.3 9.7 1.0 A– (mEq/L) 1.0 0.5 6.4 0.5 4.1 0.7 0.2 1.6 4.2 1.1 4.6 1.0 Creatinine (mg/dL) NA 0.9 0.1 2.7 0.8 1.2 0.3 0.8 0.1 1.4 0.8 APACHE II NA NA 25 2.8 NA NA NA A– – plasma nonvolatile weak acid buffer content; A– – plasma nonvolatile weak acid buffer deficit; DKA – diabetic ketoacidosis; HCO3–HH – actual bicarbonate; M– male; F – female; NA – data not available; SBE – standard base excess; SIDe – delta strong ion dif- ference effective; SIDa – strong ion difference apparent; SIDe – strong ion difference effective; SIG – strong ion gap; APACHE – Acute Physiology and Chronic Health Evaluation. Data are expressed as mean 95% confidence interval. the development of a marked metabolic acidosis mEq/L and SIDe = –10.9 1.8 mEq/L (P < .0001). postoperatively with significant loss of plasma weak Plasma nonvolatile weak-acid buffer content was acid buffer content, mostly from hypoalbuminemia decreased, A– = 4.1 0.7 mEq/L, mostly from ([albumin–]pre-CABG = 4.0 0.2, [albumin–]post-CABG = 2.4 hypoalbuminemia ([albumin–] = 2.8 0.3 g/dL). 0.2 g/dL). The SBE was equivalent to the sum of The SBE was equivalent to the sum of the SIDe the SIDe and A– in post-CABG surgery patients. and A–. The SIG = 9.4 1.3 mEq/L and adjusted There were marked changes in electrolytes post- ANG = 22 2 were elevated, indicating the presence operatively with [Na+] decreasing, [Cl–] increasing, of significant unmeasured anions. The ANG = 18 2 and [albumin–] and inorganic phosphate decreasing was only marginally elevated. Univariate logistic (Table 1). The SIG decreased postoperatively from regression analysis was performed between survi- 4.9 0.9 mEq/L to 1.8 0.6 mEq/L, indicating mini- vors and nonsurvivors in the severe sepsis patients. mal presence of unmeasured anions or possibly the The adjusted ANG (odds ratio = 12.2, P = .17, area presence of unmeasured/unidentified cations. The under receiver operating characteristic curve = ANG and adjusted ANG decreased postoperatively 0.67) and SIG (odds ratio = 4.4, P = .4, area under from 16 1 to 9 1 mmol/L and 17 1 to 14 1 receiver operating characteristic curve = 0.57) were mmol/L, respectively. not significant predictors of mortality. In the 30 severe sepsis patients (Table 1), age = In the 15 diabetic ketoacidosis patients (Table 1), 61 4 years, APACHE II score = 25 3, and over- age = 34 11 years. All patients were serum acetone all mortality = 12/30 (40%). The pH = 7.35 0.03, and urine ketone positive with hyperglycemia, the PaCO2 = 32.5 2.4 mm Hg, and the [HCO3–]HH = glucose = 436 75 mg/dL. Admission pH = 7.15 17.7 1.5 mmol/L indicated the presence of a 0.11, PaCO2 = 19.4 5.0 mm Hg, and [HCO3–]HH = metabolic acidosis with acute respiratory compen- 8.3 3.4 mmol/L indicated the presence of a severe sation. The magnitude of the metabolic acidosis metabolic acidosis with acute respiratory compensa- was markedly disparate between SBE = –6.8 1.7 tion. Both SIDe = –17.9 3.4 mEq/L and SBE = 272 Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009
  6. 6. Comparative Quantitative Acid-Base Analysis –18.6 4.5 mEq/L were not statistically different Pre- CABG Post- CABG Severe Sepsis DKA Admission 12 hours Resolution (P = .81) and were thus equivalent measures of the 10 n = 30 n = 30 n = 30 n = 15 n = 10 n = 11 magnitude of the metabolic acidosis. Plasma weak 5 acid buffer content was only slightly reduced, A– = 0 0.2 1.6 mEq/L, from normal baseline secondary to -5 mEq/L preserved albumin concentration ([albumin–] = 4.2 -10 0.5 mg/dL). The SIG = 22.1 3.7 mEq/L, adjusted Delta SIDe -15 ANG = 32 3 mmol/L, and ANG = 31 5 mmol/L SBE -20 were markedly elevated on admission indicating Delta A- the presence of a significant organic acidosis. -25 At DKA resolution, pH = 7.37 0.04, PaCO2 = 33.0 *Values expressed as mean 95% CI 3.7 mm Hg, and [HCO3–]HH = 18.9 3.1 mmol/L Fig 1. In pre- and post-coronary artery bypass graft (CABG) consistent with a mild metabolic acidosis with respira- surgery, severe sepsis, and diabetic ketoacidosis (DKA) tory compensation. The magnitude of the metabolic patients, standard base excess (SBE) equals the algebraic acidosis was disparate between SIDe = –10.1 sum of the delta strong ion difference effective ( SIDe) and plasma nonvolatile weak acid buffer deficit ( A–). 3.0 mEq/L and SBE = –5.5 3.3 mEq/L (P < .0001). The plasma nonvolatile weak acid buffer content acidoses by restoring pH and bicarbonate toward was decreased, A– = 4.6 1.0 mEq/L, mostly from normal. For example, by physicochemical analy- hypoalbuminemia ([albumin–] = 3.1 0.4 g/dL). sis with PCO2 set to 40 mm Hg, an excess of 10 The SBE was equivalent to the sum of the SIDe mEq/L of plasma anions ( SIDe = –10) at serum and A–. The SIG = 6.0 1.8 mEq/L, adjusted ANG = [albumin–] = 4.4 g/dL results in a pH of 7.21 and 16 2, and ANG = 12 2 returned to normal levels. an [HCO3–]HH = 15.6 mmol/L; at [albumin–] = 2.4 There was a marked hyperchloremia, [Cl–] = 114 g/dL, pH = 7.32 and an [HCO3–]HH = 20.1 mmol/L; 6 mEq/L, at DKA resolution. and at [albumin–] = 1.4 g/dL, pH = 7.37 and an [HCO3–]HH = 22.6 mmol/L. This appears to be an adaptive physiologic response in acute illness. The Discussion hazard of fully correcting severe hypoalbuminemia becomes apparent by acute worsening of a concur- In the post-CABG surgery, severe sepsis, and DKA rent metabolic acidosis, which may partially explain patients in recovery, the author found a marked the absence of mortality benefit with replacement decrease in plasma nonvolatile weak acid buffer therapy [29,30]. The mechanism of hypoalbumin- content (Fig 1). The decrement in plasma nonvola- emia in acute illness and major surgery is likely tile weak acid buffer content is equal to a gain in multifactorial. Impaired hepatic synthesis, acute base, and the A– reflects the magnitude of the phase protein down-regulation, increased capillary metabolic alkalosis. The metabolic alkalosis that permeability, and expansion of the intravascular results is not intuitive but exists by the laws of elec- volume by crystalloid/colloid resuscitation are all trical neutrality, conservation of mass, and dissocia- potential mechanisms [31–33]. tion equilibria that determine acid-base physiology Physicochemical analysis reveals that strong cation/ [8]. Mechanistically, this is understood by realizing anion imbalance is a pervasive cause of metabolic that albumin is a major determinant of A–. A acid-base disorders in acute illness and major decrease in plasma albumin by 1 g/dL results in an surgery. In 1981, Dr Peter Stewart [8] introduced increase in bicarbonate by 2.8 mmol/L, alkalinizing the term strong ion difference as the quantitative the plasma compartment, mitigating the effects of a estimate of strong cation/anion balance within the concurrent metabolic acidosis on pH, and reducing plasma compartment and independent determinant the ANG [26]. Simple deduction would predict that of pH. Historically, plasma buffer base is equiva- if an elevated ANG results in a metabolic acidosis, lent to strong ion difference. However, changes a reduced ANG from hypoalbuminemia results in plasma buffer base were measured by recip- in a metabolic alkalosis. This conclusion remains rocal changes in bicarbonate and protein anions difficult for some clinicians to accept and is the (easily measured quantities at the time), and the focal point of contention between both acid-base clinical significance of cation/anion balance was models. largely forgotten [2]. The SIDe represents the net Hypoalbuminemia is an independent risk factor electrical charge difference of the plasma strong for poor outcome in the acutely ill [28]. However, cations minus the strong anions ([Na+] + [K+] + it is as well beneficial during concurrent metabolic [Ca2+] + [Mg2+] + unmeasured cations – [Cl–] – [lac- Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009 273
  7. 7. Omron tate–] – unmeasured anions) and is set to 0 mEq/L 10 at standard physiological state: SIDe = 39 mEq/L, pH = 7.4, and PaCO2 = 40 mm Hg. A negative 5 value indicates an excess of plasma strong anions 0 Delta SIDe + Delta A- (hyperchloremia, hyperlactatemia, ketoanions, or unmeasured anions) or a loss of plasma strong -5 cations (free water excess or hyponatremia). A positive value indicates an excess of plasma strong -10 cations (free water loss or hypernatremia) or a -15 loss of plasma strong anions (hypochloremia). The effect of an excess of plasma strong anions causing -20 a metabolic acidosis has been recognized since the first introduction of the anion gap. Physicochemical -25 analysis extends this relationship in a quantitative -30 and predictable fashion to all the major strong cat- -30 -20 -10 0 10 ions and anions in the plasma compartment. The base excess of plasma (BE(p)) and SID are SBE conceptually and mathematically related by the Van Fig 2. Metabolic acid-base status measured by stan- Slyke equation for separated plasma. Derivation dard base excess (SBE) and the sum of the SIDe of this relationship has been extensively reviewed and A– with line of identity. elsewhere [6,13]. In brief, the BE(p) and SID both relate to changes in bicarbonate concentration by the buffer value of nonbicarbonate plasma buffers. its inclusion into the equation allows restoration of This value is fixed in the base excess model but equivalence between both acid-base models. Bias variable in the physicochemical model. At a con- and correlation analysis were performed on the stant, normal plasma nonvolatile weak acid buffer post-CABG, severe sepsis, and admission DKA data concentration ( A– = 0 mEq/L), the buffer value of sets to assess the validity of this observation (n = nonbicarbonate plasma buffers is the same for both 75). SBE and SIDe + A– are symmetric along the the BE(p) and SID. Thus, a change in BE(p) corre- line of identity, suggesting that both measures are sponds to an equivalent change in SID. However, comparable (Fig 2). There is an excellent correla- at variable plasma nonvolatile weak acid buffer tion between SBE and SIDe + A– (r2 = .99, P < concentrations ( A– 0 mEq/L), the buffer value .0001), with a low bias of 0.225 and a high clinical of nonbicarbonate plasma buffers changes, and a precision of 0.77 (Fig 3). The limits of agreement change in BE(p) no longer correlates with a change between SBE and SIDe + A– are therefore –1.29 in SID; which parameter is the better measure of and 1.74, which are not clinically relevant confirm- metabolic acid-base status is a matter of conten- ing both measures are comparable. tious debate [6,14,15]. This study was performed The partitioning of complex metabolic acid-base with SBE as opposed to the BE(p) because it is the disorders in the intensive care unit by physico- more commonly reported parameter in blood gas chemical analysis is essential to understanding the analyses. Although SBE differs from BE(p) by an mechanism of the disorder and therapeutically added constant, the numerical difference was not manipulating the plasma cations and anions by clinically relevant by bias and correlation analysis prudent choice of crystalloid or colloid to normal- In pre-CABG surgery and DKA patients on ize pH. For example, by the aforementioned math- admission, the plasma nonvolatile weak acid buf- ematical relationship, SBE can be partitioned into fer content was relatively preserved and the SBE SIDe and A–, two separate and often opposing approximated the SIDe as predicted. In contrast, independent determinants of metabolic acid-base in post-CABG surgery, severe sepsis, and DKA status. At normal, nonvolatile plasma weak acid patients after admission, nonvolatile weak acid concentrations ( A– = 0 mEq/L), SBE = SIDe. buffer concentrations were variable and thus the However, at variable plasma nonvolatile weak acid SBE and SIDe were widely discordant. However, concentrations, the SIDe reflects the magnitude of simple inspection of the data sets (Table 1, Fig 1) strong cation/anion imbalance and the A– reflects revealed that the SBE = SIDe + A– or that SBE the magnitude of the hypoalbuminemic alkalosis and SIDe differ by an added constant, A–. The or possible hyperphosphatemic acidosis [34]. Like- A– reflects the change in titratable base at variable wise, SIDe and A– can be combined to yield SBE, nonvolatile weak acid buffer concentrations, and which reflects the overall magnitude of the meta- 274 Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009
  8. 8. Comparative Quantitative Acid-Base Analysis 3 losis ( A– = 6.4 0.5 mEq/L) resulting in a SBE = 2.5 –1.0 0.5 mEq/L post-CABG surgery. Difference between methods Crystalloid and colloid solutions with a strong 2 ion difference approximating normal plasma SIDe 1.5 result in less cation/anion imbalance and improved 1 metabolic acid-base status in human [35-38] and animal studies [39-41]. Replacement of plasma 0.5 strong cations/anions to correct or compensate 0 Zero bias for cation/anion imbalance is routinely performed -0.5 by hemodialysis, hemofiltration, total parenteral nutrition, and anion replacement therapy [42-45]. -1 Intuitively, patients with a low or high plasma SIDe -1.5 are optimally managed with a high or low SID -30 -20 -10 0 10 crystalloid or colloid fluids, respectively [46]. These Mean of all methods physicochemical approaches to management have been used empirically for years in acute illness and Fig 3. Bland-Altman analysis of standard base major surgery patients without clear theoretical excess and the sum of the SIDe and A– (bias, basis prior to Stewart [8]. Whether preservation of 0.225 and precision, 0.77) the plasma SIDe by balanced crystalloid or colloid resuscitation or correction of the plasma SIDe and bolic acid-base derangement relative to standard cation/anion balance by physicochemical prin- physiological state (SIDe = 39 mEq/L, pH = 7.4 and ciples results in improved patient outcome or is PaCO2 = 40 mm Hg) but provides no information on just cosmetic remains to be determined and merits mechanism. Furthermore, a simplification of physi- continued research. cochemical analysis results from this relationship. Two clinical examples reveal the heuristic value The A– calculation is unnecessary because this of the relation SBE = SIDe + A– in critical ill- value can be deduced from the difference between ness fluid, electrolyte, and acid-base management. SIDe and SBE. The magnitude and mechanism A 42-year-old male patient presents with acute of a complex metabolic acid-base disorder can respiratory distress syndrome undergoing aggres- now be extracted from only 2 derived variables: sive diuresis. His arterial laboratory studies reveal the SIDe and SBE. This relationship reveals that pH = 7.61, PaCO2 = 40.0 mm Hg, [HCO3–]HH = 39.4 neither SBE nor SIDe is the better measure of mmol/L, SBE = 16.8 mEq/L, adjusted ANG = 23, complex acid-base derangements but that both [albumin–] = 2.4 g/dL, [PI] = 3.5 mg/dL, and [lac- conventional and physicochemical methods work tate–] = 3.0 mEq/L. Conventionally, a severe mixed in a complementary fashion at constant and vari- metabolic alkalosis with high gap acidosis is pres- able plasma nonvolatile weak acid concentrations. ent. Physicochemical analysis reveals SIDe = 10.6 The mean electrolyte and plasma nonvolatile mEq/L and A– = 6.2 mEq/L. The SBE calculation weak acid buffer changes in CABG surgery patients equals the sum of both SIDe and A– and reflects reveal the heuristic value of the relation SBE = the magnitude of the metabolic acid-base derange- SIDe + A– in metabolic acid-base analysis (Table ment. The A– calculation, however, is unnecessary 1). From pre- to post-CABG surgery, the serum because this value can be deduced from the dif- sodium decreased by 7 mEq/L (143 1 to 136 ference between SBE and SIDe. Mechanistically, 1 mEq/L), the serum potassium decreased by 0.4 the SIDe reveals a metabolic alkalosis secondary mEq/L (4.1 0.2 to 3.7 0.1), the serum chloride to strong cation excess of approximately 11 mEq/L increased by 2 mEq/L (106 1 to 108 1 mEq/L), complicated by a hypoalbuminemic alkalosis of 6.2 the SIG decreased by 3.1 mEq/L (4.9 0.9 to 1.8 mEq/L. Reduction of the SIDe by 11 mEq/L would 0.5 mEq/L), and the lactate increased by 1.1 mEq/L correct the strong cation/anion imbalance. The (0.8 0.1 to 1.9 0.4). The strong cation/anion electrolyte profile is instructive: [Na+] = 144 mEq/L imbalance (–7 – 0.4 2 + 3.1 1.1 = –7.4) is the and [Cl–] = 91 mEq/L, which reveal hypochlore- physicochemical manifestation of the stress of major mia. The patient’s acid-base status would benefit surgery quantified by the negative SIDe (–7.4 by increasing serum chloride by approximately 11 0.8 mEq/L) and consequent metabolic acidosis. The mEq/L by 0.1 hydrochloric acid infusion and by strong cation/anion imbalance is nearly invisible changing maintenance or resuscitation fluids to a by conventional metabolic acid-base determination low-SID, high-chloride isotonic crystalloid (isotonic secondary to a neutralizing hypoalbuminemic alka- saline, SID = 0 mEq/L). Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009 275
  9. 9. Omron A 78-year-old male presents with severe pneumo- study of pediatric intensive care patients. Cusack nia and sepsis. His initial arterial laboratory studies et al [51] subsequently contradicted this finding in reveal pH = 7.37, PaCO2 = 26.9 mm Hg, [HCO3–]HH = a prospective study of mixed medical and surgical 15.2 mmol/L, adjusted ANG = 18, [albumin–] = 1.3 intensive care patients. They found that the pH and g/dL, and [PI] = 3.1 mg/dL. Conventionally, a non- SBE were predictors of outcome and the SIG was anion gap metabolic acidosis with acute respiratory not. Both studies however, have been criticized on compensation is present. The SIDe = –18.1 mEq/L methodology, multicollinearity of variables, and and SBE = –9.0 mEq/L reveal both marked strong sample size. Rocktaeschel et al [52] conducted a anion excess and approximately 9.0 mEq/L of buff- larger, retrospective analysis of critically ill patients ering from hypoalbuminemia ( A– = SBE – SIDe). with rigorous attention to methodology and appro- The electrolyte profile is instructive: the [Na+] = priate statistical analysis. In contrast to Cusack et 134 mmol/L and the [Cl–] = 113 mmol/L reveal the al, they found that hospital mortality rate was not origin of the strong cation/anion imbalance: free correlated with pH or BE and that the APACHE II water excess reducing [Na+] and hyperchloremia. score, ANG, adjusted ANG, BEua, and SIG were The patient’s acid-base disorder would benefit from statistically correlated with mortality. However, free water restriction by increasing [Na+]; and a the area under the receiver operator characteristic high-SID, low-chloride isotonic crystalloid for both curves was relatively small, except for APACHE II maintenance and resuscitation (1/2 normal saline score, for mortality prediction. Kaplan et al [53] with 75 mEq/L of [NaHCO3–], SID = +75 mEq/L) by conducted an observational, retrospective analysis minimizing chloride load and compensatory work of the discriminative power of the strong ion gap of breathing and restoring SIDe toward standard calculation in separating survivors from nonsurvi- physiological state. vors after major vascular trauma before significant The increment in unmeasured strong anions fluid resuscitation. The SIG and ANG were shown in acute illness and its association with mortality to be more predictive of mortality than SBE, pH, or have been the focus of several recent publications. lactate. The magnitude of the SIG value in the non- Unmeasured strong anions were identified in pre- survivors (mean = 10.8 mEq/L) was similar to that CABG (SIG = 4.9 0.9 mEq/L) and DKA patients found by Cusack et al [51] and Rocktaeschel et al (6.0 1.8 mEq/L) at resolution. The pre-CABG [52] and the severe sepsis patients presented in this patients were uncomplicated, and nonemergent article. Kaplan’s study stands apart from these other and urea-linked polygelines [47] are not used at our studies only with respect to the lower strong ion institution. Thus, unmeasured strong anions are nor- gap value in survivors (mean = 2.4 mEq/L). One mally present in the absence of disease, and normal might speculate that the decrement in the strong levels in acute illness are unknown. In severe sep- ion gap before volume resuscitation in survivors of sis patients, the major strong cation/anion concen- major vascular trauma is the more important prog- trations ([Na+], [K+], and [Cl–]) were preserved. Nev- nostic finding [54]. ertheless, severe cation/anion imbalance existed largely secondary to excessive unmeasured strong Several weaknesses in the present study are anions (SIG = 9.4 1.3 mEq/L and adjusted ANG = noted. It is retrospective and open to selection bias. 22 2) with a small component from excess lactate The small sample sizes with homogeneous patient (2.4 0.8 mEq/L) quantified by the SIDe = –10.9 groups may limit external validity. Normal SIDe 1.8 mEq/L. The close approximation of the SIG was set to 39 mEq/L ( SIDe = 0) consistent with the to the SIDe suggests that initially severe sepsis is accepted definition of standard physiologic state: essentially a pure unmeasured strong anion gap pH = 7.4 and PaCO2 = 40 mm Hg. Normal concen- acidosis in our sample population. Several other trations of albumin and inorganic phosphate were authors have identified this unmeasured acid load, set to 4.4 g/dL and 3.6 mg/dL, respectively, which and its nature remains to be defined [48,49]. Uni- reflect normal serum values at the study medical variate logistic regression analysis between survi- center. vors and nonsurvivors revealed that the adjusted ANG or SIG was not a significant predictor of mortality after admission to the intensive care unit. Conclusions Multivariate analysis was not performed because of multicollinearity. Balasubramanyan et al [50] found The main objective of this study was to assess that base excess unmeasured anion (BE(ua)), a the relationship of SBE to SIDe at variable plasma simplification of the SIG, was a better predictor of nonvolatile weak acid buffer concentrations in the mortality than BE, ANG, or lactate in a retrospective critically ill. Standard base excess is equivalent to 276 Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009
  10. 10. Comparative Quantitative Acid-Base Analysis the algebraic sum of the SIDe and A– in CABG, 3. Jorgensen K, Astrup P. Standard bicarbonate, its clinical significance, and new method for its determination. Scand severe sepsis, and DKA patients. The SBE quantifies J Clin Lab Invest. 1957;9:122. the magnitude of the metabolic acid-base derange- 4. Siggaard-Anderson O. The pH-log pCO2 blood acid-base ment, the SIDe quantifies the plasma strong nomogram revised. Scand J Clin Lab Invest. 1962;14:598- 604. cation/anion imbalance, and the A– quantifies the 5. Siggaard-Anderson O. The Acid-Base Status of Blood. 4th decrement in plasma nonvolatile weak acid buffer ed. Baltimore, Md: Williams & Wilkins; 1974:55. content. Both SBE and physicochemical analysis 6. Fencl V, Jabor A, Kazda A, et al. Diagnosis of metabolic acid-base disturbances in critically ill patients. Am J Respir are complementary in the evaluation of complex Crit Care Med. 2000;162:2246-2251. metabolic acid-base derangements in acute illness 7. Wilkes P. Hypoproteinemia, strong-ion difference, and and major surgery. acid-base status in critically ill patients. J Appl Physiol. 1998;84:1740-1748. 8. Stewart PA. How to Understand Acid-Base. A Quantitative Acid-Base Primer for Biology and Medicine. New York, NY: Elsevier; 1981. Appendix 9. Kowalchuk JM, Scheuermann BW. Acid-base regulation: A comparison of quantitative methods. Can J Physiol 1. Strong ion difference effective: Pharmacol. 1994;72:818-826. SIDe (mEq/L) = 1000 2.46 10(–11) 10. Weinstein Y, Magazanik A, Grodjinovsky A, et al. PaCO2 (mm Hg) / (10–pH) + 10 Reexamination of Stewarts’ quantitation analysis of acid- [albumin–](g/dL) (0.123 pH – 0.631) + 0.3229 base status. Med Sci Sports Exerc. 1991;23:1270-1275. [PI](mg/dL) (0.309 pH – 0.469) 11. Figge J, Rossing TH, Fencl V. The role of serum proteins in 2. Delta strong ion difference effective: acid-base equilibria. J Lab Clin Med. 1991;117:453-467. 12. Figge J, Mydosh T, Fencl V. Serum proteins and acid-base SIDe (mEq/L) = SIDe – 39 (normal strong ion equilibria: A follow up. J Lab Clin Med. 1992;120:713-719. difference effective) 13. Wooten EW. Analytic calculation of physiological acid-base 3. Strong ion difference apparent: parameters in plasma. J Appl Physiol. 1999;86:326-334. SIDa (mEq/L) = [Na+] + [K+] + [Ca2+] + [Mg2+] – 14. Schlichtig R. [Base excess] vs [strong ion difference]: Which [Cl–] – [lactate–] is more helpful? Adv Exp Med Biol. 1997; 411:91-95. Refer to Equations 11 and 12 for conversion [Ca2+] 15. Siggaard-Anderson O, Fogh-Anderson N. Base excess or and [Mg2+] to mEq/L from mg/dL. buffer base (strong ion difference) as measure of a non- 4. Strong ion gap: respiratory acid-base disturbance. Acta Anaesthesiol Scand. SIG (mEq/L) = SIDa – SIDe 1995;39:123-128. 16. Bone RC, Balk RA, Cerra FB, et al. Definitions for sepsis 5. Standard base excess: and organ failure and guidelines for the use of innovative SBE (mEq/L) = 0.9287 ([HCO3–]HH (mmol/L) – therapies in sepsis. Chest. 1992;101:1644-1655. 24.4 + 14.83 (pH – 7.4)) 17. American College of Chest Physicians/Society of Critical 6. Actual bicarbonate: Log [HCO3–](mmol/L) = pH + Care Medicine Consensus Conference Committee. Log (PaCO2 (mm Hg) 0.0307) – 6.105 Definitions for sepsis and organ failure and guidelines for 7. Plasma nonvolatile weak acid buffer content: the use of innovative therapies in sepsis. Crit Care Med. A– (mEq/L) = 10 [albumin–](g/dL) (0.123 1992;20:864-874. pH – 0.631) + 0.3229 [PI](mg/dL) (0.309 18. Knaus WA, Draper EA, Wagner DP, et al. APACHE II: A pH – 0.469) severity of disease classification system. Crit Care Med. 1985; 13: 818-829. 8. Plasma nonvolatile weak acid buffer deficit: 19. Altman DG, Bland JM. Statistical methods for assessing A– (mEq/L) (normal [albumin–] = agreement between two methods of clinical measurement. 4.4 g/dL and [PI] = 3.6 mg/dL) = Lancet. 1986;i:307-310. 10 [4.4](g/dL) (0.123 pH – 0.631) + 0.3229 20. Siggaard-Anderson O. An acid-base chart for arterial blood [3.6] (mg/dL) (0.309 pH – 0.469) – A– with normal and pathophysiological reference areas. 9. Anion gap (ANG) = [Na+] + [K+] – [Cl–] – [HCO3–] Scand J Clin Lab Invest. 1971;27:239-245. 10. Adjusted ANG = ANG + 2.5 ([normal albumin 21. Brackett NC, Cohen JJ, Schwartz WB. Carbon dioxide titra- (4.4 g/dL)] – [observed albumin]) tion curve in normal man. N Engl J Med. 1965;272: 6-12. 11. [Mg2+] (mEq/L) = Mg (mg/dL) 0.8333 22. Prys-Roberts C, Kelman GR, Nunn JF. Determination of the in-vivo carbon dioxide titration curve of anaesthetized 12. [Ca2+] (mEq/L) = a. albumin adjustment (Calcium man. Br J Anaesth. 1966;38:500-509. (mg/dL) – [albumin–](g/dL) + 4) 23. Schlichtig R, Grogono AW, Severinghaus JW. Human PaCO2 b. [Ca2+] (mEq/L) = Calcium (mg/dL) (0.2495 and standard base excess compensation for acid-base bal- (-0.2 (pH-7.4)+0.46)) 2 ance. Crit Care Med. 1998;26:1173-1179. 24. Fencl V, Leith DE. Stewart’s quantitative acid-base chemis- try: Applications in biology and medicine. Respir Physiol. 1993;91:1-16. References 25. Gabow PA. Disorders associated with an altered anion gap. Kidney Int. 1985;27:472-483. 1. Schartz WB, Relman AS. A critique of the parameters used 26. Rossing TH, Maffeo N, Fencl V. Acid-base effects of alter- in the evaluation of acid-base disorders. N Engl J Med. ing plasma protein concentration in human blood in vitro. 1963;268:1382-1388. J Appl Physiol. 1986;61:2260-2265. 2. Singer RB, Hastings AB. Improved clinical method for the 27. Figge J, Jabor A, Kazda A, et al. Anion gap and hypoalbu- estimation of disturbances of acid-base balance of human minemia. Crit Care Med. 1998;26:1807-1810. blood. Medicine. 1948; 27:223-242. 28. Vincent JL, Dubois MJ, Navickis RJ, et al. Hypoalbuminemia in acute illness: Is there a rational for intervention? A meta- Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009 277
  11. 11. Omron analysis of cohort studies and controlled trials. Ann Surg. 42. Brimioulle S, Berre J, Dufaye P, et al. Hydrochloric acid 2003;237:319-334. infusion for treatment of metabolic alkalosis associated 29. Alderson P, Bunn F, Lefebvre C, et al. Resuscitation and vol- with respiratory acidosis. Crit Care Med. 1989;17:232-236. ume expansion in critically ill patients. Cochrane Database 43. Heering P, Ivens K, Thumer O, et al. The use of differ- Syst Rev. 2002;1:CD001208. ent buffers during continuous hemofiltration in critically 30. Wilkes MM, Navickis RJ. Patient survival after human ill patients with acute renal failure. Intensive Care Med. albumin administration: A meta-analysis of randomized, 1999;25: 1244-1251. controlled trials. Ann Intern Med. 2001;135:149-164. 44. Ronco C, Bellomo R, Kellum JA. Continuous renal replace- 31. Fleck A, Raines G, Hawker F, et al. Increased vascular per- ment therapy: Opinions and evidence. Adv Ren Replace meability: A major cause of hypoalbuminemia in disease Ther. 2002;9:229-244. and injury. Lancet. 1985;1:781-784. 45. Orr PA, Case KO, Stevenson JJ, et al. Metabolic response 32. Fleck A. Computer models for metabolic studies on plasma and parenteral nutrition in trauma, sepsis, and burns. J proteins. Ann Clin Biochem. 1985;22:33-49. Infus Nurs. 2002;25:45-53. 33. Ballmer PE. Causes and mechanisms of hypoalbuminemia. 46. Kellum JA. Metabolic acidosis in the critically ill: Lessons Clin Nutr. 2001;20:271-273. from physical chemistry. Kidney Int. 1998;53:S81-86. 34. Rocktaeschel J, Morimatsu H, Uchino S, et al. Acid-base sta- 47. Hayhoe M, Bellomo R, Liu G, et al. The etiology and patho- tus of critically ill patients with acute renal failure: Analysis genesis of cardiopulmonary bypass-associated metabolic based on Stewert-Figge methodology. Crit Care. 2003;7: acidosis using polygeline pump prime. Intensive Care Med. R60-R66. 1999;25:680-685. 35. Scheingraber S, Rehm M, Sehmisch C, et al. Rapid 48. Mecher C, Rackow EC, Astiz ME, et al. Unaccounted saline infusion produces hyperchloremic acidosis in for anions in metabolic acidosis during severe sepsis in patients undergoing gynecologic surgery. Anesthesiology. humans. Crit Care Med. 1991;19:705-711. 1999;90:1265-1270. 49. Gilfix BM, Bique M, Magder S. A physical chemical 36. Waters JH, Gottlieb A, Schoenwald P, et al. Normal approach to the analysis of acid-base balance in the clinical saline versus Ringer’s lactate solutions for intraopera- setting. J Crit Care. 1993; 8:187-197. tive fluid management in patients undergoing abdominal 50. Balasubramanyan N, Havens PL, Hoffman GM. Unmeasured aortic aneurysm repair: An outcome study. Anesth Analg. anions identified by the Fencl-Stewart method predict mor- 2001;93:817-822. tality better than base excess, anion gap, and lactate in 37. Reid F. Abnormal saline and physiological Hartmann’s solu- patients in the pediatric intensive care unit. Crit Care Med. tion: A randomized double-blind crossover study. Clin Sci. 1999;27:1577-1581. 2003;104:17-24. 51. Cusack RJ, Rhodes A, Lochead P, et al. The strong ion gap 38. Gan TJ, Bennett-Guerrero E, Phillips-Bute B, et al. Hextend, does not have prognostic value in critically ill patients in a physiologically balanced plasma expander for large vol- a mixed medical/surgical adult ICU. Intensive Care Med. ume use in major surgery: A randomized phase III clinical 2002;28:864-869. trial. Anesth Analg. 1999;88:999-1003. 52. Rocktaeschel J, Morimatsu H, Uchino S, et al. Unmeasured 39. Traverso L, Lee W, Langford MJ. Fluid resuscitation after anions in critically ill patients: Can they predict mortality. otherwise fatal hemorrhage: I. Crystalloid solutions. J Crit Care Med. 2003;31:2131-2136. Trauma. 1986;26:168-175. 53. Kaplan LJ, Kellum JA. Initial pH, base deficit, lactate, 40. Traverso L, Hollenbach SJ, Bolin RB, et al. Fluid resuscita- anion gap, strong ion difference, and strong ion gap pre- tion after otherwise fatal hemorrhage: II. Colloid solutions. dict outcome from major vascular trauma. Crit Care Med. J Trauma. 1986;26:176-182. 2004;32:1120-1124. 41. Kellum JA. Fluid resuscitation and hyperchloremic acidosis 54. Omron EM, Gilbert RC. Strong ion gap. Crit Care Med. in experimental sepsis: Improved short-term survival and 2005;33:266. acid-base balance with Hextend compared with saline. Crit Care Med. 2002;30:300-305. 278 Journal of Intensive Care Medicine 20(6); 2005 Downloaded from http://jic.sagepub.com at MICHIGAN STATE UNIV LIBRARIES on September 24, 2009

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