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Acid-Base Disorders Alan You, MD Combined EM/IM Residency Program

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Presentation on theme: "Acid-Base Disorders Alan You, MD Combined EM/IM Residency Program"— Presentation transcript:

1 Acid-Base Disorders Alan You, MD Combined EM/IM Residency Program
Virginia Commonwealth University Health System

2

3 Overview Physiologic Effects of Acid-Base Disturbances
Traditional (Schwartz-Bartter) Approach Stewart Method Fluid Resuscitation

4 Physiologic Effects of Acid-Base Disturbances

5 Consequences of Severe Acid-Base Disturbances
Organ System Acidemia (pH <7.20) Alkalemia (pH >7.60) Cardiovascular ↓ contractility, arteriolar vasodilation ↓ MAP & CO; ↓ response to catecholamines ↑ risk of arrhythmias Arteriolar vasoconstriction ↓ coronary blood flow ↑ risk of arrhythmias Respiratory Hyperventilation, ↓ resp muscle strength Hypoventilation Metabolic ↑K ↓ K, ICa, Mg, PO4 Neurologic ∆ MS ∆ MS, seizures

6 Traditional (Schwartz-Bartter) Approach

7

8 Step 1: Acidosis vs Alkalosis
Normal ??? pH Alkalosis Acidosis 14

9 Step 1: Acidosis vs Alkalosis
Normal 7.36 pH 7.44 Alkalosis Acidosis 14

10 Step 2: Respiratory vs Metabolic
Primary Disorder pH HCO3 PaCO2 Metabolic Acidosis Respiratory Acidosis Metabolic Alkalosis Respiratory Alkalosis

11 Step 2: Respiratory vs Metabolic
Primary Disorder pH HCO3 PaCO2 Metabolic Acidosis Respiratory Acidosis Metabolic Alkalosis Respiratory Alkalosis

12 Step 2: Respiratory vs Metabolic
Primary Disorder pH HCO3 PaCO2 Metabolic Acidosis Respiratory Acidosis Metabolic Alkalosis Respiratory Alkalosis

13 Step 2: Respiratory vs Metabolic
Primary Disorder pH HCO3 PaCO2 Metabolic Acidosis Respiratory Acidosis Metabolic Alkalosis Respiratory Alkalosis

14 Step 2: Respiratory vs Metabolic
Primary Disorder pH HCO3 PaCO2 Metabolic Acidosis Respiratory Acidosis Metabolic Alkalosis Respiratory Alkalosis

15 Step 3: Disorder-Specific Calculations
Anion Gap AG = Na – (Cl + HCO3) Expected AG = 2.5 × [albumin]

16 Step 3: Disorder-Specific Calculations
Delta-Delta ∆∆ = ∆AG / ∆HCO3 ∆AG = measured AG – expected AG = Na – (Cl + HCO3) – 2.5 × [albumin] ∆HCO3 = 24 – measured HCO3

17 Step 3: Disorder-Specific Calculations
Osmolar Gap OG = measured osmolality – calculated osmolality Calculated osmolality = (2 × Na) + (glu / 18) + (BUN / 2.8)

18 Step 3: Disorder-Specific Calculations
Urine Anion Gap UAG = (UNa + UK) – UCl

19 Step 4: Compensation

20 Respiratory Disorders
Step 4: Compensation ∆ 10 pCO2 HCO3 1 2 Acute 4 Chronic Respiratory Disorders ∆ 10 HCO3 pCO2 7.5 12.5 Metabolic Disorders

21 pCO2 = last two digits of pH
Step 4: Compensation pCO2 = (1.5 × HCO3) + 8 ± 2 Winter’s Formula pCO2 = last two digits of pH Eyeball Method

22 Step 4: Compensation

23 Respiratory Disorders
Step 4: Compensation ∆ 10 pCO2 pH 0.08 Acute 0.03 Chronic Respiratory Disorders

24 Step 5: Mixed Disorders After adjusting for expected compensation, if the measured ________ is ________: Too Low Too High pCO2 HCO3

25 2° Respiratory Alkalosis
Step 5: Mixed Disorders After adjusting for expected compensation, if the measured ________ is ________: Too Low Too High pCO2 2° Respiratory Alkalosis HCO3

26 Step 5: Mixed Disorders After adjusting for expected compensation, if the measured ________ is ________: Too Low Too High pCO2 2° Respiratory Alkalosis 2° Respiratory Acidosis HCO3

27 Step 5: Mixed Disorders After adjusting for expected compensation, if the measured ________ is ________: Too Low Too High pCO2 2° Respiratory Alkalosis 2° Respiratory Acidosis HCO3 2° Metabolic Acidosis

28 Step 5: Mixed Disorders After adjusting for expected compensation, if the measured ________ is ________: Too Low Too High pCO2 2° Respiratory Alkalosis 2° Respiratory Acidosis HCO3 2° Metabolic Acidosis 2° Metabolic Alkalosis

29 Step 5: Mixed Disorders If the pH is normal but:
↑ pCO2 + ↑ HCO3 ↓ pCO2 + ↓ HCO3 normal pCO2 + normal HCO3 + ↑ AG normal pCO2 + normal HCO3 + normal AG

30 Step 5: Mixed Disorders If the pH is normal but:
↑ pCO2 + ↑ HCO3 respiratory acidosis + metabolic alkalosis ↓ pCO2 + ↓ HCO3 normal pCO2 + normal HCO3 + ↑ AG normal pCO2 + normal HCO3 + normal AG

31 Step 5: Mixed Disorders If the pH is normal but:
↑ pCO2 + ↑ HCO3 respiratory acidosis + metabolic alkalosis ↓ pCO2 + ↓ HCO3 respiratory alkalosis + metabolic acidosis normal pCO2 + normal HCO3 + ↑ AG normal pCO2 + normal HCO3 + normal AG

32 Step 5: Mixed Disorders If the pH is normal but:
↑ pCO2 + ↑ HCO3 respiratory acidosis + metabolic alkalosis ↓ pCO2 + ↓ HCO3 respiratory alkalosis + metabolic acidosis normal pCO2 + normal HCO3 + ↑ AG AG metabolic acidosis + metabolic alkalosis normal pCO2 + normal HCO3 + normal AG

33 Step 5: Mixed Disorders If the pH is normal but:
↑ pCO2 + ↑ HCO3 respiratory acidosis + metabolic alkalosis ↓ pCO2 + ↓ HCO3 respiratory alkalosis + metabolic acidosis normal pCO2 + normal HCO3 + ↑ AG AG metabolic acidosis + metabolic alkalosis normal pCO2 + normal HCO3 + normal AG no disturbance or non-AG metabolic acidosis + metabolic alkalosis

34 Step 5: Mixed Disorders ∆∆ = ∆AG / ∆HCO3
If there is an AG metabolic acidosis and: ∆∆ < 1 AG metabolic acidosis + non-AG metabolic acidosis ∆∆ > 2 AG metabolic acidosis + metabolic alkalosis ∆∆ = ∆AG / ∆HCO3

35

36 Metabolic Acidosis Anion Gap Metabolic Acidosis
Caused by increase in unmeasured anions such as organic acids, phosphates, and sulfates KIL-U Ketones Ingestions Lactate Uremia (Renal Failure) Ketones DM, alcoholism, starvation Ingestions Methanol, ethylene glycol, propylene glycol, salicylates, acetaminophen Lactate Type A, Type B, D-lactic acidosis Uremia Urate, phosphate, sulfate

37 Metabolic Acidosis Anion Gap Metabolic Acidosis
Delta-Delta (∆∆) used to assess for concurrent non-AG metabolic acidosis or metabolic alkalosis Osmolar gap (OG) used to differentiate different types of ingestions Normal OG ≤10 AG OG Ingestion nl Acetaminophen, salicylates Ethanol, methanol, ethylene glycol, propylene glycol Isopropyl alcohol

38 Metabolic Acidosis Non-AG Metabolic Acidosis
Caused by decrease in albumin or increase in unmeasured cations GRIPED GI loss RTA Ingestion Post-hypocapnia Early renal failure Dilution GI Loss Diarrhea, fistula RTA Type II, type I, type IV Ingestion Acetazolamide, sevelamer, cholestyramine, toluene Post-Hypocapnia Rapid correction of respiratory alkalosis Early Renal Failure Impaired generation of ammonia Dilution Rapid infusion of acidic fluids Type II – Proximal Type I – Distal Type IV - Hypoaldo

39 Metabolic Acidosis Non-AG Metabolic Acidosis
Urine Anion Gap (UAG) used to evaluate for appropriate renal response to acidemia Indirect assay for renal NH4 as ammonium is the primary unmeasured cation in UAG calculation Positive UAG Early renal failure, type I or IV RTA Negative UAG GI loss, type II RTA, ingestions, dilution More NH4 means more negative Less NH4 means more positive

40 Metabolic Alkalosis Caused by loss of H+ or gain of HCO3- by the body
Categorized as saline-responsive (UCl <20) vs saline-resistant (UCl >20) Saline-responsive GI loss, diuretics, post-hypercapnia Saline-resistant Hyperaldosteronism, severe hypokalemia, exogenous alkali

41 Respiratory Acidosis Caused by hypoventilation CNS depression
Neuromuscular disorders Upper airway abnormalities Lower airway abnormalities Lung parenchyma abnormalities Thoracic cage abnormalities

42 Respiratory Alkalosis
Caused by hyperventilation Hypoxia-driven hyperventilation CNS disorder Pain/anxiety Toxicologic Pregnancy Sepsis Hepatic failure

43 Case 1 19-year-old female presenting to ED with 2 day history of nausea, vomiting, abdominal pain, and polyuria. ABG – 7.25 / 23 / 97 / 10 Albumin – 3.6

44 Case 2 ABG – 7.50 / 20 / 92 / 15 Albumin – 4.4 Osmolality – 302
34-year-old male with no past medical history presenting to ED with a three hour history of altered mental status, vertigo, and vomiting. ABG – 7.50 / 20 / 92 / 15 Albumin – 4.4 Osmolality – 302

45 Stewart Method

46

47 Stewart Method Alternative acid-base model created by Dr. Peter A. Stewart Also referred to as quantitative acid-base Initially outlined in 1981 in his book, “How to Understand Acid-Base” followed by a 1983 paper, “Modern quantitative acid-base chemistry” in the Canadian Journal of Physiology and Pharmacology

48 1. The human body must maintain electrical neutrality.
Prime Concepts 1. The human body must maintain electrical neutrality.

49 Prime Concepts 2. The elements that comprise acid-base homeostasis can divided into two categories of variables: independent and dependent.

50 Prime Concepts 3. H+ and HCO3- ions are plentiful in the human body and can be generated at will to maintain electrical neutrality.

51 Prime Concepts 4. There are only three truly independent variables in acid-base homeostasis: strong-ion difference (SID), total weak non-volatile acids (ATOT), and pCO2.

52

53

54 Traditional (Schwartz-Bartter) Approach
Input Output pH HCO3 Metabolic Acidosis Metabolic Alkalosis Respiratory Acidosis Respiratory Alkalosis Descriptive approach to acid-base

55 Stewart Method Input Output Status SID ATOT pCO2
Two ways to describe same thing, so there will be some ability for overlap but don’t do it.

56 Stewart Approach Variables
Independent Variables SID ATOT pCO2 Dependent Variables H+ OH- HCO3- CO32- HA (weak acids) A- (weak ions) Two ways to describe same thing, so there will be some ability for overlap but don’t do it.

57 Quantitative Model [H+] × [OH-] = K'w [H+] × [A-] = KA × [HA]
The influence of the independent variables can be predicted through 6 simultaneous equations: [H+] × [OH-] = K'w Water Dissociation Equilibrium [H+] × [A-] = KA × [HA] Weak Acid [HA] + [A-] = [ATOT] Conservation of Mass for “A” [H+] × [HCO3-] = KC × pCO2 Bicarbonate Ion Formation Equilibrium [H+] × [CO32-] = K3 × [HCO3-] Carbonate Ion Formation Equilibrium [SID] + [H+] – [HCO3-] – [A-] – [CO32-] – [OH-] = 0 Electrical Neutrality Two ways to describe same thing, so there will be some ability for overlap but don’t do it.

58 Strong Ion Difference (SID)
The difference between the sums of the concentrations of the strong cations and the strong anions: SID = Na + K + Ca2+ + Mg2+ – Cl – [other strong anions]

59 Strong Ion Difference (SID)
The difference between the sums of the concentrations of the strong cations and the strong ions: SID = Na+ – Cl- ( – [other strong anions] )

60 Strong Ion Difference (SID)
The difference between the sums of the concentrations of the strong cations and the strong ions: SID = Na+ – Cl- ( – [other strong anions] ) Under normal conditions, SID ≈ 40

61 Changing SID SID = Na+ – Cl- ⇒ relative excess of Na+ cations
If SID >40 ⇒ relative excess of Na+ cations ⇒ body generates additional HCO3- anions to maintain electrical neutrality ⇒ pH increases and body becomes more alkalotic

62 Altering SID SID = Na+ – Cl- ⇒ relative excess of Cl- anions
If SID <40 ⇒ relative excess of Cl- anions ⇒ body generates additional H+ cations to maintain electrical neutrality ⇒ pH decreases and body becomes more acidotic

63 Altering SID SID = Na+ – Cl- ( – [other strong anions] )
If SID <40 ⇒ presence of other strong anions (eg. lactate, ketoacids) ⇒ body generates additional H+ cations to maintain electrical neutrality ⇒ pH decreases and body becomes more acidotic

64 Total Weak Non-Volatile Acids (ATOT)
The plasma concentration of non-volatile weak acids comprised primarily of inorganic phosphate, albumin, and other plasma proteins. ATOT = [PiTOT] + [PrTOT] + [albumin] Phosphate is PO4 3-, Albumin is negatively charged as well Remember that PO43- and [albumin-] are both negatively charged ions.

65 pCO2 As in the traditional method, pCO2 combines with H2O to form H2CO3 (carbonic acid), a highly volatile acid. Therefore: Increased pCO2 leads to increased acid formation. Decreased pCO2 leads to decreased acid formation. CO2 + H2O ⇄ H2CO3

66 Fluid Resuscitation

67

68 Fluid Resuscitation with Quantitative Acid-Base
Quantitative acid-base allows you to more easily understand how the infusion of certain fluids will affect a patient’s acid-base status Each type of IVF has its own calculable SID Ex. 0.9% sodium chloride Because of dilutionary effects on albumin, the ideal SID for a fluid to not affect acid-base status when infused is actually around 24-28

69 Fluid Resuscitation with Quantitative Acid-Base
Quantitative acid-base allows you to more easily understand how the infusion of certain fluids will affect a patient’s acid-base status Each type of IVF has its own calculable SID Ex. 0.9% sodium chloride = 154 mEq Na mEq Cl ⇒ SID = 0 Because of dilutionary effects on albumin, the ideal SID for a fluid to not affect acid-base status when infused is actually around 24-28

70 SIDs of Various IVF IVF SID Sodium chloride 0.9% Sodium chloride 0.45%
Sodium bicarbonate Lactated ringer’s Normosol-R Plasma-Lyte A Albumin Dextrose 5%

71 SIDs of Various IVF IVF SID Sodium chloride 0.9% Sodium chloride 0.45%
Sodium chloride 0.45% Sodium chloride 3% Sodium bicarbonate 892 Lactated ringer’s 28 Normosol-R 50 Plasma-Lyte A Albumin Dextrose 5%

72 Effects of IVF on Acid-Base
Direct infusion of strong ions Causes direct modification of patient’s SID Eg. Sodium chloride 0.9%, sodium bicarbonate Direct infusion of weak ions Causes direct modification of patient’s ATOT Eg. Albumin, potassium phosphate Relative dilution/concentration of plasma Causes indirect modification of patient’s SID and ATOT Eg. Dextrose 5%, sodium chloride 3%

73

74 Questions?

75 References Grogono AW. “Stewart's Strong Ion Difference.” Available at: Accessed October 3, 2017. Nickson C. “Strong Ion Difference.” Available at: Accessed October 3, 2017. Sabatine MS. Pocket Medicine. Lippincott Williams & Wilkins; 2010. Sterns RH. “Strong ions and the analysis of acid-base disturbances (Stewart approach).” Available at: Accessed October 3, 2017. Stewart PA. Modern quantitative acid-base chemistry. Can J Physiol Pharmacol. 1983;61(12): Weingart S. “EMCrit Podcast 44 – Acid Base: Part I.” Available at: Accessed October 3, 2017. Weingart S. “EMCrit Podcast 50 – Acid Base Part IV – Choose the Solution Based on the Problem.” Available at: Accessed October 3, 2017. Wikipedia, the free encyclopedia. “Peter A. Stewart”. Available at: Accessed October 3, 2017.


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