Approach to Acid-Base Disorders (Selby) Flashcards

1
Q

definition metabolic acidosis

A

low serum HCO3-

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2
Q

definition metabolic alkalosis

A

highs serum HCO3-

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3
Q

definition respiratory acidosis

A

high PCO2

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4
Q

definition respiratory alkalosis

A

low PCO2

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5
Q

Anion gap formula

A

= Na - (HCO3 + Cl)

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6
Q

When is anion gap used?

A

to differentiate HAGMA vs.

NAGMA

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7
Q

what will falsely lower anion gap?

A

hypoalbuminemia

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8
Q

what is correction factor for anion gap with hypoalbuminemia?

A

for every 1 g/dL drop in albumin, the AG drops by 2.5 mEq/L

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9
Q

normal serum osmolality

A

275- 290 mosm/L

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10
Q

formular for serum osmolality

A

= 2(Na) + (Glucose/18) + (BUN/2.8)

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11
Q

formular for osmolar gap

A

measured serum osmolality- calculated serum osmolality

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12
Q

what is osmolar gap clinically useful for?

A
  • screening for EtOH ingestions (esp. HAGMA cases)
  • screening for ketoacidosis
  • screening for lactic acidosis
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13
Q

When is delta delta gap used for?

A

in patients with HAGMA to determine if there is coexisting NAGMA or metabolic alkalosis present

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14
Q

delta delta gap formulas

A

delta gap = calculated AG -normal AG (always 12)

delta HCO3 = normal HCO3 (always 24) - delta gap

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15
Q

what if measured HCO3 is equal to delta delta gap?

A

then no additional acid base disorder is present

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16
Q

what if measured HCO3 is greater than delta delta gap?

A

metabolic alkalosis is present in addition to HAGMA

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17
Q

what if measured HCO3 is less than delta delta gap?

A

NAGMA is present in addition to HAGMA

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18
Q

normal pH on arterial blood gas

A

pH 7.35-7.44

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19
Q

normal HCO3 on ABG

A

24 mEq/L

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20
Q

normal PCO2 on ABG

A

40 mmHg

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21
Q

normal anion gap on ABG

22
Q

normal osmolality gap on ABG

23
Q

Differential Dx HAGMA

A
G- glycols (ethylene and propylene)
O- oxoproline (acetamino tox)
L- lactic acidosis (L-isomer)
D- lactic acidosis (D-isomer)
M- methanol
A- aspirin
R- renal failure
K- ketoacidosis (EtOHism, DM, starvation)
24
Q

Who is pyroglutamic (5-oxoproline) acidosis seen in?

A

women who are malnourished or critically ill

25
DDx of increased osmolar gap
``` M- methanol E- ethanol D- diethylene glycol I- isopropyl EtOH E- ethylene glycol - propylene glycol - keto/lactic acidosis ```
26
what cause of increased osmolar gap is not associated with metabolic acidosis?
isopropyl alcohol
27
What level of potassium is acidosis associated with ?
hyperkalemia
28
what level of potassium is alkalosis associated with?
hypokalemia
29
NAGMA DDx
``` D- diarrhea U- ureteral diversion R- renal tubular acidosis H- hyperalimentation A- acetazolamide A- addison's disease M- miscellaneous (glue sniffing) ```
30
respiratory alkalosis DDx
anything that increases respiratory rate or tidal volume (including pregnancy)
31
respiratory acidosis DDx
anything that lowers respiratory rate/tidal volume, increases dead space, or worsens airway obstruction
32
what is urine anion gap used for
clinically used to differentiate renal from nonrenal causes of NAGMA
33
what is UAG a marker of
NH4Cl excretion, which indicates proper urinary acidification
34
formula urine anion gap
UAG = (urine sodium + urine potassium) - urine chloride
35
negative UAG meaning
appropriate distal nephron urinary acidification
36
postive UAG meaning
inappropriate distal nephron urinary acidification
37
problem in proximal RTA (type 2)
decreased capacity of proximal tubule to reabsorb HCO3, eventually some reabsorption occurs in other parts of tubule, but at a lower level (--> acidosis)
38
Secretion of what leads to HCO3 reabsorption?
H+
39
what is most common cause of RTA type 2 in children?
cystinosis
40
Common cause of RTA type 2 in adults?
Fanconi syndrome (likely due to multiple myeloma)
41
Problem in distal RTA (type 1)
patients are unable to acidify their urine; lack of net H+ ion secretion prevents urinary acidification and excretion of ammonium
42
common etiologies type 1 RTA
Sjogren's syndrome, glue sniffing
43
clinical manifestations type 1 RTA
nephrolithiasis or nephrocalcinosis
44
4 things for diagnosis RTA type 1
1) NAGMA 2) unable to acidify urine pH <5.5 3) hypokalemia, usually severe 4) UAG is positive
45
Etiology hyperkalemic RTA (type 4)
- deficiency circulating aldosterone - aldosterone resistance in collecting ducts - BOTH lead to impaired Na+ reabsorption by principle cells (leads to hyperkalemia)
46
clinical manifestations type 4 RTA
- usually asymptomatic - NAGMA - hyperkalemia - most patients in 50-70s with h/o DM or CKD
47
Diagnosis type 4 RTA
- variable urine pH (usually >5.5) | - UAG is positive
48
DDx metabolic alkalosis (5 things)
- hypokalemia - vomiting or nasogastric tube suctioning - diuretics (loop/thiazide) - volume depletion - mineralocorticoid excess (Conn syndrome)
49
General cause of metabolic alkalosis
factors that stimulate Na+ reabsorption, secondarily increase H+ secretion and stimulate HCO3- reabsorption
50
what cell is a mirror image of alpha intercalated cells?
beta intercalated
51
Why is there hypochloremia with volume depletion (contraction alkalosis)?
The HCO3-Cl exchanger in beta intercalated cells must replete Cl- to help with HCO3- secretion
52
winters formula
PCO2 = 1.5 [HCO3]+8 +/-2