Acid Base Flashcards

1
Q

4 causes respiratory alkalosis (CO2 <40)

A

Anxiety, toxic salicylates, sympathomimetics, chf, elevated ICP, hypoxia

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2
Q

Causes respiratory alkalosis (co2 elevated)

A
Sedation, obtundation, coma
opioids
common and chronic in copd
respiratory failure
Neuromuscular disorders 
Obesity hypoventilation syndrome
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3
Q

Causes metabolic alkalosis

A
Diuretic use 
Gastric acid losses
Hypovolemia
hyperaldosteronism
bartter syndrome
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4
Q

10 causes anion gap metabolic acidosis

A
Methanol, metformin
Uremia 
Diabetic, starvation or alcoholic ketoacidosis 
Paraldehyde, propylene glycol
Iron, isoniazide, inhalant poisoning
Lactic acidosis (cyanide, sepsis, shock, hypoxia, seizures)
Ethylene glycol 
Salicylates, solvents
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5
Q

Formula for anion gap

A

Sodium - (chloride + co2)

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6
Q

What are the only three endogenous causes of anion gap metabolic acidosis

A

Ketones, uremia and lactate

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7
Q

Causes of non anion gap metabolic acidosis

A

Hypokalemic: renal losses eg renal tubular acidosis, carbonic anhydrase inhibiotors eg acetazolamide
GI losses
Hyperkalemic: adrenal insuffiency, renal insufficiency

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8
Q

Examples of causes of both anion gap metabolic acidosis and osmolar gap

A

Toxic alcohols (methanol, ethylene glycol)
Ketoacids
Paraldehyde
?sepsis

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9
Q

What are the risks of sodium bicarb administration and when should it be considered in metabolic acidosis

A

Risk is electrolyte disturbances, cerebral acidosis because can’t cross the BBB
Reserve for severe acidosis (ph<7) and very ill
Salicylate toxicity is indicated

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10
Q

Three settings of increased bicarbonate resulting in metabolic alkalosis

A

Gastric acid loss from vomiting or GN suctioning
Diuretic use
Mineralcorticoid excess

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11
Q

Why is oxygen administration potentially dangerous in respiratory alkalosis

A

Can worsen hypercapnea in heavily sedated or obtunded patients as takes away respiratory trigger

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12
Q

Presentation of alcoholic ketoacidosis

A

Chronic alcohol patient presents not intoxicated with tachycardia, tachypnea, dehydration
Fruity breath

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13
Q

Lab findings alcoholic ketoacidosis

A

Anion gap metabolic acidosis
Positive b hydroxybutyrate
Ketones often negative initially
Low or negative etoh
Concomitant hypokalemia, hyponatremia, hypomagnesemia, hyperphosphatemia
Can see low, normal or high blood glucose
Normal osmolar gap
Often elevated lactate due to conversion from Pyruvate

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14
Q

Management alcoholic ketoacidosis

A
Thiamine 100 mg iv before dextrose
Hydration with D5NS
Correct lytes
Insulin not required 
Bicarb only is severely acidotic
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15
Q

Why should thiamine be given before D5NS in alcoholic ketoacidosis

A

Can precipitate wernicke encephalopathy

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16
Q

Differential diagnosis for lactic acidosis

A

Inadequate tissue perfusion (hypotension, hypoxia)
Disorders eg diabetes, renal or hepatic failure, seizures, leukaemia, cancer
Toxins (metormin, ethanol, methanol, epinephrine, fructose)
Inborn errors of metabolism

17
Q

Three ways glucose is derived

A

Diet
Hepatic gluconeogenesis
Liver glycogen store breakdown

18
Q

Three types of ketones produced by lipolysis

A

Betahydroxybutyrate
Acetoacetate
Acetone

19
Q

10 causes of hypoglycaemia

A

Insulin
Oral hypoglycaemics eg sulfonylurea (antidote for overdose is ocreotide which inhibits insulin release)
Sepsis
Liver failure
Alcohol (inhibition gluconeogensis and depletion glycogen stores)
Malnourishment
Drugs: haldol, cimetidine, MAOi, phenothiazide
Cortisol deficiency
Endogenous hyperinsulinism eg islet cell tumor
Hypoglycaemia of infancy

20
Q

What blood tests should be ordered in non diabetic hypoglycaemic patients if cause is not obvious

A

Insulin and c peptide levels for insulinoma vs factitious hypoglycaemia

21
Q

What can be used if no iv access and patient can’t eat or drink in hypoglycaemia

A

IM glucagon (may not be effective in elderly or alcoholic)

22
Q

6 precipitants DKA

A
Lack of insulin or non compliance 
Infection
MI
Surgery
Pregnancy
Hyperthyroid
Pancreatitis
Alcohol or illicit drugs et cocaine
Steroids
23
Q

Diagnosis DKA

A

Hyperglycaemia
Ketosis
Anion gap metabolic acidosis (gap over 15,bicarb less than 18 although can be normal if concomitant vomiting, ph <7.3)
Need to ask for b hydroxybuterate assay

24
Q

Work up DKA

A

CBC lytes extended lytes bun cr lft, troponin
Vbg serum osmolality b hydroxybutyrate
Urinalysis, cxr, ecg,

25
Q

When do you start replacing potassium in DKA

A

Potassium 3.5-5 add 20-30 meq in infusion fluid

26
Q

When do you switch to half normal saline in DKA

A

When sodium has normalized

27
Q

When should bicarb be considered in DKA

A

Life threatening hyperkalemia
Ph <6.9
Shock with impending cardiovascular collapse

28
Q

Risk factors for cerebral edema with DKA management

A
Children under 5
New diagnosis
Severe acidosis 
Bicarb use
Insulin bolus
29
Q

Management cerebral edema in pediatric DKA

A

Ct head
Manage elevated ICP
Mannitol
Reduce ivf

30
Q

Differences between DKA and HHS

A

Very elevated glucose
Negative ketones
No acidosis

Can present with focal neuro deficits, altered MS, severe dehydration

Management is similar to DKA except larger water deficits
Half fluid deficit over 12 hours then switch to half normal saline
Add thiamine, correct hypo mag and hypophos