acid base + electrolytes Flashcards

1
Q

what can cause high oxoproline

A
  1. chronic acetaminophen use ( esp if renal failure present)
  2. pregnancy, malnutrition, vegan –> deplete glycine (which is required for glutathione synthesis)
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2
Q

Anion gap metabolic acidosis etiology w/ incrase osmolar gap

A

Organic alcohol poisoning:
* Methanol
* Ethylene glycol
* Paraldehyde
* Ketoacidosis (Etoh + Diabetic)
* Lactic acidosis
* Severe CKD

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3
Q

increased osmolar gap without metabolc acidosis

A

Ethanol
Isopropyl alcohol
Mannitol
Sorbitol
*pseudohyponatremia
*Early toxic alcohol!
Hyperlipidemia
Hyperproteinemia

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4
Q

in organic alcohol intox, what do you see first
osmolar gap or anion gap

A
  1. osmolar gap w/o AG
  2. AG w/o osmolar gap
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5
Q

causes of RTA 1

A

CTD ( Sjogren&raquo_space; Ra, SLE )
Hypercalciuria
Drugs (ifosfamide)

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6
Q

causes of RTA 2

A

Fanconi
Myeloma
tenofovir
Acetazolamide

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7
Q

other findings of RTA 1

A

Calcium phosphate stones

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8
Q

other findings of RTA2

A

low phospate, low vit d, glycosuria

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9
Q

hco3 levels in type 4 RTA

A

> 17

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10
Q

rta 4 etiology

A
  1. Drugs: aldost antag, RAAS blockers, heparin, CI,
  2. Adrenal insufficiency
  3. DB
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11
Q

what to tx with rta 4

A

florinef if low bp
if htn = thiazide

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12
Q

diabetes can cause which RTA

A

type 4

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13
Q

if metab alkalosis, with urine CL > 20, what’s the next step

A

your blood pressure

– HighBP:
* Hyperaldosterone (htn, hypoK, alkalosis, high aldo)
* Liddle’s (htn, hypoK, alkalosis, low aldo) * Cushings

– LowBP:
* Barter’s (mimics Loops – low K, low Mg)
* Gittleman’s (mimics thiazides – low K, low Na, high Ca)

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14
Q

similarities and difference between hyperaldosteronism state and liddle

A

both : htn, alkalosis, high urine CL, hypoK

difference : liddle has little aldosterone vs hyperaldost has high aldo

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15
Q

another causing urine CL > 20 not related to bp

A

excess bicarb ingestion

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16
Q

when do you start worrying of urine output (amount) in context of overcorrected hyponatremia ?so what to do?

A

when UO > 150 ml/hr
DDAVP, D5W

17
Q

isotonic hyponatremia (280-295) etiology

A

pseudohypo
- hypertg
- paraprot ( MM)
- obst jaundince

18
Q

hypertonic osm hyponatremia etiology ( sosm>295)

A

Mannitol
hyperglycemia
IVIG

19
Q

if hyponatremia in dialysis patient.. cause?

A

drinking ++ h20 in between dialysis sessions

20
Q

causes of nephrogenic DI

A
  1. HyperCA
  2. Lithium
  3. post resolution of obstruct nephropathy
  4. Hereditary
21
Q

how do you test for DID

A

step 1
- high serum na and low urine osm
- fail water deprivation test

step 2
- provide them with DDAVP and see response to differentiate the subtype

22
Q

how can you differentiate DI from polydipsia ?

A

water deprivation test , urine osm rises
also they have hyponatremia, not hypernatremia

23
Q

hyperosmolarity ( i.e. glucose or mannitol), would cause hyperkalemia or hypokalemia ?

A

hyperkalemia

24
Q

harmonize trial says what about K binders

A

can continue using lokelma/sodium zirconium in CKD to allow RAAS blockade meds

25
Q

dialyze study says what about K binders

A

lokelma /sodium zirconium can be used in IHD patients with chronic pre IHD hyperkalemia

26
Q

risk associated with kayexelate in terms of e+

A

hypoCa
hypoMg

27
Q

why impt to check mg with hypokameia

A

important bcs need mg for function of romk channels to reabsp K in the kidneys

28
Q

thyrotoxic periodic paralysis can cause what ?

A

hypokalemia

29
Q

u waves makes you think of which electrolyte abN ?

A

hypokalemia

30
Q

if i tell you chronic K loss in renal and you have met alkalosis, what will you check next ?

31
Q

aminoglycoside canb lead to which genetic channelopathy ?

32
Q

what does renin and aldost look like in barter and gittleman

33
Q

can use nsaid as tx for barter and gitleman ?

34
Q

defect in liddle ?

A

enac mutation –> reabsp too much na –>high bp
*low renin, low aldost

35
Q

tx for liddle ?

36
Q

K levels in liddle ?

37
Q

nocturnal dips in bp associated with what ?

A

high risk of cv events