Lecture 3 Flashcards

1
Q

Cockcroft-Gault

A

calculated measurement of CrCl
(M): (140 - age) x IBW in kg / 72 kg x Sir in mg/dL
(F): (CrCl Male) x 0.85
assumes stable renal function and normal mm mass

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2
Q

Creatinine clearance

A

Measured

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3
Q

nephrotoxic agents

A

should be avoided in pt’s at high risk for AKI

ahminoglycosides, amphotericin B, Radiocontrast agents, Cyclosporin/Tacrolimus, ACE inhibitors/ARBs and NSAIDs

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4
Q

kidney functions

A

excretory (fluid, electrolytes and solutes), metabolic (vit D and some drugs like insulin and B-lactams), endocrine (erythropoietin)

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5
Q

Diuretic classes

A

thiazides, carbonio anhydrase inhibitors, K sparing, osmotic, loop

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6
Q

important thiazide diuretics

A

chlorothiazide, hydrochlorothiazide, indapamide, metolazone and chlorthalidone

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7
Q

chlorothiazide

A

relative potency of 0.1, least potent

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8
Q

hydrochlorothiazide

A

relative potency of 1

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9
Q

indapamide

A

relative potency of 20, most potent, may be used if CrCl < 30

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10
Q

metolazone

A

relative potency of 10, may be used if CrCl <30

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11
Q

chlorothalidone

A

relative potency of 1

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12
Q

carbonic anhydrase inhibitors

A

limited usefulness as diuretic , open-angle glaucoma

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13
Q

K sparing diuretics

A

usually administered with K-losing thiazides (helps minimize K loss)

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14
Q

Na channel inhibitors (K sparing)

A

amiloride and triamterene

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15
Q

aldosterone antagonists (K sparing)

A

Spironolactone: CrCl 10-50 administer q24hr
CrCl < 10 avoid use
SE: gynecomastia and impotence

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16
Q

glycerine, isosorbide and urea

A

osmotic diuretic, little clinical use

17
Q

loop diuretics

A

most potent diuretics, individualize therapy
4 agents available both PO and IV
adverse effects: ototoxicity (tinnitus, deafness, vertigo - reversible) and hyperuricemia (rarely gout) and hyperglycemia

18
Q

Furosemide (Lasix)

A
excellent bioavailability (good oral abs)
acute pulm edema: start at 40 mg IVP over 1-2 min, then 80 mg IVP if no response
Metolazone (thiazide) can be added for pt's refractory to furosemide (synergistic effect) - double dose q24hr to desired response
19
Q

diuretic ceiling effect

A

inability of drug to prod additional effects above a certain max effective dose

20
Q

torsemide

A

preferred in its with persistence fluid retention despite high doses of other loops

21
Q

urinary acidifying agent

A

ammonium chloride

22
Q

urinary alkalinizing agent

A

inc elimination fo Aspirin

Na bicarb and K citrate

23
Q

phosphate binders

A

PO4 is retained, (Ca x PO4) pdt > 40 may precipitate (metastatic calcification aka stones in tissue) need for these

24
Q

first line phosphate binding agents

A

Ca Carbonate (Tums), Ca Acetate (PhosLo), Sevelamer HCl (Renagel) and Sevelamer Carbonate (Renvela)

25
Q

second line phosphate binding agents

A

Lanthanum Carbonate (Fosrenol)

26
Q

Ca Acetate

A

target serum PO4 < 6 mg/dL
mild hypercalcemia is >10.5 –> constipation, anorexia and N/V
severe hypercalcemia >12 –> delirium, stupor and coma
normal is 8.4-10.2
first line

27
Q

Sevelamer (Renagel)

A
may red vit D, E, K and folate abs
anion - exchange resin 
may induce metabolic acidosis in pt's on HD
target PO4 level < 6 
try after Ca Acetate
28
Q

Na Polystyrene Sulfonate (Kayexalate)

A

K-binding agent
SE: hypocalcemia, hypokalemia, hypomagnesium, N/V
monitor EKG and electrolytes listed

29
Q

oral Fe for CKD anemia

A

give 200 mg elemental Fe

titrate dose to minimize GI upset

30
Q

IV Fe

A

Ferric Gluconate and Fe Sucrose

31
Q

Ferric Pyrophosphate Citrate

A

water-sol complex Fe salt
added to hemodialysate sol
adv: progressive Fe accumulation doesn’t occur, red use of costly ESAs, inexpensive ($61/50 mL ampule so can tx multiple pt’s)

32
Q

Epoetin Alfa (Epogen, Procrit)

A
Recombinant Human Erythropoietin 
Non Dialysis CRF dose: 75-150 units/kg/wk
Dialysis CRF dose: 75 units/kg 3 x week 
round doses to nearest 1000 units
ESA
33
Q

Darbepoetin alfa

A

1/2 life is 3 x that of epoetin alfa
to convert from epoetin, add weekly units
ESA

34
Q

tx of Benign prostatic hyperplasia

A

a1 antagonists or 5a-reductase inhibitors

35
Q

Tamsulosin (Flomax)

A

adverse effects: orthostatic hypotension (16% at 0.4 mg, 19% at 0.8 mg)

36
Q

5a reductase

A

catalyzes conversion of testosterone to DHT

type II mainly in prostate and hair follicles