10/22 Flashcards

1
Q

pharm therapy

A

1st line: thiazides, ACE/ARB/renin inhibitors, CCBs
2nd line: loops, K sparing diuretics, BB, vasodilators (hydrazaline), alpha blockers
initial selection: potentially favorable effects in other disease states

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2
Q

diuretics

A
  • roles in managing fluid: correct underlying disease state, restrict Na intake, administration
  • most pts require >2 agents: a thiazide duiretic may be 1 unless CI, combo regimens often include a diuretic, resistant HTN: failure to achieve BP goal on full doses of 3 drug regimen including a diuretic
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3
Q

diuretics clinical indication

A

HTN, edema, CHF, CKD, hypercalcemia, diabetes insipidus

may slow osteoporosis

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4
Q

thiazide diuretics historically..

A

first line for most HTN pts

more effective than loops unless CrCl

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5
Q

thiazide AEs

A

hypokalemia, hypomagnesemia, hypercalcemia, hyperuricemia, hyperglycemia, hyperlipidemia, sexual dysfunction
lithium toxicity w concurrent admin
CI: sulfa allergy

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6
Q

thiazide examples

A

HCTZ, chlorthalidone, chlorothiazide, indipamide, metolazone

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7
Q

loop diuretics

A

dose in AM or afternoon to avoid nocturnal diuresis, higher doses may be needed in pts w severely dcreased GFR or HF (use in place of thiazides when CrCl

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8
Q

loop diuretics AEs

A

hypokalemia, hypomagnesemia, hypocalcemia, hyperuricemia, ototoxicity
CI: sulfa allergy (except ethacrynic acid)

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9
Q

K sparing diuretic examples

A

amiloride, triamterene

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10
Q

K sparing diuretics

A

weak diuretics, generally used in combo w thiazide to minimize hypokalemia

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11
Q

K sparing diuretics AE

A

hyperkalemia (especially w ACE/ARB or K supplements), avoid in pts w CKD or DM

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12
Q

aldosterone antagonists examples

A

spironolactone, eplerenone

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13
Q

aldosterone antagonists CI

A

due to inc hyperkalemia, eplerenone is CrCl

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14
Q

aldosterone antagonists AE

A

hyperkalemia (especially w ACE/ARB or K supplements
avoid in CKD or DM
gynecomastia: up to 10% of patients taking spironolactone

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15
Q

ACE clinical indications

A

HTN, left ventricular systolic dysfuction, MI, diabetic nephropathy, renal artery stenosis (degree of stenosis)

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16
Q

ARBs clinical indications

A

HTN (only approved use), CHF, progressive renal impairment (diabetes)

17
Q

renin inhibitors clinical indications

A

HTN

18
Q

angiotensin compelling indications

A

DM w proteinuria, HF, post MI w systolic dysfunction

19
Q

favorable effects of angiotensin inhibitors

A

DM type 1 and 2, renal insufficiency (use)

20
Q

angiotensin inhibtors CI

A

pregnancy, nursing, hx of angioedema, bilateral renal artery stenosis, hyperkalemia

21
Q

ACEI overview

A

“prils”

  • 1st line option; strongly emphasized for CKD
  • block Ang I -> Ang II
  • prevent or regress left ventricular hypertrophy (LVH) by reducing ang II myocardial stimulation
22
Q

ACEi monitoring

A

serum K+ and SCr within 4 weeks of initiation or dose increase

23
Q

ACE AE

A

dry cough, angioedema, hyperkalemia (esp in pts with CKD or DM)

24
Q

ARB overview

A

“sartans”

-inhibit Ang II from all pathways (directly block AT1 receptor)

25
Q

ARB AE

A

othostatic hypotension, renal insufficiency, hyperkalemia

26
Q

ACE/ARB warning

A
  • reduce starting dose by 50% in some patients due to hypotension risk
  • may cause hyperkalemia in CKD patients and patients on K sparing medications
  • can cause acute kidney failure in certain patients (severe bilateral renal artery stenosis)
  • CI in pregnancy
27
Q

direct renin inhibitor

A

aliskiren

-inhibits angiotensinogen -> Ang I

28
Q

renin inhibitor dosing

A

start: 150 mg po qd
main: 150 - 300 mg PO QD
max: 300 mg PO QD

29
Q

renin inhibitor adverse events

A

orthostatic hypotension, hyperkalemia, diarrhea

30
Q

monitoring for angiotensin inhibitors

A

SCr, K+, angioedema, dizziness, cough