diabetes Flashcards

1
Q

Biguanides

administration, MOA, indications/ contradictions, side effects, adverse effects

A

METFORMIN

  • increases peripheral glucose uptake and utilization - improves inuslin sensitivity
  • decreases hepatic glucose production
  • decreases intestinal absorption of glucose
  • very effective.
  • minimal risk of hypoglycemia
  • can help with weight loss
  • oral -
  • lowers lipids

risks:
- gi disturbances
- risk for vit b12 defiency with long term
- risk for lactic acidosis

dont give with

  • gfr less than 30
  • liver disease
  • alochol use
  • acute hf
  • lactic acidosis history
  • dcreaed tissue prfusion

drug interactions
- nifedipine - increase metformin
catatonic drugs - eliminated renally

cimetidine caan result in 40% increase in metformin !!!!!!!

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2
Q

sulfonyureas

administration, MOA, indications/ contradictions, side effects, adverse effects

A

1st gen

  • chlorpropamide /
  • tolbutamine
  • fallen out of favor due to high risk of hypoglycemia and more side effecs than second gen.

second gen
glipizide
- 30 mins before meals

GLYburide
- take with breaskgst

glimepiride

  • take with breakfast
  • low risk of hypoglycemia

lot of inhibitors and inducers.

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3
Q

TZD’s

administration, MOA, indications/ contradictions, side effects, adverse effects

A

PIOGLITAZONE

  • oral
  • periodici monitoring of liver function

ROSIGLITAZONE

  • rare used
  • questionable increased risk of cv death and MI
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4
Q

GLP1’S S

administration, MOA, indications/ contradictions, side effects, adverse effects

A

increases insulin, decreases glucagon, increases beta calls, decreases gsastric emptying, increases hunger, and insulin sensivity — we want to increase the glp 1 hormone.

so we either give a glip 1 agonist

or dpp4 - which inhibits breakdown of glp 1

Pros:

  • reduce fasting and post prandial BS
  • promote weight loss
  • low risk for hypoglycemia
  • long acting and short acting
  • decrease CVD outcomes
  • can be monotherapy
  • option for second ine therapy with metformin

CONS:

  • SQ administration
  • cant use with dpp4’s
  • risk of hypoglycemia increases if combined with SU or basal insulin

SIDE EFFECTS:

  • n/v/d
  • acute pancreatisis
  • caution with renal impairement

Liraglutide

  • weigt loss. SQ
  • very expensive
  • Decreases CVD risk

dulagulatide

  • no renal dose needed
  • reduced risk for non fatal MI stroke and CV death

semaglutide

  • no renal dosing - oral forms avaiailable
  • decreases non fatal stroke outcomes.

exenatide

  • short acting
  • not reccomended if GFR is less than 30.

BLACK BOX WARNING:
- THYROID C CELL TUMORS AND PANCREATISSI

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5
Q

GLP’1

dpp4
administration, MOA, indications/ contradictions, side effects, adverse effects

A

inhibit the breakdown of glp -1 by inhibiting the action of dpp4 - an enzyme that breaks down glp - 1

PROS: 
- reduce both asting and post prandial bs 
- weight neutral 
- low risk for hypoglycemia 
oral administration 
- option for secon dline therapy 

CONS:

  • many require renal dose adjustment
  • use caution in patients with HF
  • should not be used with GLP1 agonist
  • URI, HEADACHE, COST

Saxagliptin

linagliptin

alogliptin

vildafliptin

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6
Q

SGLT2’S

administration, MOA, indications/ contradictions, side effects, adverse effects

A

block reabsorption of glucose in the kidneys promoting renal excretion of glucose

PROS:

  • REDUCE a1c up to 1%
  • prmote weight loss
  • creases CVD outcomes with some formualtion
  • low risk of hypoglycemia
  • minimal GI side effects
  • oral administration

CONS:

  • avoid if GFR less than 45.
  • decreases effects at kidney function decreases

SIDE EFFECTS

  • UTI/ yeast infections
  • decreased BMD
  • increased risk of amputations
  • risk for dehydration and DKA

Canagliflozin

  • decreased CV morbidity
  • decreased of worsening GFR, esrd and renal related death

Empagliglozin

  • significant reduction in CV mortaility
  • proven HF benefit and renal benefit

DAPAGLOFLOZIN

  • avoid in bladder cancer
  • no change in athlerscerotic outcomes but does decrease hospitalizations for HF and other.
  • renal benefit

genital area infection
- can happen with these drugs.

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7
Q

INSULIN

START, RISK/ ADVERSE EFFECTS,

A

consider early therapy with metforms and or glp 1 if aic is more than 1-%
- if therapy is failing and you are ready to add a 2nd or 3rd drug.
- rarely used as monotherapy anymore
- continue metform with inuslin initiation
combo with glp 1 is reccomended
- generally preffered treatment for GDM/DM in pregnancy

downsides are that
- high risk of hypoglycemia, weight gain, BG monitoring

start with basal insulin - controls fasting blood sugars!!

weight based - titrate every 2-3 days.

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8
Q

INSULIN

BASAL VS. PRANDIAL

A

BASAL

  • reduces fasting hyperglycemia
  • long duration
  • inject morning and or evening
  • levenir NPH or lantus
  • it is possible to overbasalize - high bedtime glucose minus morning and its more than 50 thats bad. - be aware of hypoglycemia

IF FASTING SUGARS ARE GOOD BUT A1C IS HIGH THEN CHECK POST PRANDIAL SUGARS

Prandial

  • reduceds postprandial hyperglycemia
  • short acting
  • inject at meal times

apidra, humalog, novolog, regular

  • RAPID ATING - CAN BE ADDED LATER WITH MEALS
  • start with 4 units of 10% of amount of basal insulin - as prandial insulin is adjusted it may make sense to decrease bsal insulin
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9
Q

INSULIN
HOW TO INITIATE
PAT EDUCATION

A
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