Diabetes medications: Difference between revisions
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==Background== | ==Background== | ||
*Hypoglycemics | |||
**Sulfonylureas | |||
**Benzoic acid derivatives | |||
*Antihyperglycemics | |||
**Biguanides | |||
**Alpha glucosidase inhibitors | |||
**Thiazolidinediones | |||
==[[Insulin]]== | ==[[Insulin]]== | ||
Line 14: | Line 14: | ||
===Dose=== | ===Dose=== | ||
Metformin 500mg PO BID is first-line agent for type II diabetics | Metformin 500mg PO BID is first-line agent for type II diabetics | ||
*Do not prescribe if Cr > 1.4 (GFR <40), CHF, hepatic insufficiency, ETOH abuse | |||
*Should be withheld for 48hr after IV contrast | |||
===Side Effects=== | ===Side Effects=== | ||
*Lactic acidosis (due to increased lactate production) | |||
**Seen almost exclusively in patients with renal failure | |||
*Nausea, diarrhea, crampy abdominal pain | |||
===Toxicity=== | ===Toxicity=== | ||
*Almost never causes hypoglycemia when taken alone, but can exacerbate hypoglycemia when taken in combination with hypoglycemic agents | |||
*Toxic dose unknown | |||
*Management: Supportive care | |||
==Sulfonylureas== | ==Sulfonylureas== | ||
*Increases insulin secretion (glipizide, glyburide) | |||
*Hypoglycemia is the major adverse effect (esp w/ glyburide) | |||
==Alpha Glucosidase Inhibitors== | ==Alpha Glucosidase Inhibitors== | ||
*acarbose, miglitol, voglibose | |||
*competitively and reversibly inhibit alpha glucosidase brush border hydrolase enzyme- makes postprandial decrease in carbohydrate absorption since complex polysaccharides not broken down into absorbable monosaccharides | |||
*does not affect lactose absorption | |||
*if hypoG- sucrose/ table sugar will not work- use glucose- po or iv | |||
*take these meds with each meal with first bite | |||
*since limited aborption, stays in gut and side effects mostly GI- bloating, gas, diarrhea | |||
*contraindications- cirrhosis, IBD, malabsorption synd | |||
*alpha glucs do not cause hypoG when used as monotx | |||
*acarbose- can cause transaminitis/ liver inj | |||
*since min absorption- systemic tox from OD unlikely | |||
==Thiazolidinediones== | ==Thiazolidinediones== | ||
*rosiglitazone and poiglitazone | |||
*enhance insulin effect on muscle, fat, liver without increasing panc insulin secretion | |||
*protein bound and hep metab- not good if liver dz | |||
*side effects- induce ovulation, increase plasma vol bad if CHF, decrease effectiveness of OCP's | |||
==Benzoic Acid Derivatives== | ==Benzoic Acid Derivatives== | ||
*repaglinide- mono or combo tx c metformin | |||
*binds to atp dependent potassium channel like sulfonyls but at different site. | |||
*Unlike sulfonyls, it decreases insulin lvls | |||
*Dose 30 min before meal to decrease post prandial hyperglycemia | |||
==See Also== | ==See Also== | ||
*[[Diabetes Mellitus (Main)]] | *[[Diabetes Mellitus (Main)]] | ||
== | ==References== | ||
Tintinalli | Tintinalli | ||
[[Category:Endo]] | [[Category:Endo]] | ||
[[Category:Drugs]] | [[Category:Drugs]] |
Revision as of 21:17, 26 November 2015
Background
- Hypoglycemics
- Sulfonylureas
- Benzoic acid derivatives
- Antihyperglycemics
- Biguanides
- Alpha glucosidase inhibitors
- Thiazolidinediones
Insulin
Biguanides (Metformin)
Suppresses liver glucose production
Dose
Metformin 500mg PO BID is first-line agent for type II diabetics
- Do not prescribe if Cr > 1.4 (GFR <40), CHF, hepatic insufficiency, ETOH abuse
- Should be withheld for 48hr after IV contrast
Side Effects
- Lactic acidosis (due to increased lactate production)
- Seen almost exclusively in patients with renal failure
- Nausea, diarrhea, crampy abdominal pain
Toxicity
- Almost never causes hypoglycemia when taken alone, but can exacerbate hypoglycemia when taken in combination with hypoglycemic agents
- Toxic dose unknown
- Management: Supportive care
Sulfonylureas
- Increases insulin secretion (glipizide, glyburide)
- Hypoglycemia is the major adverse effect (esp w/ glyburide)
Alpha Glucosidase Inhibitors
- acarbose, miglitol, voglibose
- competitively and reversibly inhibit alpha glucosidase brush border hydrolase enzyme- makes postprandial decrease in carbohydrate absorption since complex polysaccharides not broken down into absorbable monosaccharides
- does not affect lactose absorption
- if hypoG- sucrose/ table sugar will not work- use glucose- po or iv
- take these meds with each meal with first bite
- since limited aborption, stays in gut and side effects mostly GI- bloating, gas, diarrhea
- contraindications- cirrhosis, IBD, malabsorption synd
- alpha glucs do not cause hypoG when used as monotx
- acarbose- can cause transaminitis/ liver inj
- since min absorption- systemic tox from OD unlikely
Thiazolidinediones
- rosiglitazone and poiglitazone
- enhance insulin effect on muscle, fat, liver without increasing panc insulin secretion
- protein bound and hep metab- not good if liver dz
- side effects- induce ovulation, increase plasma vol bad if CHF, decrease effectiveness of OCP's
Benzoic Acid Derivatives
- repaglinide- mono or combo tx c metformin
- binds to atp dependent potassium channel like sulfonyls but at different site.
- Unlike sulfonyls, it decreases insulin lvls
- Dose 30 min before meal to decrease post prandial hyperglycemia
See Also
References
Tintinalli