Diabetes Flashcards
Lispro (class, mechanism [3], use, risks [3])?
Class: Rapid acting insulin prep
Mechanism: Binds insulin receptor (tyrosine kinase) rapidly.
- Liver = ↑ glucose stored as glycogen
- Muscle = ↑ glycogen and protein synthesis & ↑ K+ uptake
- Fat = ↑ TG storage
Use: Postprandial glucose control in Type 1 DM, Type 2 DM, GDM
Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
Regular Insulin (class, use [3], risks)?
Class: Short acting insulin prep Use: - Type 1 DM, Type 2 DM, GDM - Diabetic Ketoacidosis (give IV) *In DKA, no insulin to take up the high serum glucose levels - Hyperkalemia (+ glucose) - Stress hyperglycemia Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
NPH (class, use, risks)?
Class: Intermediate acting insulin prep
Use: Type 1 DM, Type 2 DM, GDM
Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
Detemir (class, use, risks)?
Class: Long acting insulin prep
Use: Basal glucose control in Type 1 DM, Type 2 DM, GDM
Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
Metformin (class, mechanism [3], mode, use, side effect, risks [2])?
Class: Biguanide
Mechanism: ↓ gluconeogenesis, ↑ glycolysis, ↑ peripheral glucose uptake (due to ↑ insulin sensitivity)
Mode: Oral
Use: First-line therapy in type 2 DM
***Can be used in patients without islet function.
Side effect: Causes modest weight loss
Risks:
- GI upset
- Most serious is lactic acidosis (thus contraindicated in renal insufficiency).
Chlorpropamide (class, mechanism, use, risks [3])?
Class: 1st gen Sulfonylurea
Mechanism: Close K+ channel in β-cell
membrane → cell depolarizes → insulin release via Ca+2 influx.
Use: Stimulate release of endogenous insulin in type 2 DM (useless in type 1 DM)
Risks:
- Risk of hypoglycemia ↑ in renal failure
- Weight gain.
- Disulfiram-like effects.
Glimepiride (class, mechanism, use, risks [3])?
Class: 2nd gen Sulfonylurea
Mechanism: Close K+ channel in β-cell
membrane → cell depolarizes → insulin release via Ca+2 influx.
Use: Stimulate release of endogenous insulin in type 2 DM (useless in type 1 DM)
Risks:
- Risk of hypoglycemia ↑ in renal failure
- Weight gain.
- Hypoglycemia
Nateglinide (class, mechanism, use [2], risks [2])?
Class: Meglitinides
Mechanism: Stimulate postprandial insulin
release by binding to K+ channels on β-cell membranes (site differs from sulfonylureas).
Use:
- Monotherapy in DM2 or combined with Metformin
- Are NOT sulfa drugs (as are sulfonylureas)
Risks:
- Hypoglycemia (↑ risk in renal failure)
- Weight gain
Exenatide (class, mechanism [4], use, risks [4], note)?
Class: GLP-1 analog Mechanism: - ↑ Glucose-dependent insulin release - ↓ Glucagon release - ↓ Gastric emptying - ↑ Satiety. Use: Type 2 DM Risks: - Nausea - Vomiting - Pancreatitis - Modest weight loss Note: Does NOT cause hypoglycemia
Linagliptin (class, mechanism [5], use, risks, notes [2])?
Class: DPP-4 inhibitors Mechanism: - Inhibits DPP-4 enzyme that deactivates GLP-1 - ↑ Glucose-dependent insulin release - ↓ Glucagon release - ↓ Gastric emptying - ↑ Satiety. Use: Type 2 DM Risks: - Urinary or Respiratory infections Notes: - Weight neutral - Does NOT cause hypoglycemia
Aspart (class, mechanism [3], use, risks [3])?
Class: Rapid acting insulin prep
Mechanism: Binds insulin receptor (tyrosine kinase) rapidly.
- Liver = ↑ glucose stored as glycogen
- Muscle = ↑ glycogen and protein synthesis & ↑ K+ uptake
- Fat = ↑ TG storage
Use: Postprandial glucose control in Type 1 DM, Type 2 DM, GDM
Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
Glargine (class, use, risks)?
Class: Long acting insulin prep
Use: Basal glucose control in Type 1 DM, Type 2 DM, GDM
Risks: Hypoglycemia, lipodystrophy, rare hypersensitivity reactions
Tolbutamide (class, mechanism, use, risks [3])?
Class: 1st gen Sulfonylurea
Mechanism: Close K+ channel in β-cell
membrane → cell depolarizes → insulin release via Ca+2 influx.
Use: Stimulate release of endogenous insulin in type 2 DM (useless in type 1 DM)
Risks:
- Risk of hypoglycemia ↑ in renal failure
- Weight gain.
- Disulfiram-like effects.
Glipizide (class, mechanism, use, risks [3])?
Class: 2nd gen Sulfonylurea
Mechanism: Close K+ channel in β-cell
membrane → cell depolarizes → insulin release via Ca+2 influx.
Use: Stimulate release of endogenous insulin in type 2 DM (useless in type 1 DM)
Risks:
- Risk of hypoglycemia ↑ in renal failure
- Weight gain.
- Hypoglycemia
Repaglinide (class, mechanism, use [2], risks [2])?
Class: Meglitinides
Mechanism: Stimulate postprandial insulin
release by binding to K+ channels on β-cell membranes (site differs from sulfonylureas).
Use:
- Monotherapy in DM2 or combined with Metformin
- Are NOT sulfa drugs (as are sulfonylureas)
Risks:
- Hypoglycemia (↑ risk in renal failure)
- Weight gain