Diabetes Flashcards

1
Q

Goals of diabetes mellitus therapy

A
  1. eliminate symptoms related to hyperglycemia
  2. reduce or eliminate long-term microvascular and macrovascular complications
  3. allow patient normal life as possible
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Immunizations for diabetes patients

A

Influenza, pneumococcal, hep B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Numeric goals for DM patients

A

A1C less than 7%
Preprandial plasma glucose: 80-130 mg/dL
Peak postprandial plasma glucose: less than 180
BP: less than 140/90
Lipids: LDL less than 100
HDL greater than 40 for men and 50 for women
Triglycerides: less than 150

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Immunizations for diabetes patients

A

Influenza, pneumococcal, hep B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Diagnostic numbers for DM

A

A1C greater than 6.5%
Fasting glucose greater than or equal to 126 mg/dL
75 gm glucose tolerance test, 2 hours with glucose 300 mg/dL or greater
Random glucose greater than 200 mg/dL with symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Metformin drug class and MOA

A

Biguandes: (insulin sensitizer)

  • Reduces hepatic glucose production
  • Improves peripheral glucose utilization
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Actions of metformin

A
Reduces fasting plasma glucose (FPG)
Reduces insulin levels
Improves lipid profile
promotes modest weight loss
Slows intestinal absorption of sugars
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Contraindications of metformin

A

Renal insufficiency, GFR less than 60 mL/min
Any form of acidosis
Unstable CHF
Liver disease
Severe hypoxemia
Discontinue in acute MI, exacerbation of HF, sepsis
Or other conditions that cause acute renal failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Adverse effects of metformin

A

Largely gastrointestinal

CI in renal dysfunction due to risk of lactic acidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Adverse effects of insulin

A

Hypoglycemia is the most serious
Weight gain
local injection site reactions
Lipodystrophy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Short acting insulin prepartations

A

Insulin lispro
Insulin aspart
Insulin glulisine
Regular insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Time of injection for short acting insulin preparations

A

Lispro, aspart, glulisine: 15 min before meal or within 15 minutes of starting a meal
Regular insulin: 30 minutes before a meal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Most commonly used insulin when IV route is needed?

A

Regular insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Intermediate-acting insulin

A

Neutral protamine Hagedorn (NPH)
Used for basal control, in conjunction with fast-acting
It should never be given IV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Long-acting insulin preparations

A

Determir
Glargine
Used as basal formulations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Microvascular complications of DM

A

Nephropathy: most common cause of ESRD
Neuropathy: most common cause of peripheral neuropathy
Retinopathy: most common cause of blindness ages 20-70

17
Q

Macrovascular complications of DM

A

Coronary artery disease
Peripheral vascular disease
Cerebrovascular disease

18
Q

How to test for nephropathy in DM

A

Assess urine albumin excretion yearly
Spot urine sample
Test urine albumin/creatinine ratio
Ratio of greater than 30 considered albuminuria

19
Q

Macrovascular preventive measures for DM?

A
Glucose control (more helpful for microV)
BP reduction
LDL reduction
Aspirin therapy
ACE inhibitors
Smoking cessation
20
Q

Microvascular preventive measures for DM?

A

Glucose control
Aggressive HTN treatment
ACE inhibitor or ARB therapy

21
Q

First line treatment for HTN in DM?

A

ACE or ARB

22
Q

Lipid management with DM

A

Statin if known Cardiovascular disease
or greater than 40 with 1 or more other risk factors:
Risk factors: LDL greater than 100, HTN, smoking, overweight or obese

23
Q

Symptoms of hyperglycemia (9)

A
Polyuria
Polydipsia
Polyphagia
weight loss
fatigue
infections (yeast or skin)
blurred vision
poor healing
growth failure in children
24
Q

Initial dosing of metformin for DM

A

Start with 500 mg once daily

Build up to 1000 mg twice daily if tolerated

25
Q

Results of DKA

A
Low insulin
increased ketone bodies (measurable)
metabolic anion gap acidosis
usually increased plasma K from cells
increased glucose
dehydration
increased serum Cr from renal failure
osmotic diuresis
Total body K and PO4 depletion
26
Q

Clinical signs of DKA

A

Abdominal pain, nausea, vomiting (caused by irritation from inflammatory cytokines)
dehydration (caused by vomiting and osmotic diuresis)
Altered mental status (dehydration and metabolic acidosis)

27
Q

Treatment of DKA

A

IV fluids and insulin

28
Q

MOA of GLP-1

A
incretin mimetics
improve insulin dependent secretion
slow gastric emptying time
increase satiety
promote B-cell proliferation
29
Q

Sulfonylureas: drugs

A

Glimepiride
glipizide
glyburide (causes more hypoG, avoid use)

30
Q

Benefits of sulfonylureas

A

50 plus years of experience
Good efficacy
very effective in combination therapy
inexpensive/generic

31
Q

Disadvantages of sulfonylureas

A

Risk of hypoglycemia
Modest weight gain
May lose effect earlier

32
Q

Sulfonylureas MOA

A

Causes stimulation of insulin production regardless of glucose levels

33
Q

Short acting insulin secretagogues drugs

Meglitinides

A
Repaglinide
nateglinide
Need to be taken before each meal
MOA: similar to sulfonylureas
Short acting and expensive
34
Q

Alpha glucosidase inhibitors

A
acarbose (precose)
miglitol (Glyset)
voglibose
MOA: slow down the absorption of carbs
Primarily affect post-prandial glucose
A1C reduction: 0.4-0.9
AE: flatulence and diarrhea
Not well tolerated
35
Q
Thiazolidinediones:
Drugs
MOA
Metabolism
Benefits
SE
CI
A

MOA: insulin sensitizers
pioglitazones; Actos, rosiglitazone (black box Cardiac)
Meta: P450
Bene: good for lipid panel
SE: Risk of CV event, weight gain, density
CI: Heart disease class 3 or 4
Concern for: bladder cancer in rosi, hepatotoxicity, possible bone loss

36
Q

GLP-1 drugs

A

exenatide (Bydureon, Byetta) BID or QW for bydureon
liraglutide (Victoza) QD
dualglutide (Trulicity) QW
albiglutide (Tanzeum) QW

37
Q
GLP-1:
MOA
Benefits
SE
CI
A

MOA: incretins, increase insulin release, decrease glucagon, decrease appetite
Bene: Low risk of hypoG, decreases weight, weekly formulation
SE: N/V/D
CI: History of pancreatitis, gastroperesis, personal or family history of medullary thyroid cancer or MEN 2A or B,
(exenatide) renal GFR <30

38
Q

DPP-4 inhibitors
Drugs
MOA
AE

A

dipeptidyl peptidase-4 inhibitors
sitagliptin (Juaniva), saxagliptin, linagliptin
MOA: prolong the activity of incretin hormones which increases insulin release in response to meals
AE: HA, pharyngitis, URI, possible connection to pancreatitis, uncertain connection to pancreatic cancer

Not a lot of bang for buck according to lecture

39
Q
SGLT-2 inhibitors
MOA
Adv
CI
Disadvantanges
A

canagliflozin (Invokana): I dose: 100mg, up to 300mg daily
dapagliflozin (Farxiga): I dose: 5mg, up to 10mg daily
empagliflozin (Jardiance): in dose: 10mg, up to 25mg daily
MOA: promotes excretion of glucose in urine along with Na (can cause hypotension)
Adv: Weight loss, decreased BP, bone fracture with invokana, also slight increase risk in LE amputations with ivokana
CI: GFR <60, Ketosis-prone patients, hypotension
Dis: Expensive, yeast infection, no long term safety data