Type 2 Diabetes Mellitus Flashcards
Diagnostic test for T2DM
1. Fasting
2. Random
3. Asymptomatic
4. Prediabetes
- Fasting glucose greater than or equal to 7mmol/l
- Random glucose greater than or equal to 11.1 mmol/l
- If patient is asymptomatic the above criteria must be met on two separate occasions
- Prediabetes/Impaired Glucose Tolerance= 6.1-6.9mmol/L fasting OR 7.8-11.0 mol/L random
HbA1c use in diagnosis of DM
- a HbA1c of greater than or equal to 48 mmol/mol (6.5%) is diagnostic of diabetes mellitus
- a HbAlc value of less than 48 mmol/mol (6.5%) does not exclude diabetes (i.e. it is not as sensitive as fasting samples for detecting diabetes)
- in patients without symptoms, the test must be repeated to confirm the diagnosis
- it should be remembered that misleading HbA1c results can be caused by increased red cell turnover (due to other causes)
conditions where HbA1c cannot be used for diagnosis of DM (8)
- haemoglobinopathies
- haemolytic anaemia
- untreated iron deficiency anaemia
- suspected gestational diabetes
- children
- HIV
- chronic kidney disease
- people taking medication that may cause hyperglycaemia (for example corticosteroids)
HbA1c targets for patients with DM
1. Patients managing with lifestyle measures
2. Patients managing with lifestyle measures and metformin
3. Patients managing using any drug which may cause hypoglycaemia (e.g. sulfonylureas)
- 48mmol/l
- 48mmol/l
- 53mmol/l
Metformin
1. Drug Class
2. Mechanism(s) of action
3. Side effects
- Biguanide
2: mechanisms
1- Decreases hepatic glucose production
2- increased hepatic insulin sensitivity
3- decreased intestinal glucose absorption
- Side effects:
- GI upset
- reduced B12 absorption
- lactic acidosis
first line drug of choice in T2DM
Metformin
When should SGLT-2 inhibitors be added to metformin?
should be given in addition to metformin if:
- patient has high risk of developing CVD or established CVD
- patient has chronic heart failure
- if either of these two factors develop during treatment
first line Tx when metformin is contraindicated
1. If patient has risk of CVD, established CVD or CHF
2. If patient doesn’t have a risk of CVD, established CVD or CHF
- SGLT-2 mono therapy
- DPP-4 inhibitor or pioglitazone or sulfonylurea
SGLT-2 inhibitors
1. Examples
2. Mechanism of action
3. Side effects (3)
- canagliflozin, dapagliflozin, empagliflozin
- reversibly inhibit sodium-glucose cotransporter 2 (SGLT-2) in the renal proximal convoluted tubule to reduce glucose reabsorption and increase urinary glucose excretion
- Side effects include
(1) urinary and genital infection (secondary to glycosuria) . Fournier’s gangrene has also been reported
(2) normoglycaemic ketoacidosis
(3) increased risk of lower limb amputation- feet should be closely monitored
DPP-4 inhibitors
1. Examples
2. Mechanism of action
3. Benefit
- Vildagliptin, Sitagliptin
- increase levels of incretins (which cause increased levels of insulin release) by decreasing their peripheral breakdown
- Benefit: Do not cause weight gain
Thiazolidinediones
1.. Example
2. Mechanism of action
3. Side effects (4)
- Pioglitazone
- PPAR-gamma receptor agonist (reduces peripheral insulin resistance)
- Side effects:
- weight gain,
- liver impairment (monitor LFTs),
- Fluid retention (therefore contraindicated in HF)
-increased risk of fractures
Sulfonylureas
1. Examples
2. Mechanism of action
3. Side effects
4. Contraindication
- Gliclazide, glimepiride, glyburide, gliplizide
- increase pancreatic insulin secretion by binding to the ATP-dependent K+ channel on cell membrane of pancreatic beta cells
- side effects
- Hypoglycaemic episodes
- weight gain - Should be avoided in breastfeeding and pregnancy
Second line therapy if metformin alone is not effective
Dual therapy - add one of the following:
- metformin + DPP-4 inhibitor
- metformin + pioglitazone
- metformin + sulfonylurea
- metformin + SGLT-2 inhibitor (if NICE criteria met)
Blood pressure target for patients with T2DM
140/90
First line medications for hypertension in DM patients and why?
ACEis (‘-pril’) and ARBs (‘-sartan’), because they are renoprotective in DM
ARBs are preferred for black African/Afro-Caribbean DM patients