Cptp - Diabetes and Lipid Lowering Drugs
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Transcript of Cptp - Diabetes and Lipid Lowering Drugs
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1DIABETES AND LIPID LOWERING DRUGS
DIABETES
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2DIABETES AND LIPID LOWERING DRUGS
DIABETES MECHANISM OF ACTION INDICATION ADVERSE EFFECTS
INSU
LIN
RAPIDAspart
To mimic prandial (mealtime) insulin. Aspart must be consumed right before meal or up to
15mins after meal whereas soluble insulin 15mins prior meal or immediately after.
Subcutaneously
In emergency e.g. DKA given IV subC in regular basis usually given
with LA
Headache Anxiety Tachycardia Confusion Vertigo Diaphoresis Lipodystrophy Hypersensitivity
SHORTSoluble insulin INTERMEDIATEIsophane insulin (NPH)
Delayed absorption from its conjugation with protamine, forming less soluble complex. SubC
All type of diabetes except DKA Use for basal control and usually
given with rapid or short acting insulin for mealtime control
STANDARD TREATMENT VS INTENSIVE TREATMENT
Standard treatment involves injection of insulin twice daily. In contrast intensive treatment involves more frequent injections.
ADA recommend target mean blood glucose levels of Hba1c of 7% or less or 154mg/dL
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3DIABETES AND LIPID LOWERING DRUGS
LONGGlargine
Isoelectric point of insulin glargine is lower than that of human insulin, leading to precipitation at the injection site and extending its action.
Given subC Slower onset than NPH, and has
flat, prolonged hypoglycaemic effect with no peak
SULP
HONY
LURE
AS
GLICLAZIDE
Stimulate insulin release from β-cells by blocking the ATP sensitive K+ channel
Reduce hepatic glucose production Increase peripheral insulin sensitivityPharmacokinetics Extensively metabolised by CYP 450 enzymes in the
liver Excreted via liver and kidney To be used with caution in patients with renal or
hepatic insufficiency
Suitable for pt with DM2 that cannot be controlled with only diet
Hypoglycaemia Weight gain (as
insulin preferentially deposits calories in adipose tissue in Type 2 diabetics)
Hyperinsulinemia
BIGU
ANID
ES
METFORMIN
1. Reduction of hepatic glucose output (inhibits gluconeogenesis)
2. Slows intestinal absorption of sugars3. Improves peripheral glucose uptake and utilisation
(especially in muscle cells)4. Reduces hyperlipidemiaPharmacokinetics Not metabolised, cleared from the body by active
tubular secretion, excreted unchanged in the urine To be used with caution in patients with renal
insufficiency or those predisposed to metabolic acidosis
useful in overweight people with diabetes
Can suppress appetite and causes less weight gain than sulphonylureas
Largely gastrointestinal including anorexia, diarrhoea, nausea and abdominal discomfort
May cause lactic acidosis
TZDS
/GL
ITAZ
ONE
PIOGLITAZONE
Activate the transcription factor PPAR, which affects adipose cell differentiation and lipid metabolism
Metabolised in the liver by CYP 450 enzymes, metabolites are eliminated mainly in bile
Weight gain Fluid retention Heart failure Bladder cancer?
HYPOGLYCAEMIA Clinical Features
AUTONOMIC NEUROGLYCOPENIC1. Anxiety 2. Sweating3. Hunger 4. Tremor 5. Palpitations 6. Dizziness
1. Confusion 2. Vertigo 3. Drowsy 4. Visual trouble seizures 5. Coma
Initial Management
oral sugar or LA starch (toast)
if x swallow - 25-50ml 50% glucose IV (via larger vein with 0.9% saline flush to prevent phlebitis)
OR
glucagon 1mg IM if no IV access (SA so repeat after 20min
and follow with oral carbs)
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4DIABETES AND LIPID LOWERING DRUGS
DIABETIC KETOACIDOSIS Clinical Features Ketonaemia ≥3 mmol/L or significant ketonuria (++ on urine dipstick) Blood glucose >11 mmol/L or known diabetes mellitus Bicarbonate (HCO3-) <15 mmol/L and/or venous pH < 7.3
Intial Management
LIPID DIS. MOA INDICATION CONTRAINDICATION ADVERSE EFFECTS INTERACTION
STAT
IN SIMVASTATIN
Inhibit enzyme HMG Co A reductase in cholesterol synthesis
Primary Hyperlipidaemia (Reduce LDL by 30% & Raise HDL by 20%)
2’ Hypercholesterolemia
during pregnancy and lactation
Headache, nausea, rashes
Sleep disturbances Rise in serum
transaminase Myositis &
Rhabdomyolysis
increased statin concentrations e.g ciclosporin, clarithromycin, calcium channel blockers, antifungals
commence 0.9% NaCl via infusion
pump + K+ replacement
IV insulin infusion (0.1u/kg/hr)
50u soluble insulin (SA) made up to 50ml with 0.9% NaCl solution
Fluid replacement
systolic <90mmHg - 500ml NaCl/10-15minsystolic >90mmHg - 1000ml/60mins
Potassium
>5.5 - NIL3.5 - 5.5 - 40mmol/L<3.5 - senior review