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Mission Possible: Pharmacology made easy- Diabetes in ARRC edition

This article explores the treatment goals for diabetes, including achieving glycemic control, managing cardiovascular risk factors, and the differences in treatment options. Topics covered include aspirin therapy, metformin, sulfonylureas, pioglitazone, and alpha-glucosidase inhibitors.

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Mission Possible: Pharmacology made easy- Diabetes in ARRC edition

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  1. Mission Possible: Pharmacology made easy- Diabetes in ARRC edition Sara Salman Clinical Advisory Pharmacist Health Hawkes Bay

  2. What’s the difference from other Diabetes

  3. Treatment goals • Glycaemic target 54-70 • Avoiding hypoglycaemia • CV risk factor management • Smoking cessation • Treatment of hypertension • Treatment of dyslipidaemia • Aspirin therapy • Exercise

  4. Aspirin therapy in DM • Daily aspirin in patients with macrovascular dx is widely accepted (secondary prevention). • A meta-analysis of a large number of secondary prevention found that absolute benefit of aspirin was greatest in over 65yrs with diabetes or diastolic hypertension. • The role of aspirin for primary prevention of CV in patients with diabetes is less certain.

  5. Pathophysiologyin T2DM

  6. Metformin • Metformin is 1st line for all people with T2DM • Also prescribed to people with pre-diabetes • Evidence may provide CV protection beyond reducing HbA1c • Actions • Decreases glucose formation in liver • Increases peripheral utilisation of glucose

  7. Metformin Adverse Effects • Nausea • Vomiting • Anorexia • Diarrhoea • Malabsorption of vitamin B12 • Rash – infrequent • Lactic acidosis – rare, but often fatal- avoidance in SICK days

  8. Lactic acidosis • Risk factors • renal impairment • old age (reduced renal function) • high doses of metformin (> 2 gram/day) • Discontinue metformin temporarily: • Prior to surgery • Prior and after use of IV contrast media • Illness causing dehydration e.g. vomiting, diarrhoea

  9. Vitamin B12 deficiency • 30% patients • May present without anemia and as a peripheral neuropathy • it is often misdiagnosed as diabetic neuropathy •  Progression of central and/or peripheral neuronal damage can be arrested but not reversed with vitamin B12 replacement

  10. Sulfonylurea • Actions • Increasing insulin secretion from functional pancreatic beta-cells • Often added to metformin when HbA1c target not achieved • 3 fully-subsidised in NZ • Glipizide • Gliclazide • Glibenclamide

  11. Sulfonylureas

  12. Sulfonylurea Adverse Effects • Weight gain • Hypoglycaemia • Risk increased by advanced age, renal or hepatic impairment • Nausea, diarrhoea, metallic taste, headache, rash – infrequent • Blood disorders, allergic reaction, photosensitivity, hepatotoxicity - rare

  13. Sulfonylurea advise • Take with food to minimise hypoglycaemia risk • Drinking alcohol (advise for all patients with diabetes) • May mask hypoglycaemia symptoms • Avoid binge drinking • Eat when drinking alcohol • Know how to recognise and treat hypoglycaemia

  14. Pioglitazone (Glitazone) • Actions • ‘Insulin sensitiser’ (like metformin) • Increases body’s ability to transport glucose across cell membrane • Peroxisome proliferator-activated receptor gamma (PPAR-ɣ) agonist which regulates genes involved in lipid and glucose metabolism • Increases sensitivity of peripheral tissues to insulin • Decreases hepatic glucose output

  15. Pioglitazone Adverse Effects • Peripheral oedema & fluid retention • Weight gain (worse with insulin combination) • Headache, dizziness • Nausea/vomiting • Arthralgia • Decrease in haemoglobin and haematocrit • Fractures – infrequent • Elevated LFTs, hepatocellular injury, heart failure, pulmonary oedema, macular oedema - rare

  16. Pioglitazone • What to watch out for? • Swollen feet or ankles • Breathlessness • Fatigue • Loss of appetite • Dark urine • Refer to prescriber if family or personal history of bladder cancer

  17. Pioglitazone Practice Points • If not effective/ if achieved 5 mmol/mol reduction in HbA1c after 6 months is not achieved • Monitoring liver enzymes • Baseline & every 2 months for 1st year, then periodically • Symptoms of liver toxicity – nausea, abdominal pain, dark urine or jaundice = discontinue tx. • Limited long term safety data • Stop if heart failure diagnosed

  18. Alpha glucosidase inhibitors- Acarbose • Actions • Delays intestinal absorption of CHO by inhibiting alpha-glucosidase enzymes in small intestine • Enzyme which breaks down complex CHO into glucose • Reduced postprandial hyperglycaemia • Little effect on fasting glucose levels

  19. Acarbose adverse effects • Flatulence (75% patients affected) • Diarrhoea (or soft stools) • Abdominal pain and distention • Increased aminotransferase concentrations – infrequent (monitor monthly for 1st 6 months) • Ileus, hepatotoxicity, skin reactions, anaemia – rare NOTE: no risk of hypoglycaemia as monotherapy

  20. Acarbose is avoided in: • Contraindicated in patients with (or risk of) • Partial intestinal obstruction • Inflammatory bowel disease • Major hernia • GI disorders with malabsorption • Avoid use if CrCl<25mL/min • Hypoglycaemia (combination treatment) • Treatment: glucose NOT sucrose e.g. glucose tablets not jellybeans

  21. Acarbose Practice Points • Swallow whole • Take with liquid immediately before a meal or with first mouthfuls of food • GI adverse effects • Dose dependent(200mg tds maximum dose) • Increased by taking sucrose • Reduced by starting on low dose and slow titration(e.g. 50mg tds after 4-8 weeks 100mg tds) • Improves as treatment continues • Unlikely to be alleviated by antacids

  22. Summary • Selection based on individual patient, treatment goals and risks.

  23. Basal vs Bolus

  24. Examples

  25. Which Tom has diabetes?

  26. Questions?

  27. Gliptins- DDP4 (Dipeptidyl Peptidase-4 inhibitors) • Dipeptidyl peptidase 4 (DPP-4) inhibitors (DPP-4i) increase endogenous incretin levels by blocking the action of DPP-4 • Once-a-day oral agents with no risk of hypoglycemia • Weight-neutral, when used as monotherapy, and therefore may be attractive agents to use in older adults. • Since they are relatively weak agents and usually lower A1C levels by only 0.6 percent, DPP-4 inhibitors should only be used as monotherapy when the A1C level is relatively close to the goal level.

  28. Flozins- SGLT2 inhibitors • Sodium–glucose co-transporter 2 (SGLT-2) inhibitors. • SGLT-2i reduce renal glucose reabsorption

  29. Extra slides

  30. Extra slides

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