CKD Flashcards

1
Q

Give two examples of statins

A
  • Simvastatin
  • Atorvastatin
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2
Q

What is the primary mechanism of action of statins?

A
  • Selective, competitive inhibitor of HMG-CoA reductase responsible for converting HMG-CoA to mevalonate in cholesterol synthesis
  • Reduces hepatic cholesterol synthesis which upregulates LDL receptors and increases hepatic uptake of LDL-cholesterol from circulation
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3
Q

What is the drug target of statins?

A

HMG-CoA reductase

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4
Q

What are the main side effects of statins?

A
  • Muscle toxicity- likelihood increases with higher doses and in patients at increased risk of muscle toxicity
  • Constipation/diarrhoea and other GI symptoms
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5
Q

What are statins useful for?

A

Effective at reducing risk of adverse cardiac events in people

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6
Q

Why do patients with statins need to be regularly followed up?

A

To monitor for hyperkalaemia and acute renal failure

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7
Q

Why may a patient have increased statin serum concentrations?

A

Coadministration with potent 3A4 inhibitors may result in increased statin serum concs

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8
Q

What is the primary mechanism of action of aspirin?

A
  • Irreversible inactivation of COX
  • Prevents oxidation of arachidonic acid for prostaglandin production
  • Reduction of thromboxane A2 in platelets reduces aggregation
  • Reduction of PGE2 at sensory pain neurones reduces pain and sensation and decreases fever in brain
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9
Q

What is the drug target of aspirin?

A

COX

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10
Q

What are the main side effects of aspirin?

A
  • Dyspepsia
  • Haemorrhage
  • In elderly, avoid doses >160mg daily (increased bleeding risk)
  • Coadminister PPI if past history of peptic ulcer
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11
Q

Why is aspirin good prevention?

A

Low dose aspirin is most cost effective medicine for prevention of secondary events of thrombosis

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12
Q

Why does aspirin cause side effects such as dyspepsia?

A

COX1 blockade in gastric mucosal cells reduces mucus/bicarbonate production which can expose stomach lining to acid

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13
Q

What is the primary mechanism of action of trimethoprim?

A
  • Direct competitor of dihydrofolate reductase enzyme
  • Inhibits reduction of dihydrofolic acid to tetrahydrofolic acid (active form)- necessary part for synthesising purines required for DNA and protein production
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14
Q

What is the drug target of trimethoprim?

A

Dihydrofolate reductase

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15
Q

What are the main side effects of trimethoprim?

A
  • Diarrhoea
  • Skin reactions
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16
Q

What is trimethoprim often administered with?

A

Often administered with sulfamethoxazole aka co-trimoxazole → in combo they block 2 steps in bacterial biosynthesis of essential nucleic acids and proteins

17
Q

What needs monitoring after administration of trimethoprim?

A
  • Need to monitor blood counts in long term use or in those at risk of folate deficiency
  • Also monitor serum electrolytes in patients at risk of developing hyperkalaemia
18
Q

What is the primary mechanism of action of gentamicin?

A

Binds to bacterial 30s ribosomal subunit disturbing translation of mRNA leading to formation of dysfunctional proteins

19
Q

What is the drug target of gentamicin?

A

30s ribosomal subunit

20
Q

What are the main side effects of gentamicin?

A
  • Ototoxicity (hearing or balance problems)
  • Nephrotoxicity
21
Q

Why is gentamicin ineffective against anaerobic bacteria?

A

It’s an aminoglycoside antibiotic and can pass through gram -ve cell membrane in an oxygen dependent manner

22
Q

How is gentamicin administered?

A

More likely to be IV administered for endocarditis, septicaemia, meningitis, pneumonia or surgical prophylaxis

23
Q

What other drugs may be used for CKD?

A
  • Calcium channel blockers
  • ACE inhibitors
  • Angiotensin receptor blockers
  • Dapaglifozin
  • NSAIDs