Cardiology questions 1 Flashcards

1
Q

HYPERTENSION

An 81-year-old man attended the hypertension clinic for

review. He also had atrial fibrillation and chronic renal
impairment. He was already taking aspirin, digoxin (rate limiting CCB), indapamide (Diuretic) and ramipril.

On examination, his pulse was 65 beats/minute and irregular, and his blood pressure was 185/88 mmHg.
What is the most appropriate additional treatment for his
hypertension?

  1. Amlodipine
  2. Atenolol
  3. Dozaxosin
  4. Spironolactone
  5. Verapamil
A

Amlodipine

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2
Q

Name the steps of hypertensive drugs

A
  1. Ace inhibitor Or ARB less <55 years old, not black or have diabetes.
    Over >55 years, or patients with Afrocaribbean CCB (Amlodipine). If not tolorated, offer thiazide-like diuretic like Indapamide
  2. ACE/ARB + CCB
  3. ACE OR ARB + CCB
  4. Add Spirolactone, selective A-blocker or B-blocker
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3
Q

DISCUSS ACE INHIBITORS CLINICAL PHARM INFORMATION

A

Angiotensin converting enzyme inhibitor

Drugs: Ramipril, lisinoprol, ptrindopril

MOA: Angiotensin converting enzyme Inhibitor block the action ACE to prevent the conversion of angiotensin I to II.
Angiotensin II is a vasoconstrictor and stimulates aldosterone secretion whichh reduces vascular afterload reducing BP.

Indications:

  • Hypertension
  • Heart failure
  • IHD
  • Diabetic nephropathy & CKD (proteinuria)

Adverse effects:

  • Hypotension
  • Dry cough
  • Angioedema
  • Hyperkalaemia
  • Worsen renal failure

Warnings (Caution):

  • Monitor kidney function as it can worsen
  • Potassium elevating drugs
  • NSAIDs

Contraindications:

  • Renal artery stenosis
  • Pregnancy
  • Breastfeeding
  • Acute kidney injury

Interactions:
Potassium elevating drugs and supplements. NSAIDs increase risk of nephrotoxicity

Monitoring:
1.25 mg daily starting dose 10mg max
Explain side effects, dry cough, dizziness
Blood test monitoring for egfr 1-2 weeks into treatment and after titrating dose.

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4
Q

DISCUSS ANGIOTENSIN RECEPTOR BLOCKER

A

ARBS: Angiotensin receptor blockers

MOA: Angiotensinn receptor nlockrt block the action of angiotensin II on the angiotensin type 1 AT 1 receptor. It is also a vasoconstrictor and stimulate aldosterone secretion. Blocking afterload reduces BP.

Drugs: LOSARTAN, CADENSARTAN

  • Indications:
  • Hypertension
  • Heart failure
  • IHD
  • Diabetic nephropathy and CKD

Adverse effects:

  • Hypotension
  • Hyperkalaemia
  • Renal failure
  • Dizziness

Warnings (Caution):

  • Dose should be monitored on renal function effect
  • Potassium elevating drugs
  • NSAIDs
  • Hypertrophic cardiomyopathy
  • Angiodema

Contraindications:

  • Renal artery stenosis
  • Acute kidney injury
  • Pregnancy
  • Breastfeeding
  • Diabetes with eGFR (less than 60ml)

Interaction:

  • ▴Potassium-elevating drugs, potassium supplements
  • Potassium sparing diuretics
  • NSAIDs increase risk of nephrotoxicity

Monitoring:

Check electrolytes and renal function
Repeat this 1–2 weeks into treatment and after increasing the dose. Check if symptoms has improved

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5
Q

DISCUSS CCB CLINICAL PHARM INFORMATION

A

CALCIUM CHANNELL BLOCKER

Drugs: Dihydropyridines: Amlodipine and nifedipine for vasculature
Non-dihydropyridines: Verapamil most cardioselective, Diltiazem

MOA:

  • Calcium channel blocker relaxation and vasodilation in arterial smooth muscle, lowering arterial pressure.
  • Calcium channel blocker reduce myocardial contractility
  • Reduces cardiac contractility and myocardial oxygen demand

Indications

  • Hypertension
  • Stable angina
  • Supraventricular arrhythmias (tachycardia, atrial flutter)
  • Adverse effects:
  • Ankle swelling
  • Flushing
  • Palpitations
  • Headache
  • (Verapamil- Constipation, Heart failure, heart block)

Warnings (Cautions):
- Patients with poor left ventricular function
- AV nodal conduction delay
- CCB and B-Blockers should not be prescribed unless specialist supervision as
they can cause HF, Bradycardia.

Contraindications:
- Amlodipine and nifedipine contraindicated in unstable angina, (increase cardial
oxygen demand)
- Severe aortic stenosis, cause collapse.

Interactions:
- Verapamil and diltiazem should not be prescribed with B-blockers as both can cause HF, bradycardia

Monitoring:
Regular BP monitoring
Help reduce cardiovascular risk
HTN usual dose is 5mg - 10mg Amlodipine
Supra ventri arrhythmias: Diltiazem 90mg orally 12hr
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6
Q

DISCUSS THIAZIDE LIKE DIURETIC CLINICAL PHARM INFORMATION

A

Thiazide like diuretics:

MOA: Thiazide inhibit NA/Cl, Co transporter in distal convulated tubule of the nephron and may mediate vasodilation.

Drugs: Indapamide, Bendroflumethiazide, chloralidone

  • Indications:
  • Hypertension, first line or add on.

Adverse effects

  • Hyponatraemia
  • Hypokalaemia (excess sodium exchanged for potassium)
  • Arrhythmias
  • Impotence

Warnings (Caution)

  • NSAIDs
  • Hyponatraemia
  • Gout

Contraindication

  • Hypokalaemia
  • Hyponatraemia
  • Pregnant women

Interactions:

  • Nsaids reduces effectiveness
  • Lowers serum potassium loop diuretics

Monitoring:
Patient starting measure serum electrolyte 2-4 weeks before and after

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7
Q

A 67 year old patient is experiencing chest pain which radiates to his jaw, he was on a jogging session while this came on. He stopped at rest and used his GTN spray after 5 min and after 15 mins the pain continued. What does this patient have?

A

Unstable angina

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8
Q

Discuss Nitrates clinical pharmacology.

A

MOA: Nitrates convert into nitric oxide. NO increases cyclic guanosine monophosphate synthesis and reduces ontracellular Ca2 in vascular smooth cells causing relaxation. Relaxation of the venous vessels reduce cardiac preload, cardiac work and O2 demand.

GTN (Sublingual glyceryl trinitrate – first line instable angina

Indications:

  • Acute angina and Acute Coronary Syndrome
  • Long-acting nitrates (Isosorbide mononitrate) used for prophylaxis of angina
  • Pulmonary oedema

Adverse effects:

  • Flushing
  • Headaches
  • Light headedness
  • Hypotension
  • Tolorance

Contraindications:

  • Severe aortic stenosis
  • Haemodynamic instability
  • Hypotension

Interactions:
- Phosphodiesterase PED inhibitors (Sildenifl) prolong hypotension

Monitoring:
Patient may experience headache, flushing etc but shortlived
- Use this before doing tasks that initate chest pain
- Postural hypotension risk, patient should sit 5 mins after using
- Ensure BP monitoring should not drop below 90mmhg

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9
Q

Discuss Beta blocker clinical pharmacology.

A

Beta blocker

MOA: Mechanism of action:

  1. B1 receptors reduce force of contraction and speed of conduction in the heart relieving myocardial ischaemia.
  2. Slow down ventricular rate by prolonging the refractory period of arioventricular node.
  3. Reduces BP by reducing renin secretion
  • Indications:
  • IHD – Ischemic heart disease
  • CHF – Chronic heart failure
  • AF – Atrial fibrillation
  • SVT – supraventricular tachycardia
  • HTN – Hypertension

Drugs: B1 selective are: Bisoprolol, metoprolol. Non-selective Propranolol
and carvedilol)

  • Adverse effects:
  • Fatigue
  • Cold extremities
    Headache
    Gi disturbances (Nausea)
    Impotence
    Nightmares.

Warnings (Caution)

  • Heart failure
  • Hepatic failure
  • COPD
  • Haemodynamic instability

Contraindications

  • Asthma
  • Heart block
  • Hepatic failure

Interactions:
- Non dihydropyridine calcium channel blocker (Verapamil, diltiazem)

Monitoring:
- Should be take once daily same time each day
- Common side effects like impotence can occur impotence
- HF initial deterioration, seek medical attention
- Patients with obstructive airway diseases if breathing get worse seek medicial attention.
Review treatment in 2-4 weeks

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10
Q

Discuss Alpha blocker clinical pharmacology

A

Alpha blocker

MOA: Drugs in this class are highly selective a1-adrenoceptor found in the smooth muscles, blood vessels and urinary system. Stimulation induces contraction; blockade induces relaxation. α1-blockers therefore cause vasodilatation and a fall in blood pressure (BP), and reduced resistance to bladder outflow

Drug names: Doxazosin, Tamsulosin, Alfuzosin

Indications:

  • Benign prostate enlargement
  • Resistant hypertension (usually fourth line)

Adverse effects:

  • Postural hypertension
  • Dizziness
  • Syncope

Caution/warnings

  • Postural hypotension
  • Raynaud’s phenomenon

Contraindication
- Modified-release doxazosin tablets in people with gastrointestinal obstruction, oesophageal obstruction, or any degree of stricture.

Interactions:
- Pronounced first-dose hypotension, it may be prudent to omit doses of one or more existing antihypertensive drugs on the day the α-blocker is started.

Monitoring:
Doxazosin is licensed both for benign prostatic enlargement and hypertension; it is typically started at a dose of 1 mg daily and increased at 1–2 week intervals according to response.

Tamsulosin given for benign prostatic enlargement only. Efficacy is the patient’s urinary symptoms and/or BP, as applicable. For tolerability and safety, adverse effects such as hypotension

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11
Q

Mr. Solomon is a 63-year old gentle man who has been under your care for a variety of medical problems during the past 5 years. He has been treated for two myocardial infarctions, hypertension, non-insulin dependent diabetes and stasis dermatitis of the left leg. He had an aorto-coronary bypass one year ago. Today he presents in the office with shortness of breath which has been progressive over the past five days. He has, however, experienced episodes of shortness of breath during the past four months, especially when exerting himself. He fatigues easily and has lost “all my energy to do anything.” He also complains of anorexia. Last night he awoke suddenly from sleep because “I couldn’t catch my breath”. He sleeps on 3 pillows.

WHAT DOES HE HAVE?

A
  • Heart failure
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12
Q

How do you manage heart failure?

A
  1. Ace inhibitors: Ramipril or ARB: Losartan
  2. Beta blocker: Bisoprolol or Carvediolol (Stopped if the patient has heart rate less than 50 beats per minute)
  3. IV loop diuretics: Furosemide (first line in diuretics)
  4. Digoxin (Sinus rhythm patients symptomatic after first and second line)
  5. Thiazide diuretics: bendroflumethiazide, Cause a more gentle and slower onset diuresis.
  6. Potassium sparing diuretics: Low dose spironolactone or amiloride
  7. Amiodarone in arrhythmic patients

A stepwise approach

ACE inhibitors or ARB
ADD diuretic
ADD beta-blocker (once euvolaemia)
ADD aldosterone antagonist (spironolactone or amiloride)
then – increase all above to maximum tolerated doses
CONSIDER ARNI (and cease ACE-i) for patients who remain with an EF <40%
CONSIDER ivabridine

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13
Q

DISCUSS LOOP DIURETICS CLINICAL PHARM INFORMATION

A

Loop diuretics

MOA: Loop diuretics act principally on the ascending limb of the loop of Henle, where they inhibit the Na+/K+/2Cl− co-transporter. Loop diuretics have a direct effect on blood vessels, causing dilatation of capacitance veins.

Drug names: Furosemide, bumetanide

Indications:
Acute pulmonary oedema
Chronic heart failure
Symptomatic treatment of fluid overload (Eg. Renal disease or liver failure)

Adverse effects:

  • Dehydration
  • Hypotension
  • Low electrolyte state due to increases excretion of magnesium, calcium and hydrogen ions
  • Hearing loss
  • Tinnitus

Cautions/warnings

  • ▴Hepatic encephalopathy
  • Severe ▴hypokalaemia
  • ▴hyponatraemia
  • Gout

Contraindication

  • ✗hypovolemia
  • ✗dehydration

Interactions:

  • Potential to affect drugs that are excreted by the kidneys
  • ▴Lithium levels are increased due to reduced excretion.
  • Risk of ▴digoxin toxicity may also be increased
  • Loop diuretics can increase the ototoxicity and nephrotoxicity of ▴aminoglycosides.

Monitoring:

  • The medicine will inevitably cause them to need to pass water more often.
  • Improvements in the patient’s symptoms, tachycardia, hypertension and oxygen requirement
  • Monitoring of serum sodium, potassium and renal function
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14
Q

DISCUSS SPIRONOLACTONE CLINICAL PHARM INFORMATION

A

Spironolactone

MOA: Aldosterone antagonists inhibit the effect of aldosterone by competitively binding to the aldosterone receptor. This increases sodium and water excretion and potassium retention

Drug names: Spironolactone, eplerenone

Indications:

  • Ascites and oedema due to liver cirrhosis: spironolactone is the first-line diuretic.
  • Chronic heart failure
  • Primary hyperaldosteronism

Adverse effect:

  • Hyperkalaemia
  • Gynaecomastia
  • Liver impairment and jaundice and are a cause of Stevens–Johnson syndrome

Warnings/cautions
- ▴pregnant or lactating women.

Contraindications:

  • ✗severe renal impairment
  • ✗hyperkalaemia
  • ✗Addison’s disease

Interactions:

  • ▴potassium-elevating drugs
  • ▴ACE inhibitors and ▴ARBs, increases the risk of hyperkalaemia
  • ✗Potassium supplements

Monitoring:

  • Possibility of growth and tenderness of tissue under the nipples and impotence.
  • Reassure them that such effects are benign and reversible.
  • e.g. reduction in ascites, oedema and/or blood pressure. Safety should be monitored by checking renal function and serum potassium concentration.
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15
Q

A 54 year old female has a recent blood test which has come back with LDL cholesterol elevated beyond the normal. You have calculated her score to be QRISK 17%. What is the diagnosis and how will you treat them?

A
  • Hyperlipidemia
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16
Q

DISCUSS STATIN CLINICAL PHARM INFORMATION

A

STATINS

  • MOA: Mechanism of action
  • Reduce serum cholesterol levels inhibiting 3 hydroxy- 3 methyl- glutaryl coenzyme reductase which makes cholesterol. Decreasing the cholesterol in
    the liver reducing LDL cholesterol from the blood.

Drugs: Artovastatin, Simvastatin

  • Indications:
  • Prevention for cardiovascular events
  • Secondary prevention of cardiovascular events
  • Primary hyperlipidaemia

Adverse Effects:

  • Headache
  • Muscle ache
  • Gastro disturbances
  • Myopathy
  • Rhabdomyolysis
  • Raise in liver enzymes

Warnings (Cautions):

  • Hepatic impairment
  • Renal impairment
  • Cytochrome inhibitors (amiodarone, diltiazem)
  • Amlodipine

Contraindications:

  • Pregnant
  • Breastfeeding

Interactions:

  • Metabolism of statins is reduced by ▴cytochrome P450 inhibitors, such as amiodarone, diltiazem & and protease inhibitors
  • ▴Amlodipine all leads to accumulation of statins

Monitoring:

  • you should check a lipid profile before treatment and 3 months after initiating treatment
  • efficacy should be monitored by checking target cholesterol levels are achieved
  • For safety, check liver enzymes (e.g. ALT) at baseline and again at 3 and 12 months
17
Q

Case about blood clot in heart

A
18
Q

DISCUSS DIRECT ANTICOAGULANT CLINICAL PHARM INFORMATION

A

DIRECT ORAL ANTICOAGULANTS

MOA:
- Act on the final common pathway of the coagulation cascade, compromising the
factor X thrombin and fibrin. Apixaban, apixaban and rivaroxaban directly inhibit
the Xa factor preserving prothrombin to thrombin.Dabigatran directly inhibits thrombin. All DOACs inhibit fibrin
formation preventing clot formation.

Indications:

  • Venous thromboembolism
  • Atrial fibrillation

Adverse effects:

  • Bleeding
  • Gi bleeding
  • Anaemia
  • Gi upset
  • Dizziness
  • Elevated liver enzymes

Warnings (Cautions):

  • Hepatic or renal disease due to excretion for CYP enzyme
  • NSAIDS
  • Macrolides
  • Protease inhibitor
  • Fluconazole

Contraindications:

  • Active bleeding
  • Risk factor for haemorrhage
  • Pregnancy
  • Breastfeeding (unknown effects of harm to offspring)
  • Rifampicin
  • Phenytoin

Interactions:

  • other antithrombotic agents (e.g. ▴heparin, ▴antiplatelets and ▴NSAIDs).
  • metabolism of DOACs (e.g. CYP inducers/inhibitors) or their excretion

Monitoring:

  • DOACs do not require routine monitoring
  • main side effect is an increased risk of bleeding. Patients should be provided with an alert card and advised to show this on all healthcare contacts
  • prolonged or serious bleeding, or weakness, tiredness or breathlessness that could be signs of anaemia
  • Reversal agents for DOACs, to use if major bleeding occurs
19
Q

A 67 year old male presents to the ED with central crushing pain to the chest that radiates to the left arm and jaw. He is currently in extreme pain and stated that this pain started 2 hours ago. He has been diagnosed with hypertension and diabetes and takes medicine for that. What is this patient experiencing?

A

Myocardial infarction

20
Q

How do you treat the MI?

A

1.MONA

  • Morphine
  • Oxygen - do not routinely administer oxygen, only less than 94%. COPD patient SpO2 of 88-92%
  • Nitrates -
  • Aspirin (Antiplatelet and clopidogrel)
  • Py212- antagonist inhibitor Ticagrelor
  • Primary percutaneous coronary intervention (PCI) has emerged as the gold-standard treatment for STEMI. Unfractionated heparin is usually given for patients who’re are going to have a PCI. Alternatives include low-molecular weight heparin
  • Thrombolysis should be performed in patients without access to primary PCI
  • An ECG should be performed 90 minutes following thrombolysis to assess whether there has been a greater than 50% resolution in the ST elevation.
21
Q

DISCUSS ASPIRIN CLINICAL PHARM INFORMATION

A

ASPIRIN

MOA:
- Irreversibly inhibits cyclooxygenase (COX) reducing the pro aggregatory
factor from thromboxane to arachidonic acid reducing platelet aggregation.

Indication:

  • ACS: Acute coronary syndrome & acute ischaemic stroke
  • Cardiovascular
  • Cerebrovascular
  • Peripheral arterial disease
  • mild to moderate fever

Adverse effects:

  • Gastrointestinal irritation
  • Peptic ulceration
  • Haemorrhage
  • Bronchospasm
  • Tinnitus

Warnings (Cautions):

  • Peptic ulceration
  • Gout
  • Antiplatelet drugs
  • Anticoagulants
  • Elderly
Contraindications:
- Children under 16 – Reye’s syndrome
- Aspirin hypersensitivity
- Third trimester of pregnancy, prostaglandin inhibition leading to ductus
arteriosus.
- Renal impairment

Interactions:

  • ▴antiplatelet drugs (clopidogrel)
  • ▴anticoagulants (e.g. heparin, warfarin)

Monitoring:
- Enquiry about side effects is the most appropriate form of monitoring.

22
Q

DISCUSS CLOPIDOGREL CLINICAL PHARM INFORMATION

A

CLOPIDOGREL

MOA:
- Prevent platelet aggregation and reduce risk of arterial occlusion by binding
irreversibly to adenosine diphosphate receptors (P2Y 12) on platelet surface

Indications:

  • ACS: Acute coronary syndrome
  • Coronary artery stents
  • Cardiovascular, Cerebrovascular & Peripheral arterial disease

Adverse effects:

  • Bleeding
  • Gastrointestinal upset, dyspepsia, abdominal pain, diarrhoea
  • Thrombocytopenia.

Warnings (Caution):

  • Stopped 7 days before elective surgery
  • Renal impairment

Interactions:

  • Reduced by CYP inhibitors (Omeprazole, ciprofloxacin)
  • Antiplatelet drugs
  • Anticoagulants
  • NSAIDs

Contraindications

  • Active bleeding
  • Renal and hepatic impairment
  • Pregnancy

Monitoring:
- Monitor clinical adverse effects

23
Q

DISCUSS WARFARIN CLINICAL PHARM INFORMATION

A

WARFARIN

MOA: Warfarin inhibits hepatic production of vitamin K-dependent coagulation factors (factors II, VII, IX and X, and proteins C and S). It does this by inhibiting vitamin K epoxide reductase, the enzyme responsible for restoring vitamin K to its reduced form, necessary as a co-factor in the synthesis of these clotting factors.

Indications:

  1. Venous thromboembolisim (Both DVT and Pulmonary embolism)
  2. To prevent arterial embolism in patients with atrial fibrillation (AF) or prosthetic heart valves

Adverse effects:

  • Bleeding
  • Intracerebral haemorrhage after minor head injury
  • Can trigger a spontaneous bleed like epistaxis retroperitoneal haemorrhage.
  • Reversed with phytomenadione (vitamin K1) or dried prothrombin complex.

Contraindications:

  • Immediate risk of haemmorhage
  • ✗pregnancy due to a risk of teratogenicity (cardiac and cranial abnormalities)
  • Avoided later in pregnancy due to the risk of peripartum haemorrhage.

Cautions/warnings:

  • Patients with ▴liver disease
  • Within 48 hours postpartum
  • History of gastrointestinal bleeding.
  • History of peptic ulceration.
  • Recent ischaemic stroke.
  • Uncontrolled hypertension.

Interactions:

  • ▴CYP inducers (e.g. phenytoin, carbamazepine, rifampicin) increase warfarin metabolism and risk of clots
  • ▴CYP inhibitors (e.g. fluconazole, macrolides) decrease warfarin metabolism and increase bleeding risk.
  • Other antibiotics can increase the effect of warfarin by killing gut flora that synthesise vitamin K

Monitoring:
The target INR range varies by indication (e.g. 2.0–3.0 in AF and VTE, higher in metallic prosthetic cardiac valves). INR is measured daily in hospital inpatients and every few days in outpatients commencing warfarin.

24
Q

DISCUSS HEPARIN CLINICAL PHARM INFORMATION

A

MOA:

  • A compound occurring in the liver and other tissues which inhibits blood coagulation.
  • Antithrombin (AT) inactivates clotting factors, particularly factors IIa (thrombin) and Xa, providing a natural break to the clotting process.
  • Heparins and fondaparinux act by enhancing the anticoagulant effect of AT.

Indications:

  • Deep vein thrombosis, venous thromboembolism
  • Acute coronary syndrome

Adverse effects:

  • Haemorrhage
  • Bruising at injections site
  • Hyperkalaemia
  • Heparin-induced thrombocytopenia (HIT)

Contraindications:

  • Active bleeding
  • heparin-induced thrombocytopenia
  • Known hypersensitivity
Caution/warning:
Clotting disorders
- Severe uncontrolled hypertension
- Recent surgery or trauma
- Invasive procedures
- Renal impairment

Monitoring:

  • Where required in selected cases (e.g. renal impairment, pregnancy),plasma antifactor Xa activity is measured
  • In prolonged therapy (>4 days), platelet count and serum potassium concentration should be monitored, as the risk of thrombocytopenia and hyperkalaemia increases