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Cardio Vivasischaemic-heart-disease

Cardio Vivas · ischaemic-heart-disease

Chronic coronary syndrome medical therapy — viva

Structured viva on chronic coronary syndrome: aims of therapy, first-line and add-on antianginal drugs with their pitfalls, antithrombotic, lipid, RAAS, SGLT2 inhibitor, GLP-1 receptor agonist and colchicine rows, lifestyle, rehabilitation and vaccination, the ISCHEMIA trial and revascularisation for symptoms, and follow-up.

structured clinical oral4 min readVerification in progress

Target exams

  • EECC
  • ABIM Cardiovascular Disease Certification
On this page
Study tools

Target exams

  • EECC
  • ABIM Cardiovascular Disease Certification
Prompt
A patient with stable angina and obstructive coronary disease seen in clinic

Write your answer

Saved on this device. No marking — you are the marker.

Stem

Practice viva. The examiner describes a patient with stable angina and obstructive coronary disease seen in clinic, and works through antianginal drug choice, event prevention, lifestyle and vaccination, the place of revascularisation, and follow-up.

Branch A — Aims and first drugs

Examiner: What are you trying to achieve with medical therapy, and what do you start?[1]

Strong answer:

  • ESC 2024 says clinicians should clearly explain that certain treatments can alleviate symptoms, while others can reduce the likelihood of ischaemic events.[1]
  • Short-acting nitrates are recommended for immediate relief of angina (ESC 2024, Class I, Level B); AHA/ACC 2023 recommends sublingual nitroglycerin or nitroglycerin spray for immediate short-term relief (COR 1, LOE B-NR).[1][2]
  • ESC 2024 recommends initial treatment with beta-blockers and/or CCBs to control heart rate and symptoms for most patients (Class I, Level B), tailored to haemodynamic profile, comorbidities, interacting drugs and preferences.[1]
  • AHA/ACC 2023 recommends a beta blocker, CCB or long-acting nitrate for relief of angina (COR 1, LOE B-R).[2]

Follow-up: Which antianginal drug improves outcomes?[1]

  • ESC 2024 says there is no evidence that any antianginal medication may improve long-term cardiovascular outcomes, except beta-blockers if administered within 1 year after an acute MI.[1]

Branch B — Escalation and pitfalls

Examiner: Angina persists on a beta-blocker. What next, and what must you avoid?[1]

Strong answer:

  • ESC 2024: if angina is not controlled by a beta-blocker alone, a beta-blocker plus a dihydropyridine CCB should be considered, unless contraindicated (Class IIa, Level B).[1]
  • ESC 2024: long-acting nitrates or ranolazine should be considered as add-on therapy (Class IIa, Level B), with a nitrate-free or low-nitrate interval to reduce tolerance (Class IIa, Level B); nicorandil or trimetazidine may be considered (Class IIb, Level B).[1]
  • AHA/ACC 2023: add a second antianginal agent from a different class (COR 1, LOE B-R); ranolazine is recommended if symptoms persist despite beta blockers, CCB or long-acting nitrates (COR 1, LOE B-R).[2]
  • Avoid ivabradine as add-on with LVEF >40% and no clinical heart failure (ESC 2024, Class III), ivabradine with non-DHP-CCBs or strong CYP3A4 inhibitors (Class III), and nitrates with phosphodiesterase inhibitors or in hypertrophic cardiomyopathy (Class III).[1]

Follow-up: Why be careful adding verapamil to a beta blocker?[2]

  • AHA/ACC 2023 says non-dihydropyridine CCBs should be used with caution in patients on beta blockers because of the potential for synergistic induction or exacerbation of bradycardia and LV dysfunction.[2]
  • It adds that verapamil and diltiazem should not be used in CCD with significant LV dysfunction.[2]

Branch C — Event prevention

Examiner: Which drugs prevent events in this patient?[1]

Strong answer:

  • ESC 2024, with no clear indication for oral anticoagulation: with significant obstructive CAD and no prior MI or revascularisation, aspirin 75–100 mg daily is recommended lifelong (Class I, Level B); after prior MI or remote PCI, aspirin 75–100 mg daily lifelong after an initial period of DAPT (Class I, Level A) or clopidogrel 75 mg daily as a safe and effective alternative to aspirin monotherapy (Class I, Level A).[1]
  • ESC 2024: an LDL-C goal of <1.4 mmol/L with ≥50% reduction (Class I, Level A), a high-intensity statin to the highest tolerated dose (Class I, Level A), then ezetimibe (Class I, Level B), then a PCSK9 inhibitor (Class I, Level A).[1]
  • ESC 2024: ACE inhibitors (or ARBs) with specific comorbidities such as hypertension, diabetes or heart failure (Class I, Level A); SGLT2 inhibitors or GLP-1 receptor agonists with proven benefit in type 2 diabetes (Class I, Level A); colchicine 0.5 mg daily should be considered with atherosclerotic CAD (Class IIa, Level A).[1]

Follow-up: Where do ESC and AHA/ACC differ on colchicine?[1][2]

  • ESC 2024 says low-dose colchicine (0.5 mg daily) should be considered in CCS with atherosclerotic CAD (Class IIa, Level A); AHA/ACC 2023 says colchicine for secondary prevention may be considered (COR 2b, LOE B-R); NHFA/CSANZ 2025 gives a weak recommendation after ACS.[1][2][6]

Branch D — Lifestyle and vaccination

Examiner: What lifestyle advice and vaccines do you give?[1]

Strong answer:

  • ESC 2024: aerobic activity of at least 150–300 min per week of moderate intensity or 75–150 min per week of vigorous intensity, with less sedentary time (Class I, Level B).[1]
  • ESC 2026 cardiac rehabilitation guideline: cardiac rehabilitation is recommended after ACS or with CCS, with or without PCI or CABG, to reduce cardiovascular mortality and MI (Class I, Level A).[3]
  • AHA/ACC 2023: assess tobacco use at every visit and advise patients who regularly smoke to quit at every visit; for them, behavioural interventions plus pharmacotherapy are recommended (each COR 1, LOE A).[2]
  • AHA/ACC 2023: annual influenza vaccination (COR 1, LOE A), COVID-19 vaccination per public health guidelines (COR 1, LOE C-EO) and pneumococcal vaccine (COR 2a, LOE B-NR).[2]

Branch E — Revascularisation and follow-up

Examiner: Does PCI improve prognosis in stable disease, and how do you follow him up?[7]

Strong answer:

  • ISCHEMIA randomised 5179 patients with moderate or severe ischaemia; over a median of 3.2 years there was no evidence that an initial invasive strategy reduced ischaemic cardiovascular events or death from any cause.[7]
  • ESC 2024 reports lower spontaneous MI and better angina-related health status with the invasive strategy; ISCHEMIA-EXTEND, up to 7 years, showed a significant 2.2% absolute decrease in cardiovascular mortality favouring it, offset by a significant 1.2% absolute increase in non-cardiac mortality, with no significant difference in all-cause mortality.[1]
  • ESC 2024 recommends revascularisation of functionally significant obstructive CAD for persistent angina despite guideline-directed medical treatment (Class I, Level A).[1]
  • For follow-up, ESC 2024 recommends periodic visits (e.g. annual) regardless of symptoms (Class I, Level C); AHA/ACC 2023 says routine periodic CT coronary angiography or stress testing is not recommended to guide therapy without a change in clinical or functional status on optimised GDMT (COR 3: No benefit).[1][2]
References5ShowHide
  1. [1]Vrints C, et al. 2024 ESC Guidelines for the management of chronic coronary syndromes. Eur Heart J, 2024.PMID 39210710
  2. [2]Virani SS, et al. 2023 AHA/ACC/ACCP/ASPC/NLA/PCNA Guideline for the Management of Patients With Chronic Coronary Disease: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines. J Am Coll Cardiol, 2023.PMID 37480922
  3. [3]Bäck M, et al. 2026 ESC Guidelines on cardiac rehabilitation. Eur Heart J, 2026.PMID 42661418
  4. [6]Brieger DB, et al. National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: Australian Clinical Guideline for Diagnosing and Managing Acute Coronary Syndromes 2025. Med J Aust, 2026.PMID 41693087
  5. [7]Maron DJ, et al. Initial Invasive or Conservative Strategy for Stable Coronary Disease. N Engl J Med, 2020.PMID 32227755
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