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Cardiology Prometric exam questions

Exam-length papers covering every published domain for Cardiology.

Tell us which regulator you are sitting and we send the bank prepared for that authority's exam.

For DHA · MOHAP · SHA · SCFHS · QCHP · NHRADHA CRD5751Pass mark DHA 65% · SCFHS 65% · QCHP 65%From 3 papers · ~155 Qs each
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What is riding on this exam

~AED 1,030
DHA exam fee, per attempt
Paid again on every re-sit. Other regulators' fees are in the table below.
3
UAE attempts - in total
Shared across DHA, DOH, MOHAP and SHA, not three each. Saudi, Qatar, Oman and Kuwait rules are in the FAQ.
65%
Pass mark, by regulator
DHA 65%, SCFHS 65%, QCHP 65%. Other regulators in the table below.

One failed attempt costs you the fee again, plus months of delay on your licence, your visa and your start date. This bank costs about a third of one exam fee.

Every regulator: format, pass marks and fees for all GCC licensing exams, each from the regulator's own documents.

The Cardiology exam at a glance

DHA (UAE) publishes a Cardiology exam of 150 MCQs in 3 hours with a 65% pass mark; SCFHS (Saudi Arabia) publishes a Cardiology exam of 200 MCQs in 240 minutes with a 65% pass mark; QCHP (Qatar) publishes a Cardiology exam of 150 MCQs in 3 hours with a 65% pass mark. MOHAP, SHA, NHRA do not publish Cardiology-specific figures; their regulator-wide format and pass-mark rules are in the full table. DOH licenses the title without a published written exam (credential review, interview or an unpublished assessment). OMSB, Kuwait MOH publish no exam for this title.

DHA · UAE
Specialist Cardiology (CRD5751)
150 MCQs in 3 hours · pass mark 65% · USD 280 (about AED 1,030) · checked September 2026
SCFHS · Saudi Arabia
Saudi Classification Examination - Cardiology
200 MCQs in 240 minutes · pass mark 65% · checked October 2026
QCHP · Qatar
Specialist Cardiology
150 MCQs in 3 hours · pass mark 65% · checked September 2026

From each regulator's own exam documents; the DHA row is from the DHA CBT Guideline, Sep 2026. Every other regulator is in the full GCC table.

Try two questions from this bank

Original questions from the bank - pick an answer to see the rationale and reference.

Q1Cardiac Pharmacology and Therapeutics

A 34-year-old woman with idiopathic pulmonary arterial hypertension is started on bosentan. Which monitoring test is mandatory before and monthly during therapy?

Choose an answer to see the rationale.

Q2Cardiac Pharmacology and Therapeutics

A 57-year-old man with HFrEF started spironolactone 25 mg daily 8 weeks ago. He now reports painful gynaecomastia but has tolerated the drug well otherwise with normal potassium. What is the most appropriate management?

Choose an answer to see the rationale.

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What's inside

  • ✓3 to 6 full-length papers (~155 Q each)
  • ✓No question repeated between papers
  • ✓Four options, one unambiguous best answer
  • ✓A full rationale on every question
  • ✓A real guideline or textbook reference
  • ✓Every sub-topic in the published blueprint
  • ✓Researched by Neelim's exam research team
  • ✓Prepared for your authority's exam, not a generic set

The Cardiology exam in every GCC country

Cardiology licensing exam in every GCC country
RegulatorExamFormatPass markFee per attempt
Specialist Cardiology (CRD5751)
150 MCQs in 3 hours65%USD 280 (about AED 1,030)
SCFHS
Kingdom of Saudi Arabia
Practise →
Saudi Classification Examination - Cardiology
200 MCQs in 240 minutes65%Not published
QCHP
State of Qatar
Practise →
Specialist Cardiology
150 MCQs in 3 hours65%Not published
DOH
Abu Dhabi, Al Ain and Al Dhafra
Practise →
No written exam published
Oral assessment, 45-60 minutes; no written exam (DOH Licensing Procedure Manual 2024)
Panel / reviewNot publishedNot published
MOHAP
Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah
Practise →
MOHAP licensing exam
Regulator-wide format
Computer-basedNot publishedNot published
SHA
Emirate of Sharjah
Practise →
SHA licensing exam
Regulator-wide format
Set at assessmentNot publishedNot published
NHRA
Kingdom of Bahrain
Practise →
NHRA licensing exam
Regulator-wide format
Prometric CBTNot publishedNot published
OMSB
Sultanate of Oman
Practise →
No exam published for this title
No OMSB exam published for this title; check with OMSB
Not publishedNot publishedNot published
Kuwait MOH
State of Kuwait
Practise →
No exam published for this title
Kuwait MOH publishes no exam for this title; check with the MOH
Not publishedNot publishedNot published

Highlighted rows publish figures for this exact Cardiology exam; the others show the regulator's general rules.

From each regulator's own exam pages; anything a regulator does not publish says so. Assessment mode also depends on your licence title, so confirm your route on your eligibility notice.

Try 15 free Cardiology questions with answersDifferent from the samples on this page - each with a full explanationStart →

What the Cardiology exam covers

The published blueprint for this exam breaks into 13 domains and 232 testable sub-topics. Our bank covers every one of them - here is the full map, so you can see exactly what you are expected to know.

Coronary Artery Disease and Acute Coronary Syndromes~20% (SCFHS published: 20%; DHA lists 'Coronary Artery Disease' as a named coverage area)20 topics
  • Atherosclerosis biology, plaque rupture versus plaque erosion, vulnerable plaque
  • Stable angina: pretest probability, functional versus anatomical testing strategy, CCTA
  • Chronic coronary syndromes: optimal medical therapy versus revascularisation (COURAGE, ISCHEMIA)
  • Universal definition of myocardial infarction and the MI types 1-5
  • High-sensitivity troponin algorithms (0/1h, 0/3h) and rule-out pathways
  • STEMI: ECG criteria, STEMI equivalents, posterior MI, de Winter and Wellens patterns
  • +14 more in the bank
Heart Failure and Cardiomyopathies~14% (SCFHS: Cardiac Failure 15% and Cardiomyopathies 5% in the classification blueprint; 13% combined in the Fellowship final)20 topics
  • Classification by ejection fraction: HFrEF, HFmrEF, HFpEF and their distinct evidence bases
  • Natriuretic peptides: BNP/NT-proBNP thresholds, confounders (obesity, AF, CKD, sacubitril)
  • Four-pillar HFrEF therapy: ARNI/ACEi/ARB, beta-blocker, MRA, SGLT2 inhibitor - sequencing and titration
  • Diuretic strategy, diuretic resistance, sequential nephron blockade and ultrafiltration
  • Ivabradine, hydralazine-nitrate, vericiguat, digoxin and iron replacement (ferric carboxymaltose)
  • HFpEF: diagnosis (H2FPEF, HFA-PEFF), phenotyping and evidence-based therapy
  • +14 more in the bank
Valvular Heart Disease and Infective Endocarditis~11% (SCFHS classification: Valvular Diseases 10%; Fellowship final 17%; DHA lists Valve Disease and Infective Endocarditis separately)18 topics
  • Aortic stenosis: severity grading, low-flow low-gradient and paradoxical low-flow subtypes, dobutamine stress echo
  • AVR timing in asymptomatic severe AS; SAVR versus TAVI decision-making and heart-team process
  • TAVI complications: paravalvular leak, conduction block and pacemaker need, stroke, valve thrombosis
  • Aortic regurgitation: acute versus chronic, LV dimension and EF thresholds for surgery
  • Mitral stenosis: rheumatic aetiology, Wilkins score, percutaneous balloon mitral valvuloplasty
  • Primary (degenerative) mitral regurgitation: severity quantification, repair versus replacement
  • +12 more in the bank
Arrhythmias, Electrophysiology and ECG Interpretation~10% (SCFHS published: Cardiac Arrhythmia 10%; DHA lists Arrhythmias)20 topics
  • Systematic 12-lead ECG interpretation: axis, intervals, chamber enlargement, ischaemia patterns
  • Narrow-complex tachycardia differentiation: AVNRT, AVRT, atrial tachycardia, atrial flutter
  • Wide-complex tachycardia: VT versus SVT with aberrancy (Brugada and Vereckei algorithms)
  • Atrial fibrillation: classification, rate versus rhythm control, early rhythm control (EAST-AFNET 4)
  • AF stroke prevention: CHA2DS2-VASc, HAS-BLED, DOAC selection, dosing and renal adjustment
  • Left atrial appendage occlusion and DOAC-ineligible patients
  • +14 more in the bank
Cardiac Pharmacology and Therapeutics~7% (SCFHS published: 10% classification, 7% Fellowship final; DHA lists Cardiac Pharmacology)19 topics
  • Antiplatelet agents: mechanisms, CYP2C19 and clopidogrel resistance, perioperative interruption
  • Anticoagulants: warfarin pharmacogenetics and INR management, heparins, DOAC pharmacology
  • Reversal agents: vitamin K, PCC, protamine, idarucizumab, andexanet alfa
  • Fibrinolytics: alteplase, tenecteplase, streptokinase; absolute and relative contraindications
  • Beta-blockers: cardioselectivity, vasodilating agents, contraindications and withdrawal
  • ACE inhibitors, ARBs and ARNI: dosing, hyperkalaemia, angioedema, washout before sacubitril
  • +13 more in the bank
Cardiovascular Imaging and Diagnostic Testing~6% (est. - not a separate DHA/SCFHS classification heading; embedded across sections and heavily represented in the Fellowship blueprint via clinical examination and basic sciences)16 topics
  • Transthoracic echocardiography: standard views, chamber quantification, EF methods (Simpson biplane, 3D)
  • Doppler principles, continuity equation, pressure half-time, PISA and regurgitant quantification
  • Diastolic function assessment and estimation of LV filling pressures
  • Strain imaging and global longitudinal strain in cardio-oncology and infiltrative disease
  • Transoesophageal echocardiography: indications, safety, endocarditis, LAA thrombus, intraprocedural guidance
  • Stress echocardiography: exercise and dobutamine protocols, viability and contractile reserve
  • +10 more in the bank
Hypertension, Pulmonary Hypertension and Preventive Cardiology~6% (SCFHS Fellowship: Systemic/Pulmonary hypertension 5%; prevention content is est.)18 topics
  • Blood pressure measurement technique, staging and diagnostic thresholds across guidelines
  • Primary hypertension: initial evaluation, target organ damage and treatment targets (SPRINT)
  • Secondary hypertension: renal artery stenosis, primary aldosteronism, phaeochromocytoma, Cushing, OSA, coarctation
  • Resistant and refractory hypertension: adherence assessment, spironolactone, renal denervation
  • Hypertensive emergency versus urgency: target organ injury and controlled BP reduction
  • Hypertension in pregnancy, chronic kidney disease, diabetes and the elderly
  • +12 more in the bank
Pericardial Disease~3% (SCFHS published: Pericardial 5%; DHA lists Pericardial Disease)15 topics
  • Acute pericarditis: diagnostic criteria, ECG stages, aetiologies including tuberculous and viral
  • NSAID plus colchicine therapy, corticosteroid pitfalls and anakinra/rilonacept for refractory disease
  • Recurrent and incessant pericarditis: risk factors, tapering strategy and duration of therapy
  • Myopericarditis versus perimyocarditis: troponin elevation and exercise restriction
  • Pericardial effusion: aetiology, size grading, echocardiographic assessment
  • Cardiac tamponade: pulsus paradoxus, Beck triad, echocardiographic signs, haemodynamics
  • +9 more in the bank
Adult Congenital Heart Disease~4% (SCFHS published: Congenital Heart Disease 5%)16 topics
  • Atrial septal defect: subtypes, shunt quantification (Qp:Qs), closure indications, device versus surgery
  • Ventricular septal defect: types, natural history, closure criteria and endocarditis risk
  • Patent ductus arteriosus and patent foramen ovale; PFO closure after cryptogenic stroke (RoPE score)
  • Atrioventricular septal defect and the Down syndrome patient
  • Coarctation of the aorta: presentation, hypertension, re-coarctation, stenting and surveillance
  • Bicuspid aortic valve and associated aortopathy
  • +10 more in the bank
Aortic Disease and Peripheral Vascular Disease~5% (SCFHS Fellowship: Aortic disease/pregnancy 6%; classification blueprint lists Peripheral Vascular Disease 5%; DHA lists Peripheral Vascular Disease)16 topics
  • Acute aortic syndromes: dissection, intramural haematoma, penetrating atherosclerotic ulcer
  • Stanford and DeBakey classification; type A surgical versus type B medical/TEVAR management
  • Acute dissection medical therapy: impulse control with beta-blockade before vasodilators
  • Malperfusion syndromes, complicated type B dissection and endovascular repair
  • Thoracic and abdominal aortic aneurysm: growth rates, screening, intervention thresholds
  • Heritable thoracic aortic disease: Marfan, Loeys-Dietz, vascular Ehlers-Danlos, familial TAAD
  • +10 more in the bank
Systemic Disease, Cardio-Obstetrics and Special Populations~5% (SCFHS published: Systemic Diseases 5%; DHA lists Systemic Disease)18 topics
  • Cardiorenal syndrome types 1-5; management of heart failure in advanced CKD and dialysis
  • Cardiac manifestations of thyroid disease: thyrotoxic AF, myxoedema heart, amiodarone thyroid dysfunction
  • Diabetes and diabetic cardiomyopathy; perioperative glycaemic and antiplatelet issues
  • Connective tissue disease and the heart: SLE, Libman-Sacks endocarditis, antiphospholipid syndrome, rheumatoid arthritis
  • Systemic sclerosis: pulmonary hypertension, myocardial fibrosis, scleroderma renal crisis
  • HIV-associated cardiovascular disease and antiretroviral metabolic effects
  • +12 more in the bank
Basic Cardiovascular Sciences and Clinical Examination~4% (SCFHS Fellowship: Basic sciences/pathology/physiology 9%, Clinical examination 7%; not a separate DHA heading - est. weight for the licensure paper)17 topics
  • Cardiac anatomy: chambers, coronary anatomy and dominance, conduction system, valve apparatus
  • Cardiac cycle, pressure-volume loops, preload, afterload and contractility
  • Frank-Starling mechanism, ventricular-arterial coupling and myocardial oxygen supply-demand
  • Cardiac action potential, ion channels and the basis of antiarrhythmic drug action
  • Excitation-contraction coupling, calcium handling and myofilament biology
  • Autonomic and neurohormonal regulation: RAAS, sympathetic system, natriuretic peptides
  • +11 more in the bank
Professionalism, Ethics, Patient Safety and Quality~5% (SCFHS published: Patient Safety 5% and Professionalism and Ethics 5%; DHA lists 'Professionalism and Ethics' as a named coverage area)19 topics
  • Informed consent for cardiac procedures: PCI, TAVI, device implantation, risk disclosure
  • Capacity assessment, surrogate decision-making and advance directives
  • Confidentiality, data protection and the UAE/GCC health data regulations
  • Breaking bad news and shared decision-making in advanced heart failure and futile intervention
  • Do-not-resuscitate orders and device deactivation (ICD, LVAD) at end of life
  • Cultural and religious considerations in GCC practice: family-centred consent, gender preferences, Ramadan fasting
  • +13 more in the bank

12 worked Cardiology practice questions

Original exam-style questions from the bank, spread across the blueprint domains. They are not real or recalled exam questions. Try each one, then open the answer for the rationale and reference. None of them appear in the free mock exam, so reading them will not spoil it.

  1. Question 1 · Coronary Artery Disease and Acute Coronary Syndromes

    A 79-year-old woman weighing 60 kg with an eGFR of 55 mL/min/1.73 m2 receives tenecteplase for an anterior ST-elevation myocardial infarction at a district hospital. Enoxaparin is to be added as adjunctive anticoagulation. What is the correct enoxaparin regimen for her?

    1. A30 mg intravenous bolus followed by 1 mg/kg subcutaneously every 12 hours
    2. BNo intravenous bolus; 0.75 mg/kg subcutaneously every 12 hours
    3. C1.5 mg/kg subcutaneously once daily with no bolus
    4. DFull-dose unfractionated heparin infusion is mandatory instead, as enoxaparin is contraindicated after fibrinolysis
    Show answer and explanation

    Correct answer: B. No intravenous bolus; 0.75 mg/kg subcutaneously every 12 hours

    In patients aged 75 years or older receiving fibrinolysis, the intravenous enoxaparin bolus is omitted and the subcutaneous dose is reduced to 0.75 mg/kg twice daily to limit intracranial haemorrhage, a schedule derived from ExTRACT-TIMI 25. The standard 30 mg bolus plus 1 mg/kg twice daily applies only to patients under 75, once-daily dosing is reserved for severe renal impairment with creatinine clearance below 30 mL/min, and enoxaparin is in fact the preferred adjunct to fibrinolysis rather than being contraindicated.

    Reference: Antman EM et al., ExTRACT-TIMI 25, New England Journal of Medicine (2006); ESC Acute Coronary Syndromes Guidelines (2023)

  2. Question 2 · Valvular Heart Disease and Infective Endocarditis

    A 58-year-old woman with native aortic valve endocarditis develops severe aortic regurgitation with pulmonary oedema on day 3 of appropriate antibiotics. On the same day she suffers a middle cerebral artery ischaemic stroke; she is drowsy but has no coma, and CT of the head shows a moderate infarct with no haemorrhagic transformation. What is the most appropriate management of the valve?

    1. AProceed with urgent valve surgery without delay
    2. BDelay surgery for at least four weeks after the stroke
    3. CDelay surgery for two weeks and repeat brain imaging before deciding
    4. DManage medically and avoid surgery because of the stroke
    Show answer and explanation

    Correct answer: A. Proceed with urgent valve surgery without delay

    After an ischaemic stroke without haemorrhage and without coma, valve surgery indicated for heart failure, uncontrolled infection or high embolic risk should not be postponed, since the risk of neurological deterioration is outweighed by the haemodynamic threat. Delay of at least one month is advised after intracranial haemorrhage, not after an uncomplicated ischaemic infarct. Withholding surgery in acute heart failure from severe regurgitation carries very high mortality, and arbitrary two- or four-week delays would be inappropriate here.

    Reference: 2023 ESC Guidelines for the Management of Endocarditis; 2020 ACC/AHA Valvular Heart Disease Guideline

  3. Question 3 · Cardiac Pharmacology and Therapeutics

    Compared with alteplase, which pharmacological property best explains why tenecteplase can be given as a single weight-based intravenous bolus in ST-elevation myocardial infarction?

    1. AIt is a non-fibrin-specific agent with a broad systemic lytic effect
    2. BIt is derived from streptococci and therefore antigenic
    3. CIt activates plasminogen only after binding to platelet glycoprotein IIb/IIIa
    4. DIt has a longer plasma half-life and greater resistance to plasminogen activator inhibitor-1
    Show answer and explanation

    Correct answer: D. It has a longer plasma half-life and greater resistance to plasminogen activator inhibitor-1

    Tenecteplase is a genetically engineered variant of alteplase with amino acid substitutions that prolong plasma half-life to about 20 minutes, increase fibrin specificity and confer roughly 80-fold greater resistance to plasminogen activator inhibitor-1, permitting single-bolus administration. Streptokinase is the antigenic streptococcal-derived, non-fibrin-specific agent; tenecteplase is more, not less, fibrin specific, and it does not act via glycoprotein IIb/IIIa.

    Reference: ASSENT-2 trial, Lancet 1999; ESC Guidelines for the Management of Acute Coronary Syndromes, 2023

  4. Question 4 · Hypertension, Pulmonary Hypertension and Preventive Cardiology

    Which set of findings correctly summarises the ASPREE trial of low-dose aspirin in community-dwelling adults aged 70 years and over without cardiovascular disease?

    1. AAspirin significantly reduced cardiovascular events and all-cause mortality with no increase in bleeding
    2. BAspirin did not prolong disability-free survival, significantly increased major haemorrhage, and was associated with higher all-cause mortality driven largely by cancer deaths
    3. CAspirin reduced dementia incidence but increased ischaemic stroke
    4. DAspirin halved the incidence of colorectal cancer and reduced major bleeding
    Show answer and explanation

    Correct answer: B. Aspirin did not prolong disability-free survival, significantly increased major haemorrhage, and was associated with higher all-cause mortality driven largely by cancer deaths

    ASPREE found no benefit of aspirin 100 mg daily on its primary endpoint of disability-free survival, a significant excess of major haemorrhage, and an unexpected increase in all-cause mortality driven mainly by cancer-related deaths. Cardiovascular events were not significantly reduced, and no benefit was demonstrated on dementia or physical disability. The trial, together with ASCEND and ARRIVE, underpins the current recommendation against initiating aspirin for primary prevention in older adults.

    Reference: ASPREE Investigators, N Engl J Med 2018;379:1499-1508, 1509-1518 and 1519-1528

  5. Question 5 · Systemic Disease, Cardio-Obstetrics and Special Populations

    A 61-year-old man has taken amiodarone for 18 months for recurrent ventricular tachycardia. He develops weight loss and worsening arrhythmia. TSH is suppressed with elevated free T4 and free T3. There is no goitre, no thyroid antibodies, and colour flow Doppler of the thyroid shows absent parenchymal vascularity. What is the most appropriate treatment?

    1. AHigh-dose carbimazole alone
    2. BUrgent total thyroidectomy
    3. CPotassium perchlorate combined with methimazole
    4. DOral prednisolone
    Show answer and explanation

    Correct answer: D. Oral prednisolone

    Absent thyroidal vascularity on colour Doppler in a previously normal gland indicates type 2 amiodarone-induced thyrotoxicosis, a destructive thyroiditis releasing preformed hormone, which responds to glucocorticoids. Thionamides with or without perchlorate are the treatment for type 1 disease, which occurs in a nodular or autonomous gland with preserved or increased vascularity. Thyroidectomy is reserved for refractory or mixed disease with severe cardiac decompensation.

    Reference: 2018 European Thyroid Association Guidelines for the Management of Amiodarone-Associated Thyroid Dysfunction (Bartalena et al., European Thyroid Journal)

  6. Question 6 · Adult Congenital Heart Disease

    A 30-year-old woman with repaired tetralogy of Fallot and moderate residual pulmonary regurgitation with preserved right ventricular function is 34 weeks pregnant. She is asymptomatic and there are no obstetric complications. What is the most appropriate delivery plan?

    1. AElective caesarean section at 37 weeks to avoid haemodynamic stress
    2. BPlanned vaginal delivery with regional analgesia and an assisted second stage if needed
    3. CElective caesarean section under general anaesthesia at 39 weeks
    4. DInduction at 34 weeks with strict avoidance of any analgesia
    Show answer and explanation

    Correct answer: B. Planned vaginal delivery with regional analgesia and an assisted second stage if needed

    In most women with congenital heart disease, including well-repaired tetralogy of Fallot with preserved ventricular function, vaginal delivery is preferred because it is associated with less blood loss, lower infection and thromboembolic risk, and fewer haemodynamic swings than caesarean section; early regional analgesia blunts the sympathetic surge of labour and an assisted second stage limits prolonged Valsalva. Caesarean section is reserved for obstetric indications or specific cardiac situations such as aortic dilatation, severe obstructive lesions, decompensated heart failure or a patient anticoagulated with a vitamin K antagonist in labour. Preterm induction is not indicated in an asymptomatic, stable patient.

    Reference: 2018 ESC Guidelines for the Management of Cardiovascular Diseases During Pregnancy, European Heart Journal 2018

  7. Question 7 · Pericardial Disease

    A 39-year-old HIV-positive man not yet established on antiretroviral therapy has confirmed tuberculous pericarditis with a large effusion. Standard four-drug antituberculous therapy is started. Regarding adjunctive corticosteroids, which statement is correct?

    1. AAdjunctive prednisolone reliably reduces all-cause mortality in every patient with tuberculous pericarditis
    2. BCorticosteroids are mandatory in HIV-positive patients to prevent immune reconstitution disease
    3. CIn the IMPI trial adjunctive prednisolone did not reduce the primary composite outcome, and among HIV-positive patients it was associated with an increased incidence of HIV-associated malignancy, so it should be avoided in this group
    4. DCorticosteroids are contraindicated in HIV-negative patients with tuberculous pericarditis
    Show answer and explanation

    Correct answer: C. In the IMPI trial adjunctive prednisolone did not reduce the primary composite outcome, and among HIV-positive patients it was associated with an increased incidence of HIV-associated malignancy, so it should be avoided in this group

    The IMPI randomised trial found no reduction in the composite of death, tamponade requiring pericardiocentesis or constriction with adjunctive prednisolone, although it did reduce constrictive pericarditis and hospitalisation; in HIV-positive participants it significantly increased HIV-associated malignancy, chiefly Kaposi sarcoma. Corticosteroids may therefore be considered selectively in HIV-negative patients (particularly with large effusions or marked inflammation) but should be avoided in HIV-positive patients not on antiretroviral therapy, making options A, B and D incorrect.

    Reference: Mayosi et al., IMPI trial, New England Journal of Medicine 2014; ESC Pericardial Disease Guidelines 2015

  8. Question 8 · Heart Failure and Cardiomyopathies

    A 54-year-old woman with obstructive hypertrophic cardiomyopathy (resting LVOT gradient 68 mmHg, EF 68%) remains NYHA class III on maximally tolerated beta-blockade. She is started on mavacamten. Which monitoring requirement is most important during therapy?

    1. ASerial serum potassium because of a high risk of hyperkalaemia
    2. BSerial echocardiographic assessment of ejection fraction, with dose interruption if EF falls below 50%
    3. CWeekly liver function tests for the first 3 months
    4. DRegular ophthalmological review for retinal deposits
    Show answer and explanation

    Correct answer: B. Serial echocardiographic assessment of ejection fraction, with dose interruption if EF falls below 50%

    Mavacamten is a selective cardiac myosin inhibitor that reduces actin-myosin cross-bridge formation and hypercontractility; its principal hazard is excessive negative inotropy causing systolic dysfunction, so protocolised echocardiography with dose interruption if EF falls below 50% is mandated, along with attention to CYP2C19/CYP3A4 interactions and avoidance in pregnancy. Hyperkalaemia, hepatotoxicity and retinal deposition are not recognised class effects of mavacamten.

    Reference: EXPLORER-HCM (Lancet 2020); VALOR-HCM (JACC 2022); 2024 AHA/ACC Guideline for the Management of Hypertrophic Cardiomyopathy

  9. Question 9 · Arrhythmias, Electrophysiology and ECG Interpretation

    A 76-year-old man has had three episodes of unexplained syncope without prodrome. His ECG shows right bundle branch block with left anterior fascicular block and a PR interval of 190 ms. Ambulatory monitoring and echocardiography are unremarkable. At electrophysiology study his baseline HV interval is 85 ms. What is the most appropriate management?

    1. AReassure him; the syncope is most likely vasovagal
    2. BImplant a permanent pacemaker
    3. CImplant a loop recorder and review in 12 months
    4. DStart fludrocortisone and increase salt intake
    Show answer and explanation

    Correct answer: B. Implant a permanent pacemaker

    In a patient with bifascicular block and unexplained syncope, a baseline HV interval of 70 ms or more at electrophysiology study demonstrates infra-Hisian conduction disease and is a class I indication for permanent pacing, since intermittent complete infranodal block is the likely mechanism. Syncope without prodrome in an elderly patient with conduction disease is not typical of reflex syncope, so reassurance and fludrocortisone are inappropriate. A loop recorder is reserved for unexplained syncope when the electrophysiology study is negative; here the study has already provided the diagnosis.

    Reference: 2021 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy (European Heart Journal, 2021); 2018 ESC Guidelines for the diagnosis and management of syncope

  10. Question 10 · Cardiovascular Imaging and Diagnostic Testing

    Simultaneous high-fidelity left and right ventricular pressure recordings during quiet respiration in a patient with unexplained oedema and raised jugular venous pressure show right ventricular systolic pressure rising while left ventricular systolic pressure falls during inspiration, with the opposite pattern during expiration. What does this discordance indicate?

    1. ARestrictive cardiomyopathy
    2. BSevere pulmonary arterial hypertension
    3. CConstrictive pericarditis
    4. DChronic obstructive pulmonary disease alone
    Show answer and explanation

    Correct answer: C. Constrictive pericarditis

    Respiratory discordance of right and left ventricular systolic pressures reflects enhanced ventricular interdependence within a fixed pericardial volume and is the most accurate invasive discriminator of constrictive pericarditis, with a systolic area index above 1.1 offering high sensitivity and specificity. In restrictive cardiomyopathy the two ventricular pressures rise and fall concordantly with respiration, and the left ventricular end-diastolic pressure typically exceeds the right by more than 5 mmHg. Pulmonary hypertension and airflow obstruction do not produce this pattern of interdependence.

    Reference: Talreja DR et al., Constrictive pericarditis in the modern era: novel criteria for diagnosis in the cardiac catheterization laboratory, J Am Coll Cardiol 2008; 2015 ESC Pericardial Disease Guidelines

  11. Question 11 · Aortic Disease and Peripheral Vascular Disease

    A 73-year-old man with diffuse atherosclerosis has a 75% ostial right renal artery stenosis with a normal-sized left kidney and stable creatinine of 128 micromol/L. His blood pressure is 138/78 mmHg on two agents and he has no episodes of flash pulmonary oedema. What does the best available randomised evidence support?

    1. ARenal artery stenting reduces cardiovascular and renal events compared with medical therapy in this situation
    2. BBilateral nephrectomy with dialysis to control renin-driven hypertension
    3. CACE inhibitors are absolutely contraindicated in all unilateral renal artery stenosis
    4. DOptimal medical therapy alone, as stenting has not shown incremental benefit in this setting
    Show answer and explanation

    Correct answer: D. Optimal medical therapy alone, as stenting has not shown incremental benefit in this setting

    The ASTRAL and CORAL randomised trials showed no significant benefit of renal artery revascularisation added to optimal medical therapy for atherosclerotic renal artery stenosis in terms of blood pressure control, renal function or cardiovascular events, while procedural complications occurred. Revascularisation is therefore reserved for selected patients with recurrent flash pulmonary oedema, rapidly deteriorating renal function, or truly refractory hypertension. Nephrectomy is not a management option here, and ACE inhibitors are appropriate in unilateral stenosis with monitoring of creatinine and potassium; they are avoided principally in bilateral stenosis or stenosis in a solitary functioning kidney.

    Reference: ASTRAL trial (NEJM 2009); CORAL trial (Cooper et al., NEJM 2014); 2017 ESC/ESVS Peripheral Arterial Diseases Guidelines

  12. Question 12 · Systemic Disease, Cardio-Obstetrics and Special Populations

    A 46-year-old man presents with heart failure. Echocardiography shows a dilated left ventricle with an ejection fraction of 32%. He also has newly diagnosed diabetes, painful metacarpophalangeal joints and slate-grey skin pigmentation. Ferritin is 1900 microgram/L and transferrin saturation is 78%. He has never been transfused. What is the most appropriate next step?

    1. AStart deferasirox as first-line therapy for iron removal
    2. BPerform liver biopsy, which remains essential for diagnosis
    3. CPerform HFE genotyping and begin therapeutic venesection alongside guideline-directed heart failure therapy
    4. DAttribute the ferritin elevation to heart failure as an acute phase response and take no specific action
    Show answer and explanation

    Correct answer: C. Perform HFE genotyping and begin therapeutic venesection alongside guideline-directed heart failure therapy

    A transferrin saturation above 45% with a high ferritin in a non-transfused patient with the triad of cardiomyopathy, diabetes and arthropathy points to hereditary haemochromatosis, confirmed by HFE genotyping, and venesection is the first-line iron removal therapy in a patient who is not anaemic. Chelation is reserved for those who cannot tolerate venesection or who are anaemic, typically secondary iron overload. Liver biopsy and MRI now have a limited confirmatory role once genotyping is available, and a raised transferrin saturation is not explained by an acute phase response, which typically raises ferritin while saturation stays normal or low.

    Reference: EASL Clinical Practice Guidelines on haemochromatosis, Journal of Hepatology 2022; 2023 ESC Guidelines for the management of cardiomyopathies

Cardiology reference books and guidelines

Every question in this bank names the textbook or guideline its answer rests on. These are the sources our Cardiology questions cite most often - the reading list to revise from alongside the bank.

Textbooks

6
  1. 1

    Braunwald's Heart Disease

    12th edition2022
  2. 2

    Josephson's Clinical Cardiac Electrophysiology

    6th edition2021
  3. 3

    Grossman & Baim's Cardiac Catheterization, Angiography and Intervention

    9th edition2021
  4. 4

    Chou's Electrocardiography in Clinical Practice

    6th edition2008
  5. 5

    Guyton and Hall Textbook of Medical Physiology

    14th edition2021
  6. 6

    Goodman & Gilman's The Pharmacological Basis of Therapeutics

    14th edition2023

Guidelines and standards

10
  1. 1

    ESC Guidelines for the Management of Acute Coronary Syndromes

    2023
  2. 2

    ESC Heart Failure Guidelines

    2021
  3. 3

    ESC Guidelines for the Management of Cardiomyopathies

    2023
  4. 4

    ACC/AHA Aortic Disease Guideline

    2022
  5. 5

    ESC Guidelines on pericardial diseases

    2015
  6. 6

    ESC Guidelines for the Diagnosis and Management of Atrial Fibrillation

    2020
  7. 7

    ESC/ESVS Peripheral Arterial Diseases Guidelines

    2017
  8. 8

    AHA/ACC Guideline for the Management of Hypertrophic Cardiomyopathy

    2024
  9. 9

    ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease

    2020
  10. 10

    ESC Pericardial Disease Guidelines

    2015

Where your regulator publishes a reading list, use the editions it names. Exam questions are not taken from any one book.

Last reviewed September 2026

About these questions: every question is original, researched by Neelim's exam research team, written to the published blueprint, with a rationale and a reference. No recalled or leaked exam content is used. How we write our questions.

Frequently asked questions

Are these real Cardiology exam questions?
No. Every item is original, researched by Neelim's exam research team against the exam blueprint published by the health authorities. Real, recalled or leaked exam content breaches the testing bodies' rules and can lead to a permanent exam ban - we do not sell it, and neither should anyone else.
How many questions are in the Cardiology bank?
Every bank starts at 3 full-length papers of roughly 155 questions each (the DHA exam itself is 150 questions), and you can add papers up to 6, including a bonus paper of our hardest questions. The papers do not overlap, so every question is new, and together they cover every sub-topic in the published blueprint.
What is the pass mark for the DHA Cardiology exam?
65%. DHA publishes the pass score for each exam, and 65% is the figure for Specialist Cardiology (CRD5751) in the DHA CBT Guideline, Sep 2026. The result is posted to your Sheryan account as Pass or Fail only - your score is not shared. Elsewhere in the GCC: SCFHS 65%, QCHP 65%.
How many questions are in the DHA Cardiology exam, and how long is it?
150 multiple-choice questions in 3 hours, and the time includes registration and the introduction. It is a computer-based test delivered by Prometric at test centres in the UAE and abroad.
How much does the DHA Cardiology exam cost?
USD 280 (about AED 1,030) per attempt, paid again for every re-sit. DHA also charges a flat AED 200 credentialing fee through Sheryan.
How many attempts do I get?
In the UAE, three in total across DHA, DOH, MOHAP and SHA, not three each, under clause 1.5.4 of the Unified PQR (April 2025). Clause 1.5.5 allows one further attempt with a different authority, except on the Consultant route. Elsewhere in the GCC: SCFHS up to 4 a year, QCHP 5 per scope, OMSB no set maximum, Kuwait MOH 3, 6 weeks apart.
Which GCC regulators license the Cardiology title?
DHA sets a written exam (Specialist Cardiology (CRD5751)); SCFHS sets a written exam (Saudi Classification Examination - Cardiology); QCHP sets a written exam (Specialist Cardiology). DOH licenses the title without a published written exam (credential review, interview or an unpublished assessment). OMSB, Kuwait MOH publish no exam for this title. This bank prepares you for the written exams, and its content is the core knowledge any interview or assessment for the title draws on.
How do I receive it?
As PDF files. Card checkout is being set up, so for now you request it from this page and we send it to you directly, usually the same day.

Still unsure whether you even need this exam?

Your route depends on your profession, your licence title and the authority. We have guided over 1,000 professionals through GCC licensing - tell us your situation and we will confirm exactly what you need to sit.