Free Cardiology mock test
25 original exam-style questions from our Cardiology bank, timed at the exam’s own pace, scored against the 65% DHA pass mark. They span 11 of the 13 blueprint domains, so you will see exactly where you are weakest - free, no sign-up.
Sit 25 original exam-style questions at real exam pace
These are 25 original questions taken from our Cardiology bank, spread across 11 of the 13 domains of the published blueprint. You get 72 seconds per question, which is exactly the pace of the real CRD5751 exam (30 minutes for 25). At the end you will see which domains you are weakest in, and the full worked reasoning for every question.
- 25
- questions
- 30:00
- time limit
- 65%
- DHA pass mark
A short diagnostic cannot predict whether you will pass - only the real exam does that. It will show you, honestly, where you currently stand.
Quick answer
The Cardiology exam at a glance
The Cardiology licensing exam is a computer-based, multiple-choice test, and each GCC regulator sets its own. DHA, SCFHS and QCHP publish exact figures, listed below. DOH licenses the title without a published written exam. This free mock gives you 25 original exam-style questions at 72 seconds each, scored against the 65% DHA pass mark, then shows your weakest domains.
Published exam figures
- DHA
Specialist Cardiology (CRD5751)
UAE150 MCQs3 hours65%
pass mark
- SCFHS
Saudi Classification Examination - Cardiology
Saudi Arabia200 MCQs240 minutes65%
pass mark
- QCHP
Specialist Cardiology
Qatar150 MCQs3 hours65%
pass mark
- Attempts in the UAE
- 3 in total across DHA, DOH, MOHAP and SHA
- This free mock
- 25 questions · 30 minutes · 11 of 13 domains
- Full bank
- 465+ questions · 3 to 6 papers · AED 319
- Regulators
- DHA, SCFHS, QCHP, DOH, MOHAP, SHA, NHRA, OMSB and Kuwait MOH
How this free Cardiology mock works
- 25
- original questions
- 30 min
- time limit
- 72s
- per question
- 11 of 13
- blueprint domains
- You get 72 seconds per question, the pace of a 150-question paper in 3 hours. The timer runs in your browser and ends the sitting when it reaches zero.
- Your score is set against the 65% DHA pass mark, the published figure for this exam. No other number is invented: there is no percentile and no pass probability.
- At the end you see your score, your pace per question, every domain ranked weakest first, and the worked answer and source for all 25 questions.
- You can mark each answer “sure” or “not sure”. Wrong answers you were sure about are shown first, because they are the ones you would not stop to check in the real exam.
- Your last result is saved in your own browser only, so you can come back and compare. Nothing is sent to us.
What the real Cardiology licensing exam looks like
The Cardiology exam is a computer-based multiple-choice paper, published by 3 regulators: DHA CRD5751 (pass mark 65%), SCFHS (pass mark 65%), QCHP (pass mark 65%). DOH license the title without a published written exam. Every regulator's format, pass mark and fee is in the table below; confirm yours before booking.
Pass marks at a glance: exam codes and pass marks by regulator for every written exam in one sourced table.
Before you can book the exam at all you need Dataflow primary source verification of your degree, licence and experience, which typically runs several weeks. Candidates often underestimate this and end up sitting the exam sooner after study than they planned. Check where you stand with our free eligibility checker or confirm whether your title even requires an exam using the Prometric exam checker.
You get three attempts in total across all UAE authorities, not three each, under the Unified Professional Qualification Requirements. At roughly AED 1,030 per attempt, plus the licensing delay each failure adds to your visa and start date, the cost of going in underprepared is not really the exam fee.
| Regulator | Exam | Format | Pass mark | Fee per attempt |
|---|---|---|---|---|
Specialist Cardiology (CRD5751) | 150 MCQs in 3 hours | 65% | USD 280 (about AED 1,030) | |
Saudi Classification Examination - Cardiology | 200 MCQs in 240 minutes | 65% | Not published | |
Specialist Cardiology | 150 MCQs in 3 hours | 65% | Not published | |
No written exam published Oral assessment, 45-60 minutes; no written exam (DOH Licensing Procedure Manual 2024) | Panel / review | Not published | Not published | |
MOHAP licensing exam Regulator-wide format | Computer-based | Not published | Not published | |
SHA licensing exam Regulator-wide format | Set at assessment | Not published | Not published | |
NHRA licensing exam Regulator-wide format | Prometric CBT | Not published | Not published | |
No exam published for this title No OMSB exam published for this title; check with OMSB | Not published | Not published | Not published | |
No exam published for this title Kuwait MOH publishes no exam for this title; check with the MOH | Not published | Not published | Not published |
Highlighted rows publish figures for this exact Cardiology exam; the others show the regulator's general rules.
What is on the Cardiology exam: the full blueprint
The published blueprint splits into 13 domains and 232 testable sub-topics. For each one you can see its weight, how many questions this mock asks on it, and about how many the full bank holds.
- Coronary Artery Disease and Acute Coronary Syndromes~20%
20 sub-topics · 3 in this mock · about 93 in the full bank
SCFHS published: 20%; DHA lists 'Coronary Artery Disease' as a named coverage area
- Heart Failure and Cardiomyopathies~14%
20 sub-topics · 1 in this mock · about 65 in the full bank
SCFHS: Cardiac Failure 15% and Cardiomyopathies 5% in the classification blueprint; 13% combined in the Fellowship final
- Valvular Heart Disease and Infective Endocarditis~11%
18 sub-topics · not in this mock · about 51 in the full bank
SCFHS classification: Valvular Diseases 10%; Fellowship final 17%; DHA lists Valve Disease and Infective Endocarditis separately
- Arrhythmias, Electrophysiology and ECG Interpretation~10%
20 sub-topics · 2 in this mock · about 46 in the full bank
SCFHS published: Cardiac Arrhythmia 10%; DHA lists Arrhythmias
- Cardiac Pharmacology and Therapeutics~7%
19 sub-topics · 4 in this mock · about 32 in the full bank
SCFHS published: 10% classification, 7% Fellowship final; DHA lists Cardiac Pharmacology
- Cardiovascular Imaging and Diagnostic Testing~6%
16 sub-topics · 4 in this mock · about 28 in the full bank
est. - not a separate DHA/SCFHS classification heading; embedded across sections and heavily represented in the Fellowship blueprint via clinical examination and basic sciences
- Hypertension, Pulmonary Hypertension and Preventive Cardiology~6%
18 sub-topics · 1 in this mock · about 28 in the full bank
SCFHS Fellowship: Systemic/Pulmonary hypertension 5%; prevention content is est.
- Pericardial Disease~3%
15 sub-topics · 1 in this mock · about 14 in the full bank
SCFHS published: Pericardial 5%; DHA lists Pericardial Disease
- Adult Congenital Heart Disease~4%
16 sub-topics · not in this mock · about 19 in the full bank
SCFHS published: Congenital Heart Disease 5%
- Aortic Disease and Peripheral Vascular Disease~5%
16 sub-topics · 3 in this mock · about 23 in the full bank
SCFHS Fellowship: Aortic disease/pregnancy 6%; classification blueprint lists Peripheral Vascular Disease 5%; DHA lists Peripheral Vascular Disease
- Systemic Disease, Cardio-Obstetrics and Special Populations~5%
18 sub-topics · 1 in this mock · about 23 in the full bank
SCFHS published: Systemic Diseases 5%; DHA lists Systemic Disease
- Basic Cardiovascular Sciences and Clinical Examination~4%
17 sub-topics · 4 in this mock · about 19 in the full bank
SCFHS Fellowship: Basic sciences/pathology/physiology 9%, Clinical examination 7%; not a separate DHA heading - est. weight for the licensure paper
- Professionalism, Ethics, Patient Safety and Quality~5%
19 sub-topics · 1 in this mock · about 23 in the full bank
SCFHS published: Patient Safety 5% and Professionalism and Ethics 5%; DHA lists 'Professionalism and Ethics' as a named coverage area
Bank counts are estimates from the published weights the bank is written to, rounded.
This mock samples 11 of 13 domains. The full bank covers all 13 across 465+ questions, including the 2 domains this mock does not reach.
See the full bank - AED 319How to use your mock score
These bands are set against the 65% DHA pass mark and match the verdict on your result screen. On 25 questions, a score near the pass mark has a 95% margin of error of about ±19 points, so treat the band as a direction, not a forecast.
Below the line
On this sample you would likely fall short of the 65% pass mark today. Do not book yet. Start with your two weakest domains from the result, then sit full-length papers until you clear the line with room to spare.
Close to the line
A few questions decide it. On a 155-question paper, every 1% is one or two questions, so drill your weakest domains and build a margin on timed papers before you book.
On track
Clear of the pass mark on this sample. 25 questions is a small sample, so confirm it over full-length timed papers before you book: stamina and pacing fail candidates who know the material.
Getting an honest score
- 1Sit it cold, once. Do not look anything up. A diagnostic you help yourself through tells you nothing. The number you get is only useful if it is honest.
- 2Read every rationale, especially the ones you got right. Getting a question right by elimination is not the same as knowing it. The worked reasoning is free, whether or not you buy anything.
- 3Work on your weakest domain first. The breakdown orders your domains worst first for exactly this reason. Studying what you are already good at feels productive and moves nothing.
- 4Re-sit under full exam conditions later. The real paper is much longer than 25 questions and stamina matters. The full bank's 3 to 6 papers are written for exactly this.
A worked Cardiology exam question
Every question in the mock and in the paid bank is written to this standard: a clinical stem, four plausible options and the reasoning for the answer, with its source.
Cardiac Pharmacology and Therapeutics
A 29-year-old woman with chronic hypertension is planning pregnancy. Which of her current medications must be stopped because of fetal toxicity?
- ALabetalol
- BNifedipine modified release
- CLisinoprilCorrect
- DMethyldopa
Why: ACE inhibitors and angiotensin receptor blockers are fetotoxic, causing oligohydramnios, renal dysgenesis, skull hypoplasia and neonatal renal failure, and must be discontinued before or as soon as pregnancy is confirmed. Labetalol, nifedipine and methyldopa are the recommended antihypertensives in pregnancy.
Source: 2018 ESC Guidelines for the Management of Cardiovascular Diseases during Pregnancy
Cardiology sample questions with answers
10 more original exam-style Cardiology questions, worked in full. They are not real or recalled exam questions, and none of them is in the mock above or on the bank page, so sit the mock first if you have not.
Question 1 · Heart Failure and Cardiomyopathies
A 63-year-old man with previous mediastinal radiotherapy has ascites, raised JVP with a prominent y descent and Kussmaul sign. Echocardiography shows normal wall thickness, a septal bounce, respirophasic septal shift, medial e' of 12 cm/s exceeding lateral e' (annulus reversus), and expiratory diastolic flow reversal in the hepatic veins. Which diagnosis do these findings support?
- AConstrictive pericarditis
- BRestrictive cardiomyopathy due to amyloidosis
- CSevere tricuspid regurgitation
- DRight ventricular infarction
Show answer and explanation
Correct answer: A. Constrictive pericarditis
Septal bounce, respirophasic septal shift, annulus reversus (medial e' greater than lateral because the lateral annulus is tethered by the rigid pericardium), preserved or exaggerated medial e' and expiratory hepatic vein diastolic flow reversal are the Mayo echocardiographic criteria for constriction, and prior mediastinal radiotherapy is a classic cause. Restrictive cardiomyopathy typically shows increased wall thickness, biatrial enlargement and reduced tissue Doppler velocities at both annuli without respiratory interdependence. The findings are not those of isolated tricuspid regurgitation or right ventricular infarction.
Reference: Welch et al., Echocardiographic diagnosis of constrictive pericarditis (Circ Cardiovasc Imaging 2014); 2015 ESC Guidelines on pericardial diseases
Question 2 · Arrhythmias, Electrophysiology and ECG Interpretation
A 72-year-old man undergoes uncomplicated implantation of a Watchman left atrial appendage occlusion device. Transoesophageal echocardiography at the end of the procedure confirms good device seating with no peri-device leak. Which post-procedural antithrombotic regimen corresponds to the protocol used in the pivotal PROTECT AF and PREVAIL trials?
- AAspirin alone from the day of implantation
- BOral anticoagulation plus aspirin for 45 days, then dual antiplatelet therapy until 6 months, then aspirin alone
- CLifelong full-dose oral anticoagulation in addition to the device
- DNo antithrombotic therapy at all after implantation
Show answer and explanation
Correct answer: B. Oral anticoagulation plus aspirin for 45 days, then dual antiplatelet therapy until 6 months, then aspirin alone
The trial protocol continued oral anticoagulation with aspirin for 45 days until imaging confirmed device sealing and endothelialisation, then switched to dual antiplatelet therapy until six months, then aspirin alone indefinitely. Aspirin alone from day one or no therapy at all leaves the un-endothelialised device surface exposed and risks device-related thrombus. Lifelong full-dose anticoagulation would defeat the whole purpose of the device, which is to allow anticoagulation to be stopped.
Reference: Holmes DR et al. PROTECT AF, Lancet (2009) and PREVAIL, Journal of the American College of Cardiology (2014); 2023 ACC/AHA/ACCP/HRS Atrial Fibrillation Guideline
Question 3 · Cardiovascular Imaging and Diagnostic Testing
A 34-year-old man has concentric left ventricular hypertrophy of 16 mm, proteinuria, a history of burning pain in the hands and feet since childhood, and corneal whorling. Cardiac MRI shows basal inferolateral mid-wall late gadolinium enhancement and a reduced native myocardial T1 value. What is the most likely diagnosis?
- ACardiac AL amyloidosis
- BAnderson-Fabry disease
- CSarcomeric hypertrophic cardiomyopathy
- DHypertensive heart disease
Show answer and explanation
Correct answer: B. Anderson-Fabry disease
Reduced (low) native myocardial T1 is essentially specific to intramyocardial sphingolipid accumulation in Anderson-Fabry disease, and the basal inferolateral mid-wall late gadolinium enhancement plus acroparaesthesia, cornea verticillata and proteinuria complete a classic picture. Both AL and ATTR amyloidosis raise native T1 and extracellular volume, typically with diffuse subendocardial enhancement and difficult myocardial nulling. Sarcomeric hypertrophic cardiomyopathy and hypertensive heart disease show normal or mildly elevated native T1 and lack the extracardiac features.
Reference: Sado DM et al., Identification of Anderson-Fabry disease by T1 mapping, Circulation: Cardiovascular Imaging 2013; 2023 ESC Guidelines for the Management of Cardiomyopathies
Question 4 · Aortic Disease and Peripheral Vascular Disease
A 31-year-old woman has thin translucent skin with visible veins, easy bruising, a history of spontaneous sigmoid colon perforation at age 27, and a first-degree relative who died of a ruptured artery in the third decade. Genetic testing identifies a pathogenic COL3A1 variant. Which statement about her management is correct?
- AElective arterial surgery and routine invasive angiography are preferred because arterial tissue holds sutures well
- BAortic root replacement is indicated once the root reaches 4.0 cm, as in Loeys-Dietz syndrome
- CEctopia lentis is the characteristic ocular finding and mandates annual slit-lamp examination
- DNon-invasive imaging surveillance is preferred and celiprolol has been shown to reduce arterial events
Show answer and explanation
Correct answer: D. Non-invasive imaging surveillance is preferred and celiprolol has been shown to reduce arterial events
A COL3A1 pathogenic variant establishes vascular Ehlers-Danlos syndrome, in which arterial and hollow-viscus tissue is extremely friable; elective invasive arteriography and surgery carry high complication rates, so non-invasive imaging (CT/MR angiography, ultrasound) is preferred and intervention is generally reserved for life-threatening events at experienced centres. The BBEST trial demonstrated that celiprolol reduced arterial rupture and dissection events in vascular EDS. Ectopia lentis is a feature of Marfan syndrome, not vascular EDS, and the low-diameter surgical thresholds used in Loeys-Dietz syndrome are not the paradigm for vascular EDS, where rupture often occurs at normal diameters.
Reference: 2022 ACC/AHA Aortic Disease Guideline; BBEST trial (Ong et al., Lancet 2010); 2017 International Classification of the Ehlers-Danlos Syndromes
Question 5 · Professionalism, Ethics, Patient Safety and Quality
A 48-year-old professional heavy-goods-vehicle driver receives a secondary-prevention ICD after resuscitated ventricular fibrillation. He asks when he can return to work. What advice is correct?
- AHe may resume commercial driving after six months if he receives no shocks
- BHe may resume driving immediately, since the device now protects him
- CHe is permanently disqualified from professional/commercial driving; private driving may resume after the restriction period specified by the applicable regulations
- DRestrictions apply only if he actually receives a device therapy
Show answer and explanation
Correct answer: C. He is permanently disqualified from professional/commercial driving; private driving may resume after the restriction period specified by the applicable regulations
Across European and most international licensing frameworks, implantation of an ICD for any indication is a permanent bar to Group 2 (commercial/heavy vehicle) licensing because of the consequences of incapacity at the wheel of a large vehicle. Private (Group 1) driving is restricted for a defined period after a secondary-prevention implant and after any appropriate shock, then permitted if the patient is stable. The restriction is triggered by the underlying arrhythmic risk and the implant itself, not only by the occurrence of a shock, and requires sensitive occupational counselling and support.
Reference: ESC Consensus on Driving and Arrhythmias / 2022 ESC Guidelines for the Management of Ventricular Arrhythmias and Prevention of Sudden Cardiac Death; DVLA Assessing Fitness to Drive (current edition)
Question 6 · Basic Cardiovascular Sciences and Clinical Examination
A 39-year-old woman from a rheumatic-endemic region has mitral stenosis with a loud S1, an opening snap and a mid-diastolic rumble. Compared with her examination two years ago, the interval between the aortic component of S2 and the opening snap is now shorter. What does this change indicate?
- ASignificant aortic regurgitation has developed
- BThe stenosis has become less severe
- CThe mitral valve has become heavily calcified and immobile
- DThe stenosis has become more severe with a higher left atrial pressure
Show answer and explanation
Correct answer: D. The stenosis has become more severe with a higher left atrial pressure
The opening snap occurs when left ventricular pressure falls below left atrial pressure; as left atrial pressure rises with worsening stenosis, the valve opens earlier and the A2-opening snap interval shortens, so a short interval indicates more severe disease. A longer interval indicates milder stenosis. A heavily calcified immobile valve tends to abolish both the loud S1 and the opening snap rather than shorten the interval, and coexisting aortic regurgitation does not shorten A2-OS in this way.
Reference: 2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease; Braunwald's Heart Disease, 12th edition, 2022
Question 7 · Coronary Artery Disease and Acute Coronary Syndromes
A 51-year-old woman has recurrent rest chest pain, often in the early morning, with transient ST elevation captured on a Holter recording. Angiography shows unobstructed coronaries, and intracoronary acetylcholine provocation reproduces her pain with more than 90% focal epicardial narrowing and ST elevation, relieved by intracoronary nitrate. Which management is most appropriate?
- AA non-dihydropyridine or dihydropyridine calcium channel blocker as first-line therapy, avoiding non-selective beta-blockers
- BHigh-dose bisoprolol as first-line therapy
- CImmediate stenting of the segment that narrowed during provocation
- DLong-term dual antiplatelet therapy with no anti-anginal drug
Show answer and explanation
Correct answer: A. A non-dihydropyridine or dihydropyridine calcium channel blocker as first-line therapy, avoiding non-selective beta-blockers
The findings define epicardial vasospastic (Prinzmetal) angina, for which calcium channel blockers, often combined with long-acting nitrates, are first-line and smoking cessation is essential. Non-selective beta-blockers can worsen spasm through unopposed alpha-mediated vasoconstriction, stenting a spastic but anatomically normal segment does not treat the disorder and risks stent-related complications, and antiplatelet therapy alone does not prevent spasm.
Reference: COVADIS international standardised diagnostic criteria for vasospastic angina (2017); ESC Chronic Coronary Syndromes Guidelines (2024)
Question 8 · Valvular Heart Disease and Infective Endocarditis
A 74-year-old man with a body surface area of 2.1 m2 underwent surgical aortic valve replacement with a 19 mm bioprosthesis. At the six-week echocardiogram he has a mean gradient of 32 mmHg, normal leaflet opening on fluoroscopy, no paravalvular or transvalvular regurgitation, and an indexed effective orifice area of 0.60 cm2/m2. What is the most likely explanation?
- ASevere patient-prosthesis mismatch
- BProsthetic valve thrombosis
- CPannus ingrowth causing obstruction
- DEarly structural valve deterioration
Show answer and explanation
Correct answer: A. Severe patient-prosthesis mismatch
An indexed effective orifice area of 0.65 cm2/m2 or less in the aortic position defines severe patient-prosthesis mismatch, which produces high gradients from the first postoperative study despite a structurally normal, normally moving prosthesis, and is typical of a small prosthesis in a large patient. Thrombosis and pannus cause restricted leaflet motion and generally develop later, with thrombosis usually accompanied by subtherapeutic anticoagulation and a mass on imaging. Structural deterioration of a bioprosthesis takes years and is usually accompanied by leaflet thickening, calcification or new regurgitation.
Reference: 2021 ESC/EACTS Valvular Heart Disease Guidelines; EACVI/ASE Recommendations for the Imaging Assessment of Prosthetic Heart Valves (2016)
Question 9 · Cardiac Pharmacology and Therapeutics
A 52-year-old woman on stable warfarin for a mechanical mitral valve has an unexpectedly high INR of 6.2 without bleeding. She recently started a new medication. Which of the following is the most likely culprit through inhibition of warfarin metabolism?
- ARifampicin
- BCarbamazepine
- CFluconazole
- DCholestyramine
Show answer and explanation
Correct answer: C. Fluconazole
Fluconazole is a potent inhibitor of CYP2C9, the enzyme clearing the more active S-enantiomer of warfarin, so it raises INR sharply. Rifampicin and carbamazepine are strong enzyme inducers that lower INR, and cholestyramine reduces warfarin absorption and therefore also lowers INR.
Reference: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 14th edition, 2023; CHEST Antithrombotic Therapy Guidelines
Question 10 · Hypertension, Pulmonary Hypertension and Preventive Cardiology
A 59-year-old man with prior myocardial infarction and type 2 diabetes has LDL cholesterol at goal (1.3 mmol/L) on maximally tolerated atorvastatin, but fasting triglycerides remain 2.6 mmol/L (230 mg/dL) after alcohol and glycaemic optimisation. Which addition has randomised evidence of reducing cardiovascular events in this setting?
- AExtended-release niacin
- BFenofibrate
- CIcosapent ethyl 2 g twice daily
- DMixed omega-3 fish oil supplement 1 g daily
Show answer and explanation
Correct answer: C. Icosapent ethyl 2 g twice daily
REDUCE-IT randomised statin-treated patients with elevated triglycerides and either established cardiovascular disease or diabetes with risk factors, and showed a 25% relative reduction in the primary composite endpoint with high-dose icosapent ethyl (purified eicosapentaenoic acid), at the cost of increased atrial fibrillation and bleeding. Niacin failed to add benefit on a statin background in AIM-HIGH and HPS2-THRIVE, fibrate outcome trials such as ACCORD-Lipid and PROMINENT were neutral overall, and low-dose mixed omega-3 supplements have not reduced events.
Reference: REDUCE-IT (Bhatt et al., N Engl J Med 2019;380:11-22); PROMINENT (Das Pradhan et al., N Engl J Med 2022)
Free mock vs the full Cardiology bank
The mock tells you where you stand. The bank is how you close the gap.
| What you get | Free mock | Full bank |
|---|---|---|
| Questions | 25 | 465+ |
| Papers | 1 short timed set | 3 to 6 full-length papers, about 155 each |
| Blueprint coverage | 11 of 13 domains | All 13 domains, 232 sub-topics |
| Worked rationale | Every question | Every question |
| Reference | Every question | Every question |
| Timing | 30 minutes in your browser | Exam-length papers to sit against the clock |
| Format | Online, free | PDF sent to you, yours to keep |
| Price | Free | AED 319, paid once |
Full Cardiology bank
Close your gaps before exam day
- 465+ original questions in 3 to 6 full-length papers
- A worked rationale and a reference on every question
- Prepared for your regulator's blueprint and pass mark
One-time price
AED 319
About a third of one exam fee (about AED 1,030 per attempt)
Unlock the full bank →No subscription · yours to keep
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