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Specialist & consultant · oral assessment

Specialist & Consultant Critical Care Medicine oral assessment prep

14 panel-style scenarios with model answers structured in the three graded domains - knowledge, management, and ethics & communication.

Pass / fail panel14 scenarios
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Try a scenario from this pack

An original scenario, written the way a panel would put it to you.

Scenario 1Acute Kidney Injury and Renal Replacement Therapy

A 66-year-old woman with type 2 diabetes and baseline creatinine 95 micromol/L is on day 3 in ICU with septic shock from a perforated diverticulum, on noradrenaline 0.12 mcg/kg/min. Urine output has been 0.2 mL/kg/h for 18 hours, creatinine is 310 micromol/L, urea 24 mmol/L, potassium 5.6 mmol/L and bicarbonate 17 mmol/L. She is 7 L positive with a rising oxygen requirement. The surgical team asks why dialysis has not started. What is your assessment and plan?

What the panel is assessing

The panel is testing whether you can apply the evidence on timing of kidney replacement therapy to an individual patient and explain the decision to colleagues.

Liked those? The full pack has 14 scenarios at this standard - every one with a model answer.

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What's inside

  • ✓14 original panel-style scenarios
  • ✓Model answer in all three graded domains
  • ✓Likely panel follow-up probes
  • ✓The pitfalls that fail candidates
  • ✓4+ ethics, consent and error-disclosure cases
  • ✓How each authority runs its oral

How the consultant Critical Care Medicine oral is run, by authority

Consultant applicants who are not exempt are usually assessed by a panel rather than a computer exam. The format differs by authority.

AuthorityFormatLengthPanel and result
DHA - DubaiNot less than five clinical scenarios in your specialtyRoughly 20-30 minutesAt least two panellists, one pass or fail decision
DOH - Abu Dhabi5-6 case scenarios, including an ethical case45-60 minutesHeld on Microsoft Teams
SCFHS - Saudi ArabiaStructured consultant interview built on clinical casesTwo sessions of roughly 30 minutesSenior consultants in your specialty
OMSB - OmanViva on specialty cases, taken after the written examNot publishedRequired of every candidate

QCHP and NHRA assess most applicants by written exam and may add an interview or clinical assessment case by case. Your own eligibility notice is the final word on your route.

What a Critical Care Medicine panel is assessing

Scenarios are judged across three domains: clinical knowledge, management, and ethics and communication. In Critical Care Medicine, that looks like this:

  • •The panel is testing whether you can apply landmark trial evidence and current guidelines to an unstable patient at the bedside, and know where the evidence stops.
  • •The panel is testing whether you escalate organ support in good time, with a defined goal, and recognise when support has become non-beneficial.
  • •The panel is testing whether you can determine death by neurological criteria rigorously and keep end-of-life and donation conversations ethically separate.
  • •The panel is testing whether you make fair, transparent triage and resource decisions under pressure and document them in line with UAE law and facility policy.

How to structure an oral answer

  1. 1Say what it is and why it is dangerous. Open with the working diagnosis, the one or two alternatives you must exclude, and what will harm the patient first.
  2. 2Show the knowledge that changes the decision. Name the finding, test or trial result your plan rests on. Panels mark reasoning, not recitation.
  3. 3Manage in time order. What you do in the next ten minutes, the next hour and the next day, who you escalate to, and what would make you change course.
  4. 4Close on ethics and communication. Consent or capacity, the family conversation, disclosure if something went wrong, and what you document. Every authority examines this domain.

Worked Critical Care Medicine scenario outlines

6 original scenarios from the pack, written the way a panel would put them to you. Each outline shows the opening of the model answer in all three domains, the follow-up questions to expect and the mistakes that fail candidates.

Acute Respiratory Failure and ARDS

A 41-year-old man with a BMI of 36 is intubated in a Dubai ICU for influenza A pneumonia. After 18 hours on volume control with tidal volume 7 mL/kg predicted body weight, PEEP 14 cmH2O and FiO2 0.9, PaO2 is 62 mmHg, PaCO2 68 mmHg, pH 7.21 and plateau pressure 32 cmH2O. The chest radiograph shows bilateral opacities and echocardiography shows normal left ventricular function. He is on noradrenaline 0.15 mcg/kg/min. How would you manage him?

What the panel is testing: The panel is testing a stepwise, evidence-based approach to severe ARDS, the timing of prone positioning and ECMO referral, and avoidance of injurious ventilation.

Show the answer outline

Knowledge: This is severe ARDS from influenza pneumonia, with a PaO2/FiO2 ratio of about 69 mmHg on high PEEP and bilateral opacities not explained by cardiac failure. The threats are refractory hypoxaemia, ventilator-induced lung injury and right ventricular failure from hypercapnia and high pressures. Ventilation at 6 mL/kg predicted body weight with plateau pressure at or below 30 cmH2O reduces mortality. In PROSEVA, prone positioning for at least 16 hours a day reduced mortality when PaO2/FiO2 was below 150 mmHg. The 2023 ESICM guideline recommends prone positioning in moderate to severe ARDS and referral of eligible patients to an ECMO centre, informed partly by EOLIA. Bacterial co-infection, especially Staphylococcus aureus, must be considered.

Management: Now I would reduce tidal volume to 6 mL/kg, accept permissive hypercapnia with pH above about 7.20, titrate PEEP to oxygenation and compliance while watching haemodynamics, and aim for driving pressure below 15 cmH2O. I would deepen sedation and use neuromuscular blockade for a limited period if dyssynchrony persists, not routinely. I would prone him within hours, for at least 16 hours a session, with a trained team. I would continue oseltamivir and, after cultures, add antibiotics covering Staphylococcus aureus and pneumococcus. Repeat echocardiography assesses the right ventricle. If PaO2/FiO2 stays below about 80 mmHg or pH below 7.25 with high PaCO2 despite proning, I would call the regional ECMO centre early, before he is too unstable to move. I would use a conservative fluid strategy once shock resolves and avoid high-frequency oscillation.

Ethics and communication: His wife needs regular, honest updates on a serious prognosis, including why proning and possible ECMO are proposed. As he lacks capacity, procedures follow UAE law and facility policy, with emergency treatment not delayed. Staff need appropriate droplet and aerosol precautions. If ECMO capacity is limited, referral should follow agreed criteria rather than family pressure.

Likely panel follow-up questions

  • What were the entry criteria for EOLIA, and what did it show?
  • How do you set PEEP in this patient?
  • He desaturates to 70% during proning. What do you do?
  • Is there a role for corticosteroids in this ARDS?

Pitfalls in this case

  • Accepting a plateau pressure above 30 cmH2O to normalise PaCO2
  • Delaying prone positioning until the patient is in extremis
  • Referring for ECMO only when he is too unstable to transfer
  • Missing bacterial co-infection with Staphylococcus aureus

Reference: Grasselli G et al, ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies, Intensive Care Medicine, 2023; Guerin C et al, Prone Positioning in Severe Acute Respiratory Distress Syndrome (PROSEVA), New England Journal of Medicine, 2013; Combes A et al, Extracorporeal Membrane Oxygenation for Severe Acute Respiratory Distress Syndrome (EOLIA), New England Journal of Medicine, 2018

Neurocritical Care

A 26-year-old motorcyclist is in an Abu Dhabi trauma ICU after evacuation of an acute subdural haematoma. On day 2 he is sedated and ventilated, and the intraparenchymal monitor shows ICP 28 mmHg for 15 minutes, with mean arterial pressure 82 mmHg, PaCO2 38 mmHg, sodium 139 mmol/L and temperature 38.4 C. The right pupil is now 5 mm and sluggish. CT shows diffuse swelling and contusions without a new surgical lesion. How do you manage his intracranial hypertension?

What the panel is testing: The panel is testing a tiered, physiological approach to raised intracranial pressure, prevention of secondary brain injury and honest discussion of decompressive craniectomy outcomes.

Show the answer outline

Knowledge: He has severe traumatic brain injury with sustained ICP above the Brain Trauma Foundation threshold of 22 mmHg, a cerebral perfusion pressure of only 54 mmHg and a new pupillary change suggesting herniation. The goal is to prevent secondary injury from hypotension, hypoxaemia, hypercapnia, fever, hyponatraemia and seizures. BTF guidance targets CPP of 60 to 70 mmHg. The SIBICC consensus provides a tiered algorithm, escalating from basic measures through hyperosmolar therapy and deeper sedation to second-tier options. In RESCUEicp, decompressive craniectomy for refractory ICP reduced mortality but increased survival with severe disability. Corticosteroids are harmful in traumatic brain injury.

Management: Immediately I would check the monitor, nurse him 30 degrees head-up with a neutral neck and loose tube ties, deepen sedation and analgesia, and give hyperosmolar therapy, such as 3% saline or mannitol 0.5 to 1 g/kg. For the dilating pupil I would allow brief hyperventilation to a PaCO2 of about 30 to 35 mmHg as a bridge only. I would raise mean arterial pressure with noradrenaline to keep CPP at least 60 mmHg, treat fever toward normothermia, and consider continuous EEG for non-convulsive seizures. I would repeat CT urgently and involve the neurosurgeon. If ICP remains high, options include an external ventricular drain, neuromuscular blockade, barbiturate coma and decompressive craniectomy, decided jointly with neurosurgery. I would avoid prolonged hyperventilation, hypotonic fluids and hypotension. Once stable, he needs thromboprophylaxis when safe, nutrition and early rehabilitation planning.

Ethics and communication: His family should hear an honest account of severity and uncertainty, avoiding early prognostic certainty that can become self-fulfilling. If craniectomy is considered, survival with severe disability must be part of the discussion with his relatives, in line with UAE law and facility policy. Police reporting of the collision follows facility procedures, and medical information is shared only as legally required.

Likely panel follow-up questions

  • Why is prolonged hyperventilation harmful?
  • Mannitol or hypertonic saline: which would you choose and why?
  • What did RESCUEicp and DECRA show?
  • How would you detect and treat non-convulsive seizures?

Pitfalls in this case

  • Treating the ICP number while ignoring a CPP of 54 mmHg
  • Using prolonged hyperventilation as routine therapy
  • Failing to repeat CT before escalating to second-tier therapy
  • Giving corticosteroids for cerebral oedema in trauma

Reference: Carney N et al, Guidelines for the Management of Severe Traumatic Brain Injury, Fourth Edition, Brain Trauma Foundation, 2016; Hawryluk GWJ et al, A management algorithm for patients with intracranial pressure monitoring: the Seattle International Severe Traumatic Brain Injury Consensus Conference (SIBICC), Intensive Care Medicine, 2019; Hutchinson PJ et al, Trial of Decompressive Craniectomy for Traumatic Intracranial Hypertension (RESCUEicp), New England Journal of Medicine, 2016

Brain Death, Organ Donation and End-of-Life Care

A 34-year-old woman was admitted to a Sharjah ICU three days ago after a massive subarachnoid haemorrhage. Off sedation for 48 hours, she has fixed dilated pupils, no cough or gag and no spontaneous breaths. Blood pressure is supported with vasopressin, sodium has risen to 158 mmol/L and urine output is 400 mL/h. Her husband and brothers ask you to continue everything and pray for a miracle, and the transplant coordinator calls to ask whether she is a potential donor. How do you proceed?

What the panel is testing: The panel is testing rigorous determination of death by neurological criteria, separation of donation from the treating team's decisions, and sensitive communication with a family in shock.

Show the answer outline

Knowledge: The picture suggests death by neurological criteria, but the diagnosis requires a protocolised process. First come an established catastrophic cause and exclusion of confounders: sedatives, hypothermia, hypotension and severe electrolyte, endocrine or metabolic disturbance. Then a full examination must show coma and absent brainstem reflexes, followed by an apnoea test. The World Brain Death Project recommends a PaCO2 of at least 60 mmHg with acidaemia and no respiratory effort, and ancillary tests when the examination or apnoea test cannot be completed. Her hypernatraemia and polyuria indicate diabetes insipidus, and severe hypernatraemia is a confounder that must be corrected first. The procedure, examiners and documentation must follow UAE law and the facility's protocol.

Management: I would treat diabetes insipidus with desmopressin and replacement of free water, and optimise blood pressure, temperature and oxygenation. Once prerequisites are met, testing is done by qualified doctors independent of the transplant team, with ancillary testing if any part cannot be completed. I would meet the family before testing and explain what it involves. If death is confirmed, I would tell them clearly that she has died, using that word, and record the time of death as the protocol specifies. The donation conversation is kept separate from the determination of death and led by the trained coordinator with me present. Support continues only while donation is considered; otherwise ventilation stops after the family have had time.

Ethics and communication: Separating the treating team from transplant interests protects trust and the dead donor rule. Families may hold differing religious views on brain death, so I would offer a religious adviser and time, while explaining that continuing the ventilator cannot change the outcome. Donation must never be pressed, and a refusal must not change her care. Her dignity continues after death.

Likely panel follow-up questions

  • Which confounders must be excluded before testing?
  • How do you perform the apnoea test safely?
  • When are ancillary tests needed, and which would you choose?
  • The family refuse testing. What do you do?

Pitfalls in this case

  • Testing while hypernatraemia or residual sedation could confound the result
  • Raising donation before death is confirmed or as part of the diagnosis
  • Using ambiguous language such as she is brain dead but alive on machines
  • Involving transplant team members in the determination of death

Reference: Greer DM et al, Determination of Brain Death/Death by Neurologic Criteria: The World Brain Death Project, JAMA, 2020; WHO Guiding Principles on Human Cell, Tissue and Organ Transplantation, 2010

Cardiogenic Shock and Mechanical Circulatory Support

A 58-year-old man with diabetes is in the cardiac ICU after primary PCI to an occluded proximal left anterior descending artery, four hours after symptom onset. He is now confused, with blood pressure 82/58 on noradrenaline 0.3 mcg/kg/min and dobutamine 5 mcg/kg/min, heart rate 118, lactate 6.4 mmol/L and urine output 10 mL/h. Echocardiography shows an ejection fraction of 20% with no mechanical complication. He has not had a cardiac arrest and is not intubated. How would you manage him?

What the panel is testing: The panel is testing staging of cardiogenic shock, current evidence on mechanical circulatory support, and goal-directed escalation with a defined destination.

Show the answer outline

Knowledge: This is cardiogenic shock after anterior STEMI, SCAI stage D, deteriorating despite escalating vasoactive drugs, with end-organ hypoperfusion. Mechanical complications, right ventricular infarction and tamponade must be excluded. In multivessel disease, CULPRIT-SHOCK favoured culprit-only PCI at the index procedure. The intra-aortic balloon pump did not reduce mortality in IABP-SHOCK II. In DanGer Shock, a microaxial flow pump in selected STEMI shock without coma reduced 180-day mortality but increased bleeding, limb ischaemia and kidney replacement therapy. In ECLS-SHOCK, routine VA-ECMO did not reduce 30-day mortality.

Management: I would convene the shock team at once: interventional cardiology, cardiac surgery and intensive care. I would place arterial and central lines and a pulmonary artery catheter to measure cardiac power output and filling pressures, avoid fluid unless preload is low, and keep noradrenaline as the vasopressor with an inotrope titrated to response. Given stage D shock from an anterior infarct without coma, I would consider a microaxial flow pump, weighing vascular access, bleeding and limb ischaemia. VA-ECMO is a bridge only for refractory shock in a candidate for recovery, a durable device or transplant. With a device in place I would manage anticoagulation and monitor limb perfusion, haemolysis and kidney function, starting kidney replacement therapy if needed. Intubation, if required, is hazardous and needs a cardiostable induction. I would review escalation and de-escalation daily, and if recovery does not come, discuss durable options or a ceiling of care.

Ethics and communication: Mechanical support should be offered as a bridge to a defined destination, and the family must understand that a device does not guarantee recovery. He should consent himself if he has capacity; otherwise treatment proceeds under the emergency provisions of UAE law. Expensive, scarce therapies should follow agreed institutional criteria. I would document goals and the ceiling of care early.

Likely panel follow-up questions

  • How do you define SCAI stages C, D and E?
  • What did DanGer Shock show, and which patients did it include?
  • When would you choose VA-ECMO over a microaxial pump?
  • How would you recognise left ventricular distension on VA-ECMO?

Pitfalls in this case

  • Giving repeated fluid boluses to a congested failing ventricle
  • Escalating vasopressors indefinitely without a mechanical support plan
  • Inserting a device with no defined destination or exit strategy
  • Missing a mechanical complication on echocardiography

Reference: Naidu SS et al, SCAI SHOCK Stage Classification Expert Consensus Update, Journal of the Society for Cardiovascular Angiography and Interventions, 2022; Moller JE et al, Microaxial Flow Pump or Standard Care in Infarct-Related Cardiogenic Shock (DanGer Shock), New England Journal of Medicine, 2024; Thiele H et al, Extracorporeal Life Support in Infarct-Related Cardiogenic Shock (ECLS-SHOCK), New England Journal of Medicine, 2023; Federal Decree-Law No. 4 of 2016 on Medical Liability and Cabinet Resolution No. 40 of 2019 (UAE)

Resource Allocation and Triage

At 02:00 in a Northern Emirates ICU, one bed is free and two referrals arrive. The first is a 76-year-old man with metastatic lung cancer progressing on third-line therapy, now with pneumonia and hypoxaemic respiratory failure on 15 L/min oxygen; his son, a senior official, is calling the hospital director. The second is a woman of 29, two days after caesarean section, with suspected endometritis, lactate 4.8 mmol/L and blood pressure 84/50 after 2 L of crystalloid. Transfer to another ICU would take three hours. How do you decide?

What the panel is testing: The panel is testing fair, transparent triage based on benefit, resistance to outside influence, and continued good care for the patient who is not admitted.

Show the answer outline

Knowledge: Triage aims to give ICU care to those most likely to benefit, judged on clinical grounds and not on status, nationality, insurance or influence. The SCCM triage framework supports decisions based on potential benefit, transparent criteria and an accountable decision-maker, usually the ICU consultant. The young woman has septic shock and a high chance of full recovery. The older man has progressive metastatic cancer, and his goals, performance status and wishes are not yet known; ICU may offer limited benefit, though high-flow oxygen or non-invasive ventilation may still help. Options also include stepping down a stable ICU patient or using a high-dependency area.

Management: I would assess both patients promptly myself and start resuscitation wherever they are: for the woman, antibiotics, source assessment with obstetrics and a vasopressor through a peripheral line if needed; for the man, oxygen and senior review. I would also look for a stable ICU patient who can safely step down. I would admit the woman to the free bed on grounds of benefit and urgency. For the man, I would speak with him, if he can talk, and with his oncologist about goals and wishes. Ward-based high-flow oxygen or non-invasive ventilation with palliative support may be right, or later ICU admission or transfer. I would brief the hospital director factually and document my reasoning and plan for each patient. Continued pressure is escalated through facility procedures.

Ethics and communication: Justice requires that equal clinical need is treated equally and that connections do not decide. Transparency and documentation protect patients and clinicians. Declining ICU admission is not declining care: the man must still receive good treatment and palliation. I would speak honestly and kindly with his son, and raise recurrent bed shortages through governance.

Likely panel follow-up questions

  • What would you do if both patients had an equal chance of benefit?
  • The hospital director instructs you to admit the man. How do you respond?
  • How do you decide whether an ICU patient can safely step down?
  • Is age alone a valid triage criterion?

Pitfalls in this case

  • Admitting on status or pressure rather than clinical benefit
  • Leaving the patient not admitted without a clear plan or senior review
  • Making a ceiling-of-care decision without speaking to the patient or his oncologist
  • Failing to document the reasoning for the triage decision

Reference: Nates JL et al, ICU Admission, Discharge, and Triage Guidelines: A Framework to Enhance Clinical Operations, Development of Institutional Policies, and Further Research, Critical Care Medicine, 2016

Major Trauma and Massive Haemorrhage

A 30-year-old construction worker falls 8 metres at a Dubai site and arrives 50 minutes later with a pelvic binder. Heart rate is 138, blood pressure 74/40 and GCS 14, and FAST is positive in the hepatorenal pouch. Haemoglobin is 82 g/L, lactate 7.1 mmol/L, INR 1.6, fibrinogen 1.2 g/L, ionised calcium 0.98 mmol/L and temperature 35.2 C after two units of red cells. You are called to the resuscitation bay as the ICU consultant. How would you manage him?

What the panel is testing: The panel is testing damage control resuscitation to current evidence, correction of trauma-induced coagulopathy, and prioritising haemorrhage control over imaging in a non-responder.

Show the answer outline

Knowledge: This is haemorrhagic shock with trauma-induced coagulopathy, bleeding from the abdomen and probably the pelvis. The 2023 European guideline recommends tranexamic acid within three hours of injury, 1 g over 10 minutes then 1 g over 8 hours, and a target systolic pressure of 80 to 90 mmHg until bleeding stops when there is no brain injury. It recommends plasma at a ratio of at least 1:2 with red cells, or a fibrinogen-based strategy, and fibrinogen replacement when Clauss fibrinogen is 1.5 g/L or less. CRASH-2 showed that early tranexamic acid reduces deaths from bleeding, and PROPPR supported balanced ratios. Damage control surgery or angioembolisation, not definitive repair, is the priority.

Management: I would activate the massive haemorrhage protocol, give tranexamic acid now, and transfuse warmed products at a balanced ratio through a rapid infuser, guided by viscoelastic testing where available. I would give fibrinogen concentrate 3 to 4 g or cryoprecipitate, calcium chloride to normalise ionised calcium, and active warming, while minimising crystalloid. As he is not responding, he goes straight to theatre or a hybrid suite for damage control laparotomy, pelvic packing or angioembolisation; CT is for responders. Once bleeding is controlled I would target haemoglobin 70 to 90 g/L and monitor potassium, acid-base and lactate. In ICU I would continue rewarming and correcting coagulopathy, watch for abdominal compartment syndrome and plan the second-look operation. Pharmacological thromboprophylaxis starts within 24 hours of bleeding control, followed by tertiary survey and spinal clearance.

Ethics and communication: Emergency treatment proceeds without consent under UAE law. I would inform his family once identified, sharing only what is needed. As a migrant worker he may fear cost or losing his job, so I would involve social work and ensure his care is not shaped by insurance status. Injury reporting follows facility policy.

Likely panel follow-up questions

  • What is your target blood pressure, and how would a head injury change it?
  • How would you use viscoelastic testing to guide products?
  • When would you choose angioembolisation over laparotomy?
  • What are the complications of massive transfusion?

Pitfalls in this case

  • Sending a non-responder to CT before haemorrhage control
  • Large-volume crystalloid resuscitation
  • Ignoring hypocalcaemia and hypothermia during massive transfusion
  • Giving tranexamic acid after three hours or not at all

Reference: Rossaint R et al, The European guideline on management of major bleeding and coagulopathy following trauma: sixth edition, Critical Care, 2023; CRASH-2 trial collaborators, Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage, Lancet, 2010; Holcomb JB et al, Transfusion of Plasma, Platelets, and Red Blood Cells in a 1:1:1 vs a 1:1:2 Ratio and Mortality in Patients With Severe Trauma (PROPPR), JAMA, 2015

Common reasons candidates fail the Critical Care Medicine oral

  • ✕Ventilating with injurious tidal volumes or plateau pressures to normalise blood gases
  • ✕Delaying proning, ECMO referral or haemorrhage control until the patient is too unstable
  • ✕Escalating mechanical support without a defined destination or exit plan
  • ✕Testing for brain death without excluding confounders, or linking it to donation
  • ✕Letting status, insurance or outside pressure decide ICU admission
  • ✕Giving families false certainty or vague language about prognosis

Critical Care Medicine oral syllabus

The clinical and professional areas the scenarios in this pack are drawn from:

  • Acute Kidney Injury and Renal Replacement Therapy
  • Acute Respiratory Failure and ARDS
  • Brain Death, Organ Donation and End-of-Life Care
  • Capacity, Consent and Family Communication
  • Cardiogenic Shock and Mechanical Circulatory Support
  • Infection Control and Antimicrobial Stewardship
  • Major Trauma and Massive Haemorrhage
  • Metabolic, Endocrine and Toxicological Emergencies
  • Neurocritical Care
  • Obstetric Critical Care
  • Patient Safety, Adverse Events and Open Disclosure
  • Resource Allocation and Triage
  • Sedation, Delirium and Liberation from Ventilation
  • Sepsis and Septic Shock

Panels expect specialist-level command of the written Critical Care Medicine blueprint too, which covers:

  • Shock, resuscitation and haemodynamics
  • Respiratory failure and mechanical ventilation
  • Sepsis and infection in the ICU
  • Neurocritical care
  • Renal, metabolic, fluids and electrolytes
  • Cardiovascular critical care
  • Trauma, toxicology and environmental emergencies
  • Haematology, gastrointestinal and nutrition
  • Ethics, end-of-life care and patient safety

Sitting the written exam as well? Critical Care Medicine question bank or the free Critical Care Medicine mock exam.

Last reviewed September 2026

About these questions: every scenario and model answer is original, written for this pack, with a guideline or trial reference. No recalled or leaked exam content is used. How we write our questions.

Frequently asked questions

Are these real Consultant Critical Care Medicine - Oral Assessment 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 is the oral assessment actually run?
It varies by authority. DHA requires not less than five clinical scenarios across roughly 20-30 minutes with a minimum of two panellists, scored pass or fail. DOH Abu Dhabi runs 5-6 scenarios including an ethical case over 45-60 minutes on Microsoft Teams. SCFHS uses a structured consultant interview of two roughly 30-minute case-based sessions, and OMSB requires a viva for every candidate after the written exam. The pack briefs you on each.
Does this cover DHA, DOH, MOHAP and SCFHS?
The core clinical knowledge is shared across the GCC; what differs by regulator is the test vendor (Prometric for DHA, SCFHS, QCHP, NHRA, Kuwait MOH; Pearson VUE for DOH, OMSB), the format, the pass mark and the local-regulation slice. The pack briefs you on how each authority runs its panel.
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.

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