Free Pulmonology mock test
25 original exam-style questions from our Pulmonology bank, timed at the exam’s own pace, scored against the 60% DHA pass mark. They span 13 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 Pulmonology bank, spread across 13 of the 13 domains of the published blueprint. You get 72 seconds per question, which is exactly the pace of the real PUL5081 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
- 60%
- 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 Pulmonology exam at a glance
The Pulmonology 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 60% DHA pass mark, then shows your weakest domains.
Published exam figures
- DHA
Specialist Pulmonary Disease (PUL5081)
UAE150 MCQs3 hours60%
pass mark
- SCFHS
Saudi Classification Examination - Pulmonology
Saudi Arabia200 MCQs240 minutes65%
pass mark
- QCHP
Specialist Pulmonary
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 · 13 of 13 domains
- Full bank
- 525+ questions · 3 to 6 papers · AED 319
- Regulators
- DHA, SCFHS, QCHP, DOH, MOHAP, SHA, NHRA, OMSB and Kuwait MOH
How this free Pulmonology mock works
- 25
- original questions
- 30 min
- time limit
- 72s
- per question
- 13 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 60% 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 Pulmonology licensing exam looks like
The Pulmonology exam is a computer-based multiple-choice paper, published by 3 regulators: DHA PUL5081 (pass mark 60%), 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 Pulmonary Disease (PUL5081) | 150 MCQs in 3 hours | 60% | USD 280 (about AED 1,030) | |
Saudi Classification Examination - Pulmonology | 200 MCQs in 240 minutes | 65% | Not published | |
Specialist Pulmonary | 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 Pulmonology exam; the others show the regulator's general rules.
What is on the Pulmonology exam: the full blueprint
The published blueprint splits into 13 domains and 260 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.
- Obstructive Lung Disease~20%
20 sub-topics · 3 in this mock · about 95 in the full bank
SCFHS Pulmonology Blueprint published: 20%; DHA lists 'Obstructive Lung Disease' as its first named coverage area
- Interstitial and Inflammatory (Diffuse Parenchymal) Lung Disease~12%
20 sub-topics · 3 in this mock · about 57 in the full bank
SCFHS published: 12%; DHA lists 'Interstitial and Inflammatory Lung Disease'
- Respiratory Infections and Tuberculosis~10%
20 sub-topics · 1 in this mock · about 47 in the full bank
SCFHS published: Infections 10%; DHA lists 'Infections'
- Sleep Medicine and Sleep-Disordered Breathing~10%
20 sub-topics · 1 in this mock · about 47 in the full bank
SCFHS published: 10%; DHA lists 'Sleep Medicine'
- Pulmonary Vascular Disorders~10%
20 sub-topics · 1 in this mock · about 47 in the full bank
SCFHS published: Vascular Disorders 10%; DHA lists 'Vascular Disorders'
- Thoracic Neoplasms and Lung Cancer~8%
20 sub-topics · 1 in this mock · about 38 in the full bank
SCFHS published: Neoplasms 8%; DHA lists 'Neoplasms'
- Pleural Diseases~5%
20 sub-topics · 1 in this mock · about 24 in the full bank
SCFHS published: 5%; DHA lists 'Pleural Diseases'
- Occupational and Environmental Lung Disease~5%
20 sub-topics · 2 in this mock · about 24 in the full bank
SCFHS published: 5%; DHA lists 'Occupational and Environmental Diseases'
- Congenital, Neuromuscular, Chest Wall and Airway Structural Disorders~5%
20 sub-topics · 1 in this mock · about 24 in the full bank
SCFHS published: Congenital, Neuromuscular, and Skeletal Abnormalities 5%; DHA lists the identical heading
- Critical Care Medicine and Respiratory Failure~5%
20 sub-topics · 4 in this mock · about 24 in the full bank
SCFHS published: Critical Care Medicine 5%; DHA lists 'Critical Care Medicine'
- Respiratory Physiology, Pulmonary Function Testing and Thoracic Imaging~5%
20 sub-topics · 1 in this mock · about 24 in the full bank
est. - not a standalone SCFHS/DHA blueprint heading, but the SCFHS Respiratory Medicine curriculum devotes full appendices to Physiology, Pulmonary Function Test and Thoracic Radiology, and PFT/imaging stimulus is embedded throughout every other section
- Interventional Pulmonology, Bronchoscopy and Lung Transplantation~5%
20 sub-topics · 4 in this mock · about 24 in the full bank
est. - not a standalone SCFHS/DHA blueprint heading, but the SCFHS Respiratory Medicine curriculum mandates bronchoscopy and pleural-ultrasound workshops, a logbook of 50 bronchoscopies and 10 ultrasound-guided thoracenteses, and a full Lung Transplant appendix; heavily sampled in oral assessment
- Patient Safety, Professionalism, Ethics and Communication~10%
20 sub-topics · 2 in this mock · about 47 in the full bank
SCFHS published: Patient Safety 5% and Professionalism and Ethics 5%; DHA lists both 'Patient Safety' and 'Professionalism and Ethics' as named coverage areas
Bank counts are estimates from the published weights the bank is written to, rounded.
This mock samples 13 of 13 domains. The full bank covers all 13 across 525+ questions.
See the full bank - AED 319How to use your mock score
These bands are set against the 60% 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 60% 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 175-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 Pulmonology 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.
Sleep Medicine and Sleep-Disordered Breathing
A 45-year-old commercial heavy-goods vehicle driver is diagnosed with severe obstructive sleep apnoea (AHI 58/h). He admits to falling asleep at traffic lights and has had one near-miss. He asks you not to tell anyone as he will lose his job. What is the most appropriate action?
- ARespect confidentiality absolutely and simply start CPAP
- BAdvise him that he must stop driving until effectively treated, document this advice, and inform the licensing authority if he continues to driveCorrect
- CAllow him to continue driving provided he limits himself to daytime routes
- DDefer any advice until three months of CPAP adherence data are available
Why: Excessive sleepiness with impaired driving in a vocational driver poses a serious risk to the public, so the duty of confidentiality is outweighed by the duty to prevent foreseeable harm. The correct sequence is to advise the patient to stop driving and to notify the licensing authority himself, document that advice, and only disclose to the authority if he fails to comply. Restricting to daytime routes does not mitigate the risk, and delaying advice for three months leaves an unsafe driver on the road.
Source: ATS Clinical Practice Guideline: Sleep Apnea, Sleepiness, and Driving Risk in Noncommercial Drivers, Am J Respir Crit Care Med (2013); GMC Confidentiality: patients' fitness to drive (2017)
Pulmonology sample questions with answers
10 more original exam-style Pulmonology 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 · Interstitial and Inflammatory (Diffuse Parenchymal) Lung Disease
A 47-year-old man has a spontaneous pneumothorax. CT shows a modest number of thin-walled, oval and lentiform cysts clustered in the basal, perihilar and paramediastinal regions, some abutting vessels. He has small white papules on the face and neck, and his mother had a renal tumour. Which is the most likely diagnosis?
- ABirt-Hogg-Dube syndrome
- BPulmonary Langerhans cell histiocytosis
- CLymphangioleiomyomatosis
- DEmphysema due to alpha-1 antitrypsin deficiency
Show answer and explanation
Correct answer: A. Birt-Hogg-Dube syndrome
Birt-Hogg-Dube syndrome, caused by germline folliculin (FLCN) mutations, produces basal, perihilar and paramediastinal lentiform cysts often abutting vessels, recurrent pneumothorax, cutaneous fibrofolliculomas and a familial risk of renal tumours such as chromophobe and hybrid oncocytic carcinoma. PLCH occurs in smokers with upper-zone nodules and bizarre cysts that spare the costophrenic angles, and LAM affects women with uniform round cysts throughout all zones. Alpha-1 antitrypsin deficiency causes basal emphysema without discrete walled cysts and without skin or renal features.
Reference: Gupta N et al, Diffuse Cystic Lung Disease, Am J Respir Crit Care Med, 2015; ERS Monograph on Orphan Lung Diseases, 2023
Question 2 · Sleep Medicine and Sleep-Disordered Breathing
Which statement best explains why central apnoeas may appear at sleep onset and during unstable NREM sleep in an otherwise healthy adult?
- AThe hypoxic ventilatory drive is abolished in NREM sleep, removing the principal stimulus to breathe
- BPaCO2 falls by 8-10 mmHg on falling asleep because alveolar ventilation increases
- CThe wakefulness drive to breathe is lost, so ventilation ceases whenever PaCO2 falls below the apnoeic threshold, which lies only a few mmHg below the eupnoeic PaCO2
- DMetabolic CO2 production rises at sleep onset, widening the CO2 reserve
Show answer and explanation
Correct answer: C. The wakefulness drive to breathe is lost, so ventilation ceases whenever PaCO2 falls below the apnoeic threshold, which lies only a few mmHg below the eupnoeic PaCO2
During wakefulness a non-chemical 'wakefulness drive' maintains breathing even when PaCO2 is low; this drive disappears in NREM sleep, so ventilation becomes critically dependent on PaCO2 remaining above the apnoeic threshold, which sits only about 2-6 mmHg below eupnoeic PaCO2 (a narrow CO2 reserve). PaCO2 actually rises by roughly 2-8 mmHg in sleep because alveolar ventilation falls, so option B is wrong. Hypoxic drive is blunted rather than abolished, and metabolic rate falls in sleep, narrowing rather than widening the CO2 reserve.
Reference: Dempsey JA et al., Physiol Rev (2010), Pathophysiology of sleep apnea; Murray & Nadel's Textbook of Respiratory Medicine, 7th ed (2022)
Question 3 · Patient Safety, Professionalism, Ethics and Communication
A cluster of Pseudomonas aeruginosa isolates with an identical antibiogram is recovered from bronchoalveolar lavage samples of five patients bronchoscoped over two weeks, and none has clinical infection. Which failure of bronchoscope reprocessing is the most likely explanation and the most important to correct?
- AFailure to sterilise the bronchoscope by steam autoclaving after each patient
- BFailure to use a new sterile bite block for every procedure
- CInadequate manual cleaning with brushing and flushing of all channels before high-level disinfection, with incomplete drying and storage
- DFailure to send every bronchoscope for ethylene oxide sterilisation weekly
Show answer and explanation
Correct answer: C. Inadequate manual cleaning with brushing and flushing of all channels before high-level disinfection, with incomplete drying and storage
Pseudo-outbreaks and true outbreaks linked to flexible bronchoscopes are most often traced to inadequate manual cleaning and channel brushing before high-level disinfection, together with residual moisture that permits biofilm formation during storage, so thorough cleaning, drying and hanging vertically are the critical steps. Flexible bronchoscopes are heat-labile semicritical devices that cannot be steam autoclaved, and routine ethylene oxide sterilisation is neither standard nor a substitute for correct cleaning. Bite blocks do not contact the sampling channel and would not produce identical channel-derived isolates.
Reference: ESGE-ESGENA Guideline: Reprocessing of Flexible Endoscopes (Endoscopy, 2018); CDC/HICPAC Guideline for Disinfection and Sterilization in Healthcare Facilities (2008, updated); BTS Guideline for Diagnostic Flexible Bronchoscopy in Adults (Thorax, 2013)
Question 4 · Pleural Diseases
A 74-year-old former shipyard worker has a small right exudative effusion with focal nodular parietal pleural thickening measuring 12 mm on CT. He has severe COPD (FEV1 28% predicted) and would tolerate single-lung ventilation and pneumothorax induction poorly. Which is the most appropriate way to obtain tissue?
- AImage-guided (CT or ultrasound) cutting-needle biopsy of the thickened pleura
- BBlind Abrams closed needle biopsy of the posterior chest wall
- CVATS pleural biopsy under general anaesthesia
- DRepeat therapeutic aspiration with cell-block cytology only
Show answer and explanation
Correct answer: A. Image-guided (CT or ultrasound) cutting-needle biopsy of the thickened pleura
When there is a visible pleural target, image-guided cutting-needle biopsy achieves a sensitivity for malignancy of around 85% and avoids the pneumothorax induction and single-lung ventilation that his respiratory reserve will not tolerate. Blind Abrams biopsy is significantly less sensitive than image-guided biopsy for malignant disease because the lesions are patchy. VATS carries unacceptable anaesthetic risk here, and further cytology alone has already been shown to be low-yield for mesothelioma in particular.
Reference: Maskell NA et al., Lancet (2003), CT-guided versus Abrams pleural biopsy; BTS Pleural Disease Guideline (Thorax, 2023)
Question 5 · Congenital, Neuromuscular, Chest Wall and Airway Structural Disorders
A 58-year-old man reports severe orthopnoea developing within seconds of lying flat and breathlessness on immersion to the waist. Seated FVC is 2.4 L and supine FVC is 1.5 L. Fluoroscopic sniff testing is reported as showing no paradoxical motion of either hemidiaphragm. Which investigation is most likely to establish the diagnosis?
- ARepeat fluoroscopic sniff testing in the lateral decubitus position
- BB-mode diaphragm ultrasound with measurement of thickening fraction at the zone of apposition bilaterally
- CHigh-resolution CT of the chest with expiratory sequences
- DCardiopulmonary exercise testing with measurement of the ventilatory equivalent for CO2
Show answer and explanation
Correct answer: B. B-mode diaphragm ultrasound with measurement of thickening fraction at the zone of apposition bilaterally
Orthopnoea with a supine fall in FVC of more than 25-30% strongly suggests bilateral diaphragm paralysis, and the sniff test is unreliable in bilateral disease because accessory and abdominal muscle recruitment can move both hemidiaphragms passively downwards, producing a false-negative result. Diaphragm ultrasound showing absent or minimal thickening fraction at the zone of apposition on both sides is the most useful bedside confirmatory test, supported by low sniff nasal inspiratory pressure and, where available, phrenic nerve conduction studies. CT and exercise testing characterise other causes of dyspnoea but do not assess diaphragm function.
Reference: ERS Statement on Respiratory Muscle Testing at Rest and During Exercise (Laveneziana P et al., Eur Respir J 2019); ATS/ERS Statement on Respiratory Muscle Testing, Am J Respir Crit Care Med 2002
Question 6 · Respiratory Physiology, Pulmonary Function Testing and Thoracic Imaging
An FDG PET-CT is requested to characterise an 18 mm solid lung nodule in a 62-year-old man from a region with a high burden of tuberculosis. Which statement about the limitations of PET-CT in this setting is correct?
- APET-CT reliably distinguishes malignant from infective nodules because granulomas are not FDG-avid
- BGranulomatous disease such as tuberculosis and sarcoidosis causes false-positive FDG uptake, while carcinoid tumours, well-differentiated adenocarcinoma in situ and lesions under about 8 mm cause false negatives
- CPET-CT has near-perfect sensitivity for lesions of any size, so a negative scan excludes malignancy regardless of nodule diameter
- DPET-CT is contraindicated in diabetes because hyperglycaemia increases FDG uptake in tumour
Show answer and explanation
Correct answer: B. Granulomatous disease such as tuberculosis and sarcoidosis causes false-positive FDG uptake, while carcinoid tumours, well-differentiated adenocarcinoma in situ and lesions under about 8 mm cause false negatives
FDG uptake reflects glucose metabolism rather than malignancy specifically, so active granulomatous and other inflammatory processes - very relevant where tuberculosis is endemic - produce false positives, while slowly metabolising lesions such as carcinoid tumours and subsolid adenocarcinoma in situ, together with nodules below roughly 8 mm which fall under scanner resolution and suffer partial volume effects, produce false negatives. Sensitivity is therefore size- and histology-dependent, and hyperglycaemia reduces rather than increases tumour FDG uptake by competitive inhibition, which is why glucose control before scanning is advised rather than the test being contraindicated.
Reference: MacMahon H et al. Guidelines for Management of Incidental Pulmonary Nodules Detected on CT Images: From the Fleischner Society 2017. Radiology 2017;284:228-243; Gould MK et al. Evaluation of Individuals With Pulmonary Nodules: ACCP Evidence-Based Clinical Practice Guidelines. Chest 2013;143(5 Suppl):e93S-e120S
Question 7 · Obstructive Lung Disease
A 48-year-old man treated for 'refractory asthma' had a prolonged intubation and tracheostomy after a road traffic accident three years ago. Spirometry shows FEV1 1.9 L, FVC 3.6 L, FEV1/FVC 0.53, and the flow-volume loop demonstrates plateauing of both the inspiratory and expiratory limbs with a FEF50/FIF50 ratio of approximately 1.0. What does this pattern indicate?
- AVariable intrathoracic obstruction such as tracheomalacia
- BVariable extrathoracic obstruction such as vocal cord paralysis
- CFixed upper airway obstruction such as post-tracheostomy tracheal stenosis
- DSmall airways obstruction due to severe asthma
Show answer and explanation
Correct answer: C. Fixed upper airway obstruction such as post-tracheostomy tracheal stenosis
Plateauing of both limbs of the flow-volume loop with an FEF50/FIF50 ratio near 1.0 is the signature of a fixed upper airway obstruction, which in this history is almost certainly a post-tracheostomy or post-intubation tracheal stenosis requiring CT of the neck and chest and bronchoscopic assessment. Variable intrathoracic lesions flatten the expiratory limb only, variable extrathoracic lesions flatten the inspiratory limb only, and diffuse small airways disease produces a concave (scooped) expiratory limb rather than a plateau.
Reference: ATS/ERS Technical Standard on Interpretive Strategies for Routine Lung Function Tests, 2022
Question 8 · Respiratory Infections and Tuberculosis
In a patient with a primary lung abscess treated with appropriate intravenous antibiotics, which of the following represents the strongest indication to proceed to percutaneous or bronchoscopic drainage?
- AAny cavity larger than 3 cm on the initial CT scan
- BThe presence of an air-fluid level within the cavity
- CFoul-smelling sputum at presentation
- DA large abscess with persistent sepsis and lack of clinical improvement after 7 or more days of appropriate antibiotic therapy
Show answer and explanation
Correct answer: D. A large abscess with persistent sepsis and lack of clinical improvement after 7 or more days of appropriate antibiotic therapy
Drainage is indicated when medical therapy fails, typically signalled by persistent fever and sepsis beyond about 7 to 10 days, and is more often needed with very large cavities (commonly cited as greater than 6 to 8 cm), impending rupture, or an underlying obstructing lesion. Cavity size alone at presentation, an air-fluid level and putrid sputum are expected features of an anaerobic lung abscess and do not by themselves mandate intervention.
Reference: Murray and Nadel's Textbook of Respiratory Medicine, 7th edition, 2022, chapter on anaerobic infections and lung abscess
Question 9 · Pulmonary Vascular Disorders
A 52-year-old woman with newly diagnosed PR3-ANCA granulomatosis with polyangiitis presents with diffuse alveolar haemorrhage, hypoxaemic respiratory failure and a creatinine that has risen from 90 to 320 micromol/L over 5 days. She has completed her family and wishes to preserve fertility. In addition to high-dose glucocorticoids, which remission-induction agent is most appropriate?
- AMethotrexate 25 mg weekly
- BRituximab
- CAzathioprine 2 mg/kg daily
- DMycophenolate mofetil 2 g daily
Show answer and explanation
Correct answer: B. Rituximab
Severe, organ-threatening ANCA-associated vasculitis requires induction with glucocorticoids plus either rituximab or cyclophosphamide; the RAVE trial showed rituximab to be non-inferior to cyclophosphamide (and superior in relapsing disease) while avoiding gonadal toxicity and bladder cancer risk, making it preferable in this patient. Methotrexate is reserved for non-severe disease and is contraindicated with significant renal impairment. Azathioprine and mycophenolate are maintenance agents and are not adequate for induction in life-threatening disease.
Reference: Stone et al., RAVE trial, N Engl J Med 2010; 2021 ACR/Vasculitis Foundation Guideline for the Management of ANCA-Associated Vasculitis
Question 10 · Thoracic Neoplasms and Lung Cancer
A 71-year-old man with COPD has a right lower lobe non-small cell lung cancer and is being assessed for right lower lobectomy. His preoperative FEV1 is 60% predicted. Using the anatomical segment-counting method (19 total segments, 5 in the right lower lobe), what is his predicted postoperative FEV1?
- AApproximately 30% predicted
- BApproximately 38% predicted
- CApproximately 44% predicted
- DApproximately 55% predicted
Show answer and explanation
Correct answer: C. Approximately 44% predicted
Predicted postoperative FEV1 equals the preoperative value multiplied by (19 minus the number of segments to be removed) divided by 19, so 60 x 14/19 gives approximately 44% predicted. Values above 30% predicted for both ppoFEV1 and ppoDLCO generally indicate acceptable risk, while values below 30% mandate cardiopulmonary exercise testing with peak VO2 measurement. Segment counting overestimates loss when the resected lobe is poorly perfused, in which case quantitative perfusion scanning is more accurate.
Reference: ERS/ESTS Clinical Guidelines on Fitness for Radical Therapy in Lung Cancer Patients, Eur Respir J 2009; ACCP Physiologic Evaluation of the Patient With Lung Cancer, Chest 2013
Free mock vs the full Pulmonology 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 | 525+ |
| Papers | 1 short timed set | 3 to 6 full-length papers, about 175 each |
| Blueprint coverage | 13 of 13 domains | All 13 domains, 260 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 Pulmonology bank
Close your gaps before exam day
- 525+ 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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