MRCP(UK) Part 1 study materials
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Suspected pulmonary embolism in a patient who cannot have contrast

MRCP(UK) Part 1 · Put your knowledge to work in context.

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Suspected pulmonary embolism in a patient who cannot have contrast

A 58-year-old woman presents five days after an uncomplicated total knee replacement with sudden pleuritic chest pain and breathlessness. She is normally independent and has no prior VTE. Observations: heart rate 112/min, respiratory rate 24/min, SpO2 93% on air, blood pressure 128/78 mmHg, temperature 37.4°C. Chest examination is clear. She has known chronic kidney disease with creatinine 210 micromol/L and eGFR 28 mL/min/1.73m², and a documented anaphylactoid reaction to iodinated contrast. ECG shows sinus tachycardia. Chest radiograph is normal.

1. How would you assess the clinical probability of pulmonary embolism here, and what does that determine about the diagnostic pathway?

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Probability assessment

  • Using the Wells score: clinical signs of DVT (0), PE as likely as or more likely than an alternative diagnosis (+3), heart rate >100 (+1.5), immobilisation/surgery within 4 weeks (+1.5), previous VTE (0), haemoptysis (0), malignancy (0). Total ≈ 6 → PE likely.
  • In the 'PE likely' group, a D-dimer is not used to rule out PE: it lacks the negative predictive value needed, and the D-dimer will be raised anyway after recent surgery. The pathway goes straight to imaging.

Why this matters

  • The judgement point is that the Wells category, not the D-dimer, drives the next step. A negative D-dimer here would not be reassuring.
  • She is haemodynamically stable (BP 128/78), so she is not in high-risk PE; she does not need immediate thrombolysis, and there is time to confirm the diagnosis. But confirmation must not be so delayed that she goes untreated - if imaging is delayed, start therapeutic anticoagulation empirically unless contraindicated.

2. Which imaging strategy would you choose, and why is the obvious first-line test problematic?

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CT pulmonary angiography is the usual first-line test but is relatively contraindicated here:

  • eGFR 28 mL/min/1.73m² means contrast nephropathy risk is significant, and she has a prior anaphylactoid reaction to iodinated contrast.

Preferred option: ventilation–perfusion (V/Q) SPECT imaging.

  • V/Q imaging requires no iodinated contrast and is validated for PE diagnosis.
  • It is most useful when the chest radiograph is normal - as here - because a normal radiograph removes many causes of matched defects.
  • A normal V/Q scan effectively excludes PE; a high-probability scan with compatible clinical probability confirms it.

If V/Q is non-diagnostic:

  • Do not simply abandon imaging and treat blindly for months. Options include catheter-directed or non-contrast MR angiography where available, or a discussion weighing the risk of a second contrast exposure against the harm of missed PE.
  • Meanwhile she should be anticoagulated if there is no bleeding contraindication.

The answer being tested is the deliberate choice of a non-contrast test rather than defaulting to CTPA and accepting renal injury and a repeat allergic reaction.

3. If PE is confirmed, how does her renal function alter your choice of anticoagulant?

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Risk stratification first

  • Stable blood pressure and no troponin/BNP evidence of right ventricular strain would place her in the low-risk group, but she has multiple comorbidities, so she likely needs admission at least initially.

Anticoagulant choices with eGFR 28:

  • LMWH (enoxaparin) is acceptable but should be dose-adjusted for renal function (often 1 mg/kg once daily rather than twice daily) or monitored with anti-Xa levels; accumulation is a real risk.
  • Fondaparinux is best avoided: it is contraindicated at creatinine clearance below 30 mL/min because of accumulation and bleeding risk.
  • DOACs: apixaban is the least renally dependent and can be used with caution in this range; dabigatran and edoxaban are less suitable, and rivaroxaban should be avoided at this level of impairment.
  • Unfractionated heparin is the safest choice if renal function is unstable or likely to deteriorate further, because it is not renally cleared and is easily reversed.

Practical points: correct the eGFR for body size, recheck renal function during intercurrent illness, and give a clear sick-day plan. Duration is at least 3 months and should be reviewed against whether the provoking factor (surgery) has resolved - provoked VTE after major surgery may justify stopping at 3 months, whereas unprovoked VTE warrants consideration of extended therapy.