Pulmonary embolism: ventilation/perfusion imaging
To check whether a blood clot has lodged in the lung's blood vessels, a scan compares which parts of the lung get air (ventilation) with which parts get blood flow (perfusion); a clot shows up as an area that is ventilated but not perfused.
Overview
Ventilation/perfusion (V/Q) scintigraphy diagnoses or excludes acute pulmonary embolism by comparing two maps of the lung obtained in the same sitting: a perfusion map, made by injecting Tc-99m-labelled macroaggregated albumin (MAA) particles that lodge in pulmonary capillaries in proportion to blood flow, and a ventilation map, made with an inhaled agent such as Technegas or krypton-81m gas. A pulmonary embolus blocks a branch of the pulmonary artery, so the perfusion map shows a wedge-shaped defect in that lung segment while the corresponding ventilation map remains normal - a mismatch that is the scintigraphic hallmark of embolism, as opposed to a matched defect where both are reduced together, typical of parenchymal lung disease rather than embolism.
The 2019 EANM guideline for V/Q SPECT strongly recommends tomographic (SPECT) rather than planar imaging wherever available, since SPECT has higher sensitivity and specificity, and defines a positive study as a mismatch of at least one segment or two subsegments conforming to pulmonary vascular anatomy; a normal perfusion study, respecting the anatomical boundaries of the lungs, excludes pulmonary embolism outright regardless of any other finding. Combining V/Q SPECT with a low-dose CT further improves specificity, particularly in patients with coexisting chronic obstructive pulmonary disease, heart failure or pneumonia, all of which can otherwise complicate interpretation.
V/Q scanning has a substantially lower radiation dose than CT pulmonary angiography, no iodinated contrast requirement, and virtually no absolute contraindications, which makes it the preferred first-line test in pregnancy, in patients with renal impairment or contrast allergy, and in younger patients where lifetime radiation exposure is a bigger consideration. ACR appropriateness criteria and SNMMI/EANM/ASH/ACCP/ACEP appropriate use criteria both support V/Q scanning or CT pulmonary angiography as appropriate first-line tests for suspected pulmonary embolism with intermediate or high pre-test probability, with the choice between them driven by patient factors (pregnancy, renal function, chest radiograph findings, local availability) rather than one modality being universally superior.
State of the art
- The 2019 EANM guideline for ventilation/perfusion SPECT for diagnosis of pulmonary embolism and beyond is the current European reference standard, recommending Technegas or krypton gas over Tc-99m-DTPA aerosol in patients with COPD and SPECT over planar imaging throughout.
- The SNMMI-led multi-society (with EANM, ASH, STS, ACCP, ACEP) appropriate use criteria for V/Q imaging in pulmonary embolism, most recently updated 2020, give scenario-by-scenario appropriateness ratings endorsed by both the American Society of Hematology and American College of Emergency Physicians.
- V/Q SPECT/CT combines the mismatch read with low-dose anatomical correlation, improving specificity in patients with coexisting COPD, heart failure or pneumonia that would otherwise confound interpretation.
Show survival figures (1)
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
- Pulmonary embolism has an estimated annual incidence in the United States of roughly 60-115 cases per 100,000 people, is part of a broader venous thromboembolism burden affecting up to 900,000 Americans a year, and is the third most common cause of cardiovascular death after coronary artery disease and stroke.
Ventilation/perfusion SPECT (or SPECT/CT), interpreted per EANM criteria: mismatch of at least one segment or two subsegments confirms PE, normal perfusion excludes it.
CT pulmonary angiography or V/Q scanning, either considered appropriate first-line by ACR and SNMMI/multi-society appropriate use criteria, chosen by local availability and patient factors.
Subtypes & biomarkers
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Dated changes read from the records linked to this indication: approvals, regulatory steps, reported trials, guideline versions and milestones. Newest first; no date is inferred.
All 5 changes by month →- 2026-09-22This recordPulmonary embolism: ventilation/perfusion imagingFacts on this page last checked
When this page itself was last checked or edited.
- 2023-09-29RegulatoryTechnegas (technetium Tc-99m labelled carbon inhalation aerosol)Technegas (technetium Tc-99m labelled carbon inhalation aerosol): approval (US)
FDA approval of NDA 022335 (Cyclomedica Australia), Type 3 new dosage form
- 2023ApprovalTechnegas (technetium Tc-99m labelled carbon inhalation aerosol)Technegas (technetium Tc-99m labelled carbon inhalation aerosol) approved in US
Visualisation of pulmonary ventilation, and evaluation of pulmonary embolism when paired with perfusion imaging, in adults and children aged 6 and over
- 2020ApprovalTechnetium Tc-99m albumin aggregated (MAA)Technetium Tc-99m albumin aggregated (MAA) approved in US
Lung scintigraphy as an adjunct in the evaluation of pulmonary perfusion, and peritoneovenous shunt patency
- 1987ApprovalTechnetium Tc-99m albumin aggregated (MAA)Technetium Tc-99m albumin aggregated (MAA) approved in US
Lung scintigraphy as an adjunct in the evaluation of pulmonary perfusion, and peritoneovenous shunt patency
What is in development for Pulmonary embolism: ventilation/perfusion imaging, drawn from the whole corpus: 1 items. Drugs are grouped by the most advanced trial phase they have reached anywhere; approved treatments sit under standard of care. Technologies are the methods being tested for this cancer, trials are the studies recorded here, and ideas are proposals not yet in a trial.
Trials reported · 1
- CYC-009: Technegas versus xenon-133 ventilation imaging · phase 3 · historic
Open problems and what is being done
Probabilistic (PIOPED-style) interpretation categories are now considered flawed by EANM and have been replaced by a simpler binary/nondiagnostic scheme, but older planar-based probabilistic reporting persists in some centres.
A 'nondiagnostic' or intermediate-probability result still occurs in a meaningful minority of studies and usually requires a second test (CT pulmonary angiography or clinical follow-up) to resolve.
Real-world uptake of SPECT over planar V/Q imaging, and of Technegas over older ventilation agents, remains uneven internationally, driven by equipment and radiopharmaceutical availability rather than by guideline preference alone.
Trials
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Landmark trials
Direct links plus the targets, companies, and technologies of this cancer's products.
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2technologies
3drugs
2companies
1trials
1Latest papers
topQuery for this indication: (TITLE:"Pulmonary embolism: ventilation/perfusion imaging" OR ABSTRACT:"Pulmonary embolism: ventilation/perfusion imaging") AND (treatment OR therapy OR trial OR survival OR diagnosis). Results are unfiltered search hits about Pulmonary embolism: ventilation/perfusion imaging, not a curated reading list.
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