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SPECT V/Q-based diagnostic strategy shows comparable 3-month VTE risk to CTPA and planar V/QSPECT V/Q Imaging May Be Reliable for Pulmonary Embolism

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Key Takeaway
Note that while SPECT V/Q showed comparable VTE risks to other methods, non-inferiority was not formally established.

This multicentre randomized controlled trial enrolled 603 patients with suspected pulmonary embolism requiring chest imaging. The study compared a SPECT V/Q-based diagnostic strategy against two other methods: CTPA and planar V/Q-based strategies.

The primary outcome was the 3-month risk of venous thromboembolism (VTE) in untreated patients with a negative workup. In the SPECT V/Q arm, the diagnosis rate was 20.1% (61/303), and the 3-month VTE risk was 0.5% (1/221). In the CTPA arm, the diagnosis rate was 20.7% (31/150) with a 3-month VTE risk of 0.0% (0/107). The planar V/Q arm showed a diagnosis rate of 16.0% (24/150) and a 3-month VTE risk of 0.8% (1/118). The difference in 3-month VTE risk between SPECT V/Q and the combined other arms was 0.0% (95% CI -1.2 to 1.3).

Safety data were not reported, but the trial was prematurely discontinued due to slow recruitment and funding limitations. Because of this early termination, the study did not formally demonstrate non-inferiority of SPECT V/Q to reference standards. While results suggest a low 3-month VTE risk for the SPECT V/Q algorithm, clinical application should be interpreted with caution given the incomplete trial data.

Researchers conducted a multicenter study involving 603 patients who were suspected of having a pulmonary embolism. The goal was to see if using a SPECT V/Q-based diagnostic strategy was as effective as other standard methods, such as CTPA and planar V/Q imaging.

The results showed that the diagnosis rates for pulmonary embolism were similar across different testing methods. Specifically, the SPECT V/Q group had a 20.1% diagnosis rate, while the CTPA group had 20.7% and the planar V/Q group had 16.0%. Additionally, the risk of developing other blood clots within three months was very low in all groups.

It is important to note that this study was stopped early due to slow recruitment and funding issues. Because it ended early, the researchers could not officially confirm if SPECT V/Q is equal to standard methods. While the results suggest it could be a reliable alternative for doctors to use, more complete data would be needed to reach a final conclusion.

What this means for you:
SPECT V/Q imaging shows similar diagnosis rates and low risk levels compared to other pulmonary embolism tests.

Common questions

Is SPECT V/Q a reliable way to find a pulmonary embolism?

The study included 603 patients and found that the SPECT V/Q group had a 20.1% diagnosis rate, which was very similar to the 20.7% rate seen in the CTPA group. While it appears to be a reliable alternative, the trial ended early, so it did not officially prove it is equal to standard methods.

What are the risks of using this imaging method?

The study tracked patients for three months and found very low rates of additional blood clots. The risk was 0.5% for those who had SPECT V/Q, 0.0% for those with CTPA, and 0.8% for those with planar V/Q. No specific adverse events were reported during the study.

How does this compare to other tests like CTPA?

The diagnosis rates were very similar between SPECT V/Q (20.1%) and CTPA (20.7%). The risk of new blood clots within three months was also comparable across both methods. Because the study ended early, doctors should still consult current guidelines for standard care.

Study Details

Study typeRct
Sample sizen = 603
EvidenceLevel 2
Follow-up3.0 mo
PublishedJul 2026
View Original Abstract ↓
BACKGROUND: While single-photon emission computed tomography (SPECT) ventilation/perfusion (V/Q) has been widely adopted for pulmonary embolism (PE) diagnosis, it is not currently endorsed by clinical guidelines due to insufficient evidence. METHODS: We conducted a non-inferiority randomised trial comparing SPECT V/Q-, computed tomography pulmonary angiography (CTPA)- and planar V/Q-based diagnostic strategies using a 2:1:1 allocation. The primary end-point was the 3-month risk of venous thromboembolism (VTE) in untreated patients with a negative workup, comparing SPECT V/Q to the combined CTPA and planar V/Q arms. A non-inferiority margin of 1% absolute difference in 3-month VTE risk was defined. Secondary outcomes included PE diagnosis rates. The trial ended prematurely in October 2024 due to slow recruitment and funding limitations. RESULTS: From July 2017 to October 2024, 603 patients were randomised. PE was diagnosed in 61/303 (20.1%) in the SPECT V/Q arm, 31/150 (20.7%) in the CTPA arm and 24/150 (16.0%) in the planar V/Q arm. The 3-month VTE risk in patients left untreated after a negative workup was 0.5% (1/221) for SPECT V/Q, 0.0% (0/107) for CTPA and 0.8% (1/118) for planar V/Q. The difference in outcome between SPECT V/Q and the combined arms was 0.0% (95% CI -1.2-1.3%). CONCLUSION: After being prematurely discontinued, this randomised trial did not demonstrate the non-inferiority of a SPECT V/Q-based strategy to reference standards for PE diagnosis. However, the results suggest a low 3-month VTE risk in patients managed using a SPECT V/Q-based diagnostic strategy. Among patients with clinically suspected acute PE requiring chest imaging, a SPECT V/Q-based algorithm might be a reliable alternative in clinical practice.
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