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Does intravenous technetium-99m-labeled deimmunized antifibrin Fab' fragments combined with SPECT imaging allow visualization of pulmonary emboli and deep vein thrombi in a dog model?
Does intravenous technetium-99m-labeled deimmunized antifibrin Fab' fragments combined with SPECT imaging allow visualization of pulmonary emboli and deep vein thrombi in a dog model?
Technetium-99m-labeled antifibrin Fab' fragments combined with SPECT imaging successfully visualized experimentally induced pulmonary emboli and deep vein thrombi in a canine model.
Demonstrates feasibility of antifibrin Fab' SPECT in canine PE/DVT; leaves open clinical translation.
Previous attempts to diagnose thromboemboli using radiolabeled antibodies and nuclear medicine imaging have been disappointing. We present the results of experiments with intravenous technetium-99m-labeled deimmunized antifibrin Fab' fragments to diagnose thromboemboli using single photon emission computed tomography (SPECT), a highly sensitive scintigraphic imaging technique. Pulmonary emboli (PEs) and lower extremity deep vein thrombi (DVTs) were formed in five dogs, then technetium-99m-labeled Fab' ( approximately 400 mg, approximately 260 MBq) were injected via forelimb veins. Thoracic and lower extremity SPECT scans were performed at 2-hour intervals after antibody infusion to visualize the thromboemboli. Four hours after antibody infusion, all PEs and DVTs of mass 0.4 g or greater were clearly visualized on SPECT scans as 'hot spots' within the lungs and legs, respectively. PEs (0.48 +/- 0.09 g) were intensely radiolabeled, yielding clot/blood radioactivity ratios of 22.8 +/- 5.6. DVTs (0.45 +/- 0.31 g) also had high clot/blood ratios (11.7 +/- 2.6). Infusion of these radiolabeled antibody fragments, combined with SPECT, produces clear images of PEs and DVTs within a clinically feasible time frame. The technique reliably identified even peripheral thromboemboli of relatively small size, which are difficult to diagnose with currently available imaging techniques, and may enable imaging of PEs, DVTs, or both in the same patient.
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Morris et al. (2004) studied this question.
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