Determining the lesion detectability index along the axial and radial direction for multi-pinhole SPECT

The improved resolution capabilities of pinhole SPECT makes it an ideal imaging modality to study various human disease models in small animals. However, the sensitivity profile of the sampled image space is non-uniform and depends on the relative location of the pinhole and the imaging geometry use...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Bal, G., Zixiong Cao, Acton, P.D.
Format: Tagungsbericht
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The improved resolution capabilities of pinhole SPECT makes it an ideal imaging modality to study various human disease models in small animals. However, the sensitivity profile of the sampled image space is non-uniform and depends on the relative location of the pinhole and the imaging geometry used. Hence, it will be desirable to place the target volume in the same plane as the pinhole for better count statistics. In this work we study the lesion detectability index of single pinhole (SP) and multi-pinhole (MP) for lesions placed at various locations in the field-of-view (FOV). A uniform cylinder filled with activity equivalent to those observed in a mouse scan was simulated (14 MBq, 10 minutes study). Lesions (1.4 mm) were placed at predetermined locations and multiple noise realizations were performed. The reconstructed images were evaluated using non-prewhitening (NPWF) analysis to accurately study the lesion detectability in the axial and radial directions. The overall lesion detectability of MP was found to be uniform and about 1.6 times better than that of the SP case. Our studies shows that the improved sensitivity (84 cps/MBq for SP and 612 cps/MBq for MP) and uniform sampling of the image space by the MP results in improved lesion detectability of a larger volume for the same acquisition time.
ISSN:1082-3654
2577-0829
DOI:10.1109/NSSMIC.2005.1596650