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Low-dose x-ray CT is a major research area with high clinical impact. Compressed sensing using view-based sparse sampling and sparsity-promoting regularization has shown promise in simulations, but these methods can be difficult to implement on diagnostic clinical CT scanners since the x-ray beam cannot be switched on and off rapidly enough. An alternative to view-based sparse sampling is interrupted-beam sparse sampling. SparseCT is a recently-proposed interrupted-beam scheme that achieves sparse sampling by blocking a portion of the beam using a multislit collimator (MSC). The use of an MSC necessitates a number of modifications to the standard compressed sensing reconstruction pipeline. In particular, we find that SparseCT reconstruction is feasible within a model-based image reconstruction framework that incorporates data fidelity weighting to consider penumbra effects and source jittering to consider the effect of partial source obstruction. Here, we present these modifications and demonstrate their application in simulations and real-world prototype scans. In simulations compared to conventional low-dose acquisitions, SparseCT is able to achieve smaller normalized root-mean square differences and higher structural similarity measures on two reduction factors. In prototype experiments, we successfully apply our reconstruction modifications and maintain image resolution at quarter-dose reduction level. The SparseCT design requires only small hardware modifications to current diagnostic clinical scanners, opening up new possibilities for CT dose reduction.

Determination of the effect of protocol modifications on diagnostic performance in CT with human observers is extremely time-consuming, limiting the applicability of such methods in routine clinical practice. In this work, we sought to determine whether a channelized Hotelling observer (CHO) could predict human observer performance for the task of liver lesion localization as background, reconstruction algorithm, dose, and lesion size were varied. Liver lesions (5 mm, 7 mm, and 9 mm) were digitally inserted into the CT projection data of patients with normal livers and water phantoms. The projection data were reconstructed with filtered back projection (FBP) and iterative reconstruction (IR) algorithms for three dose levels: full dose (liver CTDIvol  =  10.5  ±  8.5 mGy, water phantom CTDIvol  =  9.6  ±  0.1 mGy) and simulated half and quarter doses. For each of 36 datasets (3 dose levels  ×  2 reconstruction algorithms  ×  2 backgrounds  ×  3 sizes), 66 signal-present and 34 signal-absent 2D images were extracted from the reconstructed volumes. Three medical physicists independently reviewed each dataset and noted the lesion location and a confidence score for each image. A CHO with Gabor channels was calculated to estimate the performance for each of the 36 localization tasks. The CHO performances, quantified using localization receiver operating characteristic (LROC) analysis, were compared to the human observer performances. Performance values between human and model observers were highly correlated for equivalent parameters (same lesion size, dose, background, and reconstruction), with a Spearman's correlation coefficient of 0.93 (95% CI: 0.82-0.98). CHO performance values for the uniform background were strongly correlated (ρ  =  0.94, CI: 0.80-1.0) with the human observer performance values for the liver background. Performance values between human observers and CHO were highly correlated as dose, reconstruction type and object size were varied for the task of localization of patient liver lesions in both uniform and liver backgrounds.

The purpose of this study was to determine the correlation between human observer performance for localization of small low contrast lesions within uniform water background versus an anatomical liver background, under the conditions of varying dose, lesion size, and reconstruction algorithm. Liver lesions (5 mm, 7 mm, and 9 mm, contrast:  -21 HU) were digitally inserted into CT projection data of ten normal patients in vessel-free liver regions. Noise was inserted into the projection data to create three image sets: full dose and simulated half and quarter doses. Images were reconstructed with a standard filtered back projection (FBP) and an iterative reconstruction (IR) algorithm. Lesion and noise insertion procedures were repeated with water phantom data. Two-dimensional regions of interest (66 lesion-present, 34 lesion-absent) were selected, randomized, and independently reviewed by three medical physicists to identify the most likely location of the lesion and provide a confidence score. Locations and confidence scores were assessed using the area under the localization receiver operating characteristic curve (Az LROC ). We examined the correlation between human performance for the liver and uniform water backgrounds as dose, lesion size, and reconstruction algorithm varied. As lesion size or dose increased, reader localization performance improved. For full dose IR images, the Az LROC for 5, 7, and 9 mm lesions were 0.53, 0.91, and 0.97 (liver) and 0.51, 0.96, and 0.99 (uniform water), respectively. Similar trends were seen with other parameters. Performance values for liver and uniform backgrounds were highly correlated for both reconstruction algorithms, with a Spearman correlation of ρ  =  0.97, and an average difference in Az LROC of 0.05  ±  0.04. For the task of localizing low contrast liver lesions, human observer performance was highly correlated between anatomical and uniform backgrounds, suggesting that lesion localization studies emulating a clinical test of liver lesion detection can be performed using a uniform background.