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Thoracic Imaging 2003 - Society of Thoracic Radiology

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Multidetector CT: More Slices and Beyond<br />

Patricia J. Mergo, M.D.<br />

Associate Pr<strong>of</strong>essor<br />

University <strong>of</strong> Florida<br />

The development <strong>of</strong> multidetector CT (MDCT) represents a<br />

quantum leap in CT technology. The clinical advances made possible<br />

by the advent <strong>of</strong> MDCT represent one <strong>of</strong> the largest developments<br />

in current technology in radiologic imaging. New 16<br />

slice scanners are in production by several vendors including GE,<br />

Siemens, Philips and Toshiba. The biggest clinical advance made<br />

possible with MDCT is CT angiography. The capabilities <strong>of</strong> thoracic<br />

imaging are affected significantly with multislice CT with<br />

subsequent improved pulmonary arterial CT angiography (CTA),<br />

as well as thoracic aortic CTA and more recently coronary artery<br />

CTA, using cardiac gating. All these are accountable to the ability<br />

to obtain volumetric scanning <strong>of</strong> the region <strong>of</strong> interest, with<br />

imaging approaching now or equaling isotrophic voxels.<br />

When considering multislice CT, important technical considerations<br />

need to be taken into account including considerations<br />

for pitch, collimation, scan slice pr<strong>of</strong>ile, noise and radiation<br />

dose.<br />

Pitch is an important consideration since with a higher pitch,<br />

a given volume <strong>of</strong> tissue can be scanned in a shorter time period.<br />

The advantages for scanning at a higher pitch are well<br />

appreciated when fast scanning is needed as in CT angiography.<br />

The scanning at a higher pitch does result in widening <strong>of</strong> the<br />

slice width pr<strong>of</strong>ile, however. The dosage should remain the<br />

same, technically speaking, but dosage is in reality potentially<br />

increased if adjustments are made in the mA to compensate for<br />

limitations in slice width pr<strong>of</strong>ile. In single slice CT pitch is<br />

defined as table movement per rotation / slice collimation. For<br />

multislice CT, pitch is defined as table movement per rotation /<br />

single slice collimation. This implies that with a 0.5 second<br />

scanner, with 2 rotations per second, that if the table travels 16<br />

mm in a second and 1 mm collimation is used, then the pitch<br />

would be 8.<br />

With SDCT the true width or the "effective slice thickness"<br />

<strong>of</strong> the reconstructed image is influenced by pitch and the reconstruction<br />

algorithm used (wide vs. slim). With a pitch <strong>of</strong> 2 and a<br />

slim algorithm the "effective slice thickness" may increase by<br />

27%. With MDCT these factors are effectively corrected using<br />

axial interpolation algorithms.<br />

MDCT yields increased flexibility <strong>of</strong> scanning relative to<br />

slice collimation and slice width. With single detector CT the<br />

slice collimation and the slice width are the same and they cannot<br />

be modified once the scans are obtained. In MDCT, the<br />

detector collimation is chosen prior to scanning. Once the<br />

images are obtained, the images can be reconstructed at varying<br />

slice widths, such as 1 mm, 2.5 mm, 5 mm, and 10 mm slice<br />

thickness. The thinner section imaging allows higher resolution<br />

scanning, albeit with increased noise, for high resolution scanning<br />

<strong>of</strong> pulmonary parenchyma or CTA. The data obtained can<br />

be considered true volume data sets for reconstruction at varying<br />

slice width. The ability to volumetrically manipulate the<br />

data and reconstruct it at various slice widths is dependent on<br />

the initial collimation.<br />

Image noise is altered by several factors including mAs, kV,<br />

slice thickness, collimation and patient size. These factors are a<br />

trade <strong>of</strong> for thinner section imaging that is <strong>of</strong>ten required with<br />

CT angiographic studies.<br />

Since with MDCT the acquisition time for CT is significantly<br />

shortened, for instance, enabling acquisition <strong>of</strong> imaging <strong>of</strong><br />

the thorax for pulmonary embolism detection in time periods as<br />

short as 9 seconds, contrast material administration pr<strong>of</strong>iles are<br />

subsequently altered. New scan protocols are optimized for contrast<br />

injections depending on the organ or structure scanned. In<br />

general, higher injection rates result in higher level <strong>of</strong> arterial<br />

enhancement suitable for CT angiography. Similarly, protocols<br />

with shorter injection times with higher osmolality contrast have<br />

been proposed to yield improved imaging. Scan timing can be<br />

optimized using bolus triggering or test injection techniques.<br />

The changes in scanning that we have talked about can<br />

quickly result in information overload in terms <strong>of</strong> the amount <strong>of</strong><br />

data generated from the scans. For this reason, 3D processing <strong>of</strong><br />

scans becomes crucial in order to adequately display the findings<br />

to the clinician. This is especially important in CT angiographic<br />

studies, and in the chest can be most helpful for the<br />

evaluation <strong>of</strong> the airways or for the detection <strong>of</strong> pulmonary<br />

embolus.<br />

Ultimately, for many studies, although thin section imaging<br />

is obtained, reconstruction at thicker slices for interpretation<br />

results in a compromise for ease <strong>of</strong> interpretation <strong>of</strong> the axial<br />

images, while 3D reconstructions are performed on the thinner<br />

section images for improved display <strong>of</strong> the pertinent findings.<br />

47<br />

SUNDAY

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