Abstract
The development that has had the greatest influence on PET camera design in the last five years has undoubtedly been the introduction of full volume, septa-less acquisition and reconstruction. 3D PET, as it is now commonly referred to, was developed in the search for increased sensitivity and grew out of large area gas detector PET systems [1]. It was based on the original work of 3D reconstruction from electron micrographs of biomacromolecules by Vanstein and Orlov [2,3]. The translation of these ideas to multiring bismuth germanate (BGO) tomography was first implemented at the Hammersmith Hospital in a collaboration with groups from Geneva and Brussels, encouraged by the manufacturer CTI [4], and was quickly followed by others [5,6]. This has realised an increase in sensitivity of around fivefold for most multiring systems. It has allowed the development of full-time 3D systems based on BGO or NaI(Tl) detectors. The impact of 3D PET has been dramatic. In neuroscience, statistical mapping of 3D rCBF “activation” studies in single subjects, rather than groups, became possible. The duration over which 11C-labelled radiotracers could be studied was greatly increased and the quality of each datum was improved, which aids in better modelling and functional mapping results. At this point in time, while application of 3D PET to other regions of the body has been more protracted, it is nevertheless making slow progress [7,8,9].
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Bailey, D.L. (1998). Recent Trends in PET Camera Designs. In: Gulyás, B., Müller-Gärtner, H.W. (eds) Positron Emission Tomography: A Critical Assessment of Recent Trends. NATO ASI Series, vol 51. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-4996-9_5
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