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Journal of Nuclear Medicine Vol. 42 No. 4 633-635
© 2001 by Society of Nuclear Medicine


INVITED COMMENTARY

Merging the Instrumentation Evolution

I. George Zubal

Yale University School of Medicine, New Haven, Connecticut


    INTRODUCTION
 TOP
 INTRODUCTION
 REFERENCES
 
After reading the interesting article by Wong et al. (1) in this issue of The Journal of Nuclear Medicine on the state-of-the-art hardware developments in nuclear medicine imaging instrumentation, it is hard to keep one’s editorial comments away from historic references. The first nuclear medicine imaging device reported in the literature was the rectilinear scanner (2) and was used for imaging 131I’s single photons. That same year, time coincidence circuitry was used, allowing two opposing detectors to localize annihilation radiation detected from positron emitters (3). One can speculate (I believe correctly) that the front-ends (NaI crystal, photomultipliers [PMTs], preamplifiers, amplifiers, and energy windowing components) of these two devices were quite identical. Yet, since then, PET rings and single-photon planar cameras have been separated stereotypically into two species of instruments used in our profession. When and how did that evolve, if the very first two devices, aside from the coincidence circuitry itself, contained electronics that were virtually identical?

Entertain for a moment the oversimplified statement: PET rings and nuclear medicine Anger cameras evolved into their separate characteristic geometries and specialized electronics because of pulse pileup effects. I believe there is some interesting truth and historic perspective to this. The earliest PET instruments relied on two opposing NaI-PMT probes that electronically determined the line along which two back-to-back annihilation photons traveled. The position of each of the two photon interactions was determined by the physical position of the small detector itself. The detector is wide open (no collimator) and a very high number of events must be processed in the constant search for two simultaneous events. By comparison, the earliest camera built by Hal Anger required a lead collimator to be placed in front of the NaI crystal, and several PMTs behind the crystal determined to which position on the crystal (i.e., through approximately which hole in the collimator) the single photon traveled. A typical lead collimator stops >99% of the photons arriving to the camera face. Hence, these two different modes of photon detection (PET and planar imaging) defined the geometry and electronics into which these two instruments would separately develop. PET detectors evolved into smaller, more numerous elements (each with its own electronic processing channel or with minimal sharing). Anger camera crystals became larger in area over the years, whereas smaller, more numerous PMTs required that more radiation events be processed by shared electronics. Hence, the evolution of the two well-known species of instruments in nuclear medicine: multiple small-crystal PET rings and large-field-of-view SPECT cameras orbiting around the patient on sturdy gantries.

The hybrids of these two species have never been very popular. The multicrystal camera, made popular by Biard Atomic in the 1970s (4), found application in cardiac first-pass studies. Scinticor and thereafter Picker International (now Marconi Medical Systems) marketed this unit under the name of SIM-400 (5). Despite the parallel-hole collimator, counting rates in this camera could approach or exceed 1 million per second because the camera at times was clinically exposed to up to 1,000 MBq of activity. However, one does not see many of these in the field.

A 1976 publication (6) showed that two opposing large-field-of-view cameras could be used to acquire PET data and even suggested that the bare crystal be filtered to improve the counting rate capabilities. One major problem (it was obviously realized) with this geometry was that many nearly simultaneous events needed to be processed by the electronics behind the large-field-of-view crystals (causing pulse pileup). So, wasn’t this pulse pileup problem solved earlier? Why is this article by Wong et al. (1) such an interesting contemporary contribution to JNM? Three things come to mind:

Without a doubt, the authors have taken advantage of some of the most recent electronic innovations to make this advanced front-end possible. My only regret in reading this article is that clearly the most obvious and needed application for such acquisition hardware is for measuring 511-keV annihilation radiation. Although it is a reasonable proof of principle to operate this circuitry at 140 keV, I believe it is a nontrivial step to confirm that it also behaves as expected at higher energies. Because the authors state that "...the count-rate capability of the HYPER electronics for 18F is expected to be similar or better," clearly some adjustments must be made to accommodate the differences that will appear at higher energies. Indeed, perhaps some preliminary tests could have been presented using 511 keV. This would have relieved some apprehension as to how difficult it will be to operate this hardware at higher energies. This is akin to designing a supersonic jet and testing it at subsonic speeds. But I am confident that the investigators will break this barrier soon.

Remember also that at this same time, SPECT imaging with Anger-type cameras was first seriously being developed. The original single-head orbiting camera could not supply sufficient counts within a reasonable imaging time for acceptably low-noise SPECT images. The first triple-head camera was described in 1980 (12), and the first images using this design were reported in 1985 (13). I think it is safe to say that much effort was spent in the early to middle 1980s by the major camera manufacturers on improving the gantry designs, on securely affixing Anger-type cameras to gantries, and on designing the mechanics necessary to accurately orbit the cameras around the patient.

Finally, I will make one nontechnical point regarding nuclear medicine instruments. In the last decade, the medical care suppliers (insurance companies) have exerted a strong financial pressure to deliver clinical diagnoses as cheaply as possible. I believe this has created a strong impetus to simplify and merge imaging modalities. I reread Dr. Wagner’s Highlights of the 1995 Society of Nuclear Medicine annual meeting (14) with great interest and retrospective insight, in which he "... asked the assembled technologists at this meeting to try to stop using the terms PET and SPECT, replacing these terms with emission tomography (ET)... . Five years from now, we may not be referring to SPECT or PET scanners, only ET scanners." I believe that his prediction has to a great extent come true. Multiple-head Anger-type cameras are described as PET capable, as operating in coincidence mode, and one manufacturer uses a particularly interesting product name, "gammaPET." Is it a gamma camera? Or is it a PET instrument? The line has been blurred.

Hence, another oversimplified statement would be: The merger of PET scanners and Anger-type large-field-of-view cameras is being accomplished by solving the pulse pileup problem. And this is exactly the problem on which Wong et al. (1) focus. Clearly, other improvements, such as development of axial filters, implementation of multizone independent processing areas on the crystal face, thicker crystals, and even the national network for delivering. 18F-FDG to most hospitals, have contributed to the possibility of imaging positron emitters using upgraded nuclear medicine cameras. From an instrumentation point of view, solving the pulse pileup problem continues to be the central issue. From this point of view, the article by Wong et al. is quite central to the new developments occurring in nuclear medicine imaging and should be remembered as one of the central contributions to merging PET and SPECT into an ET scanner.

It is obvious to everyone that computers and software have been leading the improvements in nuclear medicine imaging, but faster acquisition electronics (albeit less highlighted) are making just as important an impact on the evolution of our imaging systems. Maximum counting rates of Anger-type cameras have increased from <100,000 counts per second (in the 1960s–1970s) and approached 500,000 in the 1990s. The type of acquisition hardware development presented here promises to make counting rates of a few or several millions per second routinely obtainable in the near future. It is exactly this type of engineering that promises to complete the cycle of nuclear medicine instrumentation evolution, whereby the same front-end electronics is used to detect either 511-keV coincident annihilation radiation or 140-keV single-photon events. I do not mean to say that dedicated PET rings and dedicated collimated large-field-of-view SPECT cameras will disappear. They will not. However, I do believe that perhaps, finally, one hybrid of these two species has found an environment in which it can thrive.


    FOOTNOTES
 
Received Nov. 13, 2000; revision accepted Dec. 5, 2000.

For correspondence or reprints contact: I. George Zubal, PhD, Department of Diagnostic Imaging, Yale University School of Medicine, BML 332, 333 Cedar St., New Haven, CT 06510.


    REFERENCES
 TOP
 INTRODUCTION
 REFERENCES
 

  1. Wong W-H, Li H, Uribe J, Baghaei H, Wang Y, Yokoyama S. Feasibility of a high-speed gamma-camera design using the high-yield-pileup-event-recovery method. J Nucl Med 2001;42:624–632.[Abstract/Free Full Text]
  2. Cassen B, Curtis L, Reed C, et al. Instrumentation of I-131 used in medical studies. Nucleonics 1951;9:46–50.
  3. Wrenn FR, Good ML, Handler P. The use of positron-emitting radioisotopes for the localization of brain tumors. Science 1951;113:525–527.[Free Full Text]
  4. Early PJ. Planar imaging. In: Early PJ, Sodee DB, eds. Principles and Practice of Nuclear Medicine 2nd ed. St. Louis, MO: Mosby; 1995:252.
  5. Benari B, Kiat H, Erel J, et al. Repeatability of treadmill exercise ejection fraction and wall motion using technetium 99m-labeled sestamibi first-pass radionuclide ventriculography. J Nucl Cardiol 1995;2:478–484.[Medline]
  6. Muehllehner G, Buchin MP, Dudek JH. Performance parameters of a positron imaging camera. IEEE Trans Nucl Sci 1976;23:528–537.
  7. Mankoff DA, Muehllehner G, Karp JS. The high count rate performance of a two-dimensionally position-sensitive detector for positron emission tomography. Phys Med Biol 1989;34:437–456.[Medline]
  8. Zeigler SI, Enterrottacher A, Boening G, Nieland P, Kretschko J, Schwaiger M. Performance characteristics of a dual head coincidence camera for the detection of small lesions [abstract]. J Nucl Med 1997;38.(suppl):206P.
  9. Wong WH, Li H, Uribe J. A high count rate positioned decoding and energy measuring method for nuclear cameras using Anger logic detectors. IEEE Trans Nucl Sci 1998;45:1122–1127.
  10. Ter-Pogossian MM, Ficke DC, Tamamoto M, et al. Super PETT I: a positron emission tomograph utilizing photon time of flight information. IEEE Trans Med Imaging. 1982;MI1.:179–187.
  11. Lewellen TK. Time-of-flight PET. Semin Nucl Med 1998;28:268–275.[Medline]
  12. Lim CB, Chang LT, Jaszczak RJ. Performance analysis of a three camera configuration for single photon emission computed tomography. IEEE Trans Nucl Sci 1980;27:559–568.
  13. Lim CB, Gottschalk S, Walker R, et al. Triangular SPECT system for 3-D total organ volume imaging: design concept and preliminary imaging results. IEEE Trans Nucl Sci 1985;32:741–747.
  14. Wagner HN Jr. A new era of certainty. J Nucl Med 1995;36:13N–15N., 24N–28N.[Free Full Text]




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