


Study with the several resources on Docsity
Earn points by helping other students or get them with a premium plan
Prepare for your exams
Study with the several resources on Docsity
Earn points to download
Earn points by helping other students or get them with a premium plan
Community
Ask the community for help and clear up your study doubts
Discover the best universities in your country according to Docsity users
Free resources
Download our free guides on studying techniques, anxiety management strategies, and thesis advice from Docsity tutors
A new method for obtaining scintigraphic images of the cardiac blood pool for the study of ventricular wall motion. The method involves using the electrocardiographic (ecg) signal to trigger the scintillation camera during a fixed time interval after the r wave, allowing for the recording of images during two portions of the cardiac cycle. The images obtained can be displayed on a single 8 x 10-in. Film as a set of serial images, each representing a portion of the cardiac cycle. The document also discusses the implementation of the instrument and the advantages of this method over previous approaches.
What you will learn
Typology: Study notes
1 / 4
This page cannot be seen from the preview
Don't miss anything!
The production of “gated―cardiac blood pool im
signal to turn on a scintillation camera during a fixed
occurrence of an R wave ( 1—5). By recording image
diac blood pool during a small portion of the me
ing electrical waveforms.
sive versions of this technique (6,7) make use of a
the setting of two independent intervals referenced to the R wave. This allows simultaneous recording of images during two portions of the cardiac cycle, usually end-systole and end-diastole. However, in
Received June 15, 1976; revision accepted Sept. 24, 1976. For reprints contact : E. A. Silverstein, Sect. of Medical Radiation Physics, Rush-Presbyterian-St. Luke's Medical Center, 1753 W. Congress Parkway, Chicago, IL 60612.
Film Cassette
Multi—Format imager
ControlSignals
L RESET@@J_ —I
jiUn/INSTRUMENTATION AND PHYSICS
Cardiac Blood Pool Imaging over the Complete
Cardiac Cycle with a Multiformat Imager
Edward A. Silverstein, David A. Turner, ErnestW. Fordham, and Anthony Chung-Bin Rush-Presbyterian-St. Luke's Medical Center and Rush Medical College, Chicago, illinois
A new method of obtaining scintigraphic images of the cardiac blood poo for the study of ventricular wall motion is described. The method, which is based upon an inexpensive modification of a commercial multiformat imaging device, yields a set of serial gated images covering the entire car diac cycle. These images may be converted into a film loop to yield a con tinuous motion picture of the mechanical cycle of the heart.
SILVERSTEIN, TURNER, FORDHAM, AND CHUNG-BIN
immediately produces a set of serial images covering
MATERIALS AND METHODS The technique is based on a “multiformat im ager.―* By means of this instrument the complete
To a portion of the cardiac cycle extending over some Mum- Formot preset time interval.
imager records 1, 4, 6, 9, 30, or 42 images on an
the console of the imager. The location on the film
vanced internally or by signals from the scintillation
For our application, external ADVANCEand RESET lines were added to the imager (Fig. 1 ). A pulse on the ADVANCE line moves the image forward to the next film position. A RESET pulse brings the image back to the starting point (Frame 1). The operation of the system is shown schemati
(“SYNC―on Fig. 1 ) to the Imager Control Circuit
ing a SYNC signal, the ICC resets the multiformat imager to Frame 1. The ICC then produces regular
78 RPM
tector was directly above turntable at distance of 15 cm.
all of these methods all data are lost during the por
preselected recording intervals. Another approach (8—11 ) allows recording of images of the cardiac blood pool throughout the
signal are recorded on a suitable medium, such as videotape, computer magnetic tape, or disk. By re playing the data, images of any portion of the cardiac cycle can be obtained. Motion pictures also can be produced. Although no image data are lost with this technique, the procedures involved are relatively complex, expensive, and time-consuming.
inexpensive to implement, simple to
new method of images which is use, and which
,,—..,@ 1
, I
I
, \
.__. —,
( ‘ I
2
I
@ .—
‘$.
,,.—@ f. ti ) _._,,,—..,.
I l\ / s..—,“•
@ I,f_—..._.. ,I ‘
*. * ‘ ) @@/F
. 1
_@IF/@•@@_
‘ @ (^) , I .-..#,‘___%@
@,.___,,,Fi-.
_(I _
‘&)#,...--.‘.@
‘ I ‘.-...‘@f\ “-.-@F
,,
I “@-@•-@@FIG.
_I _
@....•1F,
‘S...-...-•F@
@ (^) __.. .-.,.‘
‘_%.. _I _ ‘.--.. (^) ..—-@ 29f
@^ —.. ‘)
‘S. ‘— (^) —@,i 30ment
shown in Fig. 2. System was run for about 230 cycles.Fixed reference sourceis Counter-clockwise direction of rotation re
denoted by Si and moving source by Sa. suItsfrominversionof filmduring raphy. Dotted circles were drawn in as visual aids.
(^160) JOURNAL OF NUCLEAR MEDICINE
60'Tt sec
LLk 5yncror@zWig Signal
SILVERSTEIN, TURNER, FORDHAM, AND CHUNG-BIN
could be recorded.
ACKNOWLEDGMENTS The authors wish to express their gratitude to Lee Roenigk
ing electrical connections to the Ultimat multiformat imager and for installing the ADVANCE and RESET lines. We are also grateful to Elaine D. Salter for secretarial assistance.
FOOTNOTES
1. ZARET BL, STRAUSS HW, HURLEY PJ, et al. : Left yen tricular ejection fraction and regional myocardial perform ance in man without cardiac catheterization. Circulation 42: Suppl 3; 120, 1970 2. ZARET BL, STRAUSS HW, HURLEY PJ, et al. : A non invasive scintiphotographic method for detecting regional ventricular dysfunction in man. N Engl I Med 284: 1165— 1170, 1971 3. STRAUSS HW, ZARET BL, HURLEY PJ, et al. : A scinti
photographic method for measuring left ventricular ejection fraction in man without cardiac catheterization. Am I Car diol28:575—580, 1971
MID-EASTERNCHAPTER SOCIETY OF NUCLEAR MEDICINE 7th ANNUAL MEETING April 21—23,1977 Stouffer's Hotel Arlington, Virginia
ANNOUNCEMENT AND CALL FOR ABSTRACTS
The 7th Annual Meeting of the SNM Mid-Eastern Chapter will include two full days of scientific con tributions, including both teaching sessionsand selected papers. Prizes will be awarded for the three best individual presentations. Category 1 credit is applicable.
The Program Committee invites the submission of abstracts relevant to all fields of nuclear medicine for consideration by the Committee. Please send abstract (and three copies) containing less than 300 words with suitable supporting data to: Gerald S. Johnston, M.D. Director of Nuclear Medicine National Institutes of Health Room 1B37, Building 10 9000 Rockville Pike Bethesda, Maryland 20014 Co-directors, Scientific Program Committee: Peter T. Kirchner, M.D., and Gerald S. Johnston, M.D. Deadline for abstracts: February 15th, 1977.