Literature DB >> 11202456

Characteristics of a new fully programmable blood sampling device for monitoring blood radioactivity during PET.

R Boellaard1, A van Lingen, S C van Balen, B G Hoving, A A Lammertsma.   

Abstract

The first performance tests of a new fully programmable blood sampling device for monitoring blood radioactivity during positron emission tomography (PET) are described. Blood is withdrawn through 1-mm internal diameter tubing using an infusion pump which can be operated at rates varying from 0 to 600 ml/h. Activity in blood is measured by a 6-cm-thick bismuth germanate crystal connected to a photomultiplier tube and multichannel analyser (MCA) which are positioned within 6 cm lead shielding. Positioning of the tubing is an exact and simple procedure. The minimal readout time of the MCA is 1 s. Two independent energy windows can be set. Operation of the pump and MCA is fully controlled by a PC, i.e. sampling time, interval time and pump rate can be varied at any time during the PET scan by user-defined scripts. A number of characteristics of the new system were studied, such as sensitivity, dead time, linearity, effect of background radiation and pump rate as a function of input pressure. In addition, dispersion was measured as a function of pump rate. Finally, first clinical results were compared with manual samples. The sensitivity equalled 0.7 and 0.2 cps/Bq for 511- and 1022-keV 30% energy windows, respectively, and the system dead time was 500 ns. The system remained linear within 2% with activity concentrations up to 2.5 MBq/cc. Short-term reproducibility was better than 3% for a 1-h period. Long-term reproducibility was about 5% (ISD), which was mainly caused by variation in the diameter of the tubing. If the device was positioned in such a way that maximum shielding was directed towards the patient, the effects of background radiation from the patient on the measured activity concentration for clinically relevant conditions was minimal (<3%). Pump rate varied with input pressure, but remained constant for a given pressure. Dispersion constants smaller than 0.14 s(-1) were observed for pump rates higher than 300 ml/h, indicating that the system dispersion is small. Clinical data showed an excellent agreement to within 3% (ISD) between the results obtained with the new system and manual samples. With the continuous blood sampler radioactivity in blood can be measured accurately during the entire course of the PET scan. Furthermore, the system is fully programmable allowing adjustment of all parameters during a single PET scan.

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Year:  2001        PMID: 11202456     DOI: 10.1007/s002590000405

Source DB:  PubMed          Journal:  Eur J Nucl Med        ISSN: 0340-6997


  48 in total

Review 1.  Determination of the Input Function at the Entry of the Tissue of Interest and Its Impact on PET Kinetic Modeling Parameters.

Authors:  M'hamed Bentourkia
Journal:  Mol Imaging Biol       Date:  2015-12       Impact factor: 3.488

2.  Evaluation of basis function and linear least squares methods for generating parametric blood flow images using 15O-water and Positron Emission Tomography.

Authors:  Ronald Boellaard; Paul Knaapen; Abraham Rijbroek; Gert J J Luurtsema; Adriaan A Lammertsma
Journal:  Mol Imaging Biol       Date:  2005 Jul-Aug       Impact factor: 3.488

3.  Image-derived input functions for PET brain studies.

Authors:  Jurgen E M Mourik; Mark Lubberink; Alie Schuitemaker; Nelleke Tolboom; Bart N M van Berckel; Adriaan A Lammertsma; Ronald Boellaard
Journal:  Eur J Nucl Med Mol Imaging       Date:  2008-11-22       Impact factor: 9.236

4.  Comparison of velocity- and acceleration-selective arterial spin labeling with [15O]H2O positron emission tomography.

Authors:  Sophie Schmid; Dennis F R Heijtel; Henri J M M Mutsaerts; Ronald Boellaard; Adriaan A Lammertsma; Aart J Nederveen; Matthias J P van Osch
Journal:  J Cereb Blood Flow Metab       Date:  2015-03-18       Impact factor: 6.200

5.  Mapping human brain fatty acid amide hydrolase activity with PET.

Authors:  Pablo M Rusjan; Alan A Wilson; Romina Mizrahi; Isabelle Boileau; Sofia E Chavez; Nancy J Lobaugh; Stephen J Kish; Sylvain Houle; Junchao Tong
Journal:  J Cereb Blood Flow Metab       Date:  2012-12-05       Impact factor: 6.200

6.  Comparison of HRRT and HR+ scanners for quantitative (R)-[11C]verapamil, [11C]raclopride and [11C]flumazenil brain studies.

Authors:  Floris H P van Velden; Syahir M Mansor; Daniëlle M E van Assema; Bart N M van Berckel; Femke E Froklage; Shaonan Wang; Robert C Schuit; Marie-Claude Asselin; Adriaan A Lammertsma; Ronald Boellaard; Marc C Huisman
Journal:  Mol Imaging Biol       Date:  2015-02       Impact factor: 3.488

7.  Cerebral blood flow with [15O]water PET studies using an image-derived input function and MR-defined carotid centerlines.

Authors:  Edward K Fung; Richard E Carson
Journal:  Phys Med Biol       Date:  2013-02-27       Impact factor: 3.609

8.  Quantification of (R)-[11C]PK11195 binding in rheumatoid arthritis.

Authors:  M A Kropholler; R Boellaard; E H Elzinga; C J van der Laken; K Maruyama; R W Kloet; A E Voskuyl; B A C Dijkmans; A A Lammertsma
Journal:  Eur J Nucl Med Mol Imaging       Date:  2008-11-29       Impact factor: 9.236

9.  Test-retest variability of quantitative [11C]PIB studies in Alzheimer's disease.

Authors:  Nelleke Tolboom; Maqsood Yaqub; Ronald Boellaard; Gert Luurtsema; Albert D Windhorst; Philip Scheltens; Adriaan A Lammertsma; Bart N M van Berckel
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-04-22       Impact factor: 9.236

10.  In vivo validation of reconstruction-based resolution recovery for human brain studies.

Authors:  Jurgen E M Mourik; Mark Lubberink; Floris H P van Velden; Reina W Kloet; Bart N M van Berckel; Adriaan A Lammertsma; Ronald Boellaard
Journal:  J Cereb Blood Flow Metab       Date:  2009-10-21       Impact factor: 6.200

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