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[1520] MEASURED ACTIVITY OF F-18 FDG UNIT DOSES IN A CLINICAL MOBILE PET/CT ENVIRONMENT.

M. L. Schaffner*, A. Horabin, K. Thaggard, G. Glesinger, A. M. Zimmer; PET Section, Northern Shared Medical Services, Madison, WI; Department of Nuclear Medicine, Northwestern Memorial Hospital, Chicago, IL. (651514)
Monday, June 21, 2004, 8:45 AM, Technologist Paper Session: Technologist Abstract Track - Radiopharmaceutical/Chemistry (8:00 AM-9:30 AM) 201 B
Objectives: F-18 FDG unit doses, from different radiopharmaceutical vendors, are routinely provided to ten mobile PET and PET/CT coaches. Dose calibrator assay of received F-18 FDG doses were significantly different than assays provided by vendors. Assay differences in F-18 FDG unit doses and possible reasons for these differences were evaluated.
Methods: Capintec dose calibrators (Capintec Inc) are used by all vendors evaluated in this study. Biodex Atomlab 100 dose calibrators (Biodex Nuclear) are used on all mobile coaches. Each coach has a National Institute of Standards and Technology (NIST) traceable positron-emitting standard (Ge-68/Ga-68) which is used to evaluate dose calibrator accuracy on all coaches and also on a Capintec CRC-15 dose calibrator. Differences in measured F-18 FDG unit doses supplied by various vendors were measured for a 2 to 4 week time period.
Results: Dose calibrator assays of F-18 FDG doses were 19.6% ± 5.5 % (mean and standard deviation, n=16) and 7.3% ± 2.8% (mean and standard deviation, n=30) lower than assays provided by two different vendors. Biodex Atomlab 100 dose calibrator accuracy assessment with a NIST traceable Ge-68/Ga-68 standard deviated by -1.4% ± 0.5% (mean and standard deviation, n=7) of specified standard activity. With the same NIST traceable positron-emitting standard, the deviation in a Capintec CRC-15 dose calibrator was 5.2% of specified standard activity, resulting in a calibrated difference of 6.6% between vendor and end user assayed dose.
Conclusions: Significant differences in F-18 FDG assayed doses provided by radiopharmaceutical vendors were demonstrated; differences in assayed doses from one vendor were due to specific type of dose calibrator used. Recalibration of F-18 dial settings in commercial dose calibrators should be considered.
Keywords: Dose calibrator | Fluorine-18-fluorodeoxyglucose (FDG) | Assay


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