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Journal of Nuclear Medicine

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Meeting ReportInstrumentation & Data Analysis: Image Generation

Venous versus arterial blood samples for plasma input pharmacokinetic analysis of different radiotracer PET studies

Henri Greuter, Mark Lubberink, N. Harry Hendrikse, Astrid van der Veldt, Yeun Wong, Robert Schuit, Albert Windhorst, Ronald Boellaard and Adriaan Lammertsma
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1974;
Henri Greuter
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Mark Lubberink
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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N. Harry Hendrikse
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Astrid van der Veldt
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Yeun Wong
2Pulmonology, VU University Medical Center, Amsterdam, Netherlands
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Robert Schuit
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Albert Windhorst
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Ronald Boellaard
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Adriaan Lammertsma
1Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, Netherlands
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Abstract

1974

Objectives Full quantitative analysis of dynamic PET studies often requires a metabolite corrected arterial plasma input function. A whole blood input function can be obtained either by online arterial sampling or from an image derived input function (IDIF). Next, data from several manual arterial blood samples are used to correct for changing plasma to blood (P/B) activity concentration (AC) ratios and parent fractions (PF). Use of venous blood samples is more patient friendly especially in case of an IDIF. The purpose of this study was to validate the use of venous blood samples to generate a metabolite corrected plasma IDIF.

Methods During several PET studies with different tracers (see table) both arterial and venous manual blood samples were taken at different time points (n= 3 to 7 per study). Both sets of samples were used to measure blood and plasma ACs, P/B ratios and, if necessary, PFs. Venous data were compared with arterial data using linear regression analysis.

Results During several PET studies with different tracers (see table) both arterial and venous manual blood samples were taken at different time points (n= 3 to 7 per study). Both sets of samples were used to measure blood and plasma ACs, P/B ratios and, if necessary, PFs. Venous data were compared with arterial data using linear regression analysis.

Conclusions Manual arterial samples cannot be replaced by venous sampling without proper validation. Use of venous sampling to correct IDIFs for P/B ratios and PFs may be valid for some tracers

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Journal of Nuclear Medicine
Vol. 52, Issue supplement 1
May 2011
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Venous versus arterial blood samples for plasma input pharmacokinetic analysis of different radiotracer PET studies
Henri Greuter, Mark Lubberink, N. Harry Hendrikse, Astrid van der Veldt, Yeun Wong, Robert Schuit, Albert Windhorst, Ronald Boellaard, Adriaan Lammertsma
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1974;

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Venous versus arterial blood samples for plasma input pharmacokinetic analysis of different radiotracer PET studies
Henri Greuter, Mark Lubberink, N. Harry Hendrikse, Astrid van der Veldt, Yeun Wong, Robert Schuit, Albert Windhorst, Ronald Boellaard, Adriaan Lammertsma
Journal of Nuclear Medicine May 2011, 52 (supplement 1) 1974;
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