Evidence map›Paper›PMID 32383043›Full record

ArticleEJNMMI physics2020

Simulation study of a coincidence detection system for non-invasive determination of arterial blood time-activity curve measurements.

Yassine Toufique, Othmane Bouhali, Pauline Negre, Jim O' Doherty

Open access · goldAbstract read
In one paragraph

Article in EJNMMI physics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Yassine ToufiqueAdvanced Scientific Computing Center, Texas A&M University at Qatar, Doha, Qatar.
Othmane BouhaliAdvanced Scientific Computing Center, Texas A&M University at Qatar, Doha, Qatar.
Pauline NegreClinical Imaging Research Centre, Centre for Translational Medicine, National University of Singapore, Singapore, Singapore.
Jim O' DohertyClinical Imaging Research Centre, Centre for Translational Medicine, National University of Singapore, Singapore, Singapore. jim.odoherty@nus.edu.sg.ORCID http://orcid.org/0000-0003-2989-4485
National University of Singapore · SGHamad bin Khalifa University · QATexas A&M University at Qatar · QA

Funding

Qatar National Research Fund NPRP9-328-1-066
6 · The paper itself

Abstract

backgroundArterial sampling in PET studies for the purposes of kinetic modeling remains an invasive, time-intensive, and expensive procedure. Alternatives to derive the blood time-activity curve (BTAC) non-invasively are either reliant on large vessels in the field of view or are laborious to implement and analyze as well as being prone to many processing errors. An alternative method is proposed in this work by the simulation of a non-invasive coincidence detection unit.

resultsWe utilized GATE simulations of a human forearm phantom with a blood flow model, as well as a model for dynamic radioactive bolus activity concentration based on clinical measurements. A fixed configuration of 14 and, also separately, 8 detectors were employed around the phantom, and simulations were performed to investigate signal detection parameters. Bismuth germanate (BGO) crystals proved to show the highest count rate capability and sensitivity to a simulated BTAC with a maximum coincidence rate of 575 cps. Repeatable location of the blood vessels in the forearm allowed a half-ring design with only 8 detectors. Using this configuration, maximum coincident rates of 250 cps and 42 cps were achieved with simulation of activity concentration determined from

conclusionsInitial simulations demonstrated that the configuration of a single half-ring 8 detector of monolithic BGO crystals could describe the simulated BTAC in a clinically relevant forearm phantom with good signal properties, and an increased number of axial detection rings can provide increased sensitivity of the system. The system would find use in the derivation of the BTAC for use in the application of kinetic models without physical arterial sampling or reliance on image-based techniques.

Indexed as

Arterial input functionArterial samplingKinetic modelingPET

Identifiers

PMID32383043
PMCPMC7205938
OpenAlexW3023339037

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.