Evidence map›Paper›PMID 42039735›Full record

ArticleJournal of medical physics

Optimizing Positron Emission Tomography-Computed Tomography Image Quality with Iterative Reconstruction: A NEMA Phantom Study.

Hussein Kaafarani

Abstract read
In one paragraph

Article in Journal of medical physics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Hussein KaafaraniDepartment of Nuclear Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Purpose: Small-lesion detectability in positron emission tomography-computed tomography (PET/CT) depends on reconstruction parameters such as postreconstruction smoothing and matrix size, but practical guidance for selecting these parameters is limited. This work quantifies how iterative reconstruction settings affect contrast recovery coefficient (CRC, %), background variability (BV), and contrast-to-noise ratio (CNR) using a standardized NEMA IEC body phantom. This phantom-only study quantifies how iterative reconstruction and postreconstruction filtering affect CRC, %, BV, and CNR in a standardized NEMA IEC body phantom. Materials and Methods: A NEMA IEC body phantom with six spheres (10, 13, 17, 22, 28, and 37 mm) and a lung insert was filled to achieve nominal 4:1 and 8:1 sphere-to-background activity ratios using ¹3F. Four spheres were prepared as hot spheres and two as cold spheres (4 hot/2 cold). The phantom was scanned on a Philips Gemini PET/CT system. Images were reconstructed using ordered-subsets expectation maximization (3 iterations/16 subsets) while varying (i) Gaussian postreconstruction smoothing kernels of 3 mm, 5 mm, and 7 mm full width at half maximum, (ii) alternative filters (Hann, Butterworth, median), and (iii) matrix size (128 × 128 vs. 168 × 168). For each condition, we measured CRC, BV (expressed as % standard deviation of background VOIs), and CNR. Results: CRC increased with sharper filtering and with the larger matrix. At a 4:1 activity ratio, the 10 mm sphere reached 15% CRC with a 3 mm Gaussian filter, 12% with a 5 mm filter, and 10% with a 7 mm filter; the 37 mm sphere remained around 55% CRC across filters. At an 8:1 ratio, CRC rose overall: the 10 mm sphere reached 17% (3 mm), 14% (5 mm), and 12% (7 mm), while larger spheres maintained CRC ≥60% (for example, the 28 mm sphere reached 69% CRC with 3 mm Gaussian smoothing). Increasing matrix size from 128 × 128 to 168 × 168 improved CRC by approximately 2-7 absolute percentage points depending on sphere size (13 mm: 24% → 28%; 37 mm: 50% → 57%). These CRC gains were accompanied by increased BV and changes in CNR, which are now quantified in this revision. BV and CNR values represent within-scan spatial variability across background VOIs, not variability from repeated acquisitions. Conclusions: Image quality optimization is a trade-off. A 168 × 168 matrix combined with a 3 mm Gaussian filter maximizes CRC and CNR in the smallest spheres (10-13 mm) but increases BV. A 5 mm Gaussian filter provides a more clinically acceptable CRC-BV balance for spheres ≥17 mm (for example, CRC ≈40-46% for the 17 mm sphere) while moderating BV compared with the sharpest setting. A 7 mm filter suppresses BV further, but at the cost of CRC for the smallest spheres. Reporting CRC alone can exaggerate the benefit of aggressive reconstruction; BV and CNR must be considered together. A 168 × 168 matrix with a 3-5 mm Gaussian improved CRC for ≤13 mm spheres but at a BV penalty; for ≥17 mm spheres, a 5 mm Gaussian provided a more balanced CRC-BV profile, with similar or improved CNR relative to 3 mm. These findings are specific to this NEMA IEC phantom and may not translate directly to patient imaging. All BV and CNR values reflect spatial noise within a single acquisition rather than scan-to-scan variability.

Indexed as

18 F-fludeoxyglucosecontrast recovery coefficient %full width at half maximumGaussian filterimage reconstructionlesion detectabilitymatrix sizenoise-resolution tradeoffphantom studypositron emission tomography-computed tomographypython automationROI analysis

Identifiers

PMID42039735
PMCPMC13105374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.