Evidence map›Paper›PMID 27182080›Full record

ArticleIEEE transactions on nuclear science2016

LROC Investigation of Three Strategies for Reducing the Impact of Respiratory Motion on the Detection of Solitary Pulmonary Nodules in SPECT.

Mark S Smyczynski, Howard C Gifford, Joyoni Dey, Andre Lehovich, Joseph E McNamara, W Paul Segars, Michael A King

Open access · greenAbstract read
In one paragraph

Article in IEEE transactions on nuclear science, 2016. 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
1.1field-weighted citation impact, top 21% 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, 4 citations in OpenAlex.

  1. The imaging of small pulmonary nodules.Translational lung cancer research · 2017
    Review
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

7 authors at 5 institutions in 1 country.

Mark S SmyczynskiDepartment of Radiology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655.
Howard C GiffordBiomedical Engineering Dept., University of Houston, Houston, TX.
Joyoni DeyDepartment of Physics & Astronomy, Louisiana State University, LA.
Andre LehovichDepartment of Radiology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655.
Joseph E McNamaraSignature Science LLC, Egg Harbor Township, NJ.
W Paul SegarsDuke Advanced Imaging Laboratories, Duke University Medical Center, Durham, NC.
Michael A KingDepartment of Radiology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655 (telephone: 508-856-4255, michael.king@umassmed.edu ).
University of Massachusetts Chan Medical School · USDuke Medical Center · USLouisiana State University · USSignature Research (United States) · USUniversity of Houston · US

Funding

Simulation Tools for Dynamic CTR01EB001838 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI SAMEI, EHSAN, SEGARS, WILLIAM P · 2005 to 2023
$6.9M
PATIENT MOTION DETECTION AND COMPENSATION IN SPECTR01EB001457 · NIBIB · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KING, MICHAEL A · 2003 to 2013
$5.7M
NIBIB NIH HHS R01 EB001457NIBIB NIH HHS R01 EB001838
6 · The paper itself

Abstract

The objective of this investigation was to determine the effectiveness of three motion reducing strategies in diminishing the degrading impact of respiratory motion on the detection of small solitary pulmonary nodules (SPN) in single photon emission computed tomographic (SPECT) imaging in comparison to a standard clinical acquisition and the ideal case of imaging in the absence of respiratory motion. To do this non-uniform rational B-spline cardiac-torso (NCAT) phantoms based on human-volunteer CT studies were generated spanning the respiratory cycle for a normal background distribution of Tc-99m NeoTect. Similarly, spherical phantoms of 1.0 cm diameter were generated to model small SPN for each of 150 uniquely located sites within the lungs whose respiratory motion was based on the motion of normal structures in the volunteer CT studies. The SIMIND Monte Carlo program was used to produce SPECT projection data from these. Normal and single-lesion containing SPECT projection sets with a clinically realistic Poisson noise level were created for the cases of: 1) the end-expiration (EE) frame with all counts, 2) respiration-averaged motion with all counts, 3) one-fourth of the 32 frames centered around EE (Quarter-Binning), 4) one-half of the 32 frames centered around EE (Half-Binning), and 5) eight temporally binned frames spanning the respiratory cycle. Each of the sets of combined projection data were reconstructed with RBI-EM with system spatial-resolution compensation (RC). Based on the known motion for each of the 150 different lesions, the reconstructed volumes of respiratory bins were shifted so as to superimpose the locations of the SPN onto that in the first bin (Reconstruct and Shift). Five human-observers performed localization receiver operating characteristics (LROC) studies of SPN detection. The observer results were analyzed for statistical significance differences in SPN detection accuracy among the three correction strategies, the standard acquisition, and the ideal case of the absence of respiratory motion. Our human-observer LROC determined that Quarter-Binning and Half-Binning strategies resulted in SPN detection accuracy statistically significantly below (P < 0.05) that of standard clinical acquisition, whereas the Reconstruct and Shift strategy resulted in a detection accuracy not statistically significantly different from that of the ideal case. This investigation demonstrates that tumor detection based on acquisitions associated with less than all the counts which could potentially be employed may result in poorer detection despite limiting the motion of the lesion. The Reconstruct and Shift method results in tumor detection that is equivalent to ideal motion correction.

Indexed as

image generationimage quality assessmentsimulationSPECT data quantification and correction methods

Identifiers

PMID27182080
PMCPMC4863469
OpenAlexW2288503118

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.