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Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system

BACKGROUND: In an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processin...

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Autores principales: Hruska, Carrie B, Conners, Amy Lynn, Jones, Katie N, Weinmann, Amanda L, Lingineni, Ravi K, Carter, Rickey E, Rhodes, Deborah J, O’Connor, Michael K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900669/
https://www.ncbi.nlm.nih.gov/pubmed/24428856
http://dx.doi.org/10.1186/2191-219X-4-5
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author Hruska, Carrie B
Conners, Amy Lynn
Jones, Katie N
Weinmann, Amanda L
Lingineni, Ravi K
Carter, Rickey E
Rhodes, Deborah J
O’Connor, Michael K
author_facet Hruska, Carrie B
Conners, Amy Lynn
Jones, Katie N
Weinmann, Amanda L
Lingineni, Ravi K
Carter, Rickey E
Rhodes, Deborah J
O’Connor, Michael K
author_sort Hruska, Carrie B
collection PubMed
description BACKGROUND: In an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processing. METHODS: Eighty-two bilateral, two-view MBI studies were reviewed. Studies were performed with 300 MBq Tc-99 m sestamibi and a direct conversion molecular breast imaging (DC-MBI) system. Acquisitions were 10 min-per-view; the first half of each was extracted to create 5-min-per-view datasets, and WBR processing was applied. The 10-min-, 5-min-, and 5-min-per-view WBR studies were independently interpreted in a randomized, blinded fashion by two radiologists. Assessments of 1 to 5 were assigned; 4 and 5 were considered test positive. Background parenchymal uptake, lesion type, distribution of non-mass lesions, lesion intensity, and image quality were described. RESULTS: Considering detection of all malignant and benign lesions, 5 min-per-view MBI had lower sensitivity (mean of 70% vs. 85% (p ≤ 0.04) for two readers) and lower area under curve (AUC) (mean of 92.7 vs. 99.6, p ≤ 0.01) but had similar specificity (p = 1.0). WBR processing did not alter sensitivity, specificity, or AUC obtained at 5 min-per-view. Overall agreement in final assessment between 5-min-per-view and 10-min-per-view acquisition types was near perfect (κ = 0.82 to 0.89); however, fair to moderate agreement was observed for assessment category 3 (probably benign) (κ = 0.24 to 0.48). Of 33 malignant lesions, 6 (18%) were changed from assessment of 4 or 5 with 10-min-per-view MBI to assessment of 3 with 5-min-per-view MBI. Image quality of 5-min-per-view studies was reduced compared to 10-min-per-view studies for both readers (3.24 vs. 3.98, p < 0.0001 and 3.60 vs. 3.91, p < 0.0001). WBR processing improved image quality for one reader (3.85 vs. 3.24, p < 0.0001). CONCLUSIONS: Although similar radiologic interpretations were obtained with 10-min- and 5-min-per-view DC-MBI, resulting in substantial agreement in final assessment, notable exceptions were found: (1) perceived image quality at 5 min-per-view was lower than that for 10-min-per-view studies and (2) in a number of cases, assessment was downgraded from a recommendation of biopsy to that of short interval follow-up.
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spelling pubmed-39006692014-01-24 Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system Hruska, Carrie B Conners, Amy Lynn Jones, Katie N Weinmann, Amanda L Lingineni, Ravi K Carter, Rickey E Rhodes, Deborah J O’Connor, Michael K EJNMMI Res Original Research BACKGROUND: In an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processing. METHODS: Eighty-two bilateral, two-view MBI studies were reviewed. Studies were performed with 300 MBq Tc-99 m sestamibi and a direct conversion molecular breast imaging (DC-MBI) system. Acquisitions were 10 min-per-view; the first half of each was extracted to create 5-min-per-view datasets, and WBR processing was applied. The 10-min-, 5-min-, and 5-min-per-view WBR studies were independently interpreted in a randomized, blinded fashion by two radiologists. Assessments of 1 to 5 were assigned; 4 and 5 were considered test positive. Background parenchymal uptake, lesion type, distribution of non-mass lesions, lesion intensity, and image quality were described. RESULTS: Considering detection of all malignant and benign lesions, 5 min-per-view MBI had lower sensitivity (mean of 70% vs. 85% (p ≤ 0.04) for two readers) and lower area under curve (AUC) (mean of 92.7 vs. 99.6, p ≤ 0.01) but had similar specificity (p = 1.0). WBR processing did not alter sensitivity, specificity, or AUC obtained at 5 min-per-view. Overall agreement in final assessment between 5-min-per-view and 10-min-per-view acquisition types was near perfect (κ = 0.82 to 0.89); however, fair to moderate agreement was observed for assessment category 3 (probably benign) (κ = 0.24 to 0.48). Of 33 malignant lesions, 6 (18%) were changed from assessment of 4 or 5 with 10-min-per-view MBI to assessment of 3 with 5-min-per-view MBI. Image quality of 5-min-per-view studies was reduced compared to 10-min-per-view studies for both readers (3.24 vs. 3.98, p < 0.0001 and 3.60 vs. 3.91, p < 0.0001). WBR processing improved image quality for one reader (3.85 vs. 3.24, p < 0.0001). CONCLUSIONS: Although similar radiologic interpretations were obtained with 10-min- and 5-min-per-view DC-MBI, resulting in substantial agreement in final assessment, notable exceptions were found: (1) perceived image quality at 5 min-per-view was lower than that for 10-min-per-view studies and (2) in a number of cases, assessment was downgraded from a recommendation of biopsy to that of short interval follow-up. Springer 2014-01-15 /pmc/articles/PMC3900669/ /pubmed/24428856 http://dx.doi.org/10.1186/2191-219X-4-5 Text en Copyright © 2014 Hruska et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hruska, Carrie B
Conners, Amy Lynn
Jones, Katie N
Weinmann, Amanda L
Lingineni, Ravi K
Carter, Rickey E
Rhodes, Deborah J
O’Connor, Michael K
Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title_full Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title_fullStr Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title_full_unstemmed Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title_short Half-time Tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
title_sort half-time tc-99m sestamibi imaging with a direct conversion molecular breast imaging system
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900669/
https://www.ncbi.nlm.nih.gov/pubmed/24428856
http://dx.doi.org/10.1186/2191-219X-4-5
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