Skip to main content
European Journal of Breast Health logoLink to European Journal of Breast Health
. 2019 Jul 1;15(3):153–157. doi: 10.5152/ejbh.2019.4468

3D Automated Breast Ultrasound System: Comparison of Interpretation Time of Senior Versus Junior Radiologist

Aydan Arslan 1,, Gökhan Ertaş 2, Erkin Arıbal 1
PMCID: PMC6619783  PMID: 31312790

Abstract

Objective

This study aimed to compare the automated breast ultrasound system (ABUS) reading time of breast radiologist to a radiology resident independent of the clinical outcomes.

Materials and Methods

One hundred women who underwent screening ABUS between July and August 2017 were reviewed retrospectively. Each study was examined sequentially by a breast radiologist who has more than 20 years of experience in breast radiology and third year resident who has 6 months of experience in breast radiology. Data were analyzed with Spearman’ correlation, Wilcoxon Signed Ranks Test and Kruskal-Wallis Test and was recorded.

Results

The mean age of patients was 42.02±11.423 years (age range16–66). The average time for senior radiologist was 223.36±84.334 seconds (min 118 max 500 seconds). The average time for junior radiologist was 269.48±82.895 seconds (min 150 max 628 seconds). There was a significant difference between the mean time of two radiologists (p=0.00001). There was a significant difference regarding the decrease in the reading time throughout study with the increase of number of cases read by the breast radiologist (p<0.05); but not with the resident radiologist (p=0.687). There was a correlation between BI-RADS category and reading time for both the breast radiologist and the resident (p=0.002, p=0.00043 respectively) indicating that patients who had findings caused longer reading times.

Conclusion

ABUS reading time may differ according to the experience of the user, however the times of an experienced and non-experienced user is comparable.

Keywords: Automated breast ultrasound, breast ultrasonography, breast cancer, interpretation time of ABUS, average time of ABUS

Introduction

Mammography is the gold standard for breast cancer screening yielding 30% reduction in breast cancer mortality among women aged 50–74 years (1). Mammographic sensitivity for breast cancer decreases significantly with increasing breast density. To overcome this, ultrasonography (US) has been studied as an adjunct to mammography in dense breasts and studies showed significant increase in detection of small cancers when added to mammography (2, 3).

Hand Held Ultrasound (HHUS) is widely available and a well-tolerated method which allows detailed evaluation of the breast and the axilla and has the availability of color Doppler and elastography modes (4, 5). On the other hand, HHUS has several disadvantages. It is time consuming, operator-dependent, not reproducible and requires high level of skill and experience. It has high false positivity rate, lacks standardized techniques, allows only two-dimensional (2D) imaging with a small field of view (FOV) (4, 68).

Automated three-dimensional (3D) breast ultrasound (ABUS) was developed to obtain an operator independent system. It is reproducible and obtains three dimensional (3D) high resolution imaging with a large FOV. ABUS is reported as a comfortable and time-efficient technique (710). Multiple studies have demonstrated similar sensitivity, cancer detection rate, diagnostic accuracy rates and image quality for both ABUS and HHUS (1116). The new generation ABUS provides better detection of architectural distortions, lesion localization and typical hyperechoic rim on coronal planes (9, 17, 18). Thick hyperechoic rim is suspicious sonographic finding which suggests the presence of invasive cancer. However, ABUS has some limitations such as 10% lower cancer detection rate, higher false positive results and recalls, shadowing artefacts, incompatibility for US guided biopsy, limited evaluation of axilla, absence of elastography or Doppler techniques for further characterization of the lesions and relatively higher cost compared to HHUS (4, 1820).

To our knowledge, limited studies of reading time of US have been reported in the English literature (4, 2123). The average total time to complete a HHUS is 19 minutes (23). The aim of this study was to assess ABUS reading time and compare the reading times of a breast radiologist and a radiology resident independent of the clinical outcomes.

Materials and Methods

Institutional review board approval (No: 2018-2/9) was obtained for this study by Acıbadem Mehmet Ali Aydınlar University ethics committee. Additional informed consent was obtained from all patients for which identifying information is included in this article. One hundred women (age range 18–66 years; mean 42.02±11.423 years) who underwent screening ABUS examination between July and August 2017 were reviewed retrospectively.

We excluded twelve patients who were already diagnosed with breast cancer and had a breast surgery history, skin disorders, inflammatory conditions of the breast, breastfeeding woman and pregnancy. Patients with larger breasts which needed more than three positions were also excluded from the study. ABUS images of one hundred women were evaluated by two readers.

Automated Three-Dimensional (3D) Breast Ultrasound (ABUS)

Automated breast ultrasound studies were performed using the ABUS (Invenia ABUS, GE Healthcare) scanner by two well-trained radiology technicians with one month of experience on automatic ultrasound. The examination was performed in the supine position with the ipsilateral arm above the head. A hypoallergenic lotion and a disposable membrane were used to aid an acoustic coupling. Each breast was examined in three different positions; i) anteroposterior (AP), ii) lateral (LAT) including the pectoral muscle and iii) medial (MED). A nipple marker was placed on the coronal view to locate the nipple position for accurate location in each position.

Automated breast ultrasound system acquires 15.4 cm ×17.0 cm area with the volume from the skin to the chest wall up to 5 cm deep. The frequency of transducer varied between 6–15 MHz.

Each study included bilateral anteroposterior, medial, and upper-outer quadrant positions.

For the lateral position, the breast tissue was pushed from axilla towards the sternum and covered the upper outer breast. For the medial position, the breast tissue was pushed from sternum toward the axilla, covering the inner inferior part of the breast. Minor compression was performed to the breast to avoid breast movement and obtain better view of the volume.

All positions included the nipple as a landmark. The scanning time for the sweeping of the probe the whole volume of interest was one minute per view.

Data were sent from the ABUS to the dedicated workstation. Multiplanar compounded images in three planes (coronal, sagittal and axial reconstructions) were reviewed.

Data Evaluation

Each study was examined sequentially by a breast radiologist who has more than 20 years of experience in breast radiology, three months of experience in ABUS reading prior to the study (senior radiologist) and third year resident (junior radiologist) who has 6 months of experience in breast radiology, one-month experience in ABUS reading prior to the study blinded to each other’s results. Junior radiologist had a training for ABUS for one month prior to the study. Two radiologists participated in ABUS training via online webinars. A standard review protocol was used by both readers, which included, evaluation of coronal and transverse planes of each volume. Each plane was evaluated in the same order. The cases were evaluated in the same sequence. The reading environment was same.

Patient’s age, reading time of 2 radiologists and American College of Radiology Breast Imaging Reporting and Data System (BIRADS) Atlas category for each patient were noted. The results were classified as: BIRADS 0 (incomplete), BIRADS 1 (negative), BIRADS 2 (benign findings).

Statistical Analysis

Data were analyzed with Statistical Package for the Social Sciences version 24.0 (IBM Corp.; Armonk, NY, USA). Spearman’ correlation, Wilcoxon Signed Ranks Test and Kruskal-Wallis Test were recorded. P value <0.05 was considered for statistical significance for all tests. Wilcoxon Signed Ranks Test was used for significant difference between the mean time of two radiologists. Spearman’ correlation was used for significant difference regarding the decrease in the reading time throughout study with the increase of number of cases read by the breast radiologist. Kruskal-Wallis Test and Spearman’ correlation were used for correlation between BI-RADS category and reading time for both the breast.

Results

The average time for evaluating the ABUS data for the senior radiologist was 223.36±84.334 seconds (min 118 max 500 seconds). The average time for junior radiologist was 269.48±82.895 seconds (min 150 max 628 seconds) as detailed on Table 1. There was a significant difference between the mean time of two radiologists (p=0.00001). There was a significant difference regarding the decrease in the interpretation time throughout study with the increase of number of cases read by the breast radiologist (p<0.05); but not with the resident radiologist (p=0.687) (Figure 1). The reading time of the breast radiologist decreased throughout the study (Figure 2).

Table 1.

The average time for evaluating the ABUS data for the senior and junior radiologist

Descriptive Statistics Minimum Maximum Mean Std. Deviation
Age 16 66 42.02 11.423
Senior radiologist (seconds) 118 500 223.36 84.334
Junior radiologist (seconds) 150 628 269.48 82.895
Average time (seconds) 139.5 458.5 246.424 67.0528

Figure 1.

Figure 1

The reading time of the senior breast radiologist decreased throughout the study

Figure 2.

Figure 2

Learning curve of breast radiologist

We classified cases according to American College of Radiology BIRADS Atlas category; including BI-RADS category I in 20 patients (20%), BI-RADS category II in 65 patients (65%), BI-RADS category 0 in 15 patients (15%). All BI-RADS category 0 patients were examined with second look HHUS. Two of these changed to BI-RADS 2, seven to BI-RADS 3 and six to BI-RADS 4. One of six BI-RADS 4 cases proved to be an invasive carcinoma with a diameter of 6 mm which was detected by both readers. There was a correlation between BI-RADS category and reading time for both the breast radiologists and the resident (p=0.002, p=0.00043 respectively) indicating that patients who had findings resulted with longer reading times (Table 2). This finding was evident for the resident compared to the findings of the breast radiologist taking the BIRADS category into consideration.

Table 2.

Kruskal Wallis Test, correlation between BI-RADS category and reading time

Ranks
BIRADS N
Mean Rank
Reding Time for Breast Radiologist 0 66.50
1 27.48
2 54.27
3 56.64
4 64.57
Reading Time for Breast Radiologist 0 62.75
1 36.00
2 47.59
3 74.07
4 84.00
Mean Time (second) 0 65.25
1 28.05
2 50.89
3 69.64
4 80.71

Discussion and Conclusion

This study highlights the interpretation time of 3D ABUS by two radiologists with different experiences. Junior radiologist showed to be inferior to senior radiologist, particularly in the average time and learning curve. Our study showed that inexperienced radiologist’s learning curve and the reading time is longer, however the mean time difference is 46 seconds.

Average time for 2 radiologists in 100 cases was 246.424±67.0528 (min 139.5, max 458.5) seconds. We observed that ABUS reading is fast and shortens during the time span of learning curve. This interpretation time is agreeable when compared to hand-held bilateral screening ultrasound examination which is reported to take an approximately 19 min (23) particularly in practices where the radiologist performs. We believe that ABUS can be a good alternative as a less time-consuming examination for a radiologist in breast screening programs particularly in centers with high patient flow.

We observed a significant reading time difference between BI-RADS 1 and other BIRADS categories (BI-RADS 0,2). It would take less time to read a completely normal exam (BIRADS 1) than an abnormal exam (BIRADS 0 and 2).

Automated breast ultrasound is more promising for breast screening purposes where majority of women are BI-RADS category 1. Thus, recall is needed for category 0 lesions which will be higher in diagnostic studies but will be low in screening. Many studies have documented that the ABUS technique is independent of an operator, has standardized views, is faster to acquire images. ABUS requires less training than HHUS. Total examination time is about 10–15 minutes by a trained sonographer (7, 8, 2427). The interpretation time of ABUS varies between 2,9 and 9 minutes (2426). The reason of this variability may be the differences in experiences, presence of abnormalities, and to the filled reports or protocols (25, 26). Our study showed that readers with different experiences can perform interpretation of the images in comparable durations. However, a recent study demonstrated an average ABUS interpretation time of less than 3 minutes with 3 different experienced readers. Their study included patients with ACR BI-RADS 4 breast density classifications of C or D which in line with our findings (28).

To assess or compare radiologists’ performance in the detection of breast cancer with 3D ABUS were not part of this study. However, in another related study, the addition of ABUS to screening mammography has been found to increase in cancer detection in line with our findings (29).

Our study has several limitations: First, the number of study participants was relatively limited. Second, it would have been more objective to compare reading time with varied experienced more than 2 radiologists. A multicenter study with several readers may help to show the variability of reading times. Third, this study was a retrospective study and the clinical outcome was not included in the analysis.

In conclusion, ABUS reading time may differ according to the experience of the user; however, the times of an experienced and non-experienced users are comparable.

Footnotes

Ethics Committee Approval: Ethics committee approval was received for this study from the Ethics Committee of Acıbadem Mehmet Ali Aydınlar University (2018-2/9).

Informed Consent: Written informed consent was obtained from patients who participated in this study.

Peer-review: Externally peer-reviewed.

Author Contributions: Concept - A.A., E.A.; Design - A.A., E.A.; Supervision - A.A., E.A.; Resources - A.A., E.A.; Materials - A.A., E.A.; Data Collection and/or Processing - A.A., E.A.; Analysis and/or Interpretation - A.A., E.A., G.E.; Literature Search - A.A., E.A.; Writing Manuscript - A.A., E.A.; Critical Review - A.A., E.A.

Conflict of Interest: The authors have no conflicts of interest to declare.

Financial Disclosure: The authors declared that this study has received no financial support.

References

  • 1.Tabár L, Fagerberg CJ, Gad A, Baldetorp L, Holmberg LH, Gröntoft O, Ljungquist U, Lundström B, Månson JC, Eklund G. Reduction in mortality from breast cancer after mass screening with mammography: randomised trial from the Breast Cancer Screening Working Group of the Swedish National Board of Health and Welfare. Lancet. 1985;325:829–832. doi: 10.1016/S0140-6736(85)92204-4. [DOI] [PubMed] [Google Scholar]
  • 2.Kolb M, Lichy J, Newhouse H. Comparison of the performance of screening mammography, physical examination, and breast US and evaluation of factors that influence them: an analysis of 27,825 patient evaluations. Radiology. 2002;225:165–175. doi: 10.1148/radiol.2251011667. [DOI] [PubMed] [Google Scholar]
  • 3.Kim YW, Kim SK, Youn HJ, Choi EJ, Jung SH. The clinical utility of automated breast volume scanner: a pilot study of 139 cases. J Breast cancer. 2013;16:329–334. doi: 10.4048/jbc.2013.16.3.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Shin HJ, Kim HH, Cha JH. Current status of automated breast ultrasonography. Ultrasonography. 2015;34:165. doi: 10.14366/usg.15002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Zhang Q, Hu B, Hu B, Li WB. Detection of breast lesions using an automated breast volume scanner system. J Int Med Res. 2012;40:300–306. doi: 10.1177/147323001204000130. [DOI] [PubMed] [Google Scholar]
  • 6.Berg WA, Blume JD, Cormack JB, Mendelson EB. Operator dependence of physician-performed whole-breast US: lesion detection and characterization. Radiology. 2006;241:355–365. doi: 10.1148/radiol.2412051710. [DOI] [PubMed] [Google Scholar]
  • 7.Lin X, Wang J, Han F, Fu J, Li A. Analysis of eighty-one cases with breast lesions using automated breast volume scanner and comparison with handheld ultrasound. Eur J Radiol. 2012;81:873–878. doi: 10.1016/j.ejrad.2011.02.038. [DOI] [PubMed] [Google Scholar]
  • 8.Vourtsis A, Kachulis A. The performance of 3D ABUS versus HHUS in the visualisation and BI-RADS characterisation of breast lesions in a large cohort of 1,886 women. Eur Radiol. 2018;28:592–601. doi: 10.1007/s00330-017-5011-9. [DOI] [PubMed] [Google Scholar]
  • 9.Wojcinski S, Gyapong S, Farrokh A, Soergel P, Hillemanns P, Degenhardt F. Diagnostic performance and inter-observer concordance in lesion detection with the automated breast volume scanner (ABVS) BMC Med Imaging. 2013;13:36. doi: 10.1186/1471-2342-13-36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Maturo VG, Zusmer NR, Gilson AJ, Smoak WM, Janowitz WR, Bear BE, Goddard J, Dick DE. Ultrasound of the whole breast utilizing a dedicated automated breast scanner. Radiology. 1980;137:457–463. doi: 10.1148/radiology.137.2.6254110. [DOI] [PubMed] [Google Scholar]
  • 11.Choi JJ, Kim SH, Kang BJ, Song BJ. Detectability and usefulness of automated whole breast ultrasound in patients with suspicious microcalcifications on mammography: comparison with handheld breast ultrasound. J Breast cancer. 2016;19:429–437. doi: 10.4048/jbc.2016.19.4.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Kim SH, Kang BJ, Choi BG, Choi JJ, Lee JH, Song BJ, Choe BJ, Park S, Kim H. Radiologists’ performance for detecting lesions and the interobserver variability of automated whole breast ultrasound. Korean J Radiol. 2013;14:154–163. doi: 10.3348/kjr.2013.14.2.154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Shin HJ, Kim HH, Cha JH, Park JH, Lee KE, Kim JH. Automated ultrasound of the breast for diagnosis: interobserver agreement on lesion detection and characterization. AJR Am J Roentgenol. 2011;197:747–754. doi: 10.2214/AJR.10.5841. [DOI] [PubMed] [Google Scholar]
  • 14.Wang HY, Jiang YX, Zhu QL, Zhang J, Dai Q, Liu H, Lai XJ, Sun Q. Differentiation of benign and malignant breast lesions: a comparison between automatically generated breast volume scans and handheld ultrasound examinations. Eur J Radiol. 2012;81:3190–3200. doi: 10.1016/j.ejrad.2012.01.034. [DOI] [PubMed] [Google Scholar]
  • 15.Kotsianos-Hermle D, Hiltawsky KM, Wirth S, Fischer T, Friese K, Reiser M. Analysis of 107 breast lesions with automated 3D ultrasound and comparison with mammography and manual ultrasound. Eur J Radiol. 2009;71:109–115. doi: 10.1016/j.ejrad.2008.04.001. [DOI] [PubMed] [Google Scholar]
  • 16.An YY, Kim SH, Kang BJ. The image quality and lesion characterization of breast using automated whole-breast ultrasound: a comparison with handheld ultrasound. Eur J Radiol. 2015;84:1232–1235. doi: 10.1016/j.ejrad.2015.04.007. [DOI] [PubMed] [Google Scholar]
  • 17.Zheng FY, Yan LX, Huang BJ, Xia HS, Wang X, Lu Q, et al. Comparison of retraction phenomenon and BI-RADS-US descriptors in differentiating benign and malignant breast masses using an automated breast volume scanner. Eur J Radiol. 2015;84:2123–2129. doi: 10.1016/j.ejrad.2015.07.028. [DOI] [PubMed] [Google Scholar]
  • 18.Mundinger A. 3D supine automated ultrasound (saus, abus, abvs) for supplemental screening women with dense breasts. Eur J Breast Health. 2016;12:52. doi: 10.5152/tjbh.2016.2940. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Berg WA, Bandos AI, Mendelson EB, Lehrer D, Jong RA, Pisano ED. Ultrasound as the primary screening test for breast cancer: analysis from ACRIN 6666. J Natl Cancer Inst. 2015;108:djv367. doi: 10.1093/jnci/djv367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Scheel JR, Lee JM, Sprague BL, Lee CI, Lehman CD. Screening ultrasound as an adjunct to mammography in women with mammographically dense breasts. Am J Obstet Gynecol. 2015;212:9–17. doi: 10.1016/j.ajog.2014.06.048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Merry GM, Mendelson EB. Update on screening breast ultrasonography. Radiol Clin North Am. 2014;52:527–537. doi: 10.1016/j.rcl.2013.12.003. [DOI] [PubMed] [Google Scholar]
  • 22.Kelly KM, Dean J, Lee SJ, Comulada WS. Breast cancer detection: radiologists’ performance using mammography with and without automated whole-breast ultrasound. Eur J Radiol. 2010;20:2557–2564. doi: 10.1007/s00330-010-1844-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Berg WA, Blume JD, Cormack JB, Mendelson EB, Lehrer D, Böhm-Vélez M, Pisano ED, Jong RA, Evans WP, Morton MJ, Mahoney MC, Larsen LH, Barr RG, Farria DM, Marques HS, Boparai K. Combined Screening with Ultrasound and mammography compared to mammography alone in women at elevated risk of breast cancer: results of the first-year screen in ACRIN 6666. JAMA. 2008;299:2151–2163. doi: 10.1001/jama.299.18.2151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Brem RF, Tabár L, Duffy SW, Inciardi MF, Guingrich JA, Hashimoto BE, Lander MR, Lapidus RL, Peterson MK, Rapelyea JA, Roux S, Schilling KJ, Shah BA, Torrente J, Wynn RT, Miller DP. Assessing improvement in detection of breast cancer with three-dimensional automated breast US in women with dense breast tissue: the SomoInsight Study. Radiology. 2014;274:663–673. doi: 10.1148/radiol.14132832. [DOI] [PubMed] [Google Scholar]
  • 25.Skaane P, Gullien R, Eben EB, Sandhaug M, Schulz-Wendtland R, Stoeblen F. Interpretation of automated breast ultrasound (ABUS) with and without knowledge of mammography: a reader performance study. Acta Radiol. 2015;56:404–412. doi: 10.1177/0284185114528835. [DOI] [PubMed] [Google Scholar]
  • 26.Wilczek B, Wilczek HE, Rasouliyan L, Leifland K. Adding 3D automated breast ultrasound to mammography screening in women with heterogeneously and extremely dense breasts: Report from a hospital-based, high-volume, single-center breast cancer screening program. Eur J Radiol. 2016;85:1554–1563. doi: 10.1016/j.ejrad.2016.06.004. [DOI] [PubMed] [Google Scholar]
  • 27.Tozaki M, Isobe S, Yamaguchi M, Ogawa Y, Kohara M, Joo C, Fukuma E. Optimal scanning technique to cover the whole breast using an automated breast volume scanner. Jpn J Radiol. 2010;28:325–328. doi: 10.1007/s11604-010-0424-2. [DOI] [PubMed] [Google Scholar]
  • 28.Huppe AI, Inciardi MF, Redick M, Carroll M, Buckley J, Hill JD, Gatewood JB. Automated Breast Ultrasound Interpretation Times: A Reader Performance Study. Acad Radiol. 2018;25:1577–1581. doi: 10.1016/j.acra.2018.03.010. [DOI] [PubMed] [Google Scholar]
  • 29.Giger ML, Inciardi MF, Edwards A, Papaioannou J, Drukker K, Jiang Y, Brem R, Brown JB. Automated breast ultrasound in breast cancer screening of women with dense breasts: reader study of mammography-negative and mammography-positive cancers. AJR Am J Roentgenol. 2016;206:1341–1350. doi: 10.2214/AJR.15.15367. [DOI] [PubMed] [Google Scholar]

Articles from European Journal of Breast Health are provided here courtesy of Turkish Federation of Breast Diseases Societies

RESOURCES