Literature DB >> 36084083

Simplification of 2D shear wave elastography by enlarged SWE box and multiple regions of interest in one acquisition.

Moritz Weiher1, Felix Gunnar Richtering1, Yvonne Dörffel1, Hans-Peter Müller1.   

Abstract

Two-dimensional (2D) Shear Wave Elastography (SWE) is an easy to perform technique to evaluate the liver stiffness. To simplify the procedure and reduce the acquisition time we enlarged the size of the SWE-box and set ten regions of interest (ROI) in one acquisition. We compare the accuracy of this method to ten separate acquisitions in a small box each with a single ROI measurement. Sixty-nine volunteers with diffuse chronic liver disease were studied with 2D-SWE using a Canon Aplio i800 ultrasound system. The shear-wave-speed was measured in the right lobe in ten separate acquisitions and compared to one acquisition with increased size of the SWE-box and ten different ROI measurements. A Bland-Altmann plot was drawn and the interclass correlation coefficient (ICC) was calculated to compare both methods. Finally, 2D-SWE was successfully performed thru both methods in sixty-six participants. Between both methods the ICC is 0.82. The results of this study show a good reliability between ten separate measures and one grouped measure with ten ROI if the mean is below 1.6m/s (7.7kPa). For higher degrees of fibrosis (≥F2) further investigations are needed.

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Year:  2022        PMID: 36084083      PMCID: PMC9462759          DOI: 10.1371/journal.pone.0273769

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.752


Introduction

The management of patients with chronic liver disease requires easier and harmless approaches to monitor disease progressions [1]. In the last two decades many ultrasound-based methods and systems are available to follow the fibrotic changes in the liver [2-4]. The best validated method is the transient elastography [5, 6], which is easy to perform but is neither guided by B-mode picture nor enables the user to choose the area of measurement because of fixed settings. Some of these problems can be avoided by using two-dimensional (2D) shear wave elastography (SWE), which has become more available and popular in the last years [7, 8]. An advantage of 2D-SWE is the possibility to see the elasticity in an area of tissue as a coloured map inside the SWE-box, which is also named analysis-box or field-of-view and can be adjusted in size and location by the operator. It is possible to measure the elasticity in different, operator-chosen areas, inside the SWE-box by using different regions of interest (ROI). Chung et al. recently compared five separate acquired elasticity maps with single ROI measurements with five so-called grouped measurements in two separate acquired elasticity maps with two to three ROIs in one small SWE-box in the liver [9]. The operator can increase the size of the SWE-box. This allows seeing the elasticity of a greater liver area, shortens the examination time by setting more ROI in the SWE-box and makes the examination easier. On the other hand, it causes an increase in artefacts. In this study we compare ten separate acquisitions each with one ROI to one acquisition with an increased size of the SWE-box containing ten ROI.

Materials and methods

Study population

Our institutional Ethics Committee approved the study (case number: EA1/206/19) and all participants gave written informed consent. This prospective study includes 69 patients who underwent an ultrasound examination because of a known diffuse chronic liver disease in our outpatient department. The age, sex, weight, height and cause of liver disease were recorded for every participant. The participants were asked not to eat three hours before the examination [10].

Equipment and methods

2D SWE studies were performed using the Aplio i800 ultrasound system of Canon (Canon Medical Systems, Tokyo, Japan) with a convex broadband probe (i8CX1). The pre-set “Fibrosis i8CX1” was selected before the SWE mode was started. The physical and technical specifications of SWE are written in detail elsewhere [2, 11]. The examinations were performed on the right lobe of the liver with an intercostal approach at the 7th or 8th intercostal space. In B-mode an area was chosen without artefacts of ribs and without larger vessels. Two different methods of data acquisition were used. In the first method, we conducted ten separated acquisitions with the standard size SWE-box (22x18mm) as the pre-set and a single ROI measurement per scan. In the second approach the size of the SWE-box was increased to maximum (56x50mm) and ten ROI were selected in the SWE-box. The SWE-box was placed with the upper border 15–20 mm below the liver surface. In both approaches the real-time SWE modus (“Multi-Shot”) was used and the image was paused after the whole SWE-box was colour filled and the propagation map showed parallel wave fronts. The measurements for each method were obtained with a circle shaped ROI of 10 mm diameter which was placed manually by the operator in an area of lowest standard deviation (SD) and parallel wave fronts in the propagation map. The ROI never overlapped each other. An example of the methods is given in Figs 1 and 2. The calculated value and the SD in m/s and kPa for each ROI were recorded and the mean and SD of ten measurements were calculated. The operator had more than three-years of experience in abdominal ultrasound exams and more than one year of experience in real-time elastography studies. The training and supervision of ultrasound and SWE was conducted by a highly experienced operator with more than forty years of experience in abdominal ultrasound exams and more than twelve years of experience in ultrasound based elastographic techniques.
Fig 1

Example of single ROI methods.

The example picture of one of the ten acquisitions with a single ROI for measurements. The shear wave elastography (SWE)-box is shown on the left side and the corresponding propagation map on the right. Figs 1 and 2 are examples from the same patient.

Fig 2

Example of the ten ROI in one acquisition.

Example picture of one acquisition with ten measurements in the enlarged SWE-box. On the left side the SWE-box with colour-coded elastographic measurements and on the right side the corresponding propagation map are shown. Note that the Aplio ultrasound system does not show the first region of interest (ROI) after setting the tenth. Figs 1 and 2 show the results of an 86-year-old male patient with haemochromatosis, mean results are 1.16 m/s (3.9 kPa) and 1.21 m/s (4.3 kPa) for the ten acquisitions and one acquisition with ten measurements respectively.

Example of single ROI methods.

The example picture of one of the ten acquisitions with a single ROI for measurements. The shear wave elastography (SWE)-box is shown on the left side and the corresponding propagation map on the right. Figs 1 and 2 are examples from the same patient.

Example of the ten ROI in one acquisition.

Example picture of one acquisition with ten measurements in the enlarged SWE-box. On the left side the SWE-box with colour-coded elastographic measurements and on the right side the corresponding propagation map are shown. Note that the Aplio ultrasound system does not show the first region of interest (ROI) after setting the tenth. Figs 1 and 2 show the results of an 86-year-old male patient with haemochromatosis, mean results are 1.16 m/s (3.9 kPa) and 1.21 m/s (4.3 kPa) for the ten acquisitions and one acquisition with ten measurements respectively.

Statistical analysis

All statistical tests were done with SPSS Statistics version 27.0.0.0 (IBM, Armonk, USA). For comparison of the two methods a Bland-Altman plot was drawn and the interclass correlation coefficient (ICC) was calculated. The Bland-Altman plot shows the difference of two measurements, which is plotted against the mean of the two measurements [12]. In this plot the 95%-confidence interval is given as dotted lines. ICC estimates and their 95% confident intervals were calculated based on a mean-rating (k = 2), absolute-agreement, 2-way mixed-effects model. The inter-method agreement was classified as poor (ICC < 0.50), moderate (ICC = 0.50–0.75), good (ICC = 0.75–0.90) or excellent (ICC > 0.9) [13].

Results

Demographics

Sixty-nine volunteers were included in this study. For three participants (4%) the 2D-SWE failed because of obesity (BMI of more than 37 kg/m2). The demographics of the 66 successful examined participants are as follows. Fifty-five women took part (83%). The mean age was 62 with a SD of ±13 years and a range of 22 to 86 years. The mean BMI was 25.3 with a SD of ±4.8 kg/m2 and a range of 16 to 40 kg/m2. The ultrasound was performed to monitor the primary biliary cholangitis (33, 50%), primary sclerosing cholangitis (11, 17%), autoimmune-hepatitis (9, 14%), haemochromatosis (5, 8%), Wilson’s disease (3, 5%), non-alcoholic-fatty-liver (3, 5%) or autoimmune cholangitis (2, 3%).

SWE measurement

The statistical analysis of the mean value of each participant separated in both methods is shown in Table 1. The difference in mean is not statistically significant (p = 0.9). The method of one acquisition has a slight smaller range compared to ten single acquisitions with a lower maximum and a higher minimal value.
Table 1

Statistical data of both methods.

Ten single acquisitions, single ROIOne acquisition, ten ROIs
n 6666
Mean 1.300 m/s (5.16 kPa)1.301 m/s (5.17 kPa)
Mean standard deviation 0.156 m/s (1.39 kPa)0.133 m/s (1.28 kPa)
Minimal value 1.083 m/s (3.37 kPa)1.115 m/s (3.53 kPa)
Median value 1.265 m/s (4.84 kPa)1.280 m/s (4.94 kPa)
Maximum value 1.749 m/s (9.33 kPa)1.807 m/s (11.24 kPa)

Table 1 shows the statistical data compared for both methods. The difference in mean is not statistically significant (p = 0.9).

Table 1 shows the statistical data compared for both methods. The difference in mean is not statistically significant (p = 0.9).

Intermethod comparability

According to the Bland-Altman plot, the mean difference between the two methods was -0.0016 m/s with a SD of 0.121 and upper and lower limits of agreement of 0.206 and -0.209 respectively. The plot is shown in Fig 3. The ICC is 0.85 with lower and upper value of the 95th confidence interval of 0.75 and 0.91 respectively. According to Koo and Li it is a good reliability for an ICC [13].
Fig 3

Bland-Altman plot for comparison of individual measurements and the grouped-measurement method.

The horizontal axis shows the mean of both measurements and the vertical axis shows the difference between both measurements drawn. The red dotted lines are the upper and lower limits of agreement and the red stashed line is the mean of all differences. The plot shows the spread between the results of both methods which increases with higher mean values.

Bland-Altman plot for comparison of individual measurements and the grouped-measurement method.

The horizontal axis shows the mean of both measurements and the vertical axis shows the difference between both measurements drawn. The red dotted lines are the upper and lower limits of agreement and the red stashed line is the mean of all differences. The plot shows the spread between the results of both methods which increases with higher mean values.

Discussion

Grouping ten ROIs in one acquisition allows a simpler examination in shorter time compared to multiple acquisitions and a single ROI and is comparable in mean and median value with a good ICC. To simplify the procedure and reduce the amount of required time, one study showed that the mean or the median of five measurements are comparable to ten measurements [14]. Another study shows a good reliability for the median of just three valid measurements [15]. Both studies reduce the number of measurements, which increases the risk of statistical uncertainty and sampling bias. Current guidelines recommend three to five measurements and acquisitions respectively [2, 16, 17]. To the best of our knowledge exist only two studies of the liver which use multiple ROI in one acquisition. In the latest report Chung et al. (2019) [9] used grouped measurements of two to three ROIs. In the other study by O’Hara et al. (2017) [18], two ROIs in one acquisition are used. Both did not increase the SWE-box size, but they did increase the ROI area in a single measurement as suggested previously by Thiele et al. to improve the validity of measurements [19]. The easiest approach is to increase the size of the ROI, which was done by Wang et al. in a different 2D-SWE ultrasound system, but this approach increases the median and the range of the results [20] and keeps a small SWE-box. Similar approaches with different SWE systems have been studied in lymph nodes [21] and breast lesions [22]. In these entities the maximal stiffness distinguished the best between malignant and benign lesions. This approach needs further examination to validate the applicability to determine the grade of liver fibrosis. Increasing the size of the SWE-box as suggested in our study has beneficial side effects. The examiner does get a better overview and can choose areas with good to excellent quality of elastographic measurements. Additionally, it gives a better impression of the elastographic pattern of the liver because of a greater area of view. Multiple ROIs assure to measure different areas in the liver. Single acquisitions und measurements bear the risk to repeat the procedure on the same area of liver, because of the limited anatomical options to perform a good SWE measurement. In this study the good correlation could be shown for values below 1.6 m/s equal to 7.7 kPa, because most of our participants are well treated outpatients with low grades of fibrosis (≤F2). At higher values the spread between both methods increases, which is seen in most elastographic studies as well. Further research is needed to compare both methods for patients with higher grade of fibrosis or cirrhosis. Please note that the patients have mixed causes of liver disease, which could have influence on the kind of fibrotic changes and the results of the elastography.

Conclusion

To conclude, maximizing the SWE-box and setting multiple ROIs is as good as performing ten acquisitions to confirm no or low grades of fibrosis (below 1.6m/s or 7.7 kPa, F0/1 fibrosis). In practical terms the suggested method shows more area of the liver tissue and the corresponding elastographic pattern and at the same time it is simpler and faster for daily routine. For higher grades of fibrosis (≥F2) further studies are needed to be performed to prove the applicability of this method. (XLSX) Click here for additional data file. 4 May 2022
PONE-D-21-33726
Simplification of 2D shear wave elastography by an enlarged SWE box and multiple regions of interest in one acquisition
PLOS ONE Dear Dr. Weiher, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ============================== ACADEMIC EDITOR: Dear author, my feeling is that your work may be published in this journal after major revisions. In order to get this, please provide the following required changes:
Editing and language revisions are needed.
Revise and shorten Introduction and Discussion.
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Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Partly ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: Abstract Line 26 : Please correct “Thru” Introduction Line 52-54 : Please rephrase Line 55 : Please correct “collated” Materials and methods Line 64-65 : Please rephrase Results Linea 124 : Please correct “statistical” Reviewer #2: Thank you for giving me the opportunity to review the article you submitted with the title "Simplification of 2D shear wave elastography by an enlarged SWE box and multiple regions of interest in one acquisition". The topic of the manuscript refers to the use of larger SWE-box and setting ten regions of interest (ROI) in one acquisition to semplify the procedure and reduce the acquisition time. The study presents data of primary scientific research and I found that the reported results have not been published elsewhere. The research meets all applicable standards for the ethics and research integrity. The article is presented in an intelligible fashion and adheres to appropriate reporting guidelines. Summary of results is given concisely are clearly supported by accurate and good quality images. Conclusions are appropriate and the results as well as the discussion supports them. My comments on the manuscript are listed below: - The discussion should be strengthened and in this regard we recommend multiple articles that have already dealt with this issue which in fact does not represent a particular clinical innovation. Among the recommended articles:https://doi.org/10.1371/journal.pone.0265802. - "Choosing ten different ROIs in one acquisition ALWAYS involves different parts of the liver" is not scientifically correct. Describe why you say this. - The lateral ROI position contributed as much as the acquisition depth to the total variance in SWD. Locations close to the initial shear-wave excitation pulse were more robust to biases because of inaccurate probe – phantom coupling. The size of the ROI and acquisition box did not introduce significant variations. How do you refute this statement? - Many technical errors and need for vocabulary corrections are identified. A quick review is recommended. In conclusion, despite my remarks and the inaccuracies found, the proposed study is substantiated and presented concisely. The stated aim is schieved. I would recommend the proposed article to be accepted for publication but after clearance of my comments. I would recommend the authors to pay more attention when preparing their manuscripts on methodology and punctuation. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 12 Jul 2022 ACADEMIC EDITOR: Dear author, my feeling is that your work may be published in this journal after major revisions. In order to get this, please provide the following required changes: Editing and language revisions are needed. Revise and shorten Introduction and Discussion. Additional Editor Comments: The paper deals with the use of larger SWE-box and setting ten regions of interest (ROI) in one acquisition to improve the procedure and reduce the acquisition time. The subject is timely and interesting. Reviewers remarked the need of editing and language revision. Moreover, reviewer 2 suggested to re-organize the section Discussion. I suggest to revise in a more focused way the section Introduction, too. ----The introduction is shortened and the focus is set to a more technical point to address the reviewer’s comment that this method is not a clinical innovation. Redundant sentences and phrases are deleted in the discussion. A new part with perspective in SWE in LN and breast lesions has been included, which opens an interesting point of view (maximal stiffness). Reviewer #1: Abstract Line 26 : Please correct “Thru” -- It is corrected. Introduction Line 52-54 : Please rephrase -- The lines are rephrased. Line 55 : Please correct “collated” -- The correction is applied. Materials and methods Line 64-65 : Please rephrase -- The sentences are rephrased. Results Linea 124 : Please correct “statistical” -- It’s corrected. -- I apologize for the language mistakes and I am grateful for the kind remarks. Reviewer #2: Thank you for giving me the opportunity to review the article you submitted with the title "Simplification of 2D shear wave elastography by an enlarged SWE box and multiple regions of interest in one acquisition". The topic of the manuscript refers to the use of larger SWE-box and setting ten regions of interest (ROI) in one acquisition to simplify the procedure and reduce the acquisition time. The study presents data of primary scientific research and I found that the reported results have not been published elsewhere. The research meets all applicable standards for the ethics and research integrity. The article is presented in an intelligible fashion and adheres to appropriate reporting guidelines. Summary of results is given concisely are clearly supported by accurate and good quality images. Conclusions are appropriate and the results as well as the discussion supports them. My comments on the manuscript are listed below: - The discussion should be strengthened and in this regard we recommend multiple articles that have already dealt with this issue which in fact does not represent a particular clinical innovation. Among the recommended articles: https://doi.org/10.1371/journal.pone.0265802. ---- I revised the discussion. Redundancies were deleted and some aspects of the mentioned articles were included. The mentioned articles are quite interesting and expand my horizon, because I never dealt with lymph nodes nor mamma lesions. - "Choosing ten different ROIs in one acquisition ALWAYS involves different parts of the liver" is not scientifically correct. Describe why you say this. I apologize for using incorrect wording and being redundant with the sentences before. The liver doesn’t get homogenous fibrotic. Like in histological examinations a sampling error exists. By choosing a larger SWE-box you gain a better overview and avoid to acquire elasticity in the same area of the liver by mistake. - The lateral ROI position contributed as much as the acquisition depth to the total variance in SWD. Locations close to the initial shear-wave excitation pulse were more robust to biases because of inaccurate probe – phantom coupling. The size of the ROI and acquisition box did not introduce significant variations. How do you refute this statement? ----- It's correct. Due to technical problems the signal from the shear wave gets more unreliable on its way through the liver. That depends partly because of hepatic fibrosis. In soft liver tissue the difference isn’t high as shown in this study. Therefore, it would be interesting if the results change in more fibrotic and cirrhotic livers. - Many technical errors and need for vocabulary corrections are identified. A quick review is recommended. ---- I apologize for the language mistakes and corrections and reformulations have been applied. In conclusion, despite my remarks and the inaccuracies found, the proposed study is substantiated and presented concisely. The stated aim is achieved. I would recommend the proposed article to be accepted for publication but after clearance of my comments. I would recommend the authors to pay more attention when preparing their manuscripts on methodology and punctuation. ---- Thank you very much for your kind remarks. Submitted filename: RESPONSE to Reviewers.docx Click here for additional data file. 16 Aug 2022 Simplification of 2D shear wave elastography by an enlarged SWE box and multiple regions of interest in one acquisition PONE-D-21-33726R1 Dear Dr. Weiher, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Francesco Somma Academic Editor PLOS ONE 1 Sep 2022 PONE-D-21-33726R1 Simplification of 2D shear wave elastography by enlarged SWE box and multiple regions of interest in one acquisition Dear Dr. Weiher: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Francesco Somma Academic Editor PLOS ONE
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