Peer Review History
| Original SubmissionFebruary 13, 2021 |
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PONE-D-21-04965Diagnostic Performance Of Optical Coherence Tomography Macular Ganglion Cell Inner Plexiform Layer And Retinal Nerve Fiber Layer Thickness In Glaucoma Suspect And Early Glaucoma Patients At St. Paul’s Hospital Millennium Medical College, EthiopiaPLOS ONE Dear Dr. Abera, 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. Please submit your revised manuscript by Nov 22 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript:
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All PLOS journals require that the minimal data set be made fully available. For more information about our data policy, please see http://journals.plos.org/plosone/s/data-availability. Upon re-submitting your revised manuscript, please upload your study’s minimal underlying data set as either Supporting Information files or to a stable, public repository and include the relevant URLs, DOIs, or accession numbers within your revised cover letter. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories. Any potentially identifying patient information must be fully anonymized. Important: If there are ethical or legal restrictions to sharing your data publicly, please explain these restrictions in detail. Please see our guidelines for more information on what we consider unacceptable restrictions to publicly sharing data: http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. Note that it is not acceptable for the authors to be the sole named individuals responsible for ensuring data access. We will update your Data Availability statement to reflect the information you provide in your cover letter. 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) The manuscript describes diagnostic performance of clinical available OCT system (Cirrus HD-OCT) with thickness measurement for detecting glaucoma. Both macular and peri-papillary scans were performed on 188 eyes for discrimination among early glaucoma, glaucoma suspect, and healthy control groups. Thickness of ganglion cell inner plexiform layer (GCIPL)and retinal never fiber layer (RNFL) was measured for macular scan and peri-papillary scan respectively. The study is finely designed, but the content of the manuscript is more suitable for a clinical journal. I also have major concerns about the presentation of the results and the quantification methods for data analysis, which I think the authors must address. I also offer some detailed comments to help improve the manuscript. Major comments: 1. Missing important technical details prevents proper evaluation of the results. The authors used specificity and sensitivity to evaluate the diagnostic performance, however, how the two parameters were calculated from the layer thickness measurement was not explained. Other details about AUROC, GCIPL and RNFL parameter extraction from OCT images, OR-logic approach for analysis were missing as well. The necessary detailed information shall be provided. 2. Plots for AUROC and representative OCT images shall be presented to help the readers understand the analysis method and results. See detailed comments. 3. Segmentation errors may occur in the clinical OCT devices. Did the authors verify the segmentation accuracy? Detailed comments: 1. Please make sure all the abbreviation are defined in the first place they appear in the main texts. Some undefined terms are: POAG, RNFL, AUROC, SD, VCDR, ONH. 2. Page 10, Study population section: please explain the meaning of the equation (Eq. xx) and what each parameter are in the formula. 3. Page 10, last paragraph: Please clarify the threshold for normal MD and PSD. 4. Page 10, last paragraph: Please provide reference for the disease classification. 5. Page 11, OCT imaging procedure section: Please explain how the OCT thickness was extracted for different quadrants, and how the quadrants are defined. A representative OCT image should be provided for clarity purpose to help the readers understand the data analysis strategy. 6. Page 11, first paragraph: The unit is missing for refractive error. 7. Page 11, Statistical analysis section: Please explain the ‘Or-logic’ approach. 8. Page 11, Statistical analysis section: Please clarify how ‘specificities’ and ‘sensitivities’ are calculated. 9. Page 13, Result section: Are the enrolled groups age-matched? Inner retinal thickness also decreases with aging. 10. Page 14 table 2: It is not clear how the GCIPL and RNFL parameters are extracted at different regions. Example of OCT image shall be provided to explain the methods and data analysis strategy. 11. Page 14 table 2: Units are missing for the parameters. 12. Page 14 paragraph after table 2: ROC plots shall be provided for data visualization and evaluation. 13. Page 14 paragraph after table 2: Please explain what ‘or logic’ is and how ‘or logic’ is determined and used in your analysis. 14. Page 16 second paragraph: Please define ‘b/n’. 15. Page 18, Discussion section, the first sentence. I believe it is still a debatable question what loss first in glaucoma. [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. |
| Revision 1 |
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Diagnostic performance of optical coherence tomography macular ganglion cell inner plexiform layer&retinal nerve fiber layer thickness in glaucoma suspect&early glaucoma patients at St. Paul’s hospital millennium medical college, Addis Ababa,Ethiopia PONE-D-21-04965R1 Dear Dr. Abera, 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, Akram Belghith Academic Editor PLOS ONE |
| Formally Accepted |
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PONE-D-21-04965R1 Diagnostic performance of optical coherence tomography macular ganglion cell inner plexiform layer&retinal nerve fiber layer thickness in glaucoma suspect&early glaucoma patients at St. Paul’s hospital millennium medical college, Addis Ababa,Ethiopia Dear Dr. Abera: 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. Akram Belghith Academic Editor PLOS ONE |
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