Peer Review History
| Original SubmissionNovember 22, 2019 |
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PONE-D-19-32474 Botulinum toxin in the treatment of high AC/A ratio accommodative esotropia PLOS ONE Dear Dr. Tejedor, 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. We would appreciate receiving your revised manuscript by Jan 24 2020 11:59PM. When you are 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. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols Please include the following items when submitting your revised manuscript:
Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out. We look forward to receiving your revised manuscript. Kind regards, Ahmed Awadein, MD, Ph.D, FRCS Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements:
Please amend your current ethics statement to include the full name of the ethics committee/institutional review board(s) that approved your specific study. Once you have amended this/these statement(s) in the Methods section of the manuscript, please add the same text to the “Ethics Statement” field of the submission form (via “Edit Submission”). For additional information about PLOS ONE ethical requirements for human subjects research, please refer to http://journals.plos.org/plosone/s/submission-guidelines#loc-human-subjects-research. 3. Please amend your list of authors on the manuscript to ensure that each author is linked to an affiliation. Authors’ affiliations should reflect the institution where the work was done (if authors moved subsequently, you can also list the new affiliation stating “current affiliation:….” as necessary). [Note: HTML markup is below. 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: Partly Reviewer #2: Yes ********** 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: No Reviewer #2: No ********** 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: Re: Manuscript PONE-D-19-32474 "Botulinum toxin in the treatment of high AC/A ratio accommodative esotropia". Dependant on the author’s response to some of the questions I have posed,Irecommend that the article be accepted with Minor(?) revision,English is not the authors mother tongue, and the language needs to be corrected in many areas to diminish ambiguity. (While nevertheless appreciating that it is not easy to write in a language different to one’s home language) The study is retrospective and comparative, and includes patients with accommodative esotropia (ET) [Because of the residual deviation despite wearing the full cycloplegic correction,this should be changed to partially accommodative ET{PAET} with a high accommodative convergence/accommodation ratio (AC/A).]The patients were divided into two groups. Group one patients were treated by botulinum toxin injection to both medial rectus muscles. Group two patients were treated by bilateral medial rectus muscle recessions, augmented with posterior fixation. The motor and sensory outcomes of patients in each group were compared. While the manuscript is technically sound in most respects, I am concerned about the following: Patients received glasses based on the cycloplegic refraction at the initial visit, which were then worn for two months. The ET angle was measured at the next visit (the baseline visit). At that visit patients who had a residual distance ET of at least 10 prism dioptres (PD), and an ET at near that was larger than the distance ET by 10 PD or more were considered eligible for inclusion in Group 1 or 2(Lines 108-112). It is considered by many that if the glasses do not reduce the distance deviation to less than 10 PD, another cycloplegic refraction, which usually discloses additional hyperopic refractive error, should be performed. If this is found, the spectacle power should be increased, and the glasses worn for at least another 4 weeks. If the new spectacles reduce the ET angle the refraction should again be repeated. This process may reduce or eliminate the distance deviation ,and reduce the distance/ near disparity. From the manuscript it appears as if this was not done.(Lines 51and 52-“Cycloplegic refraction was carried out at the initial visit, at 6 months and a year after BTX injection or surgery”) Could the authors please comment? Line 82 -88 Consider changing to “ …….with additional procedures, several of which are available………….deviation at near. We had used the later procedure for several years,……… for this condition.” Line 85 Throughout the whole manuscript, change “medial recti and medial recti muscles” to “medial rectus muscles”, and change “bimedial recession” to “bilateral medial rectus muscle recessions”. Line90. “… parents did not agree to surgery. The results ………………..were considered to be satisfactory.” Line104 . Suggest change to “After a detailed explanation of the nature of the study, informed consent was obtained for BTX injection or surgery, and for collection of the relevant data……………” Line 125. Children with “………….myopia greater than -0.50D were excluded.” Were any myopic children include in the study? ( Line 174 “or myopic whose visual acuity improved with correction” )[Table 1 appears to indicate all patients were greater than +2.25 D hyperopic]) Line 133 . Cycloplegic retinoscopy ………were also part of the study.(but only “at the initial visit, at 6 months and a year after BTX injection or surgery”) ? Line 148. Suggest change to: “…of the muscle pulley. Although this was identified during surgery,we nevertheless chose to use a classical scleral fixation technique to secure the muscle, with a non-absorbable 5-0 Dacron suture, and not a modified pulley fixation technique, as described by Clarke et al5”(published in 2004 ,and not later). Line 158 -160 This is repetitive of lines 134-136 Lines 187 -192 Suggest change to “Six months after Botox injection or surgery, the deviation (with distance glasses) at distance and near, as well as stereoacuity were similar in the two groups. However, the deviations in the surgery group were significantly larger and stereoacuity in the BTX group significantly better at I year.” Lines 191-192 states “stereoacuity was significantly better in the surgery group at I year”, while lines 238-239 and 350 (the legend to figure 2) state it was “better in the BTX group”. Please correct The stereoacuity levels may have been related the duration of alignment before the constant ET developed(not studied) Line 202-208. “The percentage of success ….was similar in both groups……. at 6 months, but smaller in the surgery group at I year……...” Table 1 contains the preintervention median, minimum and maximum refractions. Line 52 indicates that cycloplegic refractions were carried at the initial visit and 6 and 12 months after BTX or surgery. The manuscript does not report if any of the patients required a stronger hyperopic correction between the 6 and 12 month post- treatment visits, or in those requiring a new procedure (line 214). Any under correction could have influenced the deviations, stereoacuity, distance near disparity and the need for bifocals. As the authors point out (lines 193-196), whether statistically significant or not, most differences were of little clinical relevance Line 255. Replace with “We had no overcorrections in either study group. In the past, while performing larger recessions of x mm (authors to add in size of recessions), combined with posterior fixation we had overcorrections. These frequently increased with time and required reoperation. In the present study we thus adhered strictly to the AAO guidelines 6 ” Line 279-284. Could the authors comment on whether they could either slightly increase the amount of medial rectus muscle recession, or alter placement of the PFS, in order to improve the result of surgery with PFS without a greater risk of overcorrection Line 280 By “more conservative(i.e.,less posterior)scleral……..” Do they mean placing the PFS more anteriorly, which should have less effect on the near deviation, but not on the distance deviation .If so how would it reduce the overcorrection rate? 955 Words Reviewer #2: The manuscript describes a novel way for treating partially-accommodative esotropia with botulinum toxin 1- Overall the manuscript needs extensive grammatical revision 2- Throughout the manuscript, consider replacing high accommodative convergence/accommodation (AC/A) ratio accommodative esotropia with partially acommodiative esotropia with high AC/A ratio 3- Can the authors clarify the relatively young group of the included patients? Why were older age groups not included? 4- Lines 101-102: What standard deviation was used to allow sample size calculation? 5- Did the authors include patients with convergence excess ET with normal AC/A ratio? and if not why were they included, though they might benefit from the same procedure. 6- Line 146 The relatively small amount of recession implies that the authors used standard recession rather than augmented recession. Usually the amounts of recession would be much higher for augmented recession 7- Line 174: Didnt you exclude myopic patients? 8- Lines 248-255 the authors are referring to pulley fixation rather than posterior scleral fixation. This section is not related to the current work and can be trimmed ********** 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 to be viewed.] 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. 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| Revision 1 |
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Botulinum toxin in the treatment of partially accommodative esotropia with high AC/A ratio PONE-D-19-32474R1 Dear Dr. Tejedor, We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements. Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication. Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. 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 enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and 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. With kind regards, Ahmed Awadein, MD, Ph.D, FRCS Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: |
| Formally Accepted |
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PONE-D-19-32474R1 Botulinum toxin in the treatment of partially accommodative esotropia with high AC/A ratio Dear Dr. Tejedor: I am 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 notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, 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. For any other questions or concerns, please email plosone@plos.org. Thank you for submitting your work to PLOS ONE. With kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Ahmed Awadein Academic Editor PLOS ONE |
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