Peer Review History
| Original SubmissionJuly 23, 2019 |
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PONE-D-19-20806 De-coding the language; how clinicians interpret resuscitation clinical care plans. A mixed methods study PLOS ONE 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 Oct 20 2019 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, Andrew Carl Miller Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at http://www.journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and http://www.journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. Please provide additional details regarding participant consent. In the Methods section, please ensure that you have specified (i) whether consent was informed and (ii) what type you obtained (for instance, written or verbal). If your study included minors, state whether you obtained consent from parents or guardians. If the need for consent was waived by the ethics committee, please include this information 3. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. 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We will update your Data Availability statement on your behalf to reflect the information you provide. Additional Editor Comments: Please ensure your work adheres to the following guideline and provide citation: Eysenbach, G. (2004). Improving the quality of web surveys: the checklist for reporting results of internet e‐surveys (cherries). Journal of medical Internet research, 6(3)e34 doi:10.2196/jmir.6.3.e34 http://www.jmir.org/2004/3/e34/ Describe the informed consent process. Where were the participants told the length of time of the survey, which data were stored and where and for how long, who the investigator was, and the purpose of the study? If any personal information was collected or stored, describe what mechanisms were used to protect unauthorized access. State how the survey was developed, including whether the usability and technical functionality of the electronic questionnaire had been tested before fielding the questionnaire. Please verify that this was a “closed survey”: An “open survey” is a survey open for each visitor of a site, while a closed survey is only open to a sample which the investigator knows (password-protected survey). In “closed” (non-open) surveys, users need to login first and it is easier to prevent duplicate entries from the same user. Describe how this was done. For example, was the survey never displayed a second time once the user had filled it in, or was the username stored together with the survey results and later eliminated? If the latter, which entries were kept for analysis (eg, the first entry or the most recent)? How/where was the survey announced or advertised? Some examples are offline media (newspapers), or online (mailing lists – If yes, which ones?) or banner ads (Where were these banner ads posted and what did they look like?). It is important to know the wording of the announcement as it will heavily influence who chooses to participate. Ideally the survey announcement should be published as an appendix. For the e-mail survey, were the responses entered manually into a database, or was there an automatic method for capturing responses? Were any incentives offered (eg, monetary, prizes, or non-monetary incentives such as an offer to provide the survey results)? Randomization of items: To prevent biases items can be randomized or alternated. Was adaptive questioning used? With adaptive questioning (certain items, or only conditionally displayed based on responses to other items) to reduce the number and complexity of the questions. What was the number of questionnaire items per page? The number of items is an important factor for the completion rate. Over how many pages was the questionnaire distributed? The number of items is an important factor for the completion rate. It is technically possible to do consistency or completeness checks before the questionnaire is submitted. Was this done, and if “yes”, how (usually JAVAScript)? An alternative is to check for completeness after the questionnaire has been submitted (and highlight mandatory items). If this has been done, it should be reported. All items should provide a non-response option such as “not applicable” or “rather not say”, and selection of one response option should be enforced. State whether respondents were able to review and change their answers (eg, through a Back button or a Review step which displays a summary of the responses and asks respondents if they are correct). How did you determined a unique visitor. There are different techniques available, based on IP addresses or cookies or both. -- Cookies: If so, mention the page on which the cookie was set and read, and how long the cookie was valid. Were duplicate entries avoided by preventing users access to the survey twice; or were duplicate database entries having the same user ID eliminated before analysis? In the latter case, which entries were kept for analysis (eg, the first entry or the most recent)? -- IP Address: Indicate whether the IP address of the client computer was used to identify potential duplicate entries from the same user. If so, mention the period of time for which no two entries from the same IP address were allowed (eg, 24 hours). Were duplicate entries avoided by preventing users with the same IP address access to the survey twice; or were duplicate database entries having the same IP address within a given period of time eliminated before analysis? If the latter, which entries were kept for analysis (eg, the first entry or the most recent)? Was log file analysis used?: Indicate whether other techniques to analyze the log file for identification of multiple entries were used. If so, please describe. Provide view rate (Ratio unique site visitors/unique survey visitors) if possible: Requires counting unique site visitors (not page views!) divided by the number of unique visitors of the first page of the survey. It is not unusual to have view rates of less than 0.1 % if the survey is voluntary. Provide participation rate (Ratio unique survey page visitors/agreed to participate) if possible: Count the unique number of visitors who visit the first page of the survey (or the informed consent page, if present) divided by the number of people who filled in the first survey page (or agreed to participate). This can also be called “recruitment” rate. Provide completion rate (Ratio agreed to participate/finished survey) if possible: The number of people agreeing to participate (or submitting the first survey page) divided by the number of people submitting the last questionnaire page. This is only relevant if there is a separate “informed consent” page or if the survey goes over several pages. This is a measure for attrition. Note that “completion” can involve leaving questionnaire items blank. This is not a measure for how completely questionnaires were filled in. (If you need a measure for this, use the word “completeness rate”.) Were only completed questionnaires analyzed? Were questionnaires which terminated early (where, for example, users did not go through all questionnaire pages) also analyzed? [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: Yes Reviewer #2: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: I Don't Know 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: No 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: This is an interesting study that I believe would be of interest to the international community involved in developing and implementing the use of emergency care and treatment plans. Whilst the paper has been presented well, I believe that some revision would improve it and increase its value to readers. I feel that the title of the paper (in particular the use of the word ‘de-coding’) does not reflect the study’s findings and paper’s content accurately in a way that will help readers to find it and know what it is about. The main message from the findings of this study is that use of ambiguous language in resuscitation plans – unsurprisingly – results in different interpretation among doctors and in different decisions about choices of emergency treatments. I suggest that the title is amended to reflect this clearly. The text states that 3 of the 4 authors ‘contributed equally to this work’. The nature and extent of their equal contributions are not stated. I suggest that this be corrected. There is a degree of irony in this paper that addresses ambiguity and misinterpretation of terminology within a document that itself has the ambiguous name ‘resuscitation plan’. Some people use or interpret ‘resuscitation’ as referring to cardiopulmonary resuscitation, whereas others will use terminology such as ‘fluid resuscitation’ and some consider other emergency treatments as being part of ‘resuscitation’. The study identifies that doctors have different perceptions of the purpose and value of a ‘resuscitation plan’. The paper could usefully discuss whether that might be resolved, at least in part, by using a different, more specific name for the plan and/or a clear statement on the form of its purpose. A weakness of this study, which should be acknowledged in the text, is that it has asked doctors to interpret (in the context of case vignettes) free-text phrases used on resuscitation plans from 2017 that were examined in a previous study. That previous study concluded that these phrases were ‘open to broad, variable interpretation’ and that ‘…ongoing education is integral to changing practice’. The present study has – unsurprisingly – validated the first of these conclusions, and – disappointingly – the current paper fails to acknowledge the crucial role of education (including audit, appraisal and feedback) in persuading doctors to record clear recommendations and stop using ambiguous phrases. If these phrases are in widespread use, that appears to indicate failure of adequate staff education in the completion of the 7-step form. In more than one place, the text states ‘Terminology was neither consistently interpreted nor applied…’. I think that the authors intended to state that terminology was neither interpreted consistently nor applied consistently, not that the ‘terminology’ was not applied. The paper refers to ‘not for Cardiopulmonary Resuscitation orders’ but does not make clear the legal status of such documents in Australia. In the UK, such documents are not legally binding ‘orders’ but are recommendations to guide those dealing with a sudden emergency to make the best possible decisions about the emergency care and treatment of the person, when the person has lost capacity to make choices about their care and treatment. The legal status of similar documents varies from country to country, so I think – especially in an international journal – that this should be acknowledged and discussed in this paper. The paper states that the 7-step form is being used in all ‘public tertiary hospitals’ in South Australia. This terminology is potentially ambiguous for an international readership, so it would be helpful for the text to define the type, size and number of hospitals covered by this term. It would be helpful and of great interest also to understand what arrangements are in place to communicate recommendations for the emergency care and treatment of patients who have not been admitted to this type of hospital, or patients transferred or discharged from a tertiary hospital. For the provision of person-centred care, I think there should be a robust process to transfer an up-to-date and relevant 7-step form with the patient or to generate current recommendations for emergency care and treatment on a different document. Whichever document is used outside the tertiary hospitals must be widely used, recognised and accepted across a range of other care settings, by a broad range of health and care professionals. Clearly, the ambiguous terminology used in this study to explore interpretation by hospital doctors would be likely to be even more ambiguous to health and care professionals if used on a form held by a patient at home or in various other care settings. The paper implies in a single sentence that the 7-step form is very similar to 'international counterparts'. This is not strictly true. There are substantial differences, and it would be appropriate to identify these in the text and to consider them in subsequent discussion of possible options for improving the design of the 7-step form to overcome the problems identified in this study. There is published evidence that using a discussion process and form that focus on and record treatments that would be wanted and should be considered to help to achieve the person’s goals of care, not primarily on treatment to be withheld, are preferred by both patients and by healthcare professionals. The ‘7-step form’ appears to focus more on withholding treatment rather than on giving realistic care and treatment to meet the person’s goals of care. As such, it does not appear truly person-centred or evidence-based. In the published report of their previous study (reference 4) the authors concluded that the current Alert Form (‘7-step form’) could be improved. The tick-box list in section 4 of the form focuses firstly on emergency treatments to be withheld, emphasised using red print. Treatments that ‘will be provided’ are relegated to a rather less prominent free-text box below. Even the wording in this box is ambiguous. This box should list treatments that would be wanted and should be considered – and provided if they are needed. I would like to see much more discussion about the substantial potential to improve the form and to try to ensure that the form is used to support good communication, good medical practice and person-centred care, rather than primarily supporting the healthcare system. In the discussion section, the paper suggests ‘To further improve clarity for junior staff, free-text options could be replaced with standardised choices e.g. non-invasive ventilation, cardiac monitoring, artificial hydration and intravenous antibiotics’. I am concerned that this would be primarily a system-focused intervention that is not truly person-centred. There are several potential ways in which the form could be modified to make it more person-centred and less likely to lead to varying interpretation and incorrect decision making in an emergency, and I would like to see the discussion expanded to consider these other options and the advantages and disadvantages of each. Trying to create a comprehensive list of tick-box treatment options to cater for every person's individual needs seems likely to make the form unduly long and cumbersome for all, and trying to limit the number of treatment options will inevitably fail to cater for all individual needs. I am sorry to raise so many suggestions and hope that they will be viewed in the constructive spirit intended, and used to develop this interesting paper to its full potential. Reviewer #2: I think you did a good job with a difficult research topic. I added a couple of comments about discussing the vignette management differences seen. I thought you addressed the language ambiguity in the second part well. ********** 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: Yes: Dr David Pitcher Reviewer #2: Yes: Michael Ritchie [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. 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 us at figures@plos.org. Please note that Supporting Information files do not need this step.
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| Revision 1 |
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The impact of language on the interpretation of resuscitation clinical care plans by doctors. A mixed methods study PONE-D-19-20806R1 Dear Dr. Dignam, 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, Andrew Carl Miller Academic Editor PLOS ONE Additional Editor Comments (optional): The authors have satisfactorily answered the reviews queries. |
| Formally Accepted |
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PONE-D-19-20806R1 The impact of language on the interpretation of resuscitation clinical care plans by doctors. A mixed methods study. Dear Dr. Dignam: 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. Andrew Carl Miller Academic Editor PLOS ONE |
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