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  • SECTION I. General Information/Document Identification

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  • SECTION II. Composition of Guideline Development/Statement Development Group (GDG/SDG)

  • NOTE: i) All members of any GDG/SDG are expected to divest themselves of financial investments they or their family members have, and may not participate in marketing activities, speakers’ bureau, or advisory boards of entities whose interests could be affected by the guideline or statement content. All GDG/SDG members will be asked to declare (and regularly update) all current and planned commercial, non-commercial, intellectual, institutional, patient/public activities pertinent to the potential scope of the CPG or Statement. Failure to comply with ATA policies may result in exclusion or termination of a member of a GDG/SDG.
    ii) All Chairs or Co-Chairs of ATA documents must be ATA members in good standing, with competing interests declared to the ATA within the last 6 months. iii) The ATA® supports diversity of authorship and relevant stakeholder representation. The inclusion of patient/lay representatives is encouraged, especially for clinical practice guidelines.  Final applications are approved by the ATA Board of Directors.

  • 7. Chairs or Co-chairs of proposed document (if known):

  • 8. Proposed additional member(s) of GDG or SDG (including methodologist or patient representatives [if relevant], add more lines as needed) (Note: Potential members should not be promised positions, without approval of the Board of Directors).

  • If you have additional proposed member(s) of GDG or SDG (including methodologist or patient representatives) Please upload a file with their Name(s), Gender(s), Institution(s), Relevant expertise, Email(s)
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  • SECTION III. Details about the planned document

  • (Please include specific details such as whether there are any systematic reviews planned (and if so, a brief description of methods planned, including who will conduct systematic reviews, information sources, electronic databases to be searched [and by whom], how data will be abstracted, and critically appraised – general information available in the Prisma-P statement available at http://prisma-statement.org/Extensions/Protocols. If recommendations are planned, then the method for grading evidence and formulating evidence must be described (e.g. GRADE method preferred by ATA for guidelines), methods of achieving consensus (if applicable) must also be described (e.g. if voting on recommendations is planned, must indicate how the vote will be conducted [email, survey monkey, face to face at meetings], and if blinded or unblinded and the quorum needed for voting, e.g. ≥75% of members vote with 100% consensus).

  • (Mandatory for guidelines, optional for Statements. Note patient stakeholder views may be incorporated by a variety of means (e.g. literature review of patient opinions, patient stakeholder representation on the panel, conducting a survey or qualitative study to inform the guideline panel). If patient stakeholders are representatives of any specific organization (e.g. patient support group leadership), please indicate the name of the group and their position in the organization).

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