Presentation on theme: "Participation Requirements for a Guideline Panel Co-Chair."— Presentation transcript:
Participation Requirements for a Guideline Panel Co-Chair
Background These slides are intended to clarify the guideline development process and illustrate expectations of a Co-Chair for participation in an ASCO guideline panel. Guideline development can be time-consuming, but the end- products are especially valued by members. We recognize that participation in development in an ASCO guideline involves significant commitment of time and energy. We hope that the material that follows provides some clarification regarding the expectations and scope of the undertaking.
ASCO’s Guidance Products Clinical Practice Guideline: Addresses specific clinical situations (disease- oriented) or use of approved medical products, procedures, or tests (modality-oriented). Systematic reviews serve as the evidentiary basis for drafting principles of clinical care. Interpretation and extrapolation of evidence are often necessary. Consensus Guideline: A systematic review is conducted. If evidence identified is limited, inconsistent, indirect, or of poor quality, then the formal consensus-based methodology may be considered. While the decision to incorporate consensus recommendation(s) may vary, the common thread is lack of sufficient evidence. ASCO utilizes a modified Delphi process for creating consensus guideline recommendations. Additional information on the methodology can be found on the ASCO Guidelines Wiki Guideline Development page.ASCO Guidelines Wiki Guideline Development page
ASCO’s Guidance Products Guideline Endorsement: ASCO can be approached by other organizations to endorse a guideline or ASCO can initiate the process. The topic should be relevant and appropriate to the mission and interests of ASCO. Endorsing other organizations’ guidelines decreases duplication of effort and allows ASCO to expand the library of recommendations available to members. Guideline Adaptation: ASCO follows a process for adapting guidelines from other organizations. Guideline recommendations can be adapted from one or multiple relevant guidelines with the intent of producing a guideline relevant to the ASCO membership. Adapting other organizations’ guidelines decreases duplication of efforts and allows ASCO to expand the library of recommendations available to members. Provisional Clinical Opinion (PCO): is intended to offer timely clinical direction to the ASCO membership following the publication or presentation of potentially practice-changing data from major studies. The PCO may serve in some cases as interim direction to the membership pending the development or updating of an ASCO clinical practice guideline. The PCO enables ASCO to provide a rapid response to key data from clinical cancer research. Additional information on the methodology can be found on the ASCO Guidelines Wiki Guideline Development page.ASCO Guidelines Wiki Guideline Development page
Appraising the Evidence and Rating the Evidence and Recommendations Quality appraisal. It is proposed that evidence informing guideline recommendations be formally appraised to evaluate the reliability and validity of the evidence. These assessments of quality will be made for individual sources of evidence (i.e., individual trials, systematic reviews, etc.) using pre-specified criteria, which are based primarily on elements of quality related to study design, methodology, and risk of bias. A sample of the study quality appraisal checklist developed/adapted for randomized controlled trials is provided in Appendix 3. Strength of evidence. The quality of the total body of evidence used to inform a given recommendation will be assessed to evaluate its validity, reliability, and consistency. This assessment will consider the individual study quality ratings, the overall risk of bias, and the overall validity and reliability of the total body of evidence. The summary rating will be an indication of the Panel’s confidence in the available evidence. Strength of recommendations. The Panel provides a rating of the strength of each recommendation. This assessment is primarily based on the strength of the available evidence for each recommendation and it is an indication of the Panel’s confidence in its guidance or recommendation. However, where evidence is lacking, it also affords panels the opportunity to comment on the strength of their conviction and uniformity of their agreement that the recommendation represents the best possible current guidance. Additional information on can be found on the ASCO Guidelines Wiki Guideline Development page.ASCO Guidelines Wiki Guideline Development page
Responsibilities Systematic Review Development Panel Co-Chairs collaborate with the ASCO Staff to develop a systematic review. The systematic review is what ensures that ASCO Guidelines are “evidenced based.” Co-Chairs work with ASCO staff in development the Guideline Development Protocol, which includes specific inclusion/exclusion criteria, search terms, and other information for the systematic review. Co-Chairs plan a strategy for the Panel to review the results of the systematic review. They assume responsibility for deciding if the panel work can be conducted via webinar/teleconference or if a face to face meeting is needed
Responsibilities for Guideline Development Panel Co-Chairs assume primary responsibility for drafting the manuscript, but may divide the work by having specific panel members draft some sections. It is recommended that no more than three to four people assume responsibility for initially drafting the manuscript. Co-Chairs work with ASCO Staff to set and enforce deadlines. Co-Chairs typically serve as first and last authors of the finished product, although there can be exceptions to this at the discretion of the Co-Chairs. Co-Chairs may be asked to review abstracts from an updated literature search to identify potentially practice-changing data based on defined criteria (see description of “signals” option for updating guidelines in the Guideline Procedures Manual). These data represent “signals” for updating a guideline.
Additional Responsibilities Co-Chairs will be asked to provide feedback or input into the development of “clinical tools and resources” such as decision aids, algorithms, or flow charts that are designed to facilitate adherence to the guideline. Co-Chairs will be asked to interface with the media at the time of publication and to assist ASCO in the development of press releases, and of materials suitable for use with patients and for publication on the cancer.net website. Co-Chairs are not expected to draft these documents, but to critically review them to ensure that the content is accurate and clear. Co-Chairs may be asked to participate in the development of quality measures from the guideline recommendations. These statements are considered by the Quality of Care Committee for use as quality measures in QOPI.
Steps in Creating an ASCO Guideline 1.Systematic review conducted by ASCO Staff (searches, abstract review, full text review, data extraction, evidence table development) 2.Panel meets, reviews evidence, develops recommendations 3.Draft manuscript assembled by the Co-Chairs or Steering Committee and ASCO Staff Co-chairs 4.Panel reviews and approves the first draft 5.Draft submitted for JCO review and sent concurrently for external review 6.Reviews incorporated into revised draft 7.Panel reviews and approves revised draft 8.Draft submitted to CPGC for review and approval 9.Panel revises draft based on CPGC review 10.Panel reviews and approves final draft. 11.Draft returned to CPGC reviewers for review and approval (if required) 12.Draft resubmitted to JCO.
Thank you for participating in the guideline development process. If you have any questions or concerns, please contact