Dissolve-E: FHIR Implementation Guide for the AWMF Guideline Registry
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Dissolve-E: FHIR Implementation Guide for the AWMF Guideline Registry - Downloaded Version 0.1.0 See the Directory of published versions
As part of the project planning for the creation or updating of a guideline, a decision should be made at an early stage about the planned level classification ("S classification") according to the AWMF's system of rules (1-3). The S-classification scheme of the AWMF differentiates between the classes S1 treatment recommendation as well as S2e, S2k and S3 guideline. The "S" stands for the extent of the applied systematic approach in the development process of a guideline. Each class thus stands for a specific methodological concept that must be presented in a way that is comprehensible to the users. The choice of class is based on the question of how much effort is appropriate and feasible. The need for legitimacy for the implementation of the guideline (convincing the target group) must be taken into account. When choosing a higher S-classification in the context of updating a guideline, the adaptation to the corresponding methodology has to be considered.
CodeSystem representing the guideline status according to the AWMF.
CodeSystem representing various body system conditions.
CodeSystem defining different care settings, including levels of care, healthcare services, and treatment contexts.
CodeSystem defining different clinical application types
CodeSystem defining types of contact points for a guideline
CodeSystem defining roles for the author of the guideline.
CodeSystem defining different guideline release types
Sections of a guideline, describing various aspects such as its intention, target patient group, care setting, and other relevant contextual information.
CodeSystem defining the values representing the level of consensus for a recommendation.
CodeSystem defining values to classify medical subjects into different categories.
CodeSystem defining values representing the synthesis type of a recommendation
CodeSystem defining codes to represent tags for recommendations
CodeSystem defining types of related artifacts that can be part of a guideline.
CodeSystem defining different types of remarks that can be associated with guidelines, including restrictions, warnings, and additional notes.
CodeSystem representing the overall judgment of risk of bias assessed by the RoB2 tool for evaluating risk of bias for randomized trials.
CodeSystem defining the intended patient population for whom the guideline is applicable.
CodeSystem representing different codes of interest for the Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften (AWMF)
CodeSystem representing the domains assessed by the AGREE II instrument for evaluating the quality of clinical practice guidelines.
CodeSystem representing the overall confidence ratings from the AMSTAR 2 critical appraisal tool.
CodeSystem for identifying evidence rating and appraisal frameworks used in systematic reviews, guideline development, and clinical decision support.
CodeSystem representing the Oxford Centre for Evidence-Based Medicine 2011 Levels of Evidence.
CodeSystem defining the grading of recommendations according to German guideline methodology as used in AWMF S3 guidelines.
CodeSystem representing the overall judgment of risk of bias assessed by the RoB2 tool for evaluating risk of bias for randomized trials.
CodeSystem representing the judgment of risk of bias assessed by the ROBIS tool for evaluating risk of bias in systematic reviews.
CodeSystem representing the domains assessed by the ROBIS tool for evaluating risk of bias in systematic reviews.
CodeSystem defining GRADE Evidence to Decision (EtD) Framework Certainty Ratings
CodeSystem defining values to represent the GRADE Evidence to Decision (EtD) Framework Certainty Type
CodeSystem defining possible intended audiences for a section
CodeSystem defining values indicating how a recommendation relates to a new version of the guideline