This page is part of the Evidence Based Medicine on FHIR Implementation Guide (v1.0.0-ballot2: STU1 Ballot 2) based on FHIR (HL7® FHIR® Standard) v6.0.0. No current official version has been published yet. For a full list of available versions, see the Directory of published versions
Generated Narrative: Evidence 236981
version: 69; Last updated: 2025-03-20 18:40:09+0000
Profile: ComparativeEvidence
RelatesTo
- type: part-of
- targetReference: MAGICapp Conversion Report: SGLT2 inhibitors and GLP-1 RA for type 2 diabetes (Identifier: FEvIR Linking Identifier/MAGIC-5288-j1Wqrn-conversion-report)
url: https://fevir.net/resources/Evidence/236981
identifier: FEvIR Object Identifier/https://fevir.net/FOI/236981, outcomeId/313965, picoId/85798, sectionId/73215
name: Severe_gastrointestinal_events_from_MAGICapp_313965
title: MAGIC-derived Evidence: Severe gastrointestinal events with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes
status: Active
publisher: Computable Publishing LLC
contact: support@computablepublishing.com
author: Computable Publishing®: MAGIC-to-FEvIR Converter:
Code | Value[x] |
Evidence Based Medicine on FHIR Implementation Guide Code System evidence-communication: Evidence Communication | ComparativeEvidence |
copyright:
https://creativecommons.org/licenses/by-nc-sa/4.0/
description:
This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.
assertion:
GLP-1 receptor agonists may increase the risk of severe gastrointestinal events compared with SGLT2 inhibitors.
variableDefinition
description:
Adults with type 2 diabetes
variableRole: Population
variableDefinition
description:
GroupAssignment: SGLT2 inhibitors vs. GLP-1 RA
variableRole: Exposure
comparatorCategory: GLP-1 RA
variableDefinition
description:
Severe gastrointestinal events
variableRole: Outcome
observed: Severe gastrointestinal events
synthesisType: SYSTEMATIC_REVIEW
studyDesign: NOTSET
statistic
description:
Risk Difference 5.8% (CI95 0.9% to 14.2%)
statisticType: Risk Difference
quantity: 0.058
SampleSizes
NumberOfStudies NumberOfParticipants 7 24638 AttributeEstimates
Type Range CI95 0.009-0.142
statistic
description:
OR 2.46 (CI95 1.22 to 4.97)
statisticType: Odds Ratio
quantity: 2.46
SampleSizes
NumberOfStudies NumberOfParticipants 7 24638 AttributeEstimates
Type Range CI95 1.22-4.97
certainty
description:
Due to serious inconsistency, Due to very serious indirectness, Due to very serious imprecision
type: Overall certainty
rating: Very low certainty
Subcomponents
Type Rating Risk of Bias NOTSET Inconsistency SERIOUS Indirectness VERY_SERIOUS Imprecision VERY_SERIOUS Publication Bias NOTSET