 0 Table of Contents |
  1 Introduction |
  2 Evidence Profiles |
  3 EvidenceVariable Profiles |
  4 Group Profiles |
  5 Citation Profiles |
  6 ArtifactAssessment Profiles |
  7 Composition Profiles |
  8 Other Profiles |
  9 Profiles |
  10 Extensions |
  11 Terminologies |
  12 Examples |
  13 Downloads |
  14 Artifacts Summary |
   14.1 AbsenceOfExposureDefinition |
   14.2 Adaptation |
   14.3 BaselineMeasureEvidence |
   14.4 BaselineMeasureReport |
   14.5 BaselineVariablesList |
   14.6 BookCitation |
   14.7 BookPartCitation |
   14.8 CertaintyOfEvidence |
   14.9 Classification |
   14.10 CohortDefinition |
   14.11 Comment |
   14.12 ComparativeBaselineMeasureEvidence |
   14.13 ComparativeEvidence |
   14.14 ComparativeEvidenceReport |
   14.15 ComparativeEvidenceReportExpanded |
   14.16 ComparativeEvidenceReportSubject |
   14.17 ComparativeEvidenceSynthesisReport |
   14.18 ComparativeParticipantFlowEvidence |
   14.19 ComparatorGroup |
   14.20 ComparatorOnlyEvidence |
   14.21 Comparison |
   14.22 CompositeRating |
   14.23 ConceptualCohortDefinition |
   14.24 ConceptualComparatorDefinition |
   14.25 ConceptualExposureDefinition |
   14.26 DatabaseCitation |
   14.27 DatabaseEntryCitation |
   14.28 DatasetCitation |
   14.29 DateAsRating |
   14.30 DichotomousIntendedOutcome |
   14.31 EndpointAnalysisPlan |
   14.32 EvidenceAssessment |
   14.33 EvidenceList |
   14.34 EvidenceReport |
   14.35 EvidenceReportPackage |
   14.36 EvidenceReportSubject |
   14.37 EvidenceSynthesisEvidence |
   14.38 ExposureGroup |
   14.39 GroupAssignment |
   14.40 GroupR6 |
   14.41 Guideline |
   14.42 InterventionOnlyEvidence |
   14.43 JournalArticleCitation |
   14.44 M11Report |
   14.45 MetaanalysisEligibilityCriteria |
   14.46 MetaanalysisOutcomeDefinition |
   14.47 MetaanalysisStudyGroup |
   14.48 NetEffectContribution |
   14.49 NetEffectContributionList |
   14.50 NetEffectContributions |
   14.51 NetEffectEstimate |
   14.52 NonComparativeEvidence |
   14.53 OutcomeDefinition |
   14.54 OutcomeImportance |
   14.55 OutcomeList |
   14.56 OutcomeMeasureReport |
   14.57 OutcomeVariablesList |
   14.58 ParticipantFlowEvidence |
   14.59 ParticipantFlowEvidenceVariable |
   14.60 ParticipantFlowReasonEvidenceVariable |
   14.61 ParticipantFlowReport |
   14.62 ParticipantFlowVariablesList |
   14.63 PreprintCitation |
   14.64 Rating |
   14.65 Recommendation |
   14.66 RecommendationAction |
   14.67 RecommendationEligibilityCriteria |
   14.68 RecommendationJustification |
   14.69 RecommendationPlan |
   14.70 RecommendationRating |
   14.71 ResearchStudyDataDictionary |
   14.72 ResearchStudySupport |
   14.73 RiskOfBias |
   14.74 SearchResults |
   14.75 SearchStrategy |
   14.76 SingleStudyEvidence |
   14.77 SoaPlanDefinition |
   14.78 SoftwareCitation |
   14.79 StatisticModel |
   14.80 StudyComponent |
   14.81 StudyDesign |
   14.82 StudyEligibilityCriteria |
   14.83 StudyGroup |
   14.84 StudyRegistryRecord |
   14.85 SummaryOfFindings |
   14.86 SummaryOfNetEffect |
   14.87 SystematicReview |
   14.88 SystematicReviewEligibilityCriteria |
   14.89 SystematicReviewExcludedStudies |
   14.90 SystematicReviewIncludedStudies |
   14.91 VariableDefinition |
   14.92 WebPageCitation |
   14.93 ArtifactAssessmentCompared |
   14.94 ArtifactAssessmentDateAsRating |
   14.95 ArtifactPublicationStatus |
   14.96 ArtifactRecorder |
   14.97 CharacteristicTiming |
   14.98 CiteAs |
   14.99 EvidenceVariableHandlingDetail |
   14.100 GuidelineRegistration |
   14.101 NumberAnalyzed |
   14.102 RelatesTo |
   14.103 RelatesToClassifier |
   14.104 RelatesToWithQuotation |
   14.105 RelativeOutcomeImportance |
   14.106 ResearchStudyExcludedStudy |
   14.107 ResearchStudyIncludedStudy |
   14.108 ResearchStudyIsLowInterventionTrial |
   14.109 ResearchStudyIsRareDisease |
   14.110 ResearchStudyNumberOfStudiesIdentified |
   14.111 ResearchStudyNumberOfStudiesIncluded |
   14.112 ResearchStudySaeReportingMethod |
   14.113 ResearchStudySearchStrategy |
   14.114 ResearchStudySponsorConfidentialityStatement |
   14.115 ResearchStudyStudyAmendment |
   14.116 ResearchStudySystematicReviewEligibilityCriteria |
   14.117 StatisticModelExpression |
   14.118 StatisticModelIncludeIf |
   14.119 Desirability Codes Value Set |
   14.120 EBMonFHIR Profile Name Value Set |
   14.121 Evidence Rating System Classifier Codes Value Set |
   14.122 Recommendation Justification Classifier Codes Value Set |
   14.123 Research Study Document Types Value Set |
   14.124 ResearchStudy Classifier Value Set |
   14.125 Search Strategy Characteristic Value Set |
   14.126 Desirability Code System |
   14.127 EBMonFHIR Profile Name Code System |
   14.128 Evidence Rating System Classifier Code System |
   14.129 Research Study Document Types Code System |
   14.130 Search Strategy Characteristic Code System |
   14.131 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes. |
   14.132 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   14.133 14706014 Chemohormonal therapy as primary treatment for metastatic prostate cancer: a randomized study of estramustine phosphate plus luteinizing hormone-releasing hormone agonist versus flutamide plus luteinizing hormone-releasing hormone agonist. |
   14.134 15832493 Spotlight on rosiglitazone in the management of type 2 diabetes mellitus. |
   14.135 15855602 Defining and reporting hypoglycemia in diabetes: a report from the American Diabetes Association Workgroup on Hypoglycemia. |
   14.136 179899 |
   14.137 18160893 Wonder woman. Like my childhood heroine, Mrs. Betty also had amazing powers. |
   14.138 18508207 A Phase 3 placebo-controlled, double-blind, multi-site trial of the alpha-2-adrenergic agonist, lofexidine, for opioid withdrawal. |
   14.139 19029421 Phase III trial of androgen ablation with or without three cycles of systemic chemotherapy for advanced prostate cancer. |
   14.140 19091394 Endocrine treatment, with or without radiotherapy, in locally advanced prostate cancer (SPCG-7/SFUO-3): an open randomised phase III trial. |
   14.141 19967827 Wonder woman was Argentine and her real name was Evita. |
   14.142 22056152 Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial. |
   14.143 22502942 Addition of radiotherapy to long-term androgen deprivation in locally advanced prostate cancer: an open randomised phase 3 trial. |
   14.144 23306100 Androgen-deprivation therapy alone or with docetaxel in non-castrate metastatic prostate cancer (GETUG-AFU 15): a randomised, open-label, phase 3 trial. |
   14.145 23452809 Long-term follow-up of a phase II trial of chemotherapy plus hormone therapy for biochemical relapse after definitive local therapy for prostate cancer. |
   14.146 23589542 Hypoglycemia and diabetes: a report of a workgroup of the American Diabetes Association and the Endocrine Society. |
   14.147 23604530 A phase II trial of androgen deprivation therapy (ADT) plus chemotherapy as initial treatment for local failures or advanced prostate cancer. |
   14.148 24598155 Long-term results of a phase II study with neoadjuvant docetaxel chemotherapy and complete androgen blockade in locally advanced and high-risk prostate cancer. |
   14.149 25301760 Survival with Newly Diagnosed Metastatic Prostate Cancer in the "Docetaxel Era": Data from 917 Patients in the Control Arm of the STAMPEDE Trial (MRC PR08, CRUK/06/019). |
   14.150 26002607 Should docetaxel be standard of care for patients with metastatic hormone-sensitive prostate cancer? Pro and contra. |
   14.151 26028518 Androgen deprivation therapy plus docetaxel and estramustine versus androgen deprivation therapy alone for high-risk localised prostate cancer (GETUG 12): a phase 3 randomised controlled trial. |
   14.152 26092557 Feasibility study of a randomized controlled trial comparing docetaxel chemotherapy and androgen deprivation therapy with sequential prostatic biopsies from patients with advanced non-castration-resistant prostate cancer. |
   14.153 26244877 Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer. |
   14.154 26502880 A novel nasal powder formulation of glucagon: toxicology studies in animal models. |
   14.155 26681725 Intranasal Glucagon for Treatment of Insulin-Induced Hypoglycemia in Adults With Type 1 Diabetes: A Randomized Crossover Noninferiority Study. |
   14.156 26859072 Emotional Distress in the Partners of Type 1 Diabetes Adults: Worries About Hypoglycemia and Other Key Concerns. |
   14.157 27222544 Metabolic Surgery in the Treatment Algorithm for Type 2 Diabetes: A Joint Statement by International Diabetes Organizations. |
   14.158 27308831 Efficacy and Safety of Combined Androgen Deprivation Therapy (ADT) and Docetaxel Compared with ADT Alone for Metastatic Hormone-Naive Prostate Cancer: A Systematic Review and Meta-Analysis. |
   14.159 27979893 6. Glycemic Targets. |
   14.160 29114761 Web Exclusives. Annals Story Slam - How Wonder Woman Became My Alter Ego. |
   14.161 29114762 Web Exclusives. Annals Story Slam - Wonder Woman Is a Cartoon Character. |
   14.162 29202628 "I Kinda Feel Like Wonder Woman": An Interpretative Phenomenological Analysis of Pole Fitness and Positive Body Image. |
   14.163 29357271 Using Hawkeye from the Avengers to communicate on the eye. |
   14.164 29694275 A regressive formula of perversity: Wertham and the women of comics. |
   14.165 29694302 Introduction: "Suffering Sappho!": Lesbian content and queer female characters in comics. |
   14.166 30467172 Finding my inner Wonder Woman. |
   14.167 30545967 Parachute use to prevent death and major trauma when jumping from aircraft: randomized controlled trial. |
   14.168 34871555 What Can Wonder Woman Teach Radiologists? |
   14.169 35243488 Bariatric surgery and cardiovascular disease: a systematic review and meta-analysis. |
   14.170 36491989 Another Georgia Wonder Woman: She Does More Astounding Tricks Than Did Lula Hurst. |
   14.171 367832 |
   14.172 367833 |
   14.173 37024129 Benefits and harms of drug treatment for type 2 diabetes: systematic review and network meta-analysis of randomised controlled trials. |
   14.174 38584159 Efficacy and safety of a four-drug, quarter-dose treatment for hypertension: the QUARTET USA randomized trial. |
   14.175 6907780 Career guide: to change what needs changing...doesn't take Wonder Woman. |
   14.176 A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus |
   14.177 A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   14.178 ADAS-Cog(11) EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   14.179 Add-on Amlodipine at 6 weeks |
   14.180 Adults with diabetes mellitus type 2 |
   14.181 Adults with type 2 diabetes and CVD and CKD |
   14.182 Adults with type 2 diabetes and established CVD (but no CKD) |
   14.183 Adverse event free and hypertension control |
   14.184 Adverse event free and hypertension control at 12 weeks |
   14.185 Adverse Events Report for NCT03421379 |
   14.186 Adverse Events Report for NCT03640312 |
   14.187 Age |
   14.188 Age with comparator |
   14.189 Age with intervention |
   14.190 Aircraft Type |
   14.191 Aircraft Type with comparator |
   14.192 Aircraft Type with intervention |
   14.193 Altitude |
   14.194 Altitude comparing intervention vs. comparator |
   14.195 Altitude for enrolled group |
   14.196 Altitude for screened group |
   14.197 Altitude with comparator |
   14.198 Altitude with intervention |
   14.199 Analyzed Group in PARACHUTE Trial |
   14.200 Anticoagulation for COVID-19 Combined RCTs in NEJM |
   14.201 Baseline Characteristics Report for NCT03421379 |
   14.202 Baseline Characteristics Report for NCT03640312 |
   14.203 Baseline Characteristics Report for QUARTET Trial |
   14.204 Baseline Measure Report: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.205 Baseline Measures List for PARACHUTE Trial |
   14.206 BaselineMeasureEvidence: Age in 2018 Norwegian Cohort Medical Group |
   14.207 BaselineMeasureEvidence: Age in 2018 Norwegian Cohort Surgical Group |
   14.208 BaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Medical Group |
   14.209 BaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Surgical Group |
   14.210 BaselineVariablesList: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.211 Benefits and harms of drug treatment for type 2 diabetes: systematic review and network meta-analysis of randomised controlled trials |
   14.212 BookCitation: Crossing the Quality Chasm: A New Health System for the 21st Century |
   14.213 BookPartCitation: Chapter 3 of Crossing the Quality Chasm: A New Health System for the 21st Century |
   14.214 BookPartCitation: Chapter 3 of Crossing the Quality Chasm: A New Health System for the 21st Century - without baseCitation |
   14.215 Candesartan 8 mg once daily |
   14.216 Certainty of Evidence Rating of 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   14.217 Change in Mean Diastolic Blood Pressure (NCT03640312) |
   14.218 Change in Mean Diastolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   14.219 Change in Mean Diastolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   14.220 Change in Mean Diastolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.221 Change in Mean Systolic Blood Pressure (NCT03640312) |
   14.222 Change in Mean Systolic Blood Pressure (NCT03640312) |
   14.223 Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312 |
   14.224 Change in Mean Systolic Blood Pressure at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.225 Change in Mean Systolic Blood Pressure at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.226 Change in Mean Systolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   14.227 Change in Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   14.228 Change in Mean Systolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.229 CIBIC+ EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   14.230 Citation for Composition: ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.231 Citation for EBMonFHIR Implementation Guide |
   14.232 Citation for FEvIR Evidence 55: 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   14.233 Citation for FEvIR Evidence 7637: Critically appraised summary of primary outcome of multi-platform RCT of anticoagulation for non-critically ill COVID-19 |
   14.234 Classification: Study Design for Association of Bariatric Surgery with Complications and Comorbidities JAMA 2018 Norwegian Cohort |
   14.235 Comment on Guideline: ADA 2021 Standards of Medical Care 8. Obesity Management for the Treatment of Type 2 Diabetes by Joanne Dehnbostel 2023-11-28T15:19:01.266Z |
   14.236 Comparative Evidence Report for QUARTET USA Trial |
   14.237 ComparativeBaselineMeasureEvidence: Age in 2018 Norwegian Cohort Surgical Group vs. Medical Group |
   14.238 ComparativeBaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Surgical Group vs. Medical Group |
   14.239 ComparativeEvidence: All-cause mortality effect of bariatric surgery in 2022 meta-analysis |
   14.240 ComparativeEvidence: Bariatric Surgery effect for ADA triple outcome at 5 years (Diabetes Surgery Study) |
   14.241 ComparativeEvidence: Bypass surgery effects on Additional GI surgical procedure in JAMA 2018 Norwegian cohort study |
   14.242 ComparativeEvidence: Bypass surgery effects on Myocardial infarction or stroke in Swedish Obese Subjects (SOS) study |
   14.243 ComparativeEvidence: Bypass surgery effects on New onset depression in JAMA 2018 Norwegian cohort study |
   14.244 ComparativeEvidence: Bypass surgery effects on Remission of diabetes in JAMA 2018 Norwegian cohort study |
   14.245 ComparativeEvidence: Bypass surgery effects on Treatment with opioids in JAMA 2018 Norwegian cohort study |
   14.246 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Courcoulas 2014 |
   14.247 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Courcoulas 2015 |
   14.248 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Cummings 2016 |
   14.249 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ding 2015 |
   14.250 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Dixon 2008 |
   14.251 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Halperin 2014 |
   14.252 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ikramuddin 2013 |
   14.253 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ikramuddin 2015 |
   14.254 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Liang 2013 |
   14.255 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Mingrone 2012 (DIBASY) trial |
   14.256 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Mingrone 2015 (DIBASY) trial |
   14.257 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Parikh 2014 |
   14.258 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Schauer 2012 (STAMPEDE) trial |
   14.259 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Schauer 2014 (STAMPEDE) trial |
   14.260 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Wentworth 2014 |
   14.261 ComparativeEvidence: Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   14.262 ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.263 ComparativeEvidenceReportSubject: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.264 ComparativeEvidenceSynthesisReport: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.265 ComparativeParticipantFlowEvidence: Dropout due to stopping intervention Lofexidine vs. Placebo in opioid detoxification trial |
   14.266 ComparatorDefinition: Glucagon-Like Peptide-1 (GLP-1) receptor agonists |
   14.267 ComparatorDefinition: Obese patients ≥ 18 years old without bariatric surgery |
   14.268 ComparatorDefinition: Standard care |
   14.269 ComparatorGroup: JAMA 2018 Norwegian cohort study Control cohort |
   14.270 ComparatorOnlyEvidence: Additional GI surgical procedure without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   14.271 ComparatorOnlyEvidence: All-cause mortality without bariatric surgery in 2022 meta-analysis |
   14.272 ComparatorOnlyEvidence: Myocardial infarction or stroke without bariatric surgery (Control Group) in Swedish Obese Subjects (SOS) study |
   14.273 ComparatorOnlyEvidence: New onset depression without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   14.274 ComparatorOnlyEvidence: Remission of diabetes without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   14.275 ComparatorOnlyEvidence: Treatment with opioids without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   14.276 Comparison: Original and Adapted Recommendation: ADA Obesity Management Recommendation 8.16 |
   14.277 Composite Rating of FOI 153881 for Project FOI 112280 |
   14.278 Computable_Publishing_LLC |
   14.279 ConceptualCohortDefinition: At least 2 risk factors for stroke |
   14.280 ConceptualCohortDefinition: BMI 27.5-32.4 in Asian Americans who do not achieve durable weight loss and improvement in comorbidities without surgery |
   14.281 ConceptualCohortDefinition: BMI 30-34.9 in persons who do not achieve durable weight loss and improvement in comorbidities without surgery |
   14.282 ConceptualCohortDefinition: BMI 32.5-37.4 in Asian Americans who do not achieve durable weight loss and improvement in comorbidities without surgery |
   14.283 ConceptualCohortDefinition: BMI 35-39.9 in persons who do not achieve durable weight loss and improvement in comorbidities without surgery |
   14.284 ConceptualCohortDefinition: BMI criteria for ADA surgery recommendation |
   14.285 ConceptualCohortDefinition: BMI ≥ 35 and at least 1 obesity-related comorbidity |
   14.286 ConceptualCohortDefinition: BMI ≥ 37.5 kg/m2 in Asian Americans |
   14.287 ConceptualCohortDefinition: Estimated glomerular filtration rate 45-59 |
   14.288 ConceptualCohortDefinition: Heart failure based on Phenotypes |
   14.289 ConceptualCohortDefinition: Lower BMI criteria for ADA surgery consideration |
   14.290 ConceptualCohortDefinition: Meet either T1DM-specific eligibility criteria or T2DM-specific eligibility criteria |
   14.291 ConceptualCohortDefinition: Nonfatal myocardial infarction |
   14.292 ConceptualCohortDefinition: Nonfatal stroke |
   14.293 ConceptualCohortDefinition: Oxygen saturation below 96% on Boots Finger Pulse Oximeter |
   14.294 ConceptualCohortDefinition: Oxygen saturation below 96% on Boots Finger Pulse Oximeter with Ranges |
   14.295 ConceptualCohortDefinition: Proxy criteria for surgical candidates |
   14.296 ConceptualCohortDefinition: Severe obesity |
   14.297 ConceptualCohortDefinition: T1DM or T2DM |
   14.298 ConceptualCohortDefinition: T1DM-specific criteria |
   14.299 ConceptualCohortDefinition: T2DM-specific criteria |
   14.300 ConceptualCohortDefinition_Cancer_of_any_kind_except_basal_cell_skin_cancer_or_cancer_in_situ_unless_documented_to_be_disease_free_for_five_years |
   14.301 ConceptualCohortDefinition_Cardiovascular_event |
   14.302 ConceptualComparatorDefinition: NOT Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   14.303 ConceptualComparatorDefinition: Usual-care pharmacologic thromboprophylaxis |
   14.304 ConceptualExposureDefinition: Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   14.305 ConceptualExposureDefinition: Therapeutic-dose anticoagulation with heparin |
   14.306 COVID_19PneumoniaHospitalizedAdult |
   14.307 Critically appraised summary of primary outcome of multi-platform RCT of anticoagulation for non-critically ill patients with COVID-19 |
   14.308 CTIS2024-516402-32-00 Eligibility Criteria |
   14.309 CTIS2024-516402-32-00 Primary Outcome 1 |
   14.310 CTIS2024-516402-32-00 Secondary Outcome 1 |
   14.311 CTIS2024-516402-32-00 Secondary Outcome 2 |
   14.312 CTIS2024-516402-32-00 Secondary Outcome 3 |
   14.313 CTIS2024-516402-32-00 Secondary Outcome 4 |
   14.314 CTIS2024-516402-32-00 Secondary Outcome 5 |
   14.315 CTIS2024-516402-32-00 Secondary Outcome 6 |
   14.316 CTIS2024-516402-32-00 Secondary Outcome 7 |
   14.317 CTIS2024-516402-32-00 Secondary Outcome 8 |
   14.318 DatabaseCitation: Citation for FEvIR Platform |
   14.319 DatabaseEntryCitation: ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.320 DatasetCitation: Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and is Associated with Worse Outcomes |
   14.321 DateOfFirstPublication Classification of FOI 153881 by Rachel Couban |
   14.322 Death or Major Traumatic Injury 30 days after Impact comparing intervention vs. comparator |
   14.323 Death or Major Traumatic Injury 30 days after Impact with comparator |
   14.324 Death or Major Traumatic Injury 30 days after Impact with intervention |
   14.325 Death or Major Traumatic Injury on Impact comparing intervention vs. comparator |
   14.326 declined randomization in PARACHUTE Study |
   14.327 deemed unsuitable by investigator in PARACHUTE Trial |
   14.328 Delany-Moretlwe 2022 clinical trial |
   14.329 Diabetes treatment medication |
   14.330 Diastolic blood pressure at 12 weeks |
   14.331 DichotomousIntendedOutcome: Death or Major Traumatic Injury within 30 days |
   14.332 Eculizumab in hypertensive emergency-associated hemolytic uremic syndrome: a randomized multicenter controlled trial (HYPERSHU) |
   14.333 Efficacy and Safety of a Quadruple Ultra-low-dose Treatment for Hypertension |
   14.334 Efficacy of Corticosteroids in COVID-19 Patients: A Systematic Review and Meta-Analysis |
   14.335 Eligibility criteria for NMA_Diabetes |
   14.336 Eligibility Criteria for QUARTET USA Trial |
   14.337 Enrolled Group for QUARTET USA Trial |
   14.338 Enrolled Group PARACHUTE Trial |
   14.339 Ethnic Group |
   14.340 Ethnic Group with comparator |
   14.341 Ethnic Group with intervention |
   14.342 Evidence Based Medicine on FHIR Implementation Guide Code System |
   14.343 Evidence for Results for Add-on Amlodipine at 6 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.344 Evidence for Results for Add-on Amlodipine at 6 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.345 Evidence for Results for Add-on Amlodipine at 6 weeks in QUARTET USA Trial Control Group |
   14.346 Evidence for Results for Add-on Amlodipine at 6 weeks in QUARTET USA Trial Quadpill group |
   14.347 Evidence for Results for Adverse event free and hypertension control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.348 Evidence for Results for Adverse event free and hypertension control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.349 Evidence for Results for Adverse event free and hypertension control at 12 weeks in QUARTET USA Trial Control Group |
   14.350 Evidence for Results for Adverse event free and hypertension control at 12 weeks in QUARTET USA Trial Quadpill group |
   14.351 Evidence for Results for Diastolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.352 Evidence for Results for Diastolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.353 Evidence for Results for Diastolic blood pressure at 12 weeks in QUARTET USA Trial Control Group |
   14.354 Evidence for Results for Diastolic blood pressure at 12 weeks in QUARTET USA Trial Quadpill group |
   14.355 Evidence for Results for Hypertension Control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.356 Evidence for Results for Hypertension Control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.357 Evidence for Results for Hypertension Control at 12 weeks in QUARTET USA Trial Control Group |
   14.358 Evidence for Results for Hypertension Control at 12 weeks in QUARTET USA Trial Quadpill group |
   14.359 Evidence for Results for Medication Adherence at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.360 Evidence for Results for Medication Adherence at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.361 Evidence for Results for Medication Adherence at 12 weeks in QUARTET USA Trial Control Group |
   14.362 Evidence for Results for Medication Adherence at 12 weeks in QUARTET USA Trial Quadpill group |
   14.363 Evidence for Results for Systolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.364 Evidence for Results for Systolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   14.365 Evidence for Results for Systolic blood pressure at 12 weeks in QUARTET USA Trial Control Group |
   14.366 Evidence for Results for Systolic blood pressure at 12 weeks in QUARTET USA Trial Quadpill group |
   14.367 Evidence List: Effect estimates for meta-analysis (Biegel 2020, Wang 2020, SOLIDARITY) |
   14.368 EvidenceList: Study results included in Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   14.369 EvidenceReportSectionCode Value Set |
   14.370 EvidenceReportSubject: Clinical Outcomes for Effects of Bariatric Surgery |
   14.371 EvidenceVariable Handling Extension Value Set |
   14.372 EvidenceVariable: case_id |
   14.373 EvidenceVariable: Patient id |
   14.374 EvidenceVariable: Time of measurement |
   14.375 Example EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   14.376 Excluded from PARACHUTE Study |
   14.377 ExposureGroup: JAMA 2018 Norwegian cohort study Surgery cohort |
   14.378 ExposureVariable: Age (as continuous variable) |
   14.379 ExposureVariable: Body Mass Index (as continuous variable) |
   14.380 ExposureVariable: pht013093.v1.p1 Age at diagnosis |
   14.381 ExposureVariable: pht013093.v1.p1 RACE |
   14.382 ExposureVariable: pht013093.v1.p1 SEX |
   14.383 ExposureVariable: pht013093.v1.p1 SUBJECT_ID |
   14.384 ExposureVariable: pht013094.v1.p1 ANALYTE_TYPE |
   14.385 ExposureVariable: pht013094.v1.p1 BODY_SITE |
   14.386 ExposureVariable: pht013094.v1.p1 IS_TUMOR |
   14.387 ExposureVariable: pht013094.v1.p1 SAMPLE_ID |
   14.388 ExposureVariable: pht013094.v1.p1 SAMPLE_USE |
   14.389 ExposureVariable: pht013094.v1.p1 Source_Type |
   14.390 Family History of Parachute Use |
   14.391 Family History of Parachute Use with comparator |
   14.392 Family History of Parachute Use with intervention |
   14.393 Frequent Flier |
   14.394 Frequent Flier with comparator |
   14.395 Frequent Flier with intervention |
   14.396 GLP-1 RA Group in Adults with type 2 diabetes |
   14.397 GLP-1 RA Group in at-risk Adults with type 2 diabetes with moderate CV risk |
   14.398 Glucagon Hydrochloride Solution (Active Comparator) |
   14.399 Glucagon Nasal Powder (Experimental) |
   14.400 Group Randomized to Comparator (empty backpack) in PARACHUTE Trial |
   14.401 Group Randomized to Intervention Group (parachute) in PARACHUTE Trial |
   14.402 GroupAssignment: Bariatric Surgery vs. no bariatric surgery |
   14.403 GroupAssignment: ExposureDefinition: Bariatric Surgery (RYGB, VSG, LAGB, BPD) vs. ComparatorDefinition: NOT Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   14.404 GroupAssignment: ExposureGroup: JAMA 2018 Norwegian cohort study Surgery cohort vs. ComparatorGroup: JAMA 2018 Norwegian cohort study Control cohort |
   14.405 GroupAssignment: GLP-1 RA vs. Standard care |
   14.406 GroupAssignment: high dose xanomeline vs. low dose xanomeline vs. placebo |
   14.407 GroupAssignment: Jumping from aircraft with parachute vs. Jumping from aircraft with empty backpack |
   14.408 GroupAssignment: Non Participants vs. Enrolled Participants |
   14.409 GroupAssignment: Quadpill vs. Candesartan |
   14.410 GroupAssignment: Roux-en-Y gastric bypass or Biliopancreatic Diversion vs. medical treatment |
   14.411 GroupAssignment: Roux-en-Y gastric bypass surgery vs. Lifestyle-intensive medical management intervention alone |
   14.412 GroupAssignment: Roux-en-Y gastric bypass vs. medical treatment |
   14.413 GroupAssignment: SGLT2 inhibitors vs. GLP-1 RA |
   14.414 GroupAssignment: Therapeutic-dose anticoagulation with heparin vs. Usual-care pharmacologic thromboprophylaxis |
   14.415 Guideline: ADA 2021 Standards of Medical Care 8. Obesity Management for the Treatment of Type 2 Diabetes |
   14.416 Health Survey Score Total |
   14.417 Health Survey Score Total comparing intervention vs. comparator |
   14.418 Health Survey Score Total with comparator |
   14.419 Health Survey Score Total with intervention |
   14.420 Health Survey Score-Mental Health Subscore |
   14.421 Health Survey Score-Mental Health Subscore comparing intervention vs. comparator |
   14.422 Health Survey Score-Mental Health Subscore with comparator |
   14.423 Health Survey Score-Mental Health Subscore with intervention |
   14.424 Health Survey Score-Physical Health Subscore |
   14.425 Health Survey Score-Physical Health Subscore comparing intervention vs. comparator |
   14.426 Health Survey Score-Physical Health Subscore with comparator |
   14.427 Health Survey Score-Physical Health Subscore with intervention |
   14.428 Health-related Quality of Life (NCT03640312) |
   14.429 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) at (NCT03640312) |
   14.430 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) for Candesartan in NCT03640312 |
   14.431 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) for QUARTET LDQT in NCT03640312 |
   14.432 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) at (NCT03640312) |
   14.433 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) for Candesartan in NCT03640312 |
   14.434 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) for QUARTET LDQT in NCT03640312 |
   14.435 Health-related Quality of Life at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.436 Health-related Quality of Life at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.437 Height |
   14.438 Height with comparator |
   14.439 Height with intervention |
   14.440 High Blood Pressure Medication Value Set |
   14.441 History of Acrophobia |
   14.442 History of Acrophobia with comparator |
   14.443 History of Acrophobia with intervention |
   14.444 History of Broken Bones |
   14.445 History of Broken Bones with comparator |
   14.446 History of Broken Bones with intervention |
   14.447 History of Parachute Use |
   14.448 History of Parachute Use with comparator |
   14.449 History of Parachute Use with intervention |
   14.450 Hypertension Control at 12 weeks |
   14.451 ICD-10-GM Terminale Codes |
   14.452 Injury Severity Score 30 days after Impact comparing intervention vs. comparator |
   14.453 Injury Severity Score 30 days after Impact with comparator |
   14.454 Injury Severity Score 30 days after Impact with intervention |
   14.455 Injury Severity Score on Impact comparing intervention vs. comparator |
   14.456 Injury Severity Score on Impact with comparator |
   14.457 Injury Severity Score on Impact with intervention |
   14.458 International vs Domestic Flight |
   14.459 International vs Domestic Flight with comparator |
   14.460 International vs Domestic Flight with intervention |
   14.461 InterventionDefinition: Glucagon-Like Peptide-1 (GLP-1) receptor agonists |
   14.462 InterventionDefinition: Sodium-Glucose Transport Protein 2 (SGLT2) inhibitors |
   14.463 InterventionOnlyEvidence: Additional GI surgical procedure with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   14.464 InterventionOnlyEvidence: New onset depression with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   14.465 InterventionOnlyEvidence: Remission of diabetes with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   14.466 InterventionOnlyEvidence: Treatment with opioids with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   14.467 Investigator |
   14.468 Investigator-by-treatment interaction for ADAS-Cog(11) ANCOVA |
   14.469 IV remdesivir 200 mg then 100 mg/day for 9 days |
   14.470 Joanne Dehnbostel's Adaptation Report of Recommendation: ADA Obesity Management Recommendation 8.16 |
   14.471 JournalArticleCitation: ADA 2021 Standards of Medical Care 8. Obesity Management for the Treatment of Type 2 Diabetes |
   14.472 JournalArticleCitation: Association of Bariatric Surgery with Complications and Comorbidities JAMA 2018 Norwegian Cohort |
   14.473 Jumping from aircraft with empty backpack |
   14.474 Jumping from aircraft with parachute |
   14.475 Justification for Recommendation: ADA Obesity Management Recommendation 8.16 |
   14.476 Justification for Recommendation: ADA Obesity Management Recommendation 8.17 |
   14.477 M11 IGBJ Protocol Example Eligibility Criteria |
   14.478 M11 IGBJ Protocol Example for EBMonFHIR IG |
   14.479 M11 Report Template Instructions |
   14.480 MAGIC-derived ComparatorOnlyEvidence: All-cause mortality in GLP-1 RA Group in Adults with type 2 diabetes |
   14.481 MAGIC-derived ComparatorOnlyEvidence: All-cause mortality in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.482 MAGIC-derived ComparatorOnlyEvidence: Body weight in GLP-1 RA Group in Adults with type 2 diabetes |
   14.483 MAGIC-derived ComparatorOnlyEvidence: Body weight in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.484 MAGIC-derived ComparatorOnlyEvidence: Cardiovascular mortality in GLP-1 RA Group in Adults with type 2 diabetes |
   14.485 MAGIC-derived ComparatorOnlyEvidence: Cardiovascular mortality in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.486 MAGIC-derived ComparatorOnlyEvidence: Diabetic ketoacidosis in GLP-1 RA Group in Adults with type 2 diabetes |
   14.487 MAGIC-derived ComparatorOnlyEvidence: End-stage kidney disease in GLP-1 RA Group in Adults with type 2 diabetes |
   14.488 MAGIC-derived ComparatorOnlyEvidence: End-stage kidney disease in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.489 MAGIC-derived ComparatorOnlyEvidence: Genital infection in GLP-1 RA Group in Adults with type 2 diabetes |
   14.490 MAGIC-derived ComparatorOnlyEvidence: Health-related quality of life in GLP-1 RA Group in Adults with type 2 diabetes |
   14.491 MAGIC-derived ComparatorOnlyEvidence: Health-related quality of life in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.492 MAGIC-derived ComparatorOnlyEvidence: Heart failure in GLP-1 RA Group in Adults with type 2 diabetes |
   14.493 MAGIC-derived ComparatorOnlyEvidence: Heart failure in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.494 MAGIC-derived ComparatorOnlyEvidence: Nonfatal myocardial infarction in GLP-1 RA Group in Adults with type 2 diabetes |
   14.495 MAGIC-derived ComparatorOnlyEvidence: Nonfatal myocardial infarction in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.496 MAGIC-derived ComparatorOnlyEvidence: Nonfatal stroke in GLP-1 RA Group in Adults with type 2 diabetes |
   14.497 MAGIC-derived ComparatorOnlyEvidence: Nonfatal stroke in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.498 MAGIC-derived ComparatorOnlyEvidence: Serious hyperglycaemia in GLP-1 RA Group in Adults with type 2 diabetes |
   14.499 MAGIC-derived ComparatorOnlyEvidence: Serious hyperglycaemia in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.500 MAGIC-derived ComparatorOnlyEvidence: Severe gastrointestinal events in GLP-1 RA Group in Adults with type 2 diabetes |
   14.501 MAGIC-derived ComparatorOnlyEvidence: Severe gastrointestinal events in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.502 MAGIC-derived Evidence: All-cause mortality with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.503 MAGIC-derived Evidence: All-cause mortality with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.504 MAGIC-derived Evidence: Body weight with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.505 MAGIC-derived Evidence: Body weight with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.506 MAGIC-derived Evidence: Cardiovascular mortality with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.507 MAGIC-derived Evidence: Cardiovascular mortality with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.508 MAGIC-derived Evidence: Diabetic ketoacidosis with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.509 MAGIC-derived Evidence: End-stage kidney disease with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.510 MAGIC-derived Evidence: End-stage kidney disease with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.511 MAGIC-derived Evidence: Genital infection with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.512 MAGIC-derived Evidence: Health-related quality of life with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.513 MAGIC-derived Evidence: Health-related quality of life with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.514 MAGIC-derived Evidence: Heart failure with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.515 MAGIC-derived Evidence: Heart failure with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.516 MAGIC-derived Evidence: Nonfatal myocardial infarction with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.517 MAGIC-derived Evidence: Nonfatal myocardial infarction with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.518 MAGIC-derived Evidence: Nonfatal stroke with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.519 MAGIC-derived Evidence: Nonfatal stroke with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.520 MAGIC-derived Evidence: Serious hyperglycaemia with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.521 MAGIC-derived Evidence: Serious hyperglycaemia with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.522 MAGIC-derived Evidence: Severe gastrointestinal events with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.523 MAGIC-derived Evidence: Severe gastrointestinal events with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.524 MAGIC-derived InterventionOnlyEvidence: All-cause mortality in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.525 MAGIC-derived InterventionOnlyEvidence: All-cause mortality in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.526 MAGIC-derived InterventionOnlyEvidence: Body weight in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.527 MAGIC-derived InterventionOnlyEvidence: Body weight in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.528 MAGIC-derived InterventionOnlyEvidence: Cardiovascular mortality in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.529 MAGIC-derived InterventionOnlyEvidence: Cardiovascular mortality in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.530 MAGIC-derived InterventionOnlyEvidence: Diabetic ketoacidosis in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.531 MAGIC-derived InterventionOnlyEvidence: End-stage kidney disease in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.532 MAGIC-derived InterventionOnlyEvidence: End-stage kidney disease in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.533 MAGIC-derived InterventionOnlyEvidence: Genital infection in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.534 MAGIC-derived InterventionOnlyEvidence: Health-related quality of life in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.535 MAGIC-derived InterventionOnlyEvidence: Health-related quality of life in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.536 MAGIC-derived InterventionOnlyEvidence: Heart failure in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.537 MAGIC-derived InterventionOnlyEvidence: Heart failure in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.538 MAGIC-derived InterventionOnlyEvidence: Nonfatal myocardial infarction in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.539 MAGIC-derived InterventionOnlyEvidence: Nonfatal myocardial infarction in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.540 MAGIC-derived InterventionOnlyEvidence: Nonfatal stroke in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.541 MAGIC-derived InterventionOnlyEvidence: Nonfatal stroke in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.542 MAGIC-derived InterventionOnlyEvidence: Serious hyperglycaemia in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.543 MAGIC-derived InterventionOnlyEvidence: Serious hyperglycaemia in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.544 MAGIC-derived InterventionOnlyEvidence: Severe gastrointestinal events in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   14.545 MAGIC-derived InterventionOnlyEvidence: Severe gastrointestinal events in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.546 Mean Change in Blood Urea Nitrogen (NCT03640312) |
   14.547 Mean Change in Blood Urea Nitrogen at 12 weeks for Candesartan in NCT03640312 |
   14.548 Mean Change in Blood Urea Nitrogen at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.549 Mean Change in Blood Urea Nitrogen at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.550 Mean Change in Serum Creatinine (NCT03640312) |
   14.551 Mean Change in Serum Creatinine at 12 weeks for Candesartan in NCT03640312 |
   14.552 Mean Change in Serum Creatinine at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.553 Mean Change in Serum Creatinine at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.554 Mean Change in Serum Potassium (NCT03640312) |
   14.555 Mean Change in Serum Potassium at 12 weeks for Candesartan in NCT03640312 |
   14.556 Mean Change in Serum Potassium at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.557 Mean Change in Serum Potassium at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.558 Mean Change in Serum Sodium (NCT03640312) |
   14.559 Mean Change in Serum Sodium at 12 weeks for Candesartan in NCT03640312 |
   14.560 Mean Change in Serum Sodium at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.561 Mean Change in Serum Sodium at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.562 Mean Diastolic Blood Pressure (NCT03640312) |
   14.563 Mean Diastolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   14.564 Mean Diastolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   14.565 Mean Diastolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.566 Mean Systolic Blood Pressure (NCT03640312) |
   14.567 Mean Systolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   14.568 Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   14.569 Mean Systolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.570 Median Age of Parachute Intervention Group |
   14.571 Medication Adherence (NCT03640312) |
   14.572 Medication Adherence at 12 weeks |
   14.573 Medication Adherence at 12 weeks for Candesartan in NCT03640312 |
   14.574 Medication Adherence at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.575 Medication Adherence at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.576 MetaanalysisEligibilityCriteria: Mean difference in HbA1c effect of bariatric surgery in type 2 diabetes and elevated BMI in 2016 meta-analysis |
   14.577 MetaanalysisOutcomeDefinition: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups at end of follow-up |
   14.578 MetaanalysisStudyGroup: Effect Estimates for Mortality at 14 days from COVID19 Remdesivir vs. Placebo RCTs |
   14.579 MetaanalysisStudyGroup: Study results included in Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   14.580 Mortality at 14 days |
   14.581 NCT03421379 Eligibility Criteria |
   14.582 NCT03640312 Eligibility Criteria |
   14.583 NetEffectContribution: Additional GI surgical procedure for Example for GIN 2022 |
   14.584 NetEffectContribution: All-cause mortality for Example for GIN 2022 |
   14.585 NetEffectContribution: New onset depression for Example for GIN 2022 |
   14.586 NetEffectContribution: Nonfatal myocardial infarction or stroke for Example for GIN 2022 |
   14.587 NetEffectContribution: Remission of diabetes for Example for GIN 2022 |
   14.588 NetEffectContribution: Treatment with opioids for Example for GIN 2022 |
   14.589 NetEffectContributionList: Bariatric Surgery Example for GIN 2022 |
   14.590 NetEffectContributions: Bariatric Surgery Example for GIN 2022 |
   14.591 NetEffectEstimate: Bariatric Surgery Example for GIN 2022 |
   14.592 NHANES LBDGLUSI Variable Definition Cohort Definition |
   14.593 NHANES LBDGLUSI: Fasting Glucose (mmol/L) |
   14.594 NHANES LBXGLU Variable Definition Cohort Definition |
   14.595 NHANES LBXGLU: Fasting Glucose (mg/dL) |
   14.596 NHANES Plasma Fasting Glucose (GLU_J) Data Dictionary |
   14.597 NHANES SEQN Respondent Sequence Number |
   14.598 NHANES WTSAF2YR Variable Definition Cohort Definition |
   14.599 NHANES WTSAF2YR: Fasting Subsample 2 Year MEC Weight |
   14.600 Norwegian Cohort Study Comparing Bariatric Surgery vs Medical Obesity Treatment for Long-term Medical Complications and Obesity-Related Comorbidities |
   14.601 NT-proBNP Study Data Dictionary |
   14.602 Number of Patients Requiring Step up Treatment (NCT03640312) |
   14.603 Number of Patients Requiring Step up Treatment at 6 weeks for Candesartan in NCT03640312 |
   14.604 Number of Patients Requiring Step up Treatment at 6 weeks for QUARTET LDQT in NCT03640312 |
   14.605 Number of Patients Requiring Step up Treatment at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.606 Organ support-free days |
   14.607 Outcome Importance Rating 100 of All-cause mortality |
   14.608 Outcome Importance Rating 30 of Nonfatal myocardial infarction or stroke |
   14.609 Outcome Importance Rating 5 of New onset depression |
   14.610 Outcome Importance Rating 5 of Remission of diabetes |
   14.611 Outcome Importance Rating 5 of Treatment with opioids |
   14.612 Outcome Importance Rating 8 of Additional GI surgical procedure |
   14.613 Outcome Measure List for QUARTET USA Trial |
   14.614 Outcome Measure Report for QUARTET USA Trial |
   14.615 Outcome Measure Report: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.616 Outcome Measures Report for NCT03421379 |
   14.617 Outcome Measures Report for NCT03640312 |
   14.618 Outcome Variables List for PARACHUTE Trial |
   14.619 Outcome: Death or Major Traumatic Injury 30 days after Impact |
   14.620 Outcome: Death or Major Traumatic Injury on Impact |
   14.621 Outcome: Injury Severity Score 30 days after Impact |
   14.622 Outcome: Injury Severity Score on Impact |
   14.623 OutcomeDefinition: Injury Severity Score on Impact |
   14.624 OutcomeDefinition: All-cause mortality |
   14.625 OutcomeDefinition: All-cause mortality |
   14.626 OutcomeDefinition: American Diabetes Association composite triple end point for metabolic control |
   14.627 OutcomeDefinition: Body weight |
   14.628 OutcomeDefinition: Body weight |
   14.629 OutcomeDefinition: Cardiovascular mortality |
   14.630 OutcomeDefinition: Cardiovascular mortality |
   14.631 OutcomeDefinition: Diabetes in remission |
   14.632 OutcomeDefinition: Diabetic ketoacidosis |
   14.633 OutcomeDefinition: End-stage kidney disease |
   14.634 OutcomeDefinition: End-stage kidney disease |
   14.635 OutcomeDefinition: Genital infection |
   14.636 OutcomeDefinition: HbA1c at 12 months |
   14.637 OutcomeDefinition: HbA1c at 24 months |
   14.638 OutcomeDefinition: HbA1c at 36 months |
   14.639 OutcomeDefinition: HbA1c at 6 months |
   14.640 OutcomeDefinition: HbA1c at 60 months |
   14.641 OutcomeDefinition: Health-related quality of life |
   14.642 OutcomeDefinition: Health-related quality of life |
   14.643 OutcomeDefinition: Heart failure |
   14.644 OutcomeDefinition: Heart failure |
   14.645 OutcomeDefinition: Mortality at 14 days |
   14.646 OutcomeDefinition: New onset depression |
   14.647 OutcomeDefinition: Nonfatal myocardial infarction |
   14.648 OutcomeDefinition: Nonfatal myocardial infarction |
   14.649 OutcomeDefinition: Nonfatal myocardial infarction or stroke |
   14.650 OutcomeDefinition: Nonfatal stroke |
   14.651 OutcomeDefinition: Nonfatal stroke |
   14.652 OutcomeDefinition: Serious hyperglycaemia |
   14.653 OutcomeDefinition: Serious hyperglycaemia |
   14.654 OutcomeDefinition: Severe gastrointestinal events |
   14.655 OutcomeDefinition: Severe gastrointestinal events |
   14.656 OutcomeList: Clinical Outcomes for Effects of Bariatric Surgery |
   14.657 OutcomeMeasureReport: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.658 OutcomeVariable: American Diabetes Association composite triple end point for metabolic control at 5 years |
   14.659 OutcomeVariable: HbA1c at 12 months |
   14.660 OutcomeVariable: HbA1c at 24 months |
   14.661 OutcomeVariable: HbA1c at 36 months |
   14.662 OutcomeVariable: HbA1c at 6 months |
   14.663 OutcomeVariable: HbA1c at 60 months |
   14.664 OutcomeVariable: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups at end of follow-up |
   14.665 OutcomeVariable: New onset depression |
   14.666 OutcomeVariable: Nonfatal myocardial infarction or stroke |
   14.667 OutcomeVariable: Remission of diabetes |
   14.668 OutcomeVariablesList: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   14.669 OutcomeVariable_Additional_GI_surgical_procedure |
   14.670 OutcomeVariable_All_cause_mortality |
   14.671 OutcomeVariable_Treatment_with_opioids |
   14.672 PARACHUTE Trial baseline characteristics |
   14.673 PARACHUTE Trial non participants |
   14.674 PARACHUTE trial participant flow report |
   14.675 PARACHUTE Trial Participants |
   14.676 PARACHUTE Trial Participants assigned an empty backpack |
   14.677 PARACHUTE trial participants assigned parachute |
   14.678 PARACHUTE Trial Participants available for randomization |
   14.679 PARACHUTE Trial Participants deemed unsuitable by investigator |
   14.680 PARACHUTE Trial Participants randomized into groups |
   14.681 PARACHUTE Trial Participants randomized into groups for screened group |
   14.682 PARACHUTE Trial Participants randomized into groups with comparator |
   14.683 PARACHUTE Trial Participants randomized into groups with intervention |
   14.684 PARACHUTE Trial Participants that completed 30 day follow up |
   14.685 PARACHUTE Trial Participants that completed 30 day follow up with comparator |
   14.686 PARACHUTE Trial Participants that completed 30 day follow up with intervention |
   14.687 PARACHUTE Trial Participants that completed jump and 5 minute follow-up |
   14.688 PARACHUTE Trial Participants that completed jump and 5 minute follow-up with comparator |
   14.689 PARACHUTE Trial Participants that completed jump and 5 minute follow-up with intervention |
   14.690 PARACHUTE Trial Participants that declined randomization |
   14.691 PARACHUTE Trial Participants with no contact at 30 days |
   14.692 PARACHUTE Trial Participants with no contact at 30 days with comparator |
   14.693 PARACHUTE Trial Participants with no contact at 30 days with intervention |
   14.694 PARACHUTE Trial Results |
   14.695 Parachute use to prevent death and major trauma when jumping from aircraft: randomized controlled trial. |
   14.696 Parachute vs Empty Backpack in PARACHUTE Trial |
   14.697 Participant Flow Report for NCT03421379 |
   14.698 Participant Flow Report for NCT03640312 |
   14.699 Participant Flow Report for QUARTET USA Trial |
   14.700 Participant Flow Variables List for PARACHUTE Trial |
   14.701 ParticipantFlow: 2018 Norwegian Cohort Included in Analysis |
   14.702 ParticipantFlow: 2018 Norwegian Cohort Medical Group Included in Analysis |
   14.703 ParticipantFlow: 2018 Norwegian Cohort Surgical Group Included in Analysis |
   14.704 ParticipantFlowEvidence: 2018 Norwegian Cohort Excluded from Analysis |
   14.705 ParticipantFlowMeasure: Dropout due to stopping intervention |
   14.706 ParticipantFlowMeasure: Exclusion from analysis |
   14.707 ParticipantFlowMeasure: Inclusion in analysis |
   14.708 Participants Excluded from PARACHUTE Study |
   14.709 Participants_in_Anticoagulation_for_COVID_19_Combined_ATTACC_ACTIV_4a_and_REMAP_CAP_RCT_hospitalized_not_critically_ill |
   14.710 Patients_who_are_hospitalized_for_COVID_19_and_who_are_not_critically_ill |
   14.711 PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   14.712 PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.713 PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.714 Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia (NCT03421379) |
   14.715 Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia at Pre-dose up to 30 minutes post each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.716 Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia at Pre-dose up to 30 minutes post each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.717 Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia at Pre-dose up to 30 minutes post each glucagon administration Statistical Analysis for Glucagon Nasal Powder vs Glucagon Hydrochloride Solution in NCT03421379 |
   14.718 Percentage of Participants With Potentially Related Adverse Events (NCT03640312) |
   14.719 Percentage of Participants With Potentially Related Adverse Events at 12 weeks for Candesartan in NCT03640312 |
   14.720 Percentage of Participants With Potentially Related Adverse Events at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.721 Percentage of Participants With Potentially Related Adverse Events at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.722 Percentage of Participants With Serious Adverse Events (SAEs) (NCT03640312) |
   14.723 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks for Candesartan in NCT03640312 |
   14.724 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.725 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.726 Pharmacodynamics (PD): Change From Baseline in Maximal Blood Glucose (BGmax) of Glucagon Nasal Powder and Glucagon Hydrochloride Intramuscular (IM) (NCT03421379) |
   14.727 Pharmacodynamics (PD): Change From Baseline in Maximal Blood Glucose (BGmax) of Glucagon Nasal Powder and Glucagon Hydrochloride Intramuscular (IM) at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.728 Pharmacodynamics (PD): Change From Baseline in Maximal Blood Glucose (BGmax) of Glucagon Nasal Powder and Glucagon Hydrochloride Intramuscular (IM) at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.729 Pharmacokinetics (PK): Change From Baseline in Area Under the Concentration Versus Time Curve From Zero to Time t (AUC [0-tLast]) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   14.730 Pharmacokinetics (PK): Change From Baseline in Area Under the Concentration Versus Time Curve From Zero to Time t (AUC [0-tLast]) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.731 Pharmacokinetics (PK): Change From Baseline in Area Under the Concentration Versus Time Curve From Zero to Time t (AUC [0-tLast]) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.732 PK: Change From Baseline in Maximal Concentration (Cmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   14.733 PK: Change From Baseline in Maximal Concentration (Cmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.734 PK: Change From Baseline in Maximal Concentration (Cmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.735 PK: Change From Baseline in Tmax of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   14.736 PK: Change From Baseline in Tmax of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 |
   14.737 PK: Change From Baseline in Tmax of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Nasal Powder in NCT03421379 |
   14.738 Placebo |
   14.739 PlanDefinition for Recommendation: ADA Obesity Management Recommendation 8.16 |
   14.740 PlanDefinition for Recommendation: ADA Obesity Management Recommendation 8.17 |
   14.741 PreprintCitation: Nigella Sativa for COVID-19 OSF Preprint |
   14.742 Proportion of Patients With Adverse Event Free Hypertension Control (NCT03640312) |
   14.743 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks for Candesartan in NCT03640312 |
   14.744 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.745 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.746 Proportion of Patients With Hypertension Control (NCT03640312) |
   14.747 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks at (NCT03640312) |
   14.748 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks for Candesartan in NCT03640312 |
   14.749 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks for QUARTET LDQT in NCT03640312 |
   14.750 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks at (NCT03640312) |
   14.751 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks for Candesartan in NCT03640312 |
   14.752 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks for QUARTET LDQT in NCT03640312 |
   14.753 Proportion of Patients With Hypertension Control at 6 and 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.754 Quadpill once daily |
   14.755 QUARTET USA Trial Control Group |
   14.756 QUARTET USA Trial Quadpill group |
   14.757 randomized into groups for PARACHUTE Trial |
   14.758 Rate of Adverse Events of Special Interest (NCT03640312) |
   14.759 Rate of Adverse Events of Special Interest at 12 weeks for Candesartan in NCT03640312 |
   14.760 Rate of Adverse Events of Special Interest at 12 weeks for QUARTET LDQT in NCT03640312 |
   14.761 Rate of Adverse Events of Special Interest at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   14.762 Rate of Death or Major Traumatic Injury on Impact with comparator |
   14.763 Rate of Death or Major Traumatic Injury on Impact with intervention |
   14.764 Reasons for exclusion from QUARTET USA Trial |
   14.765 Recommendation Eligibility Criteria for Bariatric Surgery (ADA Recommendation 8.17) |
   14.766 Recommendation Justification Code System |
   14.767 Recommendation Rating: ADA Obesity Management Recommendation 8.16 |
   14.768 Recommendation: ADA Obesity Management Recommendation 8.16 |
   14.769 Recommendation: ADA Obesity Management Recommendation 8.16-adapted |
   14.770 Recommendation: ADA Obesity Management Recommendation 8.17 |
   14.771 RecommendationEligibilityCriteria: Eligibility Criteria for Bariatric Surgery (ADA Recommendation 8.16) |
   14.772 Remdesivir |
   14.773 Remdesivir IV 200 mg once then 100 mg once daily for 9 days |
   14.774 ResearchStudy Classifier Code System |
   14.775 Results Section for NCT03421379 |
   14.776 Results Section for NCT03640312 |
   14.777 Risk of Bias Assessment of Critically appraised summary of primary outcome of multi-platform RCT of anticoagulation for non-critically ill patients with COVID-19 |
   14.778 Risk of Bias Assessment of PARACHUTE trial |
   14.779 Risk Of Bias Type Value Set |
   14.780 Screened Group PARACHUTE Trial |
   14.781 Search Strategy for NMA_Diabetes |
   14.782 SearchResults: PubMed search for Wonder Woman |
   14.783 SearchStrategy: PubMed and Embase search for van Veldhuisen 2022 systematic review |
   14.784 SearchStrategy: PubMed search for Wonder Woman |
   14.785 Sex |
   14.786 Sex with comparator |
   14.787 Sex with intervention |
   14.788 SGLT2 inhibitors Group in Adults with type 2 diabetes |
   14.789 SoaPlanDefinition: Follow-up assessment 3 months after study start |
   14.790 SoftwareCitation: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter |
   14.791 Spanish or English Value Set |
   14.792 Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   14.793 StudyCitation: 2022 Systematic Review of bariatric surgery mortality effect 35243488 |
   14.794 StudyEligibilityCriteria: Eligibility Criteria for DIBASY Trial |
   14.795 StudyEligibilityCriteria: Obese patients ≥ 18 years old |
   14.796 StudyEligibilityCriteria: Type 2 diabetes and elevated BMI in 2016 meta-analysis |
   14.797 StudyEligibilityCriteria_Eligibility_Criteria_for_Bariatric_Surgery_Randomized_Trial_Diabetes_Surgery_Study |
   14.798 StudyGroup: Diabetes Surgery Study Trial Enrollment Group |
   14.799 StudyGroup: Severely Obese Adults 2018 Norwegian Cohort |
   14.800 StudyGroup_DIBASY_Trial_Enrollment_Group |
   14.801 Summary of Findings - QUARTET USA Trial |
   14.802 SummaryOfFindings: Bariatric Surgery Summary of Findings Example for GIN 2022 |
   14.803 SummaryOfFindings: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   14.804 SummaryOfFindings: SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   14.805 SummaryOfNetEffect: Bariatric Surgery Summary of Net Effect Contributions Example for GIN 2022 |
   14.806 SystematicReviewEligibilityCriteria: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   14.807 SystematicReviewExcludedStudies: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   14.808 SystematicReviewIncludedStudies: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   14.809 Systolic blood pressure at 12 weeks |
   14.810 Time to integration of results in a recommendation |
   14.811 VariableDefinition: Comparator |
   14.812 VariableDefinition: Condition(s) |
   14.813 VariableDefinition: Date of birth |
   14.814 VariableDefinition: Date of measurement |
   14.815 VariableDefinition: Gender |
   14.816 VariableDefinition: NTproBNP |
   14.817 VariableDefinition: Unit |
   14.818 Velocity |
   14.819 Velocity comparing intervention vs. comparator |
   14.820 Velocity for enrolled group |
   14.821 Velocity for non participant group |
   14.822 Velocity with comparator |
   14.823 Velocity with intervention |
   14.824 WebPageCitation: A HEvKA Update Summary |
   14.825 Weight |
   14.826 Weight with comparator |
   14.827 Weight with intervention |