 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 Changes |
  15 Artifacts Summary |
   15.1 AbsenceOfExposureDefinition |
   15.2 Adaptation |
   15.3 BaselineMeasureEvidence |
   15.4 BaselineMeasureReport |
   15.5 BaselineVariablesList |
   15.6 BookCitation |
   15.7 BookPartCitation |
   15.8 CertaintyOfEvidence |
   15.9 Classification |
   15.10 CohortDefinition |
   15.11 Comment |
   15.12 ComparativeBaselineMeasureEvidence |
   15.13 ComparativeEvidence |
   15.14 ComparativeEvidenceReport |
   15.15 ComparativeEvidenceReportExpanded |
   15.16 ComparativeEvidenceReportSubject |
   15.17 ComparativeEvidenceSynthesisReport |
   15.18 ComparativeParticipantFlowEvidence |
   15.19 ComparatorGroup |
   15.20 ComparatorOnlyEvidence |
   15.21 Comparison |
   15.22 CompositeRating |
   15.23 ConceptualCohortDefinition |
   15.24 ConceptualComparatorDefinition |
   15.25 ConceptualExposureDefinition |
   15.26 DatabaseCitation |
   15.27 DatabaseEntryCitation |
   15.28 DatasetCitation |
   15.29 DateAsRating |
   15.30 DichotomousIntendedOutcome |
   15.31 EndpointAnalysisPlan |
   15.32 EvidenceAssessment |
   15.33 EvidenceList |
   15.34 EvidenceReport |
   15.35 EvidenceReportPackage |
   15.36 EvidenceReportSubject |
   15.37 EvidenceSynthesisEvidence |
   15.38 ExposureGroup |
   15.39 GroupAssignment |
   15.40 GroupR6 |
   15.41 Guideline |
   15.42 InterventionOnlyEvidence |
   15.43 JournalArticleCitation |
   15.44 M11ReportContainer |
   15.45 M11ReportSection01 |
   15.46 M11ReportSection02 |
   15.47 M11ReportSection03 |
   15.48 M11ReportSection04 |
   15.49 M11ReportSection05 |
   15.50 M11ReportSection06 |
   15.51 M11ReportSection07 |
   15.52 M11ReportSection08 |
   15.53 M11ReportSection09 |
   15.54 M11ReportSection10 |
   15.55 M11ReportSection11 |
   15.56 M11ReportSection12 |
   15.57 M11ReportSection13 |
   15.58 M11ReportSection14 |
   15.59 MetaanalysisEligibilityCriteria |
   15.60 MetaanalysisOutcomeDefinition |
   15.61 MetaanalysisStudyGroup |
   15.62 NetEffectContribution |
   15.63 NetEffectContributionList |
   15.64 NetEffectContributions |
   15.65 NetEffectEstimate |
   15.66 NonComparativeEvidence |
   15.67 OutcomeDefinition |
   15.68 OutcomeImportance |
   15.69 OutcomeList |
   15.70 OutcomeMeasureReport |
   15.71 OutcomeVariablesList |
   15.72 ParticipantFlowEvidence |
   15.73 ParticipantFlowEvidenceVariable |
   15.74 ParticipantFlowReasonEvidenceVariable |
   15.75 ParticipantFlowReport |
   15.76 ParticipantFlowVariablesList |
   15.77 PICOSpecification |
   15.78 PICOTaggedComposition |
   15.79 PICOTaggedEvidence |
   15.80 PreprintCitation |
   15.81 Rating |
   15.82 Recommendation |
   15.83 RecommendationAction |
   15.84 RecommendationEligibilityCriteria |
   15.85 RecommendationJustification |
   15.86 RecommendationPlan |
   15.87 RecommendationRating |
   15.88 ResearchStudyDataDictionary |
   15.89 ResearchStudySite |
   15.90 ResearchStudySupport |
   15.91 RiskOfBias |
   15.92 SearchResults |
   15.93 SearchStrategy |
   15.94 SingleStudyEvidence |
   15.95 SoaPlanDefinition |
   15.96 SoftwareCitation |
   15.97 StatisticModel |
   15.98 StudyComponent |
   15.99 StudyDesign |
   15.100 StudyEligibilityCriteria |
   15.101 StudyGroup |
   15.102 StudyRegistryRecord |
   15.103 SummaryOfFindings |
   15.104 SummaryOfNetEffect |
   15.105 SystematicReview |
   15.106 SystematicReviewEligibilityCriteria |
   15.107 SystematicReviewExcludedStudies |
   15.108 SystematicReviewIncludedStudies |
   15.109 VariableDefinition |
   15.110 WebPageCitation |
   15.111 ArtifactAssessmentCompared |
   15.112 ArtifactAssessmentDateAsRating |
   15.113 ArtifactPublicationStatus |
   15.114 ArtifactRecorder |
   15.115 CharacteristicTiming |
   15.116 CiteAs |
   15.117 EvidenceVariableHandlingDetail |
   15.118 GuidelineRegistration |
   15.119 NumberAnalyzed |
   15.120 RelatesToClassifier |
   15.121 RelatesToWithQuotation |
   15.122 RelativeOutcomeImportance |
   15.123 RelevantForAutomatedMatching |
   15.124 ResearchStudyExcludedStudy |
   15.125 ResearchStudyIncludedStudy |
   15.126 ResearchStudyIsLowInterventionTrial |
   15.127 ResearchStudyIsRareDisease |
   15.128 ResearchStudyNumberOfStudiesIdentified |
   15.129 ResearchStudyNumberOfStudiesIncluded |
   15.130 ResearchStudySaeReportingMethod |
   15.131 ResearchStudySearchStrategy |
   15.132 ResearchStudySponsorConfidentialityStatement |
   15.133 ResearchStudyStudyAmendment |
   15.134 ResearchStudySystematicReviewEligibilityCriteria |
   15.135 StatisticModelExpression |
   15.136 StatisticModelIncludeIf |
   15.137 Desirability Codes Value Set |
   15.138 EBMonFHIR Profile Name Value Set |
   15.139 Evidence Rating System Classifier Codes Value Set |
   15.140 PICO Classification Value Set |
   15.141 Recommendation Justification Classifier Codes Value Set |
   15.142 Research Study Document Types Value Set |
   15.143 ResearchStudy Classifier Value Set |
   15.144 Search Strategy Characteristic Value Set |
   15.145 Desirability Code System |
   15.146 EBMonFHIR Profile Name Code System |
   15.147 Evidence Rating System Classifier Code System |
   15.148 Research Study Document Types Code System |
   15.149 Search Strategy Characteristic Code System |
   15.150 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes. |
   15.151 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   15.152 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. |
   15.153 15832493 Spotlight on rosiglitazone in the management of type 2 diabetes mellitus. |
   15.154 15855602 Defining and reporting hypoglycemia in diabetes: a report from the American Diabetes Association Workgroup on Hypoglycemia. |
   15.155 179899 |
   15.156 18160893 Wonder woman. Like my childhood heroine, Mrs. Betty also had amazing powers. |
   15.157 18508207 A Phase 3 placebo-controlled, double-blind, multi-site trial of the alpha-2-adrenergic agonist, lofexidine, for opioid withdrawal. |
   15.158 19029421 Phase III trial of androgen ablation with or without three cycles of systemic chemotherapy for advanced prostate cancer. |
   15.159 19091394 Endocrine treatment, with or without radiotherapy, in locally advanced prostate cancer (SPCG-7/SFUO-3): an open randomised phase III trial. |
   15.160 19967827 Wonder woman was Argentine and her real name was Evita. |
   15.161 22056152 Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial. |
   15.162 22502942 Addition of radiotherapy to long-term androgen deprivation in locally advanced prostate cancer: an open randomised phase 3 trial. |
   15.163 23306100 Androgen-deprivation therapy alone or with docetaxel in non-castrate metastatic prostate cancer (GETUG-AFU 15): a randomised, open-label, phase 3 trial. |
   15.164 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. |
   15.165 23589542 Hypoglycemia and diabetes: a report of a workgroup of the American Diabetes Association and the Endocrine Society. |
   15.166 23604530 A phase II trial of androgen deprivation therapy (ADT) plus chemotherapy as initial treatment for local failures or advanced prostate cancer. |
   15.167 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. |
   15.168 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). |
   15.169 26002607 Should docetaxel be standard of care for patients with metastatic hormone-sensitive prostate cancer? Pro and contra. |
   15.170 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. |
   15.171 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. |
   15.172 26244877 Chemohormonal Therapy in Metastatic Hormone-Sensitive Prostate Cancer. |
   15.173 26502880 A novel nasal powder formulation of glucagon: toxicology studies in animal models. |
   15.174 26681725 Intranasal Glucagon for Treatment of Insulin-Induced Hypoglycemia in Adults With Type 1 Diabetes: A Randomized Crossover Noninferiority Study. |
   15.175 26859072 Emotional Distress in the Partners of Type 1 Diabetes Adults: Worries About Hypoglycemia and Other Key Concerns. |
   15.176 27222544 Metabolic Surgery in the Treatment Algorithm for Type 2 Diabetes: A Joint Statement by International Diabetes Organizations. |
   15.177 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. |
   15.178 27979893 6. Glycemic Targets. |
   15.179 29114761 Web Exclusives. Annals Story Slam - How Wonder Woman Became My Alter Ego. |
   15.180 29114762 Web Exclusives. Annals Story Slam - Wonder Woman Is a Cartoon Character. |
   15.181 29202628 "I Kinda Feel Like Wonder Woman": An Interpretative Phenomenological Analysis of Pole Fitness and Positive Body Image. |
   15.182 29357271 Using Hawkeye from the Avengers to communicate on the eye. |
   15.183 29694275 A regressive formula of perversity: Wertham and the women of comics. |
   15.184 29694302 Introduction: "Suffering Sappho!": Lesbian content and queer female characters in comics. |
   15.185 30467172 Finding my inner Wonder Woman. |
   15.186 30545967 Parachute use to prevent death and major trauma when jumping from aircraft: randomized controlled trial. |
   15.187 34871555 What Can Wonder Woman Teach Radiologists? |
   15.188 35243488 Bariatric surgery and cardiovascular disease: a systematic review and meta-analysis. |
   15.189 36491989 Another Georgia Wonder Woman: She Does More Astounding Tricks Than Did Lula Hurst. |
   15.190 367832 |
   15.191 367833 |
   15.192 37024129 Benefits and harms of drug treatment for type 2 diabetes: systematic review and network meta-analysis of randomised controlled trials. |
   15.193 38584159 Efficacy and safety of a four-drug, quarter-dose treatment for hypertension: the QUARTET USA randomized trial. |
   15.194 6907780 Career guide: to change what needs changing...doesn't take Wonder Woman. |
   15.195 A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus |
   15.196 A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.197 ADAS-Cog(11) EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   15.198 Add-on Amlodipine at 6 weeks |
   15.199 Adults with diabetes mellitus type 2 |
   15.200 Adults with type 2 diabetes and CVD and CKD |
   15.201 Adults with type 2 diabetes and established CVD (but no CKD) |
   15.202 Adverse event free and hypertension control |
   15.203 Adverse event free and hypertension control at 12 weeks |
   15.204 Adverse Events Report for NCT03421379 |
   15.205 Adverse Events Report for NCT03640312 |
   15.206 Age |
   15.207 Age with comparator |
   15.208 Age with intervention |
   15.209 Aircraft Type |
   15.210 Aircraft Type with comparator |
   15.211 Aircraft Type with intervention |
   15.212 Altitude |
   15.213 Altitude comparing intervention vs. comparator |
   15.214 Altitude for enrolled group |
   15.215 Altitude for screened group |
   15.216 Altitude with comparator |
   15.217 Altitude with intervention |
   15.218 Analyzed Group in PARACHUTE Trial |
   15.219 Anticoagulation for COVID-19 Combined RCTs in NEJM |
   15.220 Baseline Characteristics Report for NCT03421379 |
   15.221 Baseline Characteristics Report for NCT03640312 |
   15.222 Baseline Characteristics Report for QUARTET Trial |
   15.223 Baseline Measure Report: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.224 Baseline Measures List for PARACHUTE Trial |
   15.225 BaselineMeasureEvidence: Age in 2018 Norwegian Cohort Medical Group |
   15.226 BaselineMeasureEvidence: Age in 2018 Norwegian Cohort Surgical Group |
   15.227 BaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Medical Group |
   15.228 BaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Surgical Group |
   15.229 BaselineVariablesList: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.230 Benefits and harms of drug treatment for type 2 diabetes: systematic review and network meta-analysis of randomised controlled trials |
   15.231 BookCitation: Crossing the Quality Chasm: A New Health System for the 21st Century |
   15.232 BookPartCitation: Chapter 3 of Crossing the Quality Chasm: A New Health System for the 21st Century |
   15.233 BookPartCitation: Chapter 3 of Crossing the Quality Chasm: A New Health System for the 21st Century - without baseCitation |
   15.234 Candesartan 8 mg once daily |
   15.235 Certainty of Evidence Rating of 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   15.236 Change in Mean Diastolic Blood Pressure (NCT03640312) |
   15.237 Change in Mean Diastolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   15.238 Change in Mean Diastolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   15.239 Change in Mean Diastolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.240 Change in Mean Systolic Blood Pressure (NCT03640312) |
   15.241 Change in Mean Systolic Blood Pressure (NCT03640312) |
   15.242 Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312 |
   15.243 Change in Mean Systolic Blood Pressure at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.244 Change in Mean Systolic Blood Pressure at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.245 Change in Mean Systolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   15.246 Change in Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   15.247 Change in Mean Systolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.248 CIBIC+ EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   15.249 Citation for Composition: ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.250 Citation for EBMonFHIR Implementation Guide |
   15.251 Citation for FEvIR Evidence 55: 14-day mortality remdesivir vs placebo meta-analysis (ACTT-1, Wang et al, WHO SOLIDARITY) |
   15.252 Citation for FEvIR Evidence 7637: Critically appraised summary of primary outcome of multi-platform RCT of anticoagulation for non-critically ill COVID-19 |
   15.253 Classification: Study Design for Association of Bariatric Surgery with Complications and Comorbidities JAMA 2018 Norwegian Cohort |
   15.254 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 |
   15.255 Comparative Evidence Report for QUARTET USA Trial |
   15.256 ComparativeBaselineMeasureEvidence: Age in 2018 Norwegian Cohort Surgical Group vs. Medical Group |
   15.257 ComparativeBaselineMeasureEvidence: BMI in 2018 Norwegian Cohort Surgical Group vs. Medical Group |
   15.258 ComparativeEvidence: All-cause mortality effect of bariatric surgery in 2022 meta-analysis |
   15.259 ComparativeEvidence: Bariatric Surgery effect for ADA triple outcome at 5 years (Diabetes Surgery Study) |
   15.260 ComparativeEvidence: Bypass surgery effects on Additional GI surgical procedure in JAMA 2018 Norwegian cohort study |
   15.261 ComparativeEvidence: Bypass surgery effects on Myocardial infarction or stroke in Swedish Obese Subjects (SOS) study |
   15.262 ComparativeEvidence: Bypass surgery effects on New onset depression in JAMA 2018 Norwegian cohort study |
   15.263 ComparativeEvidence: Bypass surgery effects on Remission of diabetes in JAMA 2018 Norwegian cohort study |
   15.264 ComparativeEvidence: Bypass surgery effects on Treatment with opioids in JAMA 2018 Norwegian cohort study |
   15.265 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Courcoulas 2014 |
   15.266 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Courcoulas 2015 |
   15.267 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Cummings 2016 |
   15.268 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ding 2015 |
   15.269 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Dixon 2008 |
   15.270 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Halperin 2014 |
   15.271 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ikramuddin 2013 |
   15.272 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Ikramuddin 2015 |
   15.273 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Liang 2013 |
   15.274 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Mingrone 2012 (DIBASY) trial |
   15.275 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Mingrone 2015 (DIBASY) trial |
   15.276 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Parikh 2014 |
   15.277 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Schauer 2012 (STAMPEDE) trial |
   15.278 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Schauer 2014 (STAMPEDE) trial |
   15.279 ComparativeEvidence: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups in Wentworth 2014 |
   15.280 ComparativeEvidence: Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   15.281 ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.282 ComparativeEvidenceReportSubject: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.283 ComparativeEvidenceSynthesisReport: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.284 ComparativeParticipantFlowEvidence: Dropout due to stopping intervention Lofexidine vs. Placebo in opioid detoxification trial |
   15.285 ComparatorDefinition: Glucagon-Like Peptide-1 (GLP-1) receptor agonists |
   15.286 ComparatorDefinition: Obese patients ≥ 18 years old without bariatric surgery |
   15.287 ComparatorDefinition: Standard care |
   15.288 ComparatorGroup: JAMA 2018 Norwegian cohort study Control cohort |
   15.289 ComparatorOnlyEvidence: Additional GI surgical procedure without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   15.290 ComparatorOnlyEvidence: All-cause mortality without bariatric surgery in 2022 meta-analysis |
   15.291 ComparatorOnlyEvidence: Myocardial infarction or stroke without bariatric surgery (Control Group) in Swedish Obese Subjects (SOS) study |
   15.292 ComparatorOnlyEvidence: New onset depression without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   15.293 ComparatorOnlyEvidence: Remission of diabetes without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   15.294 ComparatorOnlyEvidence: Treatment with opioids without bariatric surgery (Control Group) in JAMA 2018 Norwegian cohort study |
   15.295 Comparison: Original and Adapted Recommendation: ADA Obesity Management Recommendation 8.16 |
   15.296 Composite Rating of FOI 153881 for Project FOI 112280 |
   15.297 Computable_Publishing_LLC |
   15.298 ConceptualCohortDefinition: At least 2 risk factors for stroke |
   15.299 ConceptualCohortDefinition: BMI 27.5-32.4 in Asian Americans who do not achieve durable weight loss and improvement in comorbidities without surgery |
   15.300 ConceptualCohortDefinition: BMI 30-34.9 in persons who do not achieve durable weight loss and improvement in comorbidities without surgery |
   15.301 ConceptualCohortDefinition: BMI 32.5-37.4 in Asian Americans who do not achieve durable weight loss and improvement in comorbidities without surgery |
   15.302 ConceptualCohortDefinition: BMI 35-39.9 in persons who do not achieve durable weight loss and improvement in comorbidities without surgery |
   15.303 ConceptualCohortDefinition: BMI criteria for ADA surgery recommendation |
   15.304 ConceptualCohortDefinition: BMI ≥ 35 and at least 1 obesity-related comorbidity |
   15.305 ConceptualCohortDefinition: BMI ≥ 37.5 kg/m2 in Asian Americans |
   15.306 ConceptualCohortDefinition: Estimated glomerular filtration rate 45-59 |
   15.307 ConceptualCohortDefinition: Heart failure based on Phenotypes |
   15.308 ConceptualCohortDefinition: Lower BMI criteria for ADA surgery consideration |
   15.309 ConceptualCohortDefinition: Meet either T1DM-specific eligibility criteria or T2DM-specific eligibility criteria |
   15.310 ConceptualCohortDefinition: Nonfatal myocardial infarction |
   15.311 ConceptualCohortDefinition: Nonfatal stroke |
   15.312 ConceptualCohortDefinition: Oxygen saturation below 96% on Boots Finger Pulse Oximeter |
   15.313 ConceptualCohortDefinition: Oxygen saturation below 96% on Boots Finger Pulse Oximeter with Ranges |
   15.314 ConceptualCohortDefinition: Proxy criteria for surgical candidates |
   15.315 ConceptualCohortDefinition: Severe obesity |
   15.316 ConceptualCohortDefinition: T1DM or T2DM |
   15.317 ConceptualCohortDefinition: T1DM-specific criteria |
   15.318 ConceptualCohortDefinition: T2DM-specific criteria |
   15.319 ConceptualCohortDefinition_Cancer_of_any_kind_except_basal_cell_skin_cancer_or_cancer_in_situ_unless_documented_to_be_disease_free_for_five_years |
   15.320 ConceptualCohortDefinition_Cardiovascular_event |
   15.321 ConceptualComparatorDefinition: NOT Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   15.322 ConceptualComparatorDefinition: Usual-care pharmacologic thromboprophylaxis |
   15.323 ConceptualExposureDefinition: Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   15.324 ConceptualExposureDefinition: Therapeutic-dose anticoagulation with heparin |
   15.325 COVID_19PneumoniaHospitalizedAdult |
   15.326 Critically appraised summary of primary outcome of multi-platform RCT of anticoagulation for non-critically ill patients with COVID-19 |
   15.327 CTIS2024-516402-32-00 Eligibility Criteria |
   15.328 CTIS2024-516402-32-00 Primary Outcome 1 |
   15.329 CTIS2024-516402-32-00 Secondary Outcome 1 |
   15.330 CTIS2024-516402-32-00 Secondary Outcome 2 |
   15.331 CTIS2024-516402-32-00 Secondary Outcome 3 |
   15.332 CTIS2024-516402-32-00 Secondary Outcome 4 |
   15.333 CTIS2024-516402-32-00 Secondary Outcome 5 |
   15.334 CTIS2024-516402-32-00 Secondary Outcome 6 |
   15.335 CTIS2024-516402-32-00 Secondary Outcome 7 |
   15.336 CTIS2024-516402-32-00 Secondary Outcome 8 |
   15.337 DatabaseCitation: Citation for FEvIR Platform |
   15.338 DatabaseEntryCitation: ComparativeEvidenceReport: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.339 DatasetCitation: Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and is Associated with Worse Outcomes |
   15.340 DateOfFirstPublication Classification of FOI 153881 by Rachel Couban |
   15.341 Death or Major Traumatic Injury 30 days after Impact comparing intervention vs. comparator |
   15.342 Death or Major Traumatic Injury 30 days after Impact with comparator |
   15.343 Death or Major Traumatic Injury 30 days after Impact with intervention |
   15.344 Death or Major Traumatic Injury on Impact comparing intervention vs. comparator |
   15.345 declined randomization in PARACHUTE Study |
   15.346 deemed unsuitable by investigator in PARACHUTE Trial |
   15.347 Delany-Moretlwe 2022 clinical trial |
   15.348 Diabetes treatment medication |
   15.349 Diastolic blood pressure at 12 weeks |
   15.350 DichotomousIntendedOutcome: Additional gastrointestinal surgical procedure |
   15.351 DichotomousIntendedOutcome: Death or Major Traumatic Injury within 30 days |
   15.352 DichotomousIntendedOutcome: New onset depression |
   15.353 DichotomousIntendedOutcome: Nonfatal myocardial infarction or stroke |
   15.354 DichotomousIntendedOutcome: Remission of diabetes |
   15.355 DichotomousIntendedOutcome: Treatment with opioids |
   15.356 DIO: Mortality |
   15.357 Eculizumab in hypertensive emergency-associated hemolytic uremic syndrome: a randomized multicenter controlled trial (HYPERSHU) |
   15.358 Efficacy and Safety of a Quadruple Ultra-low-dose Treatment for Hypertension |
   15.359 Efficacy of Corticosteroids in COVID-19 Patients: A Systematic Review and Meta-Analysis |
   15.360 Eligibility criteria for NMA_Diabetes |
   15.361 Eligibility Criteria for QUARTET USA Trial |
   15.362 Enrolled Group for QUARTET USA Trial |
   15.363 Enrolled Group PARACHUTE Trial |
   15.364 Ethnic Group |
   15.365 Ethnic Group with comparator |
   15.366 Ethnic Group with intervention |
   15.367 Evidence Based Medicine on FHIR Implementation Guide Code System |
   15.368 Evidence for Results for Add-on Amlodipine at 6 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.369 Evidence for Results for Add-on Amlodipine at 6 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.370 Evidence for Results for Add-on Amlodipine at 6 weeks in QUARTET USA Trial Control Group |
   15.371 Evidence for Results for Add-on Amlodipine at 6 weeks in QUARTET USA Trial Quadpill group |
   15.372 Evidence for Results for Adverse event free and hypertension control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.373 Evidence for Results for Adverse event free and hypertension control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.374 Evidence for Results for Adverse event free and hypertension control at 12 weeks in QUARTET USA Trial Control Group |
   15.375 Evidence for Results for Adverse event free and hypertension control at 12 weeks in QUARTET USA Trial Quadpill group |
   15.376 Evidence for Results for Diastolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.377 Evidence for Results for Diastolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.378 Evidence for Results for Diastolic blood pressure at 12 weeks in QUARTET USA Trial Control Group |
   15.379 Evidence for Results for Diastolic blood pressure at 12 weeks in QUARTET USA Trial Quadpill group |
   15.380 Evidence for Results for Hypertension Control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.381 Evidence for Results for Hypertension Control at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.382 Evidence for Results for Hypertension Control at 12 weeks in QUARTET USA Trial Control Group |
   15.383 Evidence for Results for Hypertension Control at 12 weeks in QUARTET USA Trial Quadpill group |
   15.384 Evidence for Results for Medication Adherence at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.385 Evidence for Results for Medication Adherence at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.386 Evidence for Results for Medication Adherence at 12 weeks in QUARTET USA Trial Control Group |
   15.387 Evidence for Results for Medication Adherence at 12 weeks in QUARTET USA Trial Quadpill group |
   15.388 Evidence for Results for Systolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.389 Evidence for Results for Systolic blood pressure at 12 weeks in GroupAssignment: Quadpill vs. Candesartan |
   15.390 Evidence for Results for Systolic blood pressure at 12 weeks in QUARTET USA Trial Control Group |
   15.391 Evidence for Results for Systolic blood pressure at 12 weeks in QUARTET USA Trial Quadpill group |
   15.392 Evidence List: Effect estimates for meta-analysis (Biegel 2020, Wang 2020, SOLIDARITY) |
   15.393 EvidenceList: Study results included in Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   15.394 EvidenceReportSectionCode Value Set |
   15.395 EvidenceReportSubject: Clinical Outcomes for Effects of Bariatric Surgery |
   15.396 EvidenceVariable Handling Extension Value Set |
   15.397 EvidenceVariable: case_id |
   15.398 EvidenceVariable: Patient id |
   15.399 EvidenceVariable: Time of measurement |
   15.400 Example EndpointAnalysisPlan from PHUSE Lilly Redacted Protocol - EBMonFHIR IG Version |
   15.401 Excluded from PARACHUTE Study |
   15.402 ExposureGroup: JAMA 2018 Norwegian cohort study Surgery cohort |
   15.403 ExposureVariable: Age (as continuous variable) |
   15.404 ExposureVariable: Body Mass Index (as continuous variable) |
   15.405 ExposureVariable: pht013093.v1.p1 Age at diagnosis |
   15.406 ExposureVariable: pht013093.v1.p1 RACE |
   15.407 ExposureVariable: pht013093.v1.p1 SEX |
   15.408 ExposureVariable: pht013093.v1.p1 SUBJECT_ID |
   15.409 ExposureVariable: pht013094.v1.p1 ANALYTE_TYPE |
   15.410 ExposureVariable: pht013094.v1.p1 BODY_SITE |
   15.411 ExposureVariable: pht013094.v1.p1 IS_TUMOR |
   15.412 ExposureVariable: pht013094.v1.p1 SAMPLE_ID |
   15.413 ExposureVariable: pht013094.v1.p1 SAMPLE_USE |
   15.414 ExposureVariable: pht013094.v1.p1 Source_Type |
   15.415 Family History of Parachute Use |
   15.416 Family History of Parachute Use with comparator |
   15.417 Family History of Parachute Use with intervention |
   15.418 Frequent Flier |
   15.419 Frequent Flier with comparator |
   15.420 Frequent Flier with intervention |
   15.421 GLP-1 RA Group in Adults with type 2 diabetes |
   15.422 GLP-1 RA Group in at-risk Adults with type 2 diabetes with moderate CV risk |
   15.423 Glucagon Hydrochloride Solution (Active Comparator) |
   15.424 Glucagon Nasal Powder (Experimental) |
   15.425 Group Randomized to Comparator (empty backpack) in PARACHUTE Trial |
   15.426 Group Randomized to Intervention Group (parachute) in PARACHUTE Trial |
   15.427 GroupAssignment: Bariatric Surgery vs. no bariatric surgery |
   15.428 GroupAssignment: ExposureDefinition: Bariatric Surgery (RYGB, VSG, LAGB, BPD) vs. ComparatorDefinition: NOT Bariatric Surgery (RYGB, VSG, LAGB, BPD) |
   15.429 GroupAssignment: ExposureGroup: JAMA 2018 Norwegian cohort study Surgery cohort vs. ComparatorGroup: JAMA 2018 Norwegian cohort study Control cohort |
   15.430 GroupAssignment: GLP-1 RA vs. Standard care |
   15.431 GroupAssignment: high dose xanomeline vs. low dose xanomeline vs. placebo |
   15.432 GroupAssignment: Jumping from aircraft with parachute vs. Jumping from aircraft with empty backpack |
   15.433 GroupAssignment: Non Participants vs. Enrolled Participants |
   15.434 GroupAssignment: Quadpill vs. Candesartan |
   15.435 GroupAssignment: Roux-en-Y gastric bypass or Biliopancreatic Diversion vs. medical treatment |
   15.436 GroupAssignment: Roux-en-Y gastric bypass surgery vs. Lifestyle-intensive medical management intervention alone |
   15.437 GroupAssignment: Roux-en-Y gastric bypass vs. medical treatment |
   15.438 GroupAssignment: SGLT2 inhibitors vs. GLP-1 RA |
   15.439 GroupAssignment: Therapeutic-dose anticoagulation with heparin vs. Usual-care pharmacologic thromboprophylaxis |
   15.440 Guideline: ADA 2021 Standards of Medical Care 8. Obesity Management for the Treatment of Type 2 Diabetes |
   15.441 Health Survey Score Total |
   15.442 Health Survey Score Total comparing intervention vs. comparator |
   15.443 Health Survey Score Total with comparator |
   15.444 Health Survey Score Total with intervention |
   15.445 Health Survey Score-Mental Health Subscore |
   15.446 Health Survey Score-Mental Health Subscore comparing intervention vs. comparator |
   15.447 Health Survey Score-Mental Health Subscore with comparator |
   15.448 Health Survey Score-Mental Health Subscore with intervention |
   15.449 Health Survey Score-Physical Health Subscore |
   15.450 Health Survey Score-Physical Health Subscore comparing intervention vs. comparator |
   15.451 Health Survey Score-Physical Health Subscore with comparator |
   15.452 Health Survey Score-Physical Health Subscore with intervention |
   15.453 Health-related Quality of Life (NCT03640312) |
   15.454 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) at (NCT03640312) |
   15.455 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) for Candesartan in NCT03640312 |
   15.456 Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) for QUARTET LDQT in NCT03640312 |
   15.457 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) at (NCT03640312) |
   15.458 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) for Candesartan in NCT03640312 |
   15.459 Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) for QUARTET LDQT in NCT03640312 |
   15.460 Health-related Quality of Life at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.461 Health-related Quality of Life at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.462 Height |
   15.463 Height with comparator |
   15.464 Height with intervention |
   15.465 High Blood Pressure Medication Value Set |
   15.466 History of Acrophobia |
   15.467 History of Acrophobia with comparator |
   15.468 History of Acrophobia with intervention |
   15.469 History of Broken Bones |
   15.470 History of Broken Bones with comparator |
   15.471 History of Broken Bones with intervention |
   15.472 History of Parachute Use |
   15.473 History of Parachute Use with comparator |
   15.474 History of Parachute Use with intervention |
   15.475 Hypertension Control at 12 weeks |
   15.476 ICD-10-GM Terminale Codes |
   15.477 Injury Severity Score 30 days after Impact comparing intervention vs. comparator |
   15.478 Injury Severity Score 30 days after Impact with comparator |
   15.479 Injury Severity Score 30 days after Impact with intervention |
   15.480 Injury Severity Score on Impact comparing intervention vs. comparator |
   15.481 Injury Severity Score on Impact with comparator |
   15.482 Injury Severity Score on Impact with intervention |
   15.483 International vs Domestic Flight |
   15.484 International vs Domestic Flight with comparator |
   15.485 International vs Domestic Flight with intervention |
   15.486 InterventionDefinition: Glucagon-Like Peptide-1 (GLP-1) receptor agonists |
   15.487 InterventionDefinition: Sodium-Glucose Transport Protein 2 (SGLT2) inhibitors |
   15.488 InterventionOnlyEvidence: Additional GI surgical procedure with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   15.489 InterventionOnlyEvidence: New onset depression with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   15.490 InterventionOnlyEvidence: Remission of diabetes with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   15.491 InterventionOnlyEvidence: Treatment with opioids with bariatric surgery (Intervention Group) in JAMA 2018 Norwegian cohort study |
   15.492 Investigator |
   15.493 Investigator-by-treatment interaction for ADAS-Cog(11) ANCOVA |
   15.494 IV remdesivir 200 mg then 100 mg/day for 9 days |
   15.495 Joanne Dehnbostel's Adaptation Report of Recommendation: ADA Obesity Management Recommendation 8.16 |
   15.496 JournalArticleCitation: ADA 2021 Standards of Medical Care 8. Obesity Management for the Treatment of Type 2 Diabetes |
   15.497 JournalArticleCitation: Association of Bariatric Surgery with Complications and Comorbidities JAMA 2018 Norwegian Cohort |
   15.498 Jumping from aircraft with empty backpack |
   15.499 Jumping from aircraft with parachute |
   15.500 Justification for Recommendation: ADA Obesity Management Recommendation 8.16 |
   15.501 Justification for Recommendation: ADA Obesity Management Recommendation 8.17 |
   15.502 M11 IGBJ Protocol Example Eligibility Criteria |
   15.503 M11 Report for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.504 M11 Report for M11ResearchStudy Template |
   15.505 M11 Report Section 1 (Protocol Summary) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.506 M11 Report Section 1 (Protocol Summary) for M11ResearchStudy Template |
   15.507 M11 Report Section 10 (Statistical Considerations) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.508 M11 Report Section 10 (Statistical Considerations) for M11ResearchStudy Template |
   15.509 M11 Report Section 11 (Trial Oversight) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.510 M11 Report Section 11 (Trial Oversight) for M11ResearchStudy Template |
   15.511 M11 Report Section 12 (Supporting Details) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.512 M11 Report Section 12 (Supporting Details) for M11ResearchStudy Template |
   15.513 M11 Report Section 13 (Glossary) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.514 M11 Report Section 13 (Glossary) for M11ResearchStudy Template |
   15.515 M11 Report Section 14 (References) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.516 M11 Report Section 14 (References) for M11ResearchStudy Template |
   15.517 M11 Report Section 2 (Introduction) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.518 M11 Report Section 2 (Introduction) for M11ResearchStudy Template |
   15.519 M11 Report Section 3 (Trial Objectives and Associated Estimands) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.520 M11 Report Section 3 (Trial Objectives and Associated Estimands) for M11ResearchStudy Template |
   15.521 M11 Report Section 4 (Trial Design) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.522 M11 Report Section 4 (Trial Design) for M11ResearchStudy Template |
   15.523 M11 Report Section 5 (Trial Population) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.524 M11 Report Section 5 (Trial Population) for M11ResearchStudy Template |
   15.525 M11 Report Section 6 (Trial Intervention) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.526 M11 Report Section 6 (Trial Intervention) for M11ResearchStudy Template |
   15.527 M11 Report Section 7 (Participant Discontinuation) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.528 M11 Report Section 7 (Participant Discontinuation) for M11ResearchStudy Template |
   15.529 M11 Report Section 8 (Trial Assessments) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.530 M11 Report Section 8 (Trial Assessments) for M11ResearchStudy Template |
   15.531 M11 Report Section 9 (Adverse Events) for A Study of Nasal Glucagon (LY900018) in Japanese Participants With Diabetes Mellitus - M11 Example |
   15.532 M11 Report Section 9 (Adverse Events) for M11ResearchStudy Template |
   15.533 M11ResearchStudy Template |
   15.534 MAGIC-derived ComparatorOnlyEvidence: All-cause mortality in GLP-1 RA Group in Adults with type 2 diabetes |
   15.535 MAGIC-derived ComparatorOnlyEvidence: All-cause mortality in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.536 MAGIC-derived ComparatorOnlyEvidence: Body weight in GLP-1 RA Group in Adults with type 2 diabetes |
   15.537 MAGIC-derived ComparatorOnlyEvidence: Body weight in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.538 MAGIC-derived ComparatorOnlyEvidence: Cardiovascular mortality in GLP-1 RA Group in Adults with type 2 diabetes |
   15.539 MAGIC-derived ComparatorOnlyEvidence: Cardiovascular mortality in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.540 MAGIC-derived ComparatorOnlyEvidence: Diabetic ketoacidosis in GLP-1 RA Group in Adults with type 2 diabetes |
   15.541 MAGIC-derived ComparatorOnlyEvidence: End-stage kidney disease in GLP-1 RA Group in Adults with type 2 diabetes |
   15.542 MAGIC-derived ComparatorOnlyEvidence: End-stage kidney disease in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.543 MAGIC-derived ComparatorOnlyEvidence: Genital infection in GLP-1 RA Group in Adults with type 2 diabetes |
   15.544 MAGIC-derived ComparatorOnlyEvidence: Health-related quality of life in GLP-1 RA Group in Adults with type 2 diabetes |
   15.545 MAGIC-derived ComparatorOnlyEvidence: Health-related quality of life in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.546 MAGIC-derived ComparatorOnlyEvidence: Heart failure in GLP-1 RA Group in Adults with type 2 diabetes |
   15.547 MAGIC-derived ComparatorOnlyEvidence: Heart failure in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.548 MAGIC-derived ComparatorOnlyEvidence: Nonfatal myocardial infarction in GLP-1 RA Group in Adults with type 2 diabetes |
   15.549 MAGIC-derived ComparatorOnlyEvidence: Nonfatal myocardial infarction in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.550 MAGIC-derived ComparatorOnlyEvidence: Nonfatal stroke in GLP-1 RA Group in Adults with type 2 diabetes |
   15.551 MAGIC-derived ComparatorOnlyEvidence: Nonfatal stroke in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.552 MAGIC-derived ComparatorOnlyEvidence: Serious hyperglycaemia in GLP-1 RA Group in Adults with type 2 diabetes |
   15.553 MAGIC-derived ComparatorOnlyEvidence: Serious hyperglycaemia in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.554 MAGIC-derived ComparatorOnlyEvidence: Severe gastrointestinal events in GLP-1 RA Group in Adults with type 2 diabetes |
   15.555 MAGIC-derived ComparatorOnlyEvidence: Severe gastrointestinal events in Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.556 MAGIC-derived Evidence: All-cause mortality with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.557 MAGIC-derived Evidence: All-cause mortality with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.558 MAGIC-derived Evidence: Body weight with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.559 MAGIC-derived Evidence: Body weight with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.560 MAGIC-derived Evidence: Cardiovascular mortality with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.561 MAGIC-derived Evidence: Cardiovascular mortality with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.562 MAGIC-derived Evidence: Diabetic ketoacidosis with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.563 MAGIC-derived Evidence: End-stage kidney disease with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.564 MAGIC-derived Evidence: End-stage kidney disease with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.565 MAGIC-derived Evidence: Genital infection with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.566 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 |
   15.567 MAGIC-derived Evidence: Health-related quality of life with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.568 MAGIC-derived Evidence: Heart failure with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.569 MAGIC-derived Evidence: Heart failure with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.570 MAGIC-derived Evidence: Nonfatal myocardial infarction with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.571 MAGIC-derived Evidence: Nonfatal myocardial infarction with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.572 MAGIC-derived Evidence: Nonfatal stroke with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.573 MAGIC-derived Evidence: Nonfatal stroke with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.574 MAGIC-derived Evidence: Serious hyperglycaemia with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.575 MAGIC-derived Evidence: Serious hyperglycaemia with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.576 MAGIC-derived Evidence: Severe gastrointestinal events with GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.577 MAGIC-derived Evidence: Severe gastrointestinal events with SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.578 MAGIC-derived InterventionOnlyEvidence: All-cause mortality in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.579 MAGIC-derived InterventionOnlyEvidence: All-cause mortality in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.580 MAGIC-derived InterventionOnlyEvidence: Body weight in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.581 MAGIC-derived InterventionOnlyEvidence: Body weight in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.582 MAGIC-derived InterventionOnlyEvidence: Cardiovascular mortality in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.583 MAGIC-derived InterventionOnlyEvidence: Cardiovascular mortality in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.584 MAGIC-derived InterventionOnlyEvidence: Diabetic ketoacidosis in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.585 MAGIC-derived InterventionOnlyEvidence: End-stage kidney disease in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.586 MAGIC-derived InterventionOnlyEvidence: End-stage kidney disease in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.587 MAGIC-derived InterventionOnlyEvidence: Genital infection in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.588 MAGIC-derived InterventionOnlyEvidence: Health-related quality of life in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.589 MAGIC-derived InterventionOnlyEvidence: Health-related quality of life in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.590 MAGIC-derived InterventionOnlyEvidence: Heart failure in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.591 MAGIC-derived InterventionOnlyEvidence: Heart failure in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.592 MAGIC-derived InterventionOnlyEvidence: Nonfatal myocardial infarction in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.593 MAGIC-derived InterventionOnlyEvidence: Nonfatal myocardial infarction in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.594 MAGIC-derived InterventionOnlyEvidence: Nonfatal stroke in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.595 MAGIC-derived InterventionOnlyEvidence: Nonfatal stroke in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.596 MAGIC-derived InterventionOnlyEvidence: Serious hyperglycaemia in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.597 MAGIC-derived InterventionOnlyEvidence: Serious hyperglycaemia in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.598 MAGIC-derived InterventionOnlyEvidence: Severe gastrointestinal events in GLP-1 RA Group in Adults with type 2 diabetes with moderate CV risk |
   15.599 MAGIC-derived InterventionOnlyEvidence: Severe gastrointestinal events in SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.600 Mean Change in Blood Urea Nitrogen (NCT03640312) |
   15.601 Mean Change in Blood Urea Nitrogen at 12 weeks for Candesartan in NCT03640312 |
   15.602 Mean Change in Blood Urea Nitrogen at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.603 Mean Change in Blood Urea Nitrogen at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.604 Mean Change in Serum Creatinine (NCT03640312) |
   15.605 Mean Change in Serum Creatinine at 12 weeks for Candesartan in NCT03640312 |
   15.606 Mean Change in Serum Creatinine at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.607 Mean Change in Serum Creatinine at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.608 Mean Change in Serum Potassium (NCT03640312) |
   15.609 Mean Change in Serum Potassium at 12 weeks for Candesartan in NCT03640312 |
   15.610 Mean Change in Serum Potassium at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.611 Mean Change in Serum Potassium at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.612 Mean Change in Serum Sodium (NCT03640312) |
   15.613 Mean Change in Serum Sodium at 12 weeks for Candesartan in NCT03640312 |
   15.614 Mean Change in Serum Sodium at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.615 Mean Change in Serum Sodium at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.616 Mean Diastolic Blood Pressure (NCT03640312) |
   15.617 Mean Diastolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   15.618 Mean Diastolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   15.619 Mean Diastolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.620 Mean Systolic Blood Pressure (NCT03640312) |
   15.621 Mean Systolic Blood Pressure at 6 weeks for Candesartan in NCT03640312 |
   15.622 Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 |
   15.623 Mean Systolic Blood Pressure at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.624 Median Age of Parachute Intervention Group |
   15.625 Medication Adherence (NCT03640312) |
   15.626 Medication Adherence at 12 weeks |
   15.627 Medication Adherence at 12 weeks for Candesartan in NCT03640312 |
   15.628 Medication Adherence at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.629 Medication Adherence at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.630 MetaanalysisEligibilityCriteria: Mean difference in HbA1c effect of bariatric surgery in type 2 diabetes and elevated BMI in 2016 meta-analysis |
   15.631 MetaanalysisOutcomeDefinition: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups at end of follow-up |
   15.632 MetaanalysisStudyGroup: Effect Estimates for Mortality at 14 days from COVID19 Remdesivir vs. Placebo RCTs |
   15.633 MetaanalysisStudyGroup: Study results included in Mean difference in HbA1c effect of bariatric surgery in 2016 meta-analysis |
   15.634 Mortality at 14 days |
   15.635 NCT03421379 Eligibility Criteria |
   15.636 NCT03640312 Eligibility Criteria |
   15.637 NetEffectContribution for ComparativeEvidence: All-cause mortality effect of bariatric surgery in 2022 meta-analysis |
   15.638 NetEffectContribution for ComparativeEvidence: Bypass surgery effects on Additional GI surgical procedure in JAMA 2018 Norwegian cohort study |
   15.639 NetEffectContribution for ComparativeEvidence: Bypass surgery effects on Myocardial infarction or stroke in Swedish Obese Subjects (SOS) study |
   15.640 NetEffectContribution for ComparativeEvidence: Bypass surgery effects on New onset depression in JAMA 2018 Norwegian cohort study |
   15.641 NetEffectContribution for ComparativeEvidence: Bypass surgery effects on Remission of diabetes in JAMA 2018 Norwegian cohort study |
   15.642 NetEffectContribution for ComparativeEvidence: Bypass surgery effects on Treatment with opioids in JAMA 2018 Norwegian cohort study |
   15.643 NetEffectContributionList: Bariatric Surgery Example for GIN 2022 |
   15.644 NetEffectContributions: Bariatric Surgery Example for GIN 2022 |
   15.645 NetEffectEstimate for SummaryOfNetEffect: Bariatric Surgery Summary of Net Effect Contributions Example for GIN 2022 |
   15.646 NHANES LBDGLUSI Variable Definition Cohort Definition |
   15.647 NHANES LBDGLUSI: Fasting Glucose (mmol/L) |
   15.648 NHANES LBXGLU Variable Definition Cohort Definition |
   15.649 NHANES LBXGLU: Fasting Glucose (mg/dL) |
   15.650 NHANES Plasma Fasting Glucose (GLU_J) Data Dictionary |
   15.651 NHANES SEQN Respondent Sequence Number |
   15.652 NHANES WTSAF2YR Variable Definition Cohort Definition |
   15.653 NHANES WTSAF2YR: Fasting Subsample 2 Year MEC Weight |
   15.654 Norwegian Cohort Study Comparing Bariatric Surgery vs Medical Obesity Treatment for Long-term Medical Complications and Obesity-Related Comorbidities |
   15.655 NT-proBNP Study Data Dictionary |
   15.656 Number of Patients Requiring Step up Treatment (NCT03640312) |
   15.657 Number of Patients Requiring Step up Treatment at 6 weeks for Candesartan in NCT03640312 |
   15.658 Number of Patients Requiring Step up Treatment at 6 weeks for QUARTET LDQT in NCT03640312 |
   15.659 Number of Patients Requiring Step up Treatment at 6 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.660 Organ support-free days |
   15.661 Outcome Importance Rating 100 of All-cause mortality |
   15.662 Outcome Importance Rating 30 of Nonfatal myocardial infarction or stroke |
   15.663 Outcome Importance Rating 5 of New onset depression |
   15.664 Outcome Importance Rating 5 of Remission of diabetes |
   15.665 Outcome Importance Rating 5 of Treatment with opioids |
   15.666 Outcome Importance Rating 8 of Additional GI surgical procedure |
   15.667 Outcome Importance Rating of DichotomousIntendedOutcome: Additional gastrointestinal surgical procedure for StudyEligibilityCriteria: Eligibility Criteria for Bariatric Surgery Randomized Trial (Diabetes Surgery Study) |
   15.668 Outcome Importance Rating of DichotomousIntendedOutcome: New onset depression for StudyEligibilityCriteria: Eligibility Criteria for Bariatric Surgery Randomized Trial (Diabetes Surgery Study) |
   15.669 Outcome Importance Rating of DichotomousIntendedOutcome: Nonfatal myocardial infarction or stroke for StudyEligibilityCriteria: Eligibility Criteria for Bariatric Surgery Randomized Trial (Diabetes Surgery Study) |
   15.670 Outcome Importance Rating of DichotomousIntendedOutcome: Remission of diabetes for StudyEligibilityCriteria: Eligibility Criteria for Bariatric Surgery Randomized Trial (Diabetes Surgery Study) |
   15.671 Outcome Importance Rating of DichotomousIntendedOutcome: Treatment with opioids for StudyEligibilityCriteria: Eligibility Criteria for Bariatric Surgery Randomized Trial (Diabetes Surgery Study) |
   15.672 Outcome Importance Rating of Mortality for Bariatric Surgery Patients |
   15.673 Outcome Measure List for QUARTET USA Trial |
   15.674 Outcome Measure Report for QUARTET USA Trial |
   15.675 Outcome Measure Report: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.676 Outcome Measures Report for NCT03421379 |
   15.677 Outcome Measures Report for NCT03640312 |
   15.678 Outcome Variables List for PARACHUTE Trial |
   15.679 Outcome: Death or Major Traumatic Injury 30 days after Impact |
   15.680 Outcome: Death or Major Traumatic Injury on Impact |
   15.681 Outcome: Injury Severity Score 30 days after Impact |
   15.682 Outcome: Injury Severity Score on Impact |
   15.683 OutcomeDefinition: Injury Severity Score on Impact |
   15.684 OutcomeDefinition: All-cause mortality |
   15.685 OutcomeDefinition: All-cause mortality |
   15.686 OutcomeDefinition: American Diabetes Association composite triple end point for metabolic control |
   15.687 OutcomeDefinition: Body weight |
   15.688 OutcomeDefinition: Body weight |
   15.689 OutcomeDefinition: Cardiovascular mortality |
   15.690 OutcomeDefinition: Cardiovascular mortality |
   15.691 OutcomeDefinition: Diabetes in remission |
   15.692 OutcomeDefinition: Diabetic ketoacidosis |
   15.693 OutcomeDefinition: End-stage kidney disease |
   15.694 OutcomeDefinition: End-stage kidney disease |
   15.695 OutcomeDefinition: Genital infection |
   15.696 OutcomeDefinition: HbA1c at 12 months |
   15.697 OutcomeDefinition: HbA1c at 24 months |
   15.698 OutcomeDefinition: HbA1c at 36 months |
   15.699 OutcomeDefinition: HbA1c at 6 months |
   15.700 OutcomeDefinition: HbA1c at 60 months |
   15.701 OutcomeDefinition: Health-related quality of life |
   15.702 OutcomeDefinition: Health-related quality of life |
   15.703 OutcomeDefinition: Heart failure |
   15.704 OutcomeDefinition: Heart failure |
   15.705 OutcomeDefinition: Mortality at 14 days |
   15.706 OutcomeDefinition: New onset depression |
   15.707 OutcomeDefinition: Nonfatal myocardial infarction |
   15.708 OutcomeDefinition: Nonfatal myocardial infarction |
   15.709 OutcomeDefinition: Nonfatal myocardial infarction or stroke |
   15.710 OutcomeDefinition: Nonfatal stroke |
   15.711 OutcomeDefinition: Nonfatal stroke |
   15.712 OutcomeDefinition: Serious hyperglycaemia |
   15.713 OutcomeDefinition: Serious hyperglycaemia |
   15.714 OutcomeDefinition: Severe gastrointestinal events |
   15.715 OutcomeDefinition: Severe gastrointestinal events |
   15.716 OutcomeList: Clinical Outcomes for Effects of Bariatric Surgery |
   15.717 OutcomeMeasureReport: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.718 OutcomeVariable: American Diabetes Association composite triple end point for metabolic control at 5 years |
   15.719 OutcomeVariable: HbA1c at 12 months |
   15.720 OutcomeVariable: HbA1c at 24 months |
   15.721 OutcomeVariable: HbA1c at 36 months |
   15.722 OutcomeVariable: HbA1c at 6 months |
   15.723 OutcomeVariable: HbA1c at 60 months |
   15.724 OutcomeVariable: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups at end of follow-up |
   15.725 OutcomeVariable: New onset depression |
   15.726 OutcomeVariable: Nonfatal myocardial infarction or stroke |
   15.727 OutcomeVariable: Remission of diabetes |
   15.728 OutcomeVariablesList: Association of Bariatric Surgery vs Medical Obesity Treatment With Long-term Medical Complications and Obesity-Related Comorbidities (2018 Norwegian Cohort) |
   15.729 OutcomeVariable_Additional_GI_surgical_procedure |
   15.730 OutcomeVariable_All_cause_mortality |
   15.731 OutcomeVariable_Treatment_with_opioids |
   15.732 PARACHUTE Trial baseline characteristics |
   15.733 PARACHUTE Trial non participants |
   15.734 PARACHUTE trial participant flow report |
   15.735 PARACHUTE Trial Participants |
   15.736 PARACHUTE Trial Participants assigned an empty backpack |
   15.737 PARACHUTE trial participants assigned parachute |
   15.738 PARACHUTE Trial Participants available for randomization |
   15.739 PARACHUTE Trial Participants deemed unsuitable by investigator |
   15.740 PARACHUTE Trial Participants randomized into groups |
   15.741 PARACHUTE Trial Participants randomized into groups for screened group |
   15.742 PARACHUTE Trial Participants randomized into groups with comparator |
   15.743 PARACHUTE Trial Participants randomized into groups with intervention |
   15.744 PARACHUTE Trial Participants that completed 30 day follow up |
   15.745 PARACHUTE Trial Participants that completed 30 day follow up with comparator |
   15.746 PARACHUTE Trial Participants that completed 30 day follow up with intervention |
   15.747 PARACHUTE Trial Participants that completed jump and 5 minute follow-up |
   15.748 PARACHUTE Trial Participants that completed jump and 5 minute follow-up with comparator |
   15.749 PARACHUTE Trial Participants that completed jump and 5 minute follow-up with intervention |
   15.750 PARACHUTE Trial Participants that declined randomization |
   15.751 PARACHUTE Trial Participants with no contact at 30 days |
   15.752 PARACHUTE Trial Participants with no contact at 30 days with comparator |
   15.753 PARACHUTE Trial Participants with no contact at 30 days with intervention |
   15.754 PARACHUTE Trial Results |
   15.755 Parachute use to prevent death and major trauma when jumping from aircraft: randomized controlled trial. |
   15.756 Parachute vs Empty Backpack in PARACHUTE Trial |
   15.757 Participant Flow Report for NCT03421379 |
   15.758 Participant Flow Report for NCT03640312 |
   15.759 Participant Flow Report for QUARTET USA Trial |
   15.760 Participant Flow Variables List for PARACHUTE Trial |
   15.761 ParticipantFlow: 2018 Norwegian Cohort Included in Analysis |
   15.762 ParticipantFlow: 2018 Norwegian Cohort Medical Group Included in Analysis |
   15.763 ParticipantFlow: 2018 Norwegian Cohort Surgical Group Included in Analysis |
   15.764 ParticipantFlowEvidence: 2018 Norwegian Cohort Excluded from Analysis |
   15.765 ParticipantFlowMeasure: Dropout due to stopping intervention |
   15.766 ParticipantFlowMeasure: Exclusion from analysis |
   15.767 ParticipantFlowMeasure: Inclusion in analysis |
   15.768 Participants Excluded from PARACHUTE Study |
   15.769 Participants_in_Anticoagulation_for_COVID_19_Combined_ATTACC_ACTIV_4a_and_REMAP_CAP_RCT_hospitalized_not_critically_ill |
   15.770 Patients_who_are_hospitalized_for_COVID_19_and_who_are_not_critically_ill |
   15.771 PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   15.772 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 |
   15.773 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 |
   15.774 Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia (NCT03421379) |
   15.775 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 |
   15.776 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 |
   15.777 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 |
   15.778 Percentage of Participants With Potentially Related Adverse Events (NCT03640312) |
   15.779 Percentage of Participants With Potentially Related Adverse Events at 12 weeks for Candesartan in NCT03640312 |
   15.780 Percentage of Participants With Potentially Related Adverse Events at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.781 Percentage of Participants With Potentially Related Adverse Events at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.782 Percentage of Participants With Serious Adverse Events (SAEs) (NCT03640312) |
   15.783 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks for Candesartan in NCT03640312 |
   15.784 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.785 Percentage of Participants With Serious Adverse Events (SAEs) at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.786 Pharmacodynamics (PD): Change From Baseline in Maximal Blood Glucose (BGmax) of Glucagon Nasal Powder and Glucagon Hydrochloride Intramuscular (IM) (NCT03421379) |
   15.787 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 |
   15.788 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 |
   15.789 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) |
   15.790 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 |
   15.791 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 |
   15.792 PK: Change From Baseline in Maximal Concentration (Cmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   15.793 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 |
   15.794 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 |
   15.795 PK: Change From Baseline in Tmax of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) |
   15.796 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 |
   15.797 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 |
   15.798 Placebo |
   15.799 PlanDefinition for Recommendation: ADA Obesity Management Recommendation 8.16 |
   15.800 PlanDefinition for Recommendation: ADA Obesity Management Recommendation 8.17 |
   15.801 PreprintCitation: Nigella Sativa for COVID-19 OSF Preprint |
   15.802 Proportion of Patients With Adverse Event Free Hypertension Control (NCT03640312) |
   15.803 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks for Candesartan in NCT03640312 |
   15.804 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.805 Proportion of Patients With Adverse Event Free Hypertension Control at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.806 Proportion of Patients With Hypertension Control (NCT03640312) |
   15.807 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks at (NCT03640312) |
   15.808 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks for Candesartan in NCT03640312 |
   15.809 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks for QUARTET LDQT in NCT03640312 |
   15.810 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks at (NCT03640312) |
   15.811 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks for Candesartan in NCT03640312 |
   15.812 Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks for QUARTET LDQT in NCT03640312 |
   15.813 Proportion of Patients With Hypertension Control at 6 and 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.814 Quadpill once daily |
   15.815 QUARTET USA Trial Control Group |
   15.816 QUARTET USA Trial Quadpill group |
   15.817 randomized into groups for PARACHUTE Trial |
   15.818 Rate of Adverse Events of Special Interest (NCT03640312) |
   15.819 Rate of Adverse Events of Special Interest at 12 weeks for Candesartan in NCT03640312 |
   15.820 Rate of Adverse Events of Special Interest at 12 weeks for QUARTET LDQT in NCT03640312 |
   15.821 Rate of Adverse Events of Special Interest at 12 weeks Statistical Analysis for QUARTET LDQT vs Candesartan in NCT03640312 |
   15.822 Rate of Death or Major Traumatic Injury on Impact with comparator |
   15.823 Rate of Death or Major Traumatic Injury on Impact with intervention |
   15.824 Reasons for exclusion from QUARTET USA Trial |
   15.825 Recommendation Eligibility Criteria for Bariatric Surgery (ADA Recommendation 8.17) |
   15.826 Recommendation Justification Code System |
   15.827 Recommendation Rating: ADA Obesity Management Recommendation 8.16 |
   15.828 Recommendation: ADA Obesity Management Recommendation 8.16 |
   15.829 Recommendation: ADA Obesity Management Recommendation 8.16-adapted |
   15.830 Recommendation: ADA Obesity Management Recommendation 8.17 |
   15.831 RecommendationEligibilityCriteria: Eligibility Criteria for Bariatric Surgery (ADA Recommendation 8.16) |
   15.832 Remdesivir |
   15.833 Remdesivir IV 200 mg once then 100 mg once daily for 9 days |
   15.834 ResearchStudy Classifier Code System |
   15.835 Results Section for NCT03421379 |
   15.836 Results Section for NCT03640312 |
   15.837 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 |
   15.838 Risk of Bias Assessment of PARACHUTE trial |
   15.839 Risk Of Bias Type Value Set |
   15.840 Screened Group PARACHUTE Trial |
   15.841 Search Strategy for NMA_Diabetes |
   15.842 SearchResults: PubMed search for Wonder Woman |
   15.843 SearchStrategy: PubMed and Embase search for van Veldhuisen 2022 systematic review |
   15.844 SearchStrategy: PubMed search for Wonder Woman |
   15.845 Sex |
   15.846 Sex with comparator |
   15.847 Sex with intervention |
   15.848 SGLT2 inhibitors Group in Adults with type 2 diabetes |
   15.849 SoaPlanDefinition: Follow-up assessment 3 months after study start |
   15.850 SoftwareCitation: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter |
   15.851 Spanish or English Value Set |
   15.852 Standard care Group in Adults with type 2 diabetes with moderate CV risk |
   15.853 StudyCitation: 2022 Systematic Review of bariatric surgery mortality effect 35243488 |
   15.854 StudyEligibilityCriteria for M11Report Example |
   15.855 StudyEligibilityCriteria: Eligibility Criteria for DIBASY Trial |
   15.856 StudyEligibilityCriteria: Obese patients ≥ 18 years old |
   15.857 StudyEligibilityCriteria: Type 2 diabetes and elevated BMI in 2016 meta-analysis |
   15.858 StudyEligibilityCriteria_Eligibility_Criteria_for_Bariatric_Surgery_Randomized_Trial_Diabetes_Surgery_Study |
   15.859 StudyGroup: Diabetes Surgery Study Trial Enrollment Group |
   15.860 StudyGroup: Severely Obese Adults 2018 Norwegian Cohort |
   15.861 StudyGroup_DIBASY_Trial_Enrollment_Group |
   15.862 Summary of Findings - QUARTET USA Trial |
   15.863 SummaryOfFindings: Bariatric Surgery Summary of Findings Example for GIN 2022 |
   15.864 SummaryOfFindings: GLP-1 RA vs. Standard care in Adults with type 2 diabetes with moderate CV risk |
   15.865 SummaryOfFindings: SGLT2 inhibitors vs. GLP-1 RA in Adults with type 2 diabetes |
   15.866 SummaryOfNetEffect: Bariatric Surgery Summary of Net Effect Contributions Example for GIN 2022 |
   15.867 SystematicReviewEligibilityCriteria: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   15.868 SystematicReviewExcludedStudies: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   15.869 SystematicReviewIncludedStudies: ADT and Docetaxel vs. ADT alone for metastatic hormone-naive prostate cancer |
   15.870 Systolic blood pressure at 12 weeks |
   15.871 Time to integration of results in a recommendation |
   15.872 VariableDefinition: Comparator |
   15.873 VariableDefinition: Condition(s) |
   15.874 VariableDefinition: Date of birth |
   15.875 VariableDefinition: Date of measurement |
   15.876 VariableDefinition: Gender |
   15.877 VariableDefinition: NTproBNP |
   15.878 VariableDefinition: Unit |
   15.879 Velocity |
   15.880 Velocity comparing intervention vs. comparator |
   15.881 Velocity for enrolled group |
   15.882 Velocity for non participant group |
   15.883 Velocity with comparator |
   15.884 Velocity with intervention |
   15.885 WebPageCitation: A HEvKA Update Summary |
   15.886 Weight |
   15.887 Weight with comparator |
   15.888 Weight with intervention |