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FHIR IG analytics

Packagehl7.fhir.uv.ebm
Resource TypeEvidence
IdEvidence-367905.json
FHIR VersionR6

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: Evidence 367905

version: 26; Last updated: 2025-08-18 13:22:42+0000; Language: en

Profile: NonComparativeEvidence

ArtifactPublicationStatus: Active

url: https://fevir.net/resources/Evidence/367905

identifier: FEvIR Object Identifier/367905, FEvIR Linking Identifier/NCT03640312-secondaryOutcomeMeasure-0--OG000

name: NCT03640312_secondaryOutcomeMeasure_0_OG000

title: Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312

citeAs:

Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367905. Revised 2025-08-18. Available at: https://fevir.net/resources/Evidence/367905. Computable resource at: https://fevir.net/resources/Evidence/367905#json.

status: Active

author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:

publisher: Computable Publishing LLC

contact: support@computablepublishing.com

copyright:

https://creativecommons.org/licenses/by-nc-sa/4.0/

description:

This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.

variableDefinition

description:

QUARTET LDQT

note: ,

Outcome Measure Population Description: Modified intent to treat whereby all those participants with data at any follow-up time point and baseline to contribute to analyses will be included in analyses according to arm to which they were randomized, regardless of adherence to the study protocol.

Outcome Measure Denominator Units: Participants

variableRole: Population

observed: Patients randomized to the intervention arm took a once daily ultra-low-dose quadruple combination therapy (QUARTET LDQT). The LDQT is an overencapsulated combination pill comprising four types of blood pressure lowering medications each at ¼ standard doses. QUARTET includes candesartan 2mg, amlodipine besylate 1.25mg, indapamide 0.625mg, and bisoprolol 2.5mg. The individual components are currently approved and marketed within the United States. QUARTET LDQT: Ultra-low-dose combination therapy comprising four different blood pressure lowering drugs at 1/4 dosages. Taken once daily for 12 weeks. (Identifier: ClinicalTrials.gov Outcome Measurement Group Id/OG000)

variableDefinition

variableRole: Outcome

observed: Mean Systolic Blood Pressure at 6 weeks - (NCT03640312)

statistic

statisticType: Least Squares Mean

quantity: 122.37 mm Hg

SampleSizes

-KnownDataCount
*32

AttributeEstimates

-TypeRange
*95% Confidence Interval118.32-126.42 mm Hg

Source1

{
  "resourceType": "Evidence",
  "id": "367905",
  "meta": {
    "versionId": "26",
    "lastUpdated": "2025-08-18T13:22:42.074Z",
    "profile": [
      "http://hl7.org/fhir/uv/ebm/StructureDefinition/non-comparative-evidence"
    ]
  },
  "language": "en",
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/uv/ebm/StructureDefinition/artifact-publication-status",
      "valueCodeableConcept": {
        "coding": [
          {
            "system": "http://terminology.hl7.org/CodeSystem/cited-artifact-status-type",
            "code": "active",
            "display": "Active"
          }
        ]
      }
    }
  ],
  "url": "https://fevir.net/resources/Evidence/367905",
  "identifier": [
    {
      "type": {
        "coding": [
          {
            "system": "http://terminology.hl7.org/CodeSystem/v2-0203",
            "code": "ACSN",
            "display": "Accession ID"
          }
        ],
        "text": "FEvIR Object Identifier"
      },
      "system": "https://fevir.net/FOI",
      "value": "367905",
      "assigner": {
        "display": "Computable Publishing LLC"
      }
    },
    {
      "type": {
        "text": "FEvIR Linking Identifier"
      },
      "system": "https://fevir.net/FLI",
      "value": "NCT03640312-secondaryOutcomeMeasure-0--OG000",
      "assigner": {
        "display": "Computable Publishing LLC"
      }
    }
  ],
  "name": "NCT03640312_secondaryOutcomeMeasure_0_OG000",
  "title": "Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312",
  "citeAs": "Mean Systolic Blood Pressure at 6 weeks for QUARTET LDQT in NCT03640312 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367905. Revised 2025-08-18. Available at: https://fevir.net/resources/Evidence/367905. Computable resource at: https://fevir.net/resources/Evidence/367905#json.",
  "status": "active",
  "author": [
    {
      "name": "Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter"
    }
  ],
  "publisher": "Computable Publishing LLC",
  "contact": [
    {
      "telecom": [
        {
          "system": "email",
          "value": "support@computablepublishing.com"
        }
      ]
    }
  ],
  "copyright": "https://creativecommons.org/licenses/by-nc-sa/4.0/",
  "description": "This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.",
  "variableDefinition": [
    {
      "description": "QUARTET LDQT",
      "note": [
        {
          "text": "Outcome Measure Population Description: Modified intent to treat whereby all those participants with data at any follow-up time point and baseline to contribute to analyses will be included in analyses according to arm to which they were randomized, regardless of adherence to the study protocol."
        },
        {
          "text": "Outcome Measure Denominator Units: Participants"
        }
      ],
      "variableRole": "population",
      "observed": {
        "identifier": {
          "type": {
            "text": "ClinicalTrials.gov Outcome Measurement Group Id"
          },
          "value": "OG000"
        },
        "display": "Patients randomized to the intervention arm took a once daily ultra-low-dose quadruple combination therapy (QUARTET LDQT). The LDQT is an overencapsulated combination pill comprising four types of blood pressure lowering medications each at ¼ standard doses. QUARTET includes candesartan 2mg, amlodipine besylate 1.25mg, indapamide 0.625mg, and bisoprolol 2.5mg. The individual components are currently approved and marketed within the United States.\n\nQUARTET LDQT: Ultra-low-dose combination therapy comprising four different blood pressure lowering drugs at 1/4 dosages. Taken once daily for 12 weeks."
      }
    },
    {
      "variableRole": "outcome",
      "observed": {
        "reference": "EvidenceVariable/367883",
        "type": "EvidenceVariable",
        "identifier": {
          "type": {
            "text": "FEvIR Linking Identifier"
          },
          "system": "https://fevir.net/FLI",
          "value": "NCT03640312-secondaryOutcome-0",
          "assigner": {
            "display": "Computable Publishing LLC"
          }
        },
        "display": "Mean Systolic Blood Pressure at 6 weeks -  (NCT03640312)"
      }
    }
  ],
  "statistic": [
    {
      "statisticType": {
        "text": "Least Squares Mean"
      },
      "quantity": {
        "value": 122.37,
        "unit": "mm Hg"
      },
      "sampleSize": {
        "knownDataCount": 32
      },
      "attributeEstimate": [
        {
          "type": {
            "text": "95% Confidence Interval"
          },
          "range": {
            "low": {
              "value": 118.32,
              "unit": "mm Hg"
            },
            "high": {
              "value": 126.42,
              "unit": "mm Hg"
            }
          }
        }
      ]
    }
  ]
}