@haste-health/hl7.fhir.r4b.test-data 0.1.3

package/examples-json/EnrollmentRequest-22345.json

@@ -0,0 +1,37 @@
+{
+  "resourceType": "EnrollmentRequest",
+  "id": "22345",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003eA human-readable rendering of the EnrollmentRequest.\u003c/div\u003e"
+  },
+  "identifier": [
+    {
+      "system": "http://happyvalley.com/enrollmentrequest",
+      "value": "EN22345"
+    }
+  ],
+  "status": "active",
+  "created": "2014-08-16",
+  "insurer": {
+    "reference": "Organization/2"
+  },
+  "provider": {
+    "reference": "Organization/1"
+  },
+  "candidate": {
+    "reference": "Patient/1"
+  },
+  "coverage": {
+    "reference": "Coverage/9876B1"
+  },
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}

package/examples-json/EnrollmentResponse-ER2500.json

@@ -0,0 +1,36 @@
+{
+  "resourceType": "EnrollmentResponse",
+  "id": "ER2500",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003eA human-readable rendering of the EnrollmentResponse\u003c/div\u003e"
+  },
+  "identifier": [
+    {
+      "system": "http://www.BenefitsInc.com/fhir/enrollmentresponse",
+      "value": "781234"
+    }
+  ],
+  "status": "active",
+  "request": {
+    "reference": "http://www.BenefitsInc.com/fhir/eligibility/225476332402"
+  },
+  "outcome": "complete",
+  "disposition": "Dependant added to policy.",
+  "created": "2014-08-16",
+  "organization": {
+    "reference": "Organization/2"
+  },
+  "requestProvider": {
+    "reference": "Organization/1"
+  },
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}

package/examples-json/EpisodeOfCare-example.json

@@ -0,0 +1,111 @@
+{
+  "resourceType": "EpisodeOfCare",
+  "id": "example",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003e\n      HACC Program for Peter James Chalmers at HL7 Healthcare 15 Sept 2014 - current\u003cbr/\u003e\n\t\t\twas on leave from 22 Sept - 24 Sept while in respite care\n    \u003c/div\u003e"
+  },
+  "identifier": [
+    {
+      "system": "http://example.org/sampleepisodeofcare-identifier",
+      "value": "123"
+    }
+  ],
+  "status": "active",
+  "statusHistory": [
+    {
+      "status": "planned",
+      "period": {
+        "start": "2014-09-01",
+        "end": "2014-09-14"
+      }
+    },
+    {
+      "status": "active",
+      "period": {
+        "start": "2014-09-15",
+        "end": "2014-09-21"
+      }
+    },
+    {
+      "status": "onhold",
+      "period": {
+        "start": "2014-09-22",
+        "end": "2014-09-24"
+      }
+    },
+    {
+      "status": "active",
+      "period": {
+        "start": "2014-09-25"
+      }
+    }
+  ],
+  "type": [
+    {
+      "coding": [
+        {
+          "system": "http://terminology.hl7.org/CodeSystem/episodeofcare-type",
+          "code": "hacc",
+          "display": "Home and Community Care"
+        }
+      ]
+    }
+  ],
+  "diagnosis": [
+    {
+      "condition": {
+        "reference": "Condition/stroke"
+      },
+      "role": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/diagnosis-role",
+            "code": "CC",
+            "display": "Chief complaint"
+          }
+        ]
+      },
+      "rank": 1
+    }
+  ],
+  "patient": {
+    "reference": "Patient/example"
+  },
+  "managingOrganization": {
+    "reference": "Organization/hl7"
+  },
+  "period": {
+    "start": "2014-09-01"
+  },
+  "referralRequest": [
+    {
+      "display": "Referral from Example Aged Care Services"
+    }
+  ],
+  "careManager": {
+    "reference": "Practitioner/14",
+    "display": "Amanda Assigned"
+  },
+  "team": [
+    {
+      "reference": "CareTeam/example",
+      "display": "example care team"
+    }
+  ],
+  "account": [
+    {
+      "reference": "Account/example",
+      "display": "example account"
+    }
+  ],
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}

package/examples-json/EventDefinition-example.json

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+{
+  "resourceType": "EventDefinition",
+  "id": "example",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003e\u003cp\u003e\u003cb\u003eGenerated Narrative\u003c/b\u003e\u003c/p\u003e\u003cdiv style\u003d\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"\u003e\u003cp style\u003d\"margin-bottom: 0px\"\u003eResource \u0026quot;example\u0026quot; \u003c/p\u003e\u003c/div\u003e\u003cp\u003e\u003cb\u003estatus\u003c/b\u003e: draft\u003c/p\u003e\u003cp\u003e\u003cb\u003epurpose\u003c/b\u003e: Monitor all admissions to Emergency\u003c/p\u003e\u003c/div\u003e"
+  },
+  "status": "draft",
+  "experimental": true,
+  "purpose": "Monitor all admissions to Emergency",
+  "trigger": [
+    {
+      "type": "named-event",
+      "name": "monitor-emergency-admissions",
+      "data": [
+        {
+          "type": "Encounter"
+        }
+      ],
+      "condition": {
+        "description": "Encounter Location \u003d emergency (active/completed encounters, current or previous)",
+        "language": "text/fhirpath",
+        "expression": "(this | %previous).location.where(location \u003d \u0027Location/emergency\u0027 and status in {\u0027active\u0027, \u0027completed\u0027}).exists()"
+      }
+    }
+  ],
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}

package/examples-json/Evidence-example-ASTRAL-12-alteplase-mRS3-6.json

@@ -0,0 +1,277 @@
+{
+  "resourceType": "Evidence",
+  "id": "example-ASTRAL-12-alteplase-mRS3-6",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003e\n      \u003cp\u003e\n        \u0026quot;Risk of mRS3-6 at 90 days after Alteplase for Stroke if ASTRAL score 12\u0026quot; is a univariate risk estimate.\n      \u003c/p\u003e\n\t\u003c/div\u003e"
+  },
+  "url": "http://hl7.org/fhir/Evidence/example-ASTRAL-12-alteplase-mRS3-6",
+  "title": "Risk of mRS3-6 at 90 days after Alteplase for Stroke if ASTRAL score 12",
+  "status": "draft",
+  "useContext": [
+    {
+      "code": {
+        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type",
+        "code": "focus"
+      },
+      "valueCodeableConcept": {
+        "text": "Stroke"
+      }
+    }
+  ],
+  "relatedArtifact": [
+    {
+      "type": "citation",
+      "label": "Cooray 2016 Validation Study",
+      "display": "External Validation of the ASTRAL and DRAGON Scores for Prediction of Functional Outcome in Stroke.",
+      "citation": "Cooray C, Mazya M, Bottai M, Dorado L, Skoda O, Toni D, Ford GA, Wahlgren N, Ahmed N. External Validation of the ASTRAL and DRAGON Scores for Prediction of Functional Outcome in Stroke. Stroke. 2016 Jun;47(6):1493-9. Epub 2016 May 12. PMID 27174528",
+      "url": "https://doi.org/10.1161/STROKEAHA.116.012802"
+    }
+  ],
+  "description": "5.3% risk of mRS 3-6 at 90 days",
+  "variableDefinition": [
+    {
+      "variableRole": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/variable-role",
+            "code": "population",
+            "display": "population"
+          }
+        ]
+      },
+      "observed": {
+        "reference": "Group/ASTRAL-Cooray-validation-cohort",
+        "type": "Group",
+        "display": "ASTRAL validation cohort"
+      },
+      "intended": {
+        "reference": "Group/ASTRAL-12",
+        "type": "Group",
+        "display": "patients 0-4.5 hours after acute ischemic stroke onset with ASTRAL score \u003d 12"
+      }
+    },
+    {
+      "description": "functionally dependent or dead at 3 months",
+      "variableRole": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/variable-role",
+            "code": "measuredVariable",
+            "display": "measured variable"
+          }
+        ]
+      },
+      "observed": {
+        "reference": "EvidenceVariable/example-mRS3-6-at-90days",
+        "type": "EvidenceVariable",
+        "display": "mRS 3-6 at 90 days"
+      },
+      "intended": {
+        "reference": "EvidenceVariable/example-dead-or-dependent-90day",
+        "type": "EvidenceVariable",
+        "display": "Dead or functionally dependent at 90 days"
+      },
+      "directnessMatch": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/directness",
+            "code": "high",
+            "display": "High quality match"
+          }
+        ]
+      }
+    },
+    {
+      "variableRole": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/variable-role",
+            "code": "exposure",
+            "display": "exposure"
+          }
+        ]
+      },
+      "observed": {
+        "reference": "EvidenceVariable/example-alteplase-for-stroke",
+        "type": "EvidenceVariable",
+        "display": "Alteplase for Stroke"
+      },
+      "intended": {
+        "reference": "EvidenceVariable/example-alteplase-for-stroke",
+        "type": "EvidenceVariable",
+        "display": "Alteplase for Stroke"
+      },
+      "directnessMatch": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/directness",
+            "code": "exact",
+            "display": "Exact match"
+          }
+        ]
+      }
+    }
+  ],
+  "studyType": {
+    "coding": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/study-type",
+        "code": "series",
+        "display": "uncontrolled cohort or case series"
+      }
+    ]
+  },
+  "statistic": [
+    {
+      "description": "5.3% risk",
+      "statisticType": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/statistic-type",
+            "code": "C44256",
+            "display": "Proportion"
+          }
+        ],
+        "text": "derived proportion"
+      },
+      "quantity": {
+        "value": 0.0525
+      },
+      "sampleSize": {
+        "note": [
+          {
+            "text": "number of participants describes number in the total study sample, known data count describes number in study sample with ASTRALscore \u003d 12, total number of events describes number of participants with ASTRAL score \u003d 12 and outcome of mRS 3-6 at 90 days"
+          }
+        ],
+        "numberOfParticipants": 36131
+      }
+    }
+  ],
+  "certainty": [
+    {
+      "type": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+            "code": "Overall",
+            "display": "Overall quality"
+          }
+        ]
+      },
+      "rating": {
+        "coding": [
+          {
+            "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+            "code": "high",
+            "display": "High quality"
+          }
+        ]
+      },
+      "subcomponent": [
+        {
+          "type": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+                "code": "RiskOfBias",
+                "display": "Risk of bias"
+              }
+            ]
+          },
+          "rating": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+                "code": "no-concern",
+                "display": "no serious concern"
+              }
+            ]
+          }
+        },
+        {
+          "description": "Estimated risk from validation calibration plot consistent with predicted risk; observed risk in subgroup with ASTRAL score \u003d 12 consistent with validation calibration plot",
+          "type": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+                "code": "Inconsistency",
+                "display": "Inconsistency"
+              }
+            ]
+          },
+          "rating": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+                "code": "no-concern",
+                "display": "no serious concern"
+              }
+            ]
+          }
+        },
+        {
+          "type": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+                "code": "Indirectness",
+                "display": "Indirectness"
+              }
+            ]
+          },
+          "rating": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+                "code": "no-concern",
+                "display": "no serious concern"
+              }
+            ]
+          }
+        },
+        {
+          "description": "Narrow confidence interval",
+          "type": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+                "code": "Imprecision",
+                "display": "Imprecision"
+              }
+            ]
+          },
+          "rating": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+                "code": "no-concern",
+                "display": "no serious concern"
+              }
+            ]
+          }
+        },
+        {
+          "type": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-type",
+                "code": "PublicationBias",
+                "display": "Publication bias"
+              }
+            ]
+          },
+          "rating": {
+            "coding": [
+              {
+                "system": "http://terminology.hl7.org/CodeSystem/certainty-rating",
+                "code": "no-concern",
+                "display": "no serious concern"
+              }
+            ]
+          }
+        }
+      ]
+    }
+  ]
+}

package/examples-json/EvidenceReport-example.json

@@ -0,0 +1,25 @@
+{
+  "resourceType": "EvidenceReport",
+  "id": "example",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003e[Put rendering here]\u003c/div\u003e"
+  },
+  "status": "draft",
+  "subject": {
+    "note": [
+      {
+        "text": "This is just an example."
+      }
+    ]
+  },
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}

package/examples-json/EvidenceVariable-example-Stroke-Thrombolysis-Trialists-2014-2016-IPD-MA-Cohort.json

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+{
+  "resourceType": "EvidenceVariable",
+  "id": "example-Stroke-Thrombolysis-Trialists-2014-2016-IPD-MA-Cohort",
+  "text": {
+    "status": "generated",
+    "div": "\u003cdiv xmlns\u003d\"http://www.w3.org/1999/xhtml\"\u003e\n      \u003cp\u003e\n        Stroke Thrombolysis Trialists’ Collaborators Group collection used for individual patient data meta-analysis\n      \u003c/p\u003e\n\t\u003c/div\u003e"
+  },
+  "name": "Stroke Thrombolysis Trialists’ 2014-2016 IPD-MA Cohort",
+  "title": "Stroke Thrombolysis Trialists’ Collaborators Group collection used for individual patient data meta-analysis",
+  "status": "draft",
+  "useContext": [
+    {
+      "code": {
+        "system": "http://terminology.hl7.org/CodeSystem/usage-context-type",
+        "code": "focus"
+      },
+      "valueCodeableConcept": {
+        "text": "Stroke"
+      }
+    }
+  ],
+  "relatedArtifact": [
+    {
+      "type": "citation",
+      "label": "Emberson 2014",
+      "display": "Effect of treatment delay, age, and stroke severity on the effects of intravenous thrombolysis with alteplase for acute ischaemic stroke: a meta-analysis of individual patient data from randomised trials.",
+      "citation": "Emberson J, Lees KR, Lyden P, Blackwell L, Albers G, Bluhmki E, et al;Stroke Thrombolysis Trialists\u0027 Collaborative Group. Effect of treatment delay, age, and stroke severity on the effects of intravenous thrombolysis with alteplase for acute ischaemic stroke: a meta-analysis of individual patient data from randomised trials. Lancet 2014 Nov 29;384(9958):1929-35 PMID 25106063",
+      "url": "https://doi.org/10.1016/S0140-6736(14)60584-5"
+    },
+    {
+      "type": "citation",
+      "label": "Lees 2016",
+      "display": "Figure 2 Lees 2016",
+      "citation": "Lees KR, Emberson J, Blackwell L, Bluhmki E, Davis SM, Donnan GA, et al; Stroke Thrombolysis Trialists’ Collaborators Group. Effects of alteplase for acute stroke on the distribution of functional outcomes: a pooled analysis of 9 trials. Stroke. 2016;47:2373-2379. PMID 27507856",
+      "url": "https://doi.org/10.1161/STROKEAHA.116.013644"
+    }
+  ],
+  "actual": true,
+  "characteristicCombination": "union",
+  "characteristic": [
+    {
+      "definitionReference": {
+        "reference": "Group/ECASSIII-Trial-Cohort",
+        "type": "Group",
+        "display": "ECASS III Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/IST3-Trial-Cohort",
+        "type": "Group",
+        "display": "IST3 Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/ECASS-Trial-Cohort",
+        "type": "Group",
+        "display": "ECASS Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/ECASSII-Trial-Cohort",
+        "type": "Group",
+        "display": "ECASSII Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/EPITHET-Trial-Cohort",
+        "type": "Group",
+        "display": "EPITHET Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/ATLANTIS-Trial-Cohort",
+        "type": "Group",
+        "display": "ATLANTIS Trial Cohort"
+      }
+    },
+    {
+      "definitionReference": {
+        "reference": "Group/NINDS-Trial-Cohort",
+        "type": "Group",
+        "display": "NINDS Trial Cohort"
+      }
+    }
+  ],
+  "meta": {
+    "tag": [
+      {
+        "system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
+        "code": "HTEST",
+        "display": "test health data"
+      }
+    ]
+  }
+}