This page is part of the Healthcare Associated Infection Implementation Guide (v1.1.0: STU 2 Ballot 1) based on FHIR R3. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
JSON Format: QuestionnaireResponse-hai-questionnaireResponse-los-event
Raw json
{ "resourceType" : "QuestionnaireResponse", "id" : "hai-questionnaireResponse-los-event", "meta" : { "versionId" : "1", "lastUpdated" : "2019-03-05T16:59:54.000-05:00", "profile" : [ "http://hl7.org/fhir/us/hai/StructureDefinition/hai-single-person-report-questionnaire-response" ] }, "text" : { "status" : "generated", "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\" lang=\"en-US\">\n <p>This QuestionnaireResponse instance is an example of a completed Late Onset Sepsis/Meningitis Event (LOS) Report and is in response to the Questionnaire instance defining this report.</p>\n <h2>Example Late Onset Sepsis/Meningitis Event (LOS)</h2>\n <h3>Authoring and Facility Information</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Authoring Device</td>\n <td>Id: 2.16.840.1.113883.3.117.1.1.5.1.1.2:anAuthorID</td>\n </tr>\n <tr>\n <td>Facility ID</td>\n <td>urn:hl7ii:2.16.840.1.113883.3.117.1.1.5.1.1:9W</td>\n </tr>\n <tr>\n <td>Event #</td>\n <td>urn:oid:2.16.840.1.113883.3.117.1.1.5.2.1.1.3:31</td>\n </tr>\n <tr>\n <td>Event Type</td>\n <td>Late onset sepsis (LOS)</td>\n </tr>\n <tr>\n <td>Date of Event</td>\n <td>2018-01-02</td>\n </tr>\n <tr>\n <td>Date Admitted to Facility</td>\n <td>2018-01-01</td>\n </tr>\n <tr>\n <td>Inborn/Outborn</td>\n <td>Inborn</td>\n </tr>\n <tr>\n <td>Location</td>\n <td>Medical/Surgical Critical Care</td>\n </tr>\n </tbody>\n </table>\n <h3>Patient</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Patient ID</td>\n <td>Medical Record Number: 12345</td>\n </tr>\n <tr>\n <td>Social Security #</td>\n <td>12345</td>\n </tr>\n <tr>\n <td>Medicaid #</td>\n <td>959595</td>\n </tr>\n <tr>\n <td>Patient Last Name</td>\n <td>Nuclear</td>\n </tr>\n <tr>\n <td>Patient First Name</td>\n <td>Ned</td>\n </tr>\n <tr>\n <td>Gender</td>\n <td>Male</td>\n </tr>\n <tr>\n <td>Date of Birth</td>\n <td>2018-01-01</td>\n </tr>\n <tr>\n <td>Ethnicity</td>\n <td>Not Hispanic or Latino</td>\n </tr>\n <tr>\n <td>Race</td>\n <td>White</td>\n </tr>\n </tbody>\n </table>\n \n <h3>Risk Factors</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Central line present prior to event, including umbilical catheter</td>\n <td>Yes</td>\n </tr>\n <tr>\n <td>Birth Weight</td>\n <td>700 g</td>\n </tr>\n <tr>\n <td>Gestational Age</td>\n <td>276 d</td>\n </tr>\n </tbody>\n </table>\n <h3>Event Details</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Specific Event</td>\n <td>Neonatal Laboratory Confirmed Bloodstream Infection (NLCBI 2)</td>\n </tr>\n <tr>\n <td>Criteria used</td>\n <td>Recognized pathogen from one or more blood specimens</td>\n </tr>\n <tr>\n <td>Died</td>\n <td>Yes</td>\n </tr>\n <tr>\n <td>LOS Contributed to Death</td>\n <td>No</td>\n </tr>\n <tr>\n <td>Discharge date</td>\n <td>2018-01-12</td>\n </tr>\n </tbody>\n </table>\n <h3>Findings</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Microorganism identified</td>\n <td>Clostridium symbiosum (organism)</td>\n </tr>\n <tr>\n <td>Pathogen Ranking</td>\n <td>First</td>\n </tr>\n <tr>\n <td>Clarithro Susc Islt</td>\n <td>Resistant</td>\n </tr>\n </tbody>\n </table>\n <h3>Comment</h3>\n <table border=\"1\">\n <tbody>\n <tr>\n <td>Comment</td>\n <td>NHSN text comment that is less than 2000 characters.</td>\n </tr>\n </tbody>\n </table>\n </div>" }, "identifier" : { "system" : "urn:oid:2.16.840.1.113883.3.117.1.1.5.2.1.1.2", "value" : "20202201" }, "questionnaire" : { "reference" : "http://hl7.org/fhir/us/hai/Questionnaire/hai-questionnaire-los-event" }, "status" : "completed", "subject" : { "reference" : "Patient/hai-patient-1", "display" : "hai-patient-1" }, "author" : { "reference" : "Device/hai-authoring-device", "display" : "hai-authoring-device" }, "item" : [ { "linkId" : "facility", "text" : "Facility ID", "answer" : [ { "valueUri" : "urn:hl7ii:2.16.840.1.113883.3.117.1.1.5.1.1:9W" } ] }, { "linkId" : "event-number", "text" : "Event #", "answer" : [ { "valueUri" : "urn:hl7ii:2.16.840.1.113883.3.117.1.1.5.2.1.1.3:31" } ] }, { "linkId" : "event-type", "text" : "Event Type", "answer" : [ { "valueCoding" : { "system" : "http://snomed.info/sct", "code" : "765107002", "display" : "Late-onset neonatal sepsis (disorder)" } } ] }, { "linkId" : "date-of-event", "text" : "Date of Event", "answer" : [ { "valueDate" : "2018-01-02" } ] }, { "linkId" : "facility-location", "text" : "Facility Location", "answer" : [ { "valueCoding" : { "system" : "http://hl7.org/fhir/us/hai/CodeSystem/2.16.840.1.113883.6.259", "code" : "1029-8", "display" : "Medical/Surgical Critical Care" } } ] }, { "linkId" : "date-admitted-to-facility", "text" : "Date Admitted to Facility:", "answer" : [ { "valueDate" : "2018-01-01" } ] }, { "linkId" : "inborn-outborn-observation", "text" : "Inborn/Outborn: If the infant was outborn (born at a location other than the reporting hospital), select true. If the infant was inborn (born at the reporting hospital) select false.", "answer" : [ { "valueBoolean" : false } ] }, { "linkId" : "risk-factors", "text" : "Risk Factors: Contains central line present, birth weight, gestational age", "item" : [ { "linkId" : "risk-factor-central-line", "text" : "Risk Factor: Central line present prior to event, including umbilical catheter", "answer" : [ { "valueBoolean" : true } ] }, { "linkId" : "risk-factor-birth-weight", "text" : "Risk Factor: Birth weight (grams)", "answer" : [ { "valueQuantity" : { "value" : 700, "unit" : "g" } } ] }, { "linkId" : "risk-factor-gestational-age", "text" : "Risk Factor: Gestational age (days)", "answer" : [ { "valueQuantity" : { "value" : 276, "unit" : "d" } } ] } ] }, { "linkId" : "event-details", "text" : "Event Details", "item" : [ { "linkId" : "infection-condition", "text" : "Specific Event", "answer" : [ { "valueCoding" : { "system" : "http://hl7.org/fhir/us/hai/CodeSystem/2.16.840.1.113883.6.277", "code" : "3067-6", "display" : "Neonatal Laboratory Confirmed Bloodstream Infection (NLCBI 2)" } } ] }, { "linkId" : "criteria-used", "text" : "Laboratory Criteria Used", "answer" : [ { "valueCoding" : { "system" : "http://hl7.org/fhir/us/hai/CodeSystem/2.16.840.1.113883.6.277", "code" : "1951-3", "display" : "Recognized pathogen from one or more blood cultures" } } ] }, { "linkId" : "died", "text" : "Died", "answer" : [ { "valueBoolean" : false } ] }, { "linkId" : "discharge-date", "text" : "Discharge Date", "answer" : [ { "valueDate" : "2018-01-12" } ] } ] }, { "linkId" : "findings-group", "text" : "Findings Group: Records whether infection organisms were identified and, if so, records details about them.", "item" : [ { "linkId" : "pathogen-identified", "text" : "Pathogen Identified", "answer" : [ { "valueCoding" : { "system" : "http://snomed.info/sct", "code" : "48321006", "display" : "Clostridium symbiosum (organism)" } } ] }, { "linkId" : "pathogen-ranking", "text" : "Pathogen Ranking", "answer" : [ { "valueCoding" : { "system" : "http://snomed.info/sct", "code" : "255216001", "display" : "First" } } ] }, { "linkId" : "drug-susceptibility-test-group", "text" : "Drug Susceptibility Test Group", "item" : [ { "linkId" : "drug-susceptibility-test", "text" : "Drug Susceptibility Test", "answer" : [ { "valueCoding" : { "system" : "http://loinc.org", "code" : "18907-6", "display" : "Clarithro Susc Islt" } } ] }, { "linkId" : "drug-susceptibility-test-interpretation", "text" : "Drug Susceptibility Test Interpretation", "answer" : [ { "valueCoding" : { "system" : "http://hl7.org/fhir/v3/ObservationInterpretation", "code" : "R", "display" : "Resistant" } } ] } ] } ] }, { "linkId" : "nhsn-comment", "text" : "Comments", "answer" : [ { "valueString" : "NHSN text comment that is less than 2000 characters." } ] } ] }