Connectathon 11 Snapshot

This page is part of the FHIR Specification (v1.2.0: STU 3 Draft). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R4 R3 R2

Specimen-example-urine.xml

Raw XML (canonical form)

VMA, Random Urine Sample (id = "vma-urine")

<Specimen xmlns="http://hl7.org/fhir">
  <id value="vma-urine"/>
  <!--   text>
    <status value="generated" />
    <div xmlns="http://www.w3.org/1999/xhtml">[Put rendering here]</div>
  </text>   -->
  <!--   
   Type is a loosely defined field because there is such a lot of variation in how it
   is used.
   The principal variation is how much information that could be represented elsewhere
   is also 
   represented here. For instance, here's some possible types:
     lithium heparin plasma   (+ .container.additive) (e.g. SNOMED CT 446272009)
     transfusion bag of blood (+ container.type) 
     Peritoneal lavage        (+ collection.bodySite)
   If the type includes other fields, it would be normal not to populate the other fields

   Note that this practice is so widespread that it's pointless to try and stop it    -->
  <text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: vma-urine</p><p><b>status</b>: available</p><p><b>type</b>: Urine, Random <span>(Details : {http://hl7.org/fhir/v2/0487 code 'RANDU' = 'Urine, Random', given as 'Urine,
           Random'})</span></p><p><b>subject</b>: <a>Patient/example</a></p><p><b>accessionIdentifier</b>: X352356</p><p><b>receivedTime</b>: 18/08/2015 5:03:00 PM</p><h3>Collections</h3><table><tr><td>-</td><td><b>Collector</b></td><td><b>Collected[x]</b></td></tr><tr><td>*</td><td><a>Practitioner/f202</a></td><td>18/08/2015 5:03:00 PM</td></tr></table><h3>Treatments</h3><table><tr><td>-</td><td><b>Description</b></td><td><b>Procedure</b></td></tr><tr><td>*</td><td>Acidify to pH &lt; 3.0 with 6 N HCl.</td><td>Acidification <span>(Details : {http://hl7.org/fhir/v2/0373 code 'ACID' = 'Acidification)</span></td></tr></table><h3>Containers</h3><table><tr><td>-</td><td><b>Type</b></td><td><b>Capacity</b></td><td><b>SpecimenQuantity</b></td></tr><tr><td>*</td><td>Non-sterile specimen container <span>(Details )</span></td><td>50 mls</td><td>10 mls</td></tr></table></div></text><status value="available"/>
  <type>
    <coding>
      <system value="http://hl7.org/fhir/v2/0487"/>
      <code value="RANDU"/>
      <display value="Urine, Random"/>
    </coding>
  </type>
  <subject>
    <reference value="Patient/example"/>
  </subject>
  <!--    accession identifier - e.g. assigned by the labaratory when it is received.
     This is common, unlike specimen identifier    -->
  <accessionIdentifier>
    <system value="http://lab.acme.org/specimens/2015"/>
    <value value="X352356"/>
  </accessionIdentifier>
  <receivedTime value="2015-08-18T07:03:00Z"/>
  <collection>
    <collector>
      <!--    in practice, collecter is almost always recorded    -->
      <reference value="Practitioner/f202"/>
    </collector>
    <!--    the time of collection is usually required. Usually a point in time, but can be a period
     
      (collectedPeriod) if it's a timed collection (e.g. a 24 hour urine)    -->
    <collectedDateTime value="2015-08-18T07:03:00Z"/>
    <!--    method is usually implied by type    -->
  </collection>
  <treatment>
    <description value="Acidify to pH &lt; 3.0 with 6 N HCl."/>
    <procedure>
      <coding>
        <system value="http://hl7.org/fhir/v2/0373"/>
        <code value="ACID"/>
      </coding>
    </procedure>
  </treatment>
  <container>
    <type>
      <text value="Non-sterile specimen container"/>
    </type>
    <capacity>
      <value value="50"/>
      <unit value="mls"/>
    </capacity>
    <specimenQuantity>
      <value value="10"/>
      <unit value="mls"/>
    </specimenQuantity>
  </container>
</Specimen>

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.