<status value="draft"/> <date value="2022-05-12T15:36:35.009-04:00"/> <publisher value="World Health Organization (WHO)"/> <description value="Clinics should report adverse events (reported and confirmed) to the central authority. This should be tracked as an aggregate tally (which should indicate the severity, and optionally the manifestation such as rash, vomiting, etc.), with severe cases being reported using case reporting forms, and should include an analysis of whether the AEFI was a direct result (confirmed) of vaccination or not (suspected). Serious cases are those which involved hospitalization, disability, or death. Investigation of AEFI events can lead to withdrawal of the vaccine from the market, or inform further guidance on administration of a particular antigen/product."/> <jurisdiction> <coding> <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/> <code value="001"/> </coding> </jurisdiction> <library value="http://fhir.org/guides/who/smart-immunization/Library/IMMZIND30"/> <scoring> <coding> <system value="http://terminology.hl7.org/CodeSystem/measure-scoring"/> <code value="proportion"/> </coding> </scoring> <type> <coding> <system value="http://terminology.hl7.org/CodeSystem/measure-type"/> <code value="process"/> </coding> </type> <improvementNotation> <coding> <system value="http://terminology.hl7.org/CodeSystem/measure-improvement-notation"/> <code value="increase"/> </coding> </improvementNotation> <group id="IMMZIND30"> <population id="numerator"> <code> <coding> <system value="http://terminology.hl7.org/CodeSystem/measure-population"/> <code value="numerator"/> </coding> </code> <description value="Number of persons which have received a vaccine dose, and have reported an adverse event"/> <criteria> <language value="text/cql"/> <expression value="numerator"/> </criteria> </population> <population id="denominator"> <code> <coding> <system value="http://terminology.hl7.org/CodeSystem/measure-population"/> <code value="denominator"/> </coding> </code> <description value="The total number of doses administered to patients of the product."/> <criteria> <language value="text/cql"/> <expression value="denominator"/> </criteria> </population> <stratifier id="vaccine-stratifier"> <criteria> <language value="text/cql"/> <expression value="Vaccine Stratifier"/> </criteria> </stratifier> <stratifier id="product/manufacturer-stratifier"> <criteria> <language value="text/cql"/> <expression value="Product/Manufacturer Stratifier"/> </criteria> </stratifier> <stratifier id="severity-stratifier"> <criteria> <language value="text/cql"/> <expression value="Severity Stratifier"/> </criteria> </stratifier> <stratifier id="geographic-region-stratifier"> <criteria> <language value="text/cql"/> <expression value="Geographic Region Stratifier"/> </criteria> </stratifier> <stratifier id="manifestation-/-event-stratifier"> <criteria> <language value="text/cql"/> <expression value="Manifestation / Event Stratifier"/> </criteria> </stratifier> <stratifier id="-stratifier"> <criteria> <language value="text/cql"/> <expression value="Stratifier"/> </criteria> </stratifier> </group> </Measure>

Generated Narrative: Measure

Resource Measure "IMMZIND30"

Profile: http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-measure-cqfm

url: http://fhir.org/guides/who/smart-immunization/Measure/IMMZIND30

version: 0.1.0

name: IMMZIND30

title: IMMZ.IND.30 Adverse Event Following Immunization (AEFI) case rate.

status: draft

date: 2022-05-12 15:36:35-0400

publisher: World Health Organization (WHO)

description: Clinics should report adverse events (reported and confirmed) to the central authority. This should be tracked as an aggregate tally (which should indicate the severity, and optionally the manifestation such as rash, vomiting, etc.), with severe cases being reported using case reporting forms, and should include an analysis of whether the AEFI was a direct result (confirmed) of vaccination or not (suspected). Serious cases are those which involved hospitalization, disability, or death. Investigation of AEFI events can lead to withdrawal of the vaccine from the market, or inform further guidance on administration of a particular antigen/product.

jurisdiction: Global (Whole world) (m49.htm#001)

library: IMMZIND30

scoring: Proportion (MeasureScoring#proportion)

type: Process (MeasureType#process)

improvementNotation: Increased score indicates improvement (MeasureImprovementNotation#increase)

group
id
IMMZIND30
population
id
numerator
code: Numerator (MeasurePopulationType#numerator)
description: Number of persons which have received a vaccine dose, and have reported an adverse event
Criteria
- Language Expression
* text/cql numerator
population
id
denominator
code: Denominator (MeasurePopulationType#denominator)
description: The total number of doses administered to patients of the product.
Criteria
- Language Expression
* text/cql denominator
stratifier
id
vaccine-stratifier
Criteria
- Language Expression
* text/cql Vaccine Stratifier
stratifier
id
product/manufacturer-stratifier
Criteria
- Language Expression
* text/cql Product/Manufacturer Stratifier
stratifier
id
severity-stratifier
Criteria
- Language Expression
* text/cql Severity Stratifier
stratifier
id
geographic-region-stratifier
Criteria
- Language Expression
* text/cql Geographic Region Stratifier
stratifier
id
manifestation-/-event-stratifier
Criteria
- Language Expression
* text/cql Manifestation / Event Stratifier
stratifier
id
-stratifier
Criteria
- Language Expression
* text/cql Stratifier