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EpiPulseCases
Reportingprotocolforintegratedrespiratoryvirussurveillance-Version1.2
June2026
REPORTINGPROTOCOL
EpiPulseCases:ReportingProtocolforintegratedrespiratoryvirussurveillance
1
Contents
Introduction 2
Howtousethisdocument 2
Findingfurtherinformation 2
Copyright 2
ReportingtoEpiPulseCases 3
Checkingthedatacollectionschedule 3
Preparingdata 3
Usinglatestmetadata 3
CheckingyourSurveillanceSystemDescriptors 4
Uploadingyourdata 4
Finalisingyoursubmission 5
EpiPulseCasesHelpdesk 6
Annex1.Overviewofreporting 7
Subjectcodes 7
Casedefinitions 7
Deadlineforreporting 7
Datasharing 7
Annex2.Reportingquantitativedata 8
SurveillanceType 8
SYND 8
PATH 8
Denominatorsforsyndromicdata 9
Testingdenominators 9
Agegroups 10
Co-infections 10
Case-baseddata 10
Aggregatedata 10
UNKvsmissing 11
Zerovsmissing 11
EHRdiagnosticcodes 11
Annex3.Reportingqualitativeindicators 12
Integratedreportingofinfluenza,SARS-CoV-2andRSV 12
Transmissibilityforinfluenza 13
Morbidityandmortalityforinfluenza 13
Otherreportingconsiderations 13
Annex4.Reportingthresholds 14
Annex5.Metadata 15
RESPICLINPC 15
RESPIAGGR 15
RESPICLINSC 16
RESPISEVERE 22
RESPICASE 26
RESPIQUAL 33
2
Introduction
Thisreportingprotocoldescribesdatacollectionin
EpiPulseCases
forrespiratoryvirussurveillance(including
influenza-likeillness(ILI),acuterespiratoryinfection(ARI),severeacuterespiratoryinfection(SARI),Influenza,SARS-CoV-2andRSV)intheEuropeanUnion/EuropeanEconomicArea(EU/EEA)andWorldHealthOrganizationEuropeanRegion.FromJune2026,allrespiratoryvirussurveillancedataarereportedtoEpiPulseCases,withtheexceptionofviruscharacterisationdatawhichcanstillbereportedviatheTESSyrecordtypesINFLANTIVIRand,optionally,
NCOVVARIANT(see
relatedreportingprotocol
).
Reportingprotocolsaredatacollectionguidelinesforthedatamanagersofreportingcountries,andtheprotocoldesignisintendedtoimproveuser-friendlinessby:
•introducingauniformstructuretomakeiteasierfordatamanagerstofinddatacollectioninformationacrossdifferentsubjects;
•removinginformationwhichisnotrelevantfordatamanagers.
Sincethedatamanagersinreportingcountriesoftenhavemultipleroles,subject-specificmaterialisdistributedinthemultipleannexestogetherwiththereportingprotocol.
Howtousethisdocument
Thisreportingprotocolprovidesinformationforthedatamanagersofreportingcountriesinthreemainsections:
•ReportingtoEpiPulseCaseswhichcontainsguidelinesonhowtopreparedataforsubmissiontoEpiPulseCasesandlinkstofurtherinformation.
•Annex1providesanintroductionandoverviewofthesubjectcodesusedforreporting.
•Annex2outlinesconsiderationsforsubmittingquantitativedata.
•Annex3outlinesconsiderationsforsubmittingqualitativeindicators(RESPIQUAL)
•Annex4outlinesconsiderationsforsubmittingthresholds.
•Annex5providesalistofallvariables.Pleasenotethatthisisautomaticallygeneratedandidenticaltothemetadataintheexcelfile.
Findingfurtherinformation
Updatedlinkstoalltheschedules,documentationandtrainingmaterialsmentionedinthisreportingprotocolareincludedinthe
EpiPulseHelp
,including:
•EpiPulseCasesMetadata
•EpiPulseCasesMachinetoMachineTechnicalDocumentation
Copyright
©EuropeanCentreforDiseasePreventionandControl,2026.Reproductionisauthorised,providedthesourceisacknowledged.
3
ReportingtoEpiPulseCases
EpiPulseCaseswasbuiltasareplacementforTESSy,withtheaimofimprovingtheprocessofreporting,reviewing,
andupdatingsurveillancedata.ThissectionprovidesbothanoverviewoftheEpiPulseCasesreportingprocessandtipsonwhereyoucanfindusefulinformation.
Theoverallprocessisasfollows:
•Familiariseyourselfwiththedatacollectiondeadlines.
•Prepare(exportandtransform)yourdata.
•CheckthatyourdatacomplieswiththeEpiPulseCasesmetadata–see
EpiPulseHelp
.
•Checkthatyourdatasourcesareuptodate.
•Submityourfile(s)toEpiPulseCases.
•Finaliseandapproveyoursubmission.
Checkingthedatacollectionschedule
Alinktothecurrentdatacollectionsschedulecanbefoundthe
EpiPulseHelp
section.
Preparingdata
Afteryouhaveexportedthedatafromyournationaldatabase,youneedtoensurethatthedataareinaformatthatEpiPulseCasescanaccept.EpiPulseCasesacceptsonlyCSVandXMLfiles,optionallyZIP-compressed.TheEpiPulseCasesmetadatahasbeendevelopedfromtheTESSyMetadata,withtheaimtomakeonlytheminimalnumberofchangesnecessary,andtohopefullyprovideabetterexperiencewhenreportingyourdatasetstoECDC.
AfileconvertertoolisalsoavailableinEpiPulseCasestosupportusersinthetransitionperiodwiththeconversionoffilesinTESSyformattoaformatthatwouldbecompatibletoEpiPulseCases,seeSection18intheEpiPulseCasesGuide–see
EpiPulseHelp
.
SpecificguidelinesfordatacollectionandpreparationforEpiPulseCasesareprovidedintheannexes.
Usinglatestmetadata
ThemetadatadefinesthefieldsanddataformatsthatarevalidasinputtoEpiPulseCasesforagivensubject.TheEpiPulseCasesmetadataincludesasectionthatcomparesandhighlightsthechangesbetweenTESSyandEpiPulseCases,tofacilitatethetransition.
AstherequirementsfordatatobesharedamongECDCstakeholderscanchange,thedataformatchangesneededtosupportthenewrequirementsareidentifiedandagreeduponbetweentheNationalSurveillanceContactPoints,theNetworkCoordinationGroupsandECDC’sdiseaseexperts.ThesechangesarethenimplementedtotheEpiPulseCasesmetadata.
ThemetadataforthesubjectofthisreportingprotocolaredescribedinAnnex2.
Itisespeciallyimportanttofocuson:
•Fieldformats
Manyfieldsrequirethedatatobeformattedinaspecificway.Forexample,datesmustbeintheYYYY-MM-DDformat;datesintheDD/MM/YYYYformatwillberejected.
•ReferenceValues(theequivalentofTESSyCodedValues)
Somefieldsonlypermittheuseofspecificvalues(referencevalues).Forexample,M,ForOTHarethecodedvaluesfor‘Sex’andanyothervalueina‘Sex’fieldwillberejected.PleasenotethatUNKisnolongeravalidcode,youmayleavethefieldemptyinstead.
TheEpiPulseCasesmetadataExcelfilecontainsallthedefinitionsandrulesnecessarytoformatdatacorrectly.TheREADMEsheetoftheExceldocumentexplainshowtoworkwiththemetadata.Itcanbedownloadedfromthe
EpiPulseHelp
.
Filteringthefieldsinthefilebysubjectwillenableyoutoseethefieldsrequiredforyoursubjectandtherulesthatapplytothesefields.
EpiPulseCases:ReportingProtocolforintegratedrespiratoryvirussurveillance
4
Checkingyoursurveillancesystemdescriptors
Beforesubmittingfile(s),pleasereviewyourdatasource(s)inEpiPulse(inthemenu,goto‘Report’->
‘Surveillance
systemsdescriptors’
)andupdatetheinformationasnecessary.
Completeandup-to-datedatasourceinformationforeachsubjectisimportantforimprovingtheinterpretationofdata–eachsurveillancesystemhasdifferentfeaturesthatneedtobeconsideredwhencomparingdataatEuropeanlevel.Ifyourdatasourceinformationisout-of-dateandyoudonothaveaccessrightstoupdateit,pleaseaskyourNationalFocalPointforSurveillanceorNationalCoordinatortodoso.
InformationondatasourcesisavailableintheEpiPulseCasesGuide–see
EpiPulseHelp
.
Uploadingyourdata
Dataissubmittedthroughthe
EpiPulsewebinterface
(inthemenu,gotoCases->EpiPulseCases).
ThevisualinterfaceforreportingnewdataandeditingexistingrecordshasremainedverysimilartothatofTESSy.SimilartoTESSy,youcanAdd/UpdateorReplacedatawithnewuploads,usingeitherCSVorXMLfiles.Youcanalsomanuallycreaterecordsforsomediseases,andreportzerocaseswhereappropriate.
Thefunctionalityformanuallyeditingexistingrecordsisalsoafamiliarexperience.Searchfortherecordyouwishtoeditandmodifytheexistinginformationasneeded.
EpiPulseCases:ReportingProtocolforintegratedrespiratoryvirussurveillance
5
Finalisingyoursubmission
Thecomplianceofyourdatawiththevalidationrulesinthemetadataischeckedautomaticallyduringthedatauploadprocess.InEpiPulseCasesthisprocessiscalled“TechnicalValidation”,anditistheonlystepwhereyouruploadcanberejectedbythesystem,forseveredataqualityissues,suchasthefileformatnotbeingreadablebythesystem,or(oneofthefew)technicallyrequiredvariableshavingmissingvalues.
Ifyourfilehasbeenrejected,therewillbeamessageexplainingeachinstanceofnon-compliancewiththemetadatathatneedscorrecting.
ThesignificantnewfeatureinEpiPulseCasesistheDataValidationReport,whichputsyourdatainthecontextofthealreadyexistinginformationforthesamedisease.Itprovidesyouadetailedoverviewofthenewdatainthefileyouhavejustuploaded,aswellasanoverallepidemiologicalsituationshowedwiththeexisting(past)datatogetherwiththenewlyuploadedfile(s).Thismeansmuchmoretimelyfeedbackonyouruploads,includingdetailsondataquality,aswellasoutputs(graphs,charts,andtables)onsomeofepidemiologicalindicators.TheDataValidationreportswillevolveandgrowbasedonyourfeedbackincollaborationwithourDiseaseExperts.ThesereportswillprovideanewandbetterwayofunderstandingandupdatingtheinformationcollectedatEuropeanlevelandwillhopefullyincreasethequalityandtimelinessofthedata,whilereducingworkloads.
BelowyoucanfindafewscreenshotsoftheDataValidationReport.
1.Beginbyopeningthereport:
2.Viewthereportinawindow,downloadthelistofeventualvalidationmessages,ordownloadthereport
6
3.Thedownloadedreportcanbeopenedfullscreenforeasierviewingandnavigation.
4.AfterreviewingtheinformationintheDataValidationReportyoucanchoosetoapproveorrejectit.YoucandownloadtheDataValidationReportfileandemailittoanyonewhoneedstocheckitbeforeapproval.
Ifyouchoosetorejectit,nodatawillbesavedintheEpiPulseCasessystem,butyourfilewillremainvisibleshouldyouwishtore-downloaditorresubmititforanewdatavalidationatalaterdateorafterfurtherchecks.Pleasecheckthe
DataValidationReportcarefully,theremightbewarningsandremarksrelatingtopossibledataqualityissuesorpotentialoverwritingofexistingrecordsthatyoushouldconsider.
Whenyourfilehasbeenvalidatedandyouaresatisfiedthatallcorrectionshavebeenmade,pleaseensurepromptapprovalorrejection.Unapproveduploadswillblocktheapprovalofotherrelateduploadsforthesamedisease.
EpiPulseCasesHelpdesk
Email:
EpiPulseCases@ecdc.europa.eu
Telephonenumber:+46-(0)8-58601601
Availability:9:00–16:00Stockholmtime,MondaytoFriday(exceptECDCholidays).
7
Annex1.Overviewofreporting
Dataforroutinerespiratorysurveillanceiscollectedinsevenintegratedsubjectcodes.Theseareoutlinedbelowtogetherwithinformationoncasedefinitions,reportingdeadlineanddatasharing.
Subjectcodes
ThefollowingsubjectcodesexistinEpiPulseCases:
1.RESPICLINPCforreportingweeklyage-disaggregatedprimarycaresyndromicdata(ILI/ARI).
2.RESPIAGGRforreportingofage-disaggregatedcountsofdetectionsandtestsfromILI/ARIsurveillanceandpathogen-specificlaboratory-basedsurveillancesystem.
3.RESPICLINSCforreportingweeklyage-disaggregatedsecondarycaresyndromicdata(SARI).Thissubjectcodecanalsobeusedforreportingweeklydenominatordataforcountriesreportingcase-basedSARIdatatoRESPICASE.
4.RESPISEVEREforreportingage-disaggregatedcountsofdetectionsandtestsfromSARIsurveillanceand
countsfrompathogen-specificlaboratory-basedsurveillanceofhospitaladmission,ICUadmissionsanddeathsduetorespiratoryillness.
5.RESPICASEforreportingcase-baseddataforseverecasescapturingbothsyndromicandvirologicaldataforasinglecase.BothSARIcasesandseverecasescapturedthroughpathogen-specificlaboratory-basedsurveillancecanbereportedtothissubjectcode.
6.RESPIQUALforreportingweeklyqualitativeindicators
7.RESPITHRESHOLDforreportingthresholddatacollectedforILI,ARIandSARI
Allsubjectcodesallowintegratedreportingofsyndrome(ILI,ARIorSARI)and/orlab-confirmedinfectionsbypathogen(s).
Furtherconsiderationsforreportingquantitativeandqualitativedataaredescribedinannex2and3respectively.
Instructionsforreportingthresholddatawillbeprovidedatalaterstageinannex4.Includedvariablesforeachsubjectcodesareoutlinedbelowintheannex5.
PleasenotethatINFLANTIVIRandNCOVVARIANTrecordtypeswillcontinuetobecollectedinTESSyuntilfurther
notice.Aseparatereportingprotocolwillremainavailable.Case-baseddataonhumaninfectionswithzoonoticinfluenzavirusesshouldbereportedtothesubjectcodeINFLZOOinEpiPulseCases.Aseparatereportingprotocolisavailable.
Casedefinitions
CasesshouldbereportedaccordingtothecurrentEUcasedefinition.Dataonprobableandpossiblecasesarenotcollected.
Deadlineforreporting
Wednesday23:59CETforallsubjectcodesexceptforRESPITHRESHOLD.
RESPITHRESHOLDsubmissiondeadlinewillbecommunicatedseparatelyviaemail.Annualupdatesareexpected.
DatathathavenotbeenuploadedandapprovedinEpiPulseCasesontimewillnotbeincludedinweeklyreports.Ifyouareunabletomeetthisdeadline,pleasecontacttheECDCRespiratoryVirusessurveillanceteam
(ecdc.influenza@ecdc.europa.eu).
Datasharing
PleaserefertotheECDC’spolicyondatagovernancetobepublishedontheECDCwebsiteforinformationondata
protectiongovernanceforEpiPulseincludingdatasharing:
DataprotectiongovernanceforEpipulse-final.pdf
.AlldatacollectedaresharedwiththeWorldHealthOrganisation–RegionalOfficeforEurope(WHO/Europe)onaweeklybasisandthereforeduplicatereportingtoWHOHQisthereforenotrequired.
8
Annex2.Reportingquantitativedata
Thisannexoutlinesconsiderationsforsubmittingdatatothefollowingsubjectcodes:RESPICLINPC,RESPIAGGR,
RESPICLINSC,RESPISEVEREorRESPICASEandisorganisedpertopic.Pleasenotethatthisisalivingdocumenttowhichadditionalconsiderationswillbeaddedovertime.ECDCisactivelyworkingtoexpandthissectionwithinthenextyear.
SurveillanceType
TheSurvTypevariable,withvaluesSYNDandPATH,isusedtodividesurveillancesystemsintotwobroadtypes,describedbelow.ExamplesareprovidedinTable1.
SYND
Insystemswheresurveillancetype=SYND,casesareidentifiedusingasyndromiccasedefinitionsuchasILI,ARI,
SARI,includingwheredataderivedfromelectronichealthrecords(EHR)areusedtotrytoreplicatethetraditionalcasedefinition.
WhenreportingaggregatedatatoEpiPulseCases,thesyndromiccomponentshouldbereportedtoRESPICLINPC(ILI/ARI)orRESPICLINSC(SARI)andvirologicaldatareportedtoRESPIAGGR(ILI/ARI),orRESPISEVERE(SARI).Alternatively,case-basedsyndromicandvirologicalSARIdatacanbereportedtoRESPICASE.
Thesedatawerepreviouslyreportedas‘sentinel’(STL)inTESSy.
PATH
Insystemswheresurveillancetype=PATH,caseidentificationoccursonthebasisofapositivetestforapathogen(influenza,RSV,SARS-CoV-2),orEHR-baseddiagnosticcodesthatreflectpathogen-specificdiagnoses.
Whenitisclearlyknownthatalaboratory-confirmeddetectionofinfluenza,RSVorSARS-CoV-2originatesfromapatientadmittedtohospital/ICUorwhohasdied,thesedatashouldbereportedtoRESPISEVERE(aggregate)orRESPICASE(case-based).
Wherepatientsaretestedoutsideofhospitalsettings,wherethesettingfortestingisnotknownorifthedataincludeamixofhospitalandnon-hospitalsettings,onlyaggregatedatashouldbereported,usingRESPIAGGR.
Thesedatawerepreviouslyreportedas‘non-sentinel’(NONSTL)inTESSy.
9
Table1.Examplesofdifferentsurveillancesystemswithineachofthesurveillancetypesandthelinkedreportingofsyndromicandvirologicaldata
Carelevel
Surveillancetype
Examplesofsystems
Datatype
Syndromicdata
Virologicaldata
Primarycare
SYND
a.SentinelILI/ARIsurveillancenetworkofGPpractices
fromwhichasubsetofcasesistested.
b.EHR-basedARI/ILI
surveillancecoveringmostGPpracticesinthecountrypairedwithasentinelGPnetwork
thattestsARI/ILIcases
Aggregate
RESPICLINPC
RESPIAGGR
Primarycareor
unknown
PATH
a.Laboratory-based
surveillanceofallSARS-CoV-
2,influenza,RSVdetectionsand(tests)
Aggregate
NA
RESPIAGGR
Secondarycare
SYND
a.Questionnaire-basedSARIsystem
b.SARIsystemthatappliesanEHR-basedcasedefinition
forSARIusingICDcodes.
Case-
based
RESPICASE
(numerator)
and
RESPICLINSC
(denominator)
RESPICASE
Aggregate
RESPICLINSC
RESPISEVERE
Secondarycare
PATH
a.Hospitallaboratory
surveillanceofSARS-CoV-2positives.
b.ICUsurveillanceofallpatientspositiveforinfluenza,RSVorSARS-CoV-2
c.EHR-baseddataindicatingdetectionofaspecific
pathogenforpatientsnotincludedwithinaSARIcasedefinition.
Case-
based
NA
RESPICASE
Aggregate
NA
RESPISEVERE
Mortality
PATH
a.Deathsoccurringamong
patientswhorecentlytestedpositiveforinfluenza,RSVorSARS-CoV-2andwhoare
notcapturedthroughSARIsurveillance
b.Cause-specificdeathregistrydata.
Aggregate
NA
RESPISEVERE
Denominatorsforsyndromicdata
Insystemswheresurveillancetype=SYND,twodifferentdenominatorscanbereported.
ForprimarycareILI/ARI-basedsystems(RESPICLINPC),all-causeconsultationsarereportedusingIndicator=DENOMCONSULTandthecatchmentpopulationisreportedusingIndicator=DENOMPOP.
ForsecondarycareSARIsystems(RESPICLINSC),all-causeadmissionsarereportedusingIndicator=DENOMADMITandthecatchmentpopulationisreportedusingIndicator=DENOMPOP.
Oneorbothdenominatorscanbereporteddependingondataavailabilityandsystemdesign.Wherepossible,catchmentpopulationsarepreferablesincetheyallowincidenceofILI/ARI/SARItobeestimated.
Insystemswheresurveillancetype=PATH,theabovedenominatorscannotbereported.
Testingdenominators
TestingdenominatorscanbereportedirrespectiveofSurvType.Theycanbeusedtocalculatetestpositivity.For
ERVISS,ininstanceswherecountriesreportmoredetectionsthantests,dataforthatweekareexcluded,testpositivityisnotcalculated,andcountrydataareexcludedfromaggregations.
10
Incase-baseddata(RESPICASE),thevariablesTestRSV,TestInfluenzaandTestSARSCOV2areusedtoreport
individualswhoaretested.Thisallowsforreportingofpatientswhoaretested,irrespectiveoftheresult.Wheretest-negativepatientsarereportedaswellaspatientswithapositivedetection,thesumoftestsreportedperpathogenisthetestingdenominatortouseforcalculatingtestpositivity.
Inaggregatesubjectcodes(RESPISEVERE,RESPIAGGR),thetestingdenominator(totalnumberoftestsperformedperpathogen)isreporteddirectly.InRESPIAGGRusingIndicator=TESTS.InRESPISEVEREusingIndicator=
HOSAD_TESTS(hospitaladmissions)orIndicator=ICU_TESTS(amongICUadmissions).Onetestingdenominatorshouldbereported(whereavailable)foreachcountry-week-pathogen-indicatorcombination.EvenifusingmultiplexPCR,separaterowsfortestsforRSV,influenzaandSARS-CoV-2shouldbereported.ThereportingofRSVTypeorInfluenzaTypeSubtypeisnotvalidwhenIndicator=TESTS.
Agegroups
WithinRESPICLINSC,RESPIAGGR,andRESPISERVE,countriesmayreportdatausingtwoalternativesetsofagegroups.
Wherepossible,pleasereportthenarrowagegroups:00–04,05–14,15–29,30–64,65–79,and80+years.Countriesthatareunabletoreportthesecanusethebroaderagegroups:00–04,05–14,15–64,and65+years.Countriesthatcannotreportanyage-disaggregateddatamayreportalldataunderAgeUnk.Thetotalacrossallagegroups,includingAgeUnk,isusedtocalculateoveralltotalsfordisplaysinERVISS.
Pleaseensurethatthesameagegroupstructureisappliedconsistentlytonumeratoranddenominatordata.
Co-infections
Co-infectionsarereporteddifferentlyforcase-based(RESPICASE)andaggregate(RESPIAGGR,RESPISEVERE)subjectcodes.
Case-baseddata
Co-infectionsinvolvingmorethanoneofinfluenza,RSVandSARS-CoV-2,e.g.RSVandInfluenza,shouldbereportedusingTestRSV=1,TestInfluenza=1,DetectionRSV=1,DetectionInfluenza=1.
Co-infectionswithtwotypesorsubtypesofthesamepathogenmakesuseofInfluenzaTypeSubtypeandRSVTypebeingrepeatableinRESPICASE.e.g.,InfluenzaA(H1N1)pdm09andinfluenzaB/Vic,wouldbereportedusing
TestInfluenza=1,DetectionInfluenza=1,InfluenzaTypeSubtype=AH1N1pdm09,InfluenzaTypeSubtype=BVic.
Co-infectionsbetweeninfluenza,RSV,SARS-CoV-2andotherrespiratorypathogenscanbereportedusingtherelevantTestandDetectionvariablesforthepathogen,togetherwithPathogenOthertoreportthedetectionoftheother
respiratorypathogen.PathogenOtherisrepeatableforRESPICASE,soco-infectionsinvolvingtwootherrespiratorypathogenscanbereportedinasimilarway.
Aggregatedata
Co-infectionsarereportedacrossmultiplerows,e.g.apatientaged66yearsco-infectedwithRSV-AandInfluenzaA(H1N1)pdm09shouldbereportedtoRESPIAGGRas:
•Pathogen=RSV,Indicator=DETECTIONS,RSVType=RSV_A,Age65_79=1
•Pathogen=RSV,Indicator=TESTS,Age65_79=1
•Pathogen=INFL,Indicator=DETECTIONS,InfluenzaTypeSubtype=AH1N1pdm09,Age65_79=1
•Pathogen=INFL,Indicator=TESTS,Age65_79=1
Co-infectionswithtwotypesorsubtypesofthesamepathogencanbereportedasaboveusingmultiplerows,e.g.apatientaged66yearsco-infectedwithInfluenzaB/VicandInfluenzaA(H1N1)pdm09shouldbereportedtoRESPIAGGRas:
•Pathogen=INFL,Indicator=DETECTIONS,InfluenzaTypeSubtype=BVic,Age65_79=1
•Pathogen=INFL,Indicator=DETECTIONS,InfluenzaTypeSubtype=AH1N1pdm09,Age65_79=1
•Pathogen=INFL,Indicator=TESTS,Age65_79=2
Theresultingdouble-countingoftestsforpatientswiththesecoinfectionsisnecessarytoavoidpotentialexclusionfromERVISS(recordsareexcludedwheredetections>tests)andwedonotexpectthistosignificantlyimpactinterpretationoftrends.
11
Itisalsopossibletoreportco-infectionsbetweeninfluenza,RSVorSARS-CoV-2andotherrespiratorypathogens.Detectionsofotherrespiratorypathogensherearereportedinthesamerowasthemainpathogendetectione.g.apatientaged66yearsco-infectedwithRSV-AandHumanmetapneumovirusshouldbereportedtoRESPIAGGRas:
•Pathogen=RSV,Indicator=DETECTIONS,RSVType=RSV_A,PathogenOther=HMPV,Age65_79=1
•Pathogen=RSV,Indicator=TESTS,Age65_79=1
PathogenOtherisnotrepeatableforaggregatedata,soco-infectionsinvolvingtwootherrespiratorypathogenswillneedtobereportedasIndicator=DETECTIONSacrossmultiplerows,similartothesecondexampleabovebutusingPathogen=OTH.
UNKvsmissing
InEpiPulseCases,wherethereisnodatatoreportforavariableoritsvalueisunknown,thefieldshouldbeleftblank.UNKcannotbereportedunlessitisexplicitlyincludedinthereferencelistforavariable.Thisonlyoccurswherethe
reportingofUNKismeaningful.
WithintheRESPIsubjectcodes,thefollowingvariablesstillincludeanUNKvalueintheirreferencelists:
•InfluenzaTypeSubtype(INFL_UNK=Influenzauntyped)
•RSVType(RSV_UNK=RSVuntyped)
Zerovsmissing
InERVISS,noassumptionsaremadeaboutmissingdata.Thismeansthatzerosmustbeexplicitlyreportedsince
missingvaluesarenotrecodedtozero.Forexample,inweekswheretestingwasperformedforapathogenbutall
werenegative,pleaseensurethatavalueof0isreportedforIndicator=DETECTIONStoensurethatthisisincludedinERVISSand0%positivityiscalculated.ThisrequiressubmittinganadditionalrowofdatainRESPIAGGRand
RESPISEVEREtocapturethezerodetections.
EHRdiagnosticcodes
EHRdiagnosticcodescanbereportedtoRESPICASEinthevariableEHRDiagnosticCodes.Thesecanbereportedto
indicatewhichcodesapplytoeachpatient,includingthosethatareusedtodefinetherespiratorydiagnosistomeetacasedefinitionorthatrelatetounderlyinghealthconditions,usingtheformatdescribedbelow.Thevariableisfree
text,buttoallowvalidationofthesubmittedcodespleasesubmitcodesusingthefollowingformat:CodeSystem:CodeSystemVersion:Code:Primary(P)/Secondary(S).Forexample,“ICD10:2019:J12.1:P”.
Onlyonecodeshouldbeprimary,capturingtheprincipalmedicalconditionthatpromptedtheadmission.Allothersshouldbemarkedassecondary.
IfCodeSystemVersionisnotapplicable,pleaseleavethisblank:e.g.SNOMEDCT::86406008:S.Formultiplecodes,pleaseensureeachcodeadherestothisformattingandseparatecodeswithasemi-colon“;”withinthesamecharacterstring.
Currently,codesfromthefollowingsystemswillbeaccepted:ICD9,ICD10,ICD11,SNOMED_CT,LOINCandICPC.
EpiPulseCases:ReportingProtocolforintegratedrespiratoryvirussurveillance
12
Annex3.Reportingqualitativeindicators
Qualitativeindicators(QI)provideanoverviewofthetransmissibility,severityandimpactofrespiratoryillness,
assessedusingthresholdsthatallowforthequalitativecategorisationofintensitylevels.ReportingofQItoRESPIQUALisbasedonthe
WHOPandemicInfluenzaSeverityAssessment(PISA)guide(2025)
withsomeadaptationstoallowforreportingofRSVandSARS-CoV-2.ThePISAframeworkincludesfourindicators:transmissibility,morbidityand
mortality,seriousnessofdiseaseandimpactonhealthcarecapacity.
WeprioritisethecollectionofasetofsixcoreQIforusein
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