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REVISTA

PAULISTA

DE

PEDIATRIA

www.rpped.com.br

ORIGINAL

ARTICLE

CLARIPED:

a

new

tool

for

risk

classification

in

pediatric

emergencies

Maria

Clara

de

Magalhães-Barbosa

a,∗

,

Arnaldo

Prata-Barbosa

a

,

Antonio

José

Ledo

Alves

da

Cunha

b

,

Cláudia

de

Souza

Lopes

c

aInstitutoD’OrdePesquisaeEnsino(Idor),RiodeJaneiro,RJ,Brazil

bDepartamentodePediatria,FaculdadedeMedicina,UniversidadeFederaldoRiodeJaneiro(UFRJ),RiodeJaneiro,RJ,Brazil cInstitutodeMedicinaSocial(IMS),UniversidadedoEstadodoRiodeJaneiro(Uerj),RiodeJaneiro,RJ,Brazil

Received13October2015;accepted29December2015 Availableonline27June2016

KEYWORDS

Triage;

Emergencymedical services;

Pediatrics

Abstract

Objective: Topresentanewpediatricriskclassificationtool,CLARIPED,anddescribeits devel-opmentsteps.

Methods: Development steps: (i) first round of discussion among experts, first prototype; (ii)pre-testofreliability,36 hypotheticalcases;(iii) secondroundofdiscussiontoperform adjustments;(iv)teamtraining;(v)pre-testwithpatientsinrealtime;(vi)thirdroundof dis-cussiontoperformnewadjustments;(vii)finalpre-testofvalidity(20%ofmedicaltreatments infivedays).

Results: CLARIPEDfeaturesfiveurgencycategories:Red(Emergency),Orange (veryurgent), Yellow(urgent),Green(littleurgent)andBlue(noturgent).Thefirstclassificationstepincludes themeasurementoffourvitalsigns(VIPEscore);thesecondstepconsistsintheurgency dis-criminationassessment.Eachstepresultsinassigningacolor,selectingthemosturgentone forthefinalclassification.Eachcolorcorrespondstoamaximumwaitingtimeformedicalcare andreferral tothemostappropriate physicalarea for thepatient’s clinicalcondition. The interobserver agreementwassubstantial (kappa=0.79)andthefinalpre-test, with82 medi-caltreatments,showedgoodcorrelationbetweentheproportionofpatientsineachurgency categoryandthenumberofusedresources(p<0.001).

Conclusions: CLARIPEDis anobjectiveandeasy-to-usetool for simple riskclassification,of which pre-testssuggestgoodreliability andvalidity.Larger-scalestudies onitsvalidityand reliabilityindifferenthealthcontextsareongoingandcancontributetotheimplementation ofanationwidepediatricriskclassificationsystem.

©2016SociedadedePediatriadeS˜aoPaulo.PublishedbyElsevierEditoraLtda.Thisisanopen accessarticleundertheCCBYlicense(http://creativecommons.org/licenses/by/4.0/).

Correspondingauthor.

E-mail:[email protected](M.C.Magalhães-Barbosa).

http://dx.doi.org/10.1016/j.rppede.2016.02.002

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PALAVRAS-CHAVE

Triagem; Servic¸osmédicos deemergência; Pediatria

CLARIPED:umnovoinstrumentoparaclassificac¸ãoderiscoememergências pediátricas

Resumo

Objetivo: Apresentarumnovoinstrumentodeclassificac¸ãoderiscopediátrico,oCLARIPED,e descreverasetapasdeseudesenvolvimento.

Métodos: Etapas do desenvolvimento:(i) primeira rodada de discussão entre especialistas, primeiroprotótipo;(ii)pré-testedeconfiabilidade,36casoshipotéticos;(iii)segundarodada dediscussãoparaajustes;(iv)treinamentodaequipe;(v)pré-testecompacientesemtempo real;(vi)terceirarodadadediscussãoparanovosajustes;(vii)pré-testefinaldevalidade(20% dosatendimentosdecincodias).

Resultados: O CLARIPED apresenta cinco categorias de urgência: Vermelha (emergência), Laranja (muitourgente), Amarela (urgente), Verde(poucourgente) eAzul (sem urgência). A primeira etapa da classificac¸ão inclui a aferic¸ão de quatro sinais vitais (escoreVIPE); a segunda etapaconsistenaavaliac¸ãodediscriminadores deurgência.Cada etaparesulta na atribuic¸ãodeumacor,selecionando-seademaiorurgênciaparaaclassificac¸ãofinal.Cadacor correspondeaumtempomáximodeesperapeloatendimentomédicoeaoencaminhamentoà áreafísicamaisadequadaàcondic¸ãoclínicadopaciente.Aconcordânciainterobservadorfoi substancial(kappa=0,79)eopré-testefinal,com82atendimentos,evidenciouboacorrelac¸ão entreaproporc¸ãodepacientesemcadacategoriadeurgênciaeonúmeroderecursosusados (p<0,001).

Conclusões: OCLARIPEDéuminstrumentoparaclassificac¸ãoderiscosimples,objetivoede fácil uso,cujospré-testessugerem boaconfiabilidadeevalidade. Estudosem maiorescala sobresuavalidadeeconfiabilidadeemdiferentescontextosdesaúdeestãoemcursoepodem contribuirparaaadoc¸ãodeumsistemadeclassificac¸ãoderiscopediátricoemâmbitonacional. ©2016SociedadedePediatriadeS˜aoPaulo. PublicadoporElsevier EditoraLtda.Este ´eum artigoOpenAccesssobumalicenc¸aCCBY(http://creativecommons.org/licenses/by/4.0/).

Introduction

Inthe lasttwodecades,amajorchallengein healthcare hasbeentofindsolutionstotheincreasedovercrowdingin emergencyservicehospitals.Oneofthestrategiesadopted inmanycountriestodealwiththisproblemwasthe imple-mentationoftriagesystemsusedtoclassifyeachpatient’s degree of clinical urgency shortly afterhis/her arrival to theEmergencyDepartment(ED),establishingawaitinglist basedonclinicalrisk,andnotinorderofarrival,toundergo medicalevaluationandtreatment.

The Australian Triage Scale (ATS), Canadian Triage & AcuityScale (CTAS),ManchesterTriageSystem (MTS),and EmergencySeverity Index(ESI) arethe tools for triagein emergencyservicesmostusedworldwide,allwithfivelevels ofurgency.1,2

In Brazil, the risk classification system developed by the Ministry of Health in the Qualisus Program has only fouremergencycategories,doesnotaddress thepediatric grouppeculiarities,andhasnotachievedsignificantnational adherence.3,4Ontheotherhand,thosedevelopedinEurope,

North America, andAustralia arecomplex,which hinders large-scaleadoptionina heterogeneoushealth contextas theBrazilian.Moreover,thereareinsufficientliteratureon thevalidityandreliabilityofthepediatricversionsofthese triagesystems.

Theaimofthisstudyistopresentanewriskclassification tool,theCLARIPED,forpediatricemergenciesanddescribe the steps of its development. The intent is to obtain a

reliableand validtool thatis best suitedtothe Brazilian healthcontext.

Method

(3)

chartsreview.ThestudywasapprovedbytheInstitutional Review Board of the Instituto D’Or de Pesquisa e Ensino (IDOR),underthenumber209075/2013.

Results

A group of experts (three doctors and two nurses) with extensiveexperiencein pediatricemergencieswas assem-bledinordertochooseandtestariskclassificationtoolfor thepediatricemergencydepartment.Afterextensive liter-aturereview,itwasconcludedthatthefourtriagesystems designedinNorthAmerica(CTASandESI),UnitedKingdom (MTS),andAustralia (ATS)werenotsuitablefor our coun-try,astheyareextensive,complexorlackspecific-pediatric features.TheSouthAfrican TriageScale (SATS),5 although

simplerandmoreadaptabletotheBrazilianhealthcontext, onlyhadfourlevelsofurgency,insufficientstratificationof pediatricagegroups,inadditiontohavingfewstudiesofits useinchildren.Itwasdecided,therefore,todesignanew triagesystemspecificforpediatricemergencies.

TheCLARIPEDsystem

CLARIPED comprises five urgency categories: Red (immi-nent life threat), Orange (very urgent), Yellow (urgent), Green(littleurgent)andBlue(noturgent). Eachcategory isassignedamaximumwaitingtimeformedicalevaluation andreferraltoanappropriateserviceareaofadequatecare tothepatient’slevelofurgency,asfollows:red,immediate careintheressucitationroom;orange,carewithin10minin theobservationroom;yellow,upto30min,waitingroom;

green,upto90min,waitingroom;andblue,upto180min, waitingroom.Theriskclassificationshouldstartina max-imumof 10min after patient’s arrival and registration; it shouldbeperformedbyanurseandlast2---5min.

Thefirststepstartswithsixquestionsaboutcomplaints, drugallergies,regular pediatric care, associated morbidi-ties,usingmedicationsand lastmeasured weight.Nextis theevaluationoffourvitalsigns:respiratoryrate(RR),heart rate(HR), oxygensaturation(SpO2),andskintemperature

(Temp).Eachvitalsignmeasuredisassignedavaluefrom0 to4,which willcomposethePediatricVitalSignals(VIPE) scorethatrangesfrom0to12,consistingofthesumofthe firstthreeparametersvaluessubtractedfromthe temper-aturevalueincaseof increasedHR(RR+HR+SpO2-Temp,if

increasedHR).TheVIPEscoreshouldthenbeassociatedwith oneof fivecolors: score 0=Blue; 1---2=Green; 3---5=Yellow; 6---9=Orange;≥10=Red(Table1).

The second stepis toconsult the tablesof discrimina-tors categorized by type or organ system involved (lines) and by urgency levels (columns). Assessment of five gen-eraldiscriminators(pain,generalappearance,feverreport, age, and return to the ED) is mandatory for all patients (Table2). The other discriminators are evaluated accord-ingtothepatient’scomplaint(Table3).Itisnotnecessary toconsultall linesandcolumns ofthe second table,only therelevantlinesassociatedwiththereportedcomplaints andthecolumnscorrespondingtolevelsofurgencyhigher thantheassignedbytheVIPEscore.Ifthereisa discrimi-natorcorrespondingtoahigherlevelofurgencythanthat assignedbytheVIPEscore,thehigherlevelofurgencywill

determinethefinalclassification.Theurgencydetermined bytheVIPEscoremaynotbedecreased,onlyincreasedfrom theevaluationofthediscriminators.

Inthe presence ofdiscriminators indicating risk of life threatening,suchassseizures,impairedlevelof conscious-ness,apnea,cyanosis,andothers,thepatientmustbesent for rapid or immediatemedical care before any adminis-trative procedure. The risk classification process is then performedretrospectively.

Pre-teststudies

Thehypotheticalclinicalscenariosdesignedbyexpertsfor training had the following distribution of urgency levels: Red11%,Orange42%,Yellow31%,Green8%,andBlue8%. Theoverallkappaformultipleobserversresultingfromthe firstpre-testwith36hypotheticalclinicalscenarioswas0.79 andkappaforeachurgencycategory was0.93(Red);0.82 (Orange);0.73(Yellow);0.65(Green),and0.93(Blue),with astandarddeviationof0.03andp<0.001,whichrepresented substantialreliability.

The second pre-test, performed with patients in real time, determined changes for the treshholds and values attributedtothephysiologicalparametersandforsome dis-criminators(newborn,returninlessthan24h,feverreport, abdominalpain,andcranialtrauma).

The final validity pre-test, included the retrospective analysisof95medicalcharts,selectedbyasystematic samp-ling of 20%of the cases attendedin thefirst fivedays of December2013. The aimwastoevaluate thedistribution ofthelevelsofurgencyandtheirassociationwithan out-come, which could work as a proxy of urgency, such as the numberofdiagnostic andtherapeutic resourcesused. The distributionofthelevelsofurgencywas: Blue(4.2%); Green(34.7%);Yellow(41%);Orange(6.3%),andRed(0%). NoneoftheattendancesclassifiedasBlueusedadiagnostic and/ortherapeuticresourceintheemergencydepartment; onethirdoftheGreenattendances,halfoftheYellowones usedoneresourceand20%usedtwoormoreresources;over 80%oftheOrangeonesusedtwoormoreresources(Table4;

p<0.001).

Discussion

The proposal todevelop asimple, objective, andeasy to use tool for risk classification in pediatric emergencies, appropriate toa Brazilian health context, resulted in the CLARIPED.Brazil’scontinentalmagnitudeand heterogene-ity make it difficult to adopt a risk classification system nationwide. The option to develop a new instrument, insteadofusingother triagesystemsalreadyevaluated, is justified. The most commonly used systems in the world weredevelopedincountriesinNorthAmerica,6,7 Europe,8

andAustralia.9Thehealthcontextofthesecountriesisquite

(4)

Table1 VIPEscorecalculation(vitalsignsinPediatrics).

Newbornto2monthsold

4 2 1 0 2 3 4

RR <16 16---19 20---29 30---60 61---80 81---90 >90 HR <81 81---90 91---110 111---149 150---179 180---189 >189 SpO2 <90 90---92 93---94 95---100

3monthsto11monthsold

4 2 1 0 2 3 4

RR <16 16---19 20---24 25---50 51---70 71---80 >80 HR <71 71---80 81---100 101---139 140---169 170---179 >179 SpO2 <90 90---92 93---94 95---100

1yearto4yearsold

4 2 1 0 2 3 4

RR <13 13---15 16---19 20---40 41---60 61---70 >70 HR <61 61---70 71---90 91---119 120---149 150---169 >169 SpO2 <90 90---92 93---94 95---100

5yearsto12yearsold

4 2 1 0 2 3 4

RR <11 11---14 15---17 18---24 25---36 37---50 >50 HR <51 50---60 61---70 71---109 110---129 130---149 >149 SpO2 <90 90---92 93---94 95---100

>12years

4 2 1 0 2 3 4

RR <10 10 11 12---16 17---22 23---29 >29 HR <41 41---50 51---60 61---99 100---119 120---139 >139 SpO2 <90 90---92 93---94 95---100

Assessmentofaxillarytemperature(regardlessofage) IfHRisincreased(score2,3or4)Subtract:

0 −1 −2

AxT 36---37.4 37.5---38.5 >38.5

VIPEscore(0---12)isthesumofthepointsassignedtoeachvitalsign.However,ifheartrateisincreased(score2,3or4);−1shouldbe subtractedfromthefinalscoreiftheaxillarytemperatureisbetween37.5and38.5◦Cand

−2iftheaxillarytemperature(AxT)is>38.5◦C. Urgencyclassification:Blue(0),Green(1---2),Yellow(3---5),Orange(6---9),andRed(≥10).

Table2 CLARIPEDgeneralandmandatorydiscriminators.

Discriminator Red Orange Yellow Green Blue Maximum

waitingtime

Immediate 10min 30min 90min 180min General

appearance

Criticallook Looksveryill Looksill Lookslittleill Verygood Importantprostration Mildtomoderate

prostration

Noprostration Doesnot looksick Pain(level)a Strong(7---10) Moderate(4---6) Mild(1---3) Nopain(0)

Fever(axillary temperature)b

Feverreport≥38.5◦C

in<3months

Feverreport≥37.5◦C

in<3monthsold Feverreport≥38.5◦C

in<3yearsold

Feverreport≥39.5◦Cat

anyage

Age Newborn(≤28days)

Return 1returnin<24h

2returnsin<72h

a Thelevelofpainshouldbeevaluatedbyappropriatescalesforthepatient’sage,suchasFLACCScaleorFacesScale(<5years)and

VisualAnalogicScale(>5years).

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Table3 CLARIPEDdiscriminatorsaccordingtoreportedcomplaints.

Discriminator Red Orange Yellow Green Blue Levelof

consciousness

Unconscious(coma) Altered (drowsinessand stupor)

Airway/breathing Cyanoticlips Dyspneaa Tachypneab Coryzaand/or

sneezing Apnea Stridorc Hoarsenessd

in<2years

Cough

Cardiovascular Absentpulses Weakpulses Cyanoticextremities Capillaryrefill>2s. Neurological Seizureatthetimeof

care

Acutefocaldeficit Seizureinthepast 12h

Postictalstate CBG:e40---60

(≤1year)or60---80

(>1year) CBG:e<40

(≤1year)or<60

(>1year) Gastrointestinal

andgenitourinary

Signsof dehydrationf

Currentseizureor reportof

persistent vomiting

Historyofvomiting and/ordiarrheain thepast72h

Urinaryretention withpalpable bladder

>5bowel

movements/dayor bloodydiarrhea Scrotalpain

and/orswelling

Currentand persistent abdominalpain Intermittent abdominal pain<2years Trauma Polytraumag TBIwithreport

oflossof consciousness and/orvomiting

TBIwith<12hand noreportofloss ofconsciousness orvomiting

TBIwith>12h withoutlossof consciousnessand withoutvomiting Openfractureor

deformity Highenergy mechanismh

Suspectedfracture orlimbdislocation Bleedingor

woundi

Uncontrolledbleeding Profusebleeding Controlled moderatebleeding

Smallbleeding Minorinjury withoutbleeding Extensiveinjury Moderateinjury Smallwoundwith

mildbleeding Burnj Faceand/orinhalation Moderate>20% Mild<10%

Electricalor circumferentialor chemicalburn Exogenous

intoxication

Present(reported)

Skin Urticarialwithstridor

andsignificant respiratorydifficulty

Urticarialwith

faceedema

Extensive urticarial

Rashwithout petechiae

Impetigoorlocal abscess

Purpurak Edemawithout

hypertension

Localurticaria

(6)

Table3 (Continued)

Discriminator Red Orange Yellow Green Blue Locomotor Claudication+fever

Acutegaitdisorder Foreignbody Present

Unspecific Unabletostand Inconsolablecrying Behaviorchange Irritability

Suspectedabuse Comorbidities Diabetes,withsevere

hypoglycemia (CBG<20)e

Diabeteswith hypo-orhyperglycemia: CBGe<60or>400

DiabeteswithCBGe

between250and400

Immunosuppression withfever

Neuromuscular diseasesm

Immunosuppressionn

withoutfever Suspecteddengue

(alwaysmeasure BPolyingand

sitting)

Signsofshock Presenceofwarning signsp

Absenceofwarning signsp

Signsofrespiratory failure

a Dyspnea:respiratorydistresswithpresenceofintercostalretractions. b Tachypnea:increasedRRaccordingtotheVIPEtable(RRscore>0).

c Stridor:noiseduringinspirationwithvaryingdegreesofrespiratorydistress. d Hoarseness:hoarsecryorvoiceorcough,withoutstridororrespiratorydistress.

e Capillarybloodglucose(CBGmg/dL):performthetestinallpatientswithalteredlevelofconsciousness,recentorcurrentseizure,

lethargyorprevioushistoryofdiabetes.

f Signsofdehydration:drymouth,sunkeneyes,noturinatinginthelast12h,decreasedskinturgor. g Polytrauma:patientswithtraumaticinjuryintwoormoreorgans.

h Highenergymechanism(intheabsenceofinformation,consideranytrafficaccidentashighenergymechanism):(a)motorvehicle

accident>60km/h(beltcollision);>40km/h(unbeltedcollision);>30km/h(motorcycle),and>10km/h(runover);(b)afallfromhigher than1m.

i Wound:(a)mild: abrasionsand contusionsrequiring nosuture; (b)moderate: contusionsrequiring sutures,butwithcontrolled

bleeding;(c)severe:extensivecontusionsrequiringsutures,profuseandcontinuousbleeding.

j Burn:Ruleofnines.

k Purpura:presenceofpetechiaand/orecchymosis.

l Urticaria:unlikeotherskinrashes;hyperemiaandelevatedplaques,usuallyveryitchy,butnotalways. m Neuromusculardiseases:chronicencephalopathy,myopathy,myelomeningocele,hydrocephalus.

n Immunosuppression:afterchemotherapy,nephroticsyndromeinactivity,chronicuseofcorticosteroids.

o Bloodpressure(BP):Alwaysmeasureincaseofalteredlevelofconsciousness,recentorcurrentseizure,suspecteddenguefever,

edemaofthelowerlimbsorgeneralized(anasarca).

p Warning signs in dengue (presence of one or more signs): abdominal pain, persistent vomiting, respiratory distress, postural

hypotensionordizziness,drowsiness,and/orirritability,spontaneousbleeding,decreasedurineoutput,suddendropintemperature, hypothermia,edema.

Table4 Pilotpre-testofvalidity:useoftreatmentresourcesinaccordancewiththelevelofriskclassification. Frequency

n(%)

0resource

n(%)

1resource

n(%)

2resources

n(%)

≥3

resources

n(%)

Total

n(%)

p-valuea

Blue 4(4.2) 4(100) 0 0 0 4(4.9) <0.001 Green 33(34.8) 17(51.5) 14(42.4) 1(3) 1(3) 33(40)

Yellow 39(41.0) 9(23) 17(43.6) 12(30.8) 1(2.6) 39(47.6) Orange 6(6.3) 0 1(16.6) 2(33.3) 3(50) 6(7.3)

Red 0 0 0 0 0 0

Missing 13(13.7)

Totaln(%) 30(36.6) 32(39) 15(18.3) 5(6) 82(100)

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thecountryasSouthAfricanTriageScale(SATS). CLAR-IPEDkeptthetwo-stepslogisticsoftheSATStriageprocess, consisting of mesurement of physiological parameters, followedbyassessmentofdiscriminators.However,several modificationswereperformedinbothstepsandaredetailed below.

AlthoughSATShasfivecolors,strictlyspeakingithasonly fourlevelsofurgency,astheBlueleveldoesnotreferto non-urgentpatients,buttopatientswhoaredeadonarrival.In theBrazilianhealthcontext,thereisalargeinfluxof outpa-tientstotheemergencyservices.3,4Thus,theexistenceof

alevelfornon-urgentpatientsisjustified,similartoother systemssuchastheMTS,8ESI-4,6PaedCTAS,7andATS.9The

triagetoolswithfiveemergencycategories showedhigher reliabilityandvaliditythantoolswithfewercategories.13

InCLARIPED,weoptedforthestratificationintofiveage groups,insteadofthethreegroupsusedbySATS.Thisoption isinagreementwiththevitalsignstablesrecommendedby pediatric textbooks14,15 and other triage instruments that

usefourormoreagegroups.6,7However,thereisalackof

studiesthatvalidatethestratificationofagegroupsforvital signsinPediatrics.TheBedsidePediatricEarlyWarning Sys-temScore---BedsidePEWSScore),atooldesignedtodetect early clinical deterioration of hospitalized children, was derivedfromstatisticalmethods andrecentlyvalidated.16

ThestratificationintofiveagegroupsofCLARIPEDwasbased onBedsidePEWSScore.

Althoughthereisnotyetaninternationalconsensuson theparameterstobeincludedinatriagetool,thereis evi-dencethatvitalsignsshouldbeanintegralpartofasafety risk classification process, particularly in children.5,17,18

However,vitalsignmeasurementscanbeextremelydifficult inemergencyscenarios,particularlyinsmallor uncoopera-tivechildren.Selectingthemostobjectiveparametersthat represent an effective contribution to the discrimination of emergency is crucial toachieve the goals of timeand processimprovement.InSATS,thefirststepincludes eval-uationofsevenparameters:RR,HR,systolicbloodpressure (SBP),Temp,levelofconsciousness,mobility,andpresence oftrauma.The pediatricrevised versionofSATS excluded theSBPassessment.ThePaedCTAS7recommendsthe

mea-surementofHR,RR,andSpO2asfirstordermodifiers,while

theESI-46recommendsthemeasurementofthesamethree

vitalsignsonlyincertaincircumstances.TheATS19leavesat

thediscretionofthetriageprofessionaltheneed to mea-surevitalsigns. InCLARIPED, thefourselectedvitalsigns andthescoreassignedtoeachofthemarebasedonstudies addressingthe developmentof twoinstrumentsthat used statisticalmethodstoassesstheabilityofsome physiolog-icalparameterstopredict clinical outcomes:the Bedside Pews16andPediatricEmergencyAssessmentTool(PEAT),20a

multivariatemodeltopredictthreelevelsofcarerequired forpediatricpatientsintheemergencydepartment.

TheinclusionofSpO2inVIPEscorewasbasednotonlyon

useofthisparameterinothervalidatedinstruments,suchas theESI-4,6 PaedCTAS,7 andBedsidePewsScore,16 but also

onevidence that patients withlow SpO2 usually have no

increasedrespiratory rate and that itsmeasurement may generatesignificantchangesinthemanagementofanumber ofpatientsattendedatpediatricemergencyservices.21,22

Theexclusionofblood pressuremeasurementfromthe VIPE score wasbased on evidence that the benefitof its

mandatory assessment in pediatric patients in the emer-gency department is limited.23 On onehand, hypotension

is a late sign of shock in children and, on the other hand,thetriageofchildrenwithhypertensioninthe emer-gency department may result in high prevalence of false positives.24 Other triage tools,such asMTS,8 PaedCTAS,7

ESI-4,6 andATS,19 donotincludemandatorymeasurement

ofbloodpressure,butonlytheinitialassessmentofclinical signsofshock,suchasthinpulses,delayedcapillaryrefill, sweating,andpallor.

HRcorrectedbythedegreeoffeverisauniqueaspectof CLARIPEDandwasbasedonthefactthattachycardiaisone ofthesystemicinflammatoryresponsesyndrome(SIRS)and sepsisparameters.25 Arecentstudyproposesasimilar

cor-rectionintheevaluationofchildrenwithacuteinfection.26

Noothertriagesystemconsidersthiscorrection.The assess-ment of the degree of fever is further considered in the discriminatorsstep,accordingtoageandfollowsthe guide-lines of the American College of Emergency Physicians.27

However,unlikeothertriagesystems,CLARIPEDtakesinto accountnotonlythecurrentfever,butthereportoffever inthelast24h.

In CLARIPED, the evaluation of patient’s level of con-sciousnessandpresenceoftraumaweremovedtothestep of discriminators assessment. Instead of considering the involvementofthepatient’slevelofconsciousnessintofour categories(awake,responsetopain,responsetovoice,and non-responsive),asrecommendedinSATS,11CLARIPED

con-sidersthatthepresenceofanyimpairmentofconsciousness placesthe patientat theOrangelevel (veryurgent).This strategy is already used in MTS,8 ESI-4,6 PaedCTAS,7 and

ATS.19

InCLARIPED,traumaisassessednotonlyforitspresence orabsence,asrecommendedinSATS,butaccordingtothe aspectsofmechanism,extension,locationandpresenceof symptoms.Themechanismandtraumaseverityassessment isalsousedinotherinstruments.PaedCTAS7andATS19assess

the presence of a high energy mechanism, regardless of clinical symptoms,toclassifypatients intohigherurgency categories.InMTS,8 thereisaspecificflowchartformajor

traumainwhichpatientsareclassifiedinemergencylevels one,two,oratleastthree,dependingonclinical manifes-tations.

Finally, the table of discriminators used in the second stepofCLARIPEDisverydifferentfromthatusedinSATS,in termsofcontentandorganization.AsinPaedCTAS,7

discrim-inators aregroupedby organsystems.The Canadiantool, however, is much more extensive and complex, covering 167complaintsgroupedinto17organsystems.

A recent study of the SATS5 demonstrated that in

pediatric triage the combination of the two steps, the evaluation of physiological parameters followed by the assessment of clinicaldiscriminators, increasedsensitivity (91%), compared with the use of each step alone (57.1% and75.6%,respectively).InCLARIPED,itisconsideredthat theVIPEscorecalculationhasalowerweightinthetool’s sensitivity, although this hypothesis has not been tested yet.

Thefinalpre-testwithasampleof82attendancesfounda distributionofemergenciessimilartootherstudies.28---30The

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Some limitationsmaybeidentifiedin thedevelopment oftheCLARIPEDsystem.Thefirstreferstothemethodology forconsensusontheproposedmodificationsandthechoice andorganizationofdiscriminators.ADelphimethod assur-ing the participating experts anonymity, interaction with controlled feedback, and statistical analysis of responses tosuccessiveroundsofinteractionwouldbethepreferred methodtominimizebiasand noiseandensure the preva-lence of the majority opinion. On the other hand, the tooldevelopmentprocessinseveralstepsensuredthe pro-cess systematization and a broad participation of the ED professionalsin thedevelopmentandimprovementof the instrument up to its last version. The second limitation relatesto the use of CLARIPED in other health care sett-ings.Itcanbearguedthatthespecificcontextinwhichthe CLARIPED was conceived limitsits application elsewhere. Morespecificdiscriminatorsrelatedtoophthalmologicalor psychiatricemergencies,for example,areabsentin CLAR-IPED.However,thesearchforthesimplicity,objectivity,and trainingfacility oftheinstrumentcanmakeitsadaptation anddisseminationviable inother less developedBrazilian regions by including more comprehensive and/or specific discriminators suitable to different settings. The concern in refining the discrimination between intermediate lev-els of urgency (Yellow [urgent] vs. Green [little urgent]) alsomakesthetool theoreticallyapplicable to intermedi-ateandlowurgencycareservices.Howevertheinstrument is not suitablefor pre-hospitaltriageduring criticalmass events.Specificinstrumentsfocusingontriageofcritically illpatientsinnon-hospitalsettingsareneededforthis pur-pose.

Itcan beconcludedthatthedevelopmentofCLARIPED for risk classification in pediatric emergenciesresulted in asimple,objective,andeasytousetool,whose pre-tests suggestagoodreliabilityandvalidity.Larger-scalestudies ofitsvalidity,reliability,andapplicationindifferenthealth contextsareunderway andmaycontributetotheuseofa pediatricriskclassificationsystemnationwide.

Funding

CNPq(Conselho Nacionalde Desenvolvimento Científico e Tecnológico, REF. No.: 448855/2014-3). Faperj (Fundac¸ão CarlosChagasFilhodeAmparoàPesquisadoEstadodoRio deJaneiro,REF.No.:E-26/010.000196/2015).

Conflicts

of

interest

Theauthorsdeclarenoconflictsofinterest.

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Imagem

Table 2 CLARIPED general and mandatory discriminators.
Table 3 CLARIPED discriminators according to reported complaints.
Table 4 Pilot pre-test of validity: use of treatment resources in accordance with the level of risk classification.

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