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  • RevisedNationalTuberculosis ControlProgramme

    (RNTCP)

    Dr.NAVPREETAssistantProf.,Deptt.ofCommunityMedicine

    GMCHChandigarh

  • ProblemStatementofTBinIndia

    India

    accounts

    for

    nearly

    1/4th

    of

    global

    burden

    of

    TB (2010).

    Mortality:

    26per1lacpopulation.

    Prevalence(old+newcases):256per1lacpopulation.

    Incidence(newcasesonly):185per1lacpopulation.

  • MillenniumDevelopmentGoals

    Goal

    6:

    Combat

    HIV/AIDS,

    malaria

    and

    other diseases

    Target

    8:

    By

    2015,

    to

    have

    halted

    and

    begun

    to reverse

    the

    incidence

    of

    malaria

    and

    other

    major

    diseases Indicator

    23:

    between

    1990

    and

    2015

    to

    halve

    prevalenceofTBdiseaseanddeathsduetoTB Indicator24:todetect70%ofnewinfectiouscasesand

    to successfully

    treat

    85%

    of

    detected

    sputum

    positive patients

  • EvolutionofTBControlinIndia

    1950s60s ImportantTBresearchatTRCandNTI

    1962 NationalTBProgramme(NTP)

    1992 ProgrammeReviewonly30%ofpatientsdiagnosed;ofthese,only30%treatedsuccessfully

    1993 RNTCP

    pilotbegan

    1998 RNTCPscaleup

    2000 >30%ofcountrycovered

    2004 >80%ofcountrycovered

    2006 EntirecountrycoveredbyRNTCP

  • NationalTuberculosisControl Programme

    NTCPwasstartedin1962withaimtodetectcasesat theearliest&treatthem.

    However, Treatmentsuccessrate

    :unacceptablylow

    Death&defaultrate

    :high

  • NeedForRevisedStartegy

    in

    1992,

    nation

    wise

    review

    was

    conducted

    with assistanceofSIDA&WHO.

    NTPsufferedfrommanagerialweakness Inadequatefunding OverrelianceonXraysfordiagnosis Frequentinterruptedsuppliesofdrugs Lowratesoftreatmentcompletion.

    In

    1993,

    GoI

    decided

    to

    give

    a

    new

    thrust

    by revitalizingNTP.

    RNTCPthusformulated

  • RevisedNational

    TuberculosisControlProgramme

    ObjectivesofRNTCP:

    1.

    To

    achieve

    and

    maintain

    a

    cure

    rate

    of

    at

    least

    85% amongnewlydetectedinfectious(newsputumsmear positive)cases

    2.Toachieveandmaintaindetectionofatleast70%of suchcasesinthepopulation.

  • Revisedstrategy:

    1.

    Augmentation

    of

    organizational

    support

    at

    centre andstatelevel.

    2.

    Usesputumtestingasprimarymethodofdiagnosis3.

    Standardizedtreatmentregimen

    4.

    Ensuringregular,uninterruptedsupplyofdrugs5.

    Emphasis

    on

    training,

    IEC,

    operational

    research

    &

    NGOinvolvement.6.

    Increasedbudgetoutlay

  • ComponentsofDOTS:

    1.

    Political

    will

    ensures

    financial

    support

    and sustainability.

    2.

    Case

    detection

    with

    the

    help

    of

    quality

    assured sputumsmearmicroscopy.

    3.

    Regularanduninterruptedsupplyofdrugs

    patientwiseboxes

    4.

    Directlyobservedtreatment

    directobservationwhilepatientisgettingtreatment.

    5.

    Systemicmonitoringandaccountability.

  • StructureofRNTCPatStatelevel

    State TB Cell

    District TB Centre

    Tuberculosis Unit

    Microscopy Centre

    DOT Centre

    STO, Deputy STOMO, Accountant, IEC Officer, SA, DEO

    DTO, MO-DTC, LT, DEO, Driver

    MO-TCSTS, STLS

    MO, LT

    DOT Provider MPW, NGO, PP, Comm Vol

    Nodal point for TB control

    One/ 5 lakh (2.5 lakh in hilly/ difficult/ tribal area)

    One/ lakh (0.5 lakh in hilly/ difficult/ tribal area)

  • RecommendationoftheRNTCPNationalLaboratory Committee(Oct2008)

    Strongly

    recommended

    that

    RNTCP

    changes

    diagnostic criteriaofSmear+vePTBasbelow:

    TB

    suspect

    is

    any

    person

    with

    cough

    for

    2

    weeks,

    or more

    Number

    of

    specimen

    required

    for

    diagnosis

    is

    2,

    with oneofthembeingamorningsputum

    One

    specimen

    positive

    out

    of

    the

    two

    is

    enough

    to declareapatientasSm+PTB

  • Basisofchanges

    The

    revised

    definition

    of

    a

    new

    sputum

    smear positivepulmonaryTBcaseisbasedonthepresence ofatleastoneacidfastbacillus(AFB)inatleastone sputum

    sample

    in

    countries

    with

    a

    well

    functioning

    EQAsystem. The

    reduction

    of

    the

    number

    of

    specimens

    to

    be

    examined

    for

    screening

    of

    TB

    cases

    from

    three

    to two,

    in

    places

    where

    workload

    is

    very

    high

    and

    humanresourcesarelimited.

  • RevisedCategories

    Treatmen tgroups

    Typeofpatient Regimen

    Intensive phase(IP)

    Continuation phase(CP)

    New(CatI)

    NewsputumsmearpositiveNewsputumsmearnegativeNewextrapulmonaryNewothers

    2H3R3Z3E3

    4H3R3

    Previously treated

    (CatII)

    SmearpositiverelapseSmearpositivefailureSmearpositivetreatment

    afterdefaultOthers

    2H3R3Z3E3

    S3/1H3R3Z3E3

    5H3R3E3

  • QualityAssurance

    RNTCPLabnetworkhasthreelevels: NationalReferenceLaboratories

    NTIBangalore TRCChennai LRSNewDelhi

    IntermediateReferenceLaboratories Statelevel

    NetworkofDesignatedMicroscopyCenters(>11,000) Includesmicroscopycentersinmedicalcolleges OneDMCcoversapopulationofabout1lakh Providequalityassuredacidfastsputumsmearmicroscopy

    services

  • RNTCPExternalQualityAssessment

    Components

    Paneltesting Onsiteevaluation Randomblindedrecheckingofroutineslides

  • ExternalQualityAssessmentactivitiesofRNTCP

  • ReportingProcedure

  • HIV&TB

    HIV

    coinfection

    strongest

    known

    risk

    factor

    for

    the progressionoflatentTBinfectiontoactiveTBdisease

    Estimated710%annualriskofreactivation,with60%lifetime risk

    (cf.

    10%

    lifetime

    risk

    in

    TB

    infected,

    nonHIV

    infected

    individual) Conversely,

    TB

    amongst

    the

    most

    common

    causes

    of

    morbidityandmortalityinpeoplelivingwithHIV/AIDS

    Immune

    response

    to

    TB

    bacilli

    increases

    HIV

    replication leadingtoarapidprogressionofHIVdisease

    Optimal

    access

    to

    DOTS

    will

    significantly

    reduce

    morbidity andmortalityinPLWHA

  • TB/HIVcollaborativeactivities

    TB/HIV

    Action

    Plan

    implemented

    by

    RNTCP

    and

    NACP jointly,focusingon:

    Trainingofserviceproviders Servicedeliverylinkages(ICTCRNTCPCrossreferrals) Monitoring Information,Education,andCommunication

    Implementationstarted: in

    2001,

    in

    6

    high

    HIV

    prevalent

    States

    (population

    311

    million) expanded

    in

    2004,

    to

    8

    additional

    States

    (population

    323

    million)

  • TB/HIVcollaboratingactivities

    National,

    State

    and

    District

    level

    coordination

    committees

    to monitorlinkages

    Guidelinesandtrainingmaterialdevelopedjointly OngoingtrainingofstaffonTB/HIV Crossreferral

    between

    ICTC

    and

    DOTS

    services

    developed,

    pilotedandimplemented InvolvementofNGOsandPPs CollaborativeIECactivities Jointmonitoringofactivities

  • TreatmentofTBinHIV

    TBcanbesuccessfullytreatedeveninHIVinfectedpts. But,cannotalonepreventpeoplefromdyingofAIDS

    InadditiontoTBtreatment,ARTandCPTneededforthose eligible

    DOTSisthetreatmentofchoice IntermittentSCCiseffective

    NationalpolicyistoprovideRNTCPCatItonewcasesand CatIItoretreatmentcases

    Higher

    relapse

    rates

    have

    been

    observed

    especially

    in

    those treatedwithnonRifampicincontainingregimen

    Whethertruerelapseorreinfection? DruginteractionsbetweenRifampicinandARVs

    National

    policy

    is

    to

    start

    ART

    after

    completing

    antiTB treatment,

    or

    modify

    ART

    by

    replacing

    Nevirapine

    with

    EfavirenzforthedurationofTBtreatment

  • LikelyimpactofHIVonTBinIndia?

    ScenariowithoutRNTCP

    HIV

    would

    increase

    TB

    prevalence

    (by

    1%),

    incidence

    (by 12%),

    and

    mortality

    rates

    (by

    33%)

    between

    1990

    and

    2015

    ScenariowithRNTCP

    Expect

    substantial

    reductions

    in

    prevalence

    (by

    68%), incidence(by41%),andmortality(by39%)between1990 and2015

    Nationally,

    RNTCP

    should

    be

    able

    to

    reverse

    the

    increases

    in

    TB

    burden duetoHIVbut,toensurethatTBmortalityisreducedby50%or

    moreby

    2015,

    HIVinfected

    TB

    patients

    should

    be

    provided

    with

    antiretroviral therapyinadditiontotherecommendedtreatmentforTB

  • PediatricTuberculosis RelatedtoadultTB

    Canoccuratanyage

    Diseasedevelopswithinoneyearofinfection Younger,earlier=

    disseminated

    PTB:EPTB::55:45

    PTBpaucibacillary,usuallyspneg

  • TreatmentofPediatricTB DOTS Categorization SAME Dosesperkgbodyweight Drugs

    to

    be

    made

    available

    as

    combipacks in

    patient

    wise

    boxes,

    linked

    to

    child's

    weight

    (

    610kg,1117kg,

    1825kg,26 30kg)

    PWB beingmadeavailable PC13yellow(610kg) PC14orange(1117kg) Prolongationpouches

    Pink(1825kg) Gray(2630kg)

  • MDRTBandDOTSPlus

    MDRTBisalabdiagnosis,NOTaclinicalone

    MDRTBlevelsoflessthan1%to3%innewcasesandof12% inretreatmentcases.

    EmergenceofresistancetoRifampicin

    inonly2%ofpatients, despite

    a

    high

    level

    (8%)

    of

    initial

    resistance

    to

    Isoniazid,

    eitheraloneorincombinationwithotherantiTB

    Quality

    assured

    laboratory

    facility

    for

    culture

    and

    Drug SusceptibilityTestmustbeavailable(NB:2 4monthsdelay beforeDSTresultsseen)

  • RNTCPCatIVtreatmentisa24monthstandardized2ndline regimengivenunderdailyDOT:

    6KmOfxEtoCsZE/18OfxEtoCsE

    MDRTBpatientadmittedtoindoorfacilityatDOTSPlussite forupto1monthfor:

    pretreatmentassessment; initiationofCategoryIVtreatmentafterdecisionofDOTS

    Plussitecommittee; monitoringtolerancetotreatmentregimen; counselingandhealtheducationtopatientandfamily; developinglinkagestodistrictservices;and contacttracing

  • AchievementsofRNTCP

    Treatmentsuccessrate:25%(1998)to88%(2010) Deathrate:29%(1998)to4%(2010) 662DTCs 2,698TUs 13,039DMCs 1,971NGOs >10,894Privatepractitioner 297Medicalcolleges >13,000peripherallaboratories

  • Thanks.

    Revised National Tuberculosis Control Programme(RNTCP)Problem Statement of TB in IndiaMillennium Development GoalsEvolution of TB Control in IndiaNational Tuberculosis Control ProgrammeNeed For Revised StartegyRevised National Tuberculosis Control ProgrammeRevised strategy:Components of DOTS:Structure of RNTCP at State levelRecommendation of the RNTCP National Laboratory Committee (Oct 2008)Basis of changesSlide Number 14Revised CategoriesQuality Assurance RNTCP External Quality AssessmentExternal Quality Assessment activities of RNTCPReporting Procedure HIV & TBTB/HIV collaborative activitiesTB/HIV collaborating activitiesTreatment of TB in HIVLikely impact of HIV on TB in India?Pediatric TuberculosisSlide Number 26Treatment of Pediatric TBMDR-TB and DOTS-Plus Slide Number 35Achievements of RNTCPSlide Number 51