Who Clinical Staging of Hiv

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    STAGE 1STAGE 2

    STAGE 3

    STAGE 4

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    Moderate unexplained weightloss

    (

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    Severe weightloss(>10% ofpresumedormeasured

    body weight)

    Unexplainedchronicdiarrhoeaforlongerthan one month

    Unexplainedpersistentfever(intermittentorconstantfor

    longerthan one month) Oralcandidiasis

    Oralhairyleukoplakia

    Pulmonarytuberculosis(TB)diagnosedin lasttwoyears

    Severepresumed bacterialinfections(e.g.pneumonia,

    empyema,pyomyositis, boneor jointinfection,meningitis, bacteraemia)

    Acute necrotizing ulcerativestomatitis,gingivitisor

    periodontitis

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    HIV wastingsyndrome

    Pneumocystis pneumonia

    Recurrentsevereorradiological bacterialpneumonia

    Chronicherpessimplexinfection (morethan one months

    duration) Oesophagealcandidiasis

    Extrapulmonary TB

    Kaposissarcoma

    Central nervoussystem (CNS)toxoplasmosis

    HIVencephalopathy

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    SEVERITY CD 4 LEVELS

    Notsignificantimmunosuppression >500/cu mm

    Mildimmunosuppression 350 499/cu mm

    Advancedimmunosuppression 200 349/cu mm

    Severeimmunosuppression

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    Clinicalcondition Recommendation

    WHOClinical Stage 1 Start ART ifCD4 350

    WHOClinical Stage 2 Start ART ifCD4 350

    WHOClinical Stage 3 or4 Start ART irrespectiveofCD4

    cellcount

    Active TB disease Start ART irrespectiveofCD4

    cellcount

    HBVco-infection requiring

    therapy

    Start ART irrespectiveofCD4

    cellcount

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    CLINICAL MONI ORING

    Monitoringofadherence

    Monitoringoftolerance

    Monitoringof fficacy

    LABORATORY MONITORING

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    Adherenceto ART isessentialand morethan95% adherenceisrequiredforeffectivenessoftherapy

    Causesofany new symptomsandsigns

    should beidentifiedafterinitiation ofART

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    Indicatorsforimprovementin thepatients

    condition would be

    Gain in body weight

    Decreasein frequencyorseverityofopportunisticinfections

    Increasein CD4 countof100-200 cellsperyear

    (this may belessifinitialCD4

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    Full bloodcountincludingplateletcount

    (patientson Zidovudine mayrequire

    frequentHb monitoring) Fasting Blood Sugar(ifthepatientison

    PIs)

    Liverfunction tests(ALT, AST)

    Renalfunction tests(Tenofovir)

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    Thefollowingtripletherapyregimensare

    recommended:

    2 NucleosideReverse TranscriptaseInhibitors

    (NRTIs)and 1 Non-NucleosideReverse Transcriptase

    Inhibitor(NNRTI)

    2 NRTIsand 1 ProteaseInhibitor(PI)

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    Zidovudine+Lamivudine+Nevirapine

    (Stavudine +Lamivudine+Nevirapine)

    (Zidovudine+Lamivudine+Efavirenz )

    Abacavir + Tenofovir +LopinavirDidanosine + Abacavir +Nelfinavir

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