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    Henie Widowati

    Bagian Penyakit Dalam

    Fakultas Kedokteran Universitas Trisakti

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    Latar Belakang

    TB masalah kesehatan masy yg besar sejak lama intervensi pcegahan & pengendalian

    Sepertiga populasi dunia terinfeksi TB

    Epidemi HIV P meningkat di Asia Tenggara

    40% tinfeksi M.Tb ancaman

    HIV/AIDS (+) & PPD(+) 60% risiko TB aktif

    HIV/AIDS (-) & PPD (+) 10% risiko TB aktif

    Sepertiga kasus HIV (+) dunia koinfeksi TB

    HIV meningkatkan kekambuhan TB

    meningkatkan risiko penularan

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    50% kematian HIV/AIDS oleh px paru dan salnapas.

    23 - 25% kematian pd HIV/AIDS o.k TB risiko kematian 6x lipat terlambat D/ & th/

    5 patogen tsering :

    - MTb 37% - criptococcus neoformans 15%

    - PCP 24% - streptococcus pneumonia 6%

    - nocardia 6% - strongiloides stercoralis 3%

    Respons thd th/ umumnya lambat & dipsulitoleh ESO dibandingkan status imunologinya

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    TB incidence closely correlated with HIV

    prevalence in Africa

    0

    200

    400

    600

    800

    1000

    0 10 20 30 40

    HIV prevalence, adults 15-49y

    E

    stimatedTB

    incidence

    (p

    er100,0

    00p

    opulation)

    WHO

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    TB meningkatkan progresi HIV

    Infeksi ganda TB-HIV viral loads

    sangat tinggi

    Progresi imunosupresi sangat cepat

    survival memendek walaupun th/ TB

    telah dilakukan

    Koinfeksi TB-HIV periode survivalmenurun dibandingkan HIV tanpa TB

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    TB Penyebab kematian utama pd

    HIV/AIDS LATE DIAGNOSIS &

    TERAPI

    Kesulitan D/ :

    - sputum sering (-)

    - >> EPTB

    - atypical radiografi & presentasi klinis- menyerupai infeksi paru oportunistik

    yg lain

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    CD4 counts >350

    Disease usually limited to the lungs Often presents like TB in HIV-uninfected persons

    typical chest X-ray findings with upper lobeinfiltrates with or without cavities

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    CD4 counts

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    Features ofpulmonary TB

    Early StageHIV infection

    Late StageHIV infection

    Clinical picture often resembles

    post-primary PTB

    often resembles

    primary PTB

    Sputum smear

    result

    often positive more likely to

    be negative

    Chest X-rayappearance

    upper lobeinfiltrates with or

    without cavitation

    infiltrates anylung zone, no

    cavitation;

    miliary; normal

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    1. Skrining 3 kombinasi gejala pada anamnesis :

    BATUK, DEMAM, KERINGAT MALAM

    lebih dari 3x seminggu2. Bila jawaban TIDAK pd 3 gejala tsb kemungkinan TB kecil

    3. Bila jawaban YA minimal 1 pada 3 gejala tsb

    evaluasi d/ lanjutan pemeriksaan sputumBTA & kultur, BJH pd kasus pbesaran kelenjar

    KGB

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    Bila sputum BTA (-)....

    Kultur BTA sputum the gold standardunt TB diagnosis

    Bila sputum BTA negative:

    Lakukan sputum BTA kultur (bilamemungkinkan) Kultur sputum meningkatkan kualitas

    perawatan & mbantu konfirmasi diagnosis Foto toraks dpt membantu diagnosis,

    mis. Ditemukan gambaran pbesarankelenjar di hilus, milier, infiltrat di lobusatas

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    TB Screening

    Tempat/lokasi prioritas untintensified TB case-finding (ICF):

    Medical and infectious disease wards

    VCT and PMTCT centres

    Out-patient and emergency roomdepartments

    Prisons and jails

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    0.00

    0.05

    0.10

    0.15

    1985 1990 1995 2000

    Annu

    alincidencei

    nAIDScases

    Pulmonary TB

    Disseminated TB

    Mono Dual Triple therapy

    TB among AIDS patients in Brazil

    www.aids.gov.br/boletim/bol_htm/boletim.htm

    Impact of ART on TBIncidence

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    Concomitant HAART markedly improves survival in HIV-infected patients with HIV/TB co-infection. Manosuthi, W et al. JAIDS. 43(1):42-46

    Effect of ART on survival

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    Abdool Karim SS, et al. NEJM 2010;362:697-706

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    Early ART (before 8 wks of

    TB treatment)

    Delayed ART (after 8

    wks o f TB treatment)

    Adh erence demand Problematic with use of 4-drug

    for TB and multidrug therapy

    for HIV

    Less problematic because

    fewer drugs necessary for

    TB treatment

    Ab i l i ty to determine

    the cause of adverse

    events

    Complex because of the large

    number of medications started

    in a short time period and

    overlapping side effects

    profiles

    Simpler because the

    number of drugs for TB

    treatment is less and there

    has been more time to

    evaluate response to TB

    treatment

    Drug-drug

    interact ion

    Problematic Problematic

    Severe imm unereconst i tu t ion

    inf lammatory events

    Risk may be increased Risk may be decreased

    HIV d isease

    prog ression (new OI

    or d eath

    Risk may be decreased Risk may be increased

    Burman WJ. Clin Chest Med 2005;26:283-294

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    TB regimens terapi SAMA (kec.

    Thiacetazon) antara HIV (-) dan (+)

    SEGERA!! HIV bhubungan dengan peningkatan

    mortaliti pberian ART SEGERA

    Pasien dengan sputum BTA (-)

    mortalitilebih tinggi dibandingkan pasien dengan

    sputum BTA (+)

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    CD4 < 50 ART 2 mg setelah th/ OAT

    CD4 > 50 dengan klinis berat ART 2 4

    mg setelah th/ OAT CD4 > 50 dgn klinis ringan sedang ART

    dpt ditunda 2 4 mg tetapi harus dimulai 8-

    12 mg setelah th/ OAT

    Pd psn HIV-MDR/XDR TBART 2 4 mgsesudah diberikan th/ TB second line.

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    PIs and RIF: NotRecommended

    Protease Inhibitor Effect of Rifampicin

    Saquinavir by 84%Ritonavir by 35%Indinavir by 89%Nelfinavir by 82%

    Amprenavir by 81%Lopinavir/ritonavir by 75%

    Rifampicin decreases blood levels of all PIs

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    In TB/HIV co-infection,ART should be initiated earlier (CD43 years old

    Avoid 1st trimester of pregnancy

    Efavirenz dose 600mg (or 800mg)

    NNRTI d Rif i i

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    Rifampicin decreases blood levels of

    NVP and EFV

    NNRTIs and Rifampicin

    NNRTI Effect of Rifampicin

    Nevirapine 3758%

    Efavirenz 22%

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    ART and RIF-based TB Rx

    Choice of nucleosides (NRTIs)to combine with efavirenz:

    Usual adult first-line therapy (mayalso be used in children >3):

    Zidovudine + lamivudine

    (AZT/3TC)Alternative in case of anemia:

    Stavudine + lamivudine (d4T/3TC)

    ART Options: RIF-based TB

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    *Tenofovir not recommended in pregnancy

    ART Options: RIF based TBRx

    More options (consider expertconsultation):

    Triple NRTI: abacavir or tenofovir* + 2NRTIs

    Not as potent, but no druginteractions

    WHO first-line for children >3

    Nevirapine + 2 NRTIs Some successful clinical experience

    Concern for low blood levels, toxicityoverlap (hepatitis, rash), and

    hypersensitivity reactions

    ART Options: RIF-based TB

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    ART Options: RIF based TBRx

    Ritonavir boosting of other PIscan achieve adequate bloodlevels but significant

    hepatotoxicity riskCan be used in children (