tbc hiv presentation
TRANSCRIPT
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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 (