tb case finding/tb prevention in hiv infected populations

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TB Case finding/TB Prevention in HIV infected populations. Helen Ayles ZAMBART Project. Before HIV. --_-_--_-. 1 Infectious case. 2 cases of TB. 20 contacts. Stability. 1 Non-Infectious. With HIV (10%). --_-_--_-. 1.2 Infectious cases. 18 HIV-ve. 2 HIV+ve. 1.8 cases. 20 contacts. - PowerPoint PPT Presentation

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TB Case finding/TB Prevention in HIV infected populations

Helen Ayles

ZAMBART Project

--_-_--_-

2 cases of TB

1 Infectious case

20 contacts

Stability

Before HIV

1 Non-Infectious

--_-_--_-

18 HIV-ve1.8 cases

1.2 Infectious cases

20 contacts

An Epidemic

With HIV (10%)

1.4 Non-Infectious

2 HIV+ve0.8

cases

New Cases of Tuberculosis in Zambia Notification Rate /100,000 /year 1964-1996

0

50

100

150

200

250

300

350

400

450

Source NASTLP/MoH

No country with a severe HIV epidemic is controlling TB

R2 = 0.7547

0

100

200

300

400

500

600

0 5 10 15 20 25 30Adult HIV seroprevalence (%) UNAIDS

estimates

TB

in

cid

ence

(/1

00

,00

0/y

r) G

TB

est

ima

tes

Reduce prevalence of HIV --_-_--_-

18 HIV-ve1.8 cases

1.1 Infectious cases

20 contacts

An Epidemic

With HIV (10%)

1.5 Non-Infectious

2 HIV+ve0.8

cases

Reduc

e tran

smiss

ion

Reduce reactivation

How does TB impact on HIV

• 750,000 PLHIV will develop TB this year

• TB is one of the leading causes of death in PLHIV

• ~200 PLHIV will die today of TB – despite the fact that TB is curable

• ART reduces the rate of developing TB but PLHIV on ART still have a massively increased risk of developing TB (4-8x that of HIV negative)

What can the HIV community do?

• Find more cases of active TB and treat them earlier

• Reduce reactivation of latent TB in those individuals who do not yet have active TB

Both will prevent TB!

TB Preventive therapy

• Cochrane review of 11 randomised trials including 8,130 HIV positive participants showed an overall reduction in TB of 33% (RR 0.67, 95% CI 0.51-0.87), and a reduction of 62% (RR 0.38, 95% CI 0.25-0.57) in people with a positive TST

• National and international policies exist to implement it

Poor uptake of policy in high burden countries

Woldehanna, Cochrane review 2004

Screen all HIV infected individuals for TB

Active TB: Treat Latent TB: Prophylaxis

How?When?Where?

No active

Expected yield 0-6%1-4 Eligibility 10-50%5,6

1. Espinal, Lancet 1995, 2.Burgess, AIDS 2001, 3. Kimmerling, IJTLD 2002,4. Mohammed, IJTLD 2004, 5. Aisu, AIDS 1995, 6. Ayles Trop Doc 2006

How to Screen for TB

• Symptoms

• Chest x-ray

• Sputum examination: smear Vs cultureCan use the same screens to EXCLUDE TB

How to Screen for Latent TB• Tuberculin skin test (TST)

• Interferon release assays

Symptomatic screen

• Most commonly done

• Screens vary – most validated include– Cough > 2/3 weeks

– Fever (>2 weeks)

– Night sweats (severe, > 2 weeks)

– Unintentional weight loss (>10%)

• Sensitivity high, specificity low7

7. Mosimaneotsile, Lancet 2003

Chest X-rays

• Less availability in low income settings

• Difficult to interpret• Lower sensitivity

than symptoms, ? Improved specificity

• Not cost effective8,9

– Places where available tend to have less TB

8. Schneider, Arch Int med 1996, 9. Ho Int J STD AIDS 1999

Sputum examination

• Sputum smear – Cheap and readily available– Poor sensitivity– High specificity

• Sputum culture– Expensive, less available– Improved sensitivity– Liquid culture may lead to increased NTM

detection

When & Where to Screen?

• On diagnosis – VCT, PMTCT, HIV care

• Every visit

Screen all HIV infected individuals for TB

Active TB No TBUnknown

VCT/PMTCT

Screen all HIV infected individuals for TB

Active TB No TBUnknown

ART/HIV Clinical setting

TST

• Over 100 years old, skin test

• Cheap, limited facilities needed

• False positives

• Anergy in HIV positives

Interferon - γ assays

• In-vitro assays using the M.tb region of difference 1 (RD1) antigens

• Higher specificity than TST• ? Better sensitivity although need to use a

variety of Ag 10

• Limited experience in HIV+ high TB prevalence areas11

• Expensive and need lab facilitiesWhat is the gold standard?

10. Pai, Lancet Inf Dis 2004, 11. Chapman, AIDS 2002

Do we need to diagnose latent TB in high prevalence

countries?

• We need to exclude active TB

BUT

• Can we assume exposure +/- infection and use the expensive RD1 assays in low prevalence, high income countries?

TB Prevention

• INH 5mg/kg daily• Duration 6-12

months ? Sufficient in high TB transmission areas

• Other regimens equally effective but higher toxicities and more potential drug interactions

• ? Value with ART

analysis time years years

0 1 2 3 4 5 6 7

.8

.9

1

Placebo

H & RZ

Summary

Screen all HIV infected populations for TB

Treat active TB

High income, low TB prevalence

Low income, high TB prevalence

Test latent TB Exclude active TB

TB Preventive therapy

Asymptomatic early HIV,

PMTCT/VCT

Acknowledgements

• ZAMBART Project Team• Peter Godfrey-Faussett &

Nulda Beyers• LSHTM & UNZA

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