Treatment Action Group TB/HIV Advocacy Toolkit NOVEMBER 2017

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Presentation transcript:

Treatment Action Group TB/HIV Advocacy Toolkit NOVEMBER 2017 TB AND HIV Treatment Action Group TB/HIV Advocacy Toolkit NOVEMBER 2017 With thanks to Adam Almeida and Andolyn Medina

overview TB and HIV Challenges to TB/HIV Integrating the TB/HIV response to improve care Advocacy priorities Main Points

TB AND HIV

Image from Médecins Sans Frontières TB/HIV The presence of HIV or TB causes the accelerated progression of the other disease HIV increases the risk of developing TB disease due to a weakened immune system TB causes the acceleration of HIV through an unknown mechanism TB is the most common co-infection in people with HIV In people with HIV, extrapulmonary TB (TB outside the lungs) is more common People with HIV tend to have worse outcomes from TB than HIV-negative people Image from Médecins Sans Frontières TB/HIV

TB AND HIV COMPARISON TB HIV MTB is a large bacterium made of a fatty cell wall and many proteins Genetic material is stored as DNA, which is stable because of its ability to proofread and regulate mutations TB is a complex organism and has approx. 4,000 genes TB has around throughout human history HIV is a tiny retrovirus made of a few proteins and a glycoprotein envelope Genetic material is stored as RNA, which has no regulating mechanism and its copies often contain changes or mutations HIV is a relatively simple organism and has 9 genes HIV has been around for about 70 years TB and HIV are two of the most important infectious diseases in the world today. While they overlap in many important ways, they are also quite different. TB is a large and complex bacteria that has been infecting humans since early civilization. HIV however is a tiny, relatively simple virus that has been infecting humans for less than a century. FUNDAMENTALS

TB/HIV Statistics People with HIV are 21 times more likely to develop TB There were 10.4 million new cases of TB worldwide in 2016, of which 1.03 million cases arose in people with HIV TB is the number one killer of people with HIV 23% of HIV deaths were due to TB disease However, under drug treatment regimens, TB/HIV co-infection is manageable and allows for long, healthy lives Number of deaths worldwide in 2016, according to the 2017 WHO Global TB Report and 2017 UNAIDS Factsheet Concept courtesy of ACTION TB/HIV

TB/HIV Global Burden of Disease Countries with the highest burden of TB/HIV co-infection*: *The HBC list is defined as the top 20 countries in terms of absolute number of incident cases and the top 10 countries with the most severe burden in terms of incidence rates per capita not captured by the top 20 and meet a minimum threshold of the absolute number of incident cases (1,000 per year for TB/HIV). TB/HIV Source: http://apps.who.int/iris/bitstream/10665/259366/1/9789241565516-eng.pdf?ua=1

Challenges in tb/hiv coinfection

challenges in preventing, diagnosing, and treating TB/HIV Vaccination The BCG (bacille Calmette-Guerin) vaccine, used to protect against TB, is not recommended for infants with HIV it can cause a potentially fatal inflammatory immune reaction Diagnostics The most commonly used TB diagnostic tools lack the sensitivity to detect smear-negative and extrapulmonary TB Treatment Pill burden of taking TB treatment and anti-retroviral treatment at the same time Coordination of timing of both treatments, due to immune reconstitution inflammatory syndrome (IRIS) Drug-drug interactions between HIV and TB medications, such as rifampicin and bedaquiline Challenges *see other modules for more information on preventing, diagnosing, and treating TB in people with HIV

Integrating TB/HIV response to improve care

WHO Policy on TB/HIV Collaborative Activities A. Establish NTP-NACP collaborative mechanisms Set up coordinating bodies for effective TB/HIV activities at all levels Conduct surveillance of HIV prevalence among TB cases Carry out joint TB/HIV planning Monitor and evaluate collaborative TB/HIV activities B. Decrease the burden of TB among PLHIV (Three I’s) Establish intensified TB case finding Introduce isoniazid preventive therapy Ensure TB infection control in health care and congregate settings C. Decrease the burden of HIV among TB patients Provide HIV testing and counselling Introduce HIV prevention methods Introduce co-trimoxazole preventive therapy Ensure HIV/AIDS care and support Introduce ARVs INTEGRATION 11

What are the Three I’s? Intensified case finding (ICF): the regular screening of all people at high risk of HIV, and their close contacts, for the symptoms and signs of TB. Isoniazid preventive therapy (IPT): the provision of daily isoniazid to people with HIV who are latently infected with TB to prevent progression to TB disease. Infection control (IC): strategies that minimize the risk of TB transmission, particularly in HIV- prevalent settings. The Three Is are the elements of the policy under section B designed to decrease the burden of tuberculosis in people living with HIV/AIDS.

What is the “fourth I”? Initiation of antiretroviral therapy in people with HIV— specifically earlier initiation of ART by increasing the minimum to start to 350 CD4 cells/mm3 provide ART to all HIV-positive people who have TB regardless of CD4 count The Temprano Study (2015) showed that starting ART immediately reduced risk of death and serious HIV related illnesses, including TB, by 44%. These recommendations can be found in the 2009 WHO’s Rapid Advice: Antiretroviral therapy for HIV in adults and adolescents which can be found at www.who.int/hiv/pub/arv/rapid_advice_art.pdf Source: Danel C, Gabillard D, Carrou JL, et al. Early ART and IPT in HIV-infected African adults with high CD4 count (Temprano trial). Paper presented at: 22nd Conference on Retroviruses and Opportunistic Infections; 2015 February 23–26; Seattle, WA.

INTEGRATIVE TOOLS Diagnostics that can work on both HIV and TB, or work well in people with TB/HIV, can help forge integration: GeneXpert contains a cartridge for detection of TB (MTB/RIF Ultra) and a cartridge for detection of HIV viral load and early infant diagnosis, as well as other diagnostic cartridges Centralized high throughput assays can be used to test for TB drug susceptibility as well as viral loading testing, such assays include Abbott’s Real Time Platform LAM test is a point-of-care diagnostic tool, which is able to test for TB in people living with HIV who have CD4 levels <100 cells/m3 or who are very sick Preventive therapy, recommended in all people with HIV without TB, also offers a path for integration: Several options now (see prevention module) Fixed dose formulation of isoniazid/co-trimoxazole/B6 INTEGRATION Source: http://www.treatmentactiongroup.org/pipeline-report/2017

Advocacy Priorities

Advocacy Priorities People with HIV need to be routinely screened for TB and given appropriate treatment or preventive therapy People with TB or at risk for TB should be counseled and tested for HIV, and be offered appropriate treatment Integration of HIV and TB services and care, as well as planning at the government level Cooperation and collaboration of HIV and TB activists Development of new tools to prevent, diagnose and treat TB For more information on the Global Plan to End TB 2016-2020: http://www.stoptb.org/global/plan/plan2/ ADVOCACY

MAIN POINTS

MAIN POINTS TB/HIV co-infection is one of the greatest hurdles towards lowering the global burden of both diseases TB develops as a opportunistic infection in people with immuno-compromised systems TB is the greatest killers of people living with HIV TB/HIV co-infection is completely manageable with the correct use of both diagnostic tools and drug treatments Integration of efforts from both TB and HIV activists is necessary to better treat people living with co-infection and help prevent infection and disease from occurring MAIN POINTS