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WHO report warns global actions and investments to end tuberculosis epidemic are falling far short

News release

New data published by WHO in its 2016 "Global Tuberculosis Report" show that countries need to move much faster to prevent, detect, and treat the disease if they are to meet global targets.

Governments have agreed on targets to end the tuberculosis (TB) epidemic both at the World Health Assembly and at the United Nations General Assembly within the context of the Sustainable Development Goals. They include a 90% reduction in TB deaths and an 80% reduction in TB cases by 2030 compared with 2015.

"We face an uphill battle to reach the global targets for tuberculosis," said Dr Margaret Chan, WHO Director General. "There must be a massive scale-up of efforts, or countries will continue to run behind this deadly epidemic and these ambitious goals will be missed."

The WHO 2016 "Global Tuberculosis Report" highlights the considerable inequalities among countries in enabling people with TB to access existing cost-effective diagnosis and treatment interventions that can accelerate the rate of decline in TB worldwide. The report also signals the need for bold political commitment and increased funding.

Higher global burden of disease and death

While efforts to respond to TB saved more than 3 million lives in 2015, the report shows that the TB burden is actually higher than previously estimated, reflecting new surveillance and survey data from India.

In 2015, there were an estimated 10.4 million new TB cases worldwide. Six countries accounted for 60% of the total burden, with India bearing the brunt, followed by Indonesia, China, Nigeria, Pakistan and South Africa.

An estimated 1.8 million people died from TB in 2015, of whom 0.4 million were co-infected with HIV. Although global TB deaths fell by 22% between 2000 and 2015, the disease was one of the top 10 causes of death worldwide in 2015, responsible for more deaths than HIV and malaria.

Gaps in testing for TB and reporting new cases remain major challenges. Of the estimated 10.4 million new cases, only 6.1 million were detected and officially notified in 2015, leaving a gap of 4.3 million. This gap is due to underreporting of TB cases especially in countries with large unregulated private sectors, and under-diagnosis in countries with major barriers to accessing care.

In addition, the rate of reduction in TB cases remained static at 1.5% from 2014 to 2015. This needs to accelerate to 4–5% by 2020 to reach the first milestones of the World Health Assembly-approved "End TB Strategy".

Tackling drug resistance and other challenges

Multidrug-resistant TB (MDR-TB) remains a public health crisis. WHO estimates that 480 000 people fell ill with MDR-TB in 20151. Three countries carry the major burden of MDR-TB – India, China, and the Russian Federation – which together account for nearly half of all cases globally.

Detection and treatment gaps continue to plague the MDR-TB response. In 2015, only 1in 5 of the people newly eligible for second-line treatment were able to access it. Cure rates continue to remain low globally at 52%.

"The dismal progress in the TB response is a tragedy for the millions of people suffering from this disease. To save more lives now, we must get newly recommended rapid tests, drugs and regimens to those who need them. Current actions and investments fall far short of what is needed," said Dr Mario Raviglione, Director of the WHO Global TB Programme. "The world is finally waking up to the threat of antimicrobial resistance – now is the time to accelerate the MDR-TB response."

In 2015, 22% of HIV-positive TB patients were not enrolled on antiretroviral therapy (ART). According to WHO recommendations, ART needs to be made available for all HIV-positive TB patients. Nearly a million children under five years of age, and people living with HIV, who are especially vulnerable to TB and who were eligible for preventive treatment, were able to access it in 2015. This needs to be rapidly expanded.

Closing critical gaps in TB financing

For TB care and prevention, investments in low- and middle-income countries fall almost US$ 2 billion short of the US$ 8.3 billion needed in 2016. This gap will widen to US$ 6 billion by 2020 if current levels of funding are not increased.

Overall, around 84% of the financing available in low- and middle-income countries in 2016 was from domestic sources, but this was mostly accounted for by the BRICS (Brazil, the Russian Federation, India, China and South Africa) group of countries. Other low- and middle- income countries continue to rely heavily on international donor financing, with more than 75% coming from The Global Fund to Fight AIDS, TB and Malaria.

In addition, WHO estimates that at least an extra US$ 1 billion per year is needed to accelerate the development of new vaccines, diagnostics, and medicines.

"The resources deployed against TB, the leading infectious killer in the world, are falling short," said Dr Ariel Pablos-Méndez, Assistant Administrator for Global Health, of the US Agency for International Development (USAID) – the leading bilateral funder of the TB response. "Everyone has a part to play in closing the gap. As the report shows, we need universal health coverage, social protection mechanisms, and public health financing in high burden countries. The development aid community needs to step up more investments now, or we will simply not end one of the world’s oldest and deadliest diseases."

For more information, please contact:

Gregory Härtl (Geneva)
WHO Department of Communications
Coordinator, News, Social Media and Monitoring
Telephone: +41 22 791 4458
Mobile : +41 79 203 6715

Hannah Monica Dias (Washington, DC)
WHO Global TB Programme
Communications and Technical Officer
Mobile : +41 79 477 0435

Dominique De Santis (Geneva)
Mobile : +41 79 467 3538

1 In addition, 100 000 people with rifampicin-resistant TB also required second line treatment in 2015. WHO recommends that all patients with rifampicin-resistant TB are treated with a second-line MDR-TB regimen. MDR-TB is defined as resistance to both rifampicin and isoniazid, two major anti-TB drugs.