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    More serious, aggressive strategy
    vital in fight vs tuberculosis
     
    By Priya Shetty
    SciDev.Net
     

    When the World Health Organization announced in 1993 that tuberculosis (TB) should be treated as a global emergency, the international community’s response was slow and uncoordinated.

    Although initial progress has since been made in controlling the disease, the emergence of a deadly HIV-TB co-infection epidemic and extensively drug-resistant (XDR) strains of TB means that a more serious and aggressive strategy is essential to fight the world’s second-biggest infectious disease.

     

    Practical action

    What needs to be done? More research is undoubtedly necessary. Understanding the social factors deterring people from seeking diagnosis or treatment, removing the barriers to accessing care, and devising new strategies to diagnose TB in children and HIV/AIDS patients are key priorities.

    When the genome of the bacterium that causes TB has been sequenced, researchers will be able to look for ways to defeat it. Understanding immunity to the disease may also help researchers who have so far been frustrated in efforts to develop a new, long-lasting vaccine.

    But there are practical measures that can be implemented using existing knowledge: integrating TB and HIV efforts—especially in sub-Saharan Africa—and strengthening health systems are just two examples.

    Two-thirds of TB cases could be detected with existing diagnostic methods if only these techniques were widely and effectively implemented. These measures will need tremendous national commitment as well as international support and guidance.

     

    Need for information

    Just as important as these actions is the need for accurate information. This means not only training health-care workers to understand the growing challenges of TB, but also educating the wider population to dispel any lingering myths about TB and combat the stigma associated with this disease. Raising awareness of the increased risk of TB infection for people with HIV and helping people know when they might be at risk of having latent or ‘hidden’ TB, are also key.

    This spotlight offers the simple facts and figures about TB but also delves into more complex issues—in particular, the obstacles confronting mandatory quarantine of patients with drug-resistant TB, the problem of overlapping HIV and TB epidemics and the clinical challenges for drug development.

    The facts show undeniably that tuberculosis (TB) is a major problem for the world’s poor. Over two billion people worldwide carry the bacterium that causes TB, with approximately 15 million people suffering from an active infection at any one time.

    The disease burden is highest in developing countries where people are especially vulnerable to TB because of poor underlying health, adverse living conditions and limited access to treatment.

    Although the disease is often treatable, for many people in these nations it is fatal. TB kills 1.6 million people every year; 4,400 people every day; one person every 20 seconds. 98 percent of all TB deaths occur in developing countries.

    The economic implications of this devastation are huge: fighting the disease drains $12 billion from the annual incomes of the world’s poorest communities. The loss of productivity attributable to TB is estimated to be 4 percent to 7 percent of gross domestic product.

    Figure 1 shows the 10 countries with the highest numbers of TB victims—including the Philippines—all are in the developing world.

    But it is important to put overall numbers into context, relative to a country’s population size. Figure 2 shows the countries that have the highest prevalence of TB sufferers per 100,000 of the population—a different picture from Figure 1. Almost all of these countries are in Africa, where resources for TB treatment and control are limited.


    About the disease

    TB is an infectious disease caused by the Mycobacterium tuberculosis bacterium, which most commonly affects the lungs. There are two forms of TB: active, where a patient has symptoms and an abnormal chest x-ray; and latent, where a person has no symptoms and their chest x-ray is normal, but a skin test gives a positive result for TB.

    The symptoms of active TB of the lungs include coughing—sometimes with sputum or blood—chest pains, weakness, weight loss, fever and night sweats. It is spread through the air when infected people cough, sneeze or speak.

    Despite its prevalence, many people are unaware of the complexities of TB—for example, that it can lie dormant in seemingly healthy people. Accurate information is key to tackling any major disease epidemic and unless people know what the symptoms of TB are, they are unlikely to get treatment before reaching the infectious stage of active disease.

    Strategies for controlling TB increasingly include education aimed at informing people of the key symptoms of TB and dispelling the common myths that surround this disease

     

    TB and HIV/AIDS

    TB is the leading infectious killer of people with HIV/AIDS, and a particular problem in sub-Saharan Africa, where a third of people with HIV are also infected with TB. In most of these countries, over half of patients presenting with TB are coinfected with HIV (see Table 1).

    Because of their weakened immune systems, HIV/AIDS patients are up to 20 times more likely to develop TB than people without HIV. TB is also more fatal in HIV/AIDS patients, with up to half of all deaths of HIV/AIDS patients due to TB. A person with both diseases can be four times more likely to die during TB treatment than someone with TB alone.

    Yet, effective treatment of HIV/AIDS patients infected with TB is still possible, principally through the addition of an antibiotic, cotrimoxazole, which can reduce the death rate during TB treatment by 40 percent.

    Still, stigma related to both diseases can mean that patients infected with one disease are reluctant to voluntarily be tested for the other. The lack of integration across national HIV/AIDS and TB control programs also means that routine screening of TB patients for HIV, and vice versa, is not in place for many developing countries

     

    TB treatment

    Current treatment consists of six- to nine-month courses using a combination of two or more of the four first-line drugs: isoniazid, ethambutol, pyrazinamide and rifampin. These regimens work for active, drug-susceptible TB—as long as the course is completed.

    Not completing the course can lead to relapse, continued transmission and the development of drug resistance—a growing concern in the fight against TB.

    One strategy that has been adopted by the World Health Organization (WHO) to help ensure that patients complete TB treatment is directly observed therapy (DOT), where a health worker watches the patient swallow each dose of TB medication.

    One of the Millennium Development Goals set for 2015 is to reduce the prevalence of and deaths due to TB by 50 percent of 1990 figures. DOT can lead to more successful treatments of infectious TB, which can, in turn, help prevent the spread of the disease.


    Drug resistance

    About 450,000 new cases of multidrug-resistant TB (MDR-TB) occur every year, with the highest prevalence in China, India and the countries of the former Soviet Union.

    These patients cannot be treated with first-line drugs and often require extensive chemotherapy for up to two years. In 1999, the WHO launched the DOTS-Plus program to manage MDR-TB with second-line drugs in resource-limited settings. This includes integrating drug resistance surveillance into TB control strategies and scaling up MDR-TB treatment.

    The major barrier to treatment of MDR-TB in developing countries is the high cost of second-line drugs, which are between 300 and 3,000 times more expensive than first-line drugs. Other barriers include the limited number of laboratories equipped for drug-susceptibility testing and the fear of developing extensively drug-resistant TB (XDR-TB)—where the disease is resistant to second-line drugs as well as first-line ones.

    Cases have been confirmed in KwaZulu-Natal, South Africa—where 52 of 53 patients diagnosed with XDR-TB died within 25 days of sputum collection—and worldwide.

    The resistance to second-line drugs makes XDR-TB extremely difficult to treat. But new drugs are in the pipeline.

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