Fatal Neglect Kala Azar

Kala Azar (leishmaniasis)

Kala azar, or visceral leishmaniasis, is the second deadliest parasitic disease in the world – only malaria kills more people.

neglected tropical disease, kala azar is caused by a parasite spread to humans through the bite of infected female sand flies. It attacks the immune system and is almost always fatal if not treated.

Also known as visceral leishmaniasis, kala azar is the most serious form of leishmaniasis and is endemic in 76 countries, with hundreds of millions at risk of infection. There are between 50,000 and 90,000 new cases a year, about 90 per cent of which occur in Brazil, Ethiopia, India, Kenya, Somalia, South Sudan and Sudan. Between 1989 and 2020, MSF teams treated nearly 150,000 people for kala-azar, over a third in South Sudan.

Diagnosis and treatment of the disease, especially of the variety found in eastern Africa, can be complex and painful.

 

About Kala Azar

Kala azar is caused by bites from female phlebotomine sandflies – the vector (or transmitter) of the leishmania parasite.

The sandflies feed on animals and humans for blood, which they need for developing their eggs.

If blood containing leishmania parasites is drawn from an animal or human, the next person to receive a bite will then become infected and develop leishmaniasis.

Months after this initial infection, the disease can progress into a more severe form, called visceral leishmaniasis or, kala azar.

Kala azar presents after two to eight months, with more generalised symptoms, including prolonged fever and weakness.

Co-infection of kala azar and HIV is a major challenge, as the diseases influence each other in a vicious spiral as they attack and weaken the immune system.
 

The most effective diagnostic tests for leishmaniasis are invasive and potentially dangerous, where tissue samples are required from the spleen, lymph nodes or bone marrow.

These tests require lab facilities and specialists not readily available in resource-poor, endemic areas.

The most common method of diagnosing kala azar is by dipstick testing. However, this method is highly problematic. In endemic areas, people can become infected with kala azar, but it may not develop into the disease.

Therefore, no treatment will be required.

Unfortunately, dipstick testing only establishes whether a patient is immune to kala azar – so if the parasite is present, it would appear that the patient has the disease. Because of this, dipstick testing can’t be used to see if the patient is cured, is re-infected or has relapsed.
 

Today, liposomal amphotericin B is becoming the primary treatment drug in Asia, either alone or as part of a combination therapy.

While safer and shorter than previously used medication, it requires intravenous administration, which remains an obstacle to its use in local clinics. An oral drug, miltefosine, is often added to optimise treatment regimens in patients.

In Africa, the best available treatment is still a combination of pentavalent antimonials and paromomycin, which is toxic and requires a number of painful injections. Research into other treatment combinations is underway.

MSF treated 9,900 patients for kala azar in 2018.
 

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