Onchocerciasis

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Onchocerciasis (River Blindness)

description

Onchocerciasis. (River Blindness). River Blindness, a parasitic disease, is the second leading infectious cause of blindness. . A Short History. 1975 : Fungus that produces chemical toxic to parasitic worms discovered in Japanese soil sample, from which scientists develop avermectins. - PowerPoint PPT Presentation

Transcript of Onchocerciasis

Page 1: Onchocerciasis

Onchocerciasis(River Blindness)

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River Blindness, a parasitic disease, is the second leading infectious cause of

blindness.

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A Short History

1875: John O’Neill first reports the presence of microfilaria in Onchocerciasis patients in Ghana

1893: Rudolf Leuckhart describes morphology of adult worms in subcutaneous nodules

1917: Rodolfo Robles publishes findings on a “new disease” which includes subcutaneous nodules, anterior ocular lesions, dermatitis, and microfilariae

1995: WHO establishes The African Program for Onchocerciasis Control (APOC)

1975: Fungus that produces chemical toxic to parasitic worms discovered in Japanese soil sample, from which scientists develop avermectins

2009: First evidence that Onchocerciasis can be eliminated with Ivermectin published in the journal Neglected Tropical Diseases

1987: Merck & Co agrees to donate Ivermectin to all countries where River Blindness is endemic

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River blindness is caused by a round worm, Onchocerca volvulus

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River blindness is transmitted to humans by the blackfly.

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Life Cycle

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Symptoms

RashesLesionsIntense itchingDepigmentation of the skinLymphadenitisGeneral debilitationSerious visual impairmentBlindness

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River Blindness primarily affects the tropics of Africa and the Americas

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•36 countries• 29 in sub-Saharan Africa• 6 in Latin America• Yemen

•120 million people at risk• 96 percent in Africa

•Estimated 18 million infected• 99 percent in Africa

99 percent of River Blindness cases occur in Africa

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Ivermectin is a broad-spectrum antiparasitic that can be used to treat River Blindness

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Ivermectin doesn’t kill adult worms, but prevents themfrom producing additional offspring

•Drug binds to and activates glutamate-gated chloride channels

•By activating channels, drug causes inhibitory postsynaptic potential

•Microfilaria experience paralysis and then death

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What is Being Done

APOC: African Programme for Onchocerciasis Control (1995)

The Carter Center (1996)

IDP: Ivermectin Distribution Program (1989-1994)

Mectizan Donation Program (1987)

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APOC countries: Angola, Burundi, Cameroon, Central African Republic, Chad, Congo, Democratic Republic of Congo, Ethiopia, Equatorial Guinea, Gabon, Kenya, Liberia, Malawi, Mozambique, Nigeria, Rwanda, Sudan, Tanzania and Uganda.

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http://www.who.int/blindness/partnerships/onchocerciasis_disease_information/en/index.html

http://emedicine.medscape.com/article/217776-overview

http://www.irishhealth.com/article.html?id=285

http://news.bbc.co.uk/2/hi/health/6753003.stm

http://www.stanford.edu/class/humbio103/ParaSites2006/Onchocerciasis/history%20of%20discovery.html

http://www.cartercenter.org/health/river_blindness/index.html

http://www.cartercenter.org/health/river_blindness/index.html

http://www.mectizan.org/onchocerciasis-maps

http://www.dpd.cdc.gov/dpdx/html/frames/af/filariasis/body_Filariasis_o_volvulus.htm

http://emedicine.medscape.com/article/224309-overview