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Human African Trypanosomiasis

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    Human trypanosomiasis (African sleeping sickness) is caused by intercellular hemoflagellated protozoa of the genus Trypanosoma and transmitted by Glossina sp (tsetse fly), the intermediate host.

    It ranks 7th on the WHO TDR list and belongs to category 1 of the current Tropical Disease Classification.

    • 60 million people in 36 countries are at risk.
    • Annually, 300,000 to 500,000 cases
    • Epidemic in 3 countries
    • Highly endemic in 12 countries
    • Endemic status is unknown in 13 countries including Nigeria.
    • Restricted to tsetse fly belts of Africa.

    There are 2 recognizable forms:

    • • The West African form (The Gambian Trypanosomiasis)
    • • The East African form (The Rhodesian trypanosomiasis.

    In the true sense, Gambian is the form more associated with sleeping sickness.

    West African Sleeping Sickness (WASS)

    Etiological agent: Trypanosoma gambiense

    Intermediate host: Glossina brucei palpalis and G. tachinoides

    Definitive host: man

    Reservoir host: man

    Disease type: chronic

    East African Sleeping Sickness (EASS)

    Etiological agent: Trypanosoma rhodesiense

    Intermediate hosts: Glossina mortisans and G. pallidepes

    Man: accidental host and plays less important role as a reservoir because he is too sick to go out and infect tsetse fly.

    Reservoir hosts: wild games (antelopes, etc.)

    Transmission: animal to animal, animal to man, man to man.

    Note: East African Sleeping Sickness in man is more or less a zoonosis.

    Transmission is by glossina species (tsetse flies) male and female.

    They are blood sucking flies found in

    • Vegetations by rivers and lakes
    • Gallery forest
    • Vast stretches of wooden savannah.
    Tse-tse fly

    Occupational disease of farmers, animal rearers, fishermen etc. who are exposed to the bites of tsetse fly in their ecological habitat, e.g. riverine forests.

    T. Brucie gambiense causes chronic infection while T. Brucie rhodesiense causes acute infection.

    For WASS, in the early phase they are:

    • Fever
    • Headache
    • Joint pain

    In the later phase when the CNS is involved,

    • Meningoencephalitis
    • Meningomyelitis
    • Emanciation
    • Mental and physical apathy
    • Tremors of the tongue
    • Speech impairment
    • Nervousness
    • Drowsness (sleeping sickness)
    • Lethargy
    • Coma and death

    For EASS, acute and very virulent. Incubation period is 2-3weeks. It is characterized by

    • Fever
    • Adenitis
    • Rash
    • Edema
    • Hepatomegaly
    • Splenomegaly
    • It is very virulent and immediately fatal before detection and commencement of treatment.

    • Xeno diagnosis
    • Intra dermal tests
    • Immunological tests including card agglutination methods (when antibody is present in the blood, there will be visible agglutination on the card).
    • Winter bottom sign (Negrolethargy) i.e. enlarged posterior cervical lymph node.

    Management of Trypanosomiasis is complex and requires careful evaluation with appropriate considerations (precautions) for the following:

    • Concommitant infections of the liver and kidney with respect to the capabilities of the liver to tolerate suramin, pentamidine etc.
    • The type and stage of the infection and the meticulous assessment of the CNS involvement.
    • Blood-Brain barrier especially when the CNS is involved as in Gambian trypanosomiasis.
    • Patient’s nutritional status because malnutrition might lead to death or worsen the disease.
    • Drug of choice:
      • Suramin (Bayer 205) = Antrypol
      • Pentamidine (not active against T. B rhodesiense)
      • Trypanrsamide
      • Mel B (Arsolbal melarsoprol) = only drug used routinely for patients with CNS involvement.
      • Furacin
    • Exceptional propensity of Trypanosomes for rapid protein turn over and mutation. This can lead to development of resistance rapidly.

    Chemotherapy

    Commonly used drugs are pentamidine, suramin and melarsoprol.

    Control of Tse-tse fly

    Chemical control: selective ground spraying of resting sites with synthetic pyrethroids (e.g., deltamethrine).

    Land use management: large scale tsetse reclamation projects are motivated by the current impact of urbanization and the need to accommodate a rapidly expanding human population aspiring to a higher standard of living.

    Biological methods: use of predators and parasites as well as genetic control. Genetic methods include release of males sterilized by irradiation or chemical means among others.

    Insecticide-impregnated traps and screens: these are playing an important role in the control of the vector. They are effective, nonpolluting and ideally suited to the primary health care concept.

    Odor attractants have been additionally used to lure G. mortisans group flies. The trap chosen must be appropriate for the tsetse specie present in the area.

    • For the palpalis group, the biconical, vavova or pyramidal trap are used.
    • For the mortisans group, Beta or F-2 traps are used.
    Tse-tse fly trap
    Tse-tse fly trap

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