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WHO program on AIDS

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AB

STRACTS AND REPORTS

W

HO PROGRAM ON AIDS

The WHO program on the acquired immunodeficiency syndrome (AIDS) was presented to and discussed by the Seventy-Seventh Session of the WHO Executive Board on 17 January 1986. The Board acknowledged that AIDS and other manifestations of LAVIHTLVIII

infection were becoming a major public health concern in many areas of the world and recognized that international alertness and preparedness were ur- gently required. The Board also considered that public information and edu- cation, as well as the assurance and use of safe blood and blood products, were at present the only measures available to limit the further spread of

AIDS. In view of these facts, the Board adopted a resolution (EB77.Rl2) urg- ing WHO Member States:

(1) to maintain vigilance and carry out public health strategies for the prevention and control of AIDS as neces- sary;

(2) to share information, in all open- ness, with the Organization and other Member States on AIDS incidence, the seroprevalence of LAVIHTIY-III, laboratory methods, clinical experience, and approaches to prevention and control of LAVIHTIY-III infection;

(3) to call upon the Organization as necessary for support in the prevention and control of AIDS and other LAV/ HTLV-III infections.

The resolution of the Executive Board also included the following requests for action by WHO:

(1) to further develop activities within the WHO program on AIDS:

(a) to ensure the exchange of infor- mation on LAVIHTLV-III, its epidemiology, laboratory and clinical aspects, and activities directed at its prevention and control;

(b) to prepare and distribute guide- lines, manuals, and educational materials;

(c) to assess commercially available

LAVIHTLY-III antibody test kits, develop a simple, inexpensive test for field application, and establish WHO reference reagents;

(d) to cooperate with Member States in the development of national programs for the containment of LAV/HTLV-

III infection;

(e) to advise Member States on the

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(f) to promote research on the devel- opment of therapeutic agents and vaccines, simian retroviruses, and epide- miologic and behavioral aspects of LAVIHTLV-111 infection;

(g) to coordinate collaborative clinical trials of antiviral and other drugs that have been demonstrated in human early-phase trials to show efficacy in the treatment of AIDS and/or the AIDS-

related complex;

(2) to seek additional funds from ex- trabudgetary sources for the support of national and collective programs of surveillance and epidemiology, laboratory services, clinical activities, and pre- vention and control measures.

Source: World Health Organization, Weekb Epidemiological Reco&61(5):35, 1986.

@World Health Organization-1985

T

HE CHEMOTHERAPY OF

SCHIS’I’OSOMIASIS CONTROL

Schistosomiasis is a complex disease transmitted to man by infection with the freshwater parasites Schis~osoma japonicum, S. baematobiam, S. intercdattzlm, S. mansoni, and S. mekongi.

Today approximately 200 million people are infected and SOO-600 million are exposed to the threat of infection. Schistosomiasis is widely distributed geographically, ranging across China, the Philippines, Indonesia, the Ara- bian peninsula, various countries of North Africa, the whole of sub-Saharan Africa, several South American countries, and certain Caribbean islands. Furthermore, with the increase in the number of agricultural, hydroelectric, and other water resource projects in endemic countries, transmission of the disease is increasing.

The primary objective of chemother- apy in schistosomiasis control is to reduce human morbidity from the disease to levels that do not present a threat to public health. In general, this goal is achieved when all remaining infections caused by S. haematobizlm are below

50 eggs per 10 ml in a random sample of urine, or when all remaining infec- tions from S. mansoni are below 100 eggs per gram of feces.

After 70 years’ experience with chemotherapeutic agents for the control of schistosomiasis, some of which were toxic, the recent development of safe and effective oral drugs makes possible a strategy aimed at the direct and rapid control of the disease. Cur- rently the following three drugs are available for this purpose:

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