Onchocerciasis continues to be a major cause of blindness, particularl
y in those sub-Saharan African countries which are outside the area of
West Africa monitored by the Onchocerciasis Control Programme (OCP).
Onchocercal ocular disease and blindness develop as a result of long e
xposure to onchocercal infection. Until 1987, suramin and diethylcarba
mazine were the only drugs available for the treatment of onchocercias
is and they could not be used for community therapy because of their t
oxicity and the dosage schedules required. The registration of Mectiza
n (ivermectin, MSD) for treatment of human onchocerciasis in 1987, and
the donation of this drug by Merck & Co. for as long as it is needed,
provided a new opportunity for the safe treatment and control of the
disease. The data available on the impact of repeated doses of Mectiza
n on ocular onchocercal disease indicate a significant reduction of oc
ular microfilarial loads and regression of early lesions of the anteri
or segment, including iridocyclitis and sclerosing keratitis. Such imp
rovements are seen more rapidly when Mectizan is used than when onchoc
erciasis is limited by vector control alone. Mectizan treatment also h
as a beneficial effect on onchocercal optic-nerve disease and visual-f
ield loss. Long-term maintenance of Mectizan therapy should lead to a
reduction in the prevalence of blindness in endemic communities.