Ft. Cutts et al., CONTROL OF RUBELLA AND CONGENITAL-RUBELLA SYNDROME (CRS) IN DEVELOPING-COUNTRIES .1. BURDEN OF DISEASE FROM CRS, Bulletin of the World Health Organization, 75(1), 1997, pp. 55-68
Congenital rubella syndrome (CRS) can lead to deafness, heart disease,
and cataracts, and a variety of other permanent manifestations. In de
veloping countries, the burden of CRS has been assessed as follows: by
surveillance of CRS; by surveillance of acquired rubella; by age-stra
tified serosurveys; and by serosurveys documenting the rubella suscept
ibility of women of childbearing age. During rubella outbreaks, rates
of CRS per 1000 live births were at least 1.7 in Israel, 1.7 in Jamaic
a, 0.7 in Oman, 2.2 in Panama, 1.5 in Singapore, 0.9 in Sri Lanka, and
0.6 in Trinidad and Tobago. These rates are similar to those reported
from industrialized countries during the pre-vaccine era. Special stu
dies of CRS have been reported from all WHO regions. Rubella surveilla
nce data show that epidemics occur every 4-7 years, similar to the sit
uation in Europe during the pre-vaccination era. In developing countri
es, the estimated average age at infection varies from 2-3 years to 8
years. For 45 developing countries we identified serosurveys of women
of childbearing age that had enrolled greater than or equal to 100 ind
ividuals. The proportion of women who remained susceptible to rubella
(e.g. seronegative) was < 10% in 13 countries, 10-24% in 20 countries,
and greater than or equal to 25% in 12 countries. Discussed are metho
ds to improve the surveillance of rubella and CRS in developing countr
ies.