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Action for child survival: elimination of Haemophilus influenzae type b meningitis in Uganda
Rosamund F Lewis1, Annet Kisakye, Bradford D Gessner
1Uganda Country Office, World Health Organization, Kampala, Uganda. rosamund_lewis@yahoo.ca
Insights
Haemophilus influenzae type b (Hib) vaccine introduction in Uganda dramatically reduced Hib meningitis incidence by nearly 90% within four years. The vaccine is highly effective, preventing thousands of deaths and cases of pneumonia and meningitis annually.
Area of Science:
- * Public Health & Epidemiology
- * Vaccinology & Infectious Diseases
Background:
- * Haemophilus influenzae type b (Hib) poses a significant threat, causing meningitis and pneumonia in young children.
- * Uganda implemented Hib vaccine to mitigate the burden of Hib disease.
Purpose of the Study:
- * To evaluate the public health impact of introducing the Hib vaccine in Uganda.
- * To estimate the effectiveness of the Hib vaccine in a real-world setting.
Main Methods:
- * Review of surveillance data for acute bacterial meningitis in children aged 0-59 months from sentinel sites (July 2001-June 2007).
- * Case-control study to determine Hib vaccine effectiveness.
- * Estimation of vaccine-preventable cases and deaths.
Main Results:
- * Hib meningitis incidence decreased from 88 to 13 cases per 100,000 children within 4 years post-vaccination.
- * Vaccine effectiveness was 93% against confirmed Hib meningitis and 53% against purulent meningitis of unknown cause.
- * Estimated annual prevention of 28,000 pneumonia/meningitis cases, 5,000 deaths, and 1,000 severe sequelae.
Conclusions:
- * Hib vaccination has nearly eliminated Hib meningitis in Uganda within five years.
- * Sustained benefits require ongoing surveillance, vaccine financing, and a strong immunization program.
Objective:
To guide immunization policy, we determined the public health benefit of introducing Haemophilus influenzae type b (Hib) vaccine in Uganda and estimated the vaccine effectiveness.
Methods:
Surveillance data for acute bacterial meningitis among children aged 0-59 months were reviewed from three hospital sentinel sites, for July 2001 to June 2007, to determine the incidence of Hib meningitis, the effectiveness of Hib vaccine with a case-control design, and the number of vaccine-preventable cases and deaths of Hib disease in Uganda.
Findings:
Of the 13 978 children from 17 districts with suspected bacterial meningitis, 269 had confirmed Hib meningitis, declining from 69 patients in the prevaccine year (2001-2002) to three in 2006-2007. Hib meningitis incidence dropped from 88 cases per 100,000 children aged < 5 years in the year before vaccine introduction to 13 within 4 years, and to near zero in the fifth year. Vaccine effectiveness for 2 or more doses was 93% (95% confidence interval, CI: 69-99) against confirmed Hib meningitis and 53% (95% CI: 11-68) against purulent meningitis of unknown cause. In Uganda, Hib vaccine prevents an estimated 28 000 cases of pneumonia and meningitis, 5000 deaths and 1000 severe meningitis sequelae each year.
Conclusion:
Infant immunization with Hib vaccine has virtually eliminated Hib meningitis in Uganda within 5 years. Ensuring long-term benefits of Hib vaccine urgently requires sustainable vaccine financing, high-quality ongoing surveillance, and a health sector able to deliver a robust immunization programme.
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