Streptococcal Pneumonia Clinical Trial
Official title:
Monitoring Pneumococcal Conjugate Vaccine Introduction in Cambodia: A Study of Streptococcus Pneumoniae Colonisation, Pneumonia and Invasive Disease in Cambodian Children
Streptococcus pneumoniae (the pneumococcus) remains a leading cause of childhood mortality
and morbidity. Between 2007 and 2012, Angkor Hospital for Children (AHC), Siem Reap, Cambodia
documented that S. pneumoniae was responsible for around 10% of bloodstream infections in
hospitalised children, with a case fatality rate of 15.6%.
The use of pneumococcal conjugate vaccines (PCV), covering between 7 and 13 of the >90
pneumococcal serotypes, has resulted in significant declines in invasive pneumococcal disease
(IPD) incidence in countries where they are included in routine childhood immunisation
schedules. Paediatric radiologic pneumonia incidence is also reduced by PCV, but the impact
on clinical pneumonia is minimal. The vaccines have had an effect on reducing the burden of
drug resistant IPD, although this may not be sustained. Given the large number of serotypes
not included in the current PCV formulations, it is not surprising that initial declines in
overall IPD incidence have been eroded by, for the time being, small increases in IPD due to
non-vaccine serotypes. To date most data on this serotype replacement disease has come from
high-income countries. It less clear how much serotype replacement will occur in low and
middle income countries, where pre-PCV disease incidence is generally higher and other
factors, such as unregulated antimicrobial consumption, may play a role in encouraging
non-vaccine serotype infections.
Nasopharyngeal colonisation by S. pneumoniae is common in childhood and is an essential
prerequisite for invasive disease. Surveillance of pneumococcal colonisation can provide
important data regarding serotype replacement and disease-associated serotypes, and may also
allow prediction of likely IPD incidence changes post-vaccine introduction. A recent study of
pneumococcal colonisation in children attending the AHC out-patients has documented an
overall colonisation prevalence of approximately 65%.
In January 2015, Cambodia will introduce the 13-valent PCV (PCV13; serotypes covered 1, 3, 4,
5, 6A, 6B, 7F, 9V, 14, 18C, 19F, 19A, 23F). The vaccine will be rolled out nationally with a
3+0 dosing schedule (6, 10 and 14 weeks) and no catch up campaign. There is no robust
national surveillance system in place to monitor the effects of PCV13 introduction.
n/a
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