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Published on: February 15, 2013
Defining the burden of pneumonia in children preventable by vaccination against Haemophilus influenzae type b
1Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Insights
The Haemophilus influenzae type b (Hib) vaccine significantly reduces pneumonia hospitalizations in young children. This Hib conjugate vaccine prevented 26% of pneumonia cases with likely bacterial infection indicators.
Area of Science:
- Pediatrics
- Infectious Diseases
- Vaccinology
Background:
- Pneumonia is a major cause of hospitalization in infants and young children.
- Haemophilus influenzae type b (Hib) is a significant bacterial pathogen.
- The impact of Hib vaccination on pneumonia burden requires further elucidation.
Purpose of the Study:
- To assess the burden of pneumonia preventable by Haemophilus influenzae type b (Hib) vaccination.
- To evaluate the efficacy of the PRP-T Hib conjugate vaccine in preventing pneumonia hospitalizations.
Main Methods:
- A randomized controlled trial was conducted in Santiago, Chile.
- Infants received either the PRP-T Hib conjugate vaccine combined with DTP or DTP vaccine alone.
- Pneumonia was defined by hospitalization with indicators of likely bacterial infection.
Main Results:
- The PRP-T vaccine reduced pneumonia incidence by 22% in children aged 4-23 months.
- Specifically, it reduced pneumonia with alveolar consolidation or pleural effusion by 22%.
- Overall protection against pneumonia with likely bacterial infection indicators was 26%, preventing 2.5 cases per 1000 children annually.
Conclusions:
- Hib vaccination offers substantial protection against nonbacteremic pneumonia, especially cases with signs of bacterial infection.
- Hib vaccination prevented significantly more nonbacteremic pneumonia cases than meningitis cases in infants.
- The full impact of Hib vaccination on pneumonia may be underestimated by traditional culture methods.
Objectives:
To determine the burden of pneumonia requiring hospitalization in infants and young children preventable by vaccination against Haemophilus influenzae type b (Hib).
Design:
Vaccination centers in Santiago, Chile, were randomly selected to administer PRP-T, an Hib conjugate vaccine, combined with diphtheria-tetanus toxoids-pertussis (DTP) vaccine or DTP alone.
Subjects:
Infants who received > or =2 doses of DTP or DTP and Hib conjugate vaccine combined.
Main Outcome Measures:
Pneumonia episodes leading to hospitalization accompanied by indicators of likely bacterial infection including radiologic evidence of alveolar consolidation or pleural effusion, an elevated erythrocyte sedimentation rate (> or =40 mm/h) or bronchial breath sounds on auscultation.
Results:
In participants age 4 to 23 months, PRP-T reduced the incidence of pneumonia associated with alveolar consolidation or pleural effusion by 22% (95% confidence interval, -7 to 43) from 5.0 to 3.9 episodes per 1000 children per year. When the pneumonia case definition included any of the following, alveolar consolidation, pleural effusion, erythrocyte sedimentation rate > or =40 mm/h or bronchial breath sounds, PRP-T provided 26% protection (95% confidence interval, 7 to 44) and prevented 2.5 episodes per 1000 children per year.
Conclusions:
Hib vaccine provides substantial protection against nonbacteremic pneumonia, particularly those cases with alveolar consolidation, pleural effusion or other signs of likely bacterial infection. Hib vaccination prevented approximately 5 times as many nonbacteremic pneumonia cases in infants as meningitis cases, thus indicating that the largest part of the effect of Hib vaccination might be undetectable by routine culture methods.
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