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Analysis of Invasive Haemophilus influenzae Infections after Extensive Vaccination against H. influenzae Type b

Authors :
Belén Aracil
José Campos
Edurne Lázaro
Jesús Oteo
María Pérez-Vázquez
Federico Román
Francisco J. de Abajo
Margarita Hernando
Source :
Journal of Clinical Microbiology. 42:524-529
Publication Year :
2004
Publisher :
American Society for Microbiology, 2004.

Abstract

Little clinical and microbiological information is available about invasive Haemophilus influenzae infection after widespread vaccination against H. influenzae type b (Hib). We conducted an active community surveillance study on invasive H. influenzae during a 2-year period in a community of more than 5 million people after vaccination against Hib in children was introduced. The median incidence was 16.3 cases/100,000 persons per year in children less than 1-year-old and 4.41 cases/100,000 persons in children less than H. influenzae -infected patients, 74.3% had underlying predisposing conditions, including impaired immunity and respiratory diseases. A total of 73.6% of the isolates were nontypeable and 16.5, 6.6, and 3.3% were types b, f, and e, respectively. Infections due to capsulated strains b, e, and f were evenly distributed between children and adults. Ampicillin and cotrimoxazole resistance occurred at frequencies of 24.2 and 48.4%, respectively. Antibiotic resistance was more prevalent in capsulated than in noncapsulated H. influenzae . Invasive isolates were highly resistant to antibiotics that were used infrequently in the community. Nontypeable H. influenzae were genetically much more heterogeneous than capsulated strains. Capsule-deficient mutants (b − ) were not detected. Plasmid carriage was linked to antibiotic resistance and capsulated strains. Over the study period, the incidence of invasive H. influenzae infections, either encapsulated or not, did not increase. In the post-Hib vaccination era, most invasive infections were due to noncapsulated strains and occurred in the extreme ages of life in patients with predisposing conditions.

Details

ISSN :
1098660X and 00951137
Volume :
42
Database :
OpenAIRE
Journal :
Journal of Clinical Microbiology
Accession number :
edsair.doi.dedup.....379f24bfdd40e8a599adae6b4cbe0434
Full Text :
https://doi.org/10.1128/jcm.42.2.524-529.2004