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Vol. 15. Issue 3.
Pages 215-219 (May - June 2011)
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Vol. 15. Issue 3.
Pages 215-219 (May - June 2011)
Open Access
Rotavirus infection in a tertiary hospital: laboratory diagnosis and impact of immunization on pediatric hospitalization
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2546
Luciane Aparecida Pereira1, Sonia Mara Raboni2,
Corresponding author
sraboni@ufpr.br//sonia
raboni@pq.cnpq.br

Sonia Mara Raboni Laboratório de Virologia, Hospital de Clínicas, UFPR Rua Padre Camargo, 280, 2nd floor, Room 202 Alto da XV, Curitiba, Paraná, Brazil 82060-240, Phone: 55 41 3360-7974, Fax: 55 41 3360-1811.
, Meri B. Nogueira3, Luine R. Vidal4, Sergio Monteiro de Almeida5, Maria C. Debur6, Cristina Cruz7
1 Biologist in the Laboratory of Virology, Universidade Federal do Paraná, Brazil
2 Associated Professor Infectious Diseases Departament, Universidade Federal do Paraná, Brazil
3 Biochemistry Laboratory of Virology, Universidade Federal do Paraná, Brazil
4 Biochemistry Laboratory of Virology, Universidade Federal do Paraná, Brazil
5 Neurologist Laboratory of Virology, Universidade Federal do Paraná, Brazil
6 Biochemistry Central Laboratory of Public Health, Secretaria Estadual de Saúde do Paraná, Brazil
7 Pediatric Infectologist Associated Professor, Universidade Federal do Paraná, Brazil
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Abstract
Background and objectives

Rotavirus (RV) is the main etiological agent of diarrhea in childhood; its laboratory diagnosis is crucial to guide the clinical management and prevention of its spread. RV immunization was introduced in Brazilian 6-month-old children in 2006. The present study was aimed to evaluate three methodologies used for human RV detection in stool samples obtained from patients hospitalized due to gastroenteritis in a teaching hospital and report the impact of RV immunization in hospitalization by diarrhea.

Methods

293 stool samples collected in the 2001-2008 period were analyzed by enzyme immunoassay (EIA), latex agglutination (LA) and polyacrylamide gel electrophoresis (PAGE).

Results

Rotavirus was detected in 34.8% of samples by LA assay, 28.3% of samples by EIA assay and in 25.6% of samples by PAGE assay. Considering the PAGE method as gold standard, the sensitivity, specificity and accuracy of EIA were 94.6%, 94.4% and 94.5%, and to LA were 82.6%, 81.6% and 81.9%, respectively.

Conclusions

These results indicate that antigen detection by EIA is a rapid, sensitive and specific method, and could be used in large-scale applications for screening stool samples suspected of RV infection. This study showed decreased incidence of RV infection in hospitalized children prior to the implementation of the national immunization program against RV.

Keywords:
rotavirus
diarrhea
immunoenzyme techniques
latex fixation tests
electrophoresis
polyacrylamide gel
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