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Pesquisa | Influenza A (H1N1)

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Resultados  1-10 de 10
1.

Contribution of a rapid influenza diagnostic test to manage hospitalized patients with suspected influenza.

Autor(es): Busson, Laurent; Mahadeb, Bhavna; De Foor, Marc; Vandenberg, Olivier; Hallin, Marie
Fonte: Diagn Microbiol Infect Dis;87(3): 238-242, 2017 Mar.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 27939284
Resumo: AIM: To evaluate the performances of the Alere i influenza A&B test and to appraise its contribution to patient management. METHODS: In total, 267 samples were tested. Influenza A and B PCR was performed as the reference. For each positive result, the supervising physician was contacted to collect data regarding patient management. FINDINGS: The overall sensitivity and specificity of the Alere i were 91.4% and 97.6% for influenza A and 54.5% and 98.8% for influenza B, respectively. More spe (mais)
2.

Prospective evaluation of the Alere i Influenza A&B nucleic acid amplification versus Xpert Flu/RSV.

Autor(es): Nguyen Van, J C; Caméléna, F; Dahoun, M; Pilmis, B; Mizrahi, A; Lourtet, J; Behillil, S; Enouf, V; Le Monnier, A
Fonte: Diagn Microbiol Infect Dis;85(1): 19-22, 2016 May.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 26899154
Resumo: The rapid and accurate detection of influenza virus in respiratory specimens is required for optimal management of patients with acute respiratory infections. Because of the variability of the symptoms and the numerous other causes of influenza-like illness, the diagnosis of influenza cannot be made on the basis of clinical criteria alone. Thus, rapid influenza diagnostic tests have been developed such as the Alere i Influenza A&B isothermal nucleic acid assay. We prospectively evaluated th (mais)
3.

Severe sensitivity loss in an influenza A molecular assay due to antigenic drift variants during the 2014/15 influenza season.

Autor(es): Overmeire, Yarah; Vanlaere, Elke; Hombrouck, Anneleen; De Beenhouwer, Hans; Simons, Guus; Brink, Antoinette; Van den Abeele, Anne-Marie; Verfaillie, Charlotte; Van Acker, Jos
Fonte: Diagn Microbiol Infect Dis;85(1): 42-6, 2016 May.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 26964723
Resumo: The 2014-2015 influenza season in Belgium was dominated by the circulation of 2 influenza A(H3N2) subgroups: 3C.2a and 3C.3b. Analysis of 166 nasopharyngeal aspirates, collected in patients with respiratory illness at the start of the epidemic season, showed a decreased sensitivity for the detection of influenza A(H3N2)/3C.2a using a commercially available multiplex assay. Gene sequencing of the matrix protein showed a point mutation (C163T) leading to a mismatch with the assay probes.
4.

Performance of rapid SOFIA Influenza A+B test compared to Luminex x-TAG respiratory viral panel assay in the diagnosis of influenza A, B, and subtype H3.

Autor(es): Selove, W; Rao, L V
Fonte: J Investig Med;64(4): 905-7, 2016 Apr.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 26911275
Resumo: Influenza is an acute respiratory illness caused by influenza A or B viruses that occur in outbreaks, mainly during the winter season. Rapid laboratory diagnosis of influenza can help guide the clinical management of suspected patients effectively. Clinical sensitivities and specificities of the rapid influenza diagnostic tests have varied considerably in the literature. Most of these studies are evaluated using previously frozen or stored specimens that had previously tested positive. This (mais)
5.

Performance of the Quidel Sofia rapid influenza diagnostic test during the 2012-2013 and 2013-2014 influenza seasons.

Autor(es): Kammerer, Peter E; Radin, Jennifer M; Hawksworth, Anthony W; Myers, Chris A; Brice, Gary T
Fonte: Influenza Other Respir Viruses;10(3): 220-3, 2016 May.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 26920652
Resumo: The Quidel Sofia Influenza A+B Fluorescent Immunoassay was used to test nasal swab specimens from patients with influenza-like illness at US-Mexico border-area clinics in the 2012-2013 and 2013-2014 influenza seasons. Compared with real-time reverse transcription polymerase chain reaction, the overall sensitivities and specificities were 83% and 81%, and 62% and 93%, respectively.
6.

Evaluation of twenty-two rapid antigen detection tests in the diagnosis of Equine Influenza caused by viruses of H3N8 subtype.

Autor(es): Yamanaka, Takashi; Nemoto, Manabu; Bannai, Hiroshi; Tsujimura, Koji; Kondo, Takashi; Matsumura, Tomio; Gildea, Sarah; Cullinane, Ann
Fonte: Influenza Other Respir Viruses;10(2): 127-33, 2016 Mar.
MEDLINE - Literatura Internacional em Ciências da Saúde PMID: 26568369
Resumo: BACKGROUND: Equine influenza (EI) is a highly contagious disease caused by viruses of the H3N8 subtype. The rapid diagnosis of EI is essential to reduce the disease spread. Many rapid antigen detection (RAD) tests for diagnosing human influenza are available, but their ability to diagnose EI has not been systematically evaluated. OBJECTIVES: The aim of this study was to compare the performance of 22 RAD tests in the diagnosis of EI. METHODS: The 22 RAD tests were performed on fivefold seria (mais)
7.

Performance of a commercial assay for the diagnosis of influenza A (H1N1) infection in comparison to the Centers for Disease Control and Prevention protocol of real time RT-PCR/ Evaluación del desempeño de un equipo comercial para el diagnóstico de influenza A (H1N1) en comparación con el protocolo de RT-PCR en tiempo real diseñado por los Centros de Control y Prevención de Enfermedades (CDC)

Autor(es): Barbás, María G; De Leon, Juan; Kademian, Silvia; Baumeister, Elsa; Castro, Gonzalo M; Gallego, Sandra V; Cudolá, Analía
Fonte: Rev Argent Microbiol;44(1): 0-0, Mar. 2012. tab
LILACS - Literatura Latino-Americana e do Caribe em Ciências da Saúde ID: 639714
Resumo: At the time of influenza A (H1N1) emergency, the WHO responded with remarkable speed by releasing guidelines and a protocol for a real-time RT-PCR assay (rRT-PCR). The aim of the present study was to evalúate the performance of the "Real Time Ready Influenza A/H1N1 Detection Set" (June 2009)-Roche kit in comparison to the CDC reference rRT-PCR protocol. The overall sensitivity of the Roche assay for detection of the Inf A gene in the presence or absence of the H1 gene was 74.5 %. The sensi (mais)
10.

Fe de erratas: encefalitis herpética. Serie clínica de 15 casos confirmados por reacción de polimerasa en cadena

Autor(es): A., Fica; Pérez, C; Reyes, P; Gallardo, S; Calvo, X; Salinas, A. M
Fonte: Rev Chilena Infectol;22(2): 215-215, jun. 2005.
LILACS - Literatura Latino-Americana e do Caribe em Ciências da Saúde ID: 417258
Resultados  1-10 de 10