22 results on '"Casas Flecha I"'
Search Results
2. Absence of SARS-CoV-2 RNA detection in tissue samples of COVID-19-related cutaneous lesions analyzed by real-time RT-PCR
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García‐Gil, M. F., Monte‐Serrano, J., García García, M., Prieto‐Torres, L., Pascual‐del‐Riquelme, A. J., Casas Flecha, I., Ara‐Martín, M., Hospital Clínico Universitario Lozano Blesa (España), and Instituto de Investigación Sanitaria Aragón
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Pathology ,medicine.medical_specialty ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Dermatology ,medicine.disease_cause ,Real-Time Polymerase Chain Reaction ,Sensitivity and Specificity ,Virus ,law.invention ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,law ,Biopsy ,Medicine ,Humans ,Letters to the Editor ,Letter to the Editor ,Polymerase chain reaction ,Coronavirus ,integumentary system ,medicine.diagnostic_test ,business.industry ,SARS-CoV-2 ,Reverse Transcriptase Polymerase Chain Reaction ,RNA ,COVID-19 ,Reverse transcriptase ,Infectious Diseases ,Real-time polymerase chain reaction ,030220 oncology & carcinogenesis ,RNA, Viral ,business - Abstract
Despite the increasing knowledge of COVID-19-related skin lesions, few studies have attempted to demonstrate the presence of the virus in skin lesions by real-time reverse transcriptase polymerase chain reaction (RT-PCR).1,2 The objective of this research was to determine through RT-PCR whether SARS-CoV-2 was present in skin biopsies of patients with cutaneous manifestations related to COVID-19.
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- 2021
3. A multicenter randomized open-label clinical trial for convalescent plasma in patients hospitalized with COVID-19 pneumonia
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Avendano-Sola, C, Ramos-Martinez, A, Munez-Rubio, E, Ruiz-Antoran, B, de Molina, RM, Torres, F, Fernandez-Cruz, A, Calderon-Parra, J, Payares-Herrera, C, de Santiago, AD, Romera-Martinez, I, Pintos, I, Lora-Tamayo, J, Mancheno-Losa, M, Paciello, ML, Martinez-Gonzalez, AL, Vidan-Estevez, J, Nunez-Orantos, MJ, Saez-Serrano, MI, Porras-Leal, ML, Jarilla-Fernandez, MC, Villares, P, de Oteyza, JP, Ramos-Garrido, A, Blanco, L, Madrigal-Sanchez, ME, Rubio-Batlles, M, Velasco-Iglesias, A, Pano-Pardo, JR, Moreno-Chulilla, JA, Muniz-Diaz, E, Casas-Flecha, I, Perez-Olmeda, M, Garcia-Perez, J, Alcami, J, Bueno, JL, Duarte, RF, Bösch A., and Villegas da Ros, Carolina
- Abstract
BACKGROUND. Passive immunotherapy with convalescent plasma (CP) is a potential treatment for COVID-19. Evidence from controlled clinical trials is inconclusive. METHODS. We conducted a randomized, open-label, controlled clinical trial at 27 hospitals in Spain. Patients had to be admitted for COVID-19 pneumonia within 7 days from symptom onset and not on mechanical ventilation or high-flow oxygen devices. Patients were randomized 1:1 to treatment with CP in addition to standard of care (SOC) or to the control arm receiving only SOC. The primary endpoint was the proportion of patients in categories 5 (noninvasive ventilation or high-flow oxygen), 6 (invasive mechanical ventilation or extracorporeal membrane oxygenation [ECMO]), or 7 (death) at 14 days. Primary analysis was performed in the intention-to-treat population. RESULTS. Between April 4, 2020, and February 5, 2021, 350 patients were randomly assigned to either CP (n = 179) or SOC (n = 171). At 14 days, proportion of patients in categories 5, 6, or 7 was 11.7% in the CP group versus 16.4% in the control group (P = 0.205). The difference was greater at 28 days, with 8.4% of patients in categories 5-7 in the CP group versus 17.0% in the control group (P = 0.021). The difference in overall survival did not reach statistical significance (HR 0.46, 95% CI 0.19-1.14, log-rank P = 0.087). CONCLUSION. CP showed a significant benefit in preventing progression to noninvasive ventilation or high-flow oxygen, invasive mechanical ventilation or ECMO, or death at 28 days. The effect on the predefined primary endpoint at 14 days and the effect on overall survival were not statistically significant.
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- 2021
4. Infecciones por bocavirus humano en niños españoles: características clínicas y epidemiológicas de un virus respiratorio emergente
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García-García, M.L., Calvo Rey, C., Pozo Sánchez, F., Vázquez Álvarez, M.C., González Vergaz, A., Pérez-Breña, P., and Casas Flecha, I.
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- 2007
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5. Absence of SARS‐CoV‐2 RNA detection in tissue samples of COVID‐19‐related cutaneous lesions analyzed by real‐time RT‐PCR
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García‐Gil, M. F., primary, Monte‐Serrano, J., additional, García García, M., additional, Prieto‐Torres, L., additional, Pascual‐del‐Riquelme, A. J., additional, Casas Flecha, I., additional, and Ara‐Martín, M., additional
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- 2021
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6. Papel del rinovirus en las infecciones respiratorias en niños hospitalizados
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Calvo Rey, C., García García, M.ªL., Casas Flecha, I., Sánchez Mateos, M.F., Rodrigo García, G., de Cea Crespo, J.M.ª, and Pérez-Breña, P.
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- 2006
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7. Infecciones por virus de la gripe en menores de dos años
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Calvo Rey, C., García García, M.ªL., Casas Flecha, I., Martín del Valle, F., Centeno Jiménez, M., and Pérez-Breña, P.
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- 2005
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8. Infecciones respiratorias por metapneumovirus en lactantes hospitalizados
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García García, M.<ce:sup loc='post">a</ce:sup>L., Calvo Rey, C., Martín del Valle, F., López Huertas, M.R., Casas Flecha, I., Díaz-Delgado, R., and Pérez-Breña, P.
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- 2004
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9. Lactancia materna y protección contra las infecciones respiratorias en los primeros meses de vida
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Bueno Campaña, M.M., Calvo Rey, C., Jimeno Ruiz, S., Faustino Sánchez, M., Quevedo Teruel, S., Martínez Granero, M.Á., Delgado Iribarren, A., and Casas Flecha, I.
- Subjects
Respiratory tract infection ,Lactancia materna ,Breastfeeding ,Lactantes ,Infección respiratoria ,Infants - Abstract
Introducción: entre las ventajas de la lactancia materna (LM) se incluye su papel protector ante infecciones respiratorias (IR). Objetivos: describir el patrón de LM de una cohorte de recién nacidos (RN) y su protección contra las IR en el lactante. Material y métodos: estudio prospectivo de 316 RN, de las áreas 8 y 9 de Madrid, desde el nacimiento mediante llamadas telefónicas quincenales durante el invierno, registrando datos clínicos y epidemiológicos. Si presentaban sintomatología compatible con IR se recogió aspirado nasofaríngeo. Resultados: mil ochocientas sesenta y cinco llamadas (mediana: 4,2 [1-11]) y 106 visitas programadas. Al mes, el 56,1% recibía LM exclusiva; a los tres meses, el 39,4%, y a los cinco meses, el 31,9%. La LM exclusiva se mantuvo 65,1 días (desviación estándar: 43,49) y ningún factor se asoció a una mayor duración. Hubo 89 episodios de IR aguda. Los hermanos escolares multiplican por 1,74 (intervalo de confianza del 95% [IC 95%]: 1,12-2,72) el riesgo de IR en todos los estratos de duración de LM exclusiva. El riesgo de infección se multiplica por cinco (IC 95%: 2,07-12,19) si la LM exclusiva dura menos de un mes, por 9,8 (IC 95%: 4,06-23,66) si dura entre 30 y 60 días y por 3,4 (IC 95%: 1,28-9,19) si dura entre 60 y 90 días. Conclusiones: aunque muchos RN inician LM exclusiva, solo la tercera parte la mantiene a los cinco meses. Ningún factor se asoció a mayor duración de la misma. La LM es un factor protector de IR cuando dura más de 90 días. Se debe fomentar el mantenimiento de la LM más allá del tercer mes, especialmente en aquellos con hermanos escolares. Background: the protective role against respiratory infections is included among the advantages of breastfeeding (BF). Objective: to describe the pattern of BF in a cohort of newborns and its protective role against respiratory infections (RI) in the infant. Material and methods: a cohort of 316 newborns (NB) from Madrid Health Districts 8 and 9 was followed by telephone calls every fortnight during the winter season recording clinical and epidemiological data. Nasopharyngeal aspirate was obtained in every patient with symptoms compatible with RI. Results: one thousand, eight hundred and sixty-five phone calls [median: 4.2 (1-11)], and 106 scheduled visits were conducted. At the age of 1 month 56.1% of the infants were exclusively breastfed, at 3 months 39.4% and at 5 months 31.9%. The duration of BF was 65.1 days (SD: 43.49) and no factors were associated to a longer duration. Eighty nine acute RI were registered. The presence of siblings in school age increased the risk of RI by 1.74 (CI 95%: 1.12-2.72) in all the strata of duration of exclusive BF. The risk of RI increased by 5 (CI 95%: 2.07-12.19) if breastfeeding lasted less than 1 month, by 9,8 (CI 95%: 4,06-23,66) between 30-60 days and by 3,4 (CI 95%: 1.28-9,19) if it lasted 60-90 days. Conclusions: though many NB begin BF, only a third part of them go on with it at the age of 5 months. No covariant was associated with a longer duration. BF is a protector factor against RI when it lasts more than 90 days. So it must be promoted specially in those infants with siblings in school age.
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- 2011
10. Lactancia materna y protección contra las infecciones respiratorias en los primeros meses de vida
- Author
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Bueno Campaña, M.M., primary, Calvo Rey, C., additional, Jimeno Ruiz, S., additional, Faustino Sánchez, M., additional, Quevedo Teruel, S., additional, Martínez Granero, M.Á., additional, Delgado Iribarren, A., additional, and Casas Flecha, I., additional
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- 2011
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11. Infecciones respiratorias por metapneumovirus en lactantes hospitalizados
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Calvo Rey, C, primary, Martín del Valle, F, additional, López Huertas, MR, additional, Casas Flecha, I, additional, Díaz-Delgado, R, additional, Pérez-Breña, P, additional, and García García, MªL, additional
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- 2004
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12. Viral epidemic outbreaks and public health alerts studied at the National Centre of Microbiology during a two-year period (2012-2013,Brotes epidémicos y situaciones de alerta sanitaria de probable etiología vírica estudiados en el Centro Nacional de Microbiología durante el período 2012-2013
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Echevarría Mayo, J. M., Avellón Calvo, A. A., Cabrerizo Sanz, M., Casas Flecha, I., Echevarría Mayo, J. E., Ory Manchón, Fd Eo, ANA Negredo, Pozo Sánchez, F., Sánchez-Seco Fariñas, M. P., Tarragó Asensio, D., and Trallero Masó, G.
13. Excretion and viability of SARS-CoV-2 in feces and its association with the clinical outcome of COVID-19.
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Cerrada-Romero C, Berastegui-Cabrera J, Camacho-Martínez P, Goikoetxea-Aguirre J, Pérez-Palacios P, Santibáñez S, José Blanco-Vidal M, Valiente A, Alba J, Rodríguez-Álvarez R, Pascual Á, Oteo JA, Miguel Cisneros J, Pachón J, Casas-Flecha I, Cordero E, Pozo F, and Sánchez-Céspedes J
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- Adult, Cohort Studies, Feces, Humans, Prospective Studies, RNA, Viral genetics, COVID-19 diagnosis, SARS-CoV-2 genetics
- Abstract
The main objective was to evaluate the viability of the SARS-CoV-2 viral particles excreted in stools. In addition, we aimed to identify clinical factors associated with the detection of SARS-CoV-2 RNA in feces, and to determine if its presence is associated with an unfavorable clinical outcome, defined as intensive care unit (ICU) admission and/or death. A prospective multicenter cohort study of COVID-19 adult patients, with confirmed SARS-CoV-2 infection by RT-PCR assay in nasopharyngeal (NP) swabs admitted to four hospitals in Spain, from March 2020 to February 2021. Sixty-two adult COVID-19 patients had stool samples collected at admission and/or during the follow up, with a total of 79 stool samples. SARS-CoV-2 RNA was detected in stool samples from 27 (43.5%) out of the 62 patients. Replicative virus, measured by the generation of cytopathic effect in cell culture and subsequent RT-PCR confirmation of a decrease in the Ct values, was not found in any of these stool samples. Fecal virus excretion was not associated with the presence of gastrointestinal symptoms, or with differences in the evolution of COVID-19 patients. Our results suggest that SARS-CoV-2 replicative capacity is null or very limited in stool samples, and thus, the fecal-oral transmission of SARS-CoV-2 as an alternative infection route is highly unlikely. In our study, the detection of SARS-CoV-2 RNA in feces at the beginning of the disease is not associated with any clinical factor nor with an unfavorable clinical outcome., (© 2022. The Author(s).)
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- 2022
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14. A multicenter randomized open-label clinical trial for convalescent plasma in patients hospitalized with COVID-19 pneumonia.
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Avendaño-Solá C, Ramos-Martínez A, Muñez-Rubio E, Ruiz-Antorán B, Malo de Molina R, Torres F, Fernández-Cruz A, Calderón-Parra J, Payares-Herrera C, Díaz de Santiago A, Romera-Martínez I, Pintos I, Lora-Tamayo J, Mancheño-Losa M, Paciello ML, Martínez-González AL, Vidán-Estévez J, Nuñez-Orantos MJ, Saez-Serrano MI, Porras-Leal ML, Jarilla-Fernández MC, Villares P, de Oteyza JP, Ramos-Garrido A, Blanco L, Madrigal-Sánchez ME, Rubio-Batllés M, Velasco-Iglesias A, Paño-Pardo JR, Moreno-Chulilla JA, Muñiz-Díaz E, Casas-Flecha I, Pérez-Olmeda M, García-Pérez J, Alcamí J, Bueno JL, and Duarte RF
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- Aged, COVID-19 mortality, COVID-19 physiopathology, Combined Modality Therapy, Disease Progression, Female, Hospitalization, Humans, Immunization, Passive adverse effects, Kaplan-Meier Estimate, Male, Middle Aged, Odds Ratio, Pandemics, Spain epidemiology, Treatment Outcome, COVID-19 Serotherapy, COVID-19 therapy, SARS-CoV-2
- Abstract
BACKGROUNDPassive immunotherapy with convalescent plasma (CP) is a potential treatment for COVID-19. Evidence from controlled clinical trials is inconclusive.METHODSWe conducted a randomized, open-label, controlled clinical trial at 27 hospitals in Spain. Patients had to be admitted for COVID-19 pneumonia within 7 days from symptom onset and not on mechanical ventilation or high-flow oxygen devices. Patients were randomized 1:1 to treatment with CP in addition to standard of care (SOC) or to the control arm receiving only SOC. The primary endpoint was the proportion of patients in categories 5 (noninvasive ventilation or high-flow oxygen), 6 (invasive mechanical ventilation or extracorporeal membrane oxygenation [ECMO]), or 7 (death) at 14 days. Primary analysis was performed in the intention-to-treat population.RESULTSBetween April 4, 2020, and February 5, 2021, 350 patients were randomly assigned to either CP (n = 179) or SOC (n = 171). At 14 days, proportion of patients in categories 5, 6, or 7 was 11.7% in the CP group versus 16.4% in the control group (P = 0.205). The difference was greater at 28 days, with 8.4% of patients in categories 5-7 in the CP group versus 17.0% in the control group (P = 0.021). The difference in overall survival did not reach statistical significance (HR 0.46, 95% CI 0.19-1.14, log-rank P = 0.087).CONCLUSIONCP showed a significant benefit in preventing progression to noninvasive ventilation or high-flow oxygen, invasive mechanical ventilation or ECMO, or death at 28 days. The effect on the predefined primary endpoint at 14 days and the effect on overall survival were not statistically significant.TRIAL REGISTRATIONClinicaltrials.gov, NCT04345523.FUNDINGGovernment of Spain, Instituto de Salud Carlos III.
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- 2021
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15. Granuloma annulare triggered by SARS-CoV-2 infection: Immunohistochemical staining.
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Monte-Serrano J, García-Gil MF, García-García M, Casas-Flecha I, Matovelle-Ochoa C, and Ara-Martín M
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- Consensus, Humans, Prospective Studies, SARS-CoV-2, Spain, Staining and Labeling, COVID-19, Granuloma Annulare diagnosis, Granuloma Annulare etiology
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- 2021
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16. [Viral epidemic outbreaks and public health alerts studied at the National Centre of Microbiology during a two-year period (2012-2013].
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Echevarría Mayo JM, Avellón Calvo AA, Cabrerizo Sanz M, Casas Flecha I, Echevarría Mayo JE, de Ory Manchón Fde O, Negredo Antón A, Pozo Sánchez F, Sánchez-Seco Fariñas MP, Tarragó Asensio D, and Trallero Masó G
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- Humans, Public Health, Spain epidemiology, Virus Diseases virology, Disease Outbreaks statistics & numerical data, Virus Diseases epidemiology
- Published
- 2016
17. Epidemiology of the 2009 influenza pandemic in Spain. The Spanish Influenza Surveillance System.
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Larrauri Cámara A, Jiménez-Jorge S, Mateo Ontañón Sd, Pozo Sánchez F, Ledesma Moreno J, and Casas Flecha I
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- Adolescent, Adult, Aged, Child, Child, Preschool, Humans, Influenza, Human complications, Middle Aged, Population Surveillance, Severity of Illness Index, Spain epidemiology, Young Adult, Influenza A Virus, H1N1 Subtype, Influenza, Human epidemiology, Pandemics
- Abstract
In accordance with European Centre for Disease Prevention and Control recommendations, the Spanish Influenza Surveillance System (SISS) maintained its activity during the summer of 2009, and since July 2009 the pandemic virus activity was monitored by the SISS. In this paper, we describe the epidemiological and virological characteristics of the 2009 pandemic in the Spain through the SISS. Spain experienced a transmission of the new A(H1N1)pdm09 influenza virus during the summer of 2009, which gradually increased, resulting in the pandemic wave in early autumn of that year. The reproductive number R0, estimated during the growth phase of the pandemic wave (1.32; 95% confidence interval [95%CI], 1.29-1.36), showed a transmissibility comparable to preceding pandemics. There was an almost complete replacement of the previous seasonal A(H1N1) influenza virus by the pandemic virus A(H1N1)pdm09. The pandemic virus produced a greater burden of illness than seasonal influenza in children younger than 15 years old, while the incidence in those older than 64 years was lower compared with previous inter-pandemic seasons. Nevertheless, in Spain the 2009 pandemic was characterized as mild, considering the duration of the pandemic period and the influenza detection rate, both in the range of those observed in previous inter-pandemic seasons. Also, the case fatality ratio (CFR) was estimated at 0.58 deaths/1,000 confirmed ILI cases (95%CI, 0.52-0.64), in the range of the two previous pandemics of 1957 and 1968, with the highest CFR observed in the older than 64 years age group. In the 2009 pandemic there was a higher percentage of pandemic confirmed deaths in the younger ages, compared to seasonal influenza, since only 28% of the reported deaths occurred in persons aged 64 years and older., (Copyright © 2012 Elsevier España, S.L. All rights reserved.)
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- 2012
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18. [Asymptomatic infection by influenza AH1N1 virus in healthcare workers: MARBEGRIP study, preliminary results].
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Olalla Sierra J, Ory Manchón Fd, Casas Flecha I, Montiel Quezel-Guerraz N, and Salas Bravo D
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- Humans, Prevalence, Prospective Studies, Asymptomatic Infections epidemiology, Health Personnel, Influenza A Virus, H1N1 Subtype, Influenza, Human epidemiology
- Abstract
Background: The proportion of asymptomatic individuals infected by influenza AH1N1v varies depending on the studies. Health personnel were exposed to the AH1N1v virus due to their professional activity, thus an high seroprevalence to the virus could be expected in the absence of symptomatology. The objective of this study was to determine the prevalence of asymptomatic individuals serologically positive for influenza AH1N1v virus., Methods: A cohort based prospective study on hospital staff was proposed according to an hypothetic decreasing gradient of exposure to the virus, from emergency personnel to medical and surgical areas, and auxiliary staff other than emergency personnel. Serum sample from each participant was taken in September-October, 2009, November-December, 2009, and in April-May, 2010; and a health questionnaire was simultaneously filled out. Specific antibodies against influenza AH1N1v were detected by hemagglutination inhibition test. Eighteen hospitals (1,371 individuals) participated in the study., Results: Health questionnaire and serological results from four hospitals are available. A variable proportion of non vaccinated individuals showed positive serology (5.6-83%). Only 19.4% of subjects received vaccine, with a variable rate of positive serology (18.8-64.7%). Positive serology was significantly lower in non medical participants. In addition, vaccine coverage was higher in medical personnel than in the rest of professional categories., Conclusions: There was a variable percentage of influenza AH1N1v seropositive individuals who had not suffered clinical symptomatology. This serological study detects differences on vaccine efficacy.
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- 2011
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19. [Pandemic influenza A(H1N1): the experience of the Spanish Laboratories of Influenza Network (ReLEG)].
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Cuevas González-Nicolás MT, Ledesma Moreno J, Pozo Sánchez F, Casas Flecha I, and Pérez-Breña P
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- Humans, Influenza, Human prevention & control, Influenza, Human virology, Spain epidemiology, Time Factors, Influenza A Virus, H1N1 Subtype, Influenza, Human diagnosis, Influenza, Human epidemiology, Laboratories, Pandemics, Population Surveillance methods, Virology
- Abstract
There are three types of influenza viruses: A, B, C. These viruses evolves constantly due to two main characteristics: the first one is the lack of the correction ability of the viral polymerase which causes the accumulation of single nucleotide mutations in the viral genes introduced by an error-prone viral RNA polymerase, (antigenic shift). The second one is the nature of their genome, formed by eight segments, which allows the interchange of genes between two different viral strains (antigenic drift). This viral plasticity, has allowed to the influenza A viruses to infect new host species and to cause infections with a pandemic characteristics. The Spanish influenza surveillance system, SVGE (its Spanish acronym), arises as a response to the possibility of facing a pandemic situation, especially after the transmission of avian influenza viruses to humans. This surveillance system is formed by sixteen physician and paediatrics network, nineteen epidemiological services coordinated by the National Epidemiological Centre (CNE) and eighteen laboratories , the Spanish Laboratories of Influenza network (ReLEG), coordinated by the National Centre of Microbiology. The aim of this article is to show the action of the ReLEG, in the pandemic caused by the influenza virus A(H1N1) during the season 2009-2010. The main objective of this network is the surveillance of the circulating viruses by means of their detection and their subsequent antigenic and genetic characterization, including the detection of resistance mutations against the main drugs, such as Oseltamivir.
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- 2010
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20. [Human bocavirus infections in Spanish 0-14 year-old: clinical and epidemiological characteristics of an emerging respiratory virus].
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García-García ML, Calvo Rey C, Pozo Sánchez F, Vázquez Alvarez MC, González Vergaz A, Pérez-Breña P, and Casas Flecha I
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- Child, Child, Preschool, Female, Humans, Infant, Infant, Newborn, Male, Prospective Studies, Spain epidemiology, Bocavirus, Communicable Diseases, Emerging diagnosis, Communicable Diseases, Emerging epidemiology, Parvoviridae Infections diagnosis, Parvoviridae Infections epidemiology, Respiratory Tract Infections diagnosis, Respiratory Tract Infections epidemiology
- Abstract
Introduction: In 2005 a new respiratory virus, called human bocavirus (HBoV), was cloned from respiratory samples from Swedish infants and children with lower respiratory tract infections., Objectives: To determine whether HBoV has circulated in Spain, estimate the frequency of HBoV infections in patients hospitalized for respiratory infection and describe the clinical and epidemiological characteristics of these patients., Patients and Methods: We performed a descriptive prospective study of confirmed HBoV infections in patients aged < 14 years old, hospitalized for respiratory infections between October 2004 and June 2005. Virologic diagnosis was based on multiple RT-PCR for respiratory syncytial virus (RSV) A and B, influenza A,B, and C, parainfluenza 1-4, adenovirus and rhinovirus; PCR was used for human metapneumovirus (hMPV) and PCR in nasopharyngeal aspirates was used for HBoV. The clinical and epidemiological characteristics of patients were analyzed., Results: Fifty-two cases of HBoV infection were detected, representing 17.1% (95% CI: 13% a 21%) of patients hospitalized for respiratory infections. HBoV was the third most frequent viral agent after RSV (30%) and rhinovirus (25%). In 39 patients (71.1%) coinfection with another respiratory virus was detected. Fifty percent of the patients were aged less than 13.6 months and 75% were aged less than 2 years. The most frequent diagnoses were recurrent wheezing (55.8%), bronchiolitis (21.2%) and pneumonia (15.4%). Clinical sepsis with petechial exanthema was found in two patients. Fever > 38 degrees C was found in 72.1% and radiological infiltrate in 44%. Hypoxia was present in 55.8 % of the patients. HBoV was isolated in distinct episodes in two patients. Coinfections were similar to simple infections except that hypoxia was more frequent in the former (p = 0.038)., Conclusions: HBoV is one of the most frequent viruses in severe respiratory infections in patients aged less than 14 years old. Only RSV and rhinovirus are more frequent. Coinfections are highly frequent. Most patients are infants with recurrent wheezing and bronchiolitis.
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- 2007
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21. [Biodefense: a new challenge for microbiology and public health].
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Buitrago Serna MJ, Casas Flecha I, Eiros-Bouza JM, Escudero Nieto R, Giovanni Fedele C, Jado García I, Pozo Sánchez F, Rubio Muñoz JM, Sánchez-Seco Fariñas MP, Valdezate Ramos S, and Verdejo Ortes J
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- Anthrax prevention & control, Civil Defense methods, Communicable Diseases diagnosis, Communicable Diseases transmission, Early Diagnosis, Government Agencies, Humans, Infection Control methods, Medical History Taking, Population Surveillance, Spain, Toxins, Biological analysis, Toxins, Biological poisoning, Bioterrorism, Civil Defense trends, Disaster Planning, Infection Control trends, Microbiology trends, Public Health
- Abstract
Bioterrorism and the potential use of biological weapons has become an important concern of governments and responsible authorities. An example of this threat occurred in 2001 in the USA, when letters were sent containing spores of the agent that produces anthrax; this resulted in some deaths, and caused panic and negative effects on the world economy. If this small-scale event was able to cause such a huge impact, the repercussions of a massive attack could be catastrophic. In many countries, these events have resulted in the implementation of measures directed toward preventing and responding to bioterrorist threats and acts. As a whole, these measures are known as biodefense. This article briefly analyzes several aspects related to detecting and identifying acts of bioterrorism, and considers the biological agents that are implicated. The microbiological diagnosis that allows identification of the causal agent, a key point for taking suitable control measures, is also included.
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- 2007
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22. [Respiratory infections due to metapneumovirus in hospitalized infants].
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García García ML, Calvo Rey C, Martín del Valle F, López Huertas MR, Casas Flecha I, Díaz-Delgado R, and Pérez-Breña P
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- Female, Hospital Units statistics & numerical data, Hospitalization, Humans, Infant, Male, Oxygen Inhalation Therapy, Paramyxoviridae Infections diagnosis, Paramyxoviridae Infections therapy, Prospective Studies, Respiratory Tract Infections diagnosis, Respiratory Tract Infections therapy, Reverse Transcriptase Polymerase Chain Reaction, Spain epidemiology, Metapneumovirus isolation & purification, Paramyxoviridae Infections virology, Respiratory Tract Infections virology
- Abstract
Background: Human metapneumovirus (hPMV) is a recently identified virus that is recognized as a cause of respiratory tract illness in the pediatric population., Objectives: To determine the incidence of respiratory tract infections caused by hPMV in hospitalized infants and to describe the clinical characteristics and possible presence of coinfection with other viral agents., Patients and Methods: We performed a prospective study from September to June 2003 in all children aged less than 24 months who were admitted to the Severo Ochoa Hospital (Leganés, Madrid) with a respiratory tract infection. Virological diagnosis was made with a direct immunofluorescent assay and/or reverse transcriptase-polymerase chain reaction on specimens obtained from nasopharyngeal washing. Demographic and clinical data from patients with an hPMV respiratory tract infection were analyzed., Results: During the study period, 200 infants were admitted with a respiratory tract infection, of which 18 (9 %) had an hPMV infection. HPMV was the viral agent isolated in 13.8 % of positive nasopharyngeal washings. All patients were admitted between March and April. The mean age was 6.7 +/- 6.1 months. The most common diagnoses were recurrent wheezing (55.5 %) and bronchiolitis (38.8 %). Oxygen therapy was required by 55.5 % of infants during hospitalization. Coinfection with other respiratory viruses was confirmed in 33.3 % of the patients., Conclusions: Human metapneumovirus is a major cause of respiratory tract illness in hospitalized infants. This virus causes mainly bronchiolitis and recurrent wheezing and is more frequent in spring. Coinfection with other respiratory viruses is frequent.
- Published
- 2004
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