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2.
Enferm Infecc Microbiol Clin ; 25(3): 177-83, 2007 Mar.
Article in Spanish | MEDLINE | ID: mdl-17335696

ABSTRACT

INTRODUCTION: Influenza infection in infants and children has been classically underestimated due to its non-specific symptoms, which sometimes overlap those of other respiratory viruses. Infants under 24 months are a risk group and school-aged children are a major source of influenza infection. The aim of this study was to describe the clinical and epidemiological characteristics of children hospitalized for flu, including co-infections and the differences as compared to other respiratory viruses. The effectiveness of a test for rapid diagnosis of this condition was assessed. MATERIAL AND METHODS: Prospective, descriptive study in children < 5 years of age hospitalized from 1 December 2003 to 28 February 2004 with respiratory processes or fever of unknown origin. Polymerase chain reaction (PCR) testing for influenza A (IA) and B, respiratory syncytial virus A (RSV-A) and B, and parainfluenza 1, 2 and 3 was performed in nasopharyngeal aspirate, as well as a test for rapid diagnosis of influenza. RESULTS: A total of 203 samples were included. PCR was positive for influenza in 11.3% (23/203); IA in 21 cases (20 H3N2, 1 H1N1). Co-infections were frequent (10/23), mainly IA with RSV-A. The rapid diagnostic test had a sensitivity of 45.5%. Median age of patients with flu was 4.87 months (5 days-3.5 years); 69.5% were < 24 months. Gastrointestinal symptoms were associated with fever and respiratory symptoms more often than in other viral infections (P < 0.05). Only 2.9% of patients with a recommendation for flu vaccination had received the vaccination. CONCLUSIONS: Flu is a major cause of hospitalization in infants and children, particularly those aged < 24 months. Early diagnosis of this condition may avoid unnecessary use of additional tests and antibiotics. Vaccination coverage is low; vaccination between 6 and 24 months seems advisable.


Subject(s)
Hospitalization/statistics & numerical data , Influenza, Human/epidemiology , Adolescent , Child , Child, Preschool , Comorbidity , Early Diagnosis , Female , Hospitals, Maternity/statistics & numerical data , Hospitals, Pediatric/statistics & numerical data , Humans , Infant , Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza A Virus, H3N2 Subtype/isolation & purification , Influenza Vaccines , Influenza, Human/diagnosis , Influenza, Human/virology , Male , Nasopharynx/virology , Polymerase Chain Reaction , Prospective Studies , RNA, Viral/blood , Risk Factors , Spain/epidemiology , Vaccination/statistics & numerical data , Viremia/diagnosis , Viremia/epidemiology , Viremia/virology
3.
Enferm. infecc. microbiol. clín. (Ed. impr.) ; 25(3): 177-183, mar. 2007. tab, graf
Article in Es | IBECS | ID: ibc-053160

ABSTRACT

Introducción. La gripe en pediatría ha sido clásicamente infradiagnosticada, por su clínica inespecífica y solapable con otros virus respiratorios. Los menores de 24 meses constituyen un grupo de riesgo y los escolares son una fuente importante de contagio. El objetivo de este estudio es describir la clínica y epidemiología de niños ingresados por gripe, estudiando coinfecciones y comparando con otros virus respiratorios. Se valoró la efectividad de un test de diagnóstico rápido. Material y métodos. Estudio descriptivo prospectivo en menores de 5 años hospitalizados entre el 1 de diciembre de 2003 y el 28 de febrero de 2004 por cuadro respiratorio o fiebre sin foco aparente. Se realizó reacción en cadena de polimerasa (PCR) a virus de la gripe A (IA) y B, virus respiratorio sincitial A (VRS-A) y B y parainfluenza 1, 2 y 3 en aspirado nasofaríngeo y test de diagnóstico rápido de gripe. Resultados. Se incluyeron 203 muestras, siendo la PCR positiva a virus de la gripe en un 11,3% (23/203): IA 21 casos (20 H3N2, 1 H1N1). Las coinfecciones fueron frecuentes (10/23), destacando la asociación IA y VRS-A. El test de diagnóstico rápido tuvo una sensibilidad del 45,5%. La mediana de edad de los pacientes con gripe fue 4,87 meses (5 días-3,5 años); un 69,5% eran menores 24 meses. A la fiebre y síntomas respiratorios, asociaron síntomas gastrointestinales con más frecuencia que los otros virus (p < 0,05). Sólo un 2,9% de los pacientes con indicación de vacunación antigripal la había recibido. Conclusiones. La gripe es causa importante de hospitalización en pediatría, especialmente en menores 24 meses. Su diagnóstico precoz evitaría el uso innecesario de pruebas complementarias y antibióticos. Existe una baja cobertura vacunal. Sería interesante la vacunación entre los 6 y los 24 meses (AU)


Introduction. Influenza infection in infants and children has been classically underestimated due to its non-specific symptoms, which sometimes overlap those of other respiratory viruses. Infants under 24 months are a risk group and school-aged children are a major source of influenza infection. The aim of this study was to describe the clinical and epidemiological characteristics of children hospitalized for flu, including co-infections and the differences as compared to other respiratory viruses. The effectiveness of a test for rapid diagnosis of this condition was assessed. Material and methods. Prospective, descriptive study in children < 5 years of age hospitalized from 1 December 2003 to 28 February 2004 with respiratory processes or fever of unknown origin. Polymerase chain reaction (PCR) testing for influenza A (IA) and B, respiratory syncytial virus A (RSV-A) and B, and parainfluenza 1, 2 and 3 was performed in nasopharyngeal aspirate, as well as a test for rapid diagnosis of influenza. Results. A total of 203 samples were included. PCR was positive for influenza in 11.3% (23/203); IA in 21 cases (20 H3N2, 1 H1N1). Co-infections were frequent (10/23), mainly IA with RSV-A. The rapid diagnostic test had a sensitivity of 45.5%. Median age of patients with flu was 4.87 months (5 days-3.5 years); 69.5% were < 24 months. Gastrointestinal symptoms were associated with fever and respiratory symptoms more often than in other viral infections (P < 0.05). Only 2.9% of patients with a recommendation for flu vaccination had received the vaccination. Conclusions. Flu is a major cause of hospitalization in infants and children, particularly those aged < 24 months. Early diagnosis of this condition may avoid unnecessary use of additional tests and antibiotics. Vaccination coverage is low; vaccination between 6 and 24 months seems advisable (AU)


Subject(s)
Child, Preschool , Child , Adolescent , Humans , Hospitalization/statistics & numerical data , Viremia/diagnosis , Viremia/epidemiology , Influenza, Human/epidemiology , Comorbidity , Hospitals, Pediatric/statistics & numerical data , Nasopharynx/virology , Polymerase Chain Reaction , Prospective Studies , Viremia/virology , Early Diagnosis , Influenza Vaccines
6.
Radiología (Madr., Ed. impr.) ; 45(3): 151-155, mayo 2003. ilus
Article in Spanish | IBECS | ID: ibc-141672

ABSTRACT

La ataxia telangiectasia de Louis Barr (AT) es una enfermedad autosómica recesiva caracterizada por ataxia cerebelosa progresiva, telangiectasias oculocutáneas, inmunodeficiencia combinada con susceptibilidad a infecciones sinopulmonares y alta incidencia de desarrollo neoplásico. El síndrome de Nijmegen (SNJ) es una variante de la AT, también autosómico recesivo, que presenta ataxia cerebelosa, inmunodeficiencia combinada y tendencia al desarrollo tumoral. A diferencia de la AT no muestra telangiectasias y exhibe un fenotipo característico (talla corta, cara «de pájaro» y microcefalia). Ambas entidades se incluyen dentro de la clasificación de los síndromes con fragilidad o inestabilidad cromosómica que agrupan además al síndrome de Bloom y la anemia de Fanconi. Todos ellos muestran un aumento en la frecuencia de presentación neoplásica, principalmente tumores del sistema linfoide. Presentamos tres pacientes, dos con AT y uno con SNJ, que han desarrollado diferentes tipos de linfoma en el curso de la enfermedad, indicando los aspectos más relevantes desde el punto de vista clinicorradiológico (AU)


Ataxia-telangiectasia (AT), or Louis-Bar syndrome, is an autosomal recessive illness characterized by progressive cerebellar ataxia, oculocutaneous telangiectasias, immunodeficiency combined with susceptibility to sinopulmonary infections and high incidence of neoplastic development. Nijmegen breakage syndrome (NBS) is a variant of AT, is also an autosomal recessive illness that presents cerebellar ataxia, as well as combined immunodeficiency and a tendency toward tumor development. Contrary to Louis-Bar syndrome, it doesn't present telangiectasia and exhibits a characteristic phenotype (short stature, bird-like face and microcephaly). Both entities are classified as syndromes of chromosomal instability or chromosomal fragility, a group which also includes Bloom syndrome and Fanconi anemia. All of these show an increase in the frequency of neoplastic pathologies, mainly lymphoid tumors. We present three patients, two with AT and one with NBS, who developed different lymphoma types in the course of the illness. We highlight the most outstanding aspects from a clinical-radiological point of view (AU)


Subject(s)
Child , Female , Humans , Male , Ataxia Telangiectasia/classification , Ataxia Telangiectasia/diagnosis , Ataxia Telangiectasia , Nijmegen Breakage Syndrome/diagnosis , Medical Records , Radiation
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