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1.
Rev. méd. Urug ; 34(2): 76-81, jun. 2018. tab, ilus
Article in Spanish | LILACS | ID: biblio-904977

ABSTRACT

Introducción: en Uruguay se ofrece gratuitamente una vacuna tetravalente contra el virus del papiloma humano (VPH) a todas las adolescentes de 12 años o mayores. Las coberturas logradas no han sido las esperadas. Objetivo: describir el estado vacunal contra el VPH, motivos de no vacunación y reporte de efectos adversos en las adolescentes hospitalizadas en un centro de referencia en Uruguay. Material y método: estudio descriptivo mediante encuesta anónima a adolescentes de 12 años o mayores hospitalizadas en cuidados moderados del Hospital Pediátrico del Centro Hospitalario Pereira Rossell durante el segundo semestre de 2016. Se excluyeron las adolescentes que se negaron a participar, las portadoras de retardo mental o pasibles de cuidados paliativos. Se analizó: edad, estado vacunal contra VPH, motivos de no vacunación y de rechazo a la vacuna, efectos adversos. Fue aprobado por el Comité de Ética de la institución. Resultados: se encuestaron 112 adolescentes. Edad media: 13,5 años (12-14,6). Reportaron recibir al menos una dosis de la vacuna contra VPH: 45/112 (40,1%). Motivo de no vacunación más frecuente reportado: desconocimiento de la existencia de la vacuna: 48/67 (71,6%), seguido de rechazo o negativa de la adolescente o adulto responsable: 13/67 (19,4%). El principal motivo de rechazo a recibir la vacuna fue la falta de información: 7/13. No se registraron efectos adversos graves. Conclusiones: se observó una cobertura vacunal similar a datos nacionales. El conocimiento y la información de las adolescentes y sus cuidadores sobre esta vacuna fueron los principales motivos de no vacunación detectados.


Introduction: Uruguay offers a free HPV quadrivalent vaccine to adolescents 12 years of age or older. However, the vaccination rate was not as expected. Objective: to describe the human papillomavirus (HPV) vaccination status, the reasons for non-vaccination and to report adverse effects in hospitalized adolescents in a reference center in Uruguay. Materials and methods: descriptive study by means of an anonymous survey of adolescents of 12 years of age or older hospitalized in moderate care at Pereira Rossell Hospital Center during the second half of 2016. Adolescents who refused to participate were excluded from the study, as well as those with mental retardation and / or subject to palliative care. We analyzed: age, vaccination status against HPV, reasons for non-vaccination and vaccine hesitancy, and adverse effects. The research conducted was approved by the institution's ethics committee. Results: the survey was answered by 112 adolescents who met the inclusion criteria. Mean age was 13.5 years old (12-14.6). 45/112 (40.1%). Adolescents reported having received at least one dose of the HPV vaccine. The most frequent reason for non-vaccination was: lack of knowledge of the vaccine in 48 out of 67 (71.6%), followed by rejection or rejection by the adolescent or responsible adult in 13 out of 67 (19.4%). The main reason for refusal to receive the vaccine reported was: lack of information (7/13). No serious adverse events were reported. Conclusions: vaccination coverage found was similar to national data. Knowledge and information of adolescents and their caregivers about this vaccine were the main reasons detected for non-vaccination.


Introdução: no Uruguai una vacina tetravalente contra o Vírus do Papiloma Humano (VPH) é oferecida gratuitamente a todas as adolescentes com 12 ou mais anos. A cobertura obtida não foi a esperada. Objetivo: descrever o estado vacinal contra o VPH, motivos de não vacinação e informação sobre efeitos adversos nas adolescentes hospitalizadas em um centro de referencia no Uruguai. Materiais e métodos: estudo descritivo, realizado com questionário anônimo respondido por adolescentes com 12 ou mais anos, internadas em cuidados intermediários do Hospital Pediátrico do Centro Hospitalario Pereira Rossell, durante o segundo semestre de 2016. Foram excluídas as adolescentes que não quiseram participar, as portadoras de deficiência mental e/ou passiveis de cuidados paliativos. As seguintes variáveis foram analisadas: idade, estado vacinal contra VPH, motivos de não vacinação e de rejeição à vacina e efeitos adversos. O estudo foi aprovado pelo comité de ética da instituição. Resultados: participaram 112 adolescentes com idade média 13,5 anos (12-14,6). 45 informaram ter recebido pelo menos uma dose da vacina contra VPH (45/112 - 40,1%). O motivo de não vacinação mais frequente foi o desconhecimento da existência da vacina 48/67 (71,6%), seguido de rejeição ou negativa da adolescente ou do adulto responsável 13/67 (19,4%). O motivo principal de rejeição a ser vacinada foi a falta de informação 7/13. Não foram registrados efeitos adversos graves. Conclusões: a cobertura vacinal registrada foi similar aos dados nacionais. O conhecimento e a informação das adolescentes e de seus cuidadores sobre esta vacina foram os principais motivos de não vacinação detectados.


Subject(s)
Adolescent , Adolescent , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/adverse effects , Papillomavirus Vaccines/supply & distribution , Hospitals, Pediatric , Vaccination Coverage , Vaccination Refusal
2.
Arch. pediatr. Urug ; 88(1): 6-11, feb. 2017. tab
Article in Spanish | LILACS | ID: biblio-838634

ABSTRACT

Objetivo: determinar la incidencia del síndrome de abstinencia (SA), describir presentación clínica e identificar la presencia de factores de riesgo. Metodología: se realizó un estudio prospectivo, observacional, de evaluaciones reiteradas usando la Sophia Observation Withdrawal Symptoms Scale (SOWS), en la Unidad de Cuidado Intensivo de Niños (UCIN) de 20 camas, del Centro Hospitalario Pereira Rossell (CHPR). Se incluyeron los niños ingresados en UCIN entre el 1 de noviembre de 2013 y el 30 de setiembre de 2014 tratados con benzodiacepinas y/o opiáceos por cinco días o más. Se registró: duración de la estadía, fármacos utilizados para sedación y analgesia, días de uso, máximo de dosis, dosis total acumulada. El diagnóstico de SA se realizó a través del uso de la SOWS. Los pacientes fueron divididos en dos grupos, con y sin SA. Se analizaron y compararon las características de ambos grupos. Resultados: se incluyeron 39 niños. La incidencia de SA fue 18% (7/39). Los ítems del SOWS más frecuentes fueron ansiedad y sueño menor a 1 hora. Los niños que desarrollaron SA presentaron dosis acumulativas más elevadas tanto de midazolam (54,1 mg/kg vs 44,2 mg/kg) como de fentanilo (464,2 mg/kg vs 380,1 mg/kg). Conclusiones: el SA fue frecuente en este grupo de niños. Las dosis acumulativas fueron mayores en el grupo con SA. La SOWS es una herramienta útil y de fácil aplicación para el diagnóstico de SA.


Objective: The study aims to determine the incidence of withdrawal syndrome, its clinical features and the presence of risk factors. Methodology: An observational and prospective study. Assessment was repeated and the Sophia Observation Withdrawal Symptoms Scale (SOWS) was used. The study was conducted at the Pediatric Intensive Care Unit (PICU) of Centro Hospitalario Pereira Rossell (CHPR). Hospitalized children in PICU between 1/11/2013- 30/9/2014 and treated with benzodiazepines and opioids during 5 days or more were included in the study. Days of stay at the PICU, agents used for sedation (dose, duration) and cumulative doses were recorded. Withdrawal syndrome diagnosis was done using the SOWS. Results: 39 children were included in the study. The incidence of withdrawal syndrome was 18% (7/39). Children who developed withdrawal syndrome presented higher cumulative doses of midazolam (54.1 mg/kg vs. 44.2 mg/kg) and fentanyl (464.2µg/kg vs. 380.1 µg/kg) than those without withdrawal syndrome. Conclusions: the withdrawal syndrome was frequent in this population. Cumulative doses of midazolam and fentanyl were higher in those with withdrawal symptoms. The SOWS is a useful resource for diagnosis.


Subject(s)
Humans , Male , Substance Withdrawal Syndrome/epidemiology , Benzodiazepines/adverse effects , Analgesics, Opioid/adverse effects , Opioid-Related Disorders/diagnosis , Substance Withdrawal Syndrome/diagnosis , Incidence , Prospective Studies , Critical Care/methods , Observational Study , Hypnotics and Sedatives/adverse effects
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