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1.
Ophthalmology ; 126(1): 137-143, 2019 01.
Artículo en Inglés | MEDLINE | ID: mdl-30180976

RESUMEN

PURPOSE: Outbreaks of adenovirus in neonatal intensive care units (NICUs) can lead to widespread transmission and serious adverse outcomes. We describe the investigation, response, and successful containment of an adenovirus outbreak in a NICU associated with contaminated handheld ophthalmologic equipment used during retinopathy of prematurity (ROP) screening. DESIGN: Epidemiologic outbreak investigation. PARTICIPANTS: A total of 23 hospitalized neonates, as well as NICU staff and parents of affected infants. MAIN OUTCOME MEASURES: Routine surveillance identified an adenovirus outbreak in a level IV NICU in August 2016. Epidemiologic investigation followed, including chart review, staff interviews, and observations. Cases were defined as hospital-acquired adenovirus identified from any clinical specimen (NICU patient or employee) or compatible illness in a family member. Real-time polymerase chain reaction (PCR) and partial- and whole-genome sequencing assays were used for testing of clinical and environmental specimens. RESULTS: We identified 23 primary neonatal cases and 9 secondary cases (6 employees and 3 parents). All neonatal case-patients had respiratory symptoms. Of these, 5 developed pneumonia and 12 required increased respiratory support. Less than half (48%) had ocular symptoms. All neonatal case-patients (100%) had undergone a recent ophthalmologic examination, and 54% of neonates undergoing examinations developed adenovirus infection. All affected employees and parents had direct contact with infected neonates. Observations revealed inconsistent disinfection of bedside ophthalmologic equipment and limited glove use. Sampling of 2 handheld lenses and 2 indirect ophthalmoscopes revealed adenovirus serotype 3 DNA on each device. Sequence analysis of 16 neonatal cases, 2 employees, and 2 lenses showed that cases and equipment shared 100% identity across the entire adenovirus genome. Infection control interventions included strict hand hygiene, including glove use; isolation precautions; enhanced cleaning of lenses and ophthalmoscopes between all examinations; and staff furlough. We identified no cases of secondary transmission among neonates. CONCLUSIONS: Adenovirus outbreaks can result from use of contaminated ophthalmologic equipment. Even equipment that does not directly contact patients can facilitate indirect transmission. Patient-to-patient transmission can be prevented with strict infection control measures and equipment cleaning. Ophthalmologists performing inpatient examinations should take measures to avoid adenoviral spread from contaminated handheld equipment.


Asunto(s)
Infecciones por Adenovirus Humanos/epidemiología , Brotes de Enfermedades , Contaminación de Equipos , Infecciones Virales del Ojo/epidemiología , Unidades de Cuidado Intensivo Neonatal/estadística & datos numéricos , Oftalmología/instrumentación , Infecciones del Sistema Respiratorio/epidemiología , Infecciones por Adenovirus Humanos/tratamiento farmacológico , Infecciones por Adenovirus Humanos/transmisión , Infecciones por Adenovirus Humanos/virología , Adenovirus Humanos/genética , Infección Hospitalaria/tratamiento farmacológico , Infección Hospitalaria/epidemiología , Infección Hospitalaria/transmisión , Infección Hospitalaria/virología , ADN Viral/genética , Transmisión de Enfermedad Infecciosa/prevención & control , Transmisión de Enfermedad Infecciosa/estadística & datos numéricos , Infecciones Virales del Ojo/tratamiento farmacológico , Infecciones Virales del Ojo/transmisión , Infecciones Virales del Ojo/virología , Femenino , Edad Gestacional , Humanos , Lactante , Control de Infecciones , Pacientes Internos , Masculino , Reacción en Cadena en Tiempo Real de la Polimerasa , Infecciones del Sistema Respiratorio/tratamiento farmacológico , Infecciones del Sistema Respiratorio/transmisión , Infecciones del Sistema Respiratorio/virología , Retinopatía de la Prematuridad/diagnóstico , Secuenciación Completa del Genoma
2.
Clin Nutr ; 23(4): 691-6, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15297107

RESUMEN

BACKGROUND & AIM: Feeding jejunostomy is recommended to facilitate early enteral nutrition after major upper gastrointestinal surgery. We aimed to determine the benefits and risks associated with routine practice of feeding needle catheter jejunostomy (NCJ) in high-risk upper gastrointestinal surgery. METHOD: This is a prospective consecutive cohort study of 84 patients underwent feeding NCJ over a 3 years period in an Upper Gastrointestinal Surgical Unit. RESULTS: Feeding NCJ was placed after two-stage oesophago-gastrectomy in 24 patients (28.6%), after gastrectomy in 29 patients (34.5%), after liver resections in 7 patients (8.3%), pancreatic resection in 6 patients (7.1%), bile duct reconstruction in 8 patients (9.5%) and other operations in 10 patients (12%). The mean (SE) estimated nutritional requirement per 24 h was 1791 (31)kcal. Eighty-two patients (98%) started enteral feed on day 1 after surgery. Fifty-seven patients (68%) achieved the target nutritional requirements in 3 days. Four patients were discharged home on jejunal feed whilst only two patients required parenteral nutrition support. The rest tolerated full oral diet. There was no procedure related mortality. The morbidity related to feeding tube and feeding were 12.9% and 20%, respectively. CONCLUSIONS: Routine practice of feeding NCJ is safe. Their benefits outweigh the risks in a specialist centre.


Asunto(s)
Nutrición Enteral/métodos , Enfermedades Gastrointestinales/cirugía , Enfermedades Gastrointestinales/terapia , Intubación Gastrointestinal/métodos , Yeyunostomía/métodos , Cateterismo , Estudios de Cohortes , Nutrición Enteral/efectos adversos , Femenino , Humanos , Intubación Gastrointestinal/efectos adversos , Yeyunostomía/efectos adversos , Masculino , Persona de Mediana Edad , Necesidades Nutricionales , Cuidados Posoperatorios , Estudios Prospectivos , Medición de Riesgo , Factores de Riesgo , Seguridad , Resultado del Tratamiento
3.
Trib. méd. (Bogotá) ; 86(1): 44-47, jul. 1992. ilus, tab
Artículo en Español | LILACS | ID: lil-183431

RESUMEN

Es posible que próximamente las mujeres tengan su propio condón: un nuevo dispositivo anticonceptivo que también podría ofrecer protección contra las enfermedades de transmisión sexual (ETS). El "condón femenino" es una funda desechable de látex o plástico blando, que se coloca dentro de la vagina. Muchos de los métodos eficaces para el control de la natalidad son controlados por las mujeres, pero el principal método para la protección contra las ETS (el condón masculino) no lo está. En la estela de la pandemia del SIDA, el brindar a las mujeres el potencial de proteger su salud sexual tiene mayor urgencia que nunca.


Asunto(s)
Femenino , Enfermedades de Transmisión Sexual/prevención & control , Planificación Familiar/métodos , Planificación Familiar/tendencias
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