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1.
Indian Pediatr ; 58(6): 568-571, 2021 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-33612486

RESUMO

OBJECTIVE: To evaluate if Healthcare workers (HCWs) at the frontline of COVID-19 response in a pediatric hospital are at an increased risk of acquiring SARS-CoV-2. METHODS: The Hospital Infection Control Committee (HICC) and virology testing records were combined to identify SARS-CoV-2 positive HCWs and study the transmission dynamics of COVID-19 over 6 months. RESULTS: COVID-19 cases in our HCWs cohort rose and declined parallel to community cases. Forty two out of 534 HCWs (8%) were SARS-CoV-2 positive with no fatalities. No clinical staff in the special COVID ward or ICU was positive. Significant proportion of non-clinical staff (30%) were SARS-CoV-2 positive. About 70% of SARS-CoV-2 positive staff had likely community acquisition, with a significant proportion having travelled by public transport or having a contact history with a positive case in the community. Twenty four percent of positive staff were asymptomatic and detected positive on re-joining test. CONCLUSIONS: Sustained transmission of SARS-CoV-2 did not occur in our cohort beyond community transmission. Appropriate PPE use, strict and constantly improving infection control measures and testing of both clinical and non-clinical staff were essential methods for restricting transmission amongst HCWs.


Assuntos
COVID-19/diagnóstico , COVID-19/transmissão , Transmissão de Doença Infecciosa/estatística & dados numéricos , Pessoal de Saúde/estatística & dados numéricos , Adulto , COVID-19/epidemiologia , Criança , Transmissão de Doença Infecciosa/prevenção & controle , Feminino , Hospitais Pediátricos , Humanos , Controle de Infecções , Masculino , Pessoa de Meia-Idade , Equipamento de Proteção Individual , SARS-CoV-2
2.
Indian J Pediatr ; 74(10): 953-5, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17978458

RESUMO

Congenital Central Hypoventilation Syndrome is a rare disorder of autonomic dysfunction where the body "forgets to breathe". The primitive responses to hypoxia and hypercapnia are sluggish to absent. Since, it was first described in 1970, not much has been discovered about its etiology and pathophysiology except its relationship with PHOX2B gene mutations and associations with disorders of neural crest origin like Hirschprung's Disease. Here, we describe such a case where the diagnosis of anything other than CCHS seems unlikely.


Assuntos
Doenças em Gêmeos/congênito , Doenças do Prematuro/diagnóstico , Apneia do Sono Tipo Central/congênito , Sistema Nervoso Autônomo/fisiopatologia , Diagnóstico Diferencial , Doenças em Gêmeos/diagnóstico , Doenças em Gêmeos/fisiopatologia , Doenças em Gêmeos/terapia , Humanos , Lactente , Recém-Nascido , Doenças do Prematuro/fisiopatologia , Doenças do Prematuro/terapia , Masculino , Respiração com Pressão Positiva , Apneia do Sono Tipo Central/diagnóstico , Apneia do Sono Tipo Central/fisiopatologia , Apneia do Sono Tipo Central/terapia , Traqueostomia
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