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1.
J Hosp Infect ; 132: 46-51, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-36473554

RESUMO

AIM: To estimate the incidence, timing and severity of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) breakthrough infections in fully vaccinated healthcare personnel (HCP). METHODS: In total, 6496 fully vaccinated HCP were analysed prospectively from 15th November 2021 to 17th April 2022. Full coronavirus disease 2019 (COVID-19) vaccination was defined as a complete primary vaccination series followed by a booster dose at least 6 months later. RESULTS: Overall, 1845 SARS-CoV-2 breakthrough infections occurred (28.4 episodes per 100 HCP), of which 1493 (80.9%) were COVID-19 cases and 352 (19.1%) were asymptomatic infections. Of the 1493 HCP with COVID-19, four were hospitalized for 3-6 days (hospitalization rate among HCP with COVID-19: 0.3%). No intubations or deaths occurred. SARS-CoV-2 breakthrough infections occurred at a mean of 16.2 weeks after the last vaccine dose. Multi-variable regression analyses showed that among the 1845 HCP with a breakthrough infection, the administration of a COVID-19 vaccine dose ≥16.2 weeks before the infection was associated with increased likelihood of developing COVID-19 rather than asymptomatic SARS-CoV-2 infection [odds ratio (OR) 1.58, 95% confidence interval (CI) 1.01-2.46; P=0.045] compared with administering a vaccine dose later. The likelihood of developing COVID-19 compared with asymptomatic infection increased by 7% weekly after the last COVID-19 vaccine dose (OR 1.07, 95% CI 1.03-1.11; P=0.001). CONCLUSION: SARS-CoV-2 breakthrough infections are common among fully (boosted) vaccinated HCP. However, full COVID-19 vaccination offered considerable protection against hospitalization. These findings may contribute to defining the optimal timing for booster vaccinations. More efficient COVID-19 vaccines that will also confer protection against SARS-CoV-2 infection are needed urgently.


Assuntos
Vacinas contra COVID-19 , COVID-19 , Humanos , COVID-19/epidemiologia , COVID-19/prevenção & controle , SARS-CoV-2 , Infecções Irruptivas , Infecções Assintomáticas , Vacinação , Atenção à Saúde
2.
J Paediatr Child Health ; 39(8): 635-6, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14629535

RESUMO

A 12-year-old girl with chronic otitis media complicated by petrositis and cerebellar abscess is presented. Early surgical intervention, in combination with broad-spectrum antibiotics, provided a good outcome. Life-threatening complications of otitis media, although rare, still occur in developed countries.


Assuntos
Abscesso Encefálico/etiologia , Doenças Cerebelares/etiologia , Osteíte/etiologia , Otite Média Supurativa/complicações , Osso Petroso , Abscesso Encefálico/diagnóstico , Abscesso Encefálico/patologia , Abscesso Encefálico/terapia , Doenças Cerebelares/diagnóstico , Doenças Cerebelares/terapia , Criança , Doença Crônica , Craniotomia , Feminino , Humanos , Osteíte/diagnóstico , Osteíte/terapia , Otite Média Supurativa/diagnóstico , Otite Média Supurativa/terapia , Tomografia Computadorizada por Raios X
3.
J Infect Dis ; 169(4): 853-8, 1994 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8133101

RESUMO

Four-day dexamethasone therapy has been used to treat bacterial meningitis. This prospective, randomized study compared the effect of a 2-day versus a 4-day regimen. Children (n = 118, ages 2.5 months to 15 years) were evaluated; 50% of the cases were due to Neisseria meningitidis and 40% to Haemophilus influenzae type b. Patients were treated intravenously (iv) mainly with conventional antimicrobial therapy and were randomly assigned to receive dexamethasone, 0.15 mg/kg iv every 6 h for 2 or 4 days. The clinical response was similar for both dexamethasone regimens. The meningococcal meningitis patients survived without neurologic or audiologic sequelae. On long-term follow-up, neurologic sequelae or moderate or more severe unilateral or bilateral hearing impairment (or both) were found in 1.8% and 3.8% of patients treated with dexamethasone for 2 and 4 days, respectively. The 2-day regimen appears appropriate for the treatment of H. influenzae and meningococcal meningitis.


Assuntos
Dexametasona/uso terapêutico , Meningite por Haemophilus/tratamento farmacológico , Meningite Meningocócica/tratamento farmacológico , Meningite Pneumocócica/tratamento farmacológico , Adolescente , Antibacterianos/uso terapêutico , Líquido Cefalorraquidiano/química , Líquido Cefalorraquidiano/citologia , Proteínas do Líquido Cefalorraquidiano/análise , Criança , Pré-Escolar , Dexametasona/administração & dosagem , Dexametasona/efeitos adversos , Esquema de Medicação , Quimioterapia Combinada , Feminino , Seguimentos , Hemorragia Gastrointestinal/induzido quimicamente , Glucose/líquido cefalorraquidiano , Perda Auditiva/etiologia , Humanos , Lactente , Contagem de Leucócitos , Masculino , Meningite por Haemophilus/complicações , Meningite Meningocócica/complicações , Meningite Pneumocócica/complicações , Doenças do Sistema Nervoso/etiologia , Estudos Prospectivos , Resultado do Tratamento
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