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1.
Lancet Infect Dis ; 19(2): 177-184, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30558994

RESUMO

BACKGROUND: In 2007-08, a genotype J mumps outbreak occurred among Aboriginal people in northern Western Australia, despite high vaccine coverage. In March, 2015, a second protracted mumps outbreak occurred in northern Western Australia and spread widely across rural areas of the state. This time the outbreak was caused by a genotype G virus and again primarily affected Aboriginal people. We aimed to describe the epidemiology of this outbreak. METHODS: In this population-based surveillance study, we analysed statutory notifications and public health case follow-up data from the Western Australia Notifiable Infectious Diseases Database and vaccination information from the Australian Childhood Immunisation Register. An outbreak case of mumps was notified if the affected person was living in or visiting a community in Western Australia where there was active mumps transmission, and if mumps infection was confirmed by laboratory diagnosis or by an epidemiological link. We analysed case demographics, vaccination status, and age-standardised attack rates in Aboriginal and non-Aboriginal people by region of notification. Laboratory diagnoses were made by real-time RT-PCR, serology, or both, and carried out by the sole public pathology provider in Western Australia. FINDINGS: Between March 1, 2015, and December 31, 2016, 893 outbreak cases were notified. 798 (89%) of 893 outbreak cases were reported in Aboriginal people. 40 (4%) of 893 people were admitted to hospital, and 33 (7%) of 462 men reported orchitis. Mumps attack rates increased sharply with age, peaking in the 15-19 age group. 371 (89%) of 419 people aged 1-19 years were fully vaccinated and 29 (7%) were partly vaccinated. Of the 240 people who tested positive by real-time RT-PCR and had also been tested for mumps-specific IgG and IgM, 165 (69%) were positive for IgG but negative for IgM, indicating the importance of RT-PCR testing for diagnosis in vaccinated populations. None of the cases from the 2007-08 genotype J outbreak were re-notified. INTERPRETATION: The number of mumps outbreaks reported in recent years among highly vaccinated populations, including Indigenous populations, has been growing. More widespread and pre-emptive use of the third dose of measles, mumps, and rubella vaccine might be required to control and prevent future outbreaks in high-risk populations. Research should explore the benefit of increasing the intervals between vaccine doses to strengthen the durability of vaccine protection. FUNDING: None.


Assuntos
Surtos de Doenças/prevenção & controle , Vírus da Caxumba/genética , Vírus da Caxumba/imunologia , Caxumba/epidemiologia , Caxumba/prevenção & controle , Vacinação , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Seguimentos , Genótipo , Humanos , Incidência , Lactente , Masculino , Vacina contra Sarampo-Caxumba-Rubéola , Caxumba/transmissão , Caxumba/virologia , Vírus da Caxumba/isolamento & purificação , Reação em Cadeia da Polimerase em Tempo Real , Testes Sorológicos , Austrália Ocidental/epidemiologia , Adulto Jovem
2.
Pathology ; 49(7): 765-769, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29079005

RESUMO

Certain M protein types of group A streptococcus (GAS) are known to cause acute post-streptococcal glomerulonephritis (APSGN). Outbreaks of APSGN can occur regularly in tropical regions but the emm types responsible are geographically and temporally diverse. GAS isolates from Western Australia (WA) were analysed for emm type and emm cluster during the period of increased APSGN activity in the tropical northern Kimberley region of WA. Although emm types 49, 75 and 108 and corresponding emm clusters E3, E6 and D4 were more common in WA during the outbreak there was no predominant circulating emm type or cluster found to correspond to the APSGN activity. This is consistent with the high diversity of GAS strains found during APSGN outbreaks in other countries. Potential vaccine coverage of the new 30-valent M-protein GAS vaccine was 70%.


Assuntos
Antígenos de Bactérias/genética , Proteínas da Membrana Bacteriana Externa/genética , Proteínas de Transporte/genética , Surtos de Doenças , Glomerulonefrite/microbiologia , Infecções Estreptocócicas/microbiologia , Streptococcus pyogenes/genética , Doença Aguda , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Glomerulonefrite/diagnóstico , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Infecções Estreptocócicas/diagnóstico , Streptococcus pyogenes/isolamento & purificação , Austrália Ocidental/epidemiologia , Adulto Jovem
3.
N Z Med J ; 129(1429): 57-63, 2016 Jan 29.
Artigo em Inglês | MEDLINE | ID: mdl-26914300

RESUMO

AIMS: To gauge clinical opinion about the current system and possible changes as well as providing a forum for education about Non-Invasive Prenatal Testing (NIPT). METHODS: A series of workshops for doctors and midwives, supported by the National Screening Unit of the Ministry of Health and the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, were held in the main centres of New Zealand. Following a brief education session, a structured evaluation of current screening and future possibilities was undertaken by questionnaire. RESULTS: One hundred and eight maternity carers participated in 5 workshops. Over 40% identified barriers to current screening. More than 60% would support NIPT in the first trimester. The majority of carers provided their own counselling support for women. CONCLUSIONS: The survey has shown general enthusiasm for the introduction of publically funded NIPT into prenatal screening in New Zealand. Barriers to utilisation of the current system have been identified and enhancements to screening performance with guidelines around conditions to be screened for would be supported.


Assuntos
Aneuploidia , Atitude do Pessoal de Saúde , Transtornos Cromossômicos/diagnóstico , Testes para Triagem do Soro Materno , Ultrassonografia Pré-Natal , Biomarcadores/sangue , Feminino , Humanos , Nova Zelândia , Gravidez , Primeiro Trimestre da Gravidez/sangue , Inquéritos e Questionários
4.
Aust N Z J Public Health ; 40(2): 174-80, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26259550

RESUMO

OBJECTIVES: To determine local values for environmental attributable fractions and explore their applicability and potential for public health advocacy. METHODS: Using World Health Organization (WHO) values for environmental attributable fractions, responses from a practitioner survey (73% response rate) were considered by a smaller skills-based panel to determine consensus values for Kimberley environmental attributable fractions (KEAFs). Applied to de-identified data from 17 remote primary healthcare facilities over two years, numbers and proportions of reasons for attendance directly attributable to the environment were calculated for all ages and children aged 0-4 years, including those for Aboriginal patients. RESULTS: Of 150,357 reasons for attendance for patients of all ages, 31,775 (21.1%) were directly attributable to the environment. The proportion of these directly due to the environment was significantly higher for Aboriginal patients than others (23.1% v 14.6%; p<0.001). Of 29,706 reasons for attendance by Aboriginal children aged 0-4 years, 7,599 (25.6%) were directly attributable to the environment, significantly higher than for non-Aboriginal children aged 0-4 years (25.6% v 18.6%; p<0.001). CONCLUSIONS: By addressing environmental factors, 20% of total primary healthcare demand could be prevented and, importantly, some 25% of presentations by Aboriginal children. IMPLICATIONS: KEAFs have potential to monitor impact of local environmental investments.


Assuntos
Meio Ambiente , Exposição Ambiental , Havaiano Nativo ou Outro Ilhéu do Pacífico , Saúde Pública , Determinantes Sociais da Saúde , Austrália , Pré-Escolar , Humanos , Lactente , Recém-Nascido , Atenção Primária à Saúde
5.
Arch Dis Child ; 97(3): 279-82, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21965813

RESUMO

BACKGROUND: Paracetamol is the most commonly prescribed medicine for children. Age-based dosing guidelines can lead to inappropriate dosing. METHODS: A review of age-based guidelines for paracetamol in the British National Formulary for Children (BNFC) 2011-2012 was undertaken. Single and cumulative daily doses of paracetamol for boys and girls at 9th, 50th and 91st centiles for weight were calculated for the age groups 1-3 months, 3-12 months, 1-6 years and 6-12 years. RESULTS: For children at the 9th centile, aged 3 months and above, doses were above recommended single and cumulative daily dose therapeutic limits when given the highest dose specified for their age. For children at the 91st centile at all ages, doses were below recommended single and cumulative daily dose therapeutic limits when given the lowest dose specified for their age. CONCLUSIONS: Underweight and overweight children are at risk of inappropriate paracetamol administration based on BNFC age-based dosing instructions.


Assuntos
Acetaminofen/administração & dosagem , Analgésicos não Narcóticos/administração & dosagem , Antipiréticos/administração & dosagem , Prescrição Inadequada/estatística & dados numéricos , Farmacopeias como Assunto , Fatores Etários , Peso Corporal/fisiologia , Criança , Pré-Escolar , Esquema de Medicação , Feminino , Humanos , Prescrição Inadequada/prevenção & controle , Lactente , Masculino , Guias de Prática Clínica como Assunto , Medição de Risco/métodos , Fatores Sexuais , Reino Unido
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