Paediatrics (RCH) - Research Publications

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    Recurrent 6th nerve palsy in a child following different live attenuated vaccines: case report
    Cheng, DR ; Crawford, NW ; Hayman, M ; Buckley, C ; Buttery, JP (BMC, 2012-04-30)
    BACKGROUND: Recurrent benign 6th nerve palsy in the paediatric age group is uncommon, but has been described following viral and bacterial infections. It has also been temporally associated with immunization, but has not been previously described following two different live attenuated vaccines. CASE PRESENTATION: A case is presented of a 12 month old Caucasian boy with recurrent benign 6th nerve palsy following measles-mumps-rubella and varicella vaccines, given on separate occasions with complete recovery following each episode. No alternate underlying etiology was identified despite extensive investigations and review. CONCLUSIONS: The majority of benign 6th nerve palsies do not have a sinister cause and have an excellent prognosis, with recovery expected in most cases. The exact pathophysiology is unknown, although hypotheses including autoimmune mechanisms and direct viral invasion could explain the pathophysiology behind immunization related nerve palsies. It is important to rule out other aetiologies with thorough history, physical examination and investigations. There is limited information in the literature regarding the safety of a repeat dose of a live vaccine in this setting. Future immunizations should be considered on a case-by-case basis.
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    An australian audit of vaccination status in children and adolescents with inflammatory bowel disease
    Crawford, NW ; Catto-Smith, AG ; Oliver, MR ; Cameron, DJS ; Buttery, JP (BMC, 2011-07-29)
    BACKGROUND: Children and adolescents with inflammatory bowel disease (IBD) are at increased risk of vaccine preventable diseases (VPD). This includes invasive pneumococcal disease and influenza. The primary aim of this study was to describe compliance with current Australian guidelines for vaccination of children and adolescents diagnosed with IBD. A secondary aim was to review the serological screening for VPD. METHODS: A random sample of patients (0-18 years at diagnosis), were selected from the Victoria Australia state based Pediatric Inflammatory Bowel Disease Register. A multi-faceted retrospective review of immunization status was undertaken, with hospital records audited, a telephone interview survey conducted with consenting parents and the vaccination history was checked against the primary care physician and Australian Childhood Immunization Register (ACIR) records. The routine primary childhood vaccinations and administration of the recommended additional influenza and pneumococcal vaccines was clarified. RESULTS: This 2007 audit reviewed the immunization status of 101 individuals on the Victorian Pediatric IBD database. Median age at diagnosis was 12.1 years, 50% were on active immunosuppressive therapy. 90% (38/42) [95% confidence intervals (CI) 77%; 97%] with complete immunization information were up-to-date with routine primary immunizations. Only 5% (5/101) [95% CI 2%; 11%] received a recommended pneumococcal vaccine booster and 10% (10/101) [95% CI 5%; 17%] had evidence of having ever received a seasonal influenza vaccine. Those living in rural Victoria (p = 0.005) and younger at the age of diagnosis (p = 0.002) were more likely to have ever received an influenza vaccine Serological testing, reviewing historical protection from VPD, identified 18% (17/94) with evidence of at least one serology sample. CONCLUSION: This study highlights poor compliance in IBD patients for additional recommended vaccines. A multi-faceted approach is required to maximize protection from VPD in this vulnerable special risk population.
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    Allergic adverse events following 2015 seasonal influenza vaccine, Victoria, Australia
    Clothier, HJ ; Crawford, N ; Russell, MA ; Buttery, JP (EUR CENTRE DIS PREVENTION & CONTROL, 2017-05-18)
    Australia was alerted to a possible increase in allergy-related adverse events following immunisation (AEFI) with 2015 seasonal trivalent influenza vaccines (TIV) by the Victorian state vaccine safety service, SAEFVIC. We describe SAEFVIC's initial investigation and upon conclusion of the 2015 influenza vaccination programme, to define the signal event and implications for vaccine programmes. Allergy-related AEFI were defined as anaphylaxis, angioedema, urticaria or generalised allergic reaction. Investigations compared 2015 TIV AEFI reports to previous years as proportions and reporting risk (RR) per 100,000, stratified by influenza vaccine brand. The initial investigation showed an increased proportion of allergy-related AEFI compared with 2014 (25% vs 12%), predominantly in adults, with insufficient clinical severity to alter the programme risk-benefit. While overall TIV AEFI RR in 2015 was similar to previous years (RR: 1.07, 95% confidence interval (CI): 0.88-1.29), we identified a near-doubling RR for allergy-related AEFI in 2015 (RR: 1.78, 95% CI: 1.14-- 2.80) from 2011 to 2014 with no difference by vaccine brand or severity increase identified. This increase in generalised allergy-related AEFI, across all used vaccine brands, supports evidence of variable reactogenicity arising from influenza vaccine strain variations. This investigation underlines the importance of effective seasonal influenza vaccine pharmacovigilance.
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    Invasive group A Streptococcus disease in Australian children: 2016 to 2018-a descriptive cohort study
    Oliver, J ; Thielemans, E ; McMinn, A ; Baker, C ; Britton, PN ; Clark, JE ; Marshall, HS ; Blyth, CC ; Francis, J ; Buttery, J ; Steer, AC ; Crawford, NW ; Booy, R ; Connell, J ; Dale, R ; Deverell, M ; Dinsmore, N ; Dougherty, S ; Finucane, C ; Gibson, M ; Gold, M ; Heath, C ; Hickie, L ; Hutchinson, T ; Jones, C ; Jones, J ; Kent, J ; Knight, H ; Kynaston, A ; Lee, D ; Lewis, G ; Low, S ; Maclean, N ; Macartney, K ; McDonald, F ; McLaren, N ; Mcrae, J ; Murphy, J ; Meredith, K ; Nissen, M ; Orr, C ; Orr, K ; Phillips, N ; Pym, M ; Quinn, J ; Richmond, P ; Rhind, L ; Roberts, A ; Robins, C ; Rost, L ; Royle, J ; Saravanos, G ; Snelling, T ; Talbott, C ; Tan, S ; Trinh, L ; Vidler, L ; Walker, M ; West, R ; Wharton, C ; Wood, N ; Zurynski, Y (BMC, 2019-12-30)
    OBJECTIVES: Invasive group A Streptococcus (iGAS) disease is serious and sometimes life-threatening. The Paediatric Active Enhanced Disease Surveillance (PAEDS) Network collects voluntary notifications from seven major Australian paediatric hospitals on patients with certain conditions, including iGAS disease. Our aims were to: 1) Describe the epidemiological distribution of paediatric iGAS disease in Australia and correlate this with influenza notifications, 2) Identify GAS strains commonly associated with invasive disease in children. METHODS: IGAS and influenza notification data were obtained (from the PAEDS Network and the Australian Institute of Health and Welfare, respectively, for the period 1 July 2016 to 30 June 2018). Included iGAS patients had GAS isolated from a normally sterile body site. Data were described according to selected clinical and demographic characteristics, including by age group and Australian State, with proportions and minimum incidence rates estimated. RESULTS: A total of 181 patients were identified, with most (115, 63.5%) <5 years old. The mean annual minimum incidence rate was 1.6 (95% confidence interval: 1.1-2.3) per 100,000 children across the study period. An epidemiological correlation with the seasonal burden of influenza was noted. Contact prophylaxis was not consistently offered. Of 96 patients with emm-typing results available, 72.9% showed emm-1, -4 or - 12. CONCLUSIONS: Robust surveillance systems and cohesive patient management guidelines are needed. Making iGAS disease nationally notifiable would help facilitate this. Influenza vaccination may contribute to reducing seasonal increases in iGAS incidence. The burden of disease emphasises the need for ongoing progress in GAS vaccine development.
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    Mass psychogenic response to human papillomavirus vaccination
    Buttery, JP ; Madin, S ; Crawford, NW ; Elia, S ; La Vincente, S ; Hanieh, S ; Smith, L ; Bolam, B (AUSTRALASIAN MED PUBL CO LTD, 2008-09-01)