J Massie

Summary

Affiliation: Royal Children's Hospital
Country: Australia

Publications

  1. ncbi request reprint Sweat testing for cystic fibrosis: How good is your laboratory?
    John Massie
    J Paediatr Child Health 42:153-4. 2006
  2. ncbi request reprint Lessons learned from 20 years of newborn screening for cystic fibrosis
    R John H Massie
    Department of Respiratory Medicine, Royal Children s Hospital Melbourne, Melbourne, Vic
    Med J Aust 196:67-70. 2012
  3. doi request reprint Declining prevalence of cystic fibrosis since the introduction of newborn screening
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Victoria 3052, Australia
    Arch Dis Child 95:531-3. 2010
  4. doi request reprint Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience
    John Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute Unit, Royal Children s Hospital, Melbourne, Victoria 3052, Australia
    Aust N Z J Obstet Gynaecol 49:484-9. 2009
  5. pmc Implementation of evidence based guidelines for paediatric asthma management in a teaching hospital
    J Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute, Royal Children s Hospital, Parkville, Victoria 3052, Australia
    Arch Dis Child 89:660-4. 2004
  6. ncbi request reprint Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Victoria, Australia
    J Paediatr Child Health 43:721-3. 2007
  7. ncbi request reprint Diagnosis of cystic fibrosis after newborn screening: the Australasian experience--twenty years and five million babies later: a consensus statement from the Australasian Paediatric Respiratory Group
    John Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute and University of Melbourne Royal Children s Hospital, Melbourne, Australia
    Pediatr Pulmonol 39:440-6. 2005
  8. ncbi request reprint Cough in children: when does it matter?
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Flemington Road, Parkville, Victoria 3052, Australia
    Paediatr Respir Rev 7:9-14. 2006
  9. pmc Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing
    J Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Victoria, Australia
    Arch Dis Child 91:222-5. 2006
  10. ncbi request reprint Sweat testing following newborn screening for cystic fibrosis
    J Massie
    Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Sydney, Australia
    Pediatr Pulmonol 29:452-6. 2000

Collaborators

Detail Information

Publications39

  1. ncbi request reprint Sweat testing for cystic fibrosis: How good is your laboratory?
    John Massie
    J Paediatr Child Health 42:153-4. 2006
  2. ncbi request reprint Lessons learned from 20 years of newborn screening for cystic fibrosis
    R John H Massie
    Department of Respiratory Medicine, Royal Children s Hospital Melbourne, Melbourne, Vic
    Med J Aust 196:67-70. 2012
    ..To compare three cystic fibrosis (CF) newborn screening strategies used in Victoria since 1989...
  3. doi request reprint Declining prevalence of cystic fibrosis since the introduction of newborn screening
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Victoria 3052, Australia
    Arch Dis Child 95:531-3. 2010
    ..The aim of this study was to assess the evidence for changes in the live-birth prevalence of CF since the introduction of newborn screening for CF...
  4. doi request reprint Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience
    John Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute Unit, Royal Children s Hospital, Melbourne, Victoria 3052, Australia
    Aust N Z J Obstet Gynaecol 49:484-9. 2009
    ..The carrier frequency is one per 25 and most babies with CF are born to parents with no family history. Carrier testing is possible before a couple has an affected infant...
  5. pmc Implementation of evidence based guidelines for paediatric asthma management in a teaching hospital
    J Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute, Royal Children s Hospital, Parkville, Victoria 3052, Australia
    Arch Dis Child 89:660-4. 2004
    ..To evaluate a systematic approach to the development and implementation of evidence based asthma management guidelines...
  6. ncbi request reprint Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Victoria, Australia
    J Paediatr Child Health 43:721-3. 2007
    ..Waiting for couples to have a baby with CF before they are identified as carriers denies them choice. A national policy on CF carrier screening in Australia, and determination to equitably fund such a programme, is required...
  7. ncbi request reprint Diagnosis of cystic fibrosis after newborn screening: the Australasian experience--twenty years and five million babies later: a consensus statement from the Australasian Paediatric Respiratory Group
    John Massie
    Department of Respiratory Medicine, Murdoch Children s Research Institute and University of Melbourne Royal Children s Hospital, Melbourne, Australia
    Pediatr Pulmonol 39:440-6. 2005
    ..The aim of this paper is to provide some consensus on the important issues of a cystic fibrosis diagnosis arising from newborn screening, based on the experience gained in Australia and New Zealand over the last 20 years...
  8. ncbi request reprint Cough in children: when does it matter?
    John Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Flemington Road, Parkville, Victoria 3052, Australia
    Paediatr Respir Rev 7:9-14. 2006
    ..In most cases cause can be identified or a satisfactory label given. This review will cover the approach to cough in children and cover some specific causes of troublesome cough not discussed elsewhere in this mini-symposium...
  9. pmc Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing
    J Massie
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Victoria, Australia
    Arch Dis Child 91:222-5. 2006
    ....
  10. ncbi request reprint Sweat testing following newborn screening for cystic fibrosis
    J Massie
    Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Sydney, Australia
    Pediatr Pulmonol 29:452-6. 2000
    ..Infants with sweat Cl(-) levels of 40-60 mmol/L require further investigation and review, but they almost certainly have CF. The Cl(-):Na(+) ratio does not appear useful in establishing a diagnosis of CF in infants...
  11. pmc Genetic counselling after carrier detection by newborn screening when one parent carries DeltaF508 and the other R117H
    L Curnow
    Genetic Health Services Victoria, Murdoch Children s Research Institute, Royal Children s Hospital, Melbourne, Victoria, Australia
    Arch Dis Child 88:886-8. 2003
    ..Owing to the variable phenotype associated with R117H we have developed an approach to this difficult genetic counselling situation. Centres offering or considering NBS for CF will need an approach to this problem...
  12. doi request reprint Population-based genetic screening for cystic fibrosis: attitudes and outcomes
    L Ioannou
    Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, Vic, Australia
    Public Health Genomics 13:449-56. 2010
    ..We conclude that participants' attitude towards carrier screening for CF was generally very positive. Our model of screening could be applied on a larger scale...
  13. doi request reprint Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schools
    L Ioannou
    Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, Victoria, Australia
    Clin Genet 78:21-31. 2010
    ..This has implications for multi-disease screening programmes that will increase in frequency as more conditions can be screened for and costs diminish...
  14. ncbi request reprint Double aortic arch presenting as severe bronchiolitis in a 2-week-old infant
    Amanda L Griffiths
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Victoria, Australia
    J Paediatr Child Health 41:297-9. 2005
    ..This case report emphasizes the importance of clinical history, examination findings and interpretation of the ventilator waveforms in the differential diagnosis of a difficult-to-ventilate infant with bronchiolitis...
  15. doi request reprint Chylothorax: diagnosis and management in children
    Manuel Soto-Martinez
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Parkville, Melbourne, Victoria 3052, Australia
    Paediatr Respir Rev 10:199-207. 2009
    ..Surgical intervention may be attempted thoracoscopically with repair or ligation of the thoracic duct...
  16. ncbi request reprint Polyflex stenting of tracheomalacia after surgery for congenital tracheal stenosis
    James Tibballs
    Department of Intensive Care, Royal Children s Hospital, Parkville, Melbourne, Victoria 3052, Australia
    Int J Pediatr Otorhinolaryngol 71:159-63. 2007
    ..Complications of granuloma, stent migration or dislodgement occurred in all cases. A fatal tracheo-aortic fistula occurred in one child. Granuloma in one was treated successfully with steroids. One child survives...
  17. doi request reprint A home respiratory support programme for children by parents and layperson carers
    James Tibballs
    Intensive Care Unit, University of Melbourne, Melbourne, Victoria, Australia
    J Paediatr Child Health 46:57-62. 2010
    ..To describe a respiratory support programme for children at home by parents and layperson carers...
  18. ncbi request reprint Changing their minds with time: a comparison of hypothetical and actual reproductive behaviors in parents of children with cystic fibrosis
    Susan M Sawyer
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Victoria, Australia
    Pediatrics 118:e649-56. 2006
    ..We aimed to measure parent attitudes to reproductive technologies and to compare prospectively these attitudes with later reproductive behaviors...
  19. ncbi request reprint Parental attitudes to the identification of their infants as carriers of cystic fibrosis by newborn screening
    Sharon Lewis
    Murdoch Childrens Research Institute, Royal Children s Hospital, Melbourne, Australia
    J Paediatr Child Health 42:533-7. 2006
    ..To investigate parental attitudes to cystic fibrosis (CF) carrier detection of their infant by newborn screening (NBS)...
  20. doi request reprint Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals
    Avantika Mishra
    Department of Biochemical Genetics, VCGS Pathology, The Royal Children s Hospital, Parkville, Victoria, Australia
    J Pediatr 153:758-63. 2008
    ..To develop reference intervals (RIs) for sweat chloride and sodium in healthy children, adolescents, and adults...
  21. doi request reprint Problem behaviours and parenting in preschool children with cystic fibrosis
    C Ward
    Centre for Community Child Health, Royal Children s Hospital, Parkville, Australia
    Arch Dis Child 94:341-7. 2009
    ..Problems with sleep, eating and adherence to therapy may adversely affect health outcomes in children with cystic fibrosis (CF). Data on the prevalence of such problems, associated parenting styles and caregiver mental health are limited...
  22. doi request reprint Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening
    Stephen M Stick
    Department of Respiratory Medicine, Princess Margaret Hospital for Children, School of Paediatrics and Child Health, University of Western Australia, Melbourne, Australia
    J Pediatr 155:623-8.e1. 2009
    ..To determine the prevalence of bronchiectasis in young children with cystic fibrosis (CF) diagnosed after newborn screening (NBS) and the relationship of bronchiectasis to pulmonary inflammation and infection...
  23. doi request reprint Treatment of acne with oral isotretinoin in patients with cystic fibrosis
    E Perera
    Faculty of Medicine, University of Melbourne, Melbourne, Australia
    Arch Dis Child 94:583-6. 2009
    ..Theoretical concerns about liver disease and vitamin A deficiency have limited the use of oral isotretinoin for troublesome acne in adolescents with cystic fibrosis...
  24. doi request reprint Lung function in infants with cystic fibrosis diagnosed by newborn screening
    Barry M Linnane
    Department of Respiratory Medicine, Royal Children s Hospital Melbourne, Parkville, Australia
    Am J Respir Crit Care Med 178:1238-44. 2008
    ..Progressive lung damage in cystic fibrosis (CF) starts in infancy, and early detection may aid preventative strategies...
  25. ncbi request reprint Estimating inspired oxygen concentration delivered by nasal prongs in children with bronchiolitis
    Valerie Sung
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Victoria, Australia
    J Paediatr Child Health 44:14-8. 2008
    ..We aimed to determine whether FiO(2) of oxygen delivered by nasal prongs could be predicted from nasal flow by relating arterial oxygen concentrations achieved with prongs to those achieved via head box in children with bronchiolitis...
  26. ncbi request reprint Effects of segregation on an epidemic Pseudomonas aeruginosa strain in a cystic fibrosis clinic
    Amanda L Griffiths
    Department of Respiratory Medicine, Royal Children s Hospital, Parkville, Australia
    Am J Respir Crit Care Med 171:1020-5. 2005
    ..Further studies are needed to resolve whether cohort segregation completely eliminates cross-infection and if acquisition of epidemic isolates is associated with worse outcomes...
  27. doi request reprint Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosis
    Tonia A Douglas
    Department of Respiratory Medicine, Princess Margaret Hospital for Children, Roberts Road, Subiaco, Perth, WA 6008, Australia
    Thorax 65:985-90. 2010
    ..The accuracy of serum antibodies against specific and multiple P aeruginosa antigens at predicting lower airway infection in young children with cystic fibrosis (CF) was investigated...
  28. ncbi request reprint The CT appearances of delayed amniotic fluid clearance from the lungs in an infant with absent pulmonary valve and congenital lobar emphysema
    A Michelle Fink
    Department of Medical Imaging, The Royal Children s Hospital, Flemington Road, Parkville, Victoria 3052, Australia
    Pediatr Radiol 35:891-4. 2005
    ..This resorption of fetal lung fluid via the pulmonary interstitium should not be confused with interstitial lung disease...
  29. doi request reprint Paralysis and a perihilar protuberance: an unusual presentation of sarcoidosis in a child
    Danielle F Wurzel
    Department of Respiratory Medicine, Royal Children s Hospital Melbourne, Parkville, Victoria, Australia
    Pediatr Pulmonol 44:410-4. 2009
    ..We also report the first successful use of the minimally invasive technique of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration (EBUS-TBNA) to delineate the cause of hilar lymphadenopathy in a child...
  30. doi request reprint Early bronchiectasis in cystic fibrosis detected by surveillance CT
    Naveen Pillarisetti
    Department of Respiratory Medicine, Royal Children s Hospital, Melbourne, Victoria, Australia
    Respirology 15:1009-11. 2010
    ....
  31. ncbi request reprint Pharmacokinetic profile of once daily intravenous tobramycin in children with cystic fibrosis
    John Massie
    Department of Respiratory Medicine, University of Melbourne, Melbourne, Victoria, Australia
    J Paediatr Child Health 42:601-5. 2006
    ..The aim of this study was to define the PK parameters for once-daily tobramycin in children with CF and develop an algorithm for therapeutic drug monitoring dosing...
  32. ncbi request reprint Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report
    Anne Marie Comeau
    New England Newborn Screening Program and Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts, USA
    Pediatrics 119:e495-518. 2007
    ....
  33. doi request reprint Re: acrodermatitis enteropathica-like eruption and failure to thrive as presenting signs of cystic fibrosis
    John Massie
    J Am Acad Dermatol 59:720-1. 2008
  34. pmc Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report
    Philip M Farrell
    Department of Pediatrics and Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA
    J Pediatr 153:S4-S14. 2008
    ..Their recommendations, presented herein, involve a combination of clinical presentation, laboratory testing, and genetics to confirm a diagnosis of CF...
  35. ncbi request reprint National study of infants hospitalized with pertussis in the acellular vaccine era
    Elizabeth Elliott
    Discipline of Paediatrics and Child Health, The University of Sydney and The Children s Hospital at Westmead, Sydney, Australia
    Pediatr Infect Dis J 23:246-52. 2004
    ..Few data are available on pertussis hospitalizations or sources of infection in countries exclusively using DTPa...
  36. ncbi request reprint Pleural empyema in a 14-year-old adolescent with cystic fibrosis
    Amanda L Griffiths
    J Paediatr Child Health 42:396-7. 2006
  37. pmc Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening
    Marco Cipolli
    Cystic Fibrosis Centre, Azienda Ospedaliera di Verona, Verona, Italy
    Arch Dis Child 92:842-6. 2007
    ..To determine the pancreatic phenotype of infants with cystic fibrosis (CF) diagnosed in the first week of life by a combined immunoreactive trypsin/mutation screening program...
  38. ncbi request reprint Economic evaluation of cystic fibrosis screening: a review of the literature
    Muralikrishnan Radhakrishnan
    Centre for Health Economics Research and Evaluation, University of Technology, Sydney, NSW, Australia
    Health Policy 85:133-47. 2008
    ..To critically examine the economic evidence regarding cystic fibrosis (CF) carrier screening and to understand issues relating to the transferability of international findings to any national context for policy decisions...
  39. ncbi request reprint Mobile phones and asthma: there is a correlation!
    Gaudenz M Hafen
    Med J Aust 181:712. 2004