Noni E. MacDonald
Dalhousie University
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Publication
Featured researches published by Noni E. MacDonald.
Canadian Medical Association Journal | 2011
Kevin Pottie; Christina Greenaway; John Feightner; Vivian Welch; Helena Swinkels; Meb Rashid; Lavanya Narasiah; Laurence J. Kirmayer; Erin Ueffing; Noni E. MacDonald; Ghayda Hassan; Mary McNally; Kamran Khan; R. Buhrmann; Sheila Dunn; Arunmozhi Dominic; Anne McCarthy; Anita J. Gagnon; Cécile Rousseau; Peter Tugwell
(see Appendix 2, available at [www.cmaj.ca/lookup/suppl/doi:10.1503/cmaj.090313/-/DC1][1] for summary of recommendations and clinical considerations) There are more than 200 million international migrants worldwide,[1][2] and this movement of people has implications for individual and
Pediatrics | 1999
Barbara Law; Catherine Fitzsimon; Lee Ford-Jones; Noni E. MacDonald; Pierre Déry; Wendy Vaudry; Elaine L. Mills; Scott Halperin; Andrea Michaliszyn; Marc Rivière
Objective. The purpose of this study was to assess the direct medical costs and productivity losses associated with uncomplicated chickenpox (no hospitalization) in Canada. Methods. A total of 179 otherwise healthy 1- to 9-year-old children with active chickenpox were recruited from schools, day care centers, and physician offices in 5 provinces. Direct medical (physician contacts, medication, and diagnostic tests) and nonmedical (personal expenses including child care) resources expended during the illness were determined by caregiver interview. Productivity losses attributable to the disease were determined by assessing caregiver time lost from work and daily activities. Unit costs for all resources were obtained from sources in 2 provinces, and per-patient treatment costs were determined from the patient, Ministry of Health, and societal perspectives. Results. From a societal perspective, the per-case cost for children from 1 to 4 years of age and from 5 to 9 years of age was
The Lancet | 2009
Steven Black; Juhani Eskola; Claire-Anne Siegrist; Neal A. Halsey; Noni E. MacDonald; Barbara Law; Elizabeth Miller; Nick Andrews; Julia Stowe; Daniel A. Salmon; Kirsten S. Vannice; Hector S. Izurieta; Aysha Akhtar; Michael Gold; Gabriel Wolf Oselka; Patrick Zuber; Dina Pfeifer; Claudia Vellozzi
370.2 and
The Lancet | 2005
Shawn D. Aaron; Katherine L. Vandemheen; Wendy Ferris; Dean Fergusson; Elizabeth Tullis; David Haase; Yves Berthiaume; Neil E. Brown; Pearce G. Wilcox; Veronica Yozghatlian; Peter Bye; Scott C. Bell; Francis Chan; Barbara Rose; Alphonse Jeanneret; Anne Stephenson; Mary Noseworthy; Andreas Freitag; Nigel A. M. Paterson; Steve Doucette; Colin Harbour; Michel Ruel; Noni E. MacDonald
236.5, respectively. Direct medical costs accounted for 10% of the total costs in both groups. The largest cost driver in patient care was caregiver productivity losses, which amounted to
Canadian Medical Association Journal | 2010
Anna Taddio; Mary Appleton; Robert Bortolussi; Christine T. Chambers; Vinita Dubey; Scott A. Halperin; Anita Hanrahan; Moshe Ipp; Donna Lockett; Noni E. MacDonald; Deana Midmer; Patricia Mousmanis; Valerie Palda; Karen Pielak; Rebecca Pillai Riddell; Michael J. Rieder; Jeffrey Scott; Vibhuti Shah
316.5 in the younger age group and to
Expert Review of Vaccines | 2015
Eve Dubé; Maryline Vivion; Noni E. MacDonald
182.7 in the older age group. Based on an estimated yearly incidence of 344 656 cases of uncomplicated chickenpox in Canada, the total annual societal burden of the disease can be estimated at
Canadian Medical Association Journal | 2007
Noni E. MacDonald; Tom Wong
109.2 million, with a cost to the Ministry of Health of
Journal of Autoimmunity | 2014
S. Sohail Ahmed; Peter H. Schur; Noni E. MacDonald; Lawrence Steinman
11.2 million. Conclusion. Chickenpox is one of the last common childhood diseases prevalent in Canada, and the uncomplicated disease, despite its rather benign course, imparts a large annual economic burden.
Pediatric Infectious Disease Journal | 1999
Sandra R. Arnold; Elaine E. L. Wang; Barbara J. Law; François D. Boucher; Derek Stephens; Joan Robinson; Simon Dobson; Joanne M. Langley; Jane McDonald; Noni E. MacDonald; Ian Mitchell
Because of the advent of a new influenza A H1N1 strain, many countries have begun mass immunisation programmes. Awareness of the background rates of possible adverse events will be a crucial part of assessment of possible vaccine safety concerns and will help to separate legitimate safety concerns from events that are temporally associated with but not caused by vaccination. We identified background rates of selected medical events for several countries. Rates of disease events varied by age, sex, method of ascertainment, and geography. Highly visible health conditions, such as Guillain-Barré syndrome, spontaneous abortion, or even death, will occur in coincident temporal association with novel influenza vaccination. On the basis of the reviewed data, if a cohort of 10 million individuals was vaccinated in the UK, 21.5 cases of Guillain-Barré syndrome and 5.75 cases of sudden death would be expected to occur within 6 weeks of vaccination as coincident background cases. In female vaccinees in the USA, 86.3 cases of optic neuritis per 10 million population would be expected within 6 weeks of vaccination. 397 per 1 million vaccinated pregnant women would be predicted to have a spontaneous abortion within 1 day of vaccination.
Vaccine | 2015
Eve Dubé; Dominique Gagnon; Noni E. MacDonald
BACKGROUND We did a randomised, double-blind, controlled clinical trial to prospectively assess whether use of combination antibiotic susceptibility testing improved clinical outcomes in patients with acute pulmonary exacerbations of cystic fibrosis who were infected with multiresistant bacteria. METHODS 251 patients with cystic fibrosis who were chronically infected with multiresistant gram negative bacteria gave sputum at 3-month intervals for conventional culture and sensitivity tests and for combination antibiotic susceptibility tests using multiple combination bactericidal antibiotic testing (MCBT). Patients who developed an exacerbation of pulmonary disease were randomised to receive a 14-day course of any two blinded intravenous antibiotics chosen on the basis of either results from conventional sputum culture and sensitivity testing or the result of MCBT. The primary outcome was time from randomisation until the patients next pulmonary exacerbation. Analysis was by intention-to-treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN60187870. FINDINGS 132 patients had a pulmonary exacerbation and were randomised during the 4.5-year study period. The time to next pulmonary exacerbation was not prolonged in the MCBT-treated group (hazard ratio 0.86 in favour of the conventionally-treated group, 95% CI 0.60-1.23, p=0.40). There was no difference between the groups in treatment failure rate. After 14 days of intravenous antibiotic therapy, changes in lung function, dyspnoea, and sputum bacterial density were similar in both groups. INTERPRETATION Antibiotic therapy directed by combination antibiotic susceptibility testing did not result in better clinical and bacteriological outcomes compared with therapy directed by standard culture and sensitivity techniques. The non-bactericidal effects of antibiotic therapy might play an important part in determining improvement in patients with cystic fibrosis pulmonary exacerbations.