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Dive into the research topics where Michael A. Campitelli is active.

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Featured researches published by Michael A. Campitelli.


Clinical Infectious Diseases | 2011

Obesity and Respiratory Hospitalizations During Influenza Seasons in Ontario, Canada: A Cohort Study

Jeffrey C. Kwong; Michael A. Campitelli; Laura Rosella

Evidence from the 2009 H1N1 pandemic suggests that severe obesity was a risk factor for serious complications from influenza infection. Our study identifies severe obesity as a risk factor for respiratory hospitalizations during seasonal influenza epidemics.


JAMA | 2014

Combination Long-Acting β-Agonists and Inhaled Corticosteroids Compared With Long-Acting β-Agonists Alone in Older Adults With Chronic Obstructive Pulmonary Disease

Andrea S. Gershon; Michael A. Campitelli; Ruth Croxford; Matthew B. Stanbrook; Teresa To; Ross Upshur; Anne L. Stephenson; Therese A. Stukel

IMPORTANCE Chronic obstructive pulmonary disease (COPD), a manageable respiratory condition, is the third leading cause of death worldwide. Knowing which prescription medications are the most effective in improving health outcomes for people with COPD is essential to maximizing health outcomes. OBJECTIVE To estimate the long-term benefits of combination long-acting β-agonists (LABAs) and inhaled corticosteroids compared with LABAs alone in a real-world setting. DESIGN, SETTING, AND PATIENTS Population-based, longitudinal cohort study conducted in Ontario, Canada, from 2003 to 2011. All individuals aged 66 years or older who met a validated case definition of COPD on the basis of health administrative data were included. After propensity score matching, there were 8712 new users of LABA-inhaled corticosteroid combination therapy and 3160 new users of LABAs alone who were followed up for median times of 2.7 years and 2.5 years, respectively. EXPOSURES Newly prescribed combination LABAs and inhaled corticosteroids or LABAs alone. MAIN OUTCOMES AND MEASURES Composite outcome of death and COPD hospitalization. RESULTS The main outcome was observed among 5594 new users of LABAs and inhaled corticosteroids (3174 deaths [36.4%]; 2420 COPD hospitalizations [27.8%]) and 2129 new users of LABAs alone (1179 deaths [37.3%]; 950 COPD hospitalizations [30.1%]). New use of LABAs and inhaled corticosteroids was associated with a modestly reduced risk of death or COPD hospitalization compared with new use of LABAs alone (difference in composite outcome at 5 years, -3.7%; 95% CI, -5.7% to -1.7%; hazard ratio [HR], 0.92; 95% CI, 0.88-0.96). The greatest difference was among COPD patients with a codiagnosis of asthma (difference in composite at 5 years, -6.5%; 95% CI, -10.3% to -2.7%; HR, 0.84; 95% CI, 0.77-0.91) and those who were not receiving inhaled long-acting anticholinergic medication (difference in composite at 5 years, -8.4%; 95% CI, -11.9% to -4.9%; HR, 0.79; 95% CI, 0.73-0.86). CONCLUSIONS AND RELEVANCE Among older adults with COPD, particularly those with asthma and those not receiving a long-acting anticholinergic medication, newly prescribed LABA and inhaled corticosteroid combination therapy, compared with newly prescribed LABAs alone, was associated with a significantly lower risk of the composite outcome of death or COPD hospitalization.


PLOS ONE | 2012

The Impact of Infection on Population Health: Results of the Ontario Burden of Infectious Diseases Study

Jeffrey C. Kwong; Sujitha Ratnasingham; Michael A. Campitelli; Nick Daneman; Shelley L. Deeks; Douglas G. Manuel; Vanessa Allen; Ahmed M. Bayoumi; Aamir Fazil; David N. Fisman; Andrea S. Gershon; Effie Gournis; E. Jenny Heathcote; Frances Jamieson; Prabhat Jha; Kamran Khan; Shannon E. Majowicz; Tony Mazzulli; Allison McGeer; Matthew P. Muller; Abhishek Raut; Elizabeth Rea; Robert S. Remis; Rita Shahin; Alissa J. Wright; Brandon Zagorski; Natasha S. Crowcroft

Background Evidence-based priority setting is increasingly important for rationally distributing scarce health resources and for guiding future health research. We sought to quantify the contribution of a wide range of infectious diseases to the overall infectious disease burden in a high-income setting. Methodology/Principal Findings We used health-adjusted life years (HALYs), a composite measure comprising premature mortality and reduced functioning due to disease, to estimate the burden of 51 infectious diseases and associated syndromes in Ontario using 2005–2007 data. Deaths were estimated from vital statistics data and disease incidence was estimated from reportable disease, healthcare utilization, and cancer registry data, supplemented by local modeling studies and national and international epidemiologic studies. The 51 infectious agents and associated syndromes accounted for 729 lost HALYs, 44.2 deaths, and 58,987 incident cases per 100,000 population annually. The most burdensome infectious agents were: hepatitis C virus, Streptococcus pneumoniae, Escherichia coli, human papillomavirus, hepatitis B virus, human immunodeficiency virus, Staphylococcus aureus, influenza virus, Clostridium difficile, and rhinovirus. The top five, ten, and 20 pathogens accounted for 46%, 67%, and 75% of the total infectious disease burden, respectively. Marked sex-specific differences in disease burden were observed for some pathogens. The main limitations of this study were the exclusion of certain infectious diseases due to data availability issues, not considering the impact of co-infections and co-morbidity, and the inability to assess the burden of milder infections that do not result in healthcare utilization. Conclusions/Significance Infectious diseases continue to cause a substantial health burden in high-income settings such as Ontario. Most of this burden is attributable to a relatively small number of infectious agents, for which many effective interventions have been previously identified. Therefore, these findings should be used to guide public health policy, planning, and research.


Lancet Infectious Diseases | 2013

Risk of Guillain-Barré syndrome after seasonal influenza vaccination and influenza health-care encounters: a self-controlled study

Jeffrey C. Kwong; Priya P Vasa; Michael A. Campitelli; Steven Hawken; Kumanan Wilson; Laura Rosella; Therese A. Stukel; Natasha S. Crowcroft; Allison McGeer; Lorne Zinman; Shelley L. Deeks

BACKGROUND The possible risk of Guillain-Barré syndrome from influenza vaccines remains a potential obstacle to achieving high vaccination coverage. However, influenza infection might also be associated with Guillain-Barré syndrome. We aimed to assess the risk of Guillain-Barré syndrome after seasonal influenza vaccination and after influenza-coded health-care encounters. METHODS We used the self-controlled risk interval design and linked universal health-care system databases from Ontario, Canada, with data obtained between 1993 and 2011. We used physician billing claims for influenza vaccination and influenza-coded health-care encounters to ascertain exposures. Using fixed-effects conditional Poisson regression, we estimated the relative incidence of hospitalisation for primary-coded Guillain-Barré syndrome during the risk interval compared with the control interval. FINDINGS We identified 2831 incident admissions for Guillain-Barré syndrome; 330 received an influenza vaccine and 109 had an influenza-coded health-care encounter within 42 weeks before hospitalisation. The risk of Guillain-Barré syndrome within 6 weeks of vaccination was 52% higher than in the control interval of 9-42 weeks (relative incidence 1·52; 95% CI 1·17-1·99), with the greatest risk during weeks 2-4 after vaccination. The risk of Guillain-Barré syndrome within 6 weeks of an influenza-coded health-care encounter was greater than for vaccination (15·81; 10·28-24·32). The attributable risks were 1·03 Guillain-Barré syndrome admissions per million vaccinations, compared with 17·2 Guillain-Barré syndrome admissions per million influenza-coded health-care encounters. INTERPRETATION The relative and attributable risks of Guillain-Barré syndrome after seasonal influenza vaccination are lower than those after influenza illness. Patients considering immunisation should be fully informed of the risks of Guillain-Barré syndrome from both influenza vaccines and influenza illness. FUNDING Canadian Institutes of Health Research.


Thorax | 2015

Increased risk of mycobacterial infections associated with anti-rheumatic medications

Sarah K. Brode; Frances B. Jamieson; Ryan Ng; Michael A. Campitelli; Jeffrey C. Kwong; Paterson Jm; Ping Li; Alex Marchand-Austin; Claire Bombardier; Theodore K. Marras

Rationale Anti-tumour necrosis factor (TNF) agents and other anti-rheumatic medications increase the risk of TB in rheumatoid arthritis (RA). Whether they increase the risk of infections with nontuberculous mycobacteria (NTM) is uncertain. Objectives To determine the effect of anti-TNF therapy and other anti-rheumatic drugs on the risk of NTM disease and TB in older patients with RA. Methods Population-based nested case–control study among Ontario seniors aged ≥67 years with RA who were prescribed at least one anti-rheumatic medication between 2001 and 2011. We identified cases of TB and NTM disease microbiologically and identified drug exposures using linked prescription drug claims. We estimated ORs using conditional logistic regression, controlling for several potential confounders. Measurements and main results Among 56 269 older adults with RA, we identified 37 cases of TB and 211 cases of NTM disease; each case was matched to up to 10 controls. Individuals with TB or NTM disease were both more likely to be using anti-TNF therapy (compared with non-use); adjusted ORs (95% CIs) were 5.04 (1.27 to 20.0) and 2.19 (1.10 to 4.37), respectively. Exposure to leflunomide and other anti-rheumatic drugs with high immunosuppressing potential also were associated with both TB and NTM disease, while oral corticosteroids and hydroxychloroquine were associated with NTM disease. Conclusions Anti-TNF use is associated with increased risk of both TB and NTM disease, but appears to be a relatively greater risk for TB. Several other anti-rheumatic drugs were also associated with mycobacterial infections.


Clinical Infectious Diseases | 2013

Vaccine Effectiveness Against Laboratory-Confirmed Influenza Hospitalizations Among Elderly Adults During the 2010–2011 Season

Jeffrey C. Kwong; Michael A. Campitelli; Jonathan B. Gubbay; Adriana Peci; Anne-Luise Winter; Romy Olsha; Robert Turner; Laura Rosella; Natasha S. Crowcroft

Although the benefits of influenza vaccines for preventing serious influenza outcomes in elderly adults are uncertain, the results of this study suggest that the 2010–2011 influenza vaccine was 42% effective in reducing laboratory-confirmed influenza hospitalizations in this high-risk population.


Hepatology | 2013

Health care costs associated with hepatocellular carcinoma: a population-based study.

Hla Hla Thein; Wanrudee Isaranuwatchai; Michael A. Campitelli; Jordan J. Feld; Eric M. Yoshida; Morris Sherman; Jeffrey S. Hoch; Stuart Peacock; Murray Krahn; Craig C. Earle

Although the burden of hepatocellular carcinoma (HCC) is an escalating public health problem, it has not been rigorously estimated within a Canadian context. We conducted a population‐based study using Ontario Cancer Registry linked administrative data. The mean net costs of care due to HCC were estimated using a phase of care approach and generalized estimating equations. Using an incidence approach, the mean net costs of care were applied to survival probabilities of HCC patients to estimate 5‐year net costs of care and extrapolated to the Canadian population of newly diagnosed HCC patients in 2009. During 2002‐2008, 2,341 HCC cases were identified in Ontario. The mean (95% confidence interval [CI]) net costs of HCC care per 30 patient‐days (2010 US dollars) were


Chest | 2014

Risk of Mycobacterial Infections Associated With Rheumatoid Arthritis in Ontario, Canada

Sarah K. Brode; Frances B. Jamieson; Ryan Ng; Michael A. Campitelli; Jeffrey C. Kwong; J. Michael Paterson; Ping Li; Alexandre Marchand-Austin; Claire Bombardier; Theodore K. Marras

3,204 (


PLOS ONE | 2013

Effectiveness of Inactivated Influenza Vaccines in Preventing Influenza-Associated Deaths and Hospitalizations among Ontario Residents Aged ≥65 Years: Estimates with Generalized Linear Models Accounting for Healthy Vaccinee Effects

Benjamin J. Ridenhour; Michael A. Campitelli; Jeffrey C. Kwong; Laura Rosella; Ben Armstrong; Punam Mangtani; Andrew Calzavara; David K. Shay

2,863‐


The New England Journal of Medicine | 2018

Acute Myocardial Infarction after Laboratory-Confirmed Influenza Infection

Jeffrey C. Kwong; Kevin L. Schwartz; Michael A. Campitelli; Hannah Chung; Natasha S. Crowcroft; Timothy Karnauchow; Kevin Katz; Dennis T. Ko; Allison McGeer; Dayre McNally; David Richardson; Laura Rosella; Andrew E. Simor; Marek Smieja; George Zahariadis; Jonathan B. Gubbay

3,545) in the initial phase,

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Andrea S. Gershon

Sunnybrook Health Sciences Centre

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Nick Daneman

Sunnybrook Health Sciences Centre

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