Daniel R. Ricciuto
University of Toronto
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Clinical Infectious Diseases | 2015
Anthony D. Bai; Adrienne Showler; Lisa Burry; Marilyn Steinberg; Daniel R. Ricciuto; Tania Fernandes; Anna Chiu; Sumit Raybardhan; Eshan Fernando; George Tomlinson; Chaim M. Bell; Andrew M. Morris
BACKGROUND We assessed the impact of infectious disease (ID) consultation on management and outcome in patients with Staphylococcus aureus bacteremia (SAB). METHODS A retrospective cohort study examined consecutive SAB patients from 6 academic and community hospitals between 2007 and 2010. Quality measures of management including echocardiography, repeat blood culture, removal of infectious foci, and antibiotic therapy were compared between ID consultation (IDC) and no ID consultation (NIDC) groups. A competing risk model with propensity score adjustment was used to compare in-hospital mortality and time to discharge. RESULTS Of 847 SAB patients, 506 (60%) patients received an ID consultation and 341 (40%) patients did not. Echocardiography was done for 371 (73%) IDC and 191 (56%) NIDC patients (P < .0001) in hospital. Blood cultures were repeated within 2-4 days of bacteremia in 207 (41%) IDC and 107 (31%) NIDC patients (P = .0058). The infectious foci removal rate was not statistically different between the 2 groups. For empiric therapy, 474 (94%) IDC and 297 (87%) NIDC patients received appropriate antibiotics (P = .0013). For patients who finished the planned course of antibiotics, 285 of 422 (68%) IDC and 141 of 262 (54%) NIDC patients received the appropriate duration of antibiotic therapy (P = .0004). In hospital, 204 (24%) patients died: 104 of 506 (21%) IDC and 100 of 341 (29%) NIDC patients. Matched by propensity score, ID consultation had a subdistribution hazard ratio of 0.72 (95% confidence interval [CI], .52-.99; P = .0451) for in-hospital mortality and 1.28 (95% CI, 1.06-1.56; P = .0109) for being discharged alive. CONCLUSIONS ID consultation is associated with better adherence to quality measures, reduced in-hospital mortality, and earlier discharge in patients with SAB.
Clinical Infectious Diseases | 2016
Altynay Shigayeva; Wallis Rudnick; Karen Green; Danny K. Chen; Walter Demzcuk; Wayne L. Gold; Jennie Johnstone; Ian Kitai; Sigmund Krajden; Reena Lovinsky; Matthew P. Muller; Jeff Powis; Neil Rau; Sharon Walmsley; Gregory J. Tyrrell; Ari Bitnun; Allison McGeer; Huda Almorhi; Irene Armstrong; Barbara Yaffe; Mahin Baqi; David Richardson; Abdelbaset Belhaj; Anne Matlow; Susan E. Richardson; Dat Q. Tran; Shelley Deeks; Frances Jamieson; Roslyn Devlin; Larissa M. Matukas
BACKGROUND In 2012/2013, a single dose of 13-valent pneumococcal conjugate vaccine (PCV13) was recommended for immunocompromised adults in the United States and Canada. To assess the potential benefits of this recommendation, we assessed the serotype-specific burden of invasive pneumococcal disease (IPD) among immunocompromised individuals. METHODS From 1995 to 2012, population-based surveillance for IPD was conducted in Metropolitan Toronto and Peel Region, Canada. Disease incidence and case fatality were measured in immunocompromised populations over time, and the contribution of different serotypes determined. RESULTS Overall, 2115/7604 (28%) episodes of IPD occurred in immunocompromised persons. IPD incidence was 12-fold higher (95% confidence interval [CI], 8.7-15) in immunocompromised compared to immunocompetent persons; the case fatality rate was elevated in both younger (odds ratio [OR] 1.8) and older (OR 1.3) adults. Use of immunosuppressive medications was associated with a 2.1-2.7 fold increase in the risk of IPD. Five years after PPV23 program implementation, IPD incidence had declined significantly in immunocompromised adults (IRR 0.57, 95% CI, .40-.82). Ten years after pediatric PCV7 authorization, IPD due to PCV7 serotypes had decreased by 90% (95% CI, 77%-96%) in immunocompromised persons of all ages. In 2011/2012, 37% of isolates causing IPD in immunocompromised persons were PCV13 serotypes and 27% were PPV23/not PCV13 serotypes. CONCLUSIONS Immunocompromised individuals comprised 28% of IPD. Both PPV23 and herd immunity from pediatric PCV7 were associated with reductions in IPD in immunocompromised populations. PCV13 vaccination of immunocompromised adults may substantially reduce the residual burden until herd immunity from pediatric PCV13 is fully established.
Journal of Antimicrobial Chemotherapy | 2015
Anthony D. Bai; Adrienne Showler; Lisa Burry; Marilyn Steinberg; Daniel R. Ricciuto; Tania Fernandes; Anna Chiu; Sumit Raybardhan; Eshan Fernando; George Tomlinson; Chaim M. Bell; Andrew M. Morris
OBJECTIVES We compared the effectiveness of cefazolin versus cloxacillin in the treatment of MSSA bacteraemia in terms of mortality and relapse. METHODS A retrospective cohort study examined consecutive patients with Staphylococcus aureus bacteraemia from six academic and community hospitals between 2007 and 2010. Patients with MSSA bacteraemia who received cefazolin or cloxacillin as the predominant definitive antibiotic therapy were included in the study. Ninety-day mortality was compared between the two groups matched by propensity scores. RESULTS Of 354 patients included in the study, 105 (30%) received cefazolin and 249 (70%) received cloxacillin as the definitive antibiotic therapy. In 90 days, 96 (27%) patients died: 21/105 (20%) in the cefazolin group and 75/249 (30%) in the cloxacillin group. Within 90 days, 10 patients (3%) had a relapse of S. aureus infection: 6/105 (6%) in the cefazolin group and 4/249 (2%) in the cloxacillin group. All relapses in the cefazolin group were related to a deep-seated infection. Based on the estimated propensity score, 90 patients in the cefazolin group were matched with 90 patients in the cloxacillin group. In the propensity score-matched groups, cefazolin had an HR of 0.58 (95% CI 0.31-1.08, P = 0.0846) for 90 day mortality. CONCLUSIONS There was no significant clinical difference between cefazolin and cloxacillin in the treatment of MSSA bacteraemia with respect to mortality. Cefazolin was associated with non-significantly more relapses compared with cloxacillin, especially in deep-seated S. aureus infections.
Canadian Journal of Infectious Diseases & Medical Microbiology | 2015
Anthony D. Bai; Lisa Burry; Adrienne Showler; Marilyn Steinberg; Daniel R. Ricciuto; Tânia Rg Fernandes; Anna Chiu; Sumit Raybardhan; George Tomlinson; Chaim M. Bell; Andrew M. Morris
Staphylococcus aureus bacteremia (SAB), which may be caused by methicillin-resistant S aureus (MRSA), is a leading cause of bloodstream infections. SAB and MRSA can cause an increase in mortality, result in longer hospital stays and increase medical costs. However, it is possible that MRSA colonization may predict infection. Using a retrospective cohort investigation, this study evaluated the clinical utility of past MRSA screening swabs for predicting methicillin resistance and its use in guiding empirical antibiotic therapy for SAB.
Infection Control and Hospital Epidemiology | 2018
Dhruv Nayyar; Christine Moore; Liz Mccreight; Chiana Garvida; Emily Xu; Alex Kiss; Daniel R. Ricciuto; Allison McGeer; Jerome A. Leis
In this multicenter observational study, medical and surgical inpatient rooms were randomized to receive 1 hour of continuous direct observation to determine hand hygiene opportunities (HHOs). After multivariable adjustment, HHOs were similar across inpatient units and hospitals. This estimate could serve to calibrate electronic hand hygiene monitoring systems for Canadian medical and surgical units.
Open Forum Infectious Diseases | 2014
Adrienne Showler; Lisa Burry; Anthony D. Bai; Daniel R. Ricciuto; Marilyn Steinberg; Tania Fernandes; Anna Chiu; Sumit Raybardhan; Eshan Ferndando; Chaim M. Bell; Andrew M. Morris
Infective Endocarditis in Patients with Staphylococcus aureus Bacteremia Adrienne Showler, MD; Lisa Burry, PharmD; Anthony Bai, BSc; Daniel Ricciuto, MD; Marilyn Steinberg, RN; Tania Fernandes, PharmD; Anna Chiu, PharmD; Sumit Raybardhan, BSc, Phm, MPH; Eshan Ferndando, MD; Chaim Bell, MD, PhD; Andrew Morris, MD, SM; University of Toronto, Toronto, ON, Canada; Mount Sinai Hospital, Toronto, ON, Canada; University of Ottawa, Ottawa, ON, Canada; Lakeridge Hospital, Oshawa, ON, Canada; Mount Sinai Hospital, 600 University Ave, Toronto, ON, Canada; Trillium Health Center, Toronto, ON, Canada; North York General Hospital, Toronto, ON, Canada
American Journal of Infection Control | 2015
Nisha Thampi; Adrienne Showler; Lisa Burry; Anthony D. Bai; Marilyn Steinberg; Daniel R. Ricciuto; Chaim M. Bell; Andrew M. Morris
Jacc-cardiovascular Imaging | 2015
Adrienne Showler; Lisa Burry; Anthony D. Bai; Marilyn Steinberg; Daniel R. Ricciuto; Tania Fernandes; Anna Chiu; Sumit Raybardhan; Eshan Fernando; Chaim M. Bell; Andrew M. Morris
European Journal of Clinical Microbiology & Infectious Diseases | 2017
G. Sasson; Anthony D. Bai; Adrienne Showler; Lisa Burry; Marilyn Steinberg; Daniel R. Ricciuto; Tania Fernandes; Anna Chiu; Sumit Raybardhan; Eshan Fernando; Andrew M. Morris; Chaim M. Bell
Open Forum Infectious Diseases | 2015
Tiffany Chan; Danny K. Chen; Susy Hota; Kevin Katz; Michael Lingley; Reena Lovinsky; Matthew P. Muller; Vydia Nankoosingh; Jeff Powis; Daniel R. Ricciuto; Alicia Sarabia; Andrew E. Simor; Mary Vearncombe; Allison McGeer; Andrea V. Page