Monica Taljaard

Summary

Affiliation: Ottawa Health Research Institute
Country: Canada

Publications

  1. ncbi Ethical and policy issues in cluster randomized trials: rationale and design of a mixed methods research study
    Monica Taljaard
    Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa Hospital, 1053 Carling Avenue, Civic Campus, C409, Ottawa, ON K1Y4E9, Canada
    Trials 10:61. 2009
  2. ncbi Inadequate reporting of research ethics review and informed consent in cluster randomised trials: review of random sample of published trials
    Monica Taljaard
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa Hospital, Civic Campus, 1053 Carling Avenue, Ottawa, ON, Canada K1Y 4E9
    BMJ 342:d2496. 2011
  3. ncbi When is informed consent required in cluster randomized trials in health research?
    Andrew D McRae
    Department of Epidemiology and Biostatistics, University of Western Ontario, London, ON N6A5C1, Canada
    Trials 12:202. 2011
  4. ncbi Who is the research subject in cluster randomized trials in health research?
    Andrew D McRae
    Department of Epidemiology and Biostatistics, University of Western Ontario, London, Canada
    Trials 12:183. 2011
  5. ncbi Improved delivery of cardiovascular care (IDOCC) through outreach facilitation: study protocol and implementation details of a cluster randomized controlled trial in primary care
    Clare Liddy
    C, T, Lamont Primary Health Care Research Centre, Elisabeth Bruyere Research Institute, Ottawa, Ontario, Canada
    Implement Sci 6:110. 2011
  6. ncbi Comparison of primary care models in the prevention of cardiovascular disease - a cross sectional study
    Clare Liddy
    C, T, Lamont Primary Health Care Research Centre, Elisabeth Bruyere Research Institute, 43 Bruyere St, Ottawa, Ontario, K1N 5C8, Canada
    BMC Fam Pract 12:114. 2011
  7. ncbi Rationale and design of Enhanced Angiogenic Cell Therapy in Acute Myocardial Infarction (ENACT-AMI): the first randomized placebo-controlled trial of enhanced progenitor cell therapy for acute myocardial infarction
    Monica Taljaard
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada
    Am Heart J 159:354-60. 2010
  8. ncbi Electronic search strategies to identify reports of cluster randomized trials in MEDLINE: low precision will improve with adherence to reporting standards
    Monica Taljaard
    Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada
    BMC Med Res Methodol 10:15. 2010
  9. ncbi Understanding the factors associated with differences in caesarean section rates at hospital level: the case of Latin America
    Monica Taljaard
    Ottawa Health Research Institute and University of Ottawa, Ottawa, Canada
    Paediatr Perinat Epidemiol 23:574-81. 2009
  10. ncbi Imputation strategies for missing continuous outcomes in cluster randomized trials
    Monica Taljaard
    Ottawa Health Research Institute, Clinical Epidemiology Program, Ottawa Hospital, 1053 Carling Avenue, Ottawa, Ontario, Canada
    Biom J 50:329-45. 2008

Detail Information

Publications30

  1. ncbi Ethical and policy issues in cluster randomized trials: rationale and design of a mixed methods research study
    Monica Taljaard
    Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa Hospital, 1053 Carling Avenue, Civic Campus, C409, Ottawa, ON K1Y4E9, Canada
    Trials 10:61. 2009
    ....
  2. ncbi Inadequate reporting of research ethics review and informed consent in cluster randomised trials: review of random sample of published trials
    Monica Taljaard
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa Hospital, Civic Campus, 1053 Carling Avenue, Ottawa, ON, Canada K1Y 4E9
    BMJ 342:d2496. 2011
    ....
  3. ncbi When is informed consent required in cluster randomized trials in health research?
    Andrew D McRae
    Department of Epidemiology and Biostatistics, University of Western Ontario, London, ON N6A5C1, Canada
    Trials 12:202. 2011
    ..Fifth, while health professionals may have a moral obligation to participate as subjects in research, this does not diminish the necessity of informed consent to study participation...
  4. ncbi Who is the research subject in cluster randomized trials in health research?
    Andrew D McRae
    Department of Epidemiology and Biostatistics, University of Western Ontario, London, Canada
    Trials 12:183. 2011
    ..Individuals who are indirectly affected by CRT study interventions, including patients of healthcare providers participating in knowledge translation CRTs, are not human research subjects unless at least one of these conditions is met...
  5. ncbi Improved delivery of cardiovascular care (IDOCC) through outreach facilitation: study protocol and implementation details of a cluster randomized controlled trial in primary care
    Clare Liddy
    C, T, Lamont Primary Health Care Research Centre, Elisabeth Bruyere Research Institute, Ottawa, Ontario, Canada
    Implement Sci 6:110. 2011
    ..abstract:..
  6. ncbi Comparison of primary care models in the prevention of cardiovascular disease - a cross sectional study
    Clare Liddy
    C, T, Lamont Primary Health Care Research Centre, Elisabeth Bruyere Research Institute, 43 Bruyere St, Ottawa, Ontario, K1N 5C8, Canada
    BMC Fam Pract 12:114. 2011
    ..abstract:..
  7. ncbi Rationale and design of Enhanced Angiogenic Cell Therapy in Acute Myocardial Infarction (ENACT-AMI): the first randomized placebo-controlled trial of enhanced progenitor cell therapy for acute myocardial infarction
    Monica Taljaard
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada
    Am Heart J 159:354-60. 2010
    ..However, a major limitation of autologous cell therapy is the deleterious influence of age and cardiac risk factors on progenitor cell activity...
  8. ncbi Electronic search strategies to identify reports of cluster randomized trials in MEDLINE: low precision will improve with adherence to reporting standards
    Monica Taljaard
    Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada
    BMC Med Res Methodol 10:15. 2010
    ....
  9. ncbi Understanding the factors associated with differences in caesarean section rates at hospital level: the case of Latin America
    Monica Taljaard
    Ottawa Health Research Institute and University of Ottawa, Ottawa, Canada
    Paediatr Perinat Epidemiol 23:574-81. 2009
    ..The involvement of local quality control departments is an essential component in achieving success. Our results can be used to identify institutions that can be targets for further interventions to reduce CS rates...
  10. ncbi Imputation strategies for missing continuous outcomes in cluster randomized trials
    Monica Taljaard
    Ottawa Health Research Institute, Clinical Epidemiology Program, Ottawa Hospital, 1053 Carling Avenue, Ottawa, Ontario, Canada
    Biom J 50:329-45. 2008
    ..Within-cluster multiple imputation is shown to be the least powerful among the procedures considered...
  11. ncbi Intracluster correlation coefficients from the 2005 WHO Global Survey on Maternal and Perinatal Health: implications for implementation research
    Monica Taljaard
    Ottawa Health Research Institute and University of Ottawa, Ottawa, Ontario, Canada
    Paediatr Perinat Epidemiol 22:117-25. 2008
    ..We demonstrate that ICCs generally tend to increase with higher prevalences (close to 0.5). These results can help researchers calculate the required sample size for future research studies in maternal and perinatal health...
  12. ncbi Accounting for expected attrition in the planning of community intervention trials
    Monica Taljaard
    Ottawa Health Research Institute, Clinical Epidemiology Program, The Ottawa Hospital, Ottawa, Canada
    Stat Med 26:2615-28. 2007
    ..To aid in the planning of future trials, we recommend that estimates for tau be reported in published community intervention trials...
  13. ncbi Does clinical equipoise apply to cluster randomized trials in health research?
    Ariella Binik
    Rotman Institute of Philosophy, Department of Philosophy, University of Western Ontario, London, ON, N6A 5B8, Canada
    Trials 12:118. 2011
    ..Finally, clinical equipoise provides research ethics committees with formal and procedural guidelines that form an important part of the assessment of the benefits and harms of CRTs in health research...
  14. ncbi Ethical issues posed by cluster randomized trials in health research
    Charles Weijer
    Rotman Institute of Philosophy, Department of Philosophy, University of Western Ontario, London, ON, N6A 5B8, Canada
    Trials 12:100. 2011
    ..Our hope is that these papers will serve as the basis for the creation of international ethical guidelines for the design and conduct of cluster randomized trials...
  15. ncbi International survey of emergency physicians' awareness and use of the Canadian Cervical-Spine Rule and the Canadian Computed Tomography Head Rule
    Debra Eagles
    Department of Emergency Medicine, University of Ottawa, Ottawa, Ontario, Canada
    Acad Emerg Med 15:1256-61. 2008
    ..The objectives were to determine: 1) physician awareness and use of these rules in Australasia, Canada, the United Kingdom, and the United States and 2) physician characteristics associated with awareness and use...
  16. ncbi Emergency physicians' management of transient ischemic attack and desired sensitivity of a clinical decision rule for stroke in three countries
    Jeffrey J Perry
    Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, Canada
    CJEM 13:19-27. 2011
    ....
  17. ncbi Performer fatigue and CPR quality comparing 30:2 to 15:2 compression to ventilation ratios in older bystanders: A randomized crossover trial
    Christian Vaillancourt
    Department of Emergency Medicine, University of Ottawa, Ottawa, Ontario, Canada
    Resuscitation 82:51-6. 2011
    ..We sought to compare bystander fatigue and CPR quality after 5min of CPR using the 30:2 vs. the 15:2 chest compression:ventilation ratios in a population of older participants...
  18. ncbi The independent association of provider and information continuity on outcomes after hospital discharge: implications for hospitalists
    Carl van Walraven
    Ottawa Hospital Research Institute, Ottawa, Ontario, Canada
    J Hosp Med 5:398-405. 2010
    ..To determine how this influenced patient outcomes, we examined the independent association of several physician continuity and information continuity measures on death or urgent readmission after discharge from hospital...
  19. ncbi A prospective cohort study found that provider and information continuity was low after patient discharge from hospital
    Carl van Walraven
    Ottawa Hospital Research Institute, Ottawa, Ontario, Canada
    J Clin Epidemiol 63:1000-10. 2010
    ..This study is a detailed examination of continuity of care in patients discharged from hospital that simultaneously measured separate components of continuity over time or determined the factors with which they are associated...
  20. ncbi Changes in surrogate outcomes can be translated into clinical outcomes using a Monte Carlo model
    Carl van Walraven
    Ottawa Health Research Institute, University of Ottawa, Ontario, Canada
    J Clin Epidemiol 62:1306-15. 2009
    ..Formulae to do this are uncommon because they require primary data from multiple randomized trials that measure both the surrogate and clinical outcome...
  21. ncbi Measuring acceptability of clinical decision rules: validation of the Ottawa acceptability of decision rules instrument (OADRI) in four countries
    Jamie C Brehaut
    Department of Epidemiology and Community Medicine, University of Ottawa, Ottawa, ON, Canada
    Med Decis Making 30:398-408. 2010
    ..No existing instrument measures the acceptability of a rule. The current study validated such an instrument...
  22. ncbi Information exchange among physicians caring for the same patient in the community
    Carl van Walraven
    Clinical Epidemiology Program, Ottawa Health Research Institute, ASB1 003, Ottawa Hospital, Civic Campus, 1053 Carling Ave, Ottawa, ONK1Y4E9
    CMAJ 179:1013-8. 2008
    ..This study determined the probability that patient information from previous visits with other physicians was available for a current physician visit...
  23. ncbi National survey of Canadian neurologists' current practice for transient ischemic attack and the need for a clinical decision rule
    Jeffrey J Perry
    Department of Emergency Medicine, Clinical Epidemiology Program, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada
    Stroke 41:987-91. 2010
    ..This national survey examined Canadian neurologists' current practice for managing TIA, the need for a clinical decision rule to identify high-risk patients, and the required sensitivity of such a rule...
  24. ncbi The effect of hospital-acquired infection with Clostridium difficile on length of stay in hospital
    Alan J Forster
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ont
    CMAJ 184:37-42. 2012
    ..We determined the independent impact of hospital-acquired infection with C. difficile on length of stay in hospital...
  25. ncbi Does adding risk-trends to survival models improve in-hospital mortality predictions? A cohort study
    Jenna Wong
    Clinical Epidemiology Program, Ottawa Hospital Research Institute, 1053 Carling Avenue, Ottawa, K1Y 4E9, Canada
    BMC Health Serv Res 11:171. 2011
    ..In this study, we used a unique approach to measure trends in patient hospital death risk and determined whether the incorporation of these trend measures into a survival model improved the accuracy of its risk predictions...
  26. ncbi Audit and feedback using the brief Decision Support Analysis Tool (DSAT-10) to evaluate nurse-standardized patient encounters
    Dawn Stacey
    School of Nursing, University of Ottawa, Ottawa, Ont, Canada
    Patient Educ Couns 73:519-25. 2008
    ..To evaluate the brief Decision Support Analysis Tool (DSAT-10) for auditing the quality of nurse-standardized patient encounters, structuring feedback for nurses, and testing instrument reliability...
  27. ncbi Intravenous lidocaine does not reduce length of hospital stay following abdominal hysterectomy
    Gregory L Bryson
    Department of Anesthesiology, The Ottawa Hospital Civic Campus, Ottawa, ON, Canada
    Can J Anaesth 57:759-66. 2010
    ..The purpose of this trial was to determine if intravenous lidocaine limited to the intraoperative period reduces length of hospital stay and improves functional recovery following abdominal hysterectomy...
  28. ncbi A pilot study to assess the feasibility of a multicenter cluster randomized trial for the management of asymptomatic persons with a thrombophilia
    Philip S Wells
    University of Ottawa, ON, Canada
    J Genet Couns 18:475-82. 2009
    ..The question of the best educational approach in these patients remains unanswered. The value of testing and following asymptomatic carriers of probands with VTE and thrombophilia remains unknown...
  29. ncbi Fluid resuscitation in the management of early septic shock (FINESS): a randomized controlled feasibility trial
    Lauralyn A McIntyre
    University of Ottawa Centre for Transfusion and Critical Care Research, Ottawa Hospital, Ottawa, Ontario, Canada
    Can J Anaesth 55:819-26. 2008
    ..This randomized controlled trial determined the feasibility of conducting a large trial testing resuscitation with pentastarch vs normal saline in early septic shock, powered for a difference in mortality...
  30. ncbi The merits of breaking the matches: a cautionary tale
    Allan Donner
    Department of Epidemiology and Biostatistics, Schulich School of Medicine, University of Western Ontario, London, Canada
    Stat Med 26:2036-51. 2007
    ....