Del i serien Handbook for Designing and Conducting Clinical and Translational Research

Translational Surgery

Häftad, Engelska, 2023

2 069 kr

Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt för medlemmar vid köp för minst 249 kr.

Translational Surgery covers the principles of evidence-based medicine and applies these principles to the design of translational investigations. The reader will come to fully understand important concepts including case-control studies, prospective cohort studies, randomized trials, and reliability studies. Investigators will benefit from greater confidence in their ability to initiate and execute their own investigations, avoid common pitfalls in surgical research, and know what is needed for collaboration. Further, this title is an indispensable tool in grant writing and funding efforts. The practical, straightforward approach helps the translational research navigate challenging considerations in study design and implementation. The book provides valuable discussions of the critical appraisal of published studies in surgery, allowing the reader to learn how to evaluate the quality of such studies. Thus, they will improve at measuring outcomes; making effective use of all types of evidence in patient care. In short, this practical guidebook will be of interest to every surgeon or surgical researcher who has ever had a good clinical idea, but not the knowledge of how to test it.

Focuses on translational research in Surgery, covering the principles of evidence-based medicine and applying those principles to the design of translational investigations
Provides a practical, straightforward approach to help�surgeons and researchers navigate challenging aspects of�study design and implementation
Details valuable discussions on the critical appraisal of published studies in Surgery, allowing the reader to effectively use all types of evidence for patient care

Produktinformation

Utgivningsdatum2023-03-23
Mått216 x 276 x 40 mm
Vikt2 130 g
FormatHäftad
SpråkEngelska
SerieHandbook for Designing and Conducting Clinical and Translational Research
Antal sidor768
FörlagElsevier Science
ISBN9780323903004

Tillhör följande kategorier

Biologi inom Naturvetenskap och teknik

Dr Adam E. M. Eltorai, MD, PhD completed his graduate studies in Biomedical Engineering and Biotechnology along with his medical degree from Brown University. His work has spanned the translational spectrum with a focus on medical technology innovation and development. Dr. Eltorai has published numerous articles and books.Dr. Bakal is the Program Director for Provincial Research Data Services at Alberta Health Services, which operates the Alberta Strategy for Patient Oriented Research (SPOR) data platform. He also leads the Health Service Statistical and Analytics Methods teams. Over 10 years, he has worked with health services data, including randomized clinical trials. He completed his PhD jointly through the Department of Mathematics and Statistics and the School of Physical Health and Education at Queen’s University. His work includes methodological contributions and analyses supporting international studies spanning business strategy, ophthalmology, cardiology, and geriatric medicine, as well as analyses of kinematic data, through peer-reviewed publications and conference presentations. Current interests include developing statistical methodology for time-to-event data and building classification tools to support patient decision-making processes. Paige Newell MD received her Bachelor of Arts in History of Art and Architecture from Harvard University, and subsequently received her Doctor of Medicine from Lewis Katz School of Medicine at Temple University. She started general surgery residency at Brigham and Women's Hospital in Boston, MA in 2018, and spent her two years of dedicated research time from June 2020 - June 2022 as the Vicky and Joseph Safra Cardiac Surgery Clinical Outcomes Research Fellow within the Division of Cardiac Surgery at Brigham and Women's Hospital and as a research fellow for the Center for Surgery and Public Health. Her research interests include socioeconomic disparities in cardiac surgery outcomes and barriers to access to high quality care. After completing general surgery residency she plans to complete a fellowship in cardiothoracic surgery. Adena Osband, MD is a graduate of the University of Pennsylvania and New Jersey Medical School. She is currently a transplant surgeon and director of the living donor program at Rhode Island Hospital, with over 15 years in practice. She also holds the positions of associate professor of surgery and director of surgical intern education at the Warren Alpert Medical School of Brown University.

1. Introduction; 2. Translational Process; 3. Scientific Method; 4. Basic ResearchPre-Clinical5. Overview of Preclinical Research; 6. What Problem Are You Solving?; 7. Types of Interventions; 8. Drug Discovery; 9. Drug Testing; 10. Device Discovery and Prototyping; 11. Medical Device Testing; 12. Diagnostic Discovery; 13. Diagnostic Testing; 14. Other Product Types; 15. Procedural Technique Development; 16. Behavioral InterventionClinical: Fundamentals17. Introduction to Clinical Research: What is it? Why is it needed?; 18. The Question: Types of Research Questions and How to Develop Them; 19. Study Population: Who and why them?; 20. Outcome Measurements: What data is being collected and why?; 21. Optimizing the question: Balancing significance and feasibility Statistical Principles; 22. Basic Statistical Principles; 23. Distributions; 24. Hypotheses and Error Types; 25. Power; 26. Regression; 27. Continuous Variable Analyses: T-test, Man Whitney, Wilcoxon Rank; 28. Categorical Variable Analyses: Chi-Square, fisher exact, Mantel Hanzel; 29. Analysis of Variance; 30. Correlation; 31. Biases; 32. Basic Science StatisticsClinical: Study Types33. Design Principles: Hierarchy of Study Types; 34. Case Series: Design, Measures, Classic Example; 35. Case-Control: Design, Measures, Classic Example; 36. Cohort Study: Design, Measures, Classic Example; 37. Cross-Section Study: Design, Measures, Classic Example; 38. Longitudinal Study: Design, Measures, Classic Example; 39. Clinical Trials: Design, Measures, Classic Example; 40. Meta-Analysis: Design, Measures, Classic Example; 41. Cost-Effectiveness Study: Design, Measures, Classic Example; 42. Diagnostic Test Evaluation: Design, Measures, Classic Example; 43. Reliability Study: Design, Measures, Classic Example; 44. Database Studies: Design, Measures, Classic Example; 45. Surveys and Questionnaires: Design, Measures, Classic Example; 46. Qualitative Methods and Mixed MethodsClinical Trials47. Randomized Control: Design, Measures, Classic Example; 48. Nonrandomized Control: Design, Measures, Classic Example; 49. Historical Control: Design, Measures, Classic Example; 50. Cross-Over: Design, Measures, Classic Example; 51. Withdrawal Studies: Design, Measures, Classic Example; 52. Factorial Design: Design, Measures, Classic Example; 53. Group Allocation: Design, Measures, Classic Example; 54. Hybrid Design: Design, Measures, Classic Example; 55. Large, Pragmatic: Design, Measures, Classic Example; 56. Equivalence and Noninferiority: Design, Measures, Classic Example; 57. Adaptive: Design, Measures, Classic Example; 58. Randomization: Fixed or Adaptive Procedures; 59. Blinding: Who and How?; 60. Multicenter Considerations; 61. Registries; 62. Phases of Clinical Trials; 63. IDEAL Framework; 64. Artificial Intelligence; 65. Patient PerspectivesClinical: Preparation66. Sample Size; 67. Budgeting; 68. Medical Ethics and Review Boards; 69. Regulatory Considerations for New Drugs and Devices; 70. Funding Approaches; 71. Subject Recruitment; 72. Data Management; 73. Quality Control; 74. Statistical Software; 75. Report Forms: Harm and Quality of Life; 76. Subject Adherence; 77. Survival Analysis; 78. Monitoring Committee in Clinical TrialsRegulatory Basics79. FDA Overview; 80. IND; 81. New Drug Application; 82. Devices; 83. Radiation-emitting Electronic Products; 84. Orphan Drugs; 85. Biologics; 86. Combination Products; 87. Foods; 88. Cosmetics; 89. Non-US RegulatoryClinical Implementation90. Implementation Research; 91. Design and Analysis; 92. Population and Setting Specific ImplementationPublic Health93. Public Health; 94. Epidemiology; 95. Factors in Surgical Public Health and Health Disparities Research; 96. Good Questions; 97. Population and Environmental Specific Considerations; 98. Law, Policy, and Ethics; 99. Healthcare Institutions and Systems; 100. Public Health Institutions and SystemsPractical Resources101. Presenting Data; 102. Manuscript Preparation; 103. Building a Team; 104. Patent Basics; 105. Venture Pathways; 106. SBIR/STTR; 107. Sample Forms and Templates