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    Translational Pulmonology
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      • Publisher's listprice EUR 153.99
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        65 322 Ft (62 211 Ft + 5% VAT)
      • Discount 10% (cc. 6 532 Ft off)
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    65 322 Ft

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    Product details:

    • Publisher Academic Press
    • Date of Publication 30 May 2025

    • ISBN 9780323903912
    • Binding Paperback
    • No. of pages610 pages
    • Size 276x216 mm
    • Language English
    • 700

    Categories

    Long description:

    Translational research is essential to the advancement of medicine. Translational Pulmonology is an instructional guide to translational medical research serves as a practical, step-by-step roadmap for taking a biomedical device, potential therapeutic agent, or research question from idea through demonstrated clinical benefit. Fundamentally, the volume aims to help bridge the gap between current research and practice. Written by a team of expert medical, biomedical engineering, and clinical research experts in pulmonary diseases, this volume provides a clear process for understanding, designing, executing, and analyzing clinical and translational research within the field.




    • Focusing on translational pulmonary diseases research, this volume covers the principles of evidence-based medicine and applies these principles to the design of translational investigations
    • Provides a practical, straightforward approach that will help the aspiring pulmonary researchers and pulmonologists navigate challenging considerations in study design and implementation
    • Details valuable discussions of the critical appraisal of published studies in pulmonary, allowing the reader to learn how to evaluate the quality of such studies with respect to measuring outcomes and to make effective use of all types of evidence in patient care

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    Table of Contents:

    Introduction
    1. Introduction
    2. Translational process
    3. Scientific Method

    Pre-Clinical
    4. Overview of Preclinical Research
    5. What Problem are You Solving?
    6. Types of Interventions
    7. Drug Discovery
    8. Drug Testing
    9. Device Discovery and Prototyping
    10. Device Testing
    11. Diagnostic Discovery
    12. Other Product Types
    13. Procedural Technique Development
    14. Behavioral Intervention
    15. Artificial Intelligence

    Clinical: Fundamentals
    16. Introduction to Clinical Research: What is it? Why is it Needed?
    17. The Question: Types of Research Questions and how to Development Them
    18. Study Population: Who and Why Them?
    19. Outcome Measurements: What Data is Being Collected and Why?
    20. Optimizing the Question: Balancing Significance and Feasibility

    Statistical Principles
    21. Common Issues in Analysis
    22. Basic Statistical Principles
    23. Hypotheses and Error Types
    24. Power
    25. Regression
    26. Continuous Variable Analyses
    27. Categorical Variable Analyses: Chi-square, Fisher Exact, Mantel Hanzel
    28. Correlation
    29. Biases
    30. Basic Science Statistics
    31. Sample Size
    32. Statistical Software

    Clinical: Study Types
    33. Design Principles: Hierarchy of Study Types
    34. Case Series: Design, Measures, Classic Example
    35. Case-Control Study: 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. Meta-analysis: Design, Measures, Classic Example
    40. Cost-effectiveness Study: Design, Measures, Classic Example
    41. Diagnostic Test Evaluation: Design, Measures, Classic Example
    42. Reliability Study: Design, Measures, Classic Example
    43. Database Studies: Design, Measures, Classic Example
    44. Surveys and Questionnaires: Design, Measures, Classic Example
    45. Qualitative Methods and Mixed Methods

    Clinical Trials
    46. Randomized Control: Design, Measures, Classic Example
    47. Historical Control: Design, Measures, Classic Example
    48. Cross-Over: Design, Measures, Classic Example
    49. Withdrawal Studies: Design, Measures, Classic Example
    50. Factorial Design: Design, Measures, Classic Example
    51. Group Allocation: Design, Measures, Classic Example
    52. Hybrid Design: Design, Measures, Classic Example
    53. Large, Pragmatic: Design, Measures, Classic Example
    54. Equivalence and Noninferiority: Design, Measures, Classic Example
    55. Adaptive: Design, Measures, Classic Example
    56. Phase 0 Trials: Window of Opportunity
    57. Registries
    58. Phases of Clinical Trials
    59. IDEAL Framework

    Clinical: Preparation
    60. Patient Perspectives
    61. Budgeting
    62. Ethics and Review Boards
    63. Regulatory Considerations for New Drugs and Devices
    64. Funding Approaches
    65. Conflicts of Interest
    66. Subject Recruitment
    67. Data Management
    68. Special Populations
    69. Subject Adherence
    70. Survival Analysis
    71. Monitoring Committee in Clinical Trials

    Regulatory Basics
    72. FDA Overview
    73. IND
    74. New Drug Application
    75. Devices
    76. Orphan Drugs
    77. Biologics
    78. Combination Products
    79. Foods
    80. Cosmetics
    81. CMC and GxP
    82. Non-US Regulatory
    83. Post-Market Drug Safety Monitoring
    84. Post-Market Device Safety Monitoring

    Clinical Implementation
    85. Implementation Research
    86. Design and Analysis
    87. Mixed-methods Research
    88. Population- and Setting-specific Implementation
    89. Guideline Development

    Public Health
    90. Public Health
    91. Epidemiology
    92. Factors
    93. Good Questions
    94. Population- and Environmental-specific Considerations
    95. Law, Policy, and Ethics
    96. Healthcare Institutions and Systems
    97. Public Health Institutions and Systems

    Practical Resources
    98. Presenting Data
    99. Manuscript Preparation
    100. Quality Improvement
    101. Team Science and Building a Team
    102. Patent Basics
    103. Venture Pathways
    104. SBIR/STTR
    105. Sample Forms and Templates

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