Medical Instrument Design and Development From Requirements to Market Placements.
Autor principal: | |
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Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Newark :
John Wiley & Sons, Incorporated,
2013.
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Colección: | New York Academy of Sciences Ser.
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Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- MEDICAL INSTRUMENT DESIGN AND DEVELOPMENT: from Requirements to Market Placements
- Contents
- Foreword
- Preface
- Acknowledgment
- 1 System Engineering
- Chapter Organization
- Part I: Theory
- 1.1 Introduction
- 1.2 Problem Formulation in Product Design
- 1.3 The Business Context for Design
- 1.4 The Engineering Product Design Process
- 1.5 System-subsystem Decomposition
- 1.6 The Product Development Life Cycle
- 1.7 Project Management in Product Design
- 1.8 Intellectual Property Rights and Reuse
- Part II: Implementation
- 1.11 The ECG: Introduction
- 1.11.1 The ECG's diagnostic relevance
- 1.11.2 ECG Types
- 1.12 The ECG Design Problem Formulation
- 1.13 The ECG Business Plan
- 1.13.1 Market Size and Trend
- 1.13.2 Core and Distinctive Features
- 1.14 The ECG Design Process
- 1.14.1 Transverse Activities of the ECG Design Process
- 1.14.2 Core Activities of the ECG Design Process
- 1.15 ECG System-subsystem Decomposition
- 1.15.1 Hardware Platform Decomposition
- 1.15.2 Software Application Decomposition
- 1.16 ECG Product Life Cycle
- 1.16.1 Overcoming Risk of Inadequate Visualization of ECG Signal
- 1.16.2 Overcoming Risk of Error Fixing in System Integration
- 1.16.3 Overcoming Risks for Non-stable/Unfeasible Requirements
- 1.17 The ECG Development Plan and Project Management
- 1.18 IPR and Reuse Strategy for the ECG
- References
- 2 Concepts and Requirements
- Chapter Organization
- Part I: Theory
- 2.1 Introduction
- 2.2 The Medical Instrumentation Approach
- 2.3 Extraction of Physiological Parameters
- 2.4 Pressure and Flow
- 2.4.1 Blood Pressure
- 2.4.2 Blood Flow and Hemodynamics
- 2.5 Biopotential Recording
- 2.6 Electroencephalography
- 2.7 Electromyography
- Part II: Implementation
- 2.8 Introduction
- 2.9 Requirements Management
- 2.10 Medical Instruments Requirements and Standards
- 2.11 ECG Requirements
- 2.12 The Patient Component
- 2.12.1 The Heart's Pumping Function and the Circulatory System
- 2.12.2 Heart Conduction 'Control' System
- 2.13 The ECG Method for Observation
- 2.13.1 Recording the Heart's Electrical Signals
- 2.13.2 ECG Definition and History
- 2.13.3 ECG Standard Method of Observation
- 2.14 Features of the Observations
- 2.14.1 ECG Signal
- 2.14.2 Clinically Significant Signal
- 2.14.3 Power Line Noise
- 2.14.4 Isoelectric Line Instability
- 2.14.5 Muscle Artifacts
- 2.15 Requirements Related to Measurements
- 2.16 Safety Requirements
- 2.16.1 EMC Performance
- 2.17 Usability and Marketing Requirements
- 2.18 Environment Issues
- 2.19 Economic Requirements
- References
- 3 Biomedical Engineering Design
- Chapter Organization
- Part I: Theory
- 3.1 Design Principles and Regulations
- 3.2 General Design System Model
- 3.3 Pressure and Flow Instruments
- 3.3.1 Blood Pressure Instruments
- 3.3.2 Flow Measurements
- 3.3.3 Measuring Oxygen Concentration
- 3.4 Biopotential Instruments