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Books > Medicine > General issues > Medical equipment & techniques > General
Cardiology Science and Technology comprehensively deals with the science and biomedical engineering formulations of cardiology. As a textbook, it addresses the teaching, research, and clinical aspects of cardiovascular medical engineering and computational cardiology. The books consists of two sections. The first section deals with left ventricular (LV) wall stress, cardiac contractility, ventricular remodeling, active wall stress and systolic pressure generation, and vector cardiogram characteristics, with applications in cardiology. The second section covers ECG signal analysis for arrhythmias detection, LV pumping (intra-LV, aortic and coronary flow) characteristics, and coronary bypass surgery design, with applications in cardiology and cardiac surgery. This book is like an exciting train ride through the heart and into blood flows within its chamber, the coronary tree, the aorta, and finally into coronary flow and bypass grafting. The train starts from the heart's central station and journeys through exciting places of heart wall stresses, cardiac contractility measures to characterize heart failure, and active stress generation to develop systolic heart pressure. We learn about cardiomyopathic heart remodeling and its surgical ventricular restoration, theory of ECG and vector cardiogram with medical applications, and heart rate variability signal processing to detect cardiac arrhythmias. In the heart chamber, we witness the amazing intricate intra-ventricular flow patterns. Then, we study pressure pulse wave propagation into the aorta, determination of pulse wave velocity and arterial elasticity as a measure of arteriosclerosis. We climb into the mountainous coronary terrain and look at the fascinating scenery of coronary flows and myocardial perfusion that governs cardiac contractility. Finally, we arrive at coronary bypass grafting and witness the new sequential anastomosis design for enhanced patency.
The entire scope of the BioMEMS field-at your fingertipsHelping to educate the new generation of engineers and biologists, Introduction to BioMEMS explains how certain problems in biology and medicine benefit from and often require the miniaturization of devices. The book covers the whole breadth of this dynamic field, including classical microfabrication, microfluidics, tissue engineering, cell-based and noncell-based devices, and implantable systems. It focuses on high-impact, creative work encompassing all the scales of life-from biomolecules to cells, tissues, and organisms. Brilliant color presentationAvoiding the overwhelming details found in many engineering and physics texts, this groundbreaking book-in color throughout-includes only the most essential formulas as well as many noncalculation-based exercises. Important terms are highlighted in bold and defined in a glossary. The text contains more than 400 color figures, most of which are from the original researchers. Coverage of both historical perspectives and the latest developmentsDeveloped from the author's long-running course, this classroom-tested text gives readers a vivid picture of how the field has grown by presenting historical perspectives and a timeline of seminal discoveries. It also describes numerous state-of-the-art biomedical applications that benefit from "going small," including devices that record the electrical activity of brain cells, measure the diffusion of molecules in microfluidic channels, and allow for high-throughput studies of gene expression.
Broadly tunable lasers continue to have a tremendous impact in many and diverse fields of science and technology. From a renaissance in laser spectroscopy to Bose-Einstein condensation, the one nexus is the tunable laser. Tunable Laser Applications describes the physics and architectures of widely applied tunable laser sources. Fully updated and expanded to address important advances in the science and technology, this Third Edition: Contains new chapters on tunable laser microscopy and tunable laser atomic vapor laser isotope separation Offers extended coverage of optical parametric oscillators and their application to atmospheric sensing, biomedicine, defense counter measures, microscopy, and spectroscopy Discusses exciting new applications in astronomy, defense R&D, medicine, and more Featuring fresh contributions from internationally recognized experts-including 100+ new pages and extensive reference listings-Tunable Laser Applications, Third Edition provides a timely account of the most promising tunable laser applications to date.
Bringing together the concepts of design control and reliability engineering, this book is a must for medical device manufacturers. It helps them meet the challenge of designing and developing products that meet or exceed customer expectations and also meet regulatory requirements. Part One covers motivation for design control and validation, design control requirements, process validation and design transfer, quality system for design control, and measuring design control program effectiveness. Part Two discusses risk analysis and FMEA, designing-in reliability, reliability and design verification, and reliability and design validation.
A volume in the Principles and Applications in Engineering series, Clinical Engineering focuses on managing the deployment of medical technology and integrating it appropriately with desired clinical practices. It provides a description of the wide range of responsibilities clinical engineers encounter, describes technology management and assessment in detail, and reviews the standards and regulatory agencies of interest. Then the book details various biomedical sensors, considering both biologic and electronic factors in sensor performance. Finally, the book covers bioinstrumentation, addressing traditional topics and recently developed instruments and devices such as pulse oximeters and home-care monitoring devices.
This book seeks to promote the exploitation of data science in healthcare systems. The focus is on advancing the automated analytical methods used to extract new knowledge from data for healthcare applications. To do so, the book draws on several interrelated disciplines, including machine learning, big data analytics, statistics, pattern recognition, computer vision, and Semantic Web technologies, and focuses on their direct application to healthcare. Building on three tutorial-like chapters on data science in healthcare, the following eleven chapters highlight success stories on the application of data science in healthcare, where data science and artificial intelligence technologies have proven to be very promising. This book is primarily intended for data scientists involved in the healthcare or medical sector. By reading this book, they will gain essential insights into the modern data science technologies needed to advance innovation for both healthcare businesses and patients. A basic grasp of data science is recommended in order to fully benefit from this book.
Implants into the human body, such as hip joints, heart valves and dental crowns, have been increasingly used over the last 40 years or so, and many patients have benefited from their use. But how much is known about the metals, ceramics and polymers that are used in these repairs? This book provides a state-of-the-art account of the chemistry of the synthetic materials used in medicine and dentistry. It looks at the properties and interactions of these materials within the body at a molecular level, and includes discussion of bioengineering and cell biology. In addition, there is an account of the surgical procedures used, as well as extensive coverage of the possible biological reactions to the presence of foreign materials in the body. A brief look at the emerging field of tissue engineering completes the text. Fully referenced, with detailed reviews of the current literature, The Chemistry of Medical and Dental Materials will be an essential starting-point for all those in academia and industry who are involved in the development of new and improved repair materials.
Hydrogels are networks of polymer chains which can produce a colloidal gel containing over 99 per cent water. The superabsorbency and permeability of naturally occurring and synthetic hydrogels give this class of materials an amazing array of uses. These uses range from wound dressings and skin grafts to oxygen-permeable contact lenses to biodegradable delivery systems for drugs or pesticides and scaffolds for tissue engineering and regenerative medicine. Biomedical Applications of Hydrogels Handbook provides a comprehensive description of this diverse class of materials, covering both synthesis and properties and a broad range of research and commercial applications. The Handbook is divided into four sections: Stimuli-Sensitive Hydrogels, Hydrogels for Drug Delivery, Hydrogels for Tissue Engineering, and Hydrogels with Unique Properties. Key Features:
Medical Device Safety: The Regulation of Medical Devices for Public Health and Safety examines the prospects for achieving global harmonization in medical device regulation and describes a possible future global system. Unresolved difficulties are discussed while solutions are proposed. An essential book for all those involved in health physics, engineering, and medical regulatory affairs.
Summarizing state-of-the-art developments in long-term mechanical
ventilation use, this comprehensive treatise reviews the
applications, complications, and care of breathing disorders
affecting the growing population of ventilation-assisted
individuals-including neuromuscular and chronic obstructive
pulmonary diseases (COPD) and chest wall deformities.
Under managed care, health care has become a sometimes uneasy partnership between consumers, health care providers, and the communities they serve. Empowered by a broadly held understanding of medicine and an ability to collect and use performance information to improve health services, this alliance is reshaping our local health systems. In this constantly changing environment, competitive advantage will go to those physicians who are fast-and focused-in their ability to transform their practice into accountable, cooperative business units-reshaping society's expectations of medicine and ultimately improving the delivery of health care. In The New Health Partners, physician Stephen Prather reveals
how doctors can regain stewardship of their medical practices and
strengthen their crucial role in the health care of their local
communities. Prather?a nationally known physician consultant,
educator, practitioner, and speaker--gives physicians effective
techniques and practical advice needed to deliver bottom-line
results. This groundbreaking book explores how to The New Health Partners is based on the information gathered from in-depth organizational and marketplace assessments and surveys of physician-leaders from across the country. This vital resource also includes numerous examples of best practices that have proven to be easily reproducible, cost-effective, and beneficial to patients. This hands-on volume will prove to be an invaluable aid for any physician-leader who wants to work smarter and direct a health care organization to be ethically, clinically, and fiscally sound. Discover t-he Six Dimensions of Health Systems That Can Transform Your Medical Practice The New Health Partners is an essential handbook for physicians who want to reshape their practices to prosper within the managed care environment. This key resource offers a blueprint for helping physicians, medical directors, and administrators create the needed partnerships and cooperative business alliances, put in place the best practices that will maximize accountability, and, ultimately, achieve success in disease management. "Steve Prather's book encapsulates the key forces in health care today. If followed, his practical solutions will dramatically change the way we organize and deliver care."--Henry G. Walker, president and CEO, Providence/Health System "Prather has written a book full of helpful insights, tips, and examples for thosetrying to make sense of the leadership opportunity facing doctors today and tomorrow. His strategies and stories can help those who lead physician practice today and guide those who teach tomorrow's doctors."-Paul Batalden, professor and director, Health Care Improvement Leadership Development Center for the Evaluative Clinical Sciences, Dartmouth Medical School "Using his vast experience and keen insight, Steve Prather presents exciting concepts and practices that will contribute greatly to the improvement of the delivery and quality of clinical care into the next millennium-a major concern for all health care leaders."-Dan S. Wilford, president, Memorial Hermann Healthcare System "I urge the leaders of health care systems to read and study
this enlightening book together. And, since integration, alignment,
improvement, teamwork, and partnering are relevant activities at
all levels of an organization, it would be wise for leaders to
encourage and enable the many natural work groups in their
organization to similarly study, digest, and adapt the rich
knowledge available in [this book]. Doing so will produce a much
more effective and competitive health care system."-From the
foreword by James S. Roberts, senior vice president, physician
leadership, VHA, Inc.
Medical information science requires analytic tools. This is achieved by developing and assessing methods and systems for the acquisition, processing, and interpretation of patient data, aided by scientific discovery. Cancer Informatics in Post-Genomic Era provides both the necessary methodology and practical information tools. Key challenges include integrating research and clinical care, sharing data, and establishing partnerships within and across sectors of patient diagnosis and treatment. Addressing important clinical questions in cancer research will benefit from expanding computational biology. The advent of genomic and proteomic technologies has ushered forth the era of genuine medicine. The promise of these advances is true personalized medicine where treatment strategies can be individually tailored and advance to initiating intervention before visible symptoms appear.
Through the use of new technologies, researchers, and practitioners
in health education and health communication can now provide health
information and behavior change strategies that are customized
based on the unique needs, interests, and concerns of different
individuals. These tailored health messages can be highly effective
in assisting individuals in understanding and responding to health
concerns.
Organized to serve as a resource for those just beginning to learn EEG as well as those who are already experienced, it contains concise presentations of the fundamentals of EEG technology and interpretation as well as an up-to-date review of the latest digital EEG technology and EEG clinical correlations. Unlike other EEG textbooks, the second half of this book is uniquely organized according to EEG findings rather than individual disorders. This is the best practical approach to learning interpretation because it mirrors the actual practice of EEG, the EEGer is confronted by EEG patterns, not diagnoses. All other textbooks organize findings according to clinical disorder. The book contains sufficient information to serve as a laboratory manual. The appendices contain the American Clinical Neurophysiology Society guidelines for EEG and the International Federation of Clinical Neurophysiology glossary. Each chapter begins with a summary of major concepts. An overview of EEG can be quickly obtained by those beginning the study of EEG by simply reading the introductory summaries of all chapters before reading the contents of the chapters.
This definitive source provides practicing professionals and students in the occupational, environmental, and public health and safety fields with the functional basics of biological monitoring. The author examines how environmental exposures to particular chemicals are related to concentrations of markers in body tissues and fluids. Biological Monitoring integrates the applied sciences of industrial/environmental hygiene, epidemiology, public health, occupational medicine, toxicology, biochemistry, and analytical chemistry with the basic sciences to interpret the connections between exposures and lifestyle/environmental influences, and their effects on humans. This comprehensive introduction provides dependable, detailed coverage of:
Minimally invasive medicine has the goal of providing health care with minimal trauma. When minimally invasive surgery is utilized, it reduces the length of hospital stays, lowers costs, lowers pain, and reduces blood loss. Other minimally invasive techniques minimize radiation exposure, tissue damage, and drug side effects. Collecting contributions from workers in various fields within the sphere of minimally invasive medical technology, this book provides essential information for those involved with researching, designing, and using minimally invasive devices and systems. It emphasizes the technology required to accomplish minimally invasive medicine. The book will be of interest to biomedical engineers, medical physicists, and health care providers who want to know the technical workings of their devices and instruments.
This essential reference acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents, describes the requirements listed in these documents, and provides strategies for compliance with these requirements. Medical Device Quality Assurance and Regulatory Compliance summarizes regulation activities of the FDA, the European Economic Community, and the Global Harmonization Task Force shows how to choose a standard from the ISO 9000 and ISO 14000 series teaches how to prepare your company for auditing, how to choose a notified body, and how to survive the audit reviews standards dealing specifically with medical devices such as EN 46000, ISO 13485, and ISO 13488 discusses the requirements for product submittals prior to product introduction addresses current issues such as third party approvals and more Including numerous key references, tables, and drawings, Medical Device Quality Assurance and Regulatory Compliance is ideal for biomedical, quality assurance, reliability, software, product design, manufacturing, research and development, and industrial engineers; project managers; biomedical technicians; medical device purchasing personnel; and upper-level undergraduate and graduate students in these disciplines.
This is a practical book for health and IT professionals who need to ensure that patient safety is prioritized in the design and implementation of clinical information technology. Healthcare professionals are increasingly reliant on information technology to deliver care and inform their clinical decision making. Health IT provides enormous benefits in efficiency, communication and decision making. However a number of high-profile UK and US studies have concluded that when Health IT is poorly designed or sub-optimally implemented then patient safety can be compromised. Manufacturers and healthcare organizations are increasingly required to demonstrate that their Health IT solutions are proactively assured. Surprisingly the majority of systems are not subject to regulation so there is little in the way of practical guidance as to how risk management can be achieved. The book fills that gap. The author, a doctor and IT professional, harnesses his two decades of experience to characterize the hazards that health technology can introduce. Risk can never be eliminated but by drawing on lessons from other safety-critical industries the book systematically sets out how clinical risk can be strategically controlled. The book proposes the employment of a Safety Case to articulate and justify residual risk so that not only is risk proactively managed but it is seen to be managed. These simple techniques drive product quality and allow a technology's benefits to be realized without compromising patient safety.
Thoroughly authoritative with contributions from experts in the field, this completely updated and expanded Second Edition details state-of-the-art developments in industry practices and standards relating to medical device packaging in a readily accessible format. Helps beginning and seasoned practitioners comply with recent and pending FDA Quality Systems Good Manufacturing Practices, European Medical Device Directives, ISO 14000, and other international standards and requirements The Medical Device Packaging Handbook, Second Edition offers entirely new as well as revised chapters on packaging materials sterilization techniques, such as vapor phase processes, shelf-life testing, and expriation dating package validation methods and integrity testing bar coding technology environmentally sound packaging and disposal procedures storage autoclave case systems international standards and compliance customer needs regulatory aspects and more Elucidating discussions with an extensive glossary and index as well as many novel references, tables, drawings and photographs, this timely Second Edition furnishes instructional, practical information for packaging, validation, process, and materials engineers; packaging designers; microbiologists, toxicologists; pharmacologists; pharmacists; drug manufacturers, distributors, and suppliers; quality assurance and food and drug regulatory personnel; and graduate-level students in these disciplines.
The new edition of this widely-used sourcebook details the startlingly array of diagnostic equipment available in the medical laboratory of the nineties, and also covers maintenance and quality assurance for each type of instrument. This book includes 17 completely rewritten chapters and 7 new ones, on nephelometry and turbidimetry, gas chromatography, mass spectrometry, flow cytometry, automated immunoassay systems, automated blood bank systems, and physician's office laboratory instrumentation.
This new text provides a practical guide to hydrophilic polymer coatings technology for applications in a wide range of medical materials and devices. It concisely provides both the scientific basics of this class of polymers and the up-to-date information needed for product development and evaluation, processing, manufacturing, and regulatory compliance. More than fifty schematics illustrate materials, processes, and equipment. The entire presentation is oriented to the practical needs of personnel involved in product development and evaluation, process engineering, and manufacturing management.
This new book will enable family practitioners, obstetricians and pediatricians to answer the concerns of the families in their care. It is the first book to make information on this important topic so easily accessible to clinicians. The book is firmly rooted in clinical practice and based on many years of experience, much of it involving the development and implementation of new techniques for examining the fetus in utero. The techniques now available are assessed and better ways to identify pregnancies which are eligible to their application are proposed. The authors describe both the sampling and laboratory techniques available. Other sections cover both predictable and unpredictable pregnancy risks from genetic diseases to abnormal ultrasound, including the possibilities for laboratory evaluation, and the risks and limitations. Throughout the book, the special status of the fetus as a patient is emphasized and the concerns and questions of families are considered, making this the first fully comprehensive and authoritative volume on fetal medicine. |
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