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Books > Medicine > General issues > Public health & preventive medicine > Medical screening
More than 200,000 people in the United States living with HIV/AIDS do not know they are infected. The Institute of Medicine's Committee on HIV Screening and Access to Care held a workshop and reviewed literature to explore barriers and facilitators to more widespread HIV testing. This book contains the committee's conclusions. Table of Contents Front Matter HIV Screening and Access to Care:Exploring Barriers and Facilitators to Expanded HIV Testing References Appendix A: Biographical Sketches of Committee Members Appendix B: Biographical Sketches of Workshop Speakers Appendix C: Workshop Agenda Appendix D: Workshop Attendees
Prostate cancer continues to be a major threat to men's health, the second most common cancer in men, in many countries. Therefore it is increasingly important that those faced with difficult clinical questions make the right decisions. Since the first volume was published in 2000, many debates persist but new controversies have also emerged, reflected in the chapters of this new volume. New authors have been recruited to give their insight into newer areas of this controversial topic. "Challenges in prostate cancer "provides a series of
state-of-the-art review articles, each of which addresses and
answers a contentious question. It includes chapters on medical and
surgical management of all stages of prostate cancer, clinical
investigation, epidemiology, clinical trials and basic scientific
research and covers issues such as the genetic basis of cancer,
clinical economics and influence. The authors have used their expertise to distil the available evidence into practical advice to be used by busy urologists in their day-to-day practice. And as well as being an overview of current practice many chapters attempt to give insights into the future direction of prostate cancer research and clinical management.
In 2013, the Department of Veterans Affairs (VA) estimated that about 1.5 million veterans required mental health care, including services for Major Depressive Disorder (MDD). MDD is a debilitating mental illness related to reduced quality of life and productivity, and increased risk for suicide. VA also plays a role in suicide prevention. This book begins with a brief overview of the public health framework for suicide prevention, which forms the basis for both the National Strategy for Suicide Prevention and the VHA's approach to suicide prevention. The book discusses suicide surveillance; suicide risk factors and protective factors; suicide prevention interventions; potential issues for Congress; VA's data on veterans with MDD, including those prescribed an antidepressant; the extent that veterans with MDD who are prescribed antidepressants receive recommended care and the extent to which VA monitors such care; and the quality of data VA requires VAMCs to collect on veteran suicides.
Bone mineral density (BMD) is a determinant of bone health. Phenotype, age, race, gender, activity level and overall health status all affect BMD. Recent research has shown that early pregnancy loss could be associated with bone mineral density. Reduced bone mass, bone density and consequently the pathological conditions, osteopenia and osteoporosis, represent significant health problems and contribute to disability, mortality, and reduced health related quality of life among older women and men. This book examines disorders that affect bone density, such as rickets and osteomalacia, and discusses screening and treatment options available for these and other bone disorders.
This informative book is intended to educate people about the dangers lurking in doctors
Like many words, the term "immunomics" equates to different ideas contingent on context. For a brief span, immunomics meant the study of the Immunome, of which there were, in turn, several different definitions. A now largely defunct meaning rendered the Immunome as the set of antigenic peptides or immunogenic proteins within a single microorganism - be that virus, bacteria, fungus, or parasite - or microbial population, or antigenic or allergenic proteins and peptides derived from the environment as a whole, containing also proteins from eukaryotic sources. However, times have changed and the meaning of immunomics has also changed. Other newer definitions of the Immunome have come to focus on the plethora of immunological receptors and accessory molecules that comprise the host immune arsenal. Today, Immunomics or immunogenomics is now most often used as a synonym for high-throughput genome-based immunology. This is the study of aspects of the immune system using high-throughput techniques within a conc- tual landscape borne of both clinical and biophysical thinking.
Within forty-eight hours after birth, the heel of every baby in the United States has been pricked and the blood sent for compulsory screening to detect or rule out a large number of disorders. Newborn screening is expanding rapidly, fueled by the prospect of saving lives. Yet many lives are also changed by it in ways not yet recognized. Testing Baby is the first book to draw on parents’ experiences with newborn screening in order to examine its far-reaching sociological consequences. Rachel Grob’s cautionary tale also explores the powerful ways that parents’ narratives have shaped this emotionally charged policy arena. Newborn screening occurs almost always without parents’ consent and often without their knowledge or understanding, yet it has the power to alter such things as family dynamics at the household level, the context of parenting, the way we manage disease identity, and how parents’ interests are understood and solicited in policy debates.
Within forty-eight hours after birth, the heel of every baby in the United States has been pricked and the blood sent for compulsory screening to detect or rule out a large number of disorders. Newborn screening is expanding rapidly, fueled by the prospect of saving lives. Yet many lives are also changed by it in ways not yet recognized. Testing Baby is the first book to draw on parents' experiences with newborn screening in order to examine its far-reaching sociological consequences. Rachel Grob's cautionary tale also explores the powerful ways that parents' narratives have shaped this emotionally charged policy arena. Newborn screening occurs almost always without parents' consent and often without their knowledge or understanding, yet it has the power to alter such things as family dynamics at the household level, the context of parenting, the way we manage disease identity, and how parents' interests are understood and solicited in policy debates.
Like many words, the term "immunomics" equates to different ideas contingent on context. For a brief span, immunomics meant the study of the Immunome, of which there were, in turn, several different definitions. A now largely defunct meaning rendered the Immunome as the set of antigenic peptides or immunogenic proteins within a single microorganism - be that virus, bacteria, fungus, or parasite - or microbial population, or antigenic or allergenic proteins and peptides derived from the environment as a whole, containing also proteins from eukaryotic sources. However, times have changed and the meaning of immunomics has also changed. Other newer definitions of the Immunome have come to focus on the plethora of immunological receptors and accessory molecules that comprise the host immune arsenal. Today, Immunomics or immunogenomics is now most often used as a synonym for high-throughput genome-based immunology. This is the study of aspects of the immune system using high-throughput techniques within a conc- tual landscape borne of both clinical and biophysical thinking.
The National Cancer Policy Board and the Board on Science, Engineering, and Economic Policy convened a workshop in January 2004 on a /Economic Models of Colorectal Cancer (CRC) Screening in Average-Risk Adultsa . The purpose of the workshop was to explore the reasons for differences among leading cost-effectiveness analysis (CEA) models of CRC screening, which public health policy makers increasingly rely on to help them sift through the many choices confronting them. Participants discussed the results of a collaborative pre-workshop exercise undertaken by five research teams that have developed and maintained comprehensive models of CRC screening in average-risk adults, to gain insight into each modela (TM)s structure and assumptions and possible explanations for differences in their published analyses. Workshop participants also examined the current state of knowledge on key inputs to the models with a view toward identifying areas where further research may be warranted. This document summarized the presentations and discussion at the workshop.
This volume contains refereed papers submitted by participants of the third week of a six week workshop on Statistics in the Health Sciences held by the Institute of Mathematics and its Applications in Minneapolis, Minnesota during July of 1997. This week was devoted to the closely related topics of Diagnosis and Prediction. Theoretical and applied statisticians from universities, medical and public health schools, government and private research institutions, and pharmaceutical companies involved in prediction problems in the life and social sciences and in diagnostic and screening tests were brought together to discuss and exchange new results and information on these important issues. A number of papers with applications were presented and especially lively discussions ensued involving the critical issues and difficulties in using and interpreting diagnostic tests and implementing mass screening programs. Both frequentist and Bayesian approaches were employed. The importance of predicting or controlling future events such as survival, comparative survival and survival post intervention for a disease or even for certain biological or natural events is growing rapidly. This area of concern was also represented by participants who presented work that devised predictive methodology for a variety of problems mainly from a Bayesian perspective.
This collection of six papers on the role of quantitative risk assessment in the promulgation of recent regulatory standards represents the latest contribution to a series of volumes published by Lester Lave and the Brookings Institution on regulatory decisionmaking.
This book is intended as a practical primer on the Pap test. Using bold text, tables, and highlighted areas, this book offers a user-friendly text on Pap test fundamentals so readers may find specific information effortlessly. The book is a useful tool for cytotechnologists and cytopathologists, as well as those in training. Readers preparing for various proficiency and licensing examinations will also find helpful information throughout.
Cancer screening programmes have become routine practice throughout the developed world - aiming to detect the presence of the disease prior to the manifestation of symptoms, and to increase the likelihood of successful treatment. Naturally, these programmes require regular monitoring to ensure that screening quality is maintained, and to advance the early-warning system as much as possible. Quantitative Methods for the Evaluation of Cancer Screening is a professional title designed to provide the researchers of these screening programmes with up-to-date methods and tools for improving evaluation. The book presents an introduction to cancer screening and to the methods that are employed for its monitoring, followed by an in-depth account of the more complicated modelling approaches. Each chapter is written by an international expert in the field, and imparts practical specialist information that the reader can apply to the evaluation of their own programmes. Case studies illustrate the methods in practice and provide further illumination of the fields of breast, cervix, large bowel, and neuroblastoma screening.
In this book, the authors gather and present current research in the study of the principles, analysis and benefits of screening tests. Topics discussed include the development of a screening instrument to detect common mental disorders in long-term sickness absence; a vision screening test in new-borns; nailfold capillaroscopy as a basic screening tool in Raynaud's phenomenon; the Profile of Moods Scale to assess six dimensions of mood; the Audio Recorded Cognitive Screen (ARCS) as a flexible and versatile instrument of clinical and research settings.
The secrets locked in our genes are being revealed, and we find ourselves both enthused and frightened about what that portends. We look forward to curing disease and alleviating suffering--for our children as well as for ourselves--but we also worry about delving too deeply into the double helix. Abuses perpetrated by eugenicists--from involuntary sterilization to murder--continue to taint our feelings about genetic screening. Yet, as Ruth Schwartz Cowan reveals, modern genetic screening has been practiced since 1960, benefiting millions of women and children all over the world. She persuasively argues that new forms of screening--prenatal, newborn, and carrier testing--are both morally right and politically acceptable. Medical genetics, built on the desire of parents and physicians to reduce suffering and increase personal freedom, not on the desire to "improve the human race," is in fact an entirely different enterprise from eugenics. Cowan's narrative moves from an account of the interwoven histories of genetics and eugenics in the first half of the twentieth century, to the development of new forms of genetic screening after mid-century. It includes illuminating chapters on the often misunderstood testing programs for sickle cell anemia, and on the world's only mandated premarital screening programs, both of them on the island of Cyprus. Neither minimizing the difficulty of the choices that modern genetics has created for us nor fearing them, Cowan bravely and compassionately argues that we can improve the quality of our own lives and the lives of our children by using the modern science and technology of genetic screening responsibly.
A geneticist tells the stories of men, women, and children whose genes
have shaped their lives in unexpected ways.
The Strategy of Preventive Medicine by Geoffrey Rose, first
published in 1993, remains a key text for anyone involved in
preventive medicine. Rose's insights into the inextricable
relationship between ill health, or deviance, in individuals and
populations they come from, have transformed our whole approach to
strategies for improving health. His personal and unique book,
based on many years research, sets out the case that the essential
determinants of the health of society are to be found in its mass
characteristics. The deviant minority can only be understood when
seen in its societal context, and effective prevention requires
changes which involve the population as a whole. He explores the
options for prevention, considering them from various viewpoints -
theoretical and scientific, sociological and political, practical
and ethical. The applications of his ideas are illustrated by a
variety of examples ranging from heart disease to alcoholism to
road accidents. His pioneering work focused on a population wide
approach to the prevention of common medical and behavioral
disorders has become the classic text on the subject.
This is a dynamic book that successfully combines global and local thinking with regard to an emerging technology that will contribute to the expansion of proteomics and pharmacogenomics, the science of tailored healthcare and treatments. Genetic testing and screening will change the way people understand health, diagnostic knowledge, illness but also crime, databases and private information, paternity, and self-knowledge. In addition to giving individuals the opportunity to think differently about their well-being, it installs a new taxonomy in terms of illness, because its probabilistic effects will introduce a new narrative in the health discourse of 21st century society. While in the past people could be classified as being healthy or sick, now, through genetic testing and screening, adults can be classified as being healthy, predisposed to an illness, probably at risk, at risk, or carriers of certain risks.
Screening programmes involve the systematic offer of testing for populations or groups of apparently healthy people to identify individuals who may be at future risk of a particular medical condition or disease, with the aim of offering intervention to reduce their risk. For many years, screening was practised without debate, and without evidence, but in the 1960s serious challenges were raised about many of the screening procedures then being practised. Benefits and harms of screening must be measured in high quality trials, and the benefits of screening must be weighed alongside the negative side-effects. Concerns were raised about potential and actual harm arising when people without a health problem received dangerous and unnecessary investigations and treatments as a result of routine screening tests. Controversy raged, and it took some 50 years to achieve widespread recognition that evidence-based and quality assured programme delivery was essential, coupled with provision of balanced informed to enable informed choice for potential participants. Commercially motivated provision of poor quality and non-evidence based screening tests is increasing and screening remains a highly contested topic that has relevance in all health systems including for the general public and media. This book serves as a practical and comprehensive guide to all aspects of screening. Following the international success of the first edition, this second edition brings extensive updates and new case study material. The first section deals with concepts, methods, and evidence, charts the story of screening back to 1861, and covers all aspects of a screening programme and how to research the full consequences. The second section is a practical guide to sound policy-making and to high quality delivery of best value screening. The controversies, paradoxes, uncertainties, and ethical dilemmas of screening are explained, and each chapter is packed with examples, real-life case histories, helpful summary points, and self-test questions. Reference is made to the NHS, a leader in screening, but the primary focus is on universal principles, making the book highly relevant across the globe.
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