Download or read book A Survey of Genetic Counselors Current Methods of Implementing Telegenetics written by Brenda Isabel Zuniga and published by . This book was released on 2018 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt: The field of clinical genetics is rapidly evolving, leading to an increase in demand for genetic counseling services. The use of telegenetics allows genetic counselors and other genetics providers to increase access to services by facilitating the ability to communicate with patients across long distances and reach underserved populations. The aims of this study were to characterize the various components of the telegenetics delivery model, as well as describe the perceived benefits and limitations. Full members of the National Society of Genetic Counselors (NSGC) who currently provide telegenetic services or have previously provided telegenetic services to counsel patients were invited to participate in a web-based survey. Eligible respondents were asked to complete 48 items related to the logistics of the delivery of telegenetic services, perceived benefits and limitations, useful resources, and recommendations for improvement of the delivery of telegenetic services. One-hundred fifty-nine members of the NSGC responded. Fifty-two percent and 23.4% of respondents reported providing telegenetic services in the cancer and prenatal specialties respectively, the remainder reported providing telegenetic services in a variety of other specialties. Sixty percent of respondents reported providing telegenetic services in one state and 3.8% in all 50 states, with the majority of respondents (49.4%) reporting that they hold a valid genetic counselor practice license in only one state and only 1.9% had a license in 20 states. The most common software platforms used for video and audio access were Vidyo (13.9%), Skype (12.0%), and Cisco WebEx (10.8%). Forty-three percent of respondents reported software as top barriers/limitations of the delivery of telegenetic services. Seventy-seven percent of respondents report they rely on their support staff to schedule the appointment; however, scheduling continues to be a significant barrier. Twenty-seven percent of respondents reported billing the patient for the telegenetic services and 38.0% reported not. Although this study found an increase in genetic counselors who bill for telegenetic services compared to previous studies, billing is still perceived as the biggest barrier to the delivery of telegenetic services. It is hoped that the study findings will help provide a framework for the development of telegenetic practice guidelines and service delivery logistics. In addition, it may aid in the incorporation of telegenetic services into the practice of other genetic professionals.
Download or read book Assessing Genetic Counselors Current Practice and Perceived Utility of Race Ethnicity and Ancestry REA Data Collection During Clinical Encounters written by Shontiara Darnae Johnson and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Background: Race, ethnicity, and ancestry (REA) are distinct terms that are often used interchangeably to refer to ascribed social identities. Within the medical setting, REA is commonly collected as demographic information with race and ethnicity being frequently used as surrogates for ancestral background. Currently, patient- or provider-reported REA is being used in biomedical and healthcare research instead of genetic ancestry, which is scientifically interpreted. The utilization of patient- or provider-reported REA in the clinical interpretation of potentially disease-associated variants may result in inaccurate risk assessment. Genetic counselors (GCs) often collect patient-reported REA as part of the pedigree construction process. Methods for obtaining patient-reported REA are currently not well characterized. This study aims to do the following: determine the proportion of genetic counselors who currently collect patient-reported REA during routine genetic counseling encounters, characterize how genetic counselors ask their patients about REA, and describe the characteristics of genetic counselors that do collect REA information as well as those that do not. An additional exploratory aim of investigating whether or not genetic counselors can determine race, ethnicity, and ancestry emerged during survey construction. Methods: 239 board-certified genetic counselors were recruited by electronic means to complete a 20-question online survey assessing GCs’ perception of race, ethnicity, and ancestry, the current practices of GCs, and the demographics of GCs. Data regarding GCs’ REA perception, current practices, and demographics were analyzed using descriptive statistics and chi-squared tests. Statistical analysis was not significant. Results: More participants ask patients for ancestry data (93%) in comparison to ethnicity (65%) or race data (40%). 75% of participants collect REA data from patients directly. Phrases and/or terms associated with “ethnicity”, “country”, and “ancestry” are frequently used to collect patient-reported REA (84%). More GCs were able to define REA terms as the survey progressed as 46% of participants correctly defined race, 71% of participants correctly defined ethnicity, and 93% of participants correctly defined ancestry. Most GCs claim that REA data is collected because genetic testing laboratories require this information on test requisition forms (26%). More than half (56%) of respondents feel that collecting patient REA would not change offered tests or clinical management, although 15% of respondents support that collecting REA is a “best practice”. An appreciable amount (7%) of participants experience discomfort when asking patients for REA data. More than a quarter (28.4%) of participants felt very confident regarding their understanding of race, ethnicity, and ancestry while 2.84% of participants felt very unconfident. More than a third (34%) of participants work in the oncology setting while 16% practice in a prenatal setting. Almost half (45%) of participants were aged 25-29 years and 43% had 1-4 years of experience. Most participants identified their race as White (84%) and 96% of participants identified their ethnicity as non-Hispanic. Of those responses, 10% of participants identified a race as their ethnicity. Conclusions: These results indicate that GCs employ the use of many different words, phrases, and analogies to try to elicit a family history and collect REA data directly from patients. More than half of GCs feel that collecting patient REA would not change the genetic tests they would offer or clinical management, yet an appreciable number of GCs feel that obtaining patient REA data is a genetic counseling “best practice”. There are mixed feelings regarding the collection of patient-reported REA within the genetic counseling field. This exploratory research study serves as a snapshot view that details the current characteristics and clinical practices of genetic counselors. Further characterization of GCs who practice in prenatal and oncology specialties as well as other specialties regarding clinical practices and perceptions of the lack of diversity in genomic research, REA data collection, and health disparities is necessitated. This study can serve as a basis for future research to gain more insight into the interpretations, perceptions, and feelings of genetic counselors regarding these topics as genetic counselors strive to make their interactions with patients more inclusive and meaningful and seek to provide adequate testing and services to an increasingly diverse population of patients.
Download or read book A Survey of Genetic Counseling Professionals in the Southeastern United States written by Delores James and published by . This book was released on 2019-05-31 with total page 282 pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract: This study was part of an Ethical, Legal, and Social Implications of the Human Genome Project (ELSI) grant funded by the Department of Energy (DOE) and the National Institutes of Health (NIH) . It was conducted under the aegis of the Morehouse School of Medicine in Atlanta, Georgia, and the University of Florida College of Medicine in Gainesville, Florida. As part of the project, the current study sought to answer the following questions: 1) What are the qualifications and training of professionals in the southeastern United States who provide genetic counseling? 2) Who routinely does and who should do genetic counseling? and 3) What are the educational methods used by the different health professionals in genetic counseling? A self-administered mail survey was sent to 325 potential genetic counseling professionals in the southeastern United States (Alabama, Florida, Georgia, Kentucky, Louisiana, Mississippi, North Carolina, South Carolina, and Tennessee) . Two hundred four persons volunteered for the study. Genetic associates (31%), physicians (30%), and nurses represent the three largest groups of health professionals involved in the genetic counseling process. Genetic counseling is usually a team activity. The majority of respondents reported that social workers are not and should not routinely be involved in genetic counseling. Genetic associates are well trained in human genetics and counseling techniques, but like physicians and nurses have much room for improvement in the educative aspect of counseling. Physicians have more years of experience (13 years) doing genetic counseling than genetic associates (6 years) and nurses (6 years) but the bulk of their training apparently comes from supervised clinical training rather than formal courses in human genetics, counseling techniques, and educational methods and principles. Nurses and genetic associates have comprable years of experience but nurses lack the formal courses in human genetics and counseling techniques. The majority of all respondents had no formal training in educational methods and principles. Educational techniques such as assessing clients' educational level and asking patients to repeat information in their own words were not always utilized. Recognizing professional limitations and formal training in human genetics are the only two factors perceived to increase counseling effectiveness. Policy recommendations are given. Dissertation Discovery Company and University of Florida are dedicated to making scholarly works more discoverable and accessible throughout the world. This dissertation, "A Survey of Genetic Counseling Professionals in the Southeastern United States: Actual Versus Perceived Roles" by Delores Corinne Suzette. James, was obtained from University of Florida and is being sold with permission from the author. A digital copy of this work may also be found in the university's institutional repository, IR@UF. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation.
Download or read book Genetic Counseling Practice written by Bonnie S. LeRoy and published by John Wiley & Sons. This book was released on 2020-11-16 with total page 416 pages. Available in PDF, EPUB and Kindle. Book excerpt: The second edition of Genetic Counseling Practice: Advanced Concepts and Skills, provides in-depth content regarding the advanced competencies for meeting patient needs across the changing landscape of genetic counseling practice. The content aligns with the Reciprocal Engagement Model (REM) of practice which integrates the biomedical knowledge and psychosocial aspects of genetic counseling. This edition has been revised and expanded to reflect advances made in the present-day field. Edited by a team two genetic counselors and a psychologist, the chapters offer a holistic picture of genetic counseling. Chapter authors are all recognized experts in the profession. The chapters are grounded in evidence-based practice and research. Each chapter includes learning activities to help readers apply concepts and skills. Featured topic areas include: Meeting the needs of culturally diverse patients Addressing challenging patient dynamics Working with children, adolescents and families Using emerging service delivery models for genetic counseling Engaging in self-reflective, deliberate practice Promoting genetic counselor professional development Genetic Counseling Practice is an indispensable guide to the complex and evolving field of genetic counseling, and this updated second edition will help practitioners and trainees alike navigate its most pressing and practical challenges with skill and care.
Download or read book Advanced Genetic Counseling written by Barbara B. Biesecker and published by Oxford University Press, USA. This book was released on 2019 with total page 241 pages. Available in PDF, EPUB and Kindle. Book excerpt: A CRITICAL NEW APPROACH FOR LEARNING AND THRIVING IN A FIELD OF CHANGE The scope and responsibilities of today's genetic counselors exceed the reasonable capacity of any one educational resource. While the field's first-year curriculum may be relatively fixed, the landscape of what comes after that -- a dizzying mix of practice, ethics, research design, and professional competencies -- is increasingly broad. Advanced Genetic Counseling offers an overdue extension of the field's core curriculum. From navigating ethical dilemmas and potential conflicts of interest to confronting the biases and patterns of thought that can limit counselors' interactions with clients, it prepares readers to face the profession's most challenging aspects with confidence. Drawing on techniques from psychotherapy, social psychology, and health behavior, Advanced Genetic Counseling is an essential resource for trainees and mid-career professionals. It offers a roadmap not just for addressing client needs, but for the future of genetic counseling education.
Download or read book Disparities in Cancer Prevention and Epidemiology written by Farnam Mohebi and published by Frontiers Media SA. This book was released on 2022-06-27 with total page 185 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Genetics and Public Health in the 21st Century written by Muin J. Khoury and published by Oxford University Press, USA. This book was released on 2000 with total page 661 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first broad survey of these two fields, this book deleniates a framework for integrating advances in human genetics into public health practice.
Download or read book Career Paths in Telemental Health written by Marlene M. Maheu and published by Springer. This book was released on 2016-12-24 with total page 321 pages. Available in PDF, EPUB and Kindle. Book excerpt: This visionary volume spotlights innovative mental health careers in today’s technology-driven climate while inspiring readers to create their own opportunities. Unique and engaging perspectives from professionals across disciplines and job titles describe the thought processes, ingenuity, and discipline behind matching technologies to the needs of specific populations and settings. These non-traditional paths show digital advances as used in frontline, complementary, supplemental, and alternative interventions, in academic and training settings, in private practice, and in systems facing transition. The diversity of these contributions illustrates the myriad openings technology presents for both professional fulfillment and clients’ improved well-being. Highlights of the coverage: Crisis in the behavioral health classroom: enhancing knowledge, skills, and attitudes in telehealth training. Using technology in behavior analysis: a journey into telepractice. Making iCBT available in primary care settings: bridging the gap between research and regular healthcare. Improving veterans’ access to trauma services through clinical video telehealth. Virtual reality therapy for treatment of psychological disorders. Promoting and evaluating evidence-based telepsychology interventions. For mental health practitioners, practitioners in training, researchers, academics, and policymakers, Career Paths in Telemental Health is an ideabook whose time has come—and continues to unfold.
Download or read book Personalized and Precision Medicine Informatics written by Terrence Adam and published by Springer Nature. This book was released on 2019-09-17 with total page 349 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book adopts an integrated and workflow-based treatment of the field of personalized and precision medicine (PPM). Outlined within are established, proven and mature workflows as well as emerging and highly-promising opportunities for development. Each workflow is reviewed in terms of its operation and how they are enabled by a multitude of informatics methods and infrastructures. The book goes on to describe which parts are crucial to discovery and which are essential to delivery and how each of these interface and feed into one-another. Personalized and Precision Medicine Informatics provides a comprehensive review of the integrative as well as interpretive nature of the topic and brings together a large body of literature to define the topic and ensure that this is the key reference for the topic. It is an unique contribution that is positioned to be an essential guide for both PPM experts and non-experts, and for both informatics and non-informatics professionals.
Download or read book Implementation of Genomic Medicine in Africa One continent one vision written by Maritha J. Kotze and published by Frontiers Media SA. This book was released on 2023-02-14 with total page 166 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Genetic Counseling Research written by Ian M. MacFarlane and published by Oxford University Press, USA. This book was released on 2014 with total page 305 pages. Available in PDF, EPUB and Kindle. Book excerpt: This text is devoted to research methodology in genetic counselling. The book offers step-by-step guidance for conducting research, from the development of a question to the publication of findings.
Download or read book Essentials of Medical Genetics for Health Professionals written by Laura M. Gunder McClary and published by Jones & Bartlett Publishers. This book was released on 2010-09-17 with total page 249 pages. Available in PDF, EPUB and Kindle. Book excerpt: Essentials of Medical Genetics for Health Professionals is a concise, accessible introduction to medical genetics for all health professions students. Even with limited exposure to genetics, students can use the accelerated approach in this text to attain a base foundation of genetics knowledge. This book begins with a review of chromosomes, DNA, RNA, protein synthesis, and inheritance patterns and continues with a clinical focus based on understanding different disease processes. A variety of genetic diseases are explored, including what is known about the genetics involved, the signs and symptoms of the disease, and the treatment options available. Accompanying tables and images aid comprehension. This book also covers diagnostic techniques and an overview of embryonic development and teratogens. The roles of genetic counseling and screening, as well as the ethical and legal issues related to genetic screening and genetic testing are also discussed. Complete with stated objectives, definition of key terms, references, chapter summaries and end of chapter review questions with answers, each chapter is organized for optimal learning. Essentials of Medical Genetics for Health Professionals will not only have application in the classroom setting for health professions or medical students, but practicing clinicians such as physician assistants, nurse practitioners, and physicians who want to learn more or revisit genetics will also find this book a valuable, useful resource. Instructor Resources include PowerPoint Slides, a TestBank, and an Image Bank.
Download or read book Handbook of Clinical Adult Genetics and Genomics written by Shweta Dhar and published by Academic Press. This book was released on 2020-04-10 with total page 530 pages. Available in PDF, EPUB and Kindle. Book excerpt: Handbook of Clinical Adult Genetics and Genomics: A Practice-Based Approach provides a thorough overview of genetic disorders that are commonly encountered in adult populations and supports the full translation of adult genetic and genomic modalities into clinical practice. Expert chapter authors supplement foundational knowledge with case-based strategies for the evaluation and management of genetic disorders in each organ system and specialty area. Topics discussed include employing genetic testing technologies, reporting test results, genetic counseling for adult patients, medical genetics referrals, issues of complex inheritance, gene therapy, and diagnostic and treatment criteria for developmental, cardiovascular, gastrointestinal, neuropsychiatric, pulmonary issues, and much more. Employs clinical case studies to demonstrate how to evaluate, diagnosis and treat adult patients with genetic disorders Offers a practical framework for establishing an adult genetics clinic, addressing infrastructure, billing, counseling, and challenges unique to adult clinical genetics Features chapter contributions from authors at leading adult genetics institutions in the US and abroad
Download or read book A Guide to Genetic Counseling written by Wendy R. Uhlmann and published by John Wiley & Sons. This book was released on 2011-09-20 with total page 644 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first book devoted exclusively to the principles and practice of genetic counseling—now in a new edition First published in 1998, A Guide to Genetic Counseling quickly became a bestselling and widely recognized text, used nationally and internationally in genetic counseling training programs. Now in its eagerly anticipated Second Edition, it provides a thoroughly revised and comprehensive overview of genetic counseling, focusing on the components, theoretical framework, and unique approach to patient care that are the basis of this profession. The book defines the core competencies and covers the genetic counseling process from case initiation to completion—in addition to addressing global professional issues—with an emphasis on describing fundamental principles and practices. Chapters are written by leaders in the field of genetic counseling and are organized to facilitate academic instruction and skill attainment. They provide the most up-to-date coverage of: The history and practice of genetic counseling Family history Interviewing Case preparation and management Psychosocial counseling Patient education Risk communication and decision-making Medical genetics evaluation Understanding genetic testing Medical documentation Multicultural counseling Ethical and legal issues Student supervision Genetic counseling research Professional development Genetics education and outreach Evolving roles and expanding opportunities Case examples A Guide to Genetic Counseling, Second Edition belongs on the syllabi of all medical and human genetics and genetic counseling training programs. It is an indispensable reference for both students and healthcare professionals working with patients who have or are at risk for genetic conditions.
Download or read book COMMUNITY PHARMACY AND MANAGEMENT written by Mr. Chandra Prakash Dwivedi and published by JEC PUBLICATION. This book was released on with total page 241 pages. Available in PDF, EPUB and Kindle. Book excerpt: Welcome to the field of management theory for community pharmacies. This book provides a thorough overview of the complex dynamics involved in running a community pharmacy, covering the theoretical underpinnings as well as the real-world applications necessary for success in this industry. Community pharmacies are essential to the healthcare system because they are easily accessible points of care for people living in their neighborhoods. Therefore, good management techniques are essential to both guaranteeing these pharmacies run smoothly and providing patients with high-quality medical care. We cover a wide range of topics in this book, from the foundations of pharmacy management principles to sophisticated techniques for improving workflow effectiveness, raising patient engagement, and overcoming regulatory obstacles. Based on the most recent studies and industry insights, every chapter provides insightful viewpoints and useful advice specific to the demands of running a community pharmacy. Whether you are a student hoping to work in pharmacy or an experienced professional looking to hone your management techniques, this book will give you the knowledge and resources you need to succeed in the always changing world of community pharmacy practice I urge you to approach each chapter as you begin this educational journey with an open mind and an inquisitive spirit. Accept the chances for education and development that are ahead of you, and may this book be a reliable ally in your quest for management excellence in community pharmacies.
Download or read book Benchmarking Telemedicine Improving Health Security in the Balkans written by C.S. Stone and published by IOS Press. This book was released on 2017-10-25 with total page 148 pages. Available in PDF, EPUB and Kindle. Book excerpt: Health security is dependent on many factors such as: individual government policies and regulations; budgets; management systems; and the collection, analysis, use, and protection of data. Telemedicine has the potential to change how healthcare is delivered around the world, and has developed to the point where it is possible for its use to become commonplace. The questions are, however, whether and how the use of telemedicine will improve health security in Southeast Europe. This book presents papers from the NATO Advanced Research Workshop (ARW) on Benchmarking Telemedicine: Improving Health Security in the Balkans, held in Skopje, Macedonia, in November 2016. The aim of the workshop was to bring together people from a wide range of sectors within the telemedicine community with representatives of NATO Member and Partner countries to share information and develop solutions to health security issues. Participants addressed issues such as cyber security for the implementation of telemedicine; healthcare capabilities of deployed and local medical equipment; learning methods; information sharing among local professionals; prevention and control of infectious diseases; best practices of telemedicine among NATO Member and Partner countries; integration of telemedicine across regions and borders; and telemedicine implementation. The book will be of interest to all those wishing to gain a better insight into the implications of telemedicine for health security.
Download or read book Telemedicine in Dermatology written by H. Peter Soyer and published by Springer Science & Business Media. This book was released on 2011-12-08 with total page 192 pages. Available in PDF, EPUB and Kindle. Book excerpt: Written by leading teledermatologists and telemedicine experts, this hands-on guide addresses the practical needs of the many emerging teledermatology services worldwide. It covers the medical and technical prerequisites for such services as well as the photographic imaging essentials. It also illustrates the performance of teledermatology by means of clinical examples, discusses teledermatology in underdeveloped countries, and presents specialized methods of teledermatology. The impact of telemedicine on the doctor-patient relationship is explored, and the advantages that accrue from improving access to expert knowledge are explained. In addition, quality assurance, legal assumptions, economic aspects, and the future horizons of such health care services are all considered. A comprehensive appendix provides information on training opportunities, sample protocols, consent forms, information sheets, references, and relevant web links.
