Emergency Medicine Recall is an important addition to the successful RECALL series, which uses a double-column, rapid-fire, question and answer format to help medical students, residents, nurse practitioners, physician assistants and other healthcare professionals to recall important information presented on wards. This information also is critical for USMLE test preparation. The text contains many patient management questions that are written in the emergency room setting, thus preparing students for questions that address EM-specific issues.
Written primarily for third- and fourth-year medical students in clerkships, this new edition covers the core specialty areas within internal medicine, including cardiology, pulmonology, and oncology. Each chapter is written by faculty, students, and fellows and emphasizes diagnosis and treatment.
Now in its Sixth Edition, Surgical Recall allows for rapid-fire review of surgical clerkship material for third- or fourth-year medical students preparing for the USMLE and shelf exams. Written in a concise question-and-answer format—double-column, question on the left, answer on the right—Surgical Recall addresses both general surgery and surgical subspecialties. Students on rotation or being PIMPed can quickly refer to Surgical Recall for accurate and on-the-spot answers. The book includes survival tactics and tips for success on the boards and wards as well as key information for those new to the surgical suite.
Dr. Tim Hennessy has skillfully drawn on his life experiences to put together this new book he has written. Recalled to Health functions as both a personal memoir of his path to becoming a doctor and a useful medical guide to achieving and keeping good health. Written over a five-year period in between his work as a doctor and his other professional and personal pursuits, Dr. Hennessy says the initial impetus for it came from his bimonthly e-mail health newsletter, H-mail: Medical Education Made Easy. Self-described as conservative with medicine, Hennessy's focus for this book is to promote freedom by inspiring one and all to live healthier lives, in the process becoming less dependent on medications and the flawed healthcare system, and more emboldened to live life to its fullest, unimpeded by the physical constraints of poor health. By providing a medical foundation that will lead to a better understanding of medical topics, the doctor believes that Recalled to Health can empower readers to take charge of their own health. Cholesterol, blood pressure, diet and weight management, exercise, sleeping habits, and the role of nature in health are some of the topics discussed in full here, along with suggestions for optimum actions, behaviors, and treatments. Each of the chapters end with a helpful summary of tips, and the back of the book contains numerous, fully cited references listed by chapters as well as a full index. You can use this first-rate new book to help maintain your present good health, or you can use it to help reclaim your former good health. Either way, it will help you strengthen your mind so you can strengthen your body. And what more can anyone ask of a book on health? Book jacket.
Following its acclaimed predecessor Pediatrics Recall, this new Second Edition reviews disease entities to facilitate retention and mimic verbal testing covered in a pediatric clerkship. Its unique question-and-answer format is retained. This edition is organized by disease process and involved systems. The text includes descriptions, signs, symptoms, pathophysiology essentials, treatments and possible outcomes. New to this edition are some select figures. Topics cover basic issues in neonatal and pediatric fluid management, blood products, nutrition, growth, emergencies, and intensive care. One chapter is solely devoted to issues relating to the adolescent patient. Easy access design is ideal for clinical rotation usage.
Recalls are an important tool to mitigate serious health consequences associated with defective or unsafe medical devices. Typically, a recall is voluntarily initiated by the firm that manufactured the device. The FDA oversees implementation of the recall. FDA classifies recalls based on health risks of using the recalled device. FDA also determines whether a firm has effectively implemented a recall, and when a recall can be terminated. This report identifies: (1) the numbers and characteristics of medical device recalls and FDA's use of this info. to aid its oversight; and (2) the extent to which the process ensures the effective implementation and termination of the highest-risk recalls. Charts and tables. A print on demand report.
The Food and Drug Administration (FDA) is responsible for ensuring that medical devices are safe and effective before they go on the market. Section 510(k) of the Federal Food, Drug, and Cosmetic Act requires a manufacturer of medical devices to notify FDA of its intent to market a medical device at least 90 days in advance. That window of time allows FDA to evaluate whether the device is substantially equivalent to a product already legally on the market (called a predicate), in which case the device does not need to go through the premarket approval (PMA) process. As part of its assessment of the FDA's premarket clearance process for medical devices, the Institute of Medicine (IOM) held a workshop on July 28, 2010 to discuss how medical devices are monitored for safety after they are available to consumers. Its primary focus was on monitoring the safety of marketed medical devices, including FDA's postmarket surveillance activities, analysis of safety concerns that resulted in medical device recalls, and non-FDA sources of adverse-event information. Public Health Effectiveness of the FDA 501(K) Clearance Process summarizes the views of the workshop participants.
This report contains our additional descriptive analyses and profiles of two types of medical device recalls, based on the data we collected for our August 1989 report entitled Medical Device Recalls: An Overview and Analysis 1983-88 (GAO/PEMD-89-15BR). In that report, we provided information on the overall numbers and selected characteristics of all recalls that were initiated during the 1983-88 study period. Appendix I of this report contains further background information and a description of our study's objectives, scope, and methodology. In appendices II and III, we have included the results of our further analyses of two types of recall: (1) those that involved medical devices approved for marketing by the Food and Drug Administration (FDA) through its premarket approval (PMA) process and recalled for some type of design problem (hereafter referred to as PMA-design recalls) and (2) those that FDA classified as the most serious according to health risk (class I). Our medical device recall profiles include product and manufacturer identification, the nature of the problem for which the device was recalled, the health consequences of the device problem, and a description of the recall. In our additional analyses and profile development, we found that there were 28 PMA-design and 48 classes I recalls. Six recalls fell into both groups, and taken together, the two categories accounted for 70, or 4 percent, of the universe of recalls (1,635) initiated during fiscal years 1983 through 1988. Although they are a relatively small proportion of the total, these two types of recall are probably among the most important from a public health perspective. (KT).
