The feasibility of such a program buy cheap ofloxacin 200 mg online, including the readiness of the technology buy ofloxacin 400 mg amex, willingness of the scientific community to pursue it 200 mg ofloxacin free shipping, and compelling nature of the gaps it would fill, remains to be explored. Embarking on such a program would require that existing data linking molecular, environmental, and experiential factors to disease states be surveyed and compiled, and that gaps in these data be identified and priorities set and acted upon to fill these gaps. In addition, effective and acceptable mechanisms and policies for selection, collection, storage, and management of data, as well as perception, construction, and manipulation network relationships within the data, are clearly needed. Criteria must also be established for providing or denying access to and interpretation of data. Roles of and interfaces among the involved communities (public and private funders, data contributors, clinicians, patients, industry, and others) would need to be explored and defined. And the many ethical considerations surrounding such a program would need to be addressed. Toward Precision Medicine: Building a Knowledge Network for Biomedical Research and a New Taxonomy of Disease ͺͳ Each of these areas is technically complex. Undertaking such a program would clearly require the participation and collaboration of many government and private entities over a considerable period of time. To ensure that progress is being made, goals and milestones against which program success can be measured would need to be developed. The Committee would leverage the expertise of additional scientists, clinicians, and others by holding a large (approximately 100 participants) workshop to obtain ideas from the broader scientific and medical communities. The Committee will also consider recommending a small number of case studies that might be used as an initial test for the framework. Desmond-Hellmann previously served as president of product development at Genentech, a position she held from March 2004 through April 30, 2009. In this role, she was responsible for Genentech’s pre-clinical and clinical development, process research and development, business development and product portfolio management. She also served as a member of Genentech’s executive Committee, beginning in 1996. She joined Genentech in 1995 as a clinical scientist, and she was named chief medical officer in 1996. In 1999, she was named executive vice president of development and product operations. During her time at Genentech, several of the company’s patient therapeutics (Lucentis, Avastin, Herceptin, Tarceva, Rituxan and Xolair) were approved by the U. She holds a bachelor of science degree in pre-medicine and a medical degree from the University of Nevada, Reno, and a master’s degree in public health from the University of California, Berkeley. Prior to joining Genentech, Desmond-Hellmann was associate director of clinical cancer research at Bristol-Myers Squibb Pharmaceutical Research Institute. While at Bristol-Myers Squibb, she was the project team leader for the cancer-fighting drug Taxol. She also spent two years in private practice as a medical oncologist before returning to clinical research. In January 2009, Desmond-Hellmann joined the Federal Reserve Bank of San Francisco’s Economic Advisory Council for a three-year term. In July 2008, she was appointed to the California Academy of Sciences board of trustees. Desmond-Hellmann was named to the Biotech Hall of Fame in 2007 and as the Healthcare Businesswomen’s Association Woman of the Year for 2006. She was listed among Fortune magazine’s “top 50 most powerful women in business” in 2001 and from 2003 to 2008. In 2005 and 2006, the Wall Street Journal listed Desmond-Hellmann as one of its “women to watch. Toward Precision Medicine: Building a Knowledge Network for Biomedical Research and a New Taxonomy of Disease 84 served a three-year term as a member of the American Association for Cancer Research board of directors, and from 2001 to 2009, she served on the executive Committee of the board of directors of the Biotechnology Industry Organization. Sawyers’ laboratory is currently focused on characterizing signal transduction pathway abnormalities in prostate cancer, with an eye toward translational implications. Sawyers’ work in prostate cancer has defined critical signaling pathways for disease initiation and progression through studies in mouse models and humane tissues. Sawyers is past President of the American Society of Clinical Investigation and served on the National Cancer Institute’s Board of Scientific Councilors. He has won numerous honors and awards, including: the Richard and Hinda Rosenthal Foundation Award; the Dorothy Landon Prize from the American Association of Cancer Research and the David A. Karnofsky Award from the American Society of Clinical Oncology; and the 2009 Lasker DeBakey Clinical Medical Research Award. He is a member of the Institute of Medicine and in 2010 was elected to the National Academy of Sciences. This new unit brings together human genetics, systems biology, and cell biology, combining internal capabilities with outside collaborations, to focus on increasing preclinical target validation with the aim of significantly improving clinical survival. David is a co-founder of Perlegen, and was most recently Chief Scientific Officer of the company since its formation in 2000. David was Professor of Genetics and Pediatrics at the Stanford University School of Medicine as well as the co-director of the Stanford Genome Center. He completed a Pediatric Residency at the Yale-New Haven Hospital in New Haven, Connecticut and was a Fellow in both genetics and pediatrics at the University of California, San Francisco. David is certified by the American Board of Pediatrics and the American Board of Medical Genetics. Toward Precision Medicine: Building a Knowledge Network for Biomedical Research and a New Taxonomy of Disease ͺͷ of the Human Genome Project while carrying out research involving the molecular basis of human genetic disease. He has authored over 100 peer- reviewed scientific publications and has served on numerous editorial boards. Cox’s honors include election to the Institute of Medicine of the National Academy of Sciences. Fraser-Liggett is Director of the Institute for Genome Sciences and a Professor of Medicine at the University Of Maryland School Of Medicine in Baltimore, Maryland. Previously she was the President and Director of The Institute for Genomic Research in Rockville, Maryland. Fraser-Liggett has played a role in the sequencing and analysis of human, animal, plant and microbial genomes to better understand the role that genes play in development, evolution, physiology and disease. She led the teams that sequenced the genomes of several microbial organisms, including important human and animal pathogens, and as a consequence helped to initiate the era of comparative genomics. She has served on a number of National Research Council Committees on counter-bioterrorism, domestic animal genomics, polar biology, and metagenomics. Fraser-Liggett has more than 220 scientific publications, and has served on Committees of the National Science Foundation, Department of Energy and National Institutes of Health. She received her PhD in pharmacology from State University of New York at Buffalo. He is also Co-Director of the Stanford Center for Genomics and Personalized Medicine. Galli’s research focuses on the development and function of mast cells and basophils (key players in anaphylaxis, allergies, asthma and many other biological responses), and on developing new animal models to study the diverse roles of these cells in health and disease. Galli serves on the editorial boards of several medical journals and is a co-editor of The Annual Review of Pathology: Mechanisms of Disease. Toward Precision Medicine: Building a Knowledge Network for Biomedical Research and a New Taxonomy of Disease 86 of a three year elected term, Dr. Galli was the Chair of the Advisory Board to the President and Provost of Stanford University. Goldstein is currently Professor of Molecular Genetics & Microbiology and Director of the Center for Human Genome Variation at Duke University. Goldstein is the author of over 150 scholarly publications in the areas of population and medical genetics. His work focuses on the genetics of human disease and treatment response, with a concentration on neuropsychiatric disease and host determinants of response to infectious diseases. Most recently, he was appointed the co-chair and chair of the Gordon Research Conference meeting on human genetics and genomics for 2011 and 2013. Hunter is currently the Dean for Academic Affairs at the Harvard School of Public Health and the Vincent L. Gregory Professor in Cancer Prevention in the Departments of Epidemiology and Nutrition. His research interests include cancer epidemiology and molecular and genetic epidemiology. Hunter analyzes inherited susceptibility to cancer and other chronic diseases using molecular techniques and studying molecular markers of environmental exposures. Kohane leads multiple collaborations at Harvard Medical School and its hospital affiliates in the use of genomics and computer science to study diseases (particularly cancer and autism).

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Lancet 2010 discount 400 mg ofloxacin visa; ity of single daily dosing versus multiple daily dosing of aminoglyco- 375:224–230 sides purchase 400 mg ofloxacin with visa. Ziemann M discount ofloxacin 400 mg, Sedemund-Adib B, Reiland P, et al: Increased mortal- vival in the intensive care unit: A randomized trial. Crit Care Med ity in long-term intensive care patients with active cytomegalovirus 2011; 39:2048–2058 infection. N Engl J Med 2010; 363:87–89 with moxifoxacin and meropenem vs meropenem on sepsis-related 104. Kumar A, Safdar N, Kethireddy S, et al: A survival beneft of combina- in the management of sepsis. Intensive Care Med 2001; 27 Suppl tion antibiotic therapy for serious infections associated with sepsis 1:S49–S62 and septic shock is contingent only on the risk of death: A meta-ana- lytic/meta-regression study. Boyer A, Vargas F, Coste F, et al: Infuence of surgical treatment tim- with monotherapy in septic shock: A propensity-matched analysis. Bufalari A, Giustozzi G, Moggi L: Postoperative intraabdominal therapy is associated with improved outcome against sepsis due abscesses: Percutaneous versus surgical treatment. Centers for quinolone combination antibiotic therapy for bacteremia caused Disease Control and Prevention. Klastersky J: Management of fever in neutropenic patients with vention of intravascular catheter-related infections. Martin-Loeches I, Lisboa T, Rodriguez A, et al: Combination antibi- severe necrotizing pancreatitis. Am J Surg 1997; 173:71–75 otic therapy with macrolides improves survival in intubated patients 112. Intensive Care Med 2010; atitis Study Group: A step-up approach or open necrosectomy for 36:612–620 necrotizing pancreatitis. Crit Care cal Study Group: Combination antibiotic therapy lowers mortality Med 2011; 39:1800–1818 among severely ill patients with pneumococcal bacteremia. Liberati A, D’Amico R, Pifferi S, et al: Antibiotic prophylaxis to reduce respiratory tract infections and mortality in adults receiving intensive 94. Cochrane Collaboration 2010; 9:1–72 therapy reduce mortality in Gram-negative bacteraemia? Paul M, Silbiger I, Grozinsky S, et al: Beta lactam antibiotic mono- resistant bacteria in intensive care: A randomised controlled trial. Garnacho-Montero J, Sa-Borges M, Sole-Violan J, et al: Optimal 2009; 360:20–31 management therapy for Pseudomonas aeruginosa ventilator-asso- ciated pneumonia: An observational, multicenter study comparing 118. N Engl J Med 2009; 361:1935–1944 antibiotic resistance in patients in intensive-care units: An open- 98. Lancet Infect of Pandemic (H1N1) 2009 Infuenza; Bautista E, Chotpitayasu- Dis 2011; 11:372–380 nondh T, Gao Z, et al: Clinical aspects of pandemic 2009 infuenza 120. N Engl J Med 2010; 362:1708–1719 tive decontamination on resistant gram-negative bacterial coloniza- 99. Yamazaki T, Shimada Y, Taenaka N, et al: Circulatory responses to 367:124–134 afterloading with phenylephrine in hyperdynamic sepsis. Perel P, Roberts I: Colloids versus crystalloids for fuid resuscita- tion in critically ill patients. Lancet 2007; 370:676–684 starch and gelatin on renal function in severe sepsis: A multicentre 148. Regnier B, Rapin M, Gory G, et al: Haemodynamic effects of dopa- randomised study. Ruokonen E, Takala J, Kari A, et al: Regional blood fow and oxygen Trials Group: Fluid resuscitation in the management of early sep- transport in septic shock. N Engl J Med 2008; 358:125–139 versus norepinephrine in the management of septic shock. N Engl J Med 2004; 350:2247–2256 Comparison of dopamine and norepinephrine in the treatment of 130. N Engl J Med 2010; 362:779–789 citation fuid for patients with sepsis: A systematic review and meta- analysis. De Backer D, Aldecoa C, Njimi H, et al: Dopamine versus norepi- nephrine in the treatment of septic shock: A meta-analysis*. Crit tors: A comparison of epinephrine and norepinephrine in critically ill Care Med 2004; 32:1928–1948 patients. Morelli A, Ertmer C, Rehberg S, et al: Phenylephrine versus nor- sure on tissue perfusion in septic shock. Crit Care Med 2000; epinephrine for initial hemodynamic support of patients with septic 28:2729–2732 shock: A randomized, controlled trial. Crit Care Med 2000; 28:2758–2765 term vasopressin infusion during severe septic shock. De Backer D, Creteur J, Silva E, et al: Effects of dopamine, nor- ogy 2002; 96:576–582 epinephrine, and epinephrine on the splanchnic circulation in septic 159. Crit Care Med 2003; 31:1659–1667 advanced vasodilatory shock: A prospective, randomized, controlled 138. Circulation 2003; 107:2313–2319 adrenaline infusions on acid-base balance and systemic haemody- 160. Lancet 2002; 359:1209–1210 nephrine and dobutamine to epinephrine for hemodynamics, lac- 165. Sharshar T, Blanchard A, Paillard M, et al: Circulating vasopressin tate metabolism, and gastric tonometric variables in septic shock: levels in septic shock. Confalonieri M, Urbino R, Potena A, et al: Hydrocortisone infusion 31:1394–1398 for severe community-acquired pneumonia: A preliminary random- 168. Am J Respir Crit Care Med 2005; 171:242–248 in hyperdynamic septic shock: A prospective, randomized study. Morelli A, Ertmer C, Lange M, et al: Effects of short-term simultane- monia: A randomised, double-blind, placebo-controlled trial. Bellomo R, Chapman M, Finfer S, et al: Low-dose dopamine in ized, controlled clinical trial of transfusion requirements in critical patients with early renal dysfunction: A placebo-controlled ran- care. Australian and New Zealand Intensive Care Society dian Critical Care Trials Group. Annane D, Sébille V, Charpentier C, et al: Effect of treatment with transfusion does not increase oxygen consumption in critically ill low doses of hydrocortisone and fudrocortisone on mortality in septic patients. Briegel J, Forst H, Haller M, et al: Stress doses of hydrocortisone binant human erythropoietin in the critically ill patient: A random- reverse hyperdynamic septic shock: A prospective, randomized, ized, double-blind, placebo-controlled trial. Crit Care als Group: Effcacy of recombinant human erythropoietin in Med 1998; 26:645–650 critically ill patients: A randomized controlled trial. College of American Pathologists: Practice parameter for the use 2008; 358:111–124 of fresh-frozen plasma, cryoprecipitate, and platelets. Clin Infect Dis 2009; 49:93–101 ponent Therapy: Practice guidelines for blood component therapy. Crit Care 2002; 6:251–259 transfusion on prothrombin time and bleeding in patients with mild 184. 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Flocks under the stress of egg production may suffer higher mortality compared with immature breeders generic 400mg ofloxacin with visa. Economic importance Significant economic losses may result from fatal outbreaks in commercial flocks and a drop in egg production ofloxacin 200mg lowest price. In: Field manual of wildlife websites diseases: general field procedures and diseases of birds ofloxacin 400mg for sale. Species affected Farmed and wild fish are affected worldwide, with infection confirmed in almost 80 finfish species, e. The range of susceptible species is very broad, thus many more species of fish are likely to be susceptible. Some fish species, such as common carp Cyprinus carpio and Nile tilapia Oreochromis niloticus, have been reported not to develop clinical disease during outbreaks in other species. However, experimental studies demonstrate susceptibility so their potential role in spreading the disease is currently unclear. Water salinity over two parts per thousand (ppt) can stop the spread of the agent. If the zoospores cannot find susceptible species or encounter unfavourable conditions, they can encyst in the water or pond environment waiting for conditions that favour the activation of the spores. Australia and the Philippines) have been reported to be associated with acidified run-off water from acid sulphate soil areas. The spread from wild to cultured spread between groups populations or vice versa can occur via several routes. In addition, movements of fish (cross border and domestic) for aquaculture and the ornamental fish trade are proven pathways. In some countries outbreaks occur in wild fish first and then spread to fish ponds. Once an outbreak occurs in rivers/canals, the disease can spread downstream as well as upstream where susceptible fish species exist. Infected fish may float near the surface of the water yet become hyperactive with a jerky pattern of movement. Take note of simple observations such as: abnormal fish behaviour date and time of observed outbreaks total estimate of mortalities species of fish affected and estimate of mortalities per species pattern of mortality (small number of fish dying every day, large number of fish dying at one time, etc. Aquaculture Actions should be directed firstly at prevention of the disease as subsequent control can be very difficult. The most important biosecurity measure to prevent the introduction onto farms is sourcing fish from safe, uninfected sources only. These include: All possible carriers or vectors such as freshly dead fish, birds or terrestrial animals as well as contaminated fishing gear and fish transport containers should be prevented from entering water bodies or fish ponds. In outbreaks occurring in small, closed water bodies, liming of water and improvement of water quality, together with removal of infected fish. Additional practical aquaculture biosecurity measures include: - Good farm hygiene (e. Early reporting or notification to concerned authorities of a disease outbreak or suspicion of any abnormal appearance, behaviour or other observations in fish stocks. Contact between fish-eating birds and aquaculture facilities should be minimised to reduce the risk of disease spread from an infected to an uninfected area. Indirect long- term effects may include threats to the environment and aquatic biodiversity through, for example, declining fish biomass and irreversible ecological disruption. Fisheries technical paper 402/2: Asia diagnostic guide to aquatic animal diseases. Report of the International Emergency Disease Investigation Task Force on a serious finfish disease in southern Africa. Review of biological factors relevant to import risk assessments for epizootic ulcerative syndrome (Aphanomyces invadans). Most of the hundreds of strains are harmless and some are even beneficial to humans and animals but others can cause illness. Once excreted from human and animal intestinal tracts, the bacteria may not survive, but some do find their way into lakes and streams, where they can persist for several weeks in water, sediment or sand. Dog and cat faeces may be carried along by storm sewers, deposited directly into streams and pathogens may be released into groundwater by insufficiently maintained septic systems. It is likely that widespread use of antibiotics in livestock has helped increased prevalence of E. The excretion of antibiotics into the environment directly from farms or even through sewage farms, contributes to genetically determined resistance in these and other bacteria in the environment. Infection occurs directly via contact with infected farm (or to a lesser extent wild) animals and their environments or from consumption of contaminated meat or unpasteurised milk. Scientists are now finding strong evidence that a significant amount of antibiotic resistance in human E. Environment Wetlands inhabited by susceptible species, particularly domestic ruminants. Susceptible animals include those which are immunocompromised, stressed, young, old, breeding or with associated environmental pressures. Infected animals, in particular young animals, shed the bacteria in their faeces, thus leading to exposure of other animals. In humans, incubation period ranges from 1-8 days but the duration of the illness is usually approximately 3–5 days. However, the bacteria can continue to be passed in faeces for up to three weeks post infection. Symptoms vary from mild to severe and include diarrhoea, vomiting, stomach-ache and fever. Accepting that domestic ruminants pose the greatest risk of transmission of pathogenic strains of E. If appropriate, wildlife can be kept away from possible sources of contamination e. Wetland treatment systems can also be used to reduce the risk of infection [►Environment]. Hands should be frequently washed with soap after handling animals, or working in their environment, and disposable gloves should be worn if in contact with sick animals. Wildlife populations may be in danger of fatalities or morbidity particularly if there are con-current infections or other stressors present. This is a problem of developed intensive agricultural systems and there is no evidence of widespread infection from extensive rangeland systems and natural environments. Effect on livestock Whilst domestic mammals generally only serve as carriers (or reservoirs) of the bacteria, some strains of E. Colibacillosis in pigeons and poultry is usually secondary to stress or con-current viral infection. There is now compelling evidence that animals reared for food are a reservoir for both antibiotic-resistant pathogenic and commensal E. Causal agent Toxin-producing species of algae, including: Alexandrium fundyense, Dinophysis spp, Gambierdiscus toxicus, Gymnodinium catenatum, Karenia brevis, Karenia brevisulcatum, Karlodinium veneficum, Lyngbya, Pfiesteria piscicda, Pfiesteria, Prorocentrum lima, Protoperidinium crassipes, Pseudo- nitzchia and Pyrodinium bahamense var. Environment Occur in both saltwater and freshwater environments, particularly where there are high nutrient levels (in particular high levels of nitrogen and phosphorus) but can also occur frequently in low nutrient environments. Livestock may drink contaminated water or lick themselves after bodily exposure and become ill. Affecting water quality by causing oxygen depletion from respiration and bacterial degradation, and blocking of sunlight. This may appear in conjunction with occurrence of a marine reddish/orange tide or freshwater bloom (which initially appear green and may later turn blue sometimes forming a scum/foam in the water). Signs such as irritation of the skin, vomiting, paralysis, lethargy and loss of muscle co-ordination may be observed in birds. Not all toxic algal blooms are visibly noticeable and so a sample of organisms from the bloom may be useful or necessary for diagnosis. Recommended action if Contact and seek assistance from animal and human health professionals suspected immediately if there is any illness in birds, fish, marine mammals and/or people. Diagnosis Confirmative diagnosis is difficult and relies on circumstantial evidence and supportive clinical and pathologic findings.

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Knowledge has a tendency to fade with time and non-use buy ofloxacin 400mg low cost,and there will always be situations arise that require looking up a procedure buy ofloxacin 400 mg online, a pictorial reference 200mg ofloxacin for sale, a protocol or dosing information. Healthcare practitioners undertake regular continuing education to not only stay abreast of the latest techniques but also to aid in retaining skills not often practiced. Having good reference books on hand may be critical during times when the education system is no longer working or accessible, and when you are facing a situation that calls for new knowledge or reviewing previous training. This section will be divided into three primary areas: the basic must haves; those that support the first category, and everything else. The first category lists those books which by themselves constitute a very comprehensive survival medicine library. The second group represents those works, which expand the capabilities of the library further but are not deemed first line access works. Finally, a third section will list useful references that may be considered later. These latter books round out the library of suggested works and constitute a nice-to-have as opposed to necessary collection. Any one will serve well within its area though one may be selected over another based upon your existing medical skills. These are absolute must haves for anyone just getting started with medical preparedness. The third world environment mimics in many ways the post-disaster level of development many envision should it ever come to pass. The book offers useful information for handling everyday medical problems by unskilled caregivers with minimal access to resources. How to care for the gums, extract, fill or repair teeth, manufacture your own basic dental instruments, and more. Written for remote locations where access to trained medical aid is impractical or even non-existent. Probably the weakest area in any preparedness medical prep is the ability to perform a qualifiable health exam. Having a decent reference to guide you through the more unfamiliar aspects could prove invaluable. After you acquire the first five references above fill out your primary collection with a selection from each group below. Bate’s Guide to Physical Examinations & History Taking, 8th edition (August 2002) by Lynn S. The Survival Guide: What To Do in a Biological, Chemical or Nuclear Emergency by Angelo Acquista, M. The quick, to-the-point book for the layperson seeking fast, authoritative information on dealing with nuclear, biological, or chemical attack without getting bogged down in detail. The Sanford Guide to Antimicrobial Therapy – Pocket Edition, published annually by Antimicrobial Therapy, Inc. Also available as a large print spiral-bound edition (recommended if you need bifocals) listed at $22. A very widely regarded quick reference guide for use in matching antiinfectives with conditions. Easy to read and makes liberal use of color plates to illustrate everything from anatomical references to a standard instrument array for basic patient assessment. Numerous tables present complicated information in schematic format to facilitate learning. Information on matching dosing to patient age is superior to other references examined. Includes form, strength, route, therapeutic class, approved indications, dosage, warnings, precautions, interactions, and reactions. Not a replacement for the regular drug handbook but perhaps more suited if access to prescription drugs isn’t in the picture. Recommended non-professional selection compared to the Professional’s Handbook listed in Tier Two. Good basic coverage of hygiene, nursing and medical care with limited on-hand resources. Either one covers most common medical problems but frequently offer the advice to access medical counsel via radio. Mental health diagnosis and care will be at a premium during times of significant stress. A suitable replacement, however, for Nancy Carolyn’s Emergency Care in the Streets (not updated since 1995 though copies remain currently available through many sources). If you can afford only one advanced trauma book for your library then this should be the one you select. Covers topics ranging from land mine identification to an illustrated guide of performing an emergency laparotomy without the benefit of a hospital. Everything from lists of materials for a rough field hospital to advanced surgical techniques. A valuable feature is a system of closed fracture management and an extensive chapter on the treatment of burns. They are for non-specialist doctors and for medical students and describe what a doctor can do if he cannot refer a patient. Merck Manual of Diagnosis and Therapy, 17th Edition by Robert Berkow (Editor), Mark H. It proceeds from one basic premise: that the care giver is relatively new to or even unschooled in basic care procedures required during sub-acute, long-term or recovery health care management. If you happen to be a nurse who finds themselves thrust into a role you aren’t familiar with you may find this book invaluable. Likewise any other medical care giver who doesn’t normally perform the wealth of procedures contained within this reference. Just stay away from the so-called “collector’s editions” as they have been abridged. They expand capabilities, explore subjects in greater depth, and add muscle to the first tier meat. The information as presented is often more clinical in nature and may require a good understanding of medical terminology. They are second tier because they are not essential for initial management of acute cases in the survival setting. How-to explanations and practical approaches to emergencies, and information on children and women in the wilderness. Assumes the reader has at least paramedic-level training and is familiar with the procedures. Second tier because other books offer the same info in more detailed form, making them more useful for semi-skilled personnel. However for those with a paramedic background this book bridges the gap from pre-hospital care to the full spectrum of medicine and cannot be recommended highly enough and should be a first tier reference. Surgical Care at the District Hospital Publisher: World Health Organization (2003). Though it contains much of the same content as the individual books it is essentially an abridged version within one binding. Covers such topics as knot-tying, retractor selection, and techniques for stopping bleeding. The Complete Idiot’s Guide to Dangerous Diseases and Epidemics by David Perlin, Ph. A very useful guide to rapid decision making without getting bogged down by details. A much better than average starting point when seeking quick information about specific infectious diseases. The Survival Nurse: Running An Emergency Nursing Station Under Adverse Conditions by Ragnar Benson. Not a substitute for any of the previously recommended references but it does help pull some of them together in order to form a plan of action. Worthwhile but not a high priority book when there are higher tier references to acquire first. This fifth edition includes the latest information on cryptospriosis and immunization changes. Aiello, Asa Mays (Editor) Publisher: John Wiley & Sons; 8th edition (April 15, 1998).

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