8 results on '"Walter, Frank G."'
Search Results
2. Immediate and delayed allergic reactions to Crotalidae polyvalent immune Fab (ovine) antivenom. (Case Report)
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Clark, Richard F., McKinney, Patrick E., Chase, Peter B., and Walter, Frank G.
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Allergic reaction -- Causes of ,Antivenins -- Adverse and side effects ,Bites and stings -- Care and treatment ,Health - Published
- 2002
3. Continuous Intravenous Midazolam Infusion for Centruroides exilicauda Scorpion Envenomation
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Gibly, Raquel, Williams, Michelle, Walter, Frank G., McNally, Jude, Conroy, Carol, and Berg, Robert A.
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Midazolam ,Emergency medicine ,Universities and colleges ,Emergency medical services ,Venom ,Health - Abstract
Byline: Raquel Gibly, Michelle Williams, Frank G Walter, Jude McNally, Carol Conroy, Robert A Berg Abstract: Study objective: We sought to describe the effects of continuous intravenous midazolam infusion as therapy for severe bark scorpion (Centruroides exilicauda) envenomation. Methods: A retrospective chart review from July 1, 1993, through January 1, 1998, identified all patients treated at a university hospital with International Classification of Diseases, Ninth Revision, codes 989.5 (toxic effect of venom) or E905.2 (scorpion sting causing poisoning). By using standardized collection forms, data were extracted from the medical record of every patient who had a grade III or IV envenomation and was treated with a continuous intravenous midazolam infusion. Results: Our search identified 104 patients; 34 had grade III or IV envenomation. Of these, 33 were treated in the ICU with continuous intravenous midazolam infusion. Median patient age was 4 years (range, 1 to 68 years). Midazolam dosage was adjusted to induce a light sleep state to control agitation and involuntary motor activity. The median amount of midazolam resulting in the first recorded decrease in agitation and involuntary motor activity was 0.30 mg/kg (range, 0.03 to 1.76 mg/kg). This first evidence of clinical improvement was recorded as 1.00 hour (median), with a range of 0.00 to 3.75 hours. The initial midazolam infusion rate was 0.10 mg*kg.sup.-1*h.sup.-1 (median), with a range of 0.01 to 0.31 mg*kg.sup.-1*h.sup.-1. The maximal midazolam infusion rate was 0.30 mg*kg.sup.-1*h.sup.-1 (median), with a range of 0.06 to 1.29 mg*kg.sup.-1*h.sup.-1. The median time until the maximal midazolam infusion rate was 2.5 hours (range, 0.00 to 8.50 hours). The median duration of infusion was 9.50 hours (range, 4.25 to 20.50 hours). The median length of stay in the ICU was 15.17 hours (range, 6.0 to 28.0 hours), and 85% of patients were discharged directly home. All patients had resolution of abnormal motor activity and agitation during their midazolam infusion. Transient hypoxemia without evidence of end-organ dysfunction was documented in 4 patients during midazolam therapy. Conclusion: A continuous intravenous midazolam infusion can be a safe, effective, and readily available treatment option for patients with grade III or IV C exilicauda envenomation. [Gibly R, Williams M, Walter FG, McNally J, Conroy C, Berg RA: Continuous intravenous midazolam infusion for Centruroides exilicauda scorpion envenomation. Ann Emerg Med November 1999;34:620-625.] Author Affiliation: From the Section of Medical Toxicology, Division of Emergency Medicine, Department of Surgery,.sup.* Arizona Poison and Drug Information Center,.sup.a Arizona Emergency Medicine Research Center,.sup.As. the Department of Pediatrics and the Steele Memorial Children's Research Center,.sup.a[yen] the University of Arizona Health Sciences Center, and Emergency Room Associates, Carondelet St. Joseph's Hospital,.sup.A[paragraph] Tucson, AZ Article History: Received 6 August 1998; Revised 11 May 1999; Revised 23 June 1999; Accepted 12 July 1999 Article Note: (footnote) [star] Supported in part by the Maria Mandell Emergency Medicine Research Award given by the Arizona Emergency Medicine Research Center., [star][star] Reprints not available from the authors., a 0196-0644/99/$8.00 + 0 , aa 47/1/101383
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- 1999
4. Squamous Cells as Predictors of Bacterial Contamination in Urine Samples
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Walter, Frank G., Gibly, Raquel L., Knopp, Robert K., and Roe, Denise J.
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Cell research ,Urinary tract infections ,Health - Abstract
Byline: Frank G Walter, Raquel L Gibly, Robert K Knopp, Denise J Roe Abstract: Study objective: To determine whether squamous cells in urine indicate bacterial contamination. Methods: We prospectively studied 105 consecutive women who presented to the emergency department with symptoms suggestive of a urinary tract infection. Two urine samples were collected from each woman, a midstream clean-catch (MSCC) sample and a catheterized (CATH) sample. Microscopic urinalyses to assess for squamous cells and urine cultures to assess for bacterial contamination were performed on all samples. Bacterial contamination was defined as growth of fewer than 10,000 colonies of a single species per milliliter or growth of three or more species of commensal bacteria (mixed flora) in a urine sample. Results: Squamous cells were found in 99 of 105 CATH samples (94%); however, no CATH samples had bacterial contamination. Squamous cells were found in 101 of 105 MSCC samples (96%); however, only 22 MSCC samples (21%) had bacterial contamination. Conclusion: The presence of squamous cells in CATH urine samples obtained from women is not indicative of bacterial contamination. The presence of squamous cells in MSCC urine samples obtained from women also is not a good indicator, with an overall predictive value for bacterial contamination of 21%. [Walter FG, Gibly RL, Knopp RK, Roe DJ: Squamous cells as predictors of bacterial contamination in urine samples. Ann Emerg Med April 1998;31:455-458.] Article History: Received 10 October 1996; Revised 25 June 1997; Revised 4 November 1997; Accepted 16 November 1997 Article Note: (footnote) [star] From the Department of Emergency Medicine, Valley Medical Center, Fresno, * and the Department of Medicine, University of California San Francisco School of Medicine, San Francisco,a CA; and the Division of Emergency Medicine, Department of Surgery,As. and Department of Family and Community Medicine, II The University of Arizona College of Medicine, Tucson, AZ., [star][star] Supported by a grant from the Medical Research Committee of Valley Medical Center, Fresno, CA., a Address for reprints: Raquel L Gibly, MD, Division of Emergency Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724-5057, 520-626-6312, Fax 520-626-2480, E-mail raquel@aemrc.arizona.edu, aa 47/1/88631
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- 1998
5. Loxosceles arizonica Bite Associated With Shock
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Bey, Tareg A., Walter, Frank G., Lober, William, Schmidt, Justin, Spark, Ronald, and Schlievert, Patrick M.
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Health - Abstract
Byline: Tareg A Bey, Frank G Walter, William Lober, Justin Schmidt, Ronald Spark, Patrick M Schlievert Abstract: Envenomation by the brown recluse spider (Loxosceles reclusa) is associated with shock, significant hemolysis, renal insufficiency, and disseminated intravascular coagulation (DIC). Shock has never been associated with envenomation by L arizonica, a related species indigenous to Arizona, southern California, and northwestern Mexico. We report the case of a 13-year-old girl, bitten by a specimen of L arizonica (the spider was identified by an entomologist), in whom shock and a typical cutaneous lesion developed. She did not experience renal insufficiency or disseminated intravascular coagulation. Infectious causes of shock were excluded. She recovered completely with supportive care. [Bey TA, Walter FG, Lober W, Schmidt J, Spark R, Schlievert PM: Loxosceles arizonica bite associated with shock. Ann Emerg Med November 1997;30:701-703.] Article History: Received 28 August 1996; Revised 14 January 1997; Accepted 12 April 1997 Article Note: (footnote) [star] From the Medical Toxicology Fellowship, Section of Emergency Medicine, Department of Surgery, University of Arizona Health Sciences Center,* the Department of Pathology, Tucson Medical Center,a the Carl Hayden Bee Research Center, US Department of Agriculture, Tucson, AZ,As. and the Department of Microbiology, University of Minnesota Medical School, Minneapolis, MN.a[yen] , [star][star] Reprint no. 47/1/85424 , a Address for reprints: Tareg A Bey, MD, University of Arizona Health Sciences Center, Section of Emergency Medicine, 1501 North Campbell Avenue, Tucson, AZ 85724-5057, 520-626-6312, Fax 520-626-2480, E-mail tareg@aemrc.arizona.edu
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- 1997
6. Pyridoxine does not prevent hyperbaric oxygen-induced seizures in rats
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Walter, Frank G., Chase, Peter B., Fernandez, Miguel C., Cameron, Diane, Roe, Denise J., and Wolfson, Mark
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VITAMIN B6 , *COENZYMES , *VITAMIN B complex , *THERAPEUTICS , *ANIMAL experimentation , *COMPARATIVE studies , *HYPERBARIC oxygenation , *SEIZURES (Medicine) , *INJECTIONS , *RESEARCH methodology , *MEDICAL cooperation , *PREANESTHETIC medication , *RATS , *RESEARCH , *STATISTICAL sampling , *EVALUATION research , *SPASMS , *PREVENTION , *VITAMIN therapy - Abstract
Abstract: Normobaric supplemental oxygen can prolong seizures not caused by hyperbaric oxygen therapy. In addition, hyperbaric oxygen therapy can cause seizures. The mechanism of hyperbaric oxygen-induced seizures is unknown. We hypothesized that pretreatment with pyridoxine may delay the onset of hyperbaric oxygen-induced seizures, recognizing that pyridoxine is already an antidote for some epileptogenic poisons such as isoniazid and monomethylhydrazine. Therefore, rats were pretreated with intraperitoneal injections of pyridoxine at 48, 24, and 2 h before undergoing hyperbaric oxygen (HBO) treatment at 3 atmospheres absolute with 100% oxygen and were compared to a control group of HBO-treated rats for time to onset of seizures. There was no difference in onset of seizure time between the pyridoxine-treated group of rats and the control rats. Supplemental pyridoxine pretreatment did not alter the time to onset of seizures during HBO treatment in this study. [Copyright &y& Elsevier]
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- 2006
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7. Initial Experience with F(ab')2 Antivenom Compared with Fab Antivenom for Rattlesnake Envenomations Reported to a single poison center during 2019.
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Wilson, Bryan Z., Bahadir, Alisia, Andrews, Matthew, Karpen, Jacqueline, Winkler, Garret, Smelski, Geoffrey, Dudley, Steve, Walter, Frank G., and Shirazi, Farshad Mazda
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ANTIVENINS , *POISON control centers , *RATTLESNAKES - Abstract
There are two Food and Drug Administration (FDA)-approved antivenoms available for rattlesnake envenomations in the United States: the equine-derived F (ab')2 product sold with the brand name Anavip (F (ab')2 AV) and the ovine-derived Fab product sold with the brand name Crofab (FabAV). To compare the clinical outcomes of rattlesnake envenomation patients treated either with FabAV or F (ab')2AV or a combination of these. This is a retrospective chart review of all human rattlesnake envenomations requiring antivenom reported to one regional poison control center in 2019. Patients were categorized as receiving F (ab')2 AV, FabAV, or a combination of both. Baseline characteristics included demographics, time between envenomation and administering antivenom, an abbreviated snakebite severity score (ASSS), and the presence of coagulopathy at presentation. There were a total of 123 patients requiring antivenom. Of these, 57 (46.3%) received FabAV, 53 (43.1%) received F (ab')2 AV, and 13 (10.6%) received a combination of these. Those receiving F (ab')2 AV were younger, with an average age of 40.8 (±25.0) years versus 51.3 (±19.9) years (p = 0.0161) for those receiving FabAV. Time between envenomation and antivenom administration, ASSS, and the percentage of those with coagulopathy at presentation were otherwise similar. Patients treated with F (ab')2 AV or FabAV received a similar total number of vials [16.0 vials (±6.1) vs 14.5 vials (±5.4), p = 0.189], but patients treated with F (ab')2 AV were more frequently given additional doses [31 patients (58.5%) vs. 22 FabAV patients (38.6%), p = 0.0051]. In patients with outpatient follow-up for 2 weeks, fewer patients treated with F (ab')2 AV developed late coagulopathy [5 patients (11.1%) vs 22 FabAV patients (48.9%), p = 0.0004]. Adverse events were generally mild and uncommon with no difference in frequency between patients who received either antivenom (2 F (ab')2 AV patients vs 4 FabAV patients, p = 0.6637). Other than patient age, we found no significant difference in the baseline demographics, time between envenomation and administering antivenom, an abbreviated snakebite severity score (ASSS), and the presence of coagulopathy at presentation between patients receiving F (ab')2 AV or FabAV. Patients receiving F (ab')2 AV were more likely to be given an additional dose beyond the minimum typical treatment course, but less likely to develop late coagulopathy. Adverse events were uncommon and generally mild whether patients received either antivenom. [Display omitted] • A comparison of Fab and an F (ab')2 rattlesnake antivenom in the United States. • Patients treated with either antivenom received a similar total number of vials. • Fewer patients treated with F (ab')2 antivenom developed late coagulopathy. • Adverse events were generally mild and uncommon with both antivenoms. [ABSTRACT FROM AUTHOR]
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- 2022
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8. International report: current state and development of health insurance and emergency medicine in Germany. the influence of health insurance laws on the practice of emergency medicine in a European country
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Platz, Elke, Bey, Tareg, and Walter, Frank G.
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HEALTH insurance , *MEDICALLY uninsured persons - Abstract
Germany has a comprehensive health insurance system, with only 0.183% of the population being uninsured. Access to office-based medicine and to hospitals is easy and convenient. Due to enormous financial pressures, Germany is currently decreasing the number of beds in hospitals, introducing the Diagnosis Related Groups (DRG), and restricting accessibility to specialists. In contrast to Anglo-American countries, Germany follows the concept of bringing the physician to the patient in the prehospital setting, with Emergency Medical Services (EMS) physicians responding to all Advanced Life Support (ALS) calls. Despite a mature EMS system with sophisticated medical equipment and technology, both in the prehospital and hospital setting, logistical issues such as a single emergency telephone number or multidisciplinary Emergency Departments have yet to be established. Within the hospital, this “Franco-German model” considers Emergency Medicine a practice model that does not merit specialty status. Spending restrictions in the health care system, with less access to hospital beds and office-based physicians, will increase the demand for hospital-based emergency care when patients experience problems accessing the medical system. Currently, the German hospital system is unprepared to care for greater numbers of emergency patients. This may call for changes in the German health care system as well as the medical education system, with the introduction of hospital-based Emergency Medicine as its own specialty, similar to Anglo-American countries. [Copyright &y& Elsevier]
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- 2003
- Full Text
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