Hyperthermia & Heat Stroke: Heat-Related Conditions
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Metabolomic Profiling Identifies a Novel Mechanism for Heat Stroke‑Related Acute Kidney Injury
MOLECULAR MEDICINE REPORTS 23: 241, 2021 Metabolomic profiling identifies a novel mechanism for heat stroke‑related acute kidney injury LING XUE1*, WENLI GUO2*, LI LI2, SANTAO OU2, TINGTING ZHU2, LIANG CAI3, WENFEI DING2 and WEIHUA WU2 Departments of 1Urology and 2Nephrology, Sichuan Clinical Research Center for Nephropathy, The Affiliated Hospital of Southwest Medical University;3 Department of Nuclear Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China Received April 13, 2020; Accepted August 20, 2020 DOI: 10.3892/mmr.2021.11880 Abstract. Heat stroke can induce a systemic inflammatory factor mitochondria‑associated 2 (Aifm2), high‑mobility group response, which may lead to multi‑organ dysfunction including box 1 (HMGB1) and receptor for advanced glycosylation end acute kidney injury (AKI) and electrolyte disturbances. To products (RAGE). Liquid chromatography‑mass spectrometry investigate the pathogenesis of heat stroke (HS)‑related AKI, analysis was conducted to find differential metabolites and a mouse model of HS was induced by increasing the animal's signaling pathways. The HS mouse model was built success‑ core temperature to 41˚C. Blood samples obtained from the fully, with significantly increased creatinine levels detected tail vein were used to measure plasma glucose and creati‑ in the serum of HS mice compared with controls, whereas nine levels. Micro‑positron emission tomography‑computed micro‑PET/CT revealed active metabolism in the whole tomography (micro‑PET/CT), H&E staining and trans‑ body of HS mice. H&E and TUNEL staining revealed that mission electron microscopy were conducted to examine the kidneys of HS mice exhibited signs of hemorrhage and metabolic and morphological changes in the mouse kidneys. -
Prevention and Management of Heat-Related Illness
PREVENTION AND MANAGEMENT OF HEAT-RELATED ILLNESS Federal Bureau of Prisons Clinical Guidance DECEMBER 2017 Federal Bureau of Prisons (BOP) Clinical Guidance is made available to the public for informational purposes only. The BOP does not warrant this guidance for any other purpose, and assumes no responsibility for any injury or damage resulting from the reliance thereof. Proper medical practice necessitates that all cases are evaluated on an individual basis and that treatment decisions are patient- specific. Consult the BOP Health Management Resources Web page to determine the date of the most recent update to this document: http://www.bop.gov/resources/health_care_mngmt.jsp Federal Bureau of Prisons Prevention and Management of Heat-Related Illness Clinical Guidance December 2017 TABLE OF CONTENTS 1. PURPOSE AND OVERVIEW ......................................................................................................................1 2. PATHOPHYSIOLOGY...............................................................................................................................1 3. RISK FACTORS FOR HRI ........................................................................................................................2 4. SYMPTOMS AND SIGNS ..........................................................................................................................3 5. EVALUATION.........................................................................................................................................5 6. TREATMENT..........................................................................................................................................6 -
Motion Sickness: Definition
Clinical and physiological characteristics of cybersickness Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy (Human Physiology) School of Biomedical Sciences and Pharmacy Faculty of Health and Medicine University of Newcastle, Australia This research was supported by an Australian Government Research Training Program (RTP) Scholarship. 1 STATEMENT OF ORIGINALITY I hereby certify that the work embodied in the thesis is my own work, conducted under normal supervision. The thesis contains no material which has been accepted, or is being examined, for the award of any other degree or diploma in any university or other tertiary institution and, to the best of my knowledge and belief, contains no material previously published or written by another person, except where due reference has been made. I give consent to the final version of my thesis being made available worldwide when deposited in the University’s Digital Repository, subject to the provisions of the Copyright Act 1968 and any approved embargo. Alireza Mazloumi Gavgani 2 ACKNOWLEDGMENT OF AUTHORSHIP I hereby certify that the work embodied in this thesis contains published paper/s/scholarly work of which I am a joint author. I have included as part of the thesis a written declaration endorsed in writing by my supervisor, attesting to my contribution to the joint publication/s/scholarly work. Alireza Mazloumi Gavgani 3 STATEMENT OF COLLABORATION I hereby certify that some parts of the work embodied in this thesis have been done in collaboration with other researchers. I have included as part of the thesis a statement clearly outlining the extent of collaboration, with whom and under what auspices. -
Therapeutic Hypothermia: Where Do We Stand?
5/29/2015 Therapeutic Hypothermia: Where Do We Stand? Melina Aguinaga-Meza, MD Assistant Professor of Medicine Gill Heart Institute University of Kentucky Disclosure Information Melina Aguinaga-Meza, MD “Therapeutic Hypothermia: Where Do We Stand?” • FINANCIAL DISCLOSURE: – No relevant financial relationship exists • UNLABELED/UNAPPROVED USES DISCLOSURE: – No relevant relationship exists 1 5/29/2015 The Clinical Problem • Out-of-hospital cardiac arrest (OHCA) is a leading cause of death among adults in the US • Approx. 300,000 OHCA events occur each year in the US • Resuscitation is attempted in 100,000 of these arrests • Less than 40 000 survive to hospital admission MMWR / July 29, 2011 / Vol. 60 / No. 8 2 5/29/2015 Consequences From Cardiac Arrest Myocardial Brain injury dysfunction Post-Cardiac Arrest Syndrome Systemic ischemia Disorder that + reperfusion caused the cardiac responses arrest • The effects of this syndrome are severe and pervasive MMWR / July 29, 2011 / Vol. 60 / No. 8 Survival and Neurological Outcomes after OHCA • Only one third of patients admitted to the hospital survive to hospital discharge • Approx. one out of ten people who experience OHCA survive to hospital discharge • Only 2 out of 3 of them have a good/moderate neurologic recovery MMWR / July 29, 2011 / Vol. 60 / No. 8: CARES 3 5/29/2015 “Chain of Survival” • Actions needed to improve chances of survival from out-of-hospital cardiac arrest Circulation 2010; 122:S676-84 • Try to identify and treat the precipitating causes of the arrest and prevent recurrent -
Alterations in the Specific Gravity of the Blood Plasma with Onset of Diuresis in Heart Failure
MECHANISM OF DIURESIS: ALTERATIONS IN THE SPECIFIC GRAVITY OF THE BLOOD PLASMA WITH ONSET OF DIURESIS IN HEART FAILURE Harold J. Stewart J Clin Invest. 1941;20(1):1-6. https://doi.org/10.1172/JCI101189. Research Article Find the latest version: https://jci.me/101189/pdf MECHANISM OF DIURESIS: ALTERATIONS IN THE SPECIFIC GRAVITY OF THE BLOOD PLASMA WITH ONSET OF DIURESIS IN HEART FAILURE By HAROLD J. STEWART (From the Department of Medicine of.the New York Hospital and Cornell University Medical College and the Hospital of the Rockefeller Institute for Medical Research, New York) (Received for publication July 3, 1940) There are divergent views concerning the Moreover, its duration may be brief before res- mechanism by which diuresis is initiated. Many toration is attempted, or it may be long enough of the observations on this subject relate to mer- and of such magnitude that it can be detected. curial drugs. Crawford and McIntosh (1) con- On the other hand, if diuresis is initiated at cluded that novasurol induced primary dilution, the tissue side of the system so that fluid enters followed by concentration of the blood in edema- the blood stream first, dilution of the blood would tous patients. Bryan, Evans, Fulton, and Stead occur. Equilibrium would be disturbed until the (2) thought that salyrgan resulted in concentra- kidneys began to excrete the surplus fluid. If di- tion of the blood, since sustained rise in its spe- lution of the blood was of sufficient duration and cific gravity occurred coincident with diuresis in magnitude, it might be detected. -
Critical Care in the Monoplace Hyperbaric Chamber
Critical Care in the Monoplace Hyperbaric Critical Care - Monoplace Chamber • 30 minutes, so only key points • Highly suggest critical care medicine is involved • Pitfalls Lindell K. Weaver, MD Intermountain Medical Center Murray, Utah, and • Ventilator and IV issues LDS Hospital Salt Lake City, Utah Key points Critical Care in the Monoplace Chamber • Weaver LK. Operational Use and Patient Care in the Monoplace Chamber. In: • Staff must be certified and experienced Resp Care Clinics of N Am-Hyperbaric Medicine, Part I. Moon R, McIntyre N, eds. Philadelphia, W.B. Saunders Company, March, 1999: 51-92 in CCM • Weaver LK. The treatment of critically ill patients with hyperbaric oxygen therapy. In: Brent J, Wallace KL, Burkhart KK, Phillips SD, and Donovan JW, • Proximity to CCM services (ed). Critical care toxicology: diagnosis and management of the critically poisoned patient. Philadelphia: Elsevier Mosby; 2005:181-187. • Must have study patient in chamber • Weaver, LK. Critical care of patients needing hyperbaric oxygen. In: Thom SR and Neuman T, (ed). The physiology and medicine of hyperbaric oxygen therapy. quickly Philadelphia: Saunders/Elsevier, 2008:117-129. • Weaver LK. Management of critically ill patients in the monoplace hyperbaric chamber. In: Whelan HT, Kindwall E., Hyperbaric Medicine Practice, 4th ed.. • CCM equipment North Palm Beach, Florida: Best, Inc. 2017; 65-95. • Without certain modifications, treating • Gossett WA, Rockswold GL, Rockswold SB, Adkinson CD, Bergman TA, Quickel RR. The safe treatment, monitoring and management -
20Mg Spironolactone I.P…..50Mg
For the use only of a Registered Medical Practitioner or Hospital or a Laboratory. This package insert is continually updated: Please read carefully before using a new pack Frusemide and Spironolactone Tablets Lasilactone® 50 COMPOSITION Each film coated tablet contains Frusemide I.P. …….. 20mg Spironolactone I.P…..50mg THERAPEUTIC INDICATIONS Lasilactone® contains a short-acting diuretic and a long-acting aldosterone antagonist. It is indicated in the treatment of resistant oedema where this is associated with secondary hyperaldosteronism; conditions include chronic congestive cardiac failure and hepatic cirrhosis. Treatment with Lasilactone® should be reserved for cases refractory to a diuretic alone at conventional doses. This fixed ratio combination should only be used if titration with the component drugs separately indicates that this product is appropriate. The use of Lasilactone® in the management of essential hypertension should be restricted to patients with demonstrated hyperaldosteronism. It is recommended that in these patients also, this combination should only be used if titration with the component drugs separately indicates that this product is appropriate. POSOLOGY AND METHOD OF ADMINISTRATION For oral administration. The dose must be the lowest that is sufficient to achieve the desired effect. Adults: 1-4 tablets daily. Children: The product is not suitable for use in children. Elderly: Frusemide and Spironolactone may both be excreted more slowly in the elderly. Tablets are best taken at breakfast and/or lunch with a generous amount of liquid (approx. 1 glass). An evening dose is not recommended, especially during initial treatment, because of the increased nocturnal output of urine to be expected in such cases. -
HHE Report No. HETA-2018-0154-3361, Evaluation of Rhabdomyolysis and Heat Stroke in Structural Firefighter Cadets
Evaluation of Rhabdomyolysis and Heat Stroke in Structural Firefighter Cadets HHE Report No. 2018-0154-3361 November 2019 Authors: Judith Eisenberg, MD, MS Jessica F. Li, MSPH Karl D. Feldmann, MS, CIH Desktop Publisher: Jennifer Tyrawski Editor: Cheryl Hamilton Logistics: Donnie Booher, Kevin Moore Medical Field Assistance: Nonita Dhirar Data Support: Hannah Echt Keywords: North American Industry Classification System (NAICS) 922160 (Fire Protection), Structural Firefighter Training, Structural Firefighter Cadet Course, Heat, Heat-Related Illness, Heat Stroke, Rhabdomyolysis, Texas Disclaimer The Health Hazard Evaluation Program investigates possible health hazards in the workplace under the authority of the Occupational Safety and Health Act of 1970 [29 USC 669a(6)]. The Health Hazard Evaluation Program also provides, upon request, technical assistance to federal, state, and local agencies to investigate occupational health hazards and to prevent occupational disease or injury. Regulations guiding the Program can be found in Title 42, Code of Federal Regulations, Part 85; Requests for Health Hazard Evaluations [42 CFR Part 85]. Availability of Report Copies of this report have been sent to the employer, employees, and union at the plant. The state and local health departments and the Occupational Safety and Health Administration Regional Office have also received a copy. This report is not copyrighted and may be freely reproduced. Recommended Citation NIOSH [2019]. Evaluation of rhabdomyolysis and heat stroke in structural firefighter cadets. By Eisenberg J, Li JF, Feldmann KD. Cincinnati, OH: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, Health Hazard Evaluation Report 2018-0154-3361, https://www.cdc.gov/niosh/hhe/reports/pdfs/2018-0154-3361.pdf. -
Occupational Exposure to Heat and Hot Environments
Criteria for a Recommended Standard Occupational Exposure to Heat and Hot Environments DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention National Institute for Occupational Safety and Health Cover photo by Thinkstock© Criteria for a Recommended Standard Occupational Exposure to Heat and Hot Environments Revised Criteria 2016 Brenda Jacklitsch, MS; W. Jon Williams, PhD; Kristin Musolin, DO, MS; Aitor Coca, PhD; Jung-Hyun Kim, PhD; Nina Turner, PhD DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention National Institute for Occupational Safety and Health This document is in the public domain and may be freely copied or reprinted. Disclaimer Mention of any company or product does not constitute endorsement by the National Institute for Occupational Safety and Health (NIOSH). In addition, citations of websites external to NIOSH do not constitute NIOSH endorsement of the sponsoring organizations or their programs or products. Furthermore, NIOSH is not responsible for the content of these websites. Ordering Information This document is in the public domain and may be freely copied or reprinted. To receive NIOSH documents or other information about occupational safety and health topics, contact NIOSH at Telephone: 1-800-CDC-INFO (1-800-232-4636) TTY: 1-888-232-6348 E-mail: [email protected] or visit the NIOSH website at www.cdc.gov/niosh. For a monthly update on news at NIOSH, subscribe to NIOSH eNews by visiting www.cdc.gov/ niosh/eNews. Suggested Citation NIOSH [2016]. NIOSH criteria for a recommended standard: occupational exposure to heat and hot environments. By Jacklitsch B, Williams WJ, Musolin K, Coca A, Kim J-H, Turner N. -
Preventing Dehydration
State of New Jersey Department of Human Services Division of Developmental Disabilities DDDDDD PREVENTIONPREVENTION BULLETINBULLETIN Dehydration Dehydration is a loss of too much fluid from the body. The body needs water in order to maintain normal functioning. If your body loses too much fluid - more than you are getting from your food and liquids - your body loses electrolytes. Electrolytes include important nutrients like sodium and potassium which your body needs to work normally. A person can be at risk for dehydration in any season, not just the summer months. It is also important to know that elderly individuals are at heightened risk for dehydration because their bodies have a lower water content than younger people. Why people with Common Causes and a developmental Risk Factors for disability may be Dehydration: at a higher risk for dehydration. v Diarrhea v Vomiting v People with physical limitations may v Excessive sweating not be able to get something to drink on their own and will need the assistance of v Fever others. v Burns v People who cannot speak or whose v Diabetes when blood sugar is too high speech is hard to understand may have a v hard time telling their support staff that Increased urination (undiagnosed diabetes) they are thirsty. v Not drinking enough water, especially on warm and hot days v Some people may have difficulty swal- lowing their food or drinks and may v Not drinking enough during or after exercise refuse to eat or drink. This can make v Some medications (diuretics, blood pressure them more susceptible to becoming meds, certain psychotropic and anticonvul- dehydrated. -
Diagnostic Value of Procalcitonin in Patients with Heat Stroke
Arch Microbiol Immunology 2020; 4 (1): 001-010 DOI: 10.26502/ami.93650040 Research Article Diagnostic Value of Procalcitonin in Patients with Heat Stroke Xuan Song1, Xinyan Liu1, Huairong Wang2, Xiuyan Guo2, Maopeng Yang1, Daqiang Yang1, Yahu Bai3, Nana Zhang1, Chunting Wang4* 1Department of Intensive Care Unit, DongE Hospital Affiliated to Shandong First Medical University, Liaocheng, China. 2Education Department, DongE Hospital Affiliated to Shandong First Medical University, Liaocheng, China. 3Emergency Department, DongE Hospital Affiliated to Shandong First Medical University, Liaocheng, China. 4Department of Intensive Care Unit, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Shandong, China. *Corresponding Author: Chunting Wang, Department of Intensive Care Unit, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 324 Jingwu Road, Jinan, Shandong Province, China, 250021, Tel: +86-17806359196; E-mail: [email protected] Received: 13 January 2020; Accepted: 23 January 2020; Published: 03 February 2020 Citation: Xuan Song, Xinyan Liu, Huairong Wang, Xiuyan Guo, Maopeng Yang, Daqiang Yang, Yahu Bai, Nana Zhang, Chunting Wang. Diagnostic Value of Procalcitonin in Patients with Heat Stroke. Arch Microbiol Immunology 2020; 4 (1): 001-010. Abstract (APACHE II) score and Multiple Organ Dysfunction Background: Heat stroke is a life-threatening disease, Score (MODS) were calculated within the first 24 hours but there is currently no biomarker to accurately assess of admission to the ICU. The ability of PCT, APACHE prognosis. II score, and MODS score to predict prognosis was assessed using a receiver operating characteristic curve Objective: To study whether serum procalcitonin (PCT) (ROC) and area under the curve (AUC) analyses. is an effective biomarker for evaluating the prognosis Result: There was no statistical difference in the PCT for patients with heat stroke. -
The Effect of Dehydration, Hyperthermia, and Fatigue on Landing Error Scoring System Scores
ABSTRACT THE EFFECT OF DEHYDRATION, HYPERTHERMIA, AND FATIGUE ON LANDING ERROR SCORING SYSTEM SCORES Purpose: To examine the effects of exercise-induced dehydration, hyperthermia, and fatigue on Landing Error Scoring System (LESS) scores during a jump-landing task, and the effectiveness of a personalized hydration plan. Methods: Five recreationally active heat-acclimatized males 25.4 y (SD=5.7) completed two trials: with fluid replacement, (EXP) and without fluid (CON), in a counterbalanced, randomized, cross-over fashion. Exercise was terminated when gastrointestinal temperature (Tgi) = 39.5°C and fatigue ≥ 7/10, or 90 min of exercise. Percent dehydration was determined by body mass change from pre- exercise (PRE) and post-exercise (POST). Tgi, heart rate (HR), and perceived fatigue were measured PRE, during exercise, and POST. Three jump-landing tasks were filmed in the frontal and sagittal planes. An experienced grader evaluated jump-landing tasks using the LESS. Statistical Analysis: Repeated measures ANOVA assessed primary dependent and independent variables while a priori dependent t-tests evaluated pairwise comparisons. Results: No interaction, group, or time main effects were observed for LESS scores (p=0.437). POST dehydration (%) was greater in CON (M=2.59, SD=0.52) vs. EXP (M=0.92, SD=0.41; p<0.001), whereas hyperthermia (°C) (CON, M=39.29, SD=0.31, EXP, M=39.03, SD=0.61; p=0.425), and fatigue (CON, M=9, SD=1, EXP, M=9, SD=2; p=0.424) were similar. Conclusion: LESS scores were not affected by exercise-induced dehydration, hyperthermia, and fatigue, nor by a personal hydration plan.