Oxygenation and Oxygen Therapy
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The Disappearance of IPO in Myocardium of Diabetes Mellitus Rats Is Associated with the Increase of Succinate Dehydrogenase-Flav
Deng et al. BMC Cardiovasc Disord (2021) 21:142 https://doi.org/10.1186/s12872-021-01949-z RESEARCH ARTICLE Open Access The disappearance of IPO in myocardium of diabetes mellitus rats is associated with the increase of succinate dehydrogenase-favin protein Mengyuan Deng1†, Wei Chen1†, Haiying Wang1*, Yan Wang1, Wenjing Zhou2 and Tian Yu3 Abstract Background: The aim of the present study was to investigate whether the disappearance of ischemic post-process- ing (IPO) in the myocardium of diabetes mellitus (DM) is associated with the increase of succinate dehydrogenase- favin protein (SDHA). Methods: A total of 50 Sprague Dawley rats, weighing 300–400 g, were divided into 5 groups according to the ran- dom number table method, each with 10 rats. After DM rats were fed a high-fat and -sugar diet for 4 weeks, they were injected with Streptozotocin to establish the diabetic rat model. Normal rats were fed the same regular diet for the same number of weeks. Next, the above rats were taken to establish a cardiopulmonary bypass (CPB) model. Intraperi- toneal glucose tolerance test (IPGTT) and oral glucose tolerance test (OGTT) were used to detect whether the DM rat model was established successfully. Taking blood from the femoral artery to collect the blood-gas analysis indicators, and judged whether the CPB model is established. After perfusion was performed according to the experimental strategy, the area of myocardial infarction (MI), and serum creatine kinase isoenzyme (CK-MB) and cardiac troponin (CTnI) levels were measured. Finally, the relative mRNA and protein expression of SDHA was detected. Results: The OGTT and IPGTT suggested that the DM rat model was successfully established. -
The Oxyhaemoglobin Dissociation Curve in Critical Illness
Basic sciences review The Oxyhaemoglobin Dissociation Curve in Critical Illness T. J. MORGAN Intensive Care Facility, Division of Anaesthesiology and Intensive Care, Royal Brisbane Hospital, Brisbane, QUEENSLAND ABSTRACT Objective: To review the status of haemoglobin-oxygen affinity in critical illness and investigate the potential to improve gas exchange, tissue oxygenation and outcome by manipulations of the oxyhaemoglobin dissociation curve. Data sources: Articles and published peer-review abstracts. Summary of review: The P50 of a species is determined by natural selection according to animal size, tissue metabolic requirements and ambient oxygen tension. In right to left shunting mathematical modeling indicates that an increased P50 defends capillary oxygenation, the one exception being sustained hypercapnia. Increasing the P50 should also be protective in tissue ischaemia, and this is supported by modeling and experimental evidence. Most studies of critically ill patients have indicated reduced 2,3-DPG concentrations. This is probably due to acidaemia, and the in vivo P50 is likely to be normal despite low 2,3-DPG levels. It may soon be possible to achieve significant P50 elevations without potentially harmful manipulations of acid-base balance or hazardous drug therapy. Conclusions: Despite encouraging theoretical and experimental data, it is not known whether manipulations of the P50 in critical illness can improve gas exchange and tissue oxygenation or improve outcome. The status of the P50 may warrant more routine quantification and consideration along with the traditional determinants of tissue oxygen availability. (Critical Care and Resuscitation 1999; 1: 93-100) Key words: Critical illness, haemoglobin-oxygen affinity, ischaemia, P50, tissue oxygenation, shunt In intensive care practice, manipulations to improve in the tissues. -
Mechanisms of Pulmonary Gas Exchange Abnormalities During Experimental Group B Streptococcal Infusion
003 I -3998/85/1909-0922$02.00/0 PEDIATRIC RESEARCH Vol. 19, No. 9, I985 Copyright 0 1985 International Pediatric Research Foundation, Inc. Printed in (I.S. A. Mechanisms of Pulmonary Gas Exchange Abnormalities during Experimental Group B Streptococcal Infusion GREGORY K. SORENSEN, GREGORY J. REDDING, AND WILLIAM E. TRUOG ABSTRACT. Group B streptococcal sepsis in newborns obtained from GBS (5, 6). Arterial Poz fell by 9 torr in association produces pulmonary arterial hypertension and hypoxemia. with the increase in pulmonary arterial pressure (4). In contrast, The purpose of this study was to investigate the mecha- the neonatal piglet infused with GBS demonstrated both pul- nisms by which hypoxemia occurs. Ten anesthetized, ven- monary arterial hypertension and profound arterial hypoxemia tilated piglets were infused with 2 x lo9 colony forming (7). These results suggest that the neonatal pulmonary vascula- unitstkg of Group B streptococci over a 30-min period. ture may respond to bacteremia differently from that of adults. Pulmonary arterial pressure rose from 14 ? 2.8 to 38 ? The relationship between Ppa and the matching of alveolar 6.7 torr after 20 min of the bacterial infusion (p< 0.01). ventilation and pulmonary perfusion, a major determinant of During the same period, cardiac output fell from 295 to arterial oxygenation during room air breathing (8), has not been 184 ml/kg/min (p< 0.02). Arterial Po2 declined from 97 studied in newborns. The predictable rise in Ppa with an infusion 2 7 to 56 2 11 torr (p< 0.02) and mixed venous Po2 fell of group B streptococcus offers an opportunity to delineate the from 39.6 2 5 to 28 2 8 torr (p< 0.05). -
Water Quality: a Field-Based Quality Testing Program for Middle Schools and High Schools
DOCUMENT RESUME ED 433 223 SE 062 606 TITLE Water Quality: A Field-Based Quality Testing Program for Middle Schools and High Schools. INSTITUTION Massachusetts State Water Resources Authority, Boston. PUB DATE 1999-00-00 NOTE 75p. PUB TYPE Guides Classroom - Teacher (052) EDRS PRICE MF01/PC03 Plus Postage. DESCRIPTORS Bacteria; Environmental Education; *Field Studies; High Schools; Middle Schools; Physical Environment; Pollution; *Science Activities; *Science and Society; Science Instruction; Scientific Concepts; Temperature; *Water Pollution; *Water Quality; Water Resources IDENTIFIERS pH ABSTRACT This manual contains background information, lesson ideas, procedures, data collection and reporting forms, suggestions for interpreting results, and extension activities to complement a water quality field testing program. Information on testing water temperature, water pH, dissolved oxygen content, biochemical oxygen demand, nitrates, total dissolved solids and salinity, turbidity, and total coliform bacteria is also included.(WRM) ******************************************************************************** * Reproductions supplied by EDRS are the best that can be made * * from the original document. * ******************************************************************************** SrE N N Water A Field-Based Water Quality Testing Program for Middle Schools and High Schools U.S. DEPARTMENT OF EDUCATION Office of Educational Research and Improvement PERMISSION TO REPRODUCE AND EDUCATIONAL RESOURCES INFORMATION DISSEMINATE THIS MATERIAL -
Oxygen Concentration of Blood: PO
Oxygen Concentration of Blood: PO2, Co-Oximetry, and More Gary L. Horowitz, MD Beth Israel Deaconess Medical Center Boston, MA Objectives • Define “O2 Content”, listing its 3 major variables • Define the limitations of pulse oximetry • Explain why a normal arterial PO2 at sea level on room air is ~100 mmHg (13.3 kPa) • Describe the major features of methemogobin and carboxyhemglobin O2 Concentration of Blood • not simply PaO2 – Arterial O2 Partial Pressure ~100 mm Hg (~13.3 kPa) • not simply Hct (~40%) – or, more precisely, Hgb (14 g/dL, 140 g/L) • not simply “O2 saturation” – i.e., ~89% O2 Concentration of Blood • rather, a combination of all three parameters • a value labs do not report • a value few medical people even know! O2 Content mm Hg g/dL = 0.003 * PaO2 + 1.4 * [Hgb] * [%O2Sat] = 0.0225 * PaO2 + 1.4 * [Hgb] * [%O2Sat] kPa g/dL • normal value: about 20 mL/dL Why Is the “Normal” PaO2 90-100 mmHg? • PAO2 = (FiO2 x [Patm - PH2O]) - (PaCO2 / R) – PAO2 is alveolar O2 pressure – FiO2 is fraction of inspired oxygen (room air ~0.20) – Patm is atmospheric pressure (~760 mmHg at sea level) o – PH2O is vapor pressure of water (47 mmHg at 37 C) – PaCO2 is partial pressure of CO2 – R is the respiratory quotient (typically ~0.8) – 0.21 x (760-47) - (40/0.8) – ~100 mm Hg • Alveolar–arterial (A-a) O2 gradient is normally ~ 10, so PaO2 (arterial PO2) should be ~90 mmHg NB: To convert mm Hg to kPa, multiply by 0.133 Insights from PAO2 Equation (1) • PaO2 ~ PAO2 = (0.21x[Patm-47]) - (PaCO2 / 0.8) – At lower Patm, the PaO2 will be lower • that’s -
Respiratory Support
Intensive Care Nursery House Staff Manual Respiratory Support ABBREVIATIONS FIO2 Fractional concentration of O2 in inspired gas PaO2 Partial pressure of arterial oxygen PAO2 Partial pressure of alveolar oxygen PaCO2 Partial pressure of arterial carbon dioxide PACO2 Partial pressure of alveolar carbon dioxide tcPCO2 Transcutaneous PCO2 PBAR Barometric pressure PH2O Partial pressure of water RQ Respiratory quotient (CO2 production/oxygen consumption) SaO2 Arterial blood hemoglobin oxygen saturation SpO2 Arterial oxygen saturation measured by pulse oximetry PIP Peak inspiratory pressure PEEP Positive end-expiratory pressure CPAP Continuous positive airway pressure PAW Mean airway pressure FRC Functional residual capacity Ti Inspiratory time Te Expiratory time IMV Intermittent mandatory ventilation SIMV Synchronized intermittent mandatory ventilation HFV High frequency ventilation OXYGEN (Oxygen is a drug!): A. Most infants require only enough O2 to maintain SpO2 between 87% to 92%, usually achieved with PaO2 of 40 to 60 mmHg, if pH is normal. Patients with pulmonary hypertension may require a much higher PaO2. B. With tracheal suctioning, it may be necessary to raise the inspired O2 temporarily. This should not be ordered routinely but only when the infant needs it. These orders are good for only 24h. OXYGEN DELIVERY and MEASUREMENT: A. Oxygen blenders allow O2 concentration to be adjusted between 21% and 100%. B. Head Hoods permit non-intubated infants to breathe high concentrations of humidified oxygen. Without a silencer they can be very noisy. C. Nasal Cannulae allow non-intubated infants to breathe high O2 concentrations and to be less encumbered than with a head hood. O2 flows of 0.25-0.5 L/min are usually sufficient to meet oxygen needs. -
Oxygen Saturation in High-Altitude Pulmonary Edema
Oxygen Saturation In High-Altitude Pulmonary J Am Board Fam Pract: first published as 10.3122/jabfm.5.4.429 on 1 July 1992. Downloaded from Edema James]. Bachman, M.D., Todd Beatty, M.D., and Daniel E. Levene High altitude, defined as elevations greater than Methods or equal to 8000 feet (2438 m) above sea level, is The 126 subjects for this study were all patients responsible for a variety of medical problems both who came to the Summit Medical Center Emer chronic and acute. The spectrum of altitude ill gency Department or to the Frisco Medical ness ranges from the common, mild symptoms of Center. Both units serve Summit County, Colo acute mountain sickness, such as insomnia, head rado. The base elevation of Summit County ache, and nausea, to severe and potentially fatal ranges from roughly 9000 to 11,000 feet (2743 to conditions, such as high-altitude pulmonary 3354 m). Between 1 November 1990 and 26Janu edema (HAPE) and high-altitude cerebral edema ary 1991, a record was maintained of the age, sex, (RACE).l room air pulse oximeter measure of oxygen satu HAPE is a noncardiogenic form of pulmonary ration (Sa 02)' chest radiograph findings, and final edema that predominantly affects young, physi diagnoses of all patients who underwent a chest cally active, previously healthy individuals who radiograph examination. arrived at high altitude between 1 and 4 days There were 152 patients who underwent chest before developing symptoms. Symptoms of early, radiography during the study period. Twenty-six milder cases include dry nonproductive cough, patients were excluded from the study: 18 had no decreased exercise tolerance, and dyspnea on ex oxygen saturation measurement taken or re ertion. -
Respiratory Therapy Pocket Reference
Pulmonary Physiology Volume Control Pressure Control Pressure Support Respiratory Therapy “AC” Assist Control; AC-VC, ~CMV (controlled mandatory Measure of static lung compliance. If in AC-VC, perform a.k.a. a.k.a. AC-PC; Assist Control Pressure Control; ~CMV-PC a.k.a PS (~BiPAP). Spontaneous: Pressure-present inspiratory pause (when there is no flow, there is no effect ventilation = all modes with RR and fixed Ti) PPlateau of Resistance; Pplat@Palv); or set Pause Time ~0.5s; RR, Pinsp, PEEP, FiO2, Flow Trigger, rise time, I:E (set Pocket Reference RR, Vt, PEEP, FiO2, Flow Trigger, Flow pattern, I:E (either Settings Pinsp, PEEP, FiO2, Flow Trigger, Rise time Target: < 30, Optimal: ~ 25 Settings directly or by inspiratory time Ti) Settings directly or via peak flow, Ti settings) Decreasing Ramp (potentially more physiologic) PIP: Total inspiratory work by vent; Reflects resistance & - Decreasing Ramp (potentially more physiologic) Card design by Respiratory care providers from: Square wave/constant vs Decreasing Ramp (potentially Flow Determined by: 1) PS level, 2) R, Rise Time ( rise time ® PPeak inspiratory compliance; Normal ~20 cmH20 (@8cc/kg and adult ETT); - Peak Flow determined by 1) Pinsp level, 2) R, 3)Ti (shorter Flow more physiologic) ¯ peak flow and 3.) pt effort Resp failure 30-40 (low VT use); Concern if >40. Flow = more flow), 4) pressure rise time (¯ Rise Time ® Peak v 0.9 Flow), 5) pt effort ( effort ® peak flow) Pplat-PEEP: tidal stress (lung injury & mortality risk). Target Determined by set RR, Vt, & Flow Pattern (i.e. for any set I:E Determined by patient effort & flow termination (“Esens” – PDriving peak flow, Square (¯ Ti) & Ramp ( Ti); Normal Ti: 1-1.5s; see below “Breath Termination”) < 15 cmH2O. -
Guidelines and Standard Procedures for Continuous Water-Quality Monitors: Station Operation, Record Computation, and Data Reporting
Guidelines and Standard Procedures for Continuous Water-Quality Monitors: Station Operation, Record Computation, and Data Reporting Techniques and Methods 1–D3 U.S. Department of the Interior U.S. Geological Survey Front Cover. Upper left—South Fork Peachtree Creek at Johnson Road near Atlanta, Georgia, site 02336240 (photograph by Craig Oberst, USGS) Center—Lake Mead near Sentinel Island, Nevada, site 360314114450500 (photograph by Ryan Rowland, USGS) Lower right—Pungo River at channel light 18, North Carolina, site 0208455560 (photograph by Sean D. Egen, USGS) Back Cover. Lake Mead near Sentinel Island, Nevada, site 360314114450500 (photograph by Ryan Rowland, USGS) Guidelines and Standard Procedures for Continuous Water-Quality Monitors: Station Operation, Record Computation, and Data Reporting By Richard J. Wagner, Robert W. Boulger, Jr., Carolyn J. Oblinger, and Brett A. Smith Techniques and Methods 1–D3 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior P. Lynn Scarlett, Acting Secretary U.S. Geological Survey P. Patrick Leahy, Acting Director U.S. Geological Survey, Reston, Virginia: 2006 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod Telephone: 1-888-ASK-USGS For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web: http://www.usgs.gov Telephone: 1-888-ASK-USGS Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted materials contained within this report. -
Rapid Diagnosis of Ethylene Glycol Poisoning by Urine Microscopy
University of Southern Denmark Rapid diagnosis of ethylene glycol poisoning by urine microscopy Sheta, Hussam Mahmoud; Al-Najami, Issam; Christensen, Heidi Dahl; Madsen, Jonna Skov Published in: American Journal of Case Reports DOI: 10.12659/AJCR.908569 Publication date: 2018 Document version: Final published version Document license: CC BY-NC-ND Citation for pulished version (APA): Sheta, H. M., Al-Najami, I., Christensen, H. D., & Madsen, J. S. (2018). Rapid diagnosis of ethylene glycol poisoning by urine microscopy. American Journal of Case Reports, 19, 689-693. https://doi.org/10.12659/AJCR.908569 Go to publication entry in University of Southern Denmark's Research Portal Terms of use This work is brought to you by the University of Southern Denmark. Unless otherwise specified it has been shared according to the terms for self-archiving. If no other license is stated, these terms apply: • You may download this work for personal use only. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying this open access version If you believe that this document breaches copyright please contact us providing details and we will investigate your claim. Please direct all enquiries to [email protected] Download date: 28. Sep. 2021 e-ISSN 1941-5923 © Am J Case Rep, 2018; 19: 689-693 DOI: 10.12659/AJCR.908569 Received: 2017.12.17 Accepted: 2018.03.21 Rapid Diagnosis of Ethylene Glycol Poisoning by Published: 2018.06.14 Urine Microscopy Authors’ Contribution: -
ILD Nursing and Allied Health Guide
ILD Nursing and Allied Health Guide 230 East Ohio Street, Suite 500 Chicago, Illinois 60611 844.TalkPFF (844.825.5733) pulmonaryfibrosis.org The Pulmonary Fibrosis Foundation mobilizes people and resources to provide access to high quality care and leads research for a cure so people with pulmonary fibrosis will live longer, healthier lives. © 2020 Pulmonary Fibrosis Foundation. All rights reserved. Table of Contents Dear Nurses and Allied Health Professionals ........................................................................ 2 Introduction ................................................................................................................................ 3 PART ONE: IDENTIFYING THE DISEASE ....................................................................... 4 Recognition of ILD ................................................................................................................... 4 The Diagnostic Process ............................................................................................................. 4 Idiopathic Interstitial Pneumonias .......................................................................................... 6 PART TWO: INTERPRETING TEST RESULTS ................................................................ 6 High-resolution computerized tomography scans (HRCT) ................................................. 6 Pulmonary Function Tests (PFTs) .......................................................................................... 8 Pulmonary Function Test (PFT) Report -
Diagnostic Performance of Initial Serum Albumin Level for Predicting In-Hospital Mortality Among Necrotizing Fasciitis Patients
Article Diagnostic Performance of Initial Serum Albumin Level for Predicting In-Hospital Mortality among Necrotizing Fasciitis Patients Chia-Peng Chang 1, Wen-Chih Fann 1,2, Shu-Ruei Wu 3, Chun-Nan Lin 1, I-Chuan Chen 1,2, and Cheng-Ting Hsiao 1,2,* 1 Department of Emergency Medicine, Chang Gung Memorial Hospital, No.6, Sec. W., Jiapu Rd., Puzi City, Chiayi County 613, Taiwan; [email protected] (C.-P.C.); [email protected] (W.-C.F.); [email protected] (C.-N.L.); [email protected] (I.-C.C.) 2 Department of Medicine, Chang Gung University, Taoyuan 333, Taiwan 3 Department of Pediatrics, Kaohsiung Veterans General Hospital, Kaohsiung 813, Taiwan; [email protected] * Correspondence: [email protected]; Tel.: +886-975352985, Fax: +886-53622790 Received: 16 October 2018; Accepted: 8 November 2018; Published: 10 November 2018 Abstract: Background: Hypoalbuminemia is known to be associated with adverse outcomes in critical illness. In this study, we attempted to identify whether hypoalbuminemia on emergency department (ED) arrival is a reliable predictor for in-hospital mortality in necrotizing fasciitis (NF). patients. Method: A retrospective cohort study of hospitalized adult patients with NF was conducted in a tertiary teaching hospital in Taiwan between March 2010 and March 2018. Blood samples were collected in the ED upon arrival, and serum albumin levels were determined. We evaluated the predictive value of serum albumin level at ED presentation for in-hospital mortality. All collected data were statistically analyzed. Result: Of the 707 NF patients, 40 (5.66%) died in the hospital. The mean serum albumin level was 3.1 ± 0.9 g/dL and serum albumin levels were significantly lower in the non-survivor group than in the survivor group (2.8 ± 0.7 g/dL vs.