Urine Specific Gravity
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												  Urine Specific Gravity Reference RangeUrine Specific Gravity Reference Range Richardo wonders contextually while tuppenny Maurice photographs swimmingly or unseams wholesale. Yarest Saw participate despairingly while Brett always charm his Thanet reinspiring homoeopathically, he nullifies so ruthlessly. Respirable Adolpho demising no Becky threw edgeways after Lucien sour dilatorily, quite suppliant. There is canceled by your body in the kidneys are written and specifically for your usual to. Can drinking too much it cause protein in urine? Urine Test HealthLink BC. Bananas are a candid source of potassium and none need payment be limited on a renal diet Pineapple was a kidney-friendly fruit as it contains much less potassium than is other tropical fruits. Normal results in adults generally range from 1010 to 1020 Abnormal results are generally those below 1010 or above 1020 In patients with new kidney diseases USG doesn't vary with fluid stool and is called a fixed specific gravity. In unintended venous instillation or by llamas that they breakup. They wore rubber gloves and reference ranges for people with distilled water is therefore it. Specific gravity of urine is determined inside the presence of solutes represented by. Photo courtesy of the powder is an idexx sdma is rare type of hydration status of gluteraldehyde in a part though. Thank you have a level and completed her research that urine specific gravity values. Is urine specific gravity of 1.020 normal? These two renal function will look on osmolality, crystals may need to. Excessive daily through this study is taken together for example, for your urine should be trace amounts of this study sponsor and require serially monitored to.
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												  Ketones, UrineLab Dept: Urine/Stool Test Name: KETONES, URINE General Information Lab Order Codes: UKE Synonyms: Urine Ketones; Nitroprusside Reaction for Ketones CPT Codes: 81003 – Urinalysis, by dipstick; automated, without microscopy Test Includes: Screen for urine ketones. Logistics Test Indications: Useful for evaluation of ketonuria, detection of acidosis, ketoacidosis, fasting, starvation, high protein diets, diabetes mellitus, and stress- hormone excess. Lab Testing Sections: Urinalysis Phone Numbers: MIN Lab: 612-813-6280 STP Lab: 651-220-6550 Test Availability: Daily, 24 hours Turnaround Time: 1 hour Special Instructions: Submit only one (1) of the following: Catheterized specimen or clean- catch specimen. Note: Indicate type of specimen (catheterized) on request form. Date and time of collection are required on request form for processing. Transport specimen to laboratory immediately following collection Specimen Specimen Type: Urine Container: Urine cup Draw Volume: Entire specimen collection (catheter or clean catch) Processed Volume: Minimum: 0.5 mL urine Collection: A specimen collected by catheterization is optimal; however, a clean- catch or mid-stream specimen is also acceptable. Random, voided specimens will be accepted, but are the least desirable and are not recommended if a urine culture is also being requested. Special Processing: N/A Patient Preparation: None Sample Rejection: Less than 0.5 mL urine submitted; mislabeled or unlabeled specimen Interpretive Reference Range: Negative Critical Values: N/A Limitations: Specimens containing
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												  Different Response of Body Weight Change According to Ketonuria After Fasting in the Healthy ObeseORIGINAL ARTICLE Endocrinology, Nutrition & Metabolism http://dx.doi.org/10.3346/jkms.2012.27.3.250 • J Korean Med Sci 2012; 27: 250-254 Different Response of Body Weight Change According to Ketonuria after Fasting in the Healthy Obese Hyeon-Jeong Kim1, Nam-Seok Joo1, The relationship between obesity and ketonuria is not well-established. We conducted a Kwang-Min Kim1, Duck-Joo Lee1, retrospective observational study to evaluate whether their body weight reduction response and Sang-Man Kim2 differed by the presence of ketonuria after fasting in the healthy obese. We used the data of 42 subjects, who had medical records of initial urinalysis at routine health check-up and 1Department of Family Practice and Community Health, Ajou University School of Medicine, Suwon; follow-up urinalysis in the out-patient clinic, one week later. All subjects in the initial 2Department of Family Medicine, CHA Biomedical urinalysis showed no ketonuria. However, according to the follow-up urinalysis after three Center, CHA University College of Medicine, Seoul, subsequent meals fasts, the patients were divided into a non-ketonuria group and Korea ketonuria group. We compared the data of conventional low-calorie diet programs for ± Received: 20 August 2011 3 months for both groups. Significantly greater reduction of body weight (-8.6 3.6 kg vs 2 2 Accepted: 17 January 2012 -1.1 ± 2.2 kg, P < 0.001), body mass index (-3.16 ± 1.25 kg/m vs -0.43 ± 0.86 kg/m , P < 0.001) and waist circumference (-6.92 ± 1.22 vs -2.32 ± 1.01, P < 0.001) was Address for Correspondence: observed in the ketonuria group compared to the non-ketonuria group.
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												  Deficient Diabetic MiceDiminished Loss of Proteoglycans and Lack of Albuminuria in Protein Kinase C-␣–Deficient Diabetic Mice Jan Menne,1,2 Joon-Keun Park,2 Martin Boehne,2 Marlies Elger,2 Carsten Lindschau,2 Torsten Kirsch,2 Matthias Meier,2 Faikah Gueler,2 Annette Fiebeler,3 Ferdinand H. Bahlmann,2 Michael Leitges,4 and Hermann Haller2 Activation of protein kinase C (PKC) isoforms has been implicated in the pathogenesis of diabetic nephropathy. We showed earlier that PKC-␣ is activated in the kid- iabetes affects Ͼ300 million people worldwide; -neys of hyperglycemic animals. We now used PKC-␣؊/؊ 20–40% will develop overt nephropathy. Diabe mice to test the hypothesis that this PKC isoform tes is the most common cause of end-stage mediates streptozotocin-induced diabetic nephropathy. Drenal disease. The earliest clinical sign of ne- We observed that renal and glomerular hypertrophy was phropathy is microalbuminuria. Microalbuminuria also ؊ ؊ similar in diabetic wild-type and PKC-␣ / mice. How- heralds impending cardiovascular morbidity and mortality ever, the development of albuminuria was almost absent (1–4). Microalbuminuria predicts overt proteinuria, which ؊/؊␣ in the diabetic PKC- mice. The hyperglycemia-in- is now believed to actively promote renal insufficiency (5). duced downregulation of the negatively charged base- Therefore, successful treatment of diabetic patients ment membrane heparan sulfate proteoglycan perlecan -؊ ؊ should aim for the prevention or regression of albumin was completely prevented in the PKC-␣ / mice, com- pared with controls. We then asked whether transform- uria. Hyperglycemia seems to cause microalbuminuria in   diabetic patients (6,7). However, how the metabolic dis- ing growth factor- 1 (TGF- 1) and/or vascular endothelial growth factor (VEGF) is implicated in the turbance causes cellular effects is incompletely under- PKC-␣–mediated changes in the basement membrane.
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												  Ideal Conditions for Urine Sample Handling, and Potential in Vitro Artifacts Associated with Urine StorageUrinalysis Made Easy: The Complete Urinalysis with Images from a Fully Automated Analyzer A. Rick Alleman, DVM, PhD, DABVP, DACVP Lighthouse Veterinary Consultants, LLC Gainesville, FL Ideal conditions for urine sample handling, and potential in vitro artifacts associated with urine storage 1) Potential artifacts associated with refrigeration: a) In vitro crystal formation (especially, calcium oxalate dihydrate) that increases with the duration of storage i) When clinically significant crystalluria is suspected, it is best to confirm the finding with a freshly collected urine sample that has not been refrigerated and which is analyzed within 60 minutes of collection b) A cold urine sample may inhibit enzymatic reactions in the dipstick (e.g. glucose), leading to falsely decreased results. c) The specific gravity of cold urine may be falsely increased, because cold urine is denser than room temperature urine. 2) Potential artifacts associated with prolonged storage at room temperature, and their effects: a) Bacterial overgrowth can cause: i) Increased urine turbidity ii) Altered pH (1) Increased pH, if urease-producing bacteria are present (2) Decreased pH, if bacteria use glucose to form acidic metabolites iii) Decreased concentration of chemicals that may be metabolized by bacteria (e.g. glucose, ketones) iv) Increased number of bacteria in urine sediment v) Altered urine culture results b) Increased urine pH, which may occur due to loss of carbon dioxide or bacterial overgrowth, can cause: i) False positive dipstick protein reaction ii) Degeneration of cells and casts iii) Alter the type and amount of crystals present 3) Other potential artifacts: a) Evaporative loss of volatile substances (e.g.
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												  Interpretation of Canine and Feline Urinalysis$50. 00 Interpretation of Canine and Feline Urinalysis Dennis J. Chew, DVM Stephen P. DiBartola, DVM Clinical Handbook Series Interpretation of Canine and Feline Urinalysis Dennis J. Chew, DVM Stephen P. DiBartola, DVM Clinical Handbook Series Preface Urine is that golden body fluid that has the potential to reveal the answers to many of the body’s mysteries. As Thomas McCrae (1870-1935) said, “More is missed by not looking than not knowing.” And so, the authors would like to dedicate this handbook to three pioneers of veterinary nephrology and urology who emphasized the importance of “looking,” that is, the importance of conducting routine urinalysis in the diagnosis and treatment of diseases of dogs and cats. To Dr. Carl A. Osborne , for his tireless campaign to convince veterinarians of the importance of routine urinalysis; to Dr. Richard C. Scott , for his emphasis on evaluation of fresh urine sediments; and to Dr. Gerald V. Ling for his advancement of the technique of cystocentesis. Published by The Gloyd Group, Inc. Wilmington, Delaware © 2004 by Nestlé Purina PetCare Company. All rights reserved. Printed in the United States of America. Nestlé Purina PetCare Company: Checkerboard Square, Saint Louis, Missouri, 63188 First printing, 1998. Laboratory slides reproduced by permission of Dennis J. Chew, DVM and Stephen P. DiBartola, DVM. This book is protected by copyright. ISBN 0-9678005-2-8 Table of Contents Introduction ............................................1 Part I Chapter 1 Sample Collection ...............................................5
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												  KETON.Zemia and KETONURIA in CHILDHOOD. by MURIEL JArch Dis Child: first published as 10.1136/adc.1.5.302 on 1 January 1926. Downloaded from KETON.zEMIA AND KETONURIA IN CHILDHOOD. BY MURIEL J. BROWN, M.B., Ch.B., D.P.H., AND GRACE GRAHAMI, AM.D. From the Medical Department, The Royal Hospital for Sick Children, Glasgow. The formation of ketone bodies and their excretion in the urine in albnormall amounts have for many years been problems of much interest to both physiologist and clinician. Much of our present knowledge of the subject has been gained from the study of carbohydrate metabolism in diabetes, where ketonuria in its classical formi is frequently observed. From this it has been established that an excess of ketone bodies occurs in the blood when the fats are incompletely ' combusted ' as a result of abnormal carbohydrate metabolism, and ample justification has been provided for the well-known sta.tement myiade by Rosenfeld(l) in 1895 ' that fat burns only in the fire of carbohydrate.' A good review of our present knowledge of ketone production and its prevention is to be found in Shaffer's recent lecture entitled ' Antiketo- genesis, its Mechanism and Signifiecance. '(2) A fu-ll discussion of the stubject in all its aspects is not within the scope of the present communication, but we may quote that ' there no Shaffer's statement is to-day question that http://adc.bmj.com/ ketosis is due to carbohydrate starvation,' and make special reference also to his remninder that the inhibitory effect of carbohydrate on ketone formation depends, not on the mnere existence of sufficient glucose, as glucose, in the blood (cf.
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												  [email protected][email protected] 1 • Functions of The Kidneys ❖ Remove waste products and foreign chemicals. ❖ Control acid-base balance. ❖ Control blood levels of electrolytes. ❖ Regulate fluids volume of the body, and thus, blood pressure. ❖ Secrete hormones such as erythropoietin, which is important for erythropoiesis, and without which, anemia develops. ❖ Convert 25-hydroxycholecalciferol into 1,25-dihydroxycholecalciferol (calcitriol), the most active form of vitamin D. ❖ Gluconeogenesis (conversion of non-sugar sources, particularly amino acids, into glucose). • Blood Supply of The Kidneys 2 ❖ The renal artery (the fifth branch of the aorta) enters the kidney through its hilum and divides many times to form segmental arteries, interlobar arteries, arcuate arteries, interlobular arteries (cortical radiate arteries). ❖ Interlobular arteries divide again into many afferent arterioles. ❖ Each afferent arteriole enters a glomerulus and divides to form the glomerular capillaries. ❖ The capillaries converge again to form efferent arterioles. ❖ Efferent arterioles leave the glomerulus and divide, once again, to form peritubular capillaries. ❖ Peritubular capillaries rejoin to form interlobular veins, arcuate veins, interlobar veins. ❖ Interlobar veins join to form the renal vein which leaves the kidney through its hilum. ❖ Note that the glomerular capillaries form the efferent arterioles, which divide again (instead of converging) to form other capillaries. This is known as the portal circulation. ❖ Vasa recta are peritubular capillaries that branch off the efferent arterioles of juxtamedullary nephrons (those nephrons closest to the medulla). They enter the medulla, and surround the loop of Henle. ❖ Each kidney contains one million nephrons; each of which is 6 cm long. ❖ The cortex contains the glomeruli of the nephrons, giving the cortex a granular appearance.
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												  Asymptomatic Bacteriuria and Anti-Microbial Susceptibility Patterns Among Women of Reproductive AgeArticle Asymptomatic Bacteriuria and Anti-Microbial Susceptibility Patterns among Women of Reproductive Age. A Cross-Sectional Study in Primary Care, Ghana Prince Afoakwa 1, Seth Agyei Domfeh 1, Bright Oppong Afranie 2,*, Dorcas Ohui Owusu 1, Sampson Donkor 2, Kennedy Kormla Sakyi 3, Richard Akesse Adom 3, Godfred Kyeremeh 1, Bright Afranie Okyere 4, Emmanuel Acheampong 2 and Beatrice Amoah 2 1 Department of Medical Laboratory Technology, Faculty of Health and Allied Sciences, Garden City University College, P.O. Box KS 12775, Kenyasi-Kumasi, Ghana; [email protected] (P.A.); [email protected] (S.A.D.); [email protected] (D.O.O.); [email protected] (G.K.) 2 Department of Molecular Medicine, School of Medical Sciences, Kwame Nkrumah University of Science and Technology, PMB, UPO, Kumasi, Ghana; [email protected] (S.D.); [email protected] (E.A.); [email protected] (B.A.) 3 Department of Microbiology, Tetteh Quarshie memorial hospital, Akuapem Mampong-Korforidua, P.O. Box 26, Ghana; [email protected] (K.K.S.); [email protected] (R.A.A.) 4 Department of Theoretical and Applied Biology, Faculty of Biosciences, Kwame Nkrumah University of Science and Technology, PMB, UPO, Kumasi, Ghana; [email protected] * Correspondence: [email protected]; Tel.: +233-246149286 Received: 2 November 2018; Accepted: 12 December 2018; Published: 17 December 2018 Abstract: Background: Asymptomatic bacteriuria (ASB) poses serious future clinical repercussions for reproductive women. The study determined the prevalence of asymptomatic bacteriuria along with anti-microbial susceptibility patterns among women of reproductive age in a primary care facility. Method: The study recruited a total of 300 women of reproductive age attending the Tetteh Quarshie Memorial Hospital at Akuapem-Mampong, Ghana, between January and March 2018.
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												  Plasma 'Ketone' Levelin the Diagnosis and Treatment of Diabetic AcidosisPostgrad. med. J. (October 1968) 44, 799-802. Postgrad Med J: first published as 10.1136/pgmj.44.516.799 on 1 October 1968. Downloaded from Plasma 'ketone' level in the diagnosis and treatment of diabetic acidosis M. S. KNAPP MARGARET E. HORN M.D., M.R.C.P. M.B., M.R.C.P. Lecturer in Medicine, University ofBristol Medical Registrar, Bristol Royal Hospital All patients in possible diabetic acidosis admit- Summary ted to one of the medical firms at the Bristol A simple method of estimating the plasma Royal Infirmary over a 3-year period had an 'ketone' level with 'Acetest' tablets has been used estimation of the plasma 'ketone' level performed in the diagnosis and treatment of diabetic acid- by the clinical staff in the ward side-room. In osis. The method is valuable when used in those patients treated for a moderate or severe association with full biochemical facilities, but it diabetic keto-acidosis the estimation was is especially useful in situations where these can- repeated, usually every four hours. The second not be easily obtained. and subsequent doses of insulin were based to a considerable extent on the plasma 'ketone' titre. Introduction If the titre had not fallen or had risen, an in- In a patient suspected of having diabetic keto- creased dose of insulin was given. A fall in titre acidosis it is useful to be able to rapidly confirm indicated a satisfactory response and either a Protected by copyright. the diagnosis. In this situation we have used a similar dose or a smaller one was used, depending simple side-room method for the detection of on previous blood sugar results.
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												  Medical Assessment of Drug Induced Rhabdomyolysis and Metabolic DisordersISoP Training Course- Zagreb, 3-4 April 2014 Medical assessment of drug induced rhabdomyolysis and metabolic disorders Marco Tuccori, ISoP EC member Unit of Adverse Drug Reacon Monitoring University Hospital of Pisa, Pisa, Italy At the forefront of pharmacovigilance around the world 1 ISoP training course Zagreb 3-4 April 2014 Proacve Pharmacovigilance, Risk Management and Pharmacovigilance in the Era of Personalised Medicine All presentaons provided as PDF files are protected by copyright. Prinng and storage is for scholarly research, educaonal and personal use only. Any copyright or other noces or disclaimers must not be removed, obscured or modified. If used for training the original source must be properly credited. Copying and make copies of the PDF presentaons (including through e-mail) are not permied. The PDF files must not be posted on an open- access website. At the forefront of pharmacovigilance around the world 2 Summary • Metabolic adverse reactions • Muscular adverse reactions • Definitions and classifications • Signs and symptoms • Main (alternative) causes • Drugs most frequently involved • Biological plausibility • Drug-induced lipids metabolism alterations • Drug-induced glucose metabolism alterations At the forefront of pharmacovigilance around the world 3 Metabolic Adverse Reacons Metabolism is the set of life-sustain- ing chemical transformations within the cells of living organisms. These enzyme-catalyzed reactions allow organisms to grow and reproduce, maintain their structures, ? and respond to their environments. DRUGS Lipids Myopathies Carbohydrates At the forefront of pharmacovigilance around the world 4 Muscular adverse events Definions and Classificaons Term ACC/AHA/NHLBI NLA FDA Myopathy Any disease of the Symptoms of myalgia (muscle CK > 10 ULN muscle pain or soreness), weakness.
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												  Urinary Albumin Excretion Rate Is Associated with Increased Ambulatory Blood Pressure in Normoalbuminuric Type 2 Diabetic PatientsPathophysiology/Complications ORIGINAL ARTICLE Urinary Albumin Excretion Rate Is Associated With Increased Ambulatory Blood Pressure in Normoalbuminuric Type 2 Diabetic Patients 1 1 CRISTIANE B. LEITAO˜ , MD MARCEL P. MOLON emerging evidence that patients with dia- 1 2 LU´IS H. CANANI, MD ANTONIOˆ F. PINOTTI, MD betes in the high-normal range of UAER 1 1 PATR´ICIA B. POLSON JORGE L. GROSS, MD are already at high risk for progressing to microalbuminuria or even more ad- vanced stages of renal disease (6–9). Arterial hypertension follows the es- tablishment of microalbuminuria in pa- OBJECTIVE — To evaluate the 24-h blood pressure profile in normoalbuminuric type 2 tients with type 1 diabetes (10). In type 2 diabetic patients. diabetes, this relationship is not that clear because hypertension is a common fea- RESEARCH DESIGN AND METHODS — A cross-sectional study was conducted in 90 type 2 diabetic patients with a urinary albumin excretion rate (UAER) Ͻ20 g/min on two ture in these patients, regardless of renal occasions, 6 months apart (immunoturbidimetry). Patients underwent clinical and laboratory status (11). Ambulatory 24-h blood pres- evaluations. Ambulatory blood pressure monitoring and echocardiograms were also performed. sure monitoring has a better correlation with target organ damage than doctor’s RESULTS — UAER was found to correlate positively with systolic doctor’s office blood pres- office blood pressure measurements (12) sure measurements (r ϭ 0.243, P ϭ 0.021) and ambulatory blood pressure (24 h: r ϭ 0.280, P ϭ and allows the evaluation of blood pres- 0.008) and left ventricular posterior wall thickness (r ϭ 0.359, P ϭ 0.010).