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A Dipstick Test Combined with Urine Specific Gravity Improved the Accuracy of Proteinuria Determination in Pregnancy Screening
Kobe J. Med. Sci., Vol. 56, No. 4, pp. E165-E172, 2010 A Dipstick Test Combined with Urine Specific Gravity Improved the Accuracy of Proteinuria Determination in Pregnancy Screening NATSUKO MAKIHARA1, MINEO YAMASAKI1,2, HIROKI MORITA1, and HIDETO YAMADA1* 1Division of Obstetrics and Gynecology, Department of Surgery-related, and 2Division of Integrated Medical Education, Department of Community Medicine and Social Healthcare Science, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan. Received 12 July 2010/ Accepted 20 August 2010 Key Words: dipstick test, pregnancy proteinuria, protein/creatinine ratio, urine specific gravity Proteinuria screening using a semi-quantitative dipstick test of the spot urine in antenatal clinic is known to have high false-positive rates. The aim of this study was to assess availability of a dipstick test combined with the urine specific gravity for the determination of pathological proteinuria. A dipstick test was performed on 582 urine samples obtained from 283 pregnant women comprising 260 with normal blood pressure and 23 with pregnancy-induced hypertension. The urine protein (P) and creatinine (C) concentrations, specific gravity (SG), P/C ratio were determined, and compared with dipstick test results. The P concentration increased along the stepwise augmentations in dipstick test result. Frequencies of the urine samples with 0.265 or more P/C ratio were 0.7% with − dipstick test result, 0.7% with the ± result, 3.3% with the 1+ result, and 88.9% with the ≥2+ result. However, if the urine specific gravity was low, frequencies of the high P/C ratio were 5.0% with ± dipstick test result and 9.3% with the 1+ result. -
Biochemical Profiling of Renal Diseases
INTRODUCTION TO LABORATORY PROFILING Alan H. Rebar, DVM, Ph.D., Diplomate ACVP Purdue University, Discovery Park 610 Purdue Mall, West Lafayette, IN 47907-2040 Biochemical profiling may be defined as the use of multiple blood chemistry determinations to assess the health status of various organ systems simultaneously. Biochemical profiling rapidly has become a major diagnostic aid for the practicing veterinarian for several reasons. First, a more educated clientele has come to expect increased diagnostic sophistication. Secondly, the advent of high-volume clinical pathology laboratories has resulted in low prices that make profiling in veterinary practice feasible and convenient. In addition, improved technology has resulted in the development of procedures that can be used to obtain accurate analyses on microsamples of serum. Such procedures offer obvious advantages to veterinarians, who in the past were hindered by requirements for large sample size. Although biochemical profiling offers exciting potential, it is not a panacea. Since standard chemical screens provide 12 to 30 test results, interpretation of data may be extremely complex. Interpretation is often clouded by the fact that perfectly normal animals may have, indeed, are expected to have, an occasional abnormal test result. It is estimated that in a panel of 12 chemistry tests, approximately 46% of all normal subjects will have at least one abnormal test result. Such abnormalities do not reflect inaccuracies in laboratory test procedures but rather the way in which reference (or normal) values are determined. In order to establish the "normal range" for a given test, the procedure is performed on samples from a large population of clinically normal individuals. -
Guidelines for Approach to a Child with Metabolic Acidosis (Including RTA)
Guidelines for approach to a child with Metabolic acidosis (including RTA) Children’s Kidney Centre University Hospital of Wales Cardiff CF14 4XW DISCLAIMER: These guidelines were produced in good faith by the authors reviewing available evidence/opinion. They were designed for use by paediatric nephrologists at the University Hospital of Wales, Cardiff for children under their care. They are neither policies nor protocols but are intended to serve only as guidelines. They are not intended to replace clinical judgment or dictate care of individual patients. Responsibility and decision-making (including checking drug doses) for a specific patient lie with the physician and staff caring for that particular patient. Version 1, S. Hegde/Sept 2007 Metabolic acidosis ormal acid base balance Maintaining normal PH is essential for cellular enzymatic and other metabolic functions and normal growth and development. Although it is the intracellular PH that matter for cell function, we measure extra cellular PH as 1. It is easier to measure 2. It parallels changes in intracellular PH 3. Subject to more variation because of lesser number of buffers extra cellularly. Normal PH is maintained by intra and extra cellular buffers, lungs and kidneys. Buffers attenuate changes in PH when acid or alkali is added to the body and they act by either accepting or donating Hydrogen ions. Buffers function as base when acid is added or as acid when base is added to body. Main buffers include either bicarbonate or non-bicarbonate (proteins, phosphates and bone). Source of acid load: 1. CO2- Weak acid produced from normal metabolism, dealt with by lungs pretty rapidly(within hours) 2. -
Proteinuria and Albuminuria: What’S the Difference? Cynthia A
EXPERTQ&A Proteinuria and Albuminuria: What’s the Difference? Cynthia A. Smith, DNP, CNN-NP, FNP-BC, APRN, FNKF What exactly is the difference between TABLE Q the protein-to-creatinine ratio and the Persistent Albuminuria Categories microalbumin in the lab report? How do they compare? Category Description UACR For the non-nephrology provider, the options for A1 Normal to mildly < 30 mg/g evaluating urine protein or albumin can seem con- increased (< 3 mg/mmol) fusing. The first thing to understand is the impor- tance of assessing for proteinuria, an established A2 Moderately 30-300 mg/g marker for chronic kidney disease (CKD). Higher increased (3-30 mg/mmol) protein levels are associated with more rapid pro- A3 Severely > 300 mg/g gression of CKD to end-stage renal disease and in- increased (> 30 mg/mmol) creased risk for cardiovascular events and mortality in both the nondiabetic and diabetic populations. Abbreviation: UACR, urine albumin-to-creatinine ratio. Monitoring proteinuria levels can also aid in evaluat- Source: KDIGO. Kidney Int. 2012.1 ing response to treatment.1 Proteinuria and albuminuria are not the same low-up testing. While the UACR is typically reported thing. Proteinuria indicates an elevated presence as mg/g, it can also be reported in mg/mmol.1 Other of protein in the urine (normal excretion should be options include the spot urine protein-to-creatinine < 150 mg/d), while albuminuria is defined as an “ab- ratio (UPCR) and a manual reading of a reagent strip normal loss of albumin in the urine.”1 Albumin is a (urine dipstick test) for total protein. -
Understanding What It Means to Have Protein in Your Urine Understanding What It Means to Have Protein in Your Urine
UNDERSTANDINGUnderstanding WHAT ITYour MEANS TO HAVE Hemodialysis PROTEINAccess Options IN YOUR URINE 2 AAKP: Understanding What It Means to Have Protein in Your Urine Understanding What It Means to Have Protein in Your Urine The kidneys are best known for making urine. This rather simple description does not tell the whole story. This brochure describes other important functions of the kidneys; including keeping protein in the blood and not letting any of the protein in the liquid (plasma) part of blood escape into the urine. Proteinuria is when “Proteinuria” is when kidneys allow proteins to kidneys appear in the urine and be lost from the body. allow Proteinuria is almost never normal, but it can proteins to be normal - rarely - in some healthy, active appear in the urine children or young adults. and be The kidneys are paired organs located on either lost from the body. side of the backbone. They are located at the Proteinuria level of the lowest part of the rib cage. They are is almost the size of an adult fist (4.5 – 5 inches in length). never Together the two kidneys receive a quarter of normal, but it can the blood that is pumped from the heart every be normal minute. This large blood flow is needed in order - rarely - for the kidneys to do one of the kidneys’ main in some jobs: healthy, active • remove waste products in the blood every children day or young adults. • keep the body in balance by eliminating the extra fluids and salts we consume on a regular basis. -
Tests for Abnormal Constituents in Urine
By Sandipkumar Kanazariya Tuesday, December 11, 2018 1 Under pathological conditions urine excreted by patient shows the presence of abnormal constituents along with normal constituents. Abnormal constituents of urine are sugar, proteins, blood, bile salts, bile pigments and ketone bodies. Tuesday, December 11, 2018 2 A. Physical Characteristics 1. Volume : a. Polyuria: Volume more than 3000 ml / 24 hours It is observed in Diabetes mellitus, Diabetes insipidus, Addison’s disease, Chronic progressive renal failure, excess water intake, intake of diuretics like caffeine, alcohol etc. b. Oliguria: Volume less than 400 ml / 24 hours. It is observed in fluid deprivation, excess fluid loss as in hemorrhage and neurogenic shock, dehydration, acute glomerulonephritis, obstruction in the urinary tract, disease of heart and lungs & strenuous muscular exercise. Tuesday, December 11, 2018 3 c. Anuria: Less than 150ml / 24hrs Complete absence of urine output. It is observed in shock and renal failure. Tuesday, December 11, 2018 4 2. Colour:- The colour of urine is variable in following disease conditions as given following table Sr. No Colour possible causes/ disorder 1 Colour less Fatty disease, diabetes mellitus, Polyuria 2 Yellowish brown Bile pigment, fever 3 Reddish brown Hemoglobin in urine, hemorrhage, menstrual contamination 4 Milky Presence of Fat 5 Dark Yellow Fever 6 Dark green typhoid and cholera 7 Black Due to Melanin (Melanoma) or Homogentisic acid in Tuesday, December 11, 2018 Alkaptonuria 5 3. Odour:- Normal urine has faint aromatic odour. On standing it has ammoniacal odour due to bacterial contamination. Odour of urine is variable in certain diseased condition. Sr. No Odour diseases 1 Fruity odour ketosis 2 Cabbage type odour methionine Malabsorption 3 Maple sugar odour maple sugar urine disease(MSUD) 4 Mousy phenylketonuria 5 Rancid odour tyrosine 6 Foul Urinary Tract Infection, Tuesday, December 11, 2018 Vaginitis 6 Tuesday, December 11, 2018 7 4. -
Obesity, Albuminuria, and Urinalysis Findings in US Young Adults from the Add Health Wave III Study
CJASN ePress. Published on October 17, 2007 as doi: 10.2215/CJN.00540107 Obesity, Albuminuria, and Urinalysis Findings in US Young Adults from the Add Health Wave III Study Maria Ferris,* Susan L. Hogan,* Hyunsook Chin,* David A. Shoham,† Debbie S. Gipson,* Keisha Gibson,* Sema Yilmaz,‡ Ronald J. Falk,* and J. Charles Jennette§ *University of North Carolina Kidney Center and Division of Nephrology and Hypertension and §Department of Pathology and Laboratory Animal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; †Department of Preventive Medicine and Epidemiology, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois; and ‡Department of Pediatrics, Hospital of Dumlupinar University, Kutahya, Turkey Background and objectives: Obesity has been associated with kidney disease in adults. This study was designed to evaluate the association of obesity with an early marker of kidney disease, albuminuria, among young adults. and body mass ,(4463 ؍ albumin-to-creatinine ratio (n ,(9371 ؍ Design, setting, participants, & measurements: Urinalysis (n index (kg/m2) were measured in the Add Health Wave III cohort (2001 to 2002), a multiethnic sample of young adults followed for approximately 6 yr. Multivariate logistic regression modeled the association of sex-specific albuminuria with body mass index, adjusted for sample weights, sex, race, ethnicity, and glycosuria. Results: Urinalysis revealed that 0.8% had proteinuria, 4.6% had hematuria, 0.2% had combined hematuria and proteinuria, and 1.5% had glycosuria. Albuminuria prevalence was 4.4%. Mean body mass index was higher among those with albuminuria compared with those without. There were no associations between body mass index categories of 25 to <30 or 30 to <35 kg/m2 with albuminuria compared with the lowest body mass index (<25 kg/m2); however, the highest category (>35 kg/m2) was %95 ;4.0 ؍ CI: 1.02 to 3.04). -
Storm in a Pee Cup: Hematuria and Proteinuria
Storm in a Pee Cup: Hematuria and Proteinuria Sudha Garimella MD Pediatric Nephrology, Children's Hospital-Upstate Greenville SC Conflict of Interest • I have no financial conflict of interest to disclose concerning this presentation. Objectives • Interpret the current guidelines for screening urinalysis, and when to obtain a urinalysis in the pediatric office. • Interpret the evaluation of asymptomatic/isolated proteinuria and definitions of abnormal ranges. • Explain the evaluation and differential diagnosis of microscopic hematuria. • Explain the evaluation and differential diagnosis of gross hematuria. • Explain and discuss appropriate referral patterns for hematuria. • Racial disparities in nephrology care 1. APOL-1 gene preponderance in African Americans and risk of proteinuria /progression(FSGS) 2. Race based GFR calculations which have caused harm 3. ACEI/ARB usage in AA populations: myths and reality Nephrology Problems in the Office • Hypertension • Proteinuria • Microscopic Hematuria • Abnormal Renal function The Screening Urinalysis • Choosing Wisely: • Don’t order routine screening urine analyses (UA) in healthy, asymptomatic pediatric patients as part of routine well child care. • One study showed that the calculated false positive/transient abnormality rate approaches 84%. • Population that deserves screening UA: • patients who are at high risk for chronic kidney disease (CKD), including but not necessarily limited to patients with a personal history of CKD, acute kidney injury (AKI), congenital anomalies of the urinary tract, acute nephritis, hypertension (HTN), active systemic disease, prematurity, intrauterine growth retardation, or a family history of genetic renal disease. • https://www.choosingwisely.org/societies/american-academy-of-pediatrics-section-on- nephrology-and-the-american-society-of-pediatric-nephrology/ Screening Urinalysis: Components A positive test for leukocyte esterase may be seen in genitourinary inflammation, irritation from instrumentation or catheterization, glomerulonephritis, UTIs and sexually transmitted infections. -
Hematuria in the Child
Hematuria and Proteinuria in the Pediatric Patient Laurie Fouser, MD Pediatric Nephrology Swedish Pediatric Specialty Care Hematuria in the Child • Definition • ³ 1+ on dipstick on three urines over three weeks • 5 RBCs/hpf on three fresh urines over three weeks • Prevalence • 4-6% for microscopic hematuria on a single specimen in school age children • 0.3-0.5% on repeated specimens Sources of Hematuria • Glomerular or “Upper Tract” – Dysmorphic RBCs and RBC casts – Tea or cola colored urine – Proteinuria, WBC casts, renal tubular cells • Non-Glomerular or “Lower Tract” – RBCs have normal morphology – Clots/ Bright red or pink urine The Glomerular Capillary Wall The Glomerular Capillary Wall Glomerular Causes of Hematuria • Benign or self-limiting – Benign Familial Hematuria – Exercise-Induced Hematuria – Fever-Induced Hematuria Glomerular Causes of Hematuria • Acute Glomerular Disease – Poststreptococcal/ Postinfectious – Henoch-Schönlein Purpura – Sickle Cell Disease – Hemolytic Uremic Syndrome Glomerular Causes of Hematuria • Chronic Glomerular Disease – IgA Nephropathy – Henoch-Schönlein Purpura or other Vasculitis – Alport Syndrome – SLE or other Collagen Vascular Disease – Proliferative Glomerulonephritis Non-Glomerular Hematuria • Extra-Renal • UTI • Benign urethralgia +/- meatal stenosis • Calculus • Vesicoureteral Reflux, Hydronephrosis • Foreign body • Rhabdomyosarcoma • AV M • Coagulation disorder Non-Glomerular Hematuria • Intra-Renal • Hypercalciuria • Polycystic Kidney Disease • Reflux Nephropathy with Renal Dysplasia • -
The Investigation of Symptomless Glycosuria with the Galactose and Cortisone Modified Glucose Tolerance Tests by R
J Clin Pathol: first published as 10.1136/jcp.11.5.428 on 1 September 1958. Downloaded from J. clin. Path. (1958), 11, 428. THE INVESTIGATION OF SYMPTOMLESS GLYCOSURIA WITH THE GALACTOSE AND CORTISONE MODIFIED GLUCOSE TOLERANCE TESTS BY R. B. GOUDIE, W. P. STAMM, AND S. DISCHE From the Royal Air Force Institute of Pathology and Tropical Medicine (RECEIVED FOR PUBLICATION OCTOBER 21, 1957) Glycosuria is sought in routine clinical exami- Joslin and Lawrence are two leading authorities nations in order to detect patients with early or who are representative of the two main schools of mild diabetes mellitus. There is good evidence thought. Joslin, Root, White, and Marble (1952) that early treatment may avert deterioration and gave the following criteria for the diagnosis of lead to a lower and later incidence of the vascular, diabetes mellitus with the 100 g. glucose tolerance renal, and ophthalmic complications (Dunlop, test (" true glucose " technique, capillary blood): 1954; Ricketts, 1947). a fasting blood glucose over 100 mg./100 ml., Certain occupations are unsuitable for the dia- or a peak glucose value over 170 mg./100 ml. He betic, and early diagnosis is of particular im- considered that the two-hour level was " of greatcopyright. portance in the Royal Air Force because a value " but that " one cannot disregard the height diagnosis of diabetes is a ban on aircrew duties. to which the curve goes. In borderline cases it is Since other conditions may give rise to glycos- well to be conservative and to repeat the test on uria, its discovery must be followed by a careful a later occasion." investigation in every case to determine the cause. -
Blood Or Protein in the Urine: How Much of a Work up Is Needed?
Blood or Protein in the Urine: How much of a work up is needed? Diego H. Aviles, M.D. Disclosure • In the past 12 months, I have not had a significant financial interest or other relationship with the manufacturers of the products or providers of the services discussed in my presentation • This presentation will not include discussion of pharmaceuticals or devices that have not been approved by the FDA Screening Urinalysis • Since 2007, the AAP no longer recommends to perform screening urine dipstick • Testing based on risk factors might be a more effective strategy • Many practices continue to order screening urine dipsticks Outline • Hematuria – Definition – Causes – Evaluation • Proteinuria – Definition – Causes – Evaluation • Cases You are about to leave when… • 10 year old female seen for 3 day history URI symptoms and fever. Urine dipstick showed 2+ for blood and no protein. Questions? • What is the etiology for the hematuria? • What kind of evaluation should be pursued? • Is this an indication of a serious renal condition? • When to refer to a Pediatric Nephrologist? Hematuria: Definition • Dipstick > 1+ (large variability) – RBC vs. free Hgb – RBC lysis common • > 5 RBC/hpf in centrifuged urine • Can be – Microscopic – Macroscopic Hematuria: Epidemiology • Microscopic hematuria occurs 4-6% with single urine evaluation • 0.1-0.5% of school children with repeated testing • Gross hematuria occurs in 1/1300 Localization of Hematuria • Kidney – Brown or coke-colored urine – Cellular casts • Lower tract – Terminal gross hematuria – (Blood -
Hyperglycaemia, Glycosuria and Ketonuria May Not Be Diabetes J Gray, a Bhatti, J M O'donohoe
The Ulster Medical Journal, Volume 72, No. 1, pp. 48-49, May 2003. Case Report Hyperglycaemia, glycosuria and ketonuria may not be diabetes J Gray, A Bhatti, J M O'Donohoe Accepted 20 November 2002 Diabetic ketoacidosis is a well recognised, tenderness, maximal in the lower abdomen now important, but rare differential diagnosis ofacute with associated guarding and rebound. abdominal pain in children. We report a case A presumptive diagnosis of acute appendicitis highlighting the need for complete assessment of was made and an exploratory laparotomy any child presenting with new-onset glycosuria, undertaken through a lower mid line incision. A ketonuria and hyperglycaemia. Causes other than perforated appendix was found along with pus in diabetes may rarely produce these findings. the peritoneal cavity. Appendicectomy and CASE REPORT A girl aged three years and ten peritoneal lavage were performed. months with a six-hour history ofabdominal pain Postoperative recovery was uneventful, and she and vomiting was referred to the surgical team by was discharged home on the third postoperative a general practitioner. Past medical history day. Subsequent random blood glucose was included a diagnosis of non-specific abdominal normal at 4.6mmol/L. Her HbAlc was normal pain at three years old. There was no significant while islet cell antibodies were negative. At review family history nor recent illness in the family she was well, with no complaints orcomplications. circle. DISCUSSION On examination she was restless and thirsty, but apyrexic. There was no foetor or rash. She had Rarely diabetic ketoacidosis may present with grunting respiration with tachypnoea, but the acute abdominal pain.' As this is an important lungs were clear on auscultation.