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Ischemia-Modified Albumin Level in Type 2 Diabetes Mellitus
Disease Markers 24 (2008) 311–317 311 IOS Press Ischemia-modified albumin level in type 2 diabetes mellitus – Preliminary report Agnieszka Piwowara,∗, Maria Knapik-Kordeckab and Maria Warwasa aDepartment of Pharmaceutical Biochemistry of Wroclaw Medical University, Wrocław, Poland bDepartment and Clinic of Angiology, Hypertension and Diabetology of Wroclaw Medical University, Wrocław, Poland Abstract. Aim: The main goal of the present study was the evaluation of ischemia-modified albumin (IMA) in patients with type 2 diabetes mellitus and estimation of its connection with vascular complications, glycemic control, hypertension, dyslipidemia and obesity. Methods: In 76 diabetic patients and 25 control subjects, a plasma level of IMA by manually performed, spectrophotometric Co(II)-albumin binding assay was determined. Other parameters such as glucose, fructosamine, HbA1c, total cholesterol and its fractions (HDL, LDL), triglicerydes were estimated by routine methods. Results: Diabetic patients had significantly higher level of IMA in comparison with control subjects. There were not significant differences between groups with various states of vascular complications although the lowest concentration of IMA was observed in patients with microangiopathy. Patients with poor glycemic control had higher IMA level in comparison with these with good glycemic control. Significant correlation was observed between IMA and HbA1c. Among the risk factors, only blood pressure and LDL showed a weak relationship with IMA level. Conclusions: Our results revealed, for the first time, higher level of IMA in diabetic patients which confirms that it may be of non-cardiac origin. We can suggest that the albumin molecule in plasma of diabetic patients is modified in the chronic hypoxia conditions provoked mainly by hyperglycemia and oxidative stress in diabetes. -
The Evaluation of Cardiac Markers in Myocardial Infarction Patients
Volume : 4 | Issue : 5 | May 2015 ISSN - 2250-1991 Research Paper Medical Science The Evaluation Of Cardiac Markers In Myocardial Infarction Patients Department of Medical Laboratory Science, College of Applied Ramprasad N Medical Sciences, Shaqra University, Al- Quwayiyah, Kingdom of Saudi Arabia, Corresponding Author Department of Medical Laboratory Science, College of Applied Samir Abdulkarim Medical Sciences, Shaqra University, Al- Quwayiyah, Kingdom of Alharbi Saudi Arabia Abdullah Habbab Laboratory Director, Diagnostic Laboratory, Al- Quwayiyah Gener- Alharbi al Hospital, Kingdom of Saudi Arabia. Background: Sudden cardiac death due to acute myocardial infarction (MI) is the most prevalent cause of death in young and adults. MI is a life threatening condition that needs emergency diagnosis and early treatment in the emergency room. Some researchers look for various clinical markers, which would help early diagnosis of the disease. Aim: In the present study, our aim was to investigate the lipid profile and cardiac enzymes in MI patients in Al- Quwayiyah region of Saudi Arabia. Materials and methods: This study included total 38 patients with MI and 46 age and sex matched healthy controls. Various lipid profile parameters and cardiac enzymes like Creatinine phosphokinase (CPK), Creatinine kinase- MB (CK- MB), lactate dehydrogenase (LDH), Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) levels were measured ABSTRACT and compared. This study was conducted in Al- Quwayiyah General Hospital, Saudi Arabia. Results: The significantly increased levels of cardiac enzymes (P<0.001) in MI patients when compared to control groups. Conclusion: The present study illustrated that assessing of lipid profiles and serum cardiac enzymes are the markedly very useful as it may serve as a useful monitor to judge the prognosis of the MI patients. -
CAMP Tests (Standard and Rapid) and Reverse CAMP Test
M.V.Sc. (Veterinary Microbiology), Monsoon semester Date 31.12.2020 VMC- 602 (Bacteriology II), Unit III, Practical class CAMP Tests (Standard and Rapid) and Reverse CAMP test Dr. Savita Kumari Assistant Professor-cum-Jr. Scientist Department of Veterinary Microbiology Bihar Veterinary College, BASU, Patna CAMP factor S. agalactiae contains the CAMP factor, only beta-hemolytic Streptococcus secretes Pore -forming toxin first identified in this bacterium CAMP reaction is based on the co -hemolytic activity of the CAMP factor Commonly used to identify S. agalactiae Closely related proteins present also in other Gram - positive pathogens cfb gene encodes CAMP factor CAMP test CAMP reaction- consists in a zone of strong hemolysis that is observed when S. agalactiae is streaked next to Staphylococcus aureus on blood agar S. aureus secretes sphingomyelinase Sheep red blood cells - rich in sphingomyelin, and upon exposure to sphingomyelinase become greatly sensitized to CAMP factor, which then effects hemolysis Hemolysis most pronounced in the zone between the colonies of the two bacterial species Co-hemolytic phenomenon- presumptive identification of Group B Streptococci (S. agalactiae) CAMP test First described by Christie, Atkins, and Munch –Petersen in 1944 The protein was named CAMP factor for the initials of the authors of the article that first described the phenomenon Types: Standard CAMP test Rapid CAMP test (spot test ) Standard camp test are time consuming and/or expensive compared to the CAMP spot test Principle CAMP test detects -
A Comparative Study of Creatine Kinase-MB and Troponin Levels Among Diabetic and Non Diabetic Patients with Acute MI
ORIGINAL ARTICLE A comparative study of Creatine Kinase-MB and Troponin levels among diabetic and non diabetic patients with Acute MI AWAIS ANWAR1, HASAN AKBAR KHAN2, SAMRA HAFEEZ3, KANWAL FIRDOUS4 ABSTRACT In diabetic patients myocardial infarction (MI) is a major cause of death. Weak metabolic control is very common in diabetic patients with MI and if blood glucose levels are not controlled with different treatments may produce medical complications. Hyperglycemia, CK-MB and tropanin levels are very important biomarkers for the assessment of MI. The blood glucose (325.56±23.6), CK-MB (350.6±95.23) and Tropanin (6.16±2.23) levels in diabetics individuals showed P<0.001 significant results. Key words: Myocardial infarction (MI),Creatine kinase (CK),Tropanin. INTRODUCTION produced in pregnant ladies without any diabetic history due to the stress (Kosaka et al., 2005). Commonly myocardial infarction (MI) or acute Creatine kinase (CK) is an intracellular enzyme myocardial infarction (AMI) is called heart attack and found its high quantity in skeletal muscles, it occurs by the blockages of blood supply to a part of myocardium, and brain; smaller amounts also occur the heart (Agarwall,. 2009). When supply of blood in other visceral tissues. A CK-MB test is used as stops to the heart it causes damaging of the heart biological parameter in MI (Zeller et al., 2005). In the muscle. There are many symptom of MI but the most case of MI its concentration in the blood increases common is chest pain or which may travel into the than the normal levels. Different researchers found shoulder, arm, back, neck, or jaw that creatine kinase levels increases due to heart (Aghaeishahsavari,. -
The MAS Omni QC Family
Thermo Scientific MAS Omni Quality Control Products Results you can trust The MAS Omni QC family Eliminate up to four routinely run vials Streamline your workflow Reduce your costs Streamline your workflow Consolidate multiple QC products Cardiac Panel QC STAT QC consolidated into: Omni•CARDIO Routine Immunoassay QC Tumor Marker QC Specialty Immunoassay QC General Chemistry QC consolidated into: Serum Protein / Immunology QC Omni•IMMUNE or consolidated into: Omni•IMMUNE PRO Omni•CORE MAS Omni•CARDIO™ Thermo Scientific™ MAS® Omni•CARDIO consolidates a comprehensive cardiac marker panel with the new generation of STAT analytes including D-Dimer, hCG, Myeloperoxidase and Procalcitonin. Value assignment is provided for key instrument systems including Abbott Architect, Beckman Coulter Access, AU and UniCel systems, Ortho Clinical Diagnostics VITROS, Roche Cobas and Elecsys systems and Siemens Advia, Dimension, Dimension Vista, Immulite and Stratus systems. Part Number Level Bottles & Size Storage & Stability Matrix OCRD-UL Ultra Low OCRD-L Low 36 months @ -25 to -15 ºC OCRD-101 1 15 days @ 2-8 ºC (for BNP-32, CK-MB, D-Dimer, OCRD-202 2 6 x 3 mL Assayed Digitoxin, hCG, hsCRP, Myeloperoxidase, Human Serum OCRD-303 3 Procalcitonin, Total CK, Troponin-I and Troponin-T) 10 days @ 2-8 ºC (for Myoglobin and NT-proBNP) Tri-Level Multi-Pack OCRD-MP (2 vials each level 1/2/3) Analytes Brain Natriuretic Peptide-32 (BNP-32) Beta Human Chorionic Gonadotropin (b-hCG) Procalcitonin (PCT) Creatinine Kinase-MB (CK-MB) High Sensitivity C-Reactive Protein (hsCRP) -
Use of the Diagnostic Bacteriology Laboratory: a Practical Review for the Clinician
148 Postgrad Med J 2001;77:148–156 REVIEWS Postgrad Med J: first published as 10.1136/pmj.77.905.148 on 1 March 2001. Downloaded from Use of the diagnostic bacteriology laboratory: a practical review for the clinician W J Steinbach, A K Shetty Lucile Salter Packard Children’s Hospital at EVective utilisation and understanding of the Stanford, Stanford Box 1: Gram stain technique University School of clinical bacteriology laboratory can greatly aid Medicine, 725 Welch in the diagnosis of infectious diseases. Al- (1) Air dry specimen and fix with Road, Palo Alto, though described more than a century ago, the methanol or heat. California, USA 94304, Gram stain remains the most frequently used (2) Add crystal violet stain. USA rapid diagnostic test, and in conjunction with W J Steinbach various biochemical tests is the cornerstone of (3) Rinse with water to wash unbound A K Shetty the clinical laboratory. First described by Dan- dye, add mordant (for example, iodine: 12 potassium iodide). Correspondence to: ish pathologist Christian Gram in 1884 and Dr Steinbach later slightly modified, the Gram stain easily (4) After waiting 30–60 seconds, rinse with [email protected] divides bacteria into two groups, Gram positive water. Submitted 27 March 2000 and Gram negative, on the basis of their cell (5) Add decolorising solvent (ethanol or Accepted 5 June 2000 wall and cell membrane permeability to acetone) to remove unbound dye. Growth on artificial medium Obligate intracellular (6) Counterstain with safranin. Chlamydia Legionella Gram positive bacteria stain blue Coxiella Ehrlichia Rickettsia (retained crystal violet). -
SEED Haematology Sysmex Educational Enhancement and Development October 2012
SEED Haematology Sysmex Educational Enhancement and Development October 2012 The red blood cell indices The full blood count has been used in conjunction with the traditional red The complete blood count (CBC) is central to clinical deci- cell indices in order to narrow down the possible causes sion making. This makes it one of the commonest laboratory of anaemia in an individual patient. investigations performed worldwide. Whilst the definition of what constitutes an CBC is influenced by the number Impedance technology and type of parameters measured by different haematology The RBC, HCT and MCV are all closely interrelated as they analysers, the traditional red cell indices that are widely are derived from information obtained from the passage used to classify anaemias are common to all. of cells through the aperture of the impedance channel of an automated haematology analyser. The impedance The laboratory approach to anaemia technology is based on the principle that an electrical field, Anaemia is an extremely common global healthcare prob- created between two electrodes of opposite charge, can lem. However, anaemia is merely a symptom which can be used to count and determine the size of cells. Blood result from a multitude of causes. Effective treatment is cells are poor conductors of electricity. The diluent in which only possible if the underlying cause is correctly identified. they are suspended as they pass through the aperture To this end, several classification systems have been devis- during counting is an isotonic solution which is a good ed. The most useful and widely used classification system conductor of electricity. -
Laboratory Approach to Anemia Laboratory Approach to Anemia
DOI: 10.5772/intechopen.70359 Provisional chapter Chapter 12 Laboratory Approach to Anemia Laboratory Approach to Anemia Ebru Dündar Yenilmez and Abdullah Tuli Ebru Dündar Yenilmez and Abdullah Tuli Additional information is available at the end of the chapter Additional information is available at the end of the chapter http://dx.doi.org/10.5772/intechopen.70359 Abstract Anemia is a major cause of morbidity and mortality worldwide and can be defined as a decreased quantity of circulating red blood cells (RBCs). The epidemiological studies suggested that one-third of the world’s population is affected with anemia. Anemia is not a disease, but it is instead the sign of an underlying basic pathological process. However, the sign may function as a compass in the search for the cause. Therefore, the prediag- nosis revealed by thorough investigation of this sign should be supported by laboratory parameters according to the underlying pathological process. We expect that this review will provide guidance to clinicians with findings and laboratory tests that can be followed from the initial stage in the anemia search. Keywords: anemia, complete blood count, red blood cell indices, reticulocyte 1. Introduction Anemia, the meaning of which in Greek is “without blood,” is a relatively common sign and symptom of various medical conditions. Anemia is defined as a significant decrease in the count of total erythrocyte [red blood cell (RBC)] mass, although this definition is rarely used in clinical settings. According to the World Health Organization, anemia is a condition in which the number of red blood cells (RBCs, and consequently their oxygen-carrying capacity) is insufficient to meet the body’s physiologic needs [1, 2]. -
Newborn Colonization and Antibiotic Susceptibility Patterns of Streptococcus Agalactiae at the University of Gondar Referral
Gizachew et al. BMC Pediatrics (2018) 18:378 https://doi.org/10.1186/s12887-018-1350-1 RESEARCH ARTICLE Open Access Newborn colonization and antibiotic susceptibility patterns of Streptococcus agalactiae at the University of Gondar Referral Hospital, Northwest Ethiopia Mucheye Gizachew1*, Moges Tiruneh1, Feleke Moges1, Mulat Adefris2, Zemene Tigabu3 and Belay Tessema1 Abstract Background: Group B Streptococcus (GBS) that asymptomatically colonizing the recto-vaginal area of women is the most important cause of neonatal colonization. There is paucity of evidence about newborn colonization with GBS in Ethiopia. Thus, this study was aimed to determine the prevalence of newborn colonization with GBS, antibiotic susceptibility patterns of the isolates and associated risk factors at the University of Gondar Referral Hospital in Northwest Ethiopia Methods: A prospective cross sectional study was conducted from December 2016 to November 2017. A total of 1,155 swabs from nasal, ear and umbilical areas of the newborns were collected from the 385 newborns. Identifications of the isolates and antibiotic susceptibility testing were done by using conventional methods. Results: Sixty two (16.1%, 95% CI: 12.2% - 20%) of the newborns were colonized by GBS. Seven percent of the total specimens were positive for GBS. The antibiotics susceptibility rates of GBS (average of the three body sites tested) were 95.1%, 89.6%, 88.9%, 85.7%, 85.3%, 81.3%, 76.9%, 76.1%, 73.8%, and 34.4% to ampicillin, penicillin, ciprofloxacin, chloramphenicol, vancomycin, azitromycin, erythromycin, clindamycin, ceftriaxone, and tetracycline, respectively. A multilogistic regression analyses were shown that the newborns that were from mothers whose education status was below tertiary level, and newborns from mothers who were: being employed, being nullipara and multigravida were at risk for colonization with GBS. -
Lifesign MI 3-In-1 Package Insert.Pdf
MIMyoglobin/CK-MB/Troponin I 3 IN 1 Point-of-care cardiac tests for the simultaneous qualitative detection of Myoglobin, CK-MB and Troponin I in blood, plasma and serum for the rapid diagnosis of myocardial infarction Manufactured by MF Manufactured for: EC REP Princeton BioMeditech Corp. MT Promedt Consulting GmbH 4242 U.S. Hwy 1 A PBM Group Company Altenhofstrasse 80 Monmouth Junction, NJ 08852 66386 St. Ingbert 85 Orchard Road Germany Skillman,NJ 08558 +49-68 94-58 10 20 800-526-2125, 732-246-3366 596 -4/24/12 www.lifesignmed.com P-56331-B LifeSign MI® Myoglobin/CK-MB/Troponin I Rapid Test For in vitro Diagnostic Use Only A Simple and Rapid One-Step Immunoassay for the Simultaneous Qualitative Detection of Myoglobin, CK-MB, and Cardiac Troponin I in Human Whole Blood, Serum, or Plasma. Intended Use: For the simultaneous qualitative determination of myoglobin, CK-MB, and troponin I in human whole blood, plasma or serum as an aid in the diagnosis of acute myocardial infarction in emergency room, critical care, point-of-care, and hospital settings. The LifeSign MI® Myoglobin/CK-MB/Troponin I Test provides a qualitative analytical test result. The qualitative nature of this assay does not provide infor- mation about change - either the rise or fall - in the concentration of myoglobin, CK-MB, and cardiac troponin I with single testing. A quantitative method should be used, if desired, to quantitate the concentration of myoglobin, CK-MB, and cardiac troponin I at any given time. Only with serial testing could a temporal change in the level of myoglobin, CK-MB, and cardiac troponin I be concluded. -
TRYPTIC SOY AGAR - for in Vitro Use Only
TRYPTIC SOY AGAR - For in vitro use only - Plated Media Tubed Media PT80 –Tryptic Soy Agar (TSA) TT80 – TSA Slant PT81 – TSA (SXT) TT80-18 – TSA Pour Plate [18-mL] PT89 – TSA w Yeast Extract TB75 – TSA Blood Slant PB75 – TSA w 5% Sheep Blood PB81 – TSA w 7% Sheep Blood PB69 – TSA w 5% Horse Blood PB80 – TSA w 7% Horse Blood Tryptic Soy Agar (TSA) is a general purpose The CAMP test can also be used to help identify plating medium used for the isolation, cultivation, pathogenic species of Listeria . and maintenance of a variety of fastidious and non- TSA with horse blood is used to isolate more fastidious microorganisms. fastidious organisms. Horse blood contains both X Leavitt et al. demonstrated the versatility of and V factor, which are essential growth factors for TSA by cultivating both aerobic and anaerobic some organisms such as Haemophilus species. microbes using TSA. TSA is recognized and Sheep and human blood are not suitable since they recommended by numerous agencies around the contain specific enzymes that inactivate V Factor. world. Our standard formulation is prepared Although, some laboratories prefer a plated according to the United States Pharmacopeia medium with a higher blood content (7-10%) or (USP) and recommended for various different with horse blood, these mediums should not be applications put forth by the Association of used for determination of hemolytic reactions or Official Analytical Chemists (AOAC), the for the CAMP test. The increased blood content International Dairy Federation (IDF), the United can make hemolytic reactions less distinct and States Department of Agriculture (USDA), and the more difficult to read while defibrinated horse American Public Health Association (APHA). -
Streptococci
STREPTOCOCCI Streptococci are Gram-positive, nonmotile, nonsporeforming, catalase-negative cocci that occur in pairs or chains. Older cultures may lose their Gram-positive character. Most streptococci are facultative anaerobes, and some are obligate (strict) anaerobes. Most require enriched media (blood agar). Streptococci are subdivided into groups by antibodies that recognize surface antigens (Fig. 11). These groups may include one or more species. Serologic grouping is based on antigenic differences in cell wall carbohydrates (groups A to V), in cell wall pili-associated protein, and in the polysaccharide capsule in group B streptococci. Rebecca Lancefield developed the serologic classification scheme in 1933. β-hemolytic strains possess group-specific cell wall antigens, most of which are carbohydrates. These antigens can be detected by immunologic assays and have been useful for the rapid identification of some important streptococcal pathogens. The most important groupable streptococci are A, B and D. Among the groupable streptococci, infectious disease (particularly pharyngitis) is caused by group A. Group A streptococci have a hyaluronic acid capsule. Streptococcus pneumoniae (a major cause of human pneumonia) and Streptococcus mutans and other so-called viridans streptococci (among the causes of dental caries) do not possess group antigen. Streptococcus pneumoniae has a polysaccharide capsule that acts as a virulence factor for the organism; more than 90 different serotypes are known, and these types differ in virulence. Fig. 1 Streptococci - clasiffication. Group A streptococci causes: Strep throat - a sore, red throat, sometimes with white spots on the tonsils Scarlet fever - an illness that follows strep throat. It causes a red rash on the body.