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Mean corpuscular hemoglobin concentration

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The mean corpuscular hemoglobin concentration ( MCHC ) is a measure of the concentration of hemoglobin in a given volume of packed red blood cell.

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39-697: It is calculated by dividing the hemoglobin by the hematocrit . Reference ranges for blood tests are 32 to 36 g/dL (320 to 360g/L), or between 4.81 and 5.58 mmol/L. It is thus a mass or molar concentration . Still, many instances measure MCHC in percentage (%), as if it were a mass fraction (m Hb / m RBC ). Numerically, however, the MCHC in g/dL and the mass fraction of hemoglobin in red blood cells in % are identical, assuming an RBC density of 1g/mL and negligible hemoglobin in plasma. A low MCHC can be interpreted as identifying decreased production of hemoglobin. MCHC can be normal even when hemoglobin production

78-401: A cold agglutinin , or there may be some other problem resulting in one or more artifactual results affecting the MCHC. For example, for some patients with cold agglutinins, when their blood gets colder than 37 °C, the red cells will clump together. As a result, the analyzer may incorrectly report a low number of very dense red blood cells. This will result in an impossibly high number when

117-401: A blood sample. It does not account for the mass of the red blood cells, and thus the changes in mass can alter a hematocrit level or go undetected while affecting a subject's condition. Additionally, there have been cases in which the blood for testing was inadvertently drawn proximal to an intravenous line that was infusing packed red cells or fluids. In these situations, the hemoglobin level in

156-518: A concentration of the enzyme. Other tests use colorimetric changes to determine the concentration of the chemical in question. Turbidity may also be measured. Antibodies are used by some analysers to detect many substances by immunoassay and other reactions that employ the use of antibody-antigen reactions. When concentration of these compounds is too low to cause a measurable increase in turbidity when bound to antibody, more specialised methods must be used. Recent developments include automation for

195-428: A higher hematocrit level signifies the blood sample's ability to transport oxygen, which has led to reports that an "optimal hematocrit level" may exist. Optimal hematocrit levels have been studied through combinations of assays on blood sample's hematocrit itself, viscosity, and hemoglobin level. Hematocrit levels also serve as an indicator of health conditions. Thus, tests on hematocrit levels are often carried out in

234-450: A reaction to produce a color change. Then, a photometer measures the absorbance of the sample to indirectly measure the concentration of analyte present in the sample. The use of an ion-selective electrode (ISE) is another common analytical method that specifically measures ion concentrations. This typically measures the concentrations of sodium, calcium or potassium present in the sample. There are various methods of introducing samples into

273-401: A single file line. From this stage, blood will enter the venules increasing in hematocrit, in other words the discharge hematocrit (Hd).In large vessels with low hematocrit, viscosity dramatically drops and red cells take in a lot of energy. Relationships between hematocrit, viscosity, and shear rate are important factors to put into consideration. Since blood is non-Newtonian, the viscosity of

312-485: A vertical position, with no draughts and vibration or direct sunlight allowed, an optical reader determines how far the red cells have fallen by detecting the level. Some tests and test categories are unique in their mechanism or scope, and require a separate analyser for only a few tests, or even for only one test. Other tests are esoteric in nature—they are performed less frequently than other tests, and are generally more expensive and time-consuming to perform. Even so,

351-411: Is a medical laboratory instrument designed to measure various substances and other characteristics in a number of biological samples quickly, with minimal human assistance. These measured properties of blood and other fluids may be useful in the diagnosis of disease. Photometry is the most common method for testing the amount of a specific analyte in a sample. In this technique, the sample undergoes

390-606: Is analysed by sophisticated software giving a numerical representation of the likely overall distribution of cell populations. Some of the latest hematology instruments may report Cell Population Data that consist in Leukocyte morphological information that may be used for flagging Cell abnormalities that trigger the suspect of some diseases . Reticulocyte counts can now be performed by many analysers, giving an alternative to time-consuming manual counts. Many automated reticulocyte counts, like their manual counterparts, employ

429-414: Is decreased (such as in iron deficiency) due to a calculation artifact. MCHC can be elevated ("hyperchromic") in hereditary spherocytosis , sickle cell disease and homozygous hemoglobin C disease , depending upon the hemocytometer. MCHC can be elevated in some megaloblastic anemias. MCHC can be falsely elevated when there is agglutination of red cells (falsely lowering the measured RBC count) or when there

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468-492: Is easily separated from the WBC count by the smaller impedance spikes they produce in the detector due to their lower cell volumes. Optical detection may be utilised to gain a differential count of the populations of white cell types. A dilute suspension of cells is passed through a flow cell, which passes cells one at a time through a capillary tube past a laser beam. The reflectance, transmission and scattering of light from each cell

507-472: Is flowing. The passage of cells through the current changes the impedance between the terminals (the Coulter principle ). A lytic reagent is added to the blood solution to selectively lyse the red cells (RBCs), leaving only white cells (WBCs), and platelets intact. Then the solution is passed through a second detector. This allows the counts of RBCs, WBCs, and platelets to be obtained. The platelet count

546-400: Is opacification of the plasma (falsely increasing the measured hemoglobin). Causes of plasma opacification that can falsely increase the MCHC include hyperbilirubinemia, hypertriglyceridemia, and free hemoglobin in the plasma (due to hemolysis). Because of the way automated analysers count blood cells, a very high MCHC (greater than about 370 g/L) may indicate the blood is from someone with

585-401: Is the volume percentage (vol%) of red blood cells (RBCs) in blood , measured as part of a blood test . The measurement depends on the number and size of red blood cells. It is normally 40.7–50.3% for males and 36.1–44.3% for females. It is a part of a person's complete blood count results, along with hemoglobin concentration, white blood cell count and platelet count. Because

624-452: The immunohaematology lab, also known as transfusion medicine . These are used to perform complete blood counts , erythrocyte sedimentation rates (ESRs), or coagulation tests. Automated cell counters sample the blood, and quantify, classify, and describe cell populations using both electrical and optical techniques. Electrical analysis involves passing a dilute solution of the blood through an aperture across which an electrical current

663-449: The liver function tests ), ion levels (e.g. sodium and potassium , and other tell-tale chemicals (such as glucose , serum albumin , or creatinine ). Simple ions are often measured with ion selective electrodes , which let one type of ion through, and measure voltage differences. Enzymes may be measured by the rate they change one coloured substance to another; in these tests, the results for enzymes are given as an activity, not as

702-440: The 1966–80 Health Examination Survey, there was a small rise in mean hematocrit levels in female and male adolescents that reflected a rise in annual family income. Additionally, a higher education in a parent has been put into account for a rise in mean hematocrit levels of the child. Lowered hematocrit levels also pose health impacts. These causes and impacts have been reported: Automated analyzer An automated analyser

741-628: The Erythrocyte Sedimentation Rate Test: H02-A5 and to the ICSH (International Council for Standardization in Haematology) published "ICSH review of the measurement of the erythrocyte sedimentation rate", both indicating the only reference method, being Westergren, explicitly indicating the use of diluted blood (with sodium citrate), in 200 mm pipettes, bore 2.55 mm. After 30 or 60 minutes being in

780-689: The analyser. Test tubes of samples are often loaded into racks. These racks can be inserted directly into some analysers or, in larger labs, moved along an automated track. More manual methods include inserting tubes directly into circular carousels that rotate to make the sample available. Some analysers require samples to be transferred to sample cups. However, the need to protect the health and safety of laboratory staff has prompted many manufacturers to develop analysers that feature closed tube sampling, preventing workers from direct exposure to samples. Samples can be processed singly, in batches, or continuously. The automation of laboratory testing does not remove

819-504: The analyzer calculates the MCHC. This problem is usually picked up by the laboratory before the result is reported. The blood can be warmed until the cells separate from each other, and quickly put through the machine while still warm. There are four steps to perform when a suspect increased MCHC (>370 g/L or >37.0 g/dL) is received from the analyzer: Haematocrit The hematocrit ( / h ɪ ˈ m æ t ə k r ɪ t / ) ( Ht or HCT ), also known by several other names ,

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858-487: The blood is in relation to the hematocrit, and as a function of shear rate. This is important when it comes to determining shear force, since a lower hematocrit level indicates that there is a need for more force to push the red blood cells through the system. This is because shear rate is defined as the rate to which adjacent layers of fluid move in respect to each other. Plasma is a more viscous material than typically red blood cells, since they are able to adjust their size to

897-421: The blood plasma to trigger a clotting reaction. The progress of clotting may be monitored optically by measuring the absorbance of a particular wavelength of light by the sample and how it changes over time. .. Automatic erythrocyte sedimentation rate (ESR) readers, while not strictly analysers, do preferably have to comply to the 2011-published CLSI (Clinical and Laboratory Standards Institute) "Procedures for

936-401: The blood sample will not be the true level for the patient because the sample will contain a large amount of the infused material rather than what is diluted into the circulating whole blood. That is, if packed red cells are being supplied, the sample will contain a large amount of those cells and the hematocrit will be artificially very high. Hematocrit can vary from the determining factors of

975-411: The calculated INRs commonly used for therapeutic evaluation), Lupus anticoagulant screens, D dimer assays, and factor assays. Coagulometers require blood samples that have been drawn in tubes containing sodium citrate as an anticoagulant. These are used because the mechanism behind the anticoagulant effect of sodium citrate is reversible. Depending on the test, different substances can be added to

1014-498: The character of the chemical testing laboratory by allowing significant increases in the numbers of samples that could be processed. Samples used in the analyzers include, but are not limited to, blood, serum, plasma, urine, cerebrospinal fluid, and other fluids from within the body. The design based on separating a continuously flowing stream with air bubbles largely reduced slow, clumsy, and error-prone manual methods of analysis. The types of tests include enzyme levels (such as many of

1053-542: The clinical laboratory began with the introduction of the "Robot Chemist" invented by Hans Baruch and introduced commercially in 1959 . The AutoAnalyzer is an early example of an automated chemistry analyzer using a special flow technique named "continuous flow analysis (CFA)", invented in 1957 by Leonard Skeggs, PhD and first made by the Technicon Corporation. The first applications were for clinical (medical) analysis. The AutoAnalyzer profoundly changed

1092-489: The need for human expertise (results must still be evaluated by medical technologists and other qualified clinical laboratory professionals), but it does ease concerns about error reduction, staffing concerns, and safety. These are machines that process a large portion of the samples going into a hospital or private medical laboratory . Automation of the testing process has reduced testing time for many analytes from days to minutes. The history of discrete sample analysis for

1131-429: The number of red blood cells. These factors can be from the age and sex of the subject. The normal hematocrit level is around 40% for adult women and about 45% for adult men. In newborns, it is approximately 55% and drops to around 35% by 2 months of age. After that, it gradually increases during development, reaching adult levels at puberty. Following this, the hematocrit level gradually decreases with aging. Typically,

1170-413: The process of diagnosis of such conditions, and may be conducted prior to surgery. Additionally, the health conditions associated with certain hematocrit levels are the same as ones associated with certain hemoglobin levels. As blood flows from the arterioles into the capillaries, a change in pressure occurs. In order to maintain pressure, the capillaries branch off to a web of vessels that carry blood into

1209-427: The product of the luminal diameter and hematocrit create a linear relationship that is used to measure hematocrit levels. Other than potential bruising at the puncture site, and/or dizziness, there are no complications associated with this test. While known hematocrit levels are used in detecting conditions, it may fail at times due to hematocrit being the measure of concentration of red blood cells through volume in

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1248-409: The purpose of red blood cells is to transfer oxygen from the lungs to body tissues, a blood sample's hematocrit—the red blood cell volume percentage—can become a point of reference of its capability of delivering oxygen. Hematocrit levels that are too high or too low can indicate a blood disorder, dehydration , or other medical conditions. An abnormally low hematocrit may suggest anemia , a decrease in

1287-405: The radius of a tube; the shear rate is purely dependent on the amount of red blood cells being forced in a vessel. Generally at both sea levels and high altitudes, hematocrit levels rise as children mature. These health-related causes and impacts of elevated hematocrit levels have been reported: Hematocrit levels were also reported to be correlated with social factors that influence subjects. In

1326-441: The red cells. An estimated hematocrit as a percentage may be derived by tripling the hemoglobin concentration in g / dL and dropping the units. The packed cell volume (PCV) can be determined by centrifuging EDTA -treated or heparinized blood in a capillary tube (also known as a microhematocrit tube) at 10,000  RPM for five minutes. This separates the blood into layers. The volume of packed red blood cells divided by

1365-645: The total amount of red blood cells, while an abnormally high hematocrit is called polycythemia . Both are potentially life-threatening disorders. There are other names for the hematocrit, such as packed cell volume (PCV), volume of packed red cells (VPRC), or erythrocyte volume fraction (EVF). The term hematocrit (or haematocrit in British English ) comes from the Ancient Greek words haima ( αἷμα , "blood") and kritēs ( κριτής , "judge"), and hematocrit means "to separate blood". It

1404-487: The total volume of the blood sample gives the PCV. Since a tube is used, this can be calculated by measuring the lengths of the layers. Another way of measuring hematocrit levels is by optical methods such as spectrophotometry . Through differential spectrophotometry, the differences in optical densities of a blood sample flowing through small-bore glass tubes at isosbestic wavelengths for deoxyhemoglobin and oxyhemoglobin and

1443-510: The use of a supravital dye such as new methylene blue to stain the red cells containing reticulin prior to counting. Some analysers have a modular slide maker which is able to both produce a blood film of consistent quality and stain the film, which is then reviewed by a medical laboratory professional. Automated coagulation machines or Coagulometers measure the ability of blood to clot by performing any of several types of tests including Partial thromboplastin times , Prothrombin times (and

1482-466: The venules. Through this process blood undergoes micro-circulation. In micro-circulation, the Fåhræus effect will take place, resulting in a large change in hematocrit. As blood flows through the arterioles, red cells will act a feed hematocrit (Hf), while in the capillaries, a tube hematocrit (Ht) occurs. In tube hematocrit, plasma fills most of the vessel while the red cells travel through in somewhat of

1521-462: Was coined in 1891 by Swedish physiologist Magnus Blix as haematokrit , modeled after lactokrit . With modern lab equipment, the hematocrit can be calculated by an automated analyzer or directly measured, depending on the analyzer manufacturer. Calculated hematocrit is determined by multiplying the red cell count by the mean cell volume . The hematocrit is slightly more accurate, as the PCV includes small amounts of blood plasma trapped between

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