Venous Information and Courses from MediaLab, Inc.
These are the MediaLab courses that cover Venous and links to relevant pages within the course.
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| Which one of the following parasites must migrate through the circulation before maturing in the portal venous system: | View Page |
| Diseases Associated with Proteinuria Severe proteinuria (greater than 3.5 g/day) is characteristically seen in patients with glomerulonephritis, lupus nephritis, lipoid nephrosis, and severe venous congestion of the kidney. Moderate proteinuria (0.5-3.5g/day) is seen in nephrosclerosis, multiple myeloma, diabetes nephropathy, malignant hypertension, and pyelonephritis with hypertension. Mild proteinuria (less than 0.5 g/day) may be seen with polycystic kidneys, chronic pyelonephritis, benign orthostatic proteinuria, and some renal tubular diseases. Transient proteinuria can also be due to physiologic conditions such as stress, exercise, cold exposure, and fever, in the absence of renal disease. | View Page |
| Collecting Blood Specimens for Coagulation Testing The specimen of choice for coagulation testing is plasma. Venous blood is drawn into a 3.2% buffered sodium citrate tube (blue top tube), yielding a whole blood sample with a 9:1 blood to anticoagulant ratio. Inadequate filling of the collection tube will decrease this ratio, and may affect test results. A blue top tube used for coagulation testing should be drawn before any other tubes containing additives. This includes tubes containing other anticoagulants and/or plastic serum tubes containing clot activators. A serum tube that does not contain an additive can be collected before the blue top tube. If a winged blood collection set is used in drawing a specimen for coagulation testing, a discard tube should be drawn first. The discard tube must be used to fill the blood collection tubing dead space to assure that the proper anticoagulant/blood ratio is maintained, but the discard tube does not need to be completely filled. The discard tube should be a nonadditive or a coagulation tube. If a blood specimen used for coagulation testing must be collected from an indwelling line that may contain heparin, the line should be flushed with 5 mL of saline, and the first 5 mL of blood or 6-times the line volume (dead space volume of the catheter) be drawn off and discarded before the coagulation tube is filled. | View Page |
| Fibrin/Fibrinogen Degradation Products and D-dimers The presence of D-dimers in plasma or whole blood indicates that fibrin has been formed and degraded (fibrinolysis). Plasmin can also degrade intact fibrinogen, generating fibrinogen degradation products that are detected in fibrin/fibrinogen degradation products (FDP) assays. D-dimers and FDP can become elevated whenever the coagulation and fibrinolytic systems are activated. The presence of D-dimer confirms that both thrombin and plasmin have been generated since it can only be produced as the result of the plasmin degradation of fibrin. This makes the test for D-dimers more specific for fibrinolysis than the FDP test that also detects the products of the direct proteolysis of fibrinogen (fibrinogenolysis).The D-dimer test can be useful in the diagnosis of deep venous thrombosis (DVT) or pulmonary embolism (PE), two forms of venous thromboembolism (VTE). When the test is being used for this purpose, it is important that D-dimer levels are accurately measured and accurately reported because of the serious nature of this clinical decision. If the test is positive in a patient suspected to have DVT or PE, clinicians proceed with further diagnostic tests. If the test is negative, depending on the clinical situation and the sensitivity of the D-dimer assay, DVT or PE is considered unlikely and further diagnostic tests for DVT or PE might not be pursued. D-dimer is a sensitive, but not specific, diagnostic test for disseminated intravascular coagulation, and an indicator of increased risk of future myocardial infarction in patients evaluated for chest pain. | View Page |
| Anticoagulation Therapy Anticoagulant therapy is employed in a number of clinical situations Some of these clinical situations include: After an episode of thrombosis, such as deep venous thrombosis (DVT) in the veins of the legs, to prevent reoccurrence. Prophylactically after some surgeries, especially those involving vascular repair such as coronary bypass surgery to prevent clots from blocking newly formed vasculature. In heart valve and chamber disorders where there is an increased risk of thrombosis occurring. | View Page |
| The two main compartments of the bone marrow are the venous sinuses/blood vessels and hematopoietic cords. | View Page |
| Supporting Cells Reticular cells (adventitial cells) provide structural support for the endothelial cells that line the venous sinus and the developing blood cells within the hematopoietic cord. The cytoplasm of the reticular cells is capable of extending itself in fiberlike strands deep into the hematopoietic cords. These strands provide a meshwork for the blood cells. Other types of cells which furnish support in the cord include macrophages and fat cells. | View Page |
| Location of Cells within Cord Within the hematopoietic cords each cell line has a specific location for development.
Erythroid precursors are located near a venous sinusoid and cluster around a macrophage. This is referred to as an erythroblastic island. Developing red cells obtain iron needed for hemoglobin production from macrophages.
Megakaryocytes are also located close to a venous sinus. They extend their cytoplasm in fingerlike projections through the sinus wall in order to release their platelets directly into the blood in the sinus.
Immature granulocytes lie within the hematopoietic cords.
The metamyelocyte stage is the first stage of the granulocyte series that is motile and able to move toward the sinus area. Mature neutrophils, eosinophils and basophils enter the sinusoidal blood through the basement membrane. As maturing erythrocytes also move toward the sinus wall any remaining nuclei are lost as the red cells move through small openings in the cells lining the sinus wall. | View Page |
| Location of Cells within Cord continued Another representation of the cells in a hematopoiectic cord which focuses in the appearance of various cells as well as their location within the cord is shown here.
HC: hematopoiectic cordVS: venous sinusAdv: adventitial cellEnd: endothelial cellGP: granulopoiesisF: fat cellsEi: erythroipoietic islandHist: histiocyte (macrophage)Meg: megakaryocyteA: arteriole | View Page |
| Which of the following statements are true for the blood vessel/sinus compartment of the bone marrow? (Choose ALL of the correct answers) | View Page |
| Venous sinuses alternate with hematopoietic cords in a spokelike pattern. | View Page |
| Sinuses/Blood Vessels Circulating blood enters the bone through the central artery which branches out into small arterioles. These arterioles are interspersed in the cords of hematopoietic tissue. The arterioles drain into venous sinuses (space or cavity). Sinuses have a basement membrane which is lined by endothelial cells within the sinus and surrounded by reticular (e.g. adventitial) cells on other side. Blood from several venous sinuses may combine in a collecting sinus which leads to a central vein. The venous sinuses alternate with hematopoietic cords in a spokelike pattern with the central vein as the core. | View Page |
| Tourniquets Tourniquets wrap around the arm to increase venous pressure, and fill the veins, so that they are easier to see, feel, and puncture.
They can be made of latex, Velcro, or other material.
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| Applying the tourniquet Tie the tourniquet just above the elbow.The tourniquet should be tight enough to stop venous blood flow in the superficial arm veins. | View Page |
| Butterfly needle - Butterfly needle collections Butterfly needles (also known as a winged infusion set), are available in smaller gauges, and are used to draw venous blood from children, and adults with difficult veins.
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| Heelstick - Pediatric collection procedures: Introduction Veins of small children and infants are too small for venipuncture;Safety Lancets are used to puncture the skin and collect capillary blood.Butterfly needles may be used to collect venous blood in older children.
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| Hollister system: specimen collection and labeling Positively identify the patient in the usual manner.Collect a venous blood specimen in a red top tube.Complete the specimen label and the detachable armband stub before removing them from the card.Initial, date, and time the stamped specimen label (shown on upper right), and attach it securely to the blood specimen. | View Page |
| What is phlebotomy? Phlebotomy, also known as venipuncture, means collecting blood from veins.Phlebotomists, by definition, collect venous blood, but perform a variety of other important medical tasks as well. | View Page |
| What is a phlebotomist? [continued] An experienced phlebotomist should be knowledgeable in the collection of:
- Venous blood specimens
- Capillary blood specimens
- Blood culture specimens
- Urine specimens
- Throat cultures, and
- Medico legal specimens requiring chain of custody.
He or she should also know how to:
- Process specimens
- Perform bleeding times, and
- Collection specimens from IV lines and central venous lines, under appropriate supervision.
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| Circulation: venous portion Deoxygenated (venous) blood flows from tiny capillary blood vessels within the tissues via progressively larger veins to the right side of the heart.Blood is routinely drawn from veins, but may also be drawn from arteries, or capillaries.
Illustration this screen from LifeArt Collection 2000, with permission. © Lippincott Williams & Wilkins.
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| Administration of glucose Collect venous blood for a fasting glucose level.Give the patient a standard dose of glucose, usually in the form of a beverage such as Glucola™ (Allegiance). Always follow your own procedure manual.
In general:Give a 50 gram glucose dose to screen pregnant women at 28 weeks for gestational diabetes.Give a 75 gram glucose dose to nonpregnant adults.Give a 100 gram glucose dose to confirm the diagnosis of gestational diabetes. | View Page |