Capillary fragility can be described as either weak or strong, with thin capillaries being fragile and prone to rapture, while thick capillaries are strong and can withstand pressure.
Capillaries are smaller than arteries or veins, but a little bit bigger than arteriole.
Vascular fragility particularly affects the capillary as it belongs to the vascular system.
The capillary fragility test measures the ability of small capillaries to retain blood when subjected to increased stress, such as hydrostatic pressure and anoxia.
Increased stress in the capillary fragility test includes pressure of 100mmHg for 5 minutes.
Applying in vitro pressure in the arm can constrict blood vessels, increasing intravascular pressure (blood pressure).
The capillary fragility test is a non-specific evaluation to measure capillary weakness and deficiencies in platelet number and function.
Decreased capillary resistance causes the capillaries to rupture, leading to bleeding and the formation of petechiae.
If positive for petechiae in the capillary fragility test, it indicates capillary weakness, thrombocytopenia, or both.
Repeated skin trauma can lead to increased vascular fragility.
Vitamin C deficiency is important for the immune system and helps in the integrity of blood vessels, making the blood flow smooth.
Purpuras and hemorrhage (bleeding) are signs of increased vascular fragility.
Interpretation of the Rumpel-Leede tourniquet test involves examining the forearm, hands, and fingers for the presence of petechiae, and noting the number and location of petechiae.
Platelets are thin disks, 2-4 µm in diameter and 5-7 fL in volume.
Platelets are 1/10 of the size of the RBC.
Normal platelet count is 150,000–450,000/uL.
Platelets function primarily in hemostasis and in maintaining capillary integrity.
Light Microscopy Method: Tocantin’s Method uses Rees-Ecker reagent, sodium citrate as anticoagulant, and Brilliant Cresyl Blue to stain the platelets.
Abnormally low platelet count is less than 100,000/uL.
The total volume of the entire grid of Hemocytometer is 0.9mm3.
PLT⁄cumm is the formula for platelet count, calculated by the number of platelets counted in 4 squares times the dilution factor (DF) times the volume correction factor (VCF).
VCF is calculated by dividing 1mm2 by the volume of one square used multiplied to the number of squares used.
Purpose of platelet count: to confirm if the patient is really suffering from thrombocytopenia or thrombocytosis.
Bleeding possible platelet count is 30,000–50,000/uL.
Severe spontaneous bleeding platelet count is less than 5,000/uL.
Criteria for a good diluent are that it should prevent platelet adherence to glass, should prevent platelet aggregation, should not promote premature platelet lysis, and should make platelets visible in microscope.
DF is calculated by dividing the total volume by the volume of the sample used.
Platelet numbers must be sufficient for them to play their supportive role in hemostasis.
When evaluating a bleeding problem that may be traceable to platelets, the counting of platelets is an important and logical starting point.
Spontaneous bleeding platelet count is less than 30,000/uL.
Levy chamber with improved Neubauer ruling is a feature of Hemocytometer.
Two factors that affect capillary fragility: genetics and platelet.
Phase-Contrast Microscopy Method: Brecker-Cronkite Method uses 1% NH4 oxalate as diluent, EDTA as sample, and counts platelets in 5 R squares.
HEMOCYTOMETER is an instrument used to count blood cells.