f Flashcards

1
Q

Blood Collection Additive Forms

A
  1. Liquid
  2. Spray-dried
  3. Powder forms – powdered additives should be tapped prior to use to settle the additive to the bottom of the tube
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2
Q

How many times must an additive tube be gently inverted?

A

3 to 10 times, depending on the type of additive and the manufacturer

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3
Q

How many degrees does each inversion require?

A

180 degrees and back again turning the wrist

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4
Q

What should you never do in line with additive forms?

A

Never shake or otherwise vigorously mix a specimen, as this can cause hemolysis, which makes most specimens unsuitable for testing.

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5
Q

Different Additive Types in Blood Collection Additives:

A
  1. Anticoagulants
  2. Special-use anticoagulants
  3. Antiglycotic agents
  4. Clot activators
  5. Thixotropic gel separator
  6. Trace element-free tubes
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6
Q
  • prevents blood from clotting through chelating (or binding) or precipitating calcium so it is unavailable to the coagulation process; inhibition of thrombin formation needed to convert fibrinogen to fibrin in the coagulation cascade.
  • Common examples: Ethylenediaminetetraacetic acid (EDTA),
    Citrates, Heparin and Oxalates
A

Anticoagulants

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7
Q
  • These are combined with other additives and have additional properties for special-use situations
  • Examples: Acid Citrate Dextrose (ACD); Citrate Phosphate Dextrose (CPD); Sodium Polyanethol Sulfonate (SPS)
A

Special-use Anticoagulants

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8
Q
  • Substance that prevents glycolysis (breakdown or metabolism of glucose/blood sugar by blood cells)
  • If glycolysis is not prevented, the glucose concentration in a blood specimen decreases at a rate of 10 mg/dl per hour
  • Glycolysis occurs faster in newborns because of increased metabolism and in patients with leukemia because of high metabolic activity of WBCs
  • Example: Sodium fluoride
A

Antiglycotic Agents

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9
Q
  • Enhances coagulation in tubes used to collect serum specimens
  • Includes: Silica (glass) particles, Thrombin
A

Clot Activators

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10
Q
  • Inert (non-reacting) synthetic substance initially contained in or near the bottom of certain blood collection tubes
  • Gel density is between cell and serum/plasma.
  • When a specimen in a gel tube is centrifuged, the gel undergoes a change in viscosity and moves to position between the cells and serum/plasma → barrier
A

Thixotropic gel separator

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