Get the free Point-of-care measurement of activated clotting time for ... - policyandorders cw bc
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Provincial Health Services AuthorityIdentifier:
Folder:
Subfolder:CPC ACT 0175
CW POST
ACTHemochron Activated Clotting Time Low Range Procedure for EELS
Version #:
2
Type:
Procedure (3yr)
Effective
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How to fill out point-of-care measurement of activated
How to fill out point-of-care measurement of activated
01
Ensure the testing device is properly calibrated.
02
Collect a small blood sample from the patient using a finger stick or venous blood draw.
03
Follow the manufacturer's instructions for loading the sample onto the testing device.
04
Wait for the results to be displayed on the screen of the testing device.
05
Record the activated clotting time measurement in the patient's medical record.
Who needs point-of-care measurement of activated?
01
Patients who are at risk of excessive bleeding or clotting disorders.
02
Patients undergoing surgery or other invasive procedures.
03
Patients receiving anticoagulant therapy.
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What is point-of-care measurement of activated?
Point-of-care measurement of activated is a test carried out at the patient's bedside to determine the level of coagulation or anticoagulation.
Who is required to file point-of-care measurement of activated?
Healthcare professionals such as doctors, nurses, and laboratory technicians are required to perform and document point-of-care measurement of activated.
How to fill out point-of-care measurement of activated?
Point-of-care measurement of activated is filled out by entering the test results and patient information in the designated form or electronic system.
What is the purpose of point-of-care measurement of activated?
The purpose of point-of-care measurement of activated is to quickly assess a patient's coagulation status and determine the appropriate course of treatment.
What information must be reported on point-of-care measurement of activated?
The information reported on point-of-care measurement of activated includes the test results, patient identification, date and time of the test, and any relevant patient history.
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