Transcript Chapter 5x

Chapter 5
DOCUMENTATION,
SPECIMEN HANDLING,
AND TRANSPORTATION
Documentation Basics
• Clinical/Medical Record or Electronic Medical Record
– Monitoring the quality of care
– Coordination of care
– Accrediting, licensing, research
– Legal protection
Medical Record Documentation
• The Five C’s:
– Concise– Complete– Clear– Correct– Chronologic
Reporting Errors
• Report immediately
• Include all relevant information
• Document errors & corrective actions according to facility’s policy
• Be accurate and legible
• Correct errors, but do not falsify or delete records
Documentation Basics
• Policies and Procedures
– All health care facilities have manuals that detail operating procedures to be followed.
– Health care workers may be involved in developing, writing, and practicing these procedures.
– Examples: Safety, Infection Control, QC& Preventive Maintenance, etc.
Laboratory Test Requisitions and Labels
• Transmittal of the Test Request to the Laboratory
– On-line interactive computer system
– Manual request system
• Laboratory Test Requisition Forms
– Multiple-part requisition may serve as a temporary request until the formal request can be entered into a
computer system.
– In a manual system, the multipart request forms are more subject to human error.
• Patient identification (name, unique registration or identification number, location)
• Patient’s gender, date of birth or age
• Name of physician or legally authorized person ordering the test
• Tests requested
• Time and date of specimen collection• Source of specimen• Other pertinent clinical information
when appropriate
• A “STAT” Request– In cases of emergency– Document the request appropriately
Specimen Labels and Blood Collection Lists
• Accurate specimen identification must continue from collection through disposal.
• Identification methods vary from manually copying information onto the container to using pre
numbered, bar-coded labels.
• Labeling systems can imprint a patient identification card or electronically print on to the specimen
label.
• Computer-Generated Labels Include:– Patient identification– Tests requested– Specimen collection
tubes– Transfer labels for aliquots– Accession numbers or sample numbers– Blood drawing list
• Bar Codes– Series of light and dark bands that relate to alphanumeric symbols (i.e., numbers and
letters)– When bands are placed together in a series, they can correspond to a name (patient or test) or a
number(identification or test code)– Very accurate and fast
• Radio Frequency Identification (RFID)– Silicon chip provides ID Tag– Data is transmitted to wireless
receiver– Does not require “line-of-sight”– Can track many items simultaneously
• Biometrics– Fingerprints– Face recognition– Voice prints– Iris patterns– Retinal vascular patterns–
Digitized verification
Specimen Handling and Transport
• Specimen Integrity Affected by:
– Method of transport
– Timing delays
– Temperature
– Movement/agitation
– Exposure to light
– Centrifugation methods
Centrifugation
– Not all specimens need to be centrifuged–
Standards for handling and processing of blood samples during pre-centrifugation,
centrifugation, and post-centrifugation
Specimen Handling and Transport
• Specimen Transportation Guidelines
– Leak-proof plastic bag for enclosing and transporting the specimen container.
– Transport bag may have a pouch on the outside for the laboratory request slip, thus eliminating potential
contamination.
– If possible, maintain the blood specimens in evacuated tubes and micro collection tubes in a vertical
position to promote complete clot formation and reduce the possibility of hemolysis.
– Handle blood specimens gently to reduce chances of hemolysis.
– Transport specimens as soon as possible to the clinical laboratory.
– Serum can remain at room temperature for testing, be refrigerated, be stored in a dark place, or be frozen
depending on the prescribed laboratory method.
– If from remote ambulatory sites, including home health collections, follow safe handling guidelines set in
standard precautions.
– Use an enclosed or lockable container.
– Notification procedures and a biohazard label should be on the container in case of an accident.
– Use cold packs in the container during hot weather
– The vehicle should be heated in freezing weather
Specimen Handling and Transport
• Chilled Specimens
– Fastrin
– Ammonia
– Lactic acid
– Catecholamine’s
– Parathyroid hormone
– Pyruvate
– Commercially available cool pack.
– An airtight container and ice water decrease the loss of gases from the specimen
being tested for blood gases.
– It is important to use ice water rather than solid chunks of ice; otherwise, parts of
the specimen may freeze and hemolysis will result.
Specimen Handling and Transport
Protecting Specimens from Light
• Bilirubin
• Vitamin B12
– beta-carotene
– porphyrins
– Some chemical constituents in blood, such as bilirubin, are photosensitive and decompose if exposed to
light.
– Blood collected for light-sensitive chemical analysis should be protected from bright light with an ambercolored transport bag or aluminum foil wrapping around the tube.
• Microbiological Specimens
– Blood and urine specimens for microbiological culture need to be transported to the laboratory as quickly as
possible so that the blood can be transferred to culture media and the urine analyzed.
– Specimens for blood cultures can also be collected directly into culture media, which minimizes possible
contamination and speeds the contact with the culture media.
• Warmed Specimens
– Specimens that require warming (to body temperature, 37°C) include
those for testing cold agglutinins and cryo fibrinogen.
Specimen Delivery Methods
• Courier services
• Hand delivery
• Pneumatic Tube Systems are used to transport most specimens, patient records, messages, letters,
bills, medications, x-rays, and laboratory test results.
• Transportation by Automated Vehicles uses a small motorized and/or computerized container car
attached to a network of track that is routed to appropriate sites in the laboratory and nursing stations.
Specimen Storage
• Avoid time delays whenever possible.
• Reduce turn around time (TAT) without jeopardizing safety.
• Follow manufacturer and testing guidelines.
• CLSI—Remove cells from serum or plasma in 2 hours.
• Delays in testing can have significant effects on results.
Factors for Sample Rejection
• Test request does not match labels
• Label is unreadable, partially destroyed, missing
• Anticoagulated tube has clotted
• Excessive delays
• Hemolysis
• Improper transport or storage temperature• Improper blood volume in additive tube
• Lipemic blood
• Non-fasting
• Outdated supplies were used
• Effects of posture on analyte
• Timed specimens drawn at the wrong time
• Contaminated
After Sample Rejection
• The patient may have to undergo another venipuncture or another trip to the clinic.
• The health care worker who drew the specimen and a supervisor should try to solve the problem
initially.
• Errors should be acknowledged and documented with corrective actions.
• Criterion for rejection and follow-up actions should be established by each laboratory