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Get the free LAB-GRAM #1: REDUCING SPECIMEN DISCREPANCIES - med navy

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This document provides guidelines for reducing discrepancies in urine specimen submissions to the Navy Drug Screening Laboratory, emphasizing quality assurance processes for accurate testing and compliance
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How to fill out LAB-GRAM #1: REDUCING SPECIMEN DISCREPANCIES

01
Identify the specimen to be documented.
02
Ensure all specimen information is accurate, including patient name, ID number, and date of collection.
03
Fill in the type of specimen collected, specifying any pertinent details.
04
Include the reason for the specimen collection as required.
05
Verify that the collection method and any relevant handling instructions are correctly noted.
06
Double-check all entries for clarity and accuracy to prevent discrepancies.
07
Sign and date the LAB-GRAM after completing the entries.

Who needs LAB-GRAM #1: REDUCING SPECIMEN DISCREPANCIES?

01
Laboratory personnel involved in specimen collection and processing.
02
Healthcare professionals responsible for ordering tests.
03
Quality assurance teams monitoring specimen integrity.
04
Department managers overseeing laboratory operations.
05
Anyone involved in research or clinical trials requiring accurate specimen documentation.
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Exceptional healthcare, personally delivered. Before a sample is collected ALWAYS check the patient's identity to ensure the sample is collected from the correct patient. Ensure the correct bottle is selected for the test(s) requested. Avoid haemolysis. Use the correct order of draw.
Enforce Periodic Quality Audits for Proper Labeling Be sure the label has the correct patient name, patient information, contents, and specimen source. Avoid handwritten labels, since legibility is essential, and misinterpreting handwriting can greatly impact patient safety.
What Should You do When You Encounter a Mislabeled Specimen First, notify the right people. Attempt to re-trace and re-label the specimens. Review what went wrong and correct it.
Mislabeled specimens occur frequently in healthcare and result in significant cost to the institution. Some specimen loss or mislabeling events can lead to catastrophic outcomes such as consequential delays in cancer diagnoses, or unnecessary major surgical procedures.
Enforce Periodic Quality Audits for Proper Labeling Be sure the label has the correct patient name, patient information, contents, and specimen source. Avoid handwritten labels, since legibility is essential, and misinterpreting handwriting can greatly impact patient safety.

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LAB-GRAM #1: REDUCING SPECIMEN DISCREPANCIES is a guideline designed to minimize errors and inconsistencies in the handling and processing of laboratory specimens.
Laboratory personnel involved in the collection, handling, and processing of specimens are required to file LAB-GRAM #1: REDUCING SPECIMEN DISCREPANCIES.
To fill out LAB-GRAM #1, individuals should provide complete and accurate information concerning the specimen collection process, including the type of specimen, collection date, and any discrepancies noted.
The purpose of LAB-GRAM #1 is to provide standardized procedures aimed at reducing discrepancies and improving the accuracy and reliability of laboratory test results.
The information that must be reported includes specimen identification details, collection methods, any observed discrepancies, and corrective actions taken.
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