Amending Reported Results
Amending Reported Results
Amending Reported Results
Classification :
Hospital-Wide Multidisciplinary Departmental
New Revised Renewed
PURPOSE:
To provide the laboratory staff with guidelines for amending or correcting an issued laboratory
results.
RESPONSIBILITIES:
• Reporting any erroneous result to the senior/deputy lab director or lab director, and doing
all efforts to investigate & collection of data as per the designed quality indicator, correct
the result in collaboration with Quality Manager.
1. DEFINITIONS:
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Unit:
LABORATORY DEPARTMENT Number: LAB/P/D026 ED#1
2. POLICY:
2.1. Whenever it becomes evident that erroneous laboratory test results have been reported,
an amended report must be completed with all corrections and the reason for error clearly
documented.
2.2. While the report is the end result of the testing process, the reasons for the release of an
erroneous report must be investigated whether pre-analytical phase, from test ordering
to specimen collection and handling, through the analytical phase
(instruments/reagents/staff competency), to the post-analytic phase that includes
verification of the HMIS for automated and manual results transfer. All these indicates a
problem that may involve the core issues of oversight, training, communication and
documentation.
3. PROCEDURE
3.1 Report the final corrected result, and mention clearly the previous/errors result as erroneous
and the new final result as amended/corrected result in the report.
3.2 Immediately after recognizing an erroneous result has been reported: Contact the individual
who received the original report and notify about the amendment.
3.3 When possible, retest the original specimen to obtain the correct result copy of the
erroneous report will be printed before any correction is made on the HMIS system.
3.4 The correction is made by hand on the copy, dated & signed by the person who made the
correction. If the original report is available, document on the report that the
original/previous result was in error.
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Unit:
LABORATORY DEPARTMENT Number: LAB/P/D026 ED#1
3.5 The correct result is entered to the HMIS system & printed promptly. The lab
Director/Designee will review both reports, supporting data e.g. Instrument printouts etc. &
3.7 All original & corrected reports will be maintained permanently in the corrected reports file.
3.8 Reported patient errors will be handled according to the Corrective and Preventive Action
Procedure.
3.9 All released/ verified results found to be erroneous must be reported to the ordering
physician as soon as possible to minimize the potential adverse impact on patient
management. The physician must be informed that once the error has been investigated the
3.10 All corrected results must be called to the ordering physician as soon as the results are
repeated and confirmed, all relevant quality control records have been reviewed and
checked ensuring that the quality control have been performed according to established
policy and controls are within acceptable analytical ranges and the laboratory director/
3.11 The previous test results/ information and the revised results/ information must be identified
3.12 The corrected reports guidelines as detailed above apply to all results and patient data
performed in the laboratory and any correction of any patient data must be informed either
verbally by phone and electronic laboratory report through HMIS as a part of general reporting
requirements
4 RESOURCES
CBAHI, CLSI, CAP
5 CROSS REFERENCES
6 REFERENCES
6.1 NCCLS, Using Proficiency Testing to Improve the Clinical Laboratory, Approved
Guideline GP27- A.
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Unit:
LABORATORY DEPARTMENT Number: LAB/P/D026 ED#1
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