Implementation of Laboratory Review of Test Builds Within the Electronic Health Record Reduces Errors
* Context.--As electronic health records (EHRs) become more ubiquitous, physicians have come to expect that laboratory data from a variety of sources will be incorporated into the EHR in a structured format. The Clinical Laboratory Improvement Amendments have standards for data transmission traditio...
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Published in | Archives of pathology & laboratory medicine (1976) Vol. 144; no. 6; p. 742 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
College of American Pathologists
01.06.2020
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Subjects | |
Online Access | Get full text |
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Summary: | * Context.--As electronic health records (EHRs) become more ubiquitous, physicians have come to expect that laboratory data from a variety of sources will be incorporated into the EHR in a structured format. The Clinical Laboratory Improvement Amendments have standards for data transmission traditionally met by pathologist review of their own hospital laboratory information system transmissions. However, with third-party laboratory data now being sent through external (nonhospital laboratory) interfaces, ownership of this review is less clear. Lack of an expert laboratory review process prior to changes being implemented can result in mapping and interfacing errors that could lead to misinterpretation and diagnostic errors. (Arch Pathol Lab Med. 2020;144:742-747; doi: 10.5858/arpa.2019-0239-0A) |
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ISSN: | 1543-2165 1543-2165 |
DOI: | 10.5858/arpa.2019-0239-0A |