Clinical Chemistry and Autoverification: A Path Less Traversed

Aims and background: Autoverification (AV) is an application of artificial intelligence that uses computer-based algorithmically established rules for release of patient reports. This allows effective time management, prevents probable laboratory errors, and ensures consistent results. However, not...

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Main Authors: Rashmi Rasi Datta, Anurag Bansal
Format: Article
Language:English
Published: Jaypee Brothers Medical Publisher 2024-05-01
Series:Indian Journal of Medical Biochemistry
Subjects:
Online Access:https://www.ijmb.in/doi/IJMB/pdf/10.5005/jp-journals-10054-0233
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author Rashmi Rasi Datta
Anurag Bansal
author_facet Rashmi Rasi Datta
Anurag Bansal
author_sort Rashmi Rasi Datta
collection DOAJ
description Aims and background: Autoverification (AV) is an application of artificial intelligence that uses computer-based algorithmically established rules for release of patient reports. This allows effective time management, prevents probable laboratory errors, and ensures consistent results. However, not many labs have adopted AV into practice due to hesitations concerning cost-effectiveness, lack of robust software and informatics support along with dearth of knowledge for its implementation. Additionally, there is scant published literature on AV implementation. This study has been conducted as an attempt to outline benefits of AV and address the existing gaps. Methods: The study was conducted in the Department of Clinical Chemistry of a standalone lab. Autoverification implementation was done in stepwise manner. (i) Test selection and developing algorithms, (ii) Setting-up rules in middleware to prevent release of erroneous results, (iii) User acceptance testing (UAT), (iv) Going-live. Results: Efficacy of AV system was gauged based on following factors. (i) AV passing rate—initial 53.7–85.4% later was achieved with inclusion of more parameters and extension of tolerance limit, (ii) Significant improvement was observed in TAT for both immunoassay (from 88.28 to 97.32%) and routine chemistry (from 82.7 to 95.68%), (iii) decreased error rates as evidenced by reduced number of amended reports, (iv) reduction in staff required for manual verification allowing their utilization for other departmental activities. Conclusion: Implementation of AV by laboratories provides efficient and cost-effective work opportunities with scope for continuous growth. However, it doesn’t preclude the need for careful quality control.
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spelling doaj-art-218af6c41f0a4101b235fbaa675ba31e2025-01-03T07:49:03ZengJaypee Brothers Medical PublisherIndian Journal of Medical Biochemistry2456-51642024-05-0128240010.5005/jp-journals-10054-02331Clinical Chemistry and Autoverification: A Path Less TraversedRashmi Rasi Datta0https://orcid.org/0000-0001-5485-1191Anurag Bansal1Rashmi Rasi Datta, Department of Clinical Chemistry, Agilus Diagnostics, National Reference Lab, Gurugram, Haryana, India, Phone: +91 9711310093Department of Pathology, National Reference Lab, Gurugram, Haryana, IndiaAims and background: Autoverification (AV) is an application of artificial intelligence that uses computer-based algorithmically established rules for release of patient reports. This allows effective time management, prevents probable laboratory errors, and ensures consistent results. However, not many labs have adopted AV into practice due to hesitations concerning cost-effectiveness, lack of robust software and informatics support along with dearth of knowledge for its implementation. Additionally, there is scant published literature on AV implementation. This study has been conducted as an attempt to outline benefits of AV and address the existing gaps. Methods: The study was conducted in the Department of Clinical Chemistry of a standalone lab. Autoverification implementation was done in stepwise manner. (i) Test selection and developing algorithms, (ii) Setting-up rules in middleware to prevent release of erroneous results, (iii) User acceptance testing (UAT), (iv) Going-live. Results: Efficacy of AV system was gauged based on following factors. (i) AV passing rate—initial 53.7–85.4% later was achieved with inclusion of more parameters and extension of tolerance limit, (ii) Significant improvement was observed in TAT for both immunoassay (from 88.28 to 97.32%) and routine chemistry (from 82.7 to 95.68%), (iii) decreased error rates as evidenced by reduced number of amended reports, (iv) reduction in staff required for manual verification allowing their utilization for other departmental activities. Conclusion: Implementation of AV by laboratories provides efficient and cost-effective work opportunities with scope for continuous growth. However, it doesn’t preclude the need for careful quality control.https://www.ijmb.in/doi/IJMB/pdf/10.5005/jp-journals-10054-0233algorithmsautomationautoverificationclinical chemistrylaboratory information systemsturn-around-time
spellingShingle Rashmi Rasi Datta
Anurag Bansal
Clinical Chemistry and Autoverification: A Path Less Traversed
Indian Journal of Medical Biochemistry
algorithms
automation
autoverification
clinical chemistry
laboratory information systems
turn-around-time
title Clinical Chemistry and Autoverification: A Path Less Traversed
title_full Clinical Chemistry and Autoverification: A Path Less Traversed
title_fullStr Clinical Chemistry and Autoverification: A Path Less Traversed
title_full_unstemmed Clinical Chemistry and Autoverification: A Path Less Traversed
title_short Clinical Chemistry and Autoverification: A Path Less Traversed
title_sort clinical chemistry and autoverification a path less traversed
topic algorithms
automation
autoverification
clinical chemistry
laboratory information systems
turn-around-time
url https://www.ijmb.in/doi/IJMB/pdf/10.5005/jp-journals-10054-0233
work_keys_str_mv AT rashmirasidatta clinicalchemistryandautoverificationapathlesstraversed
AT anuragbansal clinicalchemistryandautoverificationapathlesstraversed