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Chapter 40 - Verification of Specimen Identity by Double Checking with a Witness

from Section 9 - Quality Management

Published online by Cambridge University Press:  07 August 2023

Markus H. M. Montag
Affiliation:
ilabcomm GmbH, St Augustin, Germany
Dean E. Morbeck
Affiliation:
Kindbody Inc, New York City
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Summary

In our laboratory, we currently perform verification of specimen identity (VSI) by having two laboratory personnel independently check and verify the identity of each patient, gamete specimen and embryo at each step that is susceptible to a mismatch so that we can assure accurate and complete traceability throughout the processes. Since this is the system currently in place in our laboratory, this method of verification and witnessing is the main focus of discussion in this chapter. In the future, we plan to implement an electronic witnessing system following as recommended by Chapman (2019).

Type
Chapter
Information
Principles of IVF Laboratory Practice
Laboratory Set-Up, Training and Daily Operation
, pp. 293 - 300
Publisher: Cambridge University Press
Print publication year: 2023

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References

Chapman, C. W. Witnessing in ART – Has the time come to utilize technology? Col Reprod Biol Newsletter 2019; 8(2).Google Scholar
De los Santos, M. J. and Ruiz, A. Protocols for tracking and witnessing samples and patients in assisted reproductive technology. Fertil Steril 2013; 100:1499–502.CrossRefGoogle ScholarPubMed
Brison, D. R., Hooper, M., Critchlow, J. D., et al. Reducing risk in the IVF laboratory: implementation of a double witnessing system. Clin Risk 2004; 10:176–80.CrossRefGoogle Scholar
Jarman, H., Jacobs, E. and Zielinski, V. Medication study supports registered nurses’ competence for single checking. Int J Nurs Pract 2002; 8:330–5.CrossRefGoogle ScholarPubMed
Thornhill, A. R., Orriols Brunetti, X. and Bird, S. Measuring human error in the IVF laboratory using an electronic witnessing system, in Proceedings of the 17th World Congress on Controversies in Obstetrics, Gynecology & Infertility (COGI ’13), pp. 101–6 (Lisbon, Portugal: Monduzzi Editoriale, 2013).Google Scholar
Rienzi, L., Bariani, F., Dalla Zorza, M., et al. Failure mode and effects analysis of witnessing protocols for ensuring traceability during IVF. Reprod Biomed Online 2015; 31:516–22.Google Scholar
Toft, B. and Mascie-Taylor, H. Involuntary automaticity: a work-system induced risk to safe health care. Health Serv Manage Res 2005; 18:211–16.CrossRefGoogle ScholarPubMed
Armitage, G. Double checking medicines: Defense against error or contributory factor? J Eval Clin Pract 2007; 14:513–19.Google Scholar
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Novo, S., Nogues, C., Penon, O., et al. Barcode tagging of human oocytes and embryos to prevent mix-ups in assisted reproduction technologies Hum Reprod 2014; 29(1):1828.CrossRefGoogle ScholarPubMed

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