The ORLocate® aligns with the AORN recommended practices (updated July 2010)
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RP I |
A consistent multidisciplinary approach for preventing RSIs should be used during all surgical and invasive procedures
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The ORLocate® system provides a consistent multidisciplinary approach for all surgical and invasive procedures.
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RP II |
Radiopaque surgical soft goods (e.g., sponges, towels, textiles) opened onto the sterile field should be accounted for during all procedures for which soft goods are used
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The ORLocate® constantly monitors, tracks and counts all tagged soft goods before, during and at the end of the surgical procedure.
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RP III |
Sharps and other miscellaneous items that are opened onto the sterile field should be accounted for during all procedures for which sharps and miscellaneous items are used.
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The ORLocate® provides a user-friendly method to accommodate tracking untagged items using a manual count procedure
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RP IV |
Instruments should be accounted for on all procedures in which the likelihood exists that an instrument could be retained.
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The ORLocate® counts, tracks and monitors the location of all tagged surgical instruments before, during and at the end of the surgical procedure to reconcile the initial and final instrument count. |
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RP VI |
Standardized measures for investigation and reconciliation of count discrepancies should be taken during the closing count and before the end of surgery. When a discrepancy in the count(s) is identified, the surgical team should carry out steps to locate the missing item.
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In the event of a non-reconciled count, the ORLocate® mobile locator is used to locate the missing sponge/s or instrument/s and reconcile the final count. The ORLocate® prohibits the closing of a procedure if any tagged item is missing
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RP VII |
Preoperative staff members may consider the use of adjunct technologies to supplement manual count procedures.
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The ORLocate® is an adjunct technology. In fact, ORLocate® is the only RFID-based technology on the market that counts, monitors and tracks surgical instruments and sponges before, during and after a procedure to increase patient safety and reduce the occurrence of retained surgical items. |
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RP VIII |
Personnel should receive initial and ongoing
education and demonstrate competency in the performance of standardized measures to prevent RSIs.
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The ORLocate® team will help OR teams with training on best practices to reduce retained surgical items. Ongoingeducation is an integral part of the
ORLocate and hospital partnership
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RP IX |
Measures taken for the prevention of RSIs should be documented in the patient’s medical record.
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The ORLocate® provides information on the initial count of tagged instruments and sponges and non-tagged items. The system documents when and what additional items were added to the initial count and the final count reconciliation. A report can then be generated by a circulating nurse to be included in a patient’s medical record.
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RP X |
Policies and procedures for the prevention of RSIs and unretrieved device fragments should be developed, reviewed periodically, revised as necessary, and readily available in the practice setting.
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The ORLocate® provides manuals and other documents that support hospitals in better outlining their policies and procedures.
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RP XI |
A quality assurance/performance improvement process should be in place to evaluate the incident and risks of RSIs and to improve patient safety. |
Verification and validation results, as well as usability results and other data captured and produced by the ORLocate®, can be included in the documentation to support quality assurance efforts. |