Roche Infinity Patient Results Review Delta Check, Critical values, serum indices, auto dilution
Delta Check
- Access the patient's laboratory results history.
- Compare current results to previous results side by side.
- Identify any significant differences exceeding the predefined thresholds.
- Note the nature and direction of changes (increase/decrease).
- Locate the timestamp for each laboratory test.
- Verify the chronological order of tests.
- Ensure that both tests are from the same laboratory or testing method.
- Document any discrepancies in timing.
- Refer to established clinical guidelines for delta check limits.
- Cross-check current results against these limits.
- Highlight any results that fall outside acceptable ranges.
- Consult with the lab or clinical guidelines if unsure.
- Record all significant findings in the patient's file.
- Include details of the results compared and the implications.
- Notify relevant healthcare providers of significant changes.
- Ensure documentation is clear and accessible for future reference.
Critical Values
- Review patient results for critical value thresholds.
- Use the laboratory's critical value list for reference.
- Highlight or mark results that meet critical criteria.
- Double-check values for accuracy to prevent false alerts.
- Use established communication channels (phone, pager).
- Provide the healthcare provider with patient details.
- Clearly communicate the critical result and its implications.
- Confirm receipt of the information with the provider.
- Document the exact time and date of notification.
- Use the patient's chart or electronic health record.
- Ensure the entry is clear and legible.
- Include the name of the healthcare provider notified.
- Review any follow-up actions taken post-notification.
- Document interventions or changes in treatment plan.
- Include any additional tests or consultations ordered.
- Maintain accuracy and timeliness in documentation.
Serum Indices
- Review test results for serum indices.
- Identify any flags indicating abnormalities.
- Classify abnormalities as hemolysis, icterus, or lipemia.
- Record and communicate any significant findings.
- Check patient history for potential causes.
- Consult with laboratory personnel if needed.
- Evaluate sample handling and storage conditions.
- Confirm the integrity of the sample prior to testing.
- Assess the degree of abnormality in indices.
- Determine if retesting is clinically warranted.
- Follow laboratory protocols for repeat testing.
- Document the rationale for retesting.
- Record all observed serum indices and interpretations.
- Note any communication with healthcare providers.
- Include details of any repeat tests conducted.
- Ensure documentation is clear and accessible.
Auto Dilution
- Access the patient results report.
- Identify any results marked with a dilution flag.
- Cross-reference with the original sample values.
- Ensure correct identification of diluted results.
- Locate the dilution factor in the report.
- Verify the factor applied matches the protocol.
- Ensure documentation is clear and accessible.
- Record any comments regarding the dilution process.
- Compare diluted results to established reference ranges.
- Document any out-of-range findings.
- Consult with relevant guidelines for threshold values.
- Flag any results needing further investigation.
- Identify and document any inconsistencies.
- Determine the significance of discrepancies.
- Follow escalation protocol as per guidelines.
- Communicate findings to the appropriate personnel.
Use in Manifestly