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Critical Values - Mayo Medical Laboratories

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7. If this information is not included in the “readback”, specifically request it.<br />

III. Communication and Documentation of <strong>Critical</strong> Test Results to the ordering provider or designee<br />

A. Every attempt is made to speak to the ordering provider or designee. If the ordering provider is not available the<br />

result may be given to another Physician/PA/APRN or his/her designee.<br />

1. A phone call is immediately placed to the ordering provider for notification. An RN/LPN must communicate the<br />

result directly to the ordering provider or his/her designee.<br />

2. Document the time and the name of the caregiver to whom the result was reported in the patient record.<br />

3. Any telephone orders that result from the report of a critical test result to the Physician/PA/APRN should use the<br />

“readback” verification process.<br />

B. If there is an existing physician order for a protocol (ex. Insulin, Heparin) that provides direction for nursing or<br />

pharmacist intervention in response to a critical result, or treatment has already been initiated by the<br />

Physician/PA/APRN, that action is taken and/or information documented in the patient’s medical record.<br />

IV. Information to be documented includes the:<br />

A. Test name and test value/result<br />

B. Date and time the test result was received<br />

C. Date and time the test result was reported to the ordering provider or his/her designee.<br />

D. Name of the person receiving the results<br />

V. If the critical result reported is part of series (ex. Cardiac enzymes) but is moving toward the reference range, the results<br />

do not need to be reported to the ordering provider.<br />

VI. When lab staff encounter critical ED or inpatient test results that they believe are likely inaccurate (e.g. results are widely<br />

outside of expected from recent previous results; are incompatible with life; or are consistent with contamination from IV<br />

fluids), lab staff will:<br />

A. Automatically initiate a redraw for those tests<br />

B. Notify the patient’s RN that this is being done and instruct the RN to immediately inform the patient’s practitioner:<br />

1. Of the present critical result<br />

2. That those results are suspect (including rationale as to why the results are suspect); and<br />

3. That a redraw will be completed for those tests<br />

C. An exception report will be filed in Meditech documenting the suspect values, verbal read-back notification of the<br />

nurse or physician, and the follow-up action being taken.<br />

<strong>Values</strong><br />

TEST Less than Greater than<br />

Alcohol<br />

400 mg/dl<br />

Calcium 6.0 mg/dl 14.0 mg/dl<br />

CO2 10.0 mmol/L 40.0 mmol/L<br />

Carbon Monoxide 10 %<br />

Fibrinogen<br />

80 mg/dl<br />

Glucose 50 mg/dl 400 mg/dl<br />

Hematocrit 21% 60%<br />

Hemoglobin 7.0 gm/dl 20 gm/dl<br />

HIV<br />

New positive results<br />

INR 5.0<br />

Magnesuim 1.0 mg/dl 4.9 mg/dl<br />

Blood Film for Parasites<br />

Any organism seen<br />

Neonatal bilirubin<br />

VARIES BY AGE<br />

Neonatal urine glucose 3+<br />

\\Fs_2\Compliance\Policies & Procedures\Organizational Wide\General Nursing - Section 4\CURRENT\<strong>Critical</strong> Lab Results Notification [5-<br />

12].Doc<br />

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