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Reporting
Critical Test Limits
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Quick Links To Critical Test Limits
All critical, Code Blue, Trauma and O.R.
laboratory results must be called regardless of the ordering location's
printer capability (See Dept. of Pathology Policy for Verbal Orders and
Results). Each laboratory section determines its own critical value
listing (See combined critical listing below). Non-critical stat results
are reported in CIS without phone notification (See Dept. of Pathology
Policy for Requesting Stat Orders and Reporting Stat Results).
When laboratory staff verbally communicates results they should include
the following information:
Caller's name and lab section
The patient's full name
The patient's MRN
Critical or Code Blue laboratory results
Laboratory staff will request this information to be read back to them
in order to verify accuracy. The date, time and person they gave the
results to should be recorded in the Laboratory Information System (LIS).
Every effort should be made by laboratory staff to communicate critical
results to a person to ensure they are enacted upon ASAP. For DHMC
outpatient clinic locations the following process should occur in
attempting to communicate critical lab results:
- The ordering provider will be paged with any outpatient critical
results.
- During off-hours the resident covering the service will be paged.
The name and pager # of the covering resident can be determined by asking
the hospital operator.
- The pathology resident on call will be contacted in the event that
the ordering or covering provider does not return their page or can not
be reached.
- The clinic location will be called with outpatient critical results
only if the ordering physician name is missing or can not be determined.
Leaving a message on voice mail for an off-site ordering provider
indicating that critical results are available on a patient should only
be done when all reasonable efforts to contact the provider or covering
provider are exhausted. Voice message should include the lab contact
name, phone number, patient name, MRN, and name of test(s). The date and
time of the call that the voice message was left should be recorded in the
Laboratory Information System (LIS).
CHEMISTRY
Clinical Chemistry Laboratory: Guidelines for Reporting Critical
Values
Revised November 1, 2005
| ACETAMINOPHEN |
All Values |
| BUN |
Greater than 150 mg/dl |
| CALCIUM |
Less than 7.0 mg/dl, Greater than 13.0 mg/dl
|
| CARBAMAZEPINE (TEGRETOL) |
Greater than 12.0 mg/L |
| CREATININE |
Greater than 10.0 mg/dl (Except for dialysis pts.)
|
| CO2 |
Less than 10 mmol/L |
| DIGOXIN |
Greater than 2.0 ug/L (6 mos-adult)
Greater than 3.5 ug/L (0-6 mos)
|
| FREE PHENYTOIN |
Greater than 3.00 mg/L
|
| GENTAMICIN |
Peak Greater than 14.0 mg/L
Trough Greater than 2.0 mg/L |
| GLUCOSE |
Less than 40, Greater than 500 mg/dl
Greater than 300 for ICN and Newborn
|
| LIDOCAINE |
Greater than 5.0 mg/L |
| LITHIUM |
Greater than 1.5 mmol/L (chronic toxicity)
Greater than 4.0 mmol/L (acute toxicity)
|
| MAGNESIUM |
Less than 0.4 mmol/L, Greater than 2.25 mmol/L
|
| OSMOLALITY-SERUM |
Less than 250 mOs/KgH20, Greater than 330 mOs/KgH20
|
| PHENOBARBITAL |
Greater than 50.0 mg/L |
| PHENYTOIN (DILANTIN) |
Greater than 25.0 mg/L |
| PHOSPHORUS |
Less 1.5 mg/dl, Greater than 9.0 mg/dl (Except for dialysis pts.)
|
| POTASSIUM |
Less than 3.1mmol/L, Greater than 6.0 mmol/L
Less than 3.1 mmol/L for ICN and Newborn
Greater than 8.0 mmol/L for ICN and Newborn
|
| PRIMIDONE (MYSOLINE) |
Greater than 15.0 mg/L |
| SALICYLATE |
Greater than 350 mg/L |
| SODIUM |
Less than 115, Greater than 160 mmol/L
|
| THEOPHYLLINE |
Greater than 25 mg/L |
| TOBRAMYCIN |
Peak Greater than 14.0 mg/L
Trough Greater than 2.0 mg/L |
| URIC ACID |
Greater than 15.0 mg/dl |
| VALPROIC ACID |
Greater than 125 |
| VANCOMYCIN |
Peak Greater than 50 mg/L
Trough Greater than 30 mg/L |
Only OR, ER,Code and critical Blood Gas Results will be called.
BLOOD GAS CRITICAL VALUES
| pH |
Less than 7.30(pH less than 6.8 or greater
than 7.8 are incompatible with life) |
| pCO2 |
Less than 25 mmHg (0-28 days old only)
Greater than 50 mmHg |
| pO2 |
Less than 50 mmHg
|
| iCa |
Less than 0.93 and Greater than 1.53 mmol/L
|
| Na |
Less than 115 mmol/L and Greater than 160 mmol/L
|
| K |
Less than 3.1 and Greater than 6.0 mmol/L
Greater than 8.0 mmol/L for ICN
|
| Glucose |
Less than 40 mg/dl and >500mg/dl
Greater 300mg/dl for ICN
|
| Total Hemoglobin (tHb) |
See Hgb Reference Range chart below
|
Total Hemoglobin (in gm/dL)
Based on 06/29/08 DHMC Hematology Sysmex Ranges
| Age |
Refernece Range |
Critical Value Range |
| Less than 3 days |
14.5 - 22.5 |
Less than 6.0, greater than 24.6
|
| 3 days to 2 weeks |
12.5 - 20.5 |
Less than 6.0, greater than 22.6
|
| 2 weeks to 1 month |
10.0 - 18.0 |
Less than 6.0, greater than 20.0
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| 1 to 6 months |
9.4 - 14.0 |
Less than 6.0, greater than 20.0
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| 6 months to 2 years |
10.5 - 13.5 |
Less than 6.0, greater than 20.0
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| 2 to 6 years |
11.5 - 13.5 |
Less than 6.0, greater than 20.0
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| 6 to 12 years |
11.5 - 15.5 |
Less than 6.0, greater than 20.0
|
| 12 to 18 years (Female) |
12.0 - 16.0 |
Less than 6.0, greater than 20.0
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| 12 to 18 years (Male) |
13.0 - 16.0 |
Less than 6.0, greater than 20.0
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| Greater than 18 years (Female) |
11.2 - 15.7 |
Less than 6.0, greater than 20.0
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| Greater than 18 years (Male) |
13.7 - 17.5 |
Less than 6.0, greater than 20.0
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HEMATOLOGY
THE FOLLOWING VALUES MUST BE CALLED ON ALL DETERMINATIONS
| Prothrombin Time |
Greater than 49 seconds
|
| Partial Thromboplastin Time |
Greater than 130 seconds
|
| Fibrinogen |
Less than 100 mg/dl
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| Platelet Counts |
Less than 20,000/cmm (Greater than or equal to 5,000 for HSCU/1WST patients)
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| Urine Glucose |
Greater than 1,000mg/dl
NOTE: Both Ketone and Glucose must exceed critical values. |
| Urine Ketones |
Greater than 80 mg/dl
NOTE: Both Ketone and Glucose must exceed critical values. |
| Urine Clinitest |
Positive Clinitest on childeren when dipstick is negative
|
THE FIRST DETERMINATION OF THE FOLLOWING VALUES SHOULD
BE CALLED TO THE APPROPRIATE DESIGNEE
| D-Dimer |
Greater than 20,000 ng/ml
|
| Hemoglobin |
Less than 6.0gm/dl
for all age groups
Greater than 24.6 gm/dl for 0-3 days
Greater than 22.6 gm/dl for 3 days to 2 weeks
Greater than 20.0 gm/dl for greater than 2 weeks |
| White Cell Count |
Less than 2,000/cmm (<1000 for HOC patients)
Greater than 30,000/cmm
[Do not call critical WBCs to HSCU/1WST]
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Absolute Granulocytes
(Gran #)
|
Less than 0.5 X 103 cells/ul
[Do not call critical ABS granulocytes to HSCU/1WST]
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NOTE: All Platelet counts less than 20,000/cmm must be called to
the attending physician or designee. Call HSCU (Hematology Special Care)
platelets = 5,000/cmm.
REFERENCES
- Kost, G.J., JAMA, 1990; 263:704
- Howanitz, P.J., et al., Archives of Pathology and Laboratory Medicine,
2002; 126:663
- ISLH Consensus rules. http://www.islh.org
MICROBIOLOGY
For optimum patient care, the following critical isolates and test results
will be telephoned to the provider (Provider or nurse).
- Positive blood cultures
- Positive gram stains from CSF and joint fluids
- Positive CSF PCR results
- Positive Chlamydia and GC amplificiation tests
- Positive PCR for B. pertussis
- Positive culture with N. gonorrhoeae
- Positive Acid Fast stains and isolates
- Virus cultures, stains or EIA positive for respiratory viruses on in-patients
- Entamoeba histolytica
- Stronglyoides stercoralis
- Positive blood parasite slides, i.e., Malaria, Babesia and Trypanosomes
- Positive eye cultures (all sources) with P. aeruginosa and
Bacillus speciesand filamentous fungi, and all positive cultures
on vitreous fluid
ANATOMIC PATHOLOGY
All frozen section surgical pathology specimens are considered critical
and results are called regardless of the diagnosis. Please refer to the
Anatomic Pathology Physician Guidelines for specifics.
TRANSFUSION MEDICINE SERVICE*
*The Transfusion Medicine Service does not produce laboratory test results
that have the traditional critical test limits, however lisited below are
specific procedures that are performed, or products that are issued, that
are critical to the care of the patient and require immediate response.
BLOOD DONOR PROGRAM
| Pre- HPC collection |
Hemoglobin <8 gm
WBC count >65,000
Platelet count <30,000
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| Post-HPC collection |
Platelet count <20,000
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| Severe or sustained donor reactions |
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BLOOD BANK/CELLULAR THERAPY CENTER
- All suspected adverse reactions to transfusion of blood components
(or infusion of products prepared in the Cellular Therapy Center),
including those suggestive of TRALI or hemolysis (symptoms of respiratory
distress or hypotension)
- Release of Block/Uncrossmatched red blood cell units
- Release of untested or potentially incompatible blood components
- Release of ABO-incompatible platelets
- Requests for any blood component outside of standard indications
- Positive antibody screen in pre-op or surgical patients
- Positive bacterial culture of platelets or product prepared by the
Cellular Therapy Center
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