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How to Cite this article: Critical Limits of Laboratory Results for Urgent Clinician Notification, eJIFCC vol 14 no 1: http://www.ifcc.org/
ejifcc/vol14no1/140103200303n.htm
Critical limits of laboratory The laboratory should not report a criti-cal result to the
treating physician until it has been confirmed by a second
results for urgent clinician deter-mination in the same sample.
notification
The laboratory test value should be ascertained by a
Professor Dr Lothar Thomas competent member of the laboratory (laboratory doctor,
clinical chemist, senior medical laboratory tech-nician)
who should discuss the result with the treating physician.
Kirschbaumweg 8, 60489 Frankfurt
E-mail: th-books@t-online.de This is because influences and interfer-ence factors in the
preanalytical phase, e.g. sample collection for glucose
Critical limits of laboratory results need urgent notification measurement using a venous catheter that had been used
to the clinician because they are an indicator of a critical for glucose infusion, are not infrequently the cause of
or even life-threatening condition of the patient. seemingly critical values. Such cases are usually clarified by
the testing of another, properly collected sample.
The publications about this topic are mainly from the
1970s. Since then, many laboratory methods have been The specified parameters and limits are taken partly from
improved, new parameters have been added, and there [1]. The others are based on 25 years experience as a 1
have also been changes in the evaluation and treatment of doctor for laboratory medicine working in a hospital.
diseases.
References:
Against this background and at the request of the Ameri-
can Medical Association, J.G. Kost [1] conducted a survey Kost, GJ. Critical limits for urgent clinician notification at
on critical pa-rameters in the USA in 1990 and Howanitz US medical centers. JAMA 1990; 263: 704-7
et al. [2] in 2002. The spectrum of critical pa-rameters
reported in these publications does not meet the require-
ments of laboratory medicine in every respect. Howanitz PJ, Steindel SJ, Heard NV. Laboratory critical
values, policies and procedures. A College of Ameri-can
Pathologists Q-probes study in 623 institutions. Arch
I have therefore put together a new list of qualitative and Pathol Lab Med 2002; 126: 663-9.
quantitative parameters. If you think there are parameters
that should perhaps be added or deleted, limits, which
need changing, or notes that need to be amended, your
suggestions would be most welcome.
Vol 14 No 1
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Table 1: Adult and paediatric limits of laboratory results which, after confirmation
through repeat measurement in the same sample, need urgent notification of the
physician
Ammonia > 100 mg/dl (59 Risk of hepatic encephalopathy. Comatose states
mmol/l) do not usually occur unless levels exceed 300
mg/dl (176 mmol/l).
Ethanol > 3.5 g/l (76 Blood alcohol concentrations of 3-4 g/l can be
mmol/l) fatal, even in those who are not simultaneously
using medicinal products.
> 3.5 %
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Creatinine > 7.4 mg/dl (654 Acute renal failure, e.g. in multiple organ failure
mmol/l) or sepsis.
Creatine kinase > 1000 U/l Notification depends on the patient population of
the clinic or practice in question.
Vol 14 No 1
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Magnesium < 1.0 mg/dl (0.41 Characteristic symptoms are paresthesias, cramp,
mmol/l) irritability, and athetoid tetany. The patient often
shows cardiac arrhythmia in conjunction with
> 4.9 mg/dl (5.0 hypokalemia; arrhythmia is intensified by
mmol/l) digitalis.
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Osmolality < 240 mOsm/kg Cellular oedema with an increase in cell volume
H2O and development of neurological-psychiatric
symptoms.
> 330 mOsm/kg
H2O Cellular water loss and intracellular increase in
osmotically active substances, which do not
permeate the cell membrane. Result: central
symptoms and coma.
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Thromboplastin > 27 sec (approx. Decrease in the vitamin K-dependent factors II,
time (TT) 50%) VII, and X or in factor V. Since all these factors
are synthesized in the liver, a decrease in the TT
to values below the specified level indicates a
considerable disturbance of synthesis. In persons
receiving coumarin therapy, there is a risk of
haemorrhage if the TT is < 15% which
corresponds roughly to an INR of > 4.
6
Platelet count < 20,000/ml Risk of haemorrhage. Exclude EDTA-induced
thrombocytopenia.
> 1 million/ml
Risk of thrombosis.
Uric acid > 13 mg/dl (773 Acute urate nephropathy with tubular blockade
mmol/l) and renal failure. The uric acid/creatinine ratio in
spontaneous urine in such cases is > 1.0 (mg/mg).
Urea > 214 mg/dl (35.6 Indicative of acute renal failure; unlike pre-renal
mmol/l) and post-renal kidney failure, no
BUN disproportionate increase in urea compared to
> 100 mg/dl (35.6 creatinine in serum.
mmol/l)
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Cerebrospinal fluid
Suspected leukemia
7
Suspected aplastic crisis
Sickle cells
Malarial parasites
Microbiology Detection of pathogens in Gram staining of blood culture or of exudates and
transudates of body cavities
Antigenic detection of pathogens with rapid tests such as latex agglutination, immunofluorescence, or immunoassay, e.g. group B
streptococci, legionella, Pneumocystis carinii, Cryptococcus, hepatitis B
Detection of acid-fast bacilli or detection of M. tuberculosis after amplification (PCR)
Cultural detection of salmonellae, shigella, Campylobacter, C. difficile, C. perfringens, N. gonorrhoeae, B. pertussis, N.
menin-gitidis, C. diphtheriae, and pathogenic fungi such as Aspergillus, Blastomyces, Coccidioides, Histoplasma, and Cryptococcus
Detection of HIV antibodies
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Table 3: Neonatal quantitative limits of laboratory results which, after confirmation
through repeat measurement in the same sample, need urgent notification by the
physician.
Bilirubin > 14 mg/dl (239 On first day of life, e.g. in hemolytic disease of the
mmol/l) newborn; risk of kernicterus.
Hemoglobin < 8.5 g/dl Risk of multiorgan failure, especially if the patient
has a combination of ischemia and hypoxia.
Igm > 20 mg/dl A cord blood IgM concentration above the limit can
be linked to an intrauterine infection.
Leukocyte count < 5,000/ml Values below and above these limits can be
indicative of neonatal sepsis.
> 25,000/ml
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