Key pre-analytical factors in clinical biochemistry: fasting status (glucose, lipids, gastrin), posture (aldosterone, renin), time of collection (cortisol has diurnal variation — morning and afternoon samples differ), sample type (serum vs EDTA vs lithium heparin — some analytes differ significantly), haemolysis (elevates potassium, AST, LDH), lipaemia (interferes with spectrophotometric methods), and icteric samples (bilirubin interferes with some methods).
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Good practice The section head holds the three results immediately, contacts the LIS administrator, and has the calculation corrected. The eGFR values are generated: one patient has a creatinine of 132 micromol/L and an eGFR of 48 — CKD Stage 3b, which the clinician would not have identified from the creatinine value alone (132 is above the upper reference interval for females but this is not immediately obvious without clinical context). The result is released with an appropriate comment.
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Poor practice The creatinine results are released without eGFR because the LIS administrator says the calculation fix will take a day. The result of 132 micromol/L is flagged as high, but the clinician, not a nephrologist, does not know that this corresponds to an eGFR of 48 in a 68-year-old woman and does not initiate CKD management.
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