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Section 4 of 6 · Open sections

Required section · Section 4 of 6

Working the short-fill case

Return to the opening case. An adult outpatient has orders for blood cultures, PT, aPTT, a comprehensive metabolic panel, a complete blood count with differential, and plasma lactate. The collector uses a butterfly. The culture set is drawn first, correctly, at 09:08. The citrate tube is connected next without the local discard step, is visibly short filled at 1.8 mL against the 2.7 mL fill line, and is labeled with its actual collection time, 09:12. Serum, heparin, and EDTA tubes follow in the correct sequence. A separately collected prechilled gray lactate tube is drawn, placed on ice at 09:15, and its plasma is separated at 09:24, 12 minutes after the draw.

Work the coagulation result first. The citrate tube's short fill changes its blood-to-citrate ratio away from what the coagulation assay assumes, independent of anything happening inside the patient. Both PT at 16.8 s and aPTT at 43.6 s read above the teaching reference interval, but a short-fill artifact is the leading explanation for both, not a bleeding tendency. The hematocrit on the same accession is 43%, inside the 36 to 46% teaching interval, so the high-hematocrit adjustment pathway is not in play here; the short fill is a separate, sufficient explanation on its own.

Work the lactate specimen next. The prechilled gray tube stayed on ice from the moment of collection, and plasma was separated 12 minutes after the draw, inside the 15-minute limit from this method's example instructions. This specimen met that specific requirement, though it still needs to be checked against whatever the local test procedure for lactate specifies, because that instruction can differ by laboratory.

The defensible action on the coagulation panel is to hold release of PT and aPTT, communicate the short fill and the need for recollection through the local procedure, and retain the actual collection time and a record of that communication. The culture set's collection metadata, site, method, bottle volumes, time, and collector, must also be documented regardless of the coagulation issue, because that documentation is what makes the specimen traceable if it is ever questioned later.

A flagged coagulation result with a documented short fill is a specimen problem to resolve before release, not a patient result to interpret.

Illustrative drawing — this picture was drawn rather than captured.

Chart with citrate fill at 1.8 of 2.7 mL, and PT and aPTT on the same 0-50-second vertical scale. PT 16.8 s is above the 10.0-13.0 s band, and aPTT 43.6 s is above the 25.0-35.0 s band.
Figure 1The short-filled citrate tube and PT/aPTT results, with PT 16.8 s plotted above its 10.0-13.0 s band and both results on one 0-50-second scale.
Guided case specimen and result summary
Specimen or resultValue or unitTeaching reference or requirementTiming or flag
PT, citrate plasma16.8 s10.0 to 13.0 s, adult intervalShort-fill flag
aPTT, citrate plasma43.6 s25.0 to 35.0 s, adult intervalShort-fill flag
Hematocrit, EDTA whole blood43%36 to 46%, adult intervalNo high-hematocrit pathway
Lactate, plasmaNot released hereGray tube, ice, separate within 15 min, ARUP exampleSeparated at 12 min
Blood culture setNot released hereCollection metadata required by local SOPSite, method, volumes, time, collector documented

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Knowledge check 1

In the guided case, what is the leading explanation for the elevated PT and aPTT?

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Knowledge check 2

Was the lactate specimen's handling consistent with the cited method-specific example?

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