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Amylase


Plasma/Serum
Test performed by: LabPLUS Automation


Specimen Collection

Sample stability:


PST

4.5 mL PST Blood (Preferred)

Micro-PST

0.5 mL Paediatric Micro-PST Blood (Preferred)

Heparin

5 mL Heparin Blood

Plain

4 mL Plain Blood

SST

3.5 mL SST Blood

Microsample

0.5 mL Paediatric Microsample Blood

Micro-heparin

0.5 mL Paediatric Micro-heparin Blood
Reference Intervals

Units: U/L

Reference intervals:

Plasma amylase (total) : 28 - 100

Pancreatic amylase : 8 - 53

Uncertainty of measurement: 5%



Turnaround Time: Within 3 hours
Assay Method

Principle: Enzymatic/Colorimetric

Reagents: Roche P amylase kit

Analyser: Cobas c502


Diagnostic Use and Interpretation

There are 2 forms of amylase: P-amylase is specific for the pancreas as tissue of origin. S-amylase can originate from many organs, including salivary and parotid glands, breast, amniotic fluid, lungs, testes and fallopian tubes, as well as neoplasms (including pancreatic cancer).

Total amylase measures both S and P-amylase forms.

If "amylase" is requested, total amylase will be performed.

A specific assay for P-amylase is available either as a standalone test or together with total amylase. P-amylase needs to be specifically requested or test added within 6 days of collection. P-amylase is no longer automatically performed on all raised total amylase results.


In acute pancreatitis, levels peak early and decline over 3 to 4 days. For diagnosis of acute pancreatitis both the amylase level (typically 3 or 4 times greater than normal) and its time-course in relation to the abdominal pain are important. Prolonged elevation of amylase may be due to pancreatic pseudocyst formation.

Total amylase can be increased in many acute abdominal disorders including perforated peptic ulcer, acute cholecystitis, intestinal obstruction, trauma, and ectopic pregnancy.
Elevated amylase can also occur in diabetic ketoacidosis and renal failure (failure to clear the enzyme).

Ectopic pregnancy and salivary gland disorders (parotitis, mumps) cause increased total amylase, with normal P-amylase levels.

Macroamylasaemia is a cause of chronically elevated serum amylase levels, due to complexing of amylase to large proteins and reduced clearance by renal filtration. This is an incidental finding and has no clinical effects. Macroamylasaemia can be differentiated from a true raised amylase by

(a) lipase measurement

(b) PEG precipitation of serum followed by repeat amylase assay (PEG precipates macroamylase but not normal amylase). Contact the on-call chemical pathologist if you require this test.

(b) measuring urinary amylase, which is high in cases of true raised amylase and low in macroamylasemia.


Contact Information

Emails to chemicalpathologist@adhb.govt.nz will receive priority attention from the on-call chemical pathologist.

If the query concerns a specific patient please include the NHI number in your email.

If email is not a suitable option, please contact the on-call chemical pathologist via Lablink (Auckland City Hospital ext. 22000 or 09-3078995).

Individual chemical pathologists may be contacted but will not be available at all times.

After-hours : contact Lablink (Auckland City Hospital ext. 22000 or 09-3078995) or hospital operator for on duty staff after hours.


Dr Samarina Musaad (Clinical Lead) : SamarinaM@adhb.govt.nz ext. 22402

Dr Cam Kyle: CampbellK@adhb.govt.nz ext 22052

Dr Weldon Chiu: WeldonC@adhb.govt.nz ext. 23427

Dr Campbell Heron: CHeron@adhb.govt.nz ext. 23427

Dr Sakunthala Jayasinghe: Sakunthala@adhb.govt.nz ext. 23427




Last updated at 15:26:00 06/01/2025