For in vitro diagnostic use only
General Information
2-8ºC. Below -20ºC for at least 10 years (submitted Clinical
Intended Use
Chemistry November 2010). Mix samples well before
The Gentian Cystatin C Immunoassay is an in vitro diagnostic
analysing. The samples may be shipped without special
test for quantitative determination of cystatin C in human serum
cooling, but must then be analysed within 14 days after
and plasma. The measurement of cystatin C is used in
the diagnosis and treatment of renal disease.
Measuring range
The Gentian Cystatin C Assay Buffer is the Reaction Buffer R1. The buffer is ready for use.
The overall measuring range of cystatin C concentration for Gentian Cystatin C Immunoassay on the Cobas c5011 analyzer
Immunoparticles (R3)
The Gentian Cystatin C Immunoparticles are ready for use.
Reference intervals Calibrator
Gentian followed the CLSI Guideline, C28-A2 to determine the
The calibrator is ready to use and a dilution series for
transferability of the reference interval. The reference interval
calibration curve establishment is prepared automatically by
was determined from a population of ostensibly healthy
subjects with no history of renal disease. A total of 136
samples obtained from 58 males and 78 females ranging in
All reagents are stable until the expiry date given on the
age from 20 to 80 years were tested. The reference interval
labels when stored at 2-8ºC.
was calculated non-parametrically and was determined to be
0.51-1.05 mg/L. This represents the central 95 % of the
Calibrator Standardisation
population. It is recommended that every laboratory should
Gentian Cystatin C Calibrator is standardised against the
determine a local reference interval since values may vary
international calibrator standard ERM-DA471/IFCC.
depending on the population tested. In a separate study
Calibration Stability
involving 850 healthy children (46% boys, 54 % girls) in the age
The established calibration curve is stable for 4 weeks on
from 5 to 15 years, the reference range 0.51 - 1.05 mg/L was
Cobas c5011. When reagent lots are changed or measured
confirmed in all ages down to 5 years of age [5].
control values are outside the assigned range given in the
Analytical Value Sheet, a recalibration is recommended.
GFR prediction calculation Several cystatin C based prediction equations for calculation of Onboard Stability
GFR for adults and children have been published. It should
In appropriate bottles, Gentian Cystatin C Immunoparticles and
noted that these formulas were evaluated with different
Assay Buffer are stable for at least 9 weeks when stored
immunoassay PENIA or particle enhanced turbidimetric immunoassay PETIA) and may reveal inaccurate GFR results if
Assay Procedure
an inappropriate combination of formula and assay is used. For
Application Notes/Assay Installation
calculation of GFR from cystatin C values measured with the
An Instrument Parameter list is available in the section
“Instrument Settings” below. The Application Note is also
recommended using mg/L as the unit factor [4]: The equation is
available at www.gentian.no. Instrument set up, maintenance,
operation and precautions must be handled in accordance with
Reagents Preparation
Reagent is supplied ready to use. Use a suitable pipette to
Materials Provided by Gentian AS
transfer the calculated volumes (see the instruments manual)
of Reagent 1 and Reagent 3 into the appropriate compartments
Gentian Cystatin C Kit (REF1101):
of the Open Channel Reagent Cassette (cobas c pack
Gentian Cystatin C Immunoparticles, bottle of 10 mL, (R2)
MULTI1). Mix well before transfer. Use care to avoid
Gentian Cystatin C Assay Buffer, bottle of 58 mL, (R1)
contamination. Reagents should be stored capped at 2-8°C when not in use.
Gentian Cystatin C Calibrator: vial of 1 mL, REF1012 Gentian Cystatin C Calibrator Kit: 6 levels, vials of 1 mL,
Contact your distributor or Gentian to get information on how to
maximise the number of tests per reagent kit. The information
Gentian Cystatin C Control Kit: 2 vials of 1 mL, REF1019 Gentian Cystatin C Control Kit: 2 vials of 5 mL, REF1026 All materials are ready to use.
Establishment of the Calibration Curve
Use Gentian Cystatin C Calibrator, REF1012 to establish a
Specimen
6-point standard curve as defined in the instrument manuals.
Required sample material is human serum, heparinized plasma
Calibrator values are lot dependent and a new calibration must
and EDTA plasma. It is recommended to analyse the samples
be performed whenever a new calibration lot is used. The
as fresh as possible. Sample stability testing showed that
calibrator’s assigned values are given on the analytical value
cystatin C in serum and plasma samples are stable for 14 days
at room temperature (8-25ºC) and for 21 days if stored at
1A registered trademark of Roche Diagnostics Application Note for Gentian Cystatin C Immunoassay on Cobas1 c501, Roche
QC Controls
There is no interference detected with the drugs tested on
The controls low and high must be assayed each day before
any samples are assayed in order to validate the calibration
interference study was designed in accordance with the
curve. The controls have an assigned value range that must be
protocol EP7-A from CLSI [2]. There is no RF interference
met before measuring samples. The assigned values are given
present in the Gentian Cystatin C Immunoassay because the
in the Analytical Value sheet included with the Gentian Cystatin
antibodies are made from avian (chicken) [3].
C Control Kit (REF1019 or REF1026). If the control values are
not valid, repeat the control measurements. If the calibration cannot be performed without error, or valid control values
Shipping Damage
cannot be reproduced, contact the manufacturer for support.
Please notify your distributor if this product is received damaged.
Measuring Patient Samples
When a valid calibration has been performed and the control values are within the valid range, serum or plasma samples
may be measured. Check that minimum volume of sample is
Symbols Key
present and assay the samples according to the instructions given in the Instrument Manuals.
Results The results are calculated automatically by the Cobas c5011
instrument. The results are presented in mg/L.
Performance Characteristics
All results refer to the validation of Gentian Cystatin C Immunoassay on Cobas c5011.
Detection Limit
Limit of Quantification is defined as: The lowest actual amount of an analyte that can be reliably detected and at which the total error meets the requirements for accuracy. Gentian Cystatin C Immunoassay has a Limit of Quantitation of
Precision
The Gentian Cystatin C Immunoassay was used in a 5-day
precision study designed in accordance with CLSI protocol
References
EP5-A. 5 human serum pools were measured on the Cobas
[1] Sonntag O, Scholer A: Ann Clin BIochem 2001; 38:376-85.
[2] CLSI; Document EP7-A; Interference Testing in Clinical Chem.;
Mean value Within-Run Serum pool
[3] Larsson A et al: Poultry Science 1993;72:1807-1812
[4] Flodin M et al: Scand J Clin Lab Invest 2007;67:560-567 [5] Nitsch D. et al: Foetal, developmental and parental influences on
Childhood cystatin C in Childhood. Submitted for publication.
Linearity Manufacturer:
Gentian Cystatin C Immunoassay on Cobas c5011 is linear in
Gentian AS, PO BOX 733, N-1509 Moss, Norway
the range of 0.41-7.98 mg/L. Concentrations outside this range have not been tested.
Interference
EC REP Authorized European Representative in EU:
No interference is detected with Triglycerides (12.7 mmol/L)
Gentian AS, PO BOX 733, N-1509 Moss, Norway
Haemoglobin (8.0 g/L), Intralipid (14 g/L) or Bilirubin (600 mg/L)
on Cobas c5011.
1A registered trademark of Roche Diagnostics Application Note for Gentian Cystatin C Immunoassay on Cobas1 c501, Roche
For in vitro diagnostic use only
Assay/Time/Point 2 point end Wavelength (2nd /primary) S.vol (Normal) S.vol (Decrease) S.vol (Increase) Reagent (R1) T1 Reagent (R2) T2 Reagent (R3) T3 Reagent (R4) T4 Abs. Limit Increase Prozone Limit Cell Detergent Detergent 1
1A registered trademark of Roche Diagnostics Application Note for Gentian Cystatin C Immunoassay on Cobas1 c501, Roche
CALIBRATION
Calibration Type Span Point Auto calibration:
Diluent: Saline (from instrument for auto-dilution of calibrator)
1A registered trademark of Roche Diagnostics Application Note for Gentian Cystatin C Immunoassay on Cobas1 c501, Roche
Application Code: Expected Values: Standard:
CV: assigned Calibrator Value, see analytical value sheet enclosed with the calibrator
* User defined ** Calibrator Position chosen by user
1A registered trademark of Roche Diagnostics Application Note for Gentian Cystatin C Immunoassay on Cobas1 c501, Roche
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References [Ahmad01] Ahmad M, Xie T, McCulloch M, Abreo G, Runge M. Real-time three-dimensional dobutamine stress echocardiography in assessment stress echocardiography in assessment of ischemia: comparison with two-dimensional dobutamine stress echocardiography. J Am Coll Cardiol 37:1303-1309; 2001 [Alderman83] Alderman EL, Fisher LD, Litwin P, Kaiser GC, Myers WO, Maynard C, Lev