Date: 20-Apr-12 Best ResultsFor best results, ampules, cartridges and handhelds should be at the same UseWhen using cartridges that contain sensors for pH, PCO2, PO2 and ionized calcium, a separate ampule must be used for each cartridge being not use residual TriControls solution that may be in a syringe, ampule or capillary tube for additional Testing of cartridges that contain sensors for ionized calcium, pH, PCO2, or PO2. Do not use TriControls solutions past the labeled expiration date on the box and ampule Art: 723270-00A Rev. The control solutions do not contain human serum or serum products, but do contain buffers and Ingredients for TriControls MaterialsAnalyteCalibration Verification Level 1 Calibration Verification Level 2 and Control Level 1 Calibration Verification Level 3 and Control Level 2 Calibration Verification Level 4 and Control Level 3 Calibration Verification Level 5Na (mmol/L)97118124150159K (mmol/L) (mmol/L)677694119134 Glu (mg/dL)5952851606553 Urea (mg/dL) (mmol/L) (mmol/L) (mg/dL) (mmHg)9665402612PO2 (mmHg)4063120163500H+ (pH) storage at 2-8 C (35-46 F) should be maintained until the printed expiration date on the box and ampule labels.ģ TriControls solutions may also be maintained at room temperature (18-30 C 64-86 F) for up to 5 days. i-STAT TriControls Level 1, 2 and 3 are formulated at three clinically relevant levels with defined pH and hematocrit values and with known concentrations of:SodiumPCO2 GlucosePotassiumPO2 LactateChlorideTCO2 BUN/UreaIonized CalciumCreatinineEach level of control is packaged in a box containing 10 individual mL glass ampules. Date: 20-Apr-122 CONTROLS FOR BLOOD GAS/ELECTROLYTE/METABOLITE CARTRIDGES (i-STAT TriControls )Control SolutionsAqueous-based control fluids are available for verifying the integrity of newly received cartridges. Abbott List NumberDevice Name05P71-01 TriControls Control Level 105P72-01 TriControls Control Level 205P73-01 TriControls Control Level 305P70-01 TriControls Calibration Verification Set Levels 1-5 Art: 723270-00A Rev. This enables reduced control Testing in cases where all of these tests are being evaluated and : The additive used to simulate the effect of hematocrit results in reduced precision.Ģ Refer to the Precision section at the end of this document for additional details. Date: 20-Apr-12 TECHNICAL BULLETINi-STAT TriControlsControl Materials for Liquid QC and Calibration VerificationOVERVIEWAs part of the READi initiative (Responds, Enhances, And Delivers innovations), Abbott Point of Care (APOC) has released a new set of aqueous control and calibration verification materials that combine the ability to assay hematocrit, blood gases, electrolytes, and chemistries. Introduction.īefore You Use the Analyzer.1 Abbott Point of Care Inc. Summary of the Procedure.ĭata Management. Minimize ID Entry Errors.Īpril 2008 Update to the Central Data Station Version 5. Using i-STAT ® Analyzer Customization Features to Result Calibration Modes for the i-STAT 1 Analyzer. Hematocrit on the i-STAT System.ĪCT Test Result Options: Prewarmed vs. Receive Data from a Philips Clinical Data Server. Installation Guide for the Central Data Station to Hematocrit Determination in the i-STAT SystemĪnd Comparison to Other Methods. Prothrombin Time PT/INR.Ĭardiac Troponin I.Ĭreatine Kinase MB / CK-MB.ī-Type Natriuretic Peptide/BNP.Īnalyzer Coded Messages. In the event that your System Manual does not contain the current configuration, it is recommended that you contact your i-STAT support provider.Īs of April 2008, your i-STAT ®1 System Manual should be configured with the contents as listed below and in the order shown.Ĭover Sheet. Please ensure that the contents of your System Manual are complete and up to date. Windows is a registered trademark of Microsoft Corporation. Precision and PCx are trademarks of Abbott Laboratories. MediSense is a registered trademark of Abbott Laboratories. I-STAT is a registered trademark of Abbott Laboratories. Symbol Technologies Corporation is the owner of US Patent Nos.
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