PEPconnect

CLINITEK Status®+ System hCG Quality Control Cassette Test Online Training

Perform QC testing to ensure hCG Cassettes react properly and the analyzer reads accurately.

Identify how to delete records from instrument memory (Option must be enabled on analyzer; Operator must have required security access.) Identify how to recall stored results Identify products approved for use on the CLINITEK Status®+ Analyzer Identify the steps to set up and run Quality Controls on hCG Cassettes Welcome to the CLINITEK Status® Portfolio hCG Quality Control Cassette Test Online Training course. After successful completion of this course, you will be able to: Select Next to continue. Bienvenue à la formation en ligne du programme de gestion des données et de la connexion RAPIDComm®, Gestion des opérateurs. Le programme RAPIDComm® vous permet d'ajouter et de gérer des opérateurs pour les instruments connectés. La recertification des opérateurs peut également être programmée et gérée afin de garantir la certification des opérateurs travaillant sur les instruments. Cliquez sur Suivant dans le coin supérieur droit de la fenêtre pour commencer le cours. Congratulations. You have completed the CLINITEK Status®+ System hCG Quality Control Cassette Test Online Training course. In this course, you have learned how to: Identify the steps to set up and run Quality Controls for hCG Cassettes   Performing QC helps ensure that urinalysis hCG cassettes are reacting properly and that the instrument accurately reads them. QC testing also can help detect user technique errors. Run QC as determined by your facility's operating procedures at regular intervals and whenever you are when using a new shipment of reagents or cassettes, a new lot number of reagent or cassettes, opening a new bottle of reagents, test results are in doubt or training new operators. The CLINITEK Status®+ Analyzer does not discriminate between a QC sample or a patient sample.  You will be required to manually run, review, and log QC test results. The CLINTEK Status® Connect System supports new QC management capabilities.  The analyzer now can be programmed to accept quality control tests and can analyze automatically if a QC test passes based on pre-defined criteria.  The system maintains a separate database of results for QC and patient samples. The system supports Siemens or other manufacturers control materials. If using Siemens’ Chek-Stix® Urinalysis positive and negative controls, these can be prepared to verify performance. Identify products approved for use on the CLINITEK Status®+ Analyzer The CLINITEK Status®+ Analyzer uses only Siemens Healthcare Diagnostics products which include: Clinitest® Immunoassay cassettes for qualitative hCG pregnancy tests. CLINITEK Microalbumin 2 -  small levels of albumin (referred to as microalbumin) are adjusted due to creatinine values and can be important as a predictor of pre-eclampsia Identify how to recall stored results The CLINITEK Status® platform offers expanded on-board memory storage for patient results that are recalled easily for improved data management. The CLINITEK Status® Connect system also stores quality control results. The CLINITEK Status® Connect Platform stores up to 950 patient test results in the onboard memory. When the limit of 950 has been reached, the oldest test will be deleted from the analyzer. Deleted information cannot be retrieved from the analyzer. The CLINITEK Status® Connect System can store 200 QC results in the onboard memory.  As there is no QC functionality on the CLINITEK Status®+ Analyzer, QC results must be tracked manually. Identify how to delete records from instrument memory Patient and QC records stored on the analyzer can be deleted permanently from instrument memory. Individual records cannot be deleted. Before deleting records, save the database to an external source. Data stored on an LIS will not be deleted. This option must be enabled on the analyzer, and the operator must have the required security access.   Select Next to continue.     Dans cette section, vous apprendrez comment télécharger une liste d'opérateurs sur un instrument. Run QC when: Determined by your facility's operating procedures at regular intervals Using a new shipment of  hCG cassettes Using a new lot number of  hCG cassettes Opening a new bottle of reagents Test results are in doubt Training new operators Note: Depending on instrument configuration, patient tests cannot be run until the QC tests pass. Note: This course includes information on Options and Functions in the system which may require security approval from your facility in order to access.   QC Tests Learn about running QC tests on the CLINITEK Status Connect system. Tab TitleTextCLINITEK Status®+ Analyzer Quality control solutions can be tested. However, the CLINITEK Status® + Analyzer does not discriminate between a QC sample and a patient sample.  You will be required to manually run, review, and log QC test results. Clean the test table insert each time after performing QC. CLINITEK Status® Connect The CLINTEK Status Connect System supports new QC management capabilities. The analyzer now can be programmed to accept quality control tests and can analyze automatically if a QC test passes based on pre-defined criteria. The system maintains a separate database of results for QC and patient samples. The system supports Siemens or other manufacturers control materials. Clean the test table insert each time after performing QC. Note: Enable the CLINITEK Status connector platform to use these features. When complete, select the X in the upper-right corner to close the window and continue. Running hCG QC Cassette Tests Learn how to run hCG QC Cassette tests. Checklist TitleChecklist TypeChecklist ContentPrepare AnalyzerHTML   Select each checkbox to learn how to run hCG QC Tests. Verify that the test table insert is in position for a cassette test.    Select QC TestHTML From the Select Ready screen, select the QC Test button.  Select QC Cassette Test RequiredHTML   From the QC Test screen, select QC Cassette Test Required.  If the operator determines pass/fail, continue to the next step.  If the instrument is set to pass/fail, the control Lot screen will display (Skip to Prepare the Cassette step.)   Enter Control DetailsHTML   On the Enter Control Name screen, select the Enter lot and expiration date button. Follow the onscreen prompts to enter control information, using the alpha or numeric keypad. (If the Operator ID function has been enabled, you will need to enter this information prior to entering the control details.) If the lot number is available on the product as a barcode, you also can scan the information using the barcode reader on the analyzer or scan using the external barcode reader. If using a previously entered lot, press the Use last lot button.. Prepare CassetteHTML    Remove the hCG cassette from the foil package and place it into the insert on the test table.  Select STARTHTML    From the Prepare Test screen, press the START button. The instrument will calibrate automatically.  Draw SampleHTML   Once START is pressed, you have 8 seconds to draw and add the control sample. Draw the sample and completely fill the pipette stem. Any excess sample will go into the overflow reservoir of the pipette. Warning: To avoid erroneous results, you must press the START button before drawing and adding the sample.  Fill Cassette WellHTML   Empty only one pipette stem into the sample well. Do not dispense the liquid into the overflow reservoir. At the end of the 8 seconds, the test table will be drawn automatically into the analyzer.  Review ResultsHTML   After the test is completed, the Results screen displays. Select the Print button to print the results. Select Done.  Pass/Fail ResultsHTML   If the instrument is set to determine pass/fail, either the Results-QC Test: Pass or Results-QC Test: Fail screen displays. If the system is enabled for the operator to determine pass/fail, you must select either QC PASS or QC FAIL.  After completing the test, repeat the process for the second control level When complete, select the X in the upper-right corner to close the window and continue.   The CLINITEK Status®+ Analyzer used Siemens Healthcare Diagnostics Clinitest® hCG Cassettes to perform a single test and obtain qualitative results.  Other products approved for use on the analyzer for pregnancy related testing are: CLINITEK Microalbumin 2  - microalbumin results adjusted due to creatinine value and can be important as a predictor of pre-eclampsia Select Next to continue.   Al completar con éxito este curso, usted estará en la capacidad de: Vaciar el depósito de residuos, [Pausa] Revisar la botella de desbordamiento, [Pausa] Revisar y reemplazar el inventario de reactivos [Pausa] y obtener los recuentos de fondo [Pausa]. Usted también estará en la capacidad de realizar un lavado del sistema [Pausa] e identificar el procedimiento de fin de día [Pausa]. Seleccione Siguiente para continuar. When used as a standalone or in conjunction with the Connector Platform, the CLINITEK Status®+ Analyzer, stores up to 950 patient test results in the on-board memory. When the limit of 950 has been reached, the oldest test will be deleted from the analyzer. Deleted information cannot be retrieved from the analyzer. Note: The CLINITEK Status® Connect System can store 200 QC results in the on board memory.  As there is no QC functionality on the CLINITEK Status®+ Analyzer, QC results must be tracked manually.   Recall Stored Results Learn how to recall stored results. Instructions:If media does not automatically start, select the play arrow to beginFlash File:/content/generator/Course_90006181/simCSPlusRecallResults____9/simCSPlusRecallResults____9.swfHTML5 File:/content/generator/Course_90006181/simCSPlusRecallResults____9/index.htmlPDF File: Félicitations. Vous avez terminé la formation en ligne du Programme de gestion de données RAPIDComm® 4.0, Consultation des résultats. Examinez le contenu de cette page avant de procéder au quiz final. Patient and QC records stored on the analyzer can be deleted permanently from instrument memory. The CLINITEK Status®+ Analyzer stores QC records as patient tests. Data stored on an LIS will not be deleted. Save the database to an external source prior to deletion. Individual records cannot be deleted. Note: This option must be enabled on the analyzer. You must be authorized by your facility to delete any records. Deleting Stored Records Learn how to delete stored records. Checklist TitleChecklist TypeChecklist ContentSelect readyHTML Select each check box to learn more about deleting records. On the Select Ready screen, click the Recall Results Button.  Recall OptionsHTML   On the Recall Options screen, use the down arrow to highlight the Delete Records option then click Select.  Delete recordsHTML On the Delete Records screen, select Yes to delete all records and return to the Select Ready screen or select NO to return to the Recall Options screen. When complete, select the X in the upper-right corner to close the window and continue.

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  • recall stored results
  • delete records
  • human chorionic gonadotropin
  • clinical laboratory training