POCcelerator™ Client Review and Acknowledge QC Results Video

To review QC results in Poxcelerator client, begin by navigating to the QC monitor and verify the QC Chart tab is selected. Here you have the option to view QC in a graphical presentation or a tabular QC presentation. For this exercise, let's stick to the graphical presentation. In the graphical presentation, you have a few viewing options. This icon allows you to zoom in or enlarge the graphical view. This icon allows you to zoom out or minimize the graphical view. This icon returns the graphical view to its original size, and this icon shows connecting lines between measurement results for each individual device. The selection criteria filters at the top of the screen can be used to search for a desired measurement series and the QC chart and statistical values are updated according to your selection. Note the toggles in the device area of the selection criteria can be used to switch between ward or groups and model or family. Additionally, the QC monitor displays non archived measurements by default. To view archived measurements, the date filters must be updated accordingly. Once your QC results have been filtered, you can analyze the QC chart. A blue point indicates A valid QC measurement. A light blue point indicates A commented valid QC measurement. A red point indicates a QC violation. A yellow point indicates A commented QC violation, a green point indicates an approved QC measurement, and a Gray point indicates an archived QC measurement. Now let's discuss how to acknowledge QC results via the status bar. Start by double clicking on the red signal light in the status bar. The first uncommented QC violation is opened on the QC chart of the QC monitor screen and the selection criteria filters are automatically adjusted to have all affected results displayed. Then select the red QC violation on the QC chart. The Lab comment for QC window appears with additional QC result information. Enter a Lab comment. You can either enter a free text comment or right click within the text box and select Insert Template to enter an existing Lab comment or select New Template to create a new Lab comment. Then select OK to confirm your input or Select for All to assign the comment to all QC results for the measurement series. The QC result then changes status depending on the follow up QC measurement result. If the QC violation has no follow up QC result where the follow up QC result is outside of the defined range, the QC violation will change from red to yellow status and the status bar will show a decrease in one red QC violation and an increase in one yellow QC violation. If the QC violation has a follow up QC result within the defined range, the QC violation will change from red to green status and the status bar will show a decrease in one red QC violation. If you did not select for all, then you would need to repeat the steps of selecting a red QC violation, entering a comment, and selecting OK for each red QC violation in the current measurement series. Double click on the red signal light in the status bar to open the next series of uncommented QC violations. Repeat the steps of selecting the red QC violations and entering comments until all red QC violations in the status bar have been acknowledged. Note this process can be followed to view all yellow QC violations and verify the commented QC violations receive a valid follow up QC measurement result.

16/05/2023 150.00 05/06/2023 149.16 1.85 1.24 1:1 168 166 164 162 160 158 156 154 152 148 146 144 142 140 138 136 134 132 18.05.2023 26.05.2023 30.05.2023 03.06.2023 149.1 6/7 50.00 62 64 150 :1 22.05.2023 3.75 1.51 4.1 3.9 3.85 3.8 3.7 3.65 3.6 3.55 35 3.35 41 3.5 4.05 3.95 34 36 39 300292 4.15 61 3.45 3.3 31.00 30.85 0.78 33 32 31 30 29 60 30.8 Review and Acknowledge QC Results Master Template HILS2218 | Effective Date: 25 Mar 2022 File View Quality controls Setup Extra In Result Monitor QC Monitor Process Monitor EQA Monitor Device Statistical values No. of controls Ward Model Target value Mean value Parameter Control Sample type |Whole blood Level 2 Standard deviation Analytes: Glu Lot no. Variation coefficient Quality control measurements Range by law Range by manufacturer . QC result Refresh QC chart Incomplete QC data -Stat Levet Result Monito QC Monitor Extra In i-Stat from: Device / Device ID User / ward Meas. time / Transmit time Reagent lot 151 mg/dL Device User Siemens (12345) Room 1 04/06/2023 12:51:07 / 05/06/2023 15:38:58 L04260 151.07 mg/dL 148.63 mg/dL 165 mg/dL 149.15 mg/dL 146.04 mg/dL OC violations Siemens Healthineers (1000) Process Monitor | EQA Monitor mg/dL Period from L04260_CG8+_L Extra Info Level: Sample type Whole blood Sample type Whole blood 22 05.2023 POCcelerator™ Review QC Results valid QC measurement commented valid QC measurement QC violation commented QC violation approved QC measurement archived QC measurement QC result ra Info 111038_EG6+_N Process Monitor EQA Monitor File Lab comment for qc Room 1 Beeper Telephone / Fax: Device name Serial number 420N132180235 User Device User Siemens Meas. time 26/05/2023 10:17:10 Transm. time 05/06/2023 15:39:10 Comments Wrong Level Lab comment: Unlock measuring method for patient resutts For all Cancel File Vi File View Quality controls File View Quality controls Setup Extra Info Insert template New template Qk Mode Measurement Repeated POCcelerator Invalid or missing follow up QC measurement Valid follow up QC measurement To acknowledge all QC violations in a measurement series: 1. Select a red QC violation 2. Enter a comment 3. Select Ok mmHg mmH 32.5 mmHg Lab comment For a Disclaimer Please note that the learning material is for training purposes only. For the proper use of the software or hardware, please always use the Operator Manual or Instructions for Use (hereinafter collectively "Operator Manual") issued by Siemens Healthineers. This material is to be used as training material only and shall by no means substitute the Operator Manual. Any material used in this training will not be updated on a regular basis and does not necessarily reflect the latest version of the software and hardware available at the time of the training. The Operator Manual shall be used as your main reference, in particular for relevant safety information like warnings and cautions. Please note: Some functions shown in this material are optional and might not be part of your system. Certain products, product related claims or functionalities (hereinafter collectively "Functionality") may not (yet) be commercially available in your country. Due to regulatory requirements, the future availability of said Functionalities in any specific country is not guaranteed. Please contact your local Siemens Healthineers sales representative for the most current information. The reproduction, transmission or distribution of this training or its contents is not permitted without express written authority. Offenders will be liable for damages. All names and data of patients, parameters and configuration dependent designations are fictional and examples only. All rights, including rights created by patent grant or registration of a utility model or design, are reserved. POCcelerator and all associated marks are trademarks of Siemens Healthcare Diagnostics Inc ., or its affiliates. All other trademarks are the property of their respective owners. Siemens Healthcare GmbH 2023 91052 Erlangen, GermanylTelephone: +49 9131 84-Olsiemens-healthineers.com