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HAEMONETICS TEG 5000 PDF

The TEG® Hemostasis Analyzer System provides a more complete .. TEG are trademarks or registered trademarks of Haemonetics Corporation in the. Consult HAEMONETICS’s entire TEG ® catalogue on MedicalExpo. Page: 1/8. Consult HAEMONETICS’s entire TEG Hemostasis Analyzer System catalogue on MedicalExpo. Page: 1/8.

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The data panel can be invoked when it is not displayed, by clicking either p anywhere on the tracing p on the Data icon in the local toolbar p or pressing F8 and can be dismissed by clicking on Done.

The end result of the hemostasis process is a single product — the clot. Page 7 Chapter 1: Page 91 Chapter 7: Click on all of the samples you wish to report. Move through the initial screens of the program until you reach the Main Menu. If sample notes are also entered, as described in Chapter 4, then they follow the case notes.

If you are not sure, select New. During this time, any samples that are running will continue to run without interruption, but any other activity will require logging back in as described earlier under “Operator Login. We strongly recommend making a backup copy of the database using Explorer or My Computer before running Compact database.

Haemoscope Corporation recommends that the user follow locally established procedures for the collection and handling of specimens. If you access the Detail haemoneticz by hameonetics the icon, the Tracing tab is displayed as in figure 5. Each rotation cycle lasts 10 seconds. Open the catalog to page 4. By default all pages are printed.

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Pipette the following volumes of CaCl2, depending on blood sample, in the cup: QC samples are copied, if any exist, providing the option is set in the User Profile to transfer samples. Seminars in Thrombosis and Haemoetics. The tracing border, the sample ID information, and 50000 data receive a cyan blue background. Page Quality Control Chapter As part of that configuration, users are defined with security user login names and optional passwords, along with all sorts of user default settings.

If this information is not available until later, you can enter the haemonetkcs either before or after you start the sample. TMA combines the rate of clot development from the start of a sample run until the clot reaches its maximum strength.

Moront The Toledo Hospital: You can override this default for black and white printers such as lasers by clicking Print text in black under Graphics options. Click “Log In” on the Main toolbar for operator login.

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The software can be run in a configuration that allows the analyzer to be placed in a centralized location such as a laboratory, with results displayed where needed, for example, in remote operating rooms.

Hemostasis diagnosis and treatment decisions are sometimes difficult to arrive at. Transfer the blood gently from the syringe to a small non-wettable surface, e. Using the two-syringe method and observing proper technique e.

An example Figure 2. Pipette the following haemoneticd of blood to the cup. CL30 parameter Thirty minutes after MA is reached, the amplitudes of both tracings read zero due to fibrinolytic activity.

TEG Haemonetics U.S.A – HSC

The left portion of the panel displays sample identifying information: Contact your local service representative, or the main office at: Black background is useful when the captured tracing will be used on a mm slide or in an online slide presentation such as PowerPoint. To print a quick report of one sample, follow these steps: However, even if this is the case, we strongly recommend you back up your own data.

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All records related to this patient, including all samples, notes, etc. This can be described as the time needed to form a stable clot. Note that you can input sample identifying information without running the sample at this time. To maximize a single tracing, either: Press the carrier down firmly against the platform so that the plastic pusher located at the bottom of the carrier pushes the disposable cup out of the cupwell.

You will see a sample display showing how the columns are assigned. The tracing detail screen summarizes all the numerical data for the selected sample, while showing the tracing at the left. Page 3 Chapter 1: Cap and store at room temperature, without mixing until ready to assay.

PMA begins to display when amplitude reaches 5 mm, and is finalized when the rate of clot formation slows a is final.

As you select a sample, you will notice a cyan blue border in the tracing panel and highlighted numbers in the data panel for selected samples.