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cmelloh

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Posts posted by cmelloh

  1. We use preprinted, computer generated, labels. The patient also has a blood bank ID bracelet which one of the numbers MUST be attached to the specimen. We also use electronic PPID which helps prevent mislabels. The nurse will scan the patient's armband, then the medical record number on the label. If there is a mismatch then the user gets an error message. We also require sample labeling at bedside.

  2. Our Blood Bank is segregated from the rest of the lab (behind a wall) so the noise is what we generate in the room. The only rule we have about interruptions is when we dispense a product. If we are interrupted in the middle of a dispense, we have to start over. So if anyone of us is dispensing, and someone goes to talk with us, we usually hold up a finger (index) and give the "1 minute please." The joke then becomes, "I have to wait, I just got the finger." If a radio is too loud, then we politely ask them to turn it down.

  3. We ship the majority of our blood products through a pneumatic tube station. Blood Bank and the OR have the highest priority meaning if we hit the Send button, the system stops any other tubes from entering the system until the Blood Bank tube is delivered. For products that have to be hand delivered (syringe, saline resuspended, washed) the RN, LPN, or health unit coordinator can pick up blood. The paperwork, that goes with the unit, is two part so we can see who picked up the product and time and who hung the product and time.

  4. I am in the process of validating our Hematology analyzers to perform platelet counts on platelet rich plasma from our plateletphersis. Has anyone ever done this? If so, can you share what you did to validate, the statistical methods you used, and your acceptable criteria? The analyzer does not matter. I don't want to reinvent the wheel if I don't have to. Thanks!

  5. We use a second ABORh typing rack with a different manufacturer of typing reagent. A second tech performs the type recheck using the different reagents. If only one tech is in Blood Bank (mostly midnight shift) then the same tech can retype the sample since a different set of reagent is used.

  6. Our physicians order the volume they want and if the patient needs volume reduction of platelets due to volume issues. All of our products are irradiated, leukoreduced, and tested for CMV status due to our patients being oncology patients. The Blood Bank determines the patient type and CMV requirements based on testing, diagnosis, and cytogenetic data. With our sickle cell patients, the orders for RBCs are for C, E, K and Sickle negative. We perform phenotyping on these patients at admission and then give products based on the information. The Blood Bank makes the decision as to whether a patient will get CMV negative products or not.

  7. We give volume reduced (plasma reduced) plateletpheresis for incompatible platelets. We have a patient that was transplanted and requires AB plasma products. I took a call last week from the doctor stating he did not order volume reduced but he did not want the patient to have a reaction or form an antibody (duh! neither do we). I explained that because of her plasma type requirement, and the fact we rarly have AB platelets, all of her platelets would be volume reduced. He ended the conversation with "are you sure she won't have a reaction?"

    Crystal

  8. We allow our products to "rest" for one hour after collection and the rock for another hour before sample collection. By allowing the platelet to relax, does this cause any microaggregates to dissolve causing an increase in the platelet count? If so, would vortexing the sample give the same result or would it activate the platelets making the counts even lower?

  9. I am getting ready to start validation a LH 750 and DxH, both Beckman-Coulter, for platetet counts on platelet rich plasma. I have a few questions. Is there a certain amount of time that should elapse between the PRP sample being collected and the sample analyzed? How often should linearity for PRP be performed? We remove 3mL of PRP from our plateletpheresis product, place the sample in EDTA, and refrigerate. Is this the best storage option or should the samples be kept at room temp? Thanks!

  10. Hi everyone! I am new to the forum and am really excited about having someone to talk "shop" with outside of my employer. I work at St. Jude Children's Research Hospital as the Evening Shift Supervisor. I look forward to talking with you.

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