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cthherbal

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Posts posted by cthherbal

  1. I agree with the others who state to consider getting rid of the separate blood bank ID bands.

    We do not use these currently. We have Cerner LIS and Epic EMR. The nurses scan blood bags and patient armband at bedside when starting the transfusion.

    As an aside, we do bedside collection labeling in Epic. We do track Wrong Blood in Tube. When we first went live on Epic, those numbers increased, but once workflows were reinforced, the number is now very low.

    The one WBIT we had in 2021 is where someone found a way around the system I believe someone mentioned it above, "scan overrides". Problem detected in blood bank when confirmatory sample did not match original type and screen blood type. Luckily this person no longer works here. :)

  2. On 4/8/2022 at 6:29 AM, Ensis01 said:

    Sorry for my ignorance, I have never used the vision. Would you need two different cards, one for IgG and one for IS? If the cards exist why could you not validate their use? As jayinsat said automation helps the generalists especially when short staffed or they are inexperienced. 

    FDA approval came through last year.

  3. we bill CPT 86078

    from AABB website: Billing for Blood and Transfusion Services- Frequently Asked Questions and Answers (aabb.org)

    Billing for Transfusion Reactions

    Question: What is the appropriate billing date for CPT code 86078 Blood Bank physician services; investigation of transfusion reaction including suspicion of transmissible disease, interpretation and written report?

    Answer: The date the transfusion reaction workup specimen(s) was collected should be the billed date of service. This includes all services performed in conjunction with the transfusion reaction regardless of date of completion.

    Reference

    1. 68 Fed. Reg. 74607, at 74611 (Dec. 24, 2003)
    2. Negotiated Rulemaking: Coverage and Administrative Policies for Clinical Diagnostic Laboratory Services
  4. AABB 3.9 Information Systems


    The BB/TS shall have processes to support the implementation and modification of software,
    hardware, and databases relating to the requirements of these BB/TS Standards. Standard
    5.1.1 applies. These processes shall include:
    1. Risk analysis, training, validation, implementation, and evaluation of postimplementation
    performance.
    2. System maintenance and operation.
    3. Documentation written in language understandable to the user.
    4. Display and verification of data before final acceptance, when data are added, or when
    data are amended.
    5. Evaluation, authorization, and documentation of modifications to the system.

  5. I did a swiss cheese diagram after the fatality in the US a few years ago to hit home what COULD happen.

    Attaching, feel free to tweak for your use. It speaks to just one of the reasons why we require the sample confirmatory sample, and probably the most important one, WBIT.

    Swiss cheese TX incompatible transfusions patient death1.pptx

  6. On 8/15/2017 at 8:08 AM, SarahE said:

    Thank you for all your responses!  I will be doing more research, and discussing the topic with our pathologists.  Since our current method does not use any enhancement techniques, and "gel" does, the correlations are poor.  There difference is at very least 2-fold.  I agree that reproducibility and tech interpretation are two major factors with the tube technique, and I believe that "gel" would help with both of those.  What do your physicians use as a "critical" number as far as titers go?  I've read that using tube, some physicians consider a titer of 32 as "critical", where this would have to be modified for "gel."

    We have not gone "live" with our Ortho Vision testing yet, but I will keep you informed with our decisions.  :)

    Hi, Sarah. What did you end up deciding? We have a Vision but don’t currently run titers on it. We use manual gel, and haven’t had any problems with proficiency testing.

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