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clmergen

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Posts posted by clmergen

  1. I joined this page 13 years ago but haven't really looked at it in at least 5 years. Through moves and promotions, I haven't been as involved in blood banking as I used to be.  I was surprised to see my password worked (luckily I had it written down).  I was happy to see many of the members from so long ago.  I see we still need to grow the non-blood bank forums. I suggest this site to every medical laboratory scientist and student I know as it has helped me greatly in the past.  I am glad to be back. 

    Carrie 

  2. My hospital helped develop an Massive Obstetrical Hemmorhage Protocol that has garnered recognition for our multidisciplinary team.  This is an email that I sent out to my staff to help understand what is going on. 

     

     

    There are risk levels and stage levels. 

     

    A risk level is “how likely is the woman to have a hemorrhage”. Therefore, we draw and test initially based on a risk level.

    Low Risk = Band and Hold

    Medium Risk = Type and Screen

    High Risk = Type and Cross 2 units

     

    Stage levels coincide with “how is the patient doing”

                    Stage 0 = Routine delivery

                    Stage 1 = Increased bleeding but still watch and see

                    Stage 2 = Increasing bleeding. Maternal Hemorrhage called. DIC panels every 30 minutes initiated.  Products are NOT ordered at this stage.

    Stage 3 = Blood loss is >1500mL. DIC panels every 30 minutes.  Need MOH Pack (3 RBC, 2 Plasma, 1 PLP, 1 cryo), additional packs as needed.

                    Stage 4 = Modified post-partum care based  on what stage 2 or 3 hemorrhage.

     

    Patients may go through the levels quickly but remember that the physicians are trying all options to stop the hemorrhaging. Therefore patients may never go to stage 3 but stop at stage 2. And not need any blood products.

     

    We have found over the last 3 years that they will typically transfuse everything but the cryo so we have changed the policy to not give the cryo until specifically requested (which is usually with fibrinogen <200)

  3. I worked in a lab where we discovered a weak subgroup of A using Immucor Anti-A,B to retype a unit, I believe it turned out to be an Ax. Typing with Anti-A and Anti-B yielded negative results. The Anti-A,B gave weak reactions but were defintiely visible. This unit was promptly returned to the blood supplier for retyping.

  4. Belle Bonfils is a good choice in Denver for an SBB. I believe they have a reference laboratory. I would think there would be quite a few hospitals to work in depending on how far you want to travel. denver is pretty spread out.

     

    I know the hospital I worked at in Colorado Springs had a lot of SBBs and most of the day shift were dedicted blood bankers. Evenings and nights had generalists.  But much has changed there since I left in 2006.

  5. At my last hospital, we stocked enough Rhophylac to be the 1st dose in a patient with ITP. Pharmacy was expiring the IGG they used and we never expired Rhophylac. I miss Rhophylac. I suggested it here and was told "we tried that and the nurses hated it". May re-assess soon.

  6. Trying to remember from my CAP inspection days (current lab TJC only). At my last facility, we documented bench cleaning each shift. I thought it was based on the CAP general checklist but can't remember exactly. It was mandated by our Laboratory Safety Officer. As for microscope disinfection, I know we didn't have a policy in the Transfusion Services but I do not know if Hematology or Urinalysis did.

  7. We are in the process of setting this up. We will require 2 blood types for all blood/blood product transfusions. At my last facility we tried dropping the requirement for plasma but the medical directors said NO. They felt (and I agree) that having a single standard for all products was less confusing for the cross-trained generalists.

  8. We run QC on the "dipstick" part of our analyzer (Clinitek Atlas) once per day but on the Microscopic (UF100) 3 times per day as it is a laser and cell counter just like a hematology analyzer. Actually since we had problems hitting the 8 hours + 15 minutes, we went to running 4 times per day. So we QC our analyzers (including Abbott Architect electrolytes, recommended every 8 hours) at 0300, 0900, 1500, and 2100.

  9. I really recommend Last Chance Review. I did the Florida Blood Service online SBB course and then also went to Last Chance Review. The concise presentation of the material gave a really nice study guide to augment my 12 3" binders from the SBB course. Plus there is a review on how to take the test that was nice. And it's always great to meet new people and network.

  10. One thing to consider also is the technique used by the technologists performing the tests. My first thought was that it is an Immucor/Orhto reagent problem. But if the same reagents are used and one technologist let the tube sit at room temperature for an extended length of time, that may change a negative reaction to a positive reaction. I have seen this with some weak Ds although going beyond 1+ is unusual.

  11. GilTPhoto, I feel your pain. We switched to Meditech 6.0 which in my opinion is far inferior to Cerner, but I can't tell if it is the programming or the stupid standards committee at the corporate level. I know a lot of your pain is the standards committee because we didn't run into your problems when I helped build Cerner two jobs ago.

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