Jump to content

amym1586

Members
  • Posts

    249
  • Joined

  • Last visited

  • Days Won

    5
  • Country

    United States

Posts posted by amym1586

  1. Thanks for your feedback!

    I hope no one took that as me "dissing" an MLT.  There are MLTs here that have been working for as long as I've been alive.  And I believe no matter how much you study BB it's really the experience that counts.    

    I was just curious if their standards here were based on the fact that we do have majority of MLT's working here. They keep a short leash on some things and other things don't check at all.    I think they need some updating and rearranging. I just hope I have the guts to do it. 

  2. I'm coming from a hospital that only staffed MTs to a blood bank supervisor with mostly MLTs.  They make them call a pathologist for every platelet that gets issued, after 4 FFP have been issued and for every Cryo.   I was wonder if they were doing that to keep them in check or what ?  I'm just not used to that. 

  3. On ‎10‎/‎20‎/‎2015 at 9:29 AM, Maureen said:

    To ensure compliance with AABB Standard 5.16.2.2 if you use an electronic crossmatch you need to perform both front and back types (AABB 5.14.1).

    Is there anything that says you must have 2 antibody screens done before eligible for an Electronic crossmatch ?

  4. We normally have 2 cubes open at a time. with 2 different lot numbers.   One is hooked up to our cell washer and one is opened to fill our squirt bottles.

     

    How do you handle qc for that?

    Currently we are just writing down the QC for the cube lot# going to the cell washer.

    Do I need to update my qc to include the saline going into the squirt bottles?

  5. 5 minutes ago, David Saikin said:

    Unless you do these routinely your techs might have a hard time with this test.  I do them for 3 other hospitals and all my techs have to read the CAP survey slides after we submit them.  It is the only way to keep them confident.  The counting is abysmal to tell the truth.  I think the CV is around 40%.  Flow cytometry is the preferred method for quantifying the fetal/maternal hemorrhage.  Not going to happen in a small hospital like mine.

    Yeah, I've done plenty of KB stains at my old hospital ( I don't miss them :D)

    I've been here for a year and so far have not had one patient need one.

    I just wonder if that will suffice to give one dose of RhIg to an Rh Neg Weak D pos mother of an Rh Pos baby.  Or if more testing is required.

    I guess we are getting by with our procedure of them not being a candidate but I don't like that.

     

    I still don't understand why there is so much gray area in blood banking. I feel like there should be way to do it and that is the way to do it. 

  6. 23 minutes ago, goodchild said:

    Amy I would also recommend reading the manufacturer's instructions for your fetal screen kit. What does it say about weak D mothers, weak D babies, other special scenarios?

    "If the mother is D positive, including weak D, strong agglutination provides no information about the extent of fetomaternal hemorrhage"

     

    It doesn't expand any further. 

  7.  

    We only do IS on Rh Neg mom's unless it doesn't match up with what the clinic typed them. Then we add on a weak D.

     

    But when we result a Weak D pos it changes the patient to O Pos. Our procedure says Rh neg Du positive Mothers would not be a candidate to receive  rhogam.

     

    But if we had no history and simply did an IS Rh we would type her as Rh neg and she would be a candidate for Rhogam.

     

    :blink:

  8. How many of you have a Transfusion Safety officer (TSO) at your hospital?

    If you don't have one, is the role just taken by the BB supervisor ?

    I see UBS offers a TSO curriculum program.  I wonder if it would be beneficial for a BB supervisor who does not have a TSO to attend.

  9. I've just noticed we don't write an issue time on the blood tag at my new hospital.   I don't know how they are monitoring that the transfusion is started in a timely manner or if it's finished in 4 hours.     I am not in charge of monitoring this info here.

     

    Also, If you are issuing products in a cooler/refrigerator are they supposed to write in a time removed and then a time started?  

     

     

  10. 1 hour ago, AMcCord said:

    It depends on how their policy is written and how stringent the nursing reviewers are - if they documented issues with an IV (or something else legit), I wouldn't nick them for that. I would, however, make sure the infusion was complete in 4 hours.

    Gotcha,   I pull a percentage of transfusion slips every month and my pathologist checks all the info. So, I'd have to check with him I suppose about how lenient we are with those numbers.   

×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.