Search
Facebook Twitter RSS
 
 

 

Print

Submit a question to the Forum. Use our new online form below!

Subscribe to the e-Network Forum Newsletter

 

 

Routine Pre-Transfusion Testing Topics

 

Date Posted Subject
Dec. 23, 2011 Why is an AHG (serologic) crossmatch required when the antibody screen is positive?
July 19, 2011 Computer Crossmatch ADDENDA July 22 & 25
Apr. 2, 2011 Are American Transfusion Services screening for Diego(a) antibody?
Sept. 29, 2009 A problem with 12x75 glass tubes cracking when retesting blood donor units using an automated Gel-based technology ADDENDA Oct. 4 & 8
Mar. 28, 2009 Emergency transfusion of uncrossmatched blood to injured patients via helicopter personnel in the field
Dec. 26, 2008 Performance of the Direct Antiglobulin Test when doing antibody screening or crossmatching
Dec. 15, 2008 Performing the direct antiglobulin test without using tubes ADDENDA Jan. 28, 2009
Sept. 15, 2008 Why 3 months for prior transfusion history?
Mar. 5, 2008 Is incomplete re-suspension in automated cell washers acceptable?
Jan. 12, 2008 Is anyone using a micro titre tube method? ADDENDA Feb. 19
Oct. 3, 2006 The serological and/or clinical significance of indicating "strong" or "weak" notations when grading antigen-antibody reactions ADDENDA Oct. 4
Aug. 3, 2006

The medical necessity of continuing to perform crossmatches on RBC units for patients who have experienced massive transfusion of at least 8-10 RBCs in less than 24 hours ADDENDA Aug. 7

May 23, 2006 Is ABO, Rh and/or K typing routinely performed by phenotyping or genotyping by the UK National Blood Service? ADDENDA May 31
May 12, 2006 Is it considered acceptable to use a patient's historical ABO/Rh result from a previous visit when filling an order for FFP?
Mar. 30, 2006 Do transfusion service laboratories use a 'control' to check for spontaneous agglutination to rule out possible false positive results when performing a direct antiglobulin test (DAT) by GEL Test Technology? ADDENDA Apr. 6
Oct. 3, 2005 QC checks for ABO typing reagents; what is required for compliance with rules/regulations versus what is needed to assure test results are accurate for patients who might need transfusion? ADDENDA Oct. 4; Nov. 22, 2007
Aug. 5, 2005 Do transfusion service laboratories with automated equipment use the same QC reagents for the daily QC of their automated equipment and for the rack(s) of reagents that might be used in manual testing, in the event the automated equipment malfunctions?
June 24, 2005 Provision of A1 and B reagent red cells negative for M and Lewis antigens ADDENDA June 28 & July 4
May 23, 2005 How do hospital transfusion service laboratories perform quality control (QC) testing for reagent red cells that are part of an antibody identification panel? ADDENDA May 31, June 1 & Aug. 21
May 3, 2005 Blood grouping prerequisites for electronic crossmatching in a fully automated environment (including electronic transfer of results) ADDENDA May 4, 8 & 10
Mar. 22, 2005 Interpretation of AABB Standards for pre-transfusion compatibility testing of two-unit red cell apheresis products from the same donation ADDENDA Mar. 23
Mar. 9, 2005 Addressing the proposed new requirements for verification of donor-recipient ABO compatibility in organ procurement and transplantation ADDENDA Mar. 10
Aug. 15, 2004 An alternative approach to ABO/Rh donor unit confirmation testing ADDENDA Aug. 21
June 19, 2004 Revisions for the package inserts for the 0.8% Reagent Red Blood Cell product line which is used with the GEL Technology ADDENDA Jan. 16 & 18, 2006
June 17, 2004 Does a history of transient passively acquired anti-D from receipt of RhIG disqualify a patient for an electronic crossmatch? ADDENDA June 23
Mar. 27, 2004 Report of bubbles in the columns of ABD gel cards ADDENDA Mar. 30
Feb. 8, 2004 Methods to obtain appropriate reaction strength when performing daily reagent QC using gel cards ADDENDA Feb. 10, 15 & 19
May 29, 2003 What is the experience with using washed red cells for the immediate spin test to reduce the nondetection rate for ABO incompatibilityADDENDA June 3
May 3, 2003 What is a reasonable parallel testing scheme for verifying equivalence between a manual tube technique and a gel automated technique?
Apr. 2, 2003 What are the QC requirements for isotonic saline used with automatic cell washers? ADDENDA April 5
Mar. 6, 2003 Are laboratories following the requirement to use complement-coated RBCs for validating negative direct antiglobulin tests (DATs) performed with anti-C3b, -C3d reagents? ADDENDA Mar. 12 & 13
Feb. 3, 2003 Reconciling conflicting results for Rh typing using different test reagents ADDENDA Feb. 4 & 5, 2003; Mar. 25, 2007; June 11, 2008; Jan. 18, 2009
Jan. 30, 2003 Do institutions that use the Gel method for ABO grouping encounter ABO grouping discrepancies due to failure of the test system to detect expected ABO antibodiesADDENDA Jan. 31, Feb. 5 & 6
Nov. 21, 2002 How do colleagues test for and report Rh typing results of individuals who are weak D positive?
Dec. 21, 2001 Type and screen for scheduled elective surgical cases ADDENDA Dec. 26
Nov. 14, 2001 Use of immediate spin phase when crossmatching using PEG-AHG or GEL-AHG techniques
Oct. 10, 2001 Use of immediate spin phase when crossmatching using PEG technique
Sept. 20, 2001 Experience using PEG versus LISS for antibody detection ADDENDA Sept. 21
Aug. 26, 2001 What factors influence the decision to switch to tubeless techniques for compatibility testing?
Aug. 20, 2001 Strategies for STAT provision of blood for patients who bleed out in a cardiovascular OR and/or ICU ADDENDA Aug. 22
July 22, 2001 Management of Compatibility Testing When a Patient is Transferred To Another Hospital Sharing the Same Transfusion Service SOPs and Computer System. ADDENDA Aug. 1, 2001
July 13, 2001 What is the status of automated pre-transfusion compatibility testing in the USA? ADDENDA July 14, 2001; Jan. 8, 10, 19 & 25, 2006
April 14, 2001 The Need for A Physician's Order for "Keep Ahead" Crossmatched Units
Feb. 14, 2001 False-negative Results with PEG Red Cell Antibody Test - Due to Elevated Serum Globulins ADDENDA Feb. 15, 2001
Feb. 11, 2001 Antibody Detection by Gel and Solid Phase Techniques
Dec. 12, 2000 Compatibility Testing for Issuing Non-RBC Components
Oct. 30, 2000 Should a reference laboratory discontinue testing for weak D for ALL patients?
April 28, 2000 Interference of "Hextend" with Compatibility Testing?
Feb. 28, 1999 Repeat testing for weak D in females of childbearing age?
Feb. 28, 1999 Is it necessary to do daily QC of anti-C3b, C3d reagents? (Updated 3-8-99)

 

Back to Top

Submit Comments to the e-Network Forum below:

Items marked with an asterisk (*) are required entries. Please note that there is a 60 minute time-out on this form. if one anticipates taking more than 30 minutes or so to compose the submission, we recommend composing your comments in a word processing application, and performing a copy and paste of your text into the comments field. "
* Name
Title
Affiliation
* email address
* Enter email address again to verify
* Do you wish to have attribution for your comments?



* Your Comments
*Please indicate if this is a new question, or if you are commenting on an existing discussion:

New Question
Existing, Name:
 File Attachments
(2MB limit)
To help us prevent SPAM, you must enter the the validation code EXACTLY AS IT IS DISPLAYED in the image directly to the right of the text entry field below in order to submit this form. Please note that the validation code is CASE SENSITIVE.
captcha

 
 
Login Join