1996
DOI: 10.1111/j.1365-3148.1996.tb00079.x
|View full text |Cite
|
Sign up to set email alerts
|

Guidelines for pre‐transfusion compatibility procedures in blood transfusion laboratories

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
30
0
2

Year Published

2005
2005
2017
2017

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 90 publications
(32 citation statements)
references
References 13 publications
(5 reference statements)
0
30
0
2
Order By: Relevance
“…ANZSBT Guidelines also recommend providing RBCs that match for Rh and K types to chronically transfused patients where readily available 20 . Moreover, the United Kingdom even considered the need to recommend phenotype as fully as possible before transfusion and to match for Rh and K antigens before the onset of alloimmunization due to the excessive high risk of alloimmunization in sickle cell anemia patients 9,21 …”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…ANZSBT Guidelines also recommend providing RBCs that match for Rh and K types to chronically transfused patients where readily available 20 . Moreover, the United Kingdom even considered the need to recommend phenotype as fully as possible before transfusion and to match for Rh and K antigens before the onset of alloimmunization due to the excessive high risk of alloimmunization in sickle cell anemia patients 9,21 …”
Section: Discussionmentioning
confidence: 99%
“…In Hong Kong, all patients would have their pretransfusion compatibility tests at the hospital blood bank. They followed either UK standards 9 or AABB standards 10 . Pretransfusion testing included ABO group, D type, antibody screen, and compatibility testing.…”
Section: Methodsmentioning
confidence: 99%
“…Panels of reagent RBCs for identification of antibodies to RBCs are typed for a list of antigens defined by government bodies 28,29 . Whereas some European regulatory agencies require D, C, E, c, e, Fy a , Jk a , and S antigens in double dose, there is no requirement of the Food and Drug Administration in the United States to be present in double dose, 30 although the AABB technical manual indicates that it is valuable to include RBC samples with a double dose of the same antigens 31 .…”
Section: Discussionmentioning
confidence: 99%
“…The choices are based on the principle that the recipient plasma must not contain the antibodies corresponding to donor A and/or B antigens [11,12]. Ideally, the same blood group RBC which is compatible with the recipient plasma should be transfused.…”
Section: Choice Of Blood Groupmentioning
confidence: 99%