A recent CMAJ Practice article1 on modern Rhesus (Rh) typing in transfusion and pregnancy and its associated correspondence2 prompted a productive discussion on safe recommendations for pregnant patients with a weak D type 4.0 allele, originally described in 2000.3 The differing approaches1,2 represent the personal views of the respective authors. Based on our review of 20 years’ worth of literature on this specialized topic, we have agreed on the following 5 statements:
No published case reports have documented adverse clinical effects, such as hemolysis, among pregnant people with weak D type 4.0 caused by an allo- or auto-anti–D.
Similarly, no published case reports have documented adverse clinical effects, such as anemia or jaundice, among fetuses or newborns caused by such a mother’s allo- or auto-anti–D.
No published evidence has shown that Rh immunoglobulin (RhIg) is clinically effective in an individual with weak D type 4.0 (e.g., for preventing anti-D formation); RhIg can cause a positive direct antiglobulin test, which does not imply clinical harm.
The weak D type 4.0 phenotype may be associated with a proportionately larger number of anti-D than most other weak D types.4–6 The nature of these antibodies has not been well characterized (i.e., allo- v. auto-antibody). 6 A fraction of all people with a weak D type 4.0 are routinely typed as normal RhD-positive and do not receive RhIg.3,7,8
The decision of whether or not to use RhIg or RhD-negative transfusion in such mothers should be based on national guidelines.9 Both approaches have been adopted by expert groups2,6,8–10 and are considered safe. The decision may still depend on an individual patient’s circumstances. 11 If providers are unsure, consultation with a transfusion medicine physician or perinatal immunohematology reference laboratory is recommended.1,10
Footnotes
Competing interests: None declared.
Funding: Willy Albert Flegel is supported by the NIH Clinical Center, Intramural Research Program, ID ZIC CL002128.
Disclaimer: The views expressed do not necessarily represent the views of the National Institutes of Health, the Department of Health and Human Services, or the U.S. Federal Government.
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