Survey of newborn direct antiglobulin testing practice in United States and Canadian transfusion services. Issue 4 (25th February 2021)

• Record Type: Journal Article
• Authors: Crowe, Elizabeth P.; Goel, Ruchika; Andrews, Jennifer; Meyer, Erin K.; Wong, Trisha E.; Sloan, Steven R.; Delaney, Meghan; Lieberman, Lani; Cushing, Melissa M.
• Is Part Of: Transfusion. Volume 61:Issue 4(2021)
• Page Start: 1080
• Page End: 1092
• Publication Date: 2021-02-25
• Subjects: direct antiglobulin test -- hemolytic disease of the fetus and newborn -- immunohematology -- newborn; Hematology -- Periodicals; Blood -- Transfusion -- Periodicals; Blood Group Antigens -- Periodicals; Blood Preservation -- Periodicals; Blood Transfusion -- Periodicals; 615
• DOI: 10.1111/trf.16335
• Languages: English
• ISSNs: 0041-1132

Abstract

Abstract: Background: We hypothesized that variability in practice exists for newborn immunohematology testing due to lack of consensus guidelines. We report the results of a survey assessing that variability at hospitals in the United States and Canada. Study Design and Methods: An AABB Pediatric Subsection working party developed and validated a survey of newborn immunohematology testing practice. The survey was sent electronically to transfusion service leadership at teaching institutions. Results: The response rate was 67% (61/91); 56 surveys meeting inclusion criteria were analyzed. Approximately 90% (50/56) were from birth hospitals and 16.1% (9/56) were from pediatric hospitals. Newborn immunohematology testing is ordered as a panel by 66.0% (33/50) of birth hospitals. ABO group and DAT is mandated before discharge in 14/56 (25.0%) and 13/56 (23.2%), respectively. About 76.8% (43/56) selectively perform a DAT according to blood blank or clinical parameters. The most common DAT practices include anti‐IgG only testing by 73.2% (41/56) and use of umbilical cord specimen type by 67.9% (38/56). A positive DAT is a critical value for 26.8% (15/56) and followed with eluate testing when a maternal antibody screen is positive for 48.2% (27/56). In the setting of a non‐ABO maternal red cell antibody, 55.4% (31/56), phenotype neonatal red cells when the DAT is positive. Group O RBC are transfused irrespective of the DAT result for 82.1%, (46/56). Conclusion: There is variability in newborn immunohematology testing and transfusion practice and potential overutilization of the DAT. Evidence‐based consensus guidelines should be developed to standardize practice and to improve safety.