Extended phenotyping does not preclude the occurrence of delayed haemolytic transfusion reactions in sickle cell disease. (10th October 2021)
- Record Type:
- Journal Article
- Title:
- Extended phenotyping does not preclude the occurrence of delayed haemolytic transfusion reactions in sickle cell disease. (10th October 2021)
- Main Title:
- Extended phenotyping does not preclude the occurrence of delayed haemolytic transfusion reactions in sickle cell disease
- Authors:
- Gerritsma, Jorn
Bongaerts, Vera
Eckhardt, Corien
Heijboer, Harriet
Nur, Erfan
Biemond, Bart
van der Schoot, Ellen
Fijnvandraat, Karin - Abstract:
- Summary: Delayed haemolytic transfusion reaction (DHTR) is a potentially life‐threatening complication of red blood cell (RBC) transfusions in sickle cell disease (SCD) and is classically induced by reactivation of previously formed antibodies. Improved antigenic matching has reduced alloimmunization and may reduce DHTR risk. We conducted a retrospective cohort study to investigate the incidence rate of DHTR in SCD patients receiving extended matched units (ABO/RhDCcEe/K/Fy a /Jk b /S). Occasional transfusion episodes (OTE) between 2011 and 2020 were reviewed for occurrence of DHTR symptoms using four screening criteria: decreased Hb, increased lactate dehydrogenase (LDH), pain, and dark urine. We included 205 patients who received a cumulative number of 580 transfusion episodes of 1866 RBC units. During follow‐up, 10 DHTR events were observed. The incidence rate of DHTR was 13·8/1000 OTEs [95% confidence interval (CI): 7·37–22·2], with a cumulative incidence of 15·2% (95% CI: 8·4–24·0%) after 25 patients having received RBC units. One DHTR event was fatal (10%). Symptoms were misdiagnosed in four DHTR events (40%) as other acute SCD complications. Despite a lower incidence rate compared to most other studies, the incidence rate of DHTR in SCD remains high, in spite of extended matching of donor RBCs. Increased awareness of DHTR is of utmost importance to facilitate early diagnosis and, consequently, improve outcome.
- Is Part Of:
- British journal of haematology. Volume 196:Number 3(2022)
- Journal:
- British journal of haematology
- Issue:
- Volume 196:Number 3(2022)
- Issue Display:
- Volume 196, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 196
- Issue:
- 3
- Issue Sort Value:
- 2022-0196-0003-0000
- Page Start:
- 769
- Page End:
- 776
- Publication Date:
- 2021-10-10
- Subjects:
- delayed hemolytic transfusion reaction -- transfusion reaction -- red blood cell transfusion -- sickle cell disease -- alloimmunization
Hematology -- Periodicals
Blood -- Diseases -- Periodicals
616.15 - Journal URLs:
- http://www.blacksci.co.uk/%7Ecgilib/jnlpage.bin?Journal=bjh&File=bjh&Page=aims ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2141 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjh.17875 ↗
- Languages:
- English
- ISSNs:
- 0007-1048
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2309.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26818.xml