2020
DOI: 10.1111/trf.15987
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Red blood cell alloimmunization prevalence and hemolytic disease of the fetus and newborn in Israel: A retrospective study

Abstract: Background Hemolytic disease of the fetus and newborn (HDFN) is a severe form of anemia caused by maternal antibodies against fetal red blood cells (RBC) that can cause intrauterine and perinatal morbidity and mortality. The prevalence and specificities of alloantibodies among Israeli pregnant women and clinical outcomes for their fetuses and newborns are unknown. Study Design and Methods: A retrospective study of women who gave birth between January 1, 2011, and December 31, 2011, was performed. Data were obt… Show more

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Cited by 15 publications
(12 citation statements)
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“…While there have been reports suggestive of increased severity of fetal anemia based on type of antibody, especially in cases of Kell antibodies or the presence of multiple antibodies [15][16][17][18][19], our study did not demonstrate any difference in mode of transfusion based on type of antibody or number of antibodies detected. Several studies have reviewed the complications from IUTs which include preterm premature rupture of membranes, infection, preterm delivery, demise, and need for emergency cesarean section [5,[20][21][22].…”
Section: Discussioncontrasting
confidence: 93%
“…While there have been reports suggestive of increased severity of fetal anemia based on type of antibody, especially in cases of Kell antibodies or the presence of multiple antibodies [15][16][17][18][19], our study did not demonstrate any difference in mode of transfusion based on type of antibody or number of antibodies detected. Several studies have reviewed the complications from IUTs which include preterm premature rupture of membranes, infection, preterm delivery, demise, and need for emergency cesarean section [5,[20][21][22].…”
Section: Discussioncontrasting
confidence: 93%
“…This findings is in agreement with previous reports of Gothwal and colleagues reported that (3.119%) of pregnant women were alloimmunized with specificity of anti-M (9.23%), anti-c (3.076%), anti-E (1.538%), anti-e (1.538%), anti-Lewis (a) (1.538%), unspecified antibodies (1.538%), multiple antibodies anti-D and anti-C (3.076%), anti-e and anti-c (1.538%), and anti-D and anti-G (1.538%) in tertiary care centre of Western India [11] and that of Karim and colleagues in Pakistan reported the frequency of maternal alloimmunization among pregnant women was 1.8% of with specificity of non-anti-D (1.6%), anti-M (15%), anti-Lewis(a) (15%), anti-c (5%), anti-E (5%), anti-e (5%), anti-Lewis(b) (5%) and nonspecific antibodies (30%) and the prevalence of anti-D 2.9% in D negative blood type [12] as well as the report of [13] Ugandan who reported that 2•2% of pregnant women were alloimmunized to RBC antigens with specificity including anti-S, 12; anti-M, 11; anti-Lea, 6; anti-D, 4 and 1 each of anti-K, anti-Fyb, anti-Jka, anti-Lua and anti-Kpa. [14] in isreal also reported that 5.8% of the pregnant women had antibody with specificity of anti-E (23%), anti-K (16%), and anti-c (10.8%) and multiple alloantibodies were observed in 15% of women and severe HDFN developed in 6.8% of these pregnancies. "Although the subjects are not the same, the finding are also in agreement with another previous report that reported 6.5% antibody screening positive with 13 RBC antibodies against antigens in the Rh system some had multiple antibodies, M antigen, and one against a low frequency antigen of unknown specificity" [15].…”
Section: Resultsmentioning
confidence: 92%
“…The mean ± SD prevalence of Rh(D)-mediated HDFN (requiring any form of treatment) as reported in 5 studies [ 23 , 29 , 45 , 47 , 54 ] was 0.047%±0.037% among all pregnancies that were managed and delivered in the centers of the 5 selected studies (Fig. 2 ).…”
Section: Resultsmentioning
confidence: 99%