Abstract

BackgroundThe Leiden University Medical Center (LUMC) is the Dutch national referral centre for pregnancies complicated by haemolytic disease of the fetus and newborn (HDFN) caused by maternal alloimmunization. Yearly, 20-25 affected fetuses with severe anaemia are transfused with intra-uterine blood transfusions (IUT). Mothers of whom their fetus has undergone IUT for HDFN are considered high responders with regard to red blood cell (RBC) antibody formation. Most study groups report high perinatal survival, resulting in a shift in attention towards short- and long-term outcome in surviving children.Methods/DesignWe set up a large long-term observational follow-up study (LOTUS study), in cooperation with the Sanquin Blood Supply Foundation and the LUMC departments of Obstetrics, Neonatology and ImmunoHematology & Bloodtransfusion.The first part of this study addresses several putative mechanisms associated with blood group alloimmunization in these mothers. The second part of this study determines the incidence of long-term neurodevelopment impairment (NDI) and associated risk factors in children treated with IUT. All women and their life offspring who have been treated with IUT for HDFN in the LUMC from 1987-2008 are invited to participate and after consent, blood or saliva samples are taken. RBC and HLA antigen profile and antibodies are determined by serologic or molecular techniques. Microchimerism populations are tested by real time polymerase chain reaction (RT PCR).All children are tested for their neurological, cognitive and psychosocial development using standardised tests and questionnaires. The primary outcome is neurodevelopmental impairment (NDI), a composite outcome defined as any of the following: cerebral palsy, cognitive or psychomotor development < 2 standard deviation, bilateral blindness and/or bilateral deafness.DiscussionThe LOTUS study includes the largest cohort of IUT patients ever studied and is the first to investigate post-IUT long-term effects in both mother and child. The results may lead to a change in transfusion policy, in particular future avoidance of certain incompatibilities. Additionally the LOTUS study will provide clinicians and parents better insights in the long-term neurodevelopmental outcome in children with HDFN treated with IUTs, and may improve the quality of antenatal counselling and long-term guidance.

Highlights

  • The Leiden University Medical Center (LUMC) is the Dutch national referral centre for pregnancies complicated by haemolytic disease of the fetus and newborn (HDFN) caused by maternal alloimmunization

  • The LOTUS study includes the largest cohort of intra-uterine blood transfusions (IUT) patients ever studied and is the first to investigate post-IUT long-term effects in both mother and child

  • The LOTUS study will provide clinicians and parents better insights in the long-term neurodevelopmental outcome in children with HDFN treated with IUTs, and may improve the quality of antenatal counselling and long-term guidance

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Summary

Discussion

Part 1: “Long-term maternal immunological outcome” Pregnant women with Rh-D alloimmunization resulting in haemolytic disease of the fetus, receive a median of. We found that the neurodevelopmental outcome for children with HDFN treated with IUTs compared favourably with a group of high-risk, very low birth weight infants (10% versus 18%, respectively), but less favourably with a healthy control group (10% versus 6%, respectively) [10]. List of abbreviations ADCC: Antibody-Dependent Cell-mediated Cytotoxicity assay; BSID: Bayley Scales of Infant Development; FMH: Fetomaternal haemorrhage; HDFN: Haemolytic Disease of the Fetus and Newborn; HLA: Human Leucocyte Antigen; IUT: IntraUterine Transfusion; MDI: Mental Development Index; MHC: Major Histocompatibility Complex; NDI: NeuroDevelopmental Impairment; PDI: Psychomotor Development Index; RBC: Red Blood Cell; RT-PCR: Real Time Polymerase Chain Reaction; SDQ: Strenghts and Difficulties Questionnaire; TAAQOL: TNO AZL Adolescent Quality of Life; TACQOL: TNO AZL Child Quality of Life; WISC-III: Wechsler Intelligence Scale for Children-3rd edition; WPPSI-III: Wechsler Preschool Performance Scale of Intelligence-3rd edition. All authors edited the manuscript and read and approved the final draft

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