Affiliation:
1. Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland USA
2. Department of Laboratory Medicine and Pathology University of Washington Seattle Washington USA
3. Department of Laboratory Medicine Seattle Children's Hospital Seattle Washington USA
4. Department of Laboratory Medicine University of California San Francisco San Francisco California USA
5. The Johns Hopkins Center for Fetal Therapy, Department of Gynecology and Obstetrics Johns Hopkins University Baltimore Maryland USA
6. Department of Obstetrics, Gynecology and Reproductive Sciences University of California San Francisco San Francisco California USA
7. Corporate Medical Affairs Vitalant Scottsdale Arizona USA
Abstract
AbstractBackgroundIntrauterine transfusion (IUT) is an invasive but critical and potentially life‐saving intervention for severe fetal anemia with demonstrated improvement in outcomes. The fetus is vulnerable to hemodynamic alterations and transfusion‐related adverse events; therefore, special consideration must be given to blood component selection and modification. There is widespread IUT practice variability, and existing guidance primarily relies on expert opinion and single center experiences.Study Design and MethodsExperts in Maternal Fetal Medicine, Pediatric Hematology, and Transfusion Medicine from centers across the United States, collectively performing about 120 IUT annually, offer a multidisciplinary perspective on the performance of IUT and preparation of blood components. This perspective includes strategies for identifying an at‐risk fetus, communicating between disciplines, determining the necessary blood volume, selecting and processing blood components, documenting the procedure in medical record, and managing the neonate.ResultsIdentifying an at‐risk fetus relies on review of the clinical history, non‐invasive monitoring, and laboratory evaluation. We recommend the use of relatively fresh, group O, cytomegalovirus‐safe, freshly irradiated, red blood cells (RBC) that are Hemoglobin S negative and antigen‐negative for any maternal antibody, if indicated. These RBC units should be concentrated to remove additives and increase the hematocrit thus minimizing fluctuations in fetal volume status. The units intended for IUT should be labeled clearly and the documentation of transfusion differentiated in the maternal medical record.DiscussionAn awareness of the technical, logistical, and regulatory considerations for IUT performance will facilitate improved communication and patient care, especially when rare units of RBC are required.
Subject
Hematology,Immunology,Immunology and Allergy