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How do we perform intrauterine transfusions?
Crowe, Elizabeth P; Hasan, Rida; Saifee, Nabiha H; Bakhtary, Sara; Miller, Jena L; Gonzalez-Velez, Juan M; Goel, Ruchika.
Afiliação
  • Crowe EP; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Hasan R; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Saifee NH; Department of Laboratory Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Bakhtary S; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
  • Miller JL; Department of Laboratory Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
  • Gonzalez-Velez JM; Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.
  • Goel R; The Johns Hopkins Center for Fetal Therapy, Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, Maryland, USA.
Transfusion ; 63(12): 2214-2224, 2023 12.
Article em En | MEDLINE | ID: mdl-37888489
BACKGROUND: Intrauterine 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 METHODS: Experts 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. RESULTS: Identifying 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. DISCUSSION: An 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritroblastose Fetal / Doenças Fetais / Anemia Limite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Transfusion Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritroblastose Fetal / Doenças Fetais / Anemia Limite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Transfusion Ano de publicação: 2023 Tipo de documento: Article