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Læknablaðið - 01.07.2016, Blaðsíða 15

Læknablaðið - 01.07.2016, Blaðsíða 15
LÆKNAblaðið 2016/102 331 R A N N S Ó K N ENGLISH SUMMARY Introduction: Hemolytic disease of the fetus and newborn (HDFN) is caused by the destruction of fetal red blood cells due to red cell antibodies produced by the mother. HDFN can cause fetal hydrops during pregnancy or neonatal jaundice after birth. Direct Antiglobulin Test (DAT) detects antibodies bound to red cells and is a valuable test aiding in the diagnosis of HDFN. In Iceland DAT is routinely performed on cord blood or newborn blood samples if the mother is Rhesus D negati- ve or has non-A/B red cell alloantibodies. The aim of this study was to investigate the causes and consequences of positive DAT in newborns in Iceland over a period of eight years. Material and methods: The study population was infants diagnosed with a positive DAT in the Blood Bank in Iceland in the years 2005-2012. Relevant data on the blood group and antibody status of mother and child, blood transfusion and DAT results were retrieved from the Blood Bank information system ProSang. Birth records provided information on birth weight, gestational age and phototherapy. Health records from the Children's Hospital provided information on the management and fate of the newborn. Results: Over the study period 383 newborns had a positive DAT result at the Blood Bank. In 73.6% of cases the underlying cause was ABO blood group mismatch between mother and infant, in 20.4% of cases the mother had non-A/B red cell alloantibodies, in 3.9% both of above factors were present, while in 2.1% the cause was unclear. A total of 179 (47.6%) children had neonatal jaundice that required treatment, of which 167 (93.3%) only needed phototherapy. Eight infants required exchange transfusion, five of these had Rhesus antibodies and three ABO blood group mismatch. Conclusion: ABO blood group mismatch between mother and child was the most common cause for a positive DAT in neonates in Iceland in the years 2005-2012. Almost half of the neonates required treatment but usually phototherapy was sufficient. Rarely, blood transfusion or exchange transfusion was necessary in severe cases of ABO blood group mismatch or non-A/B red cell alloantibodies. Positive Coomb’s test in newborns; causes and clinical consequences Summary of cases diagnosed in the Blood Bank in the years 2005 to 2012 Thordis Kristinsdottir1, Sveinn Kjartansson2, Hildur Hardardottir1,3, Thorbjörn Jonsson4, Anna Margret Halldorsdottir4 1Faculty of Medicine, University of Iceland, 2Children's Hospital of Landspítali, 3Department of Obstetrics and Gynecology, Landspítali, 4The Blood Bank, Landspítali. Key words: Coombs test, Direct Antiglobulin Test (DAT), Hemolytic disease of the fetus and newborn (HDFN), ABO blood group mismatch, red cell alloantibodies, neonatal jaundice, exchange transfusion. Correspondence: Anna Margrét Halldórsdóttir, annamha@landspitali.is Heimildir 1. Poole J, Daniels G. Blood group antibodies and their sign- ificance in transfusion medicine. Transfus Med Rev 2007; 21: 58-71. 2. Harmening DM. Modern Blood Banking & Transfusion Practices. 5th ed. F.A. Davis Company, Fíladelfíu, Bandaríkjunum 2005. 3. Chen JY, Ling UP. Prediction of the development of neonatal hyperbilirubinemia in ABO incompatibility. Zhonghua Yi Xue Za Zhi (Taipei) 1994; 53: 13-8. 4. Petrides M, Stack G, Cooling L, Maes LY. Practical Guide to Transfusion Medicine. 2nd ed. AABB Pres, Bethesda, Maryland 2007. 5. Murray NA, Roberts IA. Haemolytic disease of the new- born. Arch Dis Child Fetal Neonatal Ed 2007; 92: F83-F88. 6. Bowman J. Thirty-five years of Rh prophylaxis. Transfusion 2003; 43: 1661-6. 7. Roberts IA. The changing face of haemolytic disease of the newborn. Early Hum Dev 2008; 84: 515-23. 8. Geifman-Holtzman O, Wojtowycz M, Kosmas E, Artal R. Female alloimmunization with antibodies known to cause hemolytic disease. Obstet Gynecol 1997; 89: 272-5. 9. Hellman-Erlingsson S. Greining blóðflokkamótefna hjá vanfærum konum og mæðrum á Íslandi 1970-1984. Læknablaðið 1986; 72: 321-9. 10. Nordvall M, Dziegel M, Hegaard HK, Bidstrup M, Jonsbo F, Christensen B, et al. Red blood cell antibodies in pregn- ancy and their clinical consequences: synergistic effects of multiple specificities. Transfusion 2009; 9: 2070-5. 11. Dinesh D. Review of positive direct antiglobulin tests found on cord blood sampling. J Paediatr Child Health 2005; 41: 504-7. 12. Coombs RRA, Mourant AE, Race RR. In-vivo isos- ensitisation of red cells in babies with hæmolytic disease. Lancet 1946; 247: 264-6. 13. Pediatrics A.A.o. Clinical practice guideline: management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics 2004; 114: 297-316. 14. Herschel M, Karrison T, Wen M, Caldarelli L, Baron B. Evaluation of the direct antiglobulin (Coombs') test for identifying newborns at risk for hemolysis as determined by end-tidal carbon monoxide concentration (ETCOc); and comparison of the Coombs' test with ETCOc for det- ecting significant jaundice. J Perinatol 2002; 22: 341-7. 15. Cortey A, Brossard Y. [Adverse effects and patient information]. J Gynecol Obstet Biol Reprod (Paris) 2006; 35(1 Suppl): 1S112-1S118. 16. Madan A, Huntsinger K, Burgos A, Benitz WE. Readmission for newborn jaundice: the value of the Coombs’ test in predicting the need for phototherapy. Clin Pediatr 2004; 43: 63-8. 17. Dillon A, Chaudhari T, Crispin P, Shadbolt B, Kent A. Has anti-D prophylaxis increased the rate of positive direct antiglobulin test results and can the direct antiglobulin test predict need for phototherapy in Rh/ABO incompati- bility? J Paediatr Child Health 2011; 47: 40-3. 18. Moise KJ. Fetal anemia due to non-Rhesus-D red-cell all- oimmunization. Sem Fetal Neonatal Med 2008; 13: 207-14. 19. McKenna DS, Nagaraja HN, O’Shaughnessy R. Management of pregnancies complicated by anti-Kell isoimmunization. Obstet Gynecol 1999; 93: 667-73. 20. Kaplan M, Hammerman C, Vreman HJ, Wong RJ, Stevenson DK. Hemolysis and hyperbilirubinemia in antiglobulin positive, direct ABO blood group hetero- specific neonates. J Pediatr 2010; 157: 772-7. 21. Daniels G, Poole J, De Silva M, Callaghan T, MacLennan S, Smith N. The clinical significance of blood group antibodies. Transfus Med 2002; 12: 287-95. 22. American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics 2004; 114: 297-316. 23. Kaplan M, Na'amad M, Kenan A, Rudensky B, Hammerman C, Vreman HJ, et al. Failure to predict hemolysis and hyperbilirubinemia by IgG Subclass in blood group A or B infants born to group O mothers. Pediatr 2009; 123: e132-e137. 24. Sgro M, Campbell D, Shah V. Incidence and causes of severe neonatal hyperbilirubinemia in Canada. CMAJ 2006; 175: 587-90. 25. Wainer S, Rabi J, Lyon M. Coombs' testing and neonatal hyperbilirubinemia. CMAJ 2007; 176: 972-3; author reply 973. 26. Elalfy MS, Elbarbary NS, Abaza HW. Early intravenous immunoglobin (two-dose regimen) in the management of severe Rh hemolytic disease of newborn--a prospective randomized controlled trial. Eur J Pediatr 2011; 170: 461-7. 27. Smits-Wintjens VE, Walther FJ, Rath ME, Lindenburg IT, te Pas AB, Kramer CM, et al. Intravenous immunoglobulin in neonates with rhesus hemolytic disease: a randomized controlled trial. Pediatr 2011; 127: 680-6.

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