Maternal alloimmunization as a risk factor of haemolytic disease of the foetus and newborn in Owerri metropolis, Nigeria
Keywords:
maternal, Alloimmunization, Rhesus, antibodies, foetus, newborn haemolytic anti-D immunoglobulin prophylaxis., maternal, Alloimmunization, Rhesus, antibodies, foetus, newborn haemolytic anti-D immunoglobulin prophylaxisAbstract
Blood group incompatibility between mother and her foetus which usually arises as a result of heterospecific pregnancy causes haemolytic disease of the foetus and newborn (HDN). Five hundred (500) pregnant women attending antenatal clinic at Federal Medical Centre (FMC), Owerri were recruited for this research work. They were aged between 17 and 40 years. All subjects gave informed consent to participate in the study. They were screened for ABO blood groups RhD status and immune alloantibodies. Anti-A and anti-B from group O subjects compared with anti-A from group B women and anti-B from group A women among the trimester. The rate of RhD negativity (5.4%) was significantly lower than the RhD positively (94.6%) (P<0.005). Haemolysin tests were positive in 110 (22.0%) cases and negative in 390 (78.0%) cases. Group O women produced more alpha and / or beta haemolysins than either A or B women (P<0.005). Anti-A titres were higher in the trimesters than anti-B. Indirect antiglobulin test (IAT) was positive in 12(80.0%) cases among ABO group and positive in 3(20.0%) cases among RhD group. There was a higher prevalence of ABO HDN than RhD HDN in the ratio of 3:1 respectively. This study illustrates the presence of immune alloantibodies in the sera of allominiunized pregnant women and the rise in the antibody titres has helped to identify pregnancies at risk of foetal and neonatal HDN. Anti-D immunoprophylaxis has made HDN caused by sensitization to the D-antigen a preventable disease and prenatal deaths from allominization by immunoprophylaxis has been primarily responsible for the dramatic reduction in the diseases, although changes in family size and the quality of prenatal care have also contributed.
References
Azubuike, J.C., 1989. Neonatal Jaundice in Eastern Nigeria. East Afr. Med. J., 56, 320-324.
Belmar, J.J.V., Carmen, B.P., Cristina, G.C., 2005. Incidence of non-Rh (D), anti-A or anti-B alloimmunization in pregnant women in Spain and clinical repercussion in the newborn. HAEMA., 6, 1108-16821106862ja.
Bowman, J.M., 1999. Haemolytic Disease ( Erythroblastosis fetalis ) In: Maternal Fetal Medicine: Principles and Practices, Creasy, R., Resnik, R., (Eds.). 3rd Edn. WB Saunder Co., Philadelphia, USA., pp, 736-76837224bc.
Bowman, J.M., 1999. Intrauterine and Neonatal Transfusion. In: Scientific Basis of Transfusion Medicine: Implications for Clinical Practice, Anderson, K.C., Ness, P.M., (Eds.). WB Saunders, Philadephia, USA., pp: 307-320.
Cariani, L., Romano, E.L, Martinez, N., Montano, R., Suarez, G., Ruiz, I., Soyano, A., 1995. ABO haemolytic disease of the feotus and newborn: Factors influencing its severity and incidence in Venezuela. J. Trop. Pediatr., 41 14-21.
Cheesbrough, M., 2000. Haemolytic Disease of the Newborn. In: District Laboratory Practice in Tropical Countries, Part 2, Cheesbrough, M. (Ed.). Cambridge University Press. Cambridge, UK., pp, 376-378.
Clarke, C.A., Tanley, P.C., Wallas, C.H., 1992. Decline in deaths from Rhesus haemolytic disease of the newborn. Roy.Coll. phys. Lond., 28, 310-311.
Dacie, J.V., Lewis, S.M., 1991. Laboratory Method used in the Investigation of Haemolytic Anaemia. In: Practical Haematology, Dacie, J.V. and S.M. Lewis (Eds.). 7th Edn. Churchhill Livingstone, Edinburg h. UK., pp, 436-445. 37227bc.
Engelfriet, C.P., Reesink, H.W., Bowman, J.M., 1995. Laboratory procedures for the prediction of the severity of haemolytic disease of the newborn (international forum). Vox Sanguinis., 69, 61-69. 1106891ja.
Filbey, D., Hanson, U., Wesstrom, G., 1995. The prevalence of red cell antibodies in pregnancy correlated to the outcome of the newborn. Acta Obstet. Gynecol. Scand., 74, 687-692. 1106892ja.
Geifman-Holtzman, O., Wojtowycz, M., Kosmas, E., Artal, R., 1997. Female alloimmunization with antibodies known to cause hemolytic disease. Obstet. Gynecol., 89, 272-275. 1106894ja.
Gorlin, J.B., 2002. Standards for Blood Banks and Transfusion Services. 21st Edn., American Associations of Blood Banks, Bethesda, MD., USA., pp, 379-391. 103431b.
Hoffbrand, A.V., Lewis, S.M., Tuddenham, E.G.D., 2001. Clinical Blood Transfusion. In: Post-Graduate Haematology, Hoffbrand, A.V., S.M. Lewis and E.G.D. Tuddenham (Eds.). 4th Edn. Blackwell Publishing. Oxfrd, UK., pp,215-234.
Howard, H.L., Martlew, V.J., McFagyen, I.R., Clarke, C.A., 1998. Preventing Rhesus (D) Haemolytic disease of the newborn by giving anti-D, Immunoglobulin; Are the guildlines being adequately followed? Bri. J. Obstet. Gynecol., 104,34-41. 37229bc.
Issitt, P.D., 1999. Antibody screening: Elimination of another piece of the test. Transfusion, 39, 229-230. 1106918ja.
Mba, G.O., 2003. Antibodies causing haemolutic disease of the foetus and Newborn in Nigerian pregnant women. Nigerian National Society of Medical Service, Marina, Lagos. Nigeria., pp, 19-21.58134an.
McDonnell, M., Hannam, S., Devane, S.P., 1998. Hydrops fetalis due to ABO incompatibility. Archiv. Dis. Child. Fetal Neonatal Edn., 78, F220-F221. 1106936ja.
Moise, K.J., 2002. The process of Alloimmunization. UNC Depart. Obstet. Gynecolog., USA.58135an.
Moise, J.r.K.J., 2005. Red blood cell alloimmunization in pregnancy. Semin. Hematol., 42, 169-178.
Mollison, P.L., Engelfriet, C.P., Contreras, M., 1997. Blood Transfusion in Clinical Medicine. Blackwell Sci. England.
Mollison, P.L., Engelfriet, C.P., Contreras, M., 2000. Rhesus Blood Group System in Blood Transfusion in Clinical Medicine. 9th Edn., Blackwell Sci.Publ. Oxford. UK., pp, 2008-2009.
Onwukeme, K.E., 1990., Blood Group Distribution in Blood donors in a Nigeria population. Niger. J. Physiol. Sci., 6, 67-70.
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