Literature DB >> 1306646

High-dose intravenous immune globulin therapy for hyperbilirubinemia caused by Rh hemolytic disease.

J Rübo1, K Albrecht, P Lasch, E Laufkötter, J Leititis, D Marsan, B Niemeyer, J Roesler, C Roll, B Roth.   

Abstract

We conducted a multicenter controlled trial to test the hypothesis that high-dose intravenous immune globulin (HDivIG) therapy can modulate bilirubin production and reduce the frequency of exchange transfusions in newborn infants with Rh hemolytic disease. Thirty-four patients with Rh incompatibility proved by positive direct antiglobulin test (Coombs test) results were randomly assigned to receive conventional treatment including phototherapy, with or without additional HDivIG therapy at 500 mg/kg given for a 2-hour period as soon as the diagnosis was established. Exchange transfusions were performed if serum bilirubin concentrations exceeded the modified curves of Polácek by more than 2 mg/dl. Two patients were excluded because of protocol violations. The results in 32 infants were analyzed. In the HDivIG group, 2 (12.5%) of 16 children required exchange transfusions, whereas it became necessary in 11 (69%) of 16 children in the control group (p less than 0.005). Bilirubin levels in the HDivIG group were lower despite reduced frequency of exchange transfusions. No side effects of HDivIG treatment were observed. We conclude that HDivIG therapy by a yet unknown mechanism reduces serum bilirubin levels and the need for blood exchange transfusions in children with Rh hemolytic disease.

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Year:  1992        PMID: 1306646     DOI: 10.1016/s0022-3476(05)82551-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  13 in total

1.  Intravenous immunoglobulins in rhesus hemolytic disease.

Authors:  Kanya Mukhopadhyay; Srinivas Murki; Anil Narang; Sourabh Dutta
Journal:  Indian J Pediatr       Date:  2003-09       Impact factor: 1.967

Review 2.  Systematic review of intravenous immunoglobulin in haemolytic disease of the newborn.

Authors:  R Gottstein; R W I Cooke
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2003-01       Impact factor: 5.747

Review 3.  Haemolytic disease of the newborn.

Authors:  Neil A Murray; Irene A G Roberts
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-03       Impact factor: 5.747

4.  Improving the management and outcome in haemolytic disease of the foetus and newborn.

Authors:  Enrico Lopriore; Mirjam E A Rath; Helen Liley; Vivianne E H J Smits-Wintjens
Journal:  Blood Transfus       Date:  2013-07-19       Impact factor: 3.443

5.  Phototherapy-induced Purpuric Eruption in a Neonate.

Authors:  Jennifer LaRusso; Joshua Wilson; Roger Ceilley
Journal:  J Clin Aesthet Dermatol       Date:  2015-03

6.  Single versus multiple dose intravenous immunoglobulin in combination with LED phototherapy in the treatment of ABO hemolytic disease in neonates.

Authors:  Gamze Demirel; Melek Akar; Istemi Han Celik; Omer Erdeve; Nurdan Uras; Serife Suna Oguz; Ugur Dilmen
Journal:  Int J Hematol       Date:  2011-05-25       Impact factor: 2.490

7.  Necrotizing enterocolitis in a term neonate following intravenous immunoglobulin therapy.

Authors:  Lalitha Krishnan; Anil Pathare
Journal:  Indian J Pediatr       Date:  2011-01-19       Impact factor: 1.967

Review 8.  Current drug treatment options in neonatal hyperbilirubinaemia and the prevention of kernicterus.

Authors:  F F Rubaltelli
Journal:  Drugs       Date:  1998-07       Impact factor: 9.546

Review 9.  Immunoglobulin for alloimmune hemolytic disease in neonates.

Authors:  Carolien Zwiers; Mirjam Ea Scheffer-Rath; Enrico Lopriore; Masja de Haas; Helen G Liley
Journal:  Cochrane Database Syst Rev       Date:  2018-03-18

10.  Phenobarbital and Phototherapy Combination Enhances Decline of Total Serum Bilirubin and May Decrease the Need for Blood Exchange Transfusion in Newborns with Isoimmune Hemolytic Disease.

Authors:  Mahmoud Af Kaabneh; Ghassan Sa Salama; Ayoub Ga Shakkoury; Ibrahim Mh Al-Abdallah; Afrah Alshamari; Ruba Aa Halaseh
Journal:  Clin Med Insights Pediatr       Date:  2015-08-09
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