Exchange transfusion in neonatal hyperbilirubinemia: A single Centre experience from Northern India.

Blood group incompatibility Exchange transfusion Hyperbilirubinemia Neonate Reconstituted blood

Journal

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis
ISSN: 1473-0502
Titre abrégé: Transfus Apher Sci
Pays: England
ID NLM: 101095653

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 30 06 2019
revised: 30 08 2019
accepted: 27 09 2019
pubmed: 23 10 2019
medline: 1 5 2020
entrez: 23 10 2019
Statut: ppublish

Résumé

To determine the indication, efficacy and adverse events related to exchange transfusion (ET) with reconstituted blood (RB) in neonatal hyperbilirubinemia (NNH). Blood bank records of neonates who underwent double volume ET for NNH from January 2013 to July 2018 were retrospectively reviewed. Demographic details, cause of NNH, details of ET and ET related adverse events were recorded. A total of 23 ET (average: 1.64/neonate) were performed in 14 neonates (9 males; 5 females) with a mean age of 9.8 ± 7.6 days. Ten (71.4%) neonates underwent 1 session of ET, while 4 (28.6%) underwent repeated sessions (average: 3.25/neonate). A total of 5912 ml of RB was transfused (average: 422 ml/neonate). A statistically significant reduction was noted in total serum bilirubin (TSB) level post-ET (p < 0.001) with overall TSB reduction/procedure being 46%. Of the 14 neonates with NNH, 11 (78.6%) had Rh haemolytic disease of foetus and new-born (HDFN), 2 (14.3%) had ABO HDFN and 1 (7.1%) had hyperbilirubinemia due to prematurity. Of the 11 neonates with Rh HDFN, only 5 underwent intrauterine transfusion (average: 1.8/neonate). Post-ET, top-up transfusions were noted in 8 (57.1%) neonates with packed red blood cell and/or platelet concentrate. ET related adverse were noted in 5 (21.7%) procedures only. Rh HDFN was the most common cause of NNH in our study population.Exchange transfusion is a safe treatment modality for treating NNH, as it results in the rapid elimination of serum bilirubin, thus, lowering the risk of kernicterus in these patients.

Identifiants

pubmed: 31636029
pii: S1473-0502(19)30219-8
doi: 10.1016/j.transci.2019.09.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102655

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Brinda Kakkar (B)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India. Electronic address: docbrindakakkar@gmail.com.

Soma Agrawal (S)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India.

Mohit Chowdhry (M)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India.

P J Muthukumaravel (PJ)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India.

Raj Nath Makroo (RN)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India.

Uday K Thakur (UK)

Department of Transfusion Medicine and Immunology, Indraprastha Apollo Hospitals, New Delhi, 110076, India.

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