Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/9018
Title: A Rare Case of Transfusion Transmission of Hepatitis A Virus to Two Patients with Haematological Disease
Authors: Silva, Suely Gonçalves Cordeiro da
Alves, Gilda
Leon, Luciane Almeida Amado
Brito, Selma Magalhães
Sandes, Valcieny de Souza
Lima, Magda Maria Adorno Ferreira
Nogueira, Marta Colares
Tavares, Rita de Cássia Barbosa da Silva
Dobbin, Jane de Almeida
Apa, Alexandre Gustavo
Paula, Vanessa Salete de
Oliveira, Jaqueline Mendes de Oliveira
Pinto, Marcelo Alves
Ferreira Júnior, Orlando da Costa
Motta, Iara de Jesus Ferreira
Keywords: Hepatite A
Hepatitis A
Imunossupressão
Immunosuppression
Período da janela
Window period
Doadores de Sangue
Blood Donors
Blood Transfusion
Transfusão de Sangue
Issue Date: 2016
Publisher: Transfus Med Hemother
Citation: SILVA, Suely Gonçalves Cordeiro da et al. A Rare Case of Transfusion Transmission of Hepatitis A Virus to Two Patients with Haematological Disease. Transfus Med Hemother, v. 43, p. 137–141, 2016.
Abstract: Background: This paper describes the transmission of hepatitis A virus (HAV) to two blood recipients from a healthy donor that later presented to the blood bank with jaundice. Methods: The RNA of HAV was detected by qualitative nested reverse transcription polymerase chain reaction (nested RT-PCR) and quantified by realtime RT-PCR. HAV RNA samples were genotyped by direct sequencing of PCR products. A sequence from a fragment of 168 bp from the VP1/2A HAV region was used to construct a phylogenetic tree. Case Report: A 31-year-old male donor accepted for donation of a whole blood unit returned to the blood bank with clinical jaundice 20 days after donation. His serological and NAT tests were negative for HBV and HCV. Serological tests for HAV IgM and IgG were negative on donation sample but positive on follow-up sample, confirming donor’s HAV acute infection. Both recipients of red blood cells (R1) and platelet concentrate (R2) from the same implicated donation were HAV IgM-negative and IgG-positive. Qualitative PCR was positive on samples from all three individuals and phylogenetic analysis of viruses proved HAV transmission to the two recipients of blood products. HAV viral load on donor follow-up sample and the platelet recipient was 1.3 and 1.5 × 103 IU/ml, respectively. The RBC recipient, also infected by HCV, was undergoing bone marrow transplantation and died from fulminant hepatitis, 26 days after the implicated HAV transfusion. Conclusion: The blood donor, a garbage collector, spontaneously returned to the blood bank when developing jaundice. This highlights the importance of donor education to immediately report to blood banks of any signs and symptoms related to infectious disease developed after blood donation. The fact that one immunocompromised patient with HCV infection died from fulminant hepatitis after receiving a HAV-contaminated platelet transfusion underpins the importance of a HAV vaccination program for these group of patients.
Description: p. 137–141.: il. p&b.
URI: http://sr-vmlxaph03:8080/jspui/handle/123456789/9018
Appears in Collections:Artigos de Periódicos da área de Farmácia



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