Literature DB >> 28279592

Older red cell units are associated with an increased incidence of infection in chronically transfused adults with sickle cell disease.

Matthew S Karafin1, Erica Carpenter2, Amy Pan2, Pippa Simpson2, Joshua J Field3.   

Abstract

BACKGROUND: In adults with sickle cell disease (SCD), the effects of the red cell storage lesion are not well defined. The objectives of this study were to: (1) describe the distribution of storage ages provided to adults with SCD, and (2) evaluate clinical outcomes associated with storage age. PATIENTS AND METHODS: We performed a retrospective cohort study of adults with SCD managed with prophylactic simple transfusion regimens. Units were universally pre-storage leukocyte reduced and CEK-matched. Age of the unit was 42 days minus the difference between the expiration and transfusion dates. A mixed effects model, which accounts for a subject's contribution to repeated transfusion encounters, was used to investigate the association between storage age and the incidence of hospital encounters for infection and pain crises prior to the next red cell transfusion.
RESULTS: Over the study interval, twenty-eight steady-state adults with SCD received 627 units via simple transfusion over 281 outpatient encounters. Overall median unit storage age was 22 days (range: 2-42 days). Receipt of older units was associated with an increased incidence of emergency department or hospital admission for infection prior to the next transfusion (p=0.04). There was no association between unit storage age and admission for pain (p=0.4). DISCUSSION: In a cohort of chronically transfused adults with SCD, we provide evidence that receipt of older units is associated with a higher rate of admission for infection. Prospective studies will need to validate these data and explore potential mechanisms by which these older units promote infection.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Red cell storage age; Sickle cell disease; Transfusion practices

Mesh:

Year:  2017        PMID: 28279592     DOI: 10.1016/j.transci.2017.01.008

Source DB:  PubMed          Journal:  Transfus Apher Sci        ISSN: 1473-0502            Impact factor:   1.764


  5 in total

Review 1.  Red blood cell storage lesion: causes and potential clinical consequences.

Authors:  Tatsuro Yoshida; Michel Prudent; Angelo D'alessandro
Journal:  Blood Transfus       Date:  2019-01       Impact factor: 3.443

2.  Hitchhiker's guide to the red blood cell storage lesion.

Authors:  Tiffany Thomas; Steven L Spitalnik
Journal:  Blood Transfus       Date:  2019-01       Impact factor: 3.443

3.  The role of policy in red blood cell storage and transfusion in children.

Authors:  Jean L Raphael
Journal:  Pediatr Res       Date:  2017-10-04       Impact factor: 3.756

4.  Transfusion Practice, Post-Transfusion Complications and Risk Factors in Sickle Cell Disease in Senegal, West Africa.

Authors:  Moussa Seck; Alioune Badara Senghor; Mossane Loum; Sokhna Aissatou Touré; Blaise Félix Faye; Alioune Badara Diallo; Mohamed Keita; Seydi Elimane Bousso; Sérigne Mourtalla Guèye; Macoura Gadji; Abibatou Sall; Awa Oumar Touré; Saliou Diop
Journal:  Mediterr J Hematol Infect Dis       Date:  2022-01-01       Impact factor: 2.576

5.  Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal.

Authors:  Swee Lay Thein; France Pirenne; Ross M Fasano; Anoosha Habibi; Pablo Bartolucci; Satheesh Chonat; Jeanne E Hendrickson; Sean R Stowell
Journal:  Haematologica       Date:  2020-02-06       Impact factor: 11.047

  5 in total

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