Evidence map›Paper›PMID 29570817›Full record

ArticleTransfusion2018

Red blood cell alloimmunization in sickle cell disease: assessment of transfusion protocols during two time periods.

Sally A Campbell-Lee, Kristina Gvozdjan, K Mia Choi, Yi-Fan Chen, Santosh L Saraf, Lewis L Hsu, Victor R Gordeuk, Ronald G Strauss, Darrell J Triulzi

Abstract read
In one paragraph

Article in Transfusion, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Sally A Campbell-LeeDepartment of Pathology, University of Illinois at Chicago College of Medicine, Chicago, IL.ORCID http://orcid.org/0000-0003-4157-2120
Kristina GvozdjanDepartment of Pathology, University of Illinois at Chicago College of Medicine, Chicago, IL.
K Mia ChoiDepartment of Pathology, University of Illinois at Chicago College of Medicine, Chicago, IL.
Yi-Fan ChenCenter for Clinical and Translational Science, University of Illinois at Chicago College of Medicine, Chicago, IL.
Santosh L SarafDepartment of Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL.
Lewis L HsuSickle Cell Center, University of Illinois at Chicago College of Medicine, Chicago, IL.
Victor R GordeukDepartment of Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL.
Ronald G StraussThe Institute for Transfusion Medicine, Chicago, Illinois.
Darrell J TriulziThe Institute for Transfusion Medicine, Chicago, Illinois.

Funding

Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
Genetics and Genomics of Sickle Cell Nephropathy.K23HL125984 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SARAF, SANTOSH · 2015 to 2018
$700k
NCATS NIH HHS UL1 TR002003NHLBI NIH HHS K23 HL125984
6 · The paper itself

Abstract

backgroundPrevention of red blood cell (RBC) alloimmunization in patients with sickle cell disease (SCD) focuses on phenotypic RBC matching. We assessed alloimmunization among transfused patients with SCD after implementing leukoreduction and prophylactic antigen matching (PAM). STUDY DESIGN AND

methodsRetrospective review of transfusion and medical records for SCD patients 18 months to 81 years of age was performed covering two 5-year periods: Period 1, no PAM, occasional leukoreduction, and Period 2, consistent leukoreduction and extended PAM (Rh, Kell, S, Fy, Jk) for patients already alloimmunized. Patients transfused in Period 1 were excluded from Period 2.

resultsA total of 293 patients were transfused in Period 1 and 183 in Period 2. Median time between first sample and last type and screen after transfusion was 2.12 years in Period 1 and 1.03 years in Period 2. Initial alloimmunization prevalence was lower in Period 2 (26.2%) versus Period 1 (37.5%) and after subsequent transfusions in Period 2 (23.8%) versus Period 1 (45.7%), although without significant difference after adjusting for number of units transfused, percentage of leukoreduced RBCs, sex, and age. Alloimmunized patients received more nonleukoreduced RBCs in Period 1 than nonalloimmunized. Patients transfused during inflammatory conditions were not significantly more likely to become alloimmunized.

conclusionsThe prevalence of initial and subsequent RBC alloimmunization in Period 2 was lower than that in Period 1; however, overall prevalence remained high. We recommend leukoreduced, hemoglobin S-negative Rh and Kell PAM RBCs for transfusion of patients with SCD. Component and recipient factors affecting alloimmunization should be studied further.

Indexed as

AdolescentAnemia, Sickle CellBlood TransfusionErythrocytesErythrocyte TransfusionFemaleHumansIsoantibodiesLogistic ModelsMaleRetrospective StudiesIsoantibodies

Identifiers

PMID29570817
PMCPMC7193458

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.