Evidence map›Paper›PMID 24960646›Full record

Trial reportBlood transfusion = Trasfusione del sangue2015

Variant RH alleles and Rh immunisation in patients with sickle cell disease.

Emilia Sippert, Claudia R Fujita, Debora Machado, Glaucia Guelsin, Ane C Gaspardi, Jordão Pellegrino, Simone Gilli, Sara S T O Saad, Lilian Castilho

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Blood transfusion = Trasfusione del sangue, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.8field-weighted citation impact, top 5% of its field
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

30 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. DNA Reference Reagents for Genotyping RH Variants.The Journal of molecular diagnostics : JMD · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. How to avoid the problem of erythrocyte alloimmunization in sickle cell disease.Hematology. American Society of Hematology. Education Program · 2021
    Review
  17. Article
  18. Article
  19. Review
  20. The Significance ofFrontiers in immunology · 2021
    Article
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 at 2 institutions in 1 country.

Emilia SippertNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Claudia R FujitaFujisan, Fortaleza, Brazil.
Debora MachadoNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Glaucia GuelsinNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Ane C GaspardiNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Jordão PellegrinoNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Simone GilliNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Sara S T O SaadNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Lilian CastilhoNational Institute of Science and Blood Technology, Campinas Centre Blood, UNICAMP, Campinas, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade de Fortaleza · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlloimmunisation is a major complication in patients with sickle cell disease (SCD) receiving red blood cell (RBC) transfusions and despite provision of Rh phenotyped RBC units, Rh antibodies still occur. These antibodies in patients positive for the corresponding Rh antigen are considered autoantibodies in many cases but variant RH alleles found in SCD patients can also contribute to Rh alloimmunisation. In this study, we characterised variant RH alleles in 31 SCD patients who made antibodies to Rh antigens despite antigen-positive status and evaluated the clinical significance of the antibodies produced. MATERIALS AND

methodsRHD and RHCE BeadChip™ from BioArray Solutions and/or amplification and sequencing of exons were used to identify the RH variants. The serological features of all Rh antibodies in antigen-positive patients were analysed and the clinical significance of the antibodies was evaluated by retrospective analysis of the haemoglobin (Hb) levels before and after transfusion; the change from baseline pre-transfusion Hb and the percentage of HbS were also determined.

resultsWe identified variant RH alleles in 31/48 (65%) of SCD patients with Rh antibodies. Molecular analyses revealed the presence of partial RHD alleles and variant RHCE alleles associated with altered C and e antigens. Five patients were compound heterozygotes for RHD and RHCE variants. Retrospective analysis showed that 42% of antibodies produced by the patients with RH variants were involved in delayed haemolytic transfusion reactions or decreased survival of transfused RBC. DISCUSSION: In this study, we found that Rh antibodies in SCD patients with RH variants can be clinically significant and, therefore, matching patients based on RH variants should be considered.

Indexed as

AllelesAnemia, Sickle CellErythrocyte TransfusionBlood Grouping and CrossmatchingFemaleHumansIsoantibodiesMaleRh-Hr Blood-Group SystemIsoantibodiesRHCE protein, humanRh-Hr Blood-Group SystemRho(D) antigen

Identifiers

PMID24960646
PMCPMC4317093
OpenAlexW38669435

What OpenQuestion holds

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Registered trials

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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.