Evidence map›Paper›PMID 19833910›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2009

Acute hemolysis after high-dose intravenous immunoglobulin therapy in highly HLA sensitized patients.

Joseph Kahwaji, Eva Barker, Sam Pepkowitz, Ellen Klapper, Rafael Villicana, Alice Peng, Robert Chang, Stanley C Jordan, Ashley A Vo

Registry-linked trialAbstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02123615 (ASIS for GAMMAGARD in Primary Immunodeficiency), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT02123615 phase1 / phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

ASIS for GAMMAGARD in Primary Immunodeficiency

TypeinterventionalSponsorASIS CorporationRan2016 to 2016Enrolled60ConditionsPrimary ImmunodeficiencyArmsGadolinium For abdomen, Gadolinium For lower back, Efficacy of Gammagard subcutaneously at Week 12, Efficacy of Gammagard subcutaneously at Week 24, Efficacy of Gammagard subcutaneously at Week 36
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 126 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Human immune globulin infusion in the management of multifocal motor neuropathy.Degenerative neurological and neuromuscular disease · 2016
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Occurrence of hemolytic anemia in patients with GBS treated with high-dose IVIg.Neurology(R) neuroimmunology & neuroinflammation · 2014
    Article
  18. American Society of Nephrology Quiz and Questionnaire 2013: transplantation.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Article
  19. Article
  20. ABO incompatible renal transplants: Good or bad?World journal of transplantation · 2014
    Review
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.

Joseph KahwajiComprehensive Transplant Center, Cedars-Sinai Medical Center, West Los Angeles, CA 90048, USA. Kahwajij@cshs.org
Eva Barker
Sam Pepkowitz
Ellen Klapper
Rafael Villicana
Alice Peng
Robert Chang
Stanley C Jordan
Ashley A Vo
Comprehensive Clinical Research · USCedars-Sinai Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesIntravenous Ig (IVIG) is used in renal transplantation for desensitization and treatment of antibody-mediated rejection (AMR). The infusion of high-dose IVIG is generally well tolerated, but there are reports of hemolytic anemia induced by anti-blood group antibodies present in IVIG. Here, we report our experience with IVIG-induced hemolytic anemia (IH) in ESRD patients receiving IVIG for desensitization or treatment of AMR. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: All patients receiving IVIG for desensitization or for treatment of AMR were monitored for evidence of acute anemia and hemolysis. Markers of hemolysis, including direct antiglobulin tests, were recorded. Five different IVIG products were tested for isohemagglutinin titers.

resultsThere were 18 cases of IH in 16 patients. All identified cases received the IVIG product Gamunex, Gammagard liquid, or Privigen. All patients developing hemolysis were non-O blood types. Isohemagglutinin titers ranged from 1:2 to 1:64 in the various IVIG products, with higher titers noted in the liquid, nonlyophilized products.

conclusionsAcute IH is a significant complication of high-dose IVIG infusion. Identified risk factors include non-O blood type of the recipient and administration of liquid IVIG preparations with high titer anti-A/B IgG antibodies. We recommend monitoring hemoglobin 48 to 72 h after IVIG infusion. If the hemoglobin decreases, a hemolytic work-up is recommended. Hemolysis could be avoided in at risk patients by choosing a low titer product. However, other complications such as acute renal failure or thrombosis may be seen because the low titer products are usually hyperosmotic.

Indexed as

Kidney TransplantationABO Blood-Group SystemAcute DiseaseAdultAgedAnemia, HemolyticAutoantibodiesCaprylatesFemaleGraft RejectionHemagglutininsHLA AntigensHumansImmunoglobulin GImmunoglobulins, IntravenousKidney Failure, ChronicABO Blood-Group SystemAutoantibodiesCaprylatesHemagglutininsHLA AntigensImmunoglobulin GImmunoglobulins, Intravenous

Identifiers

PMID19833910
PMCPMC2798878
OpenAlexW2012571571

What OpenQuestion holds

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Registered trials

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.