Evidence map›Paper›PMID 35131930›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2022

Use and Outcomes of Induction Therapy in Well-Matched Kidney Transplant Recipients.

Rhys D R Evans, James H Lan, Matthew Kadatz, Sandeep Brar, Doris T Chang, Lachlan McMichael, Jagbir Gill, John S Gill

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Guideline
  2. Article
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  5. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Rhys D R EvansDivision of Nephrology, Kidney Transplant Program, University of British Columbia, Vancouver, British Columbia, Canada.
James H LanDivision of Nephrology, Kidney Transplant Program, University of British Columbia, Vancouver, British Columbia, Canada.
Matthew KadatzDivision of Nephrology, Kidney Transplant Program, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0003-1119-9724
Sandeep BrarDivision of Nephrology, Kidney Transplant Program, University of British Columbia, Vancouver, British Columbia, Canada.
Doris T ChangProvidence Health Research Institute, Vancouver, British Columbia, Canada.
Lachlan McMichaelDivision of Nephrology, Kidney Transplant Program, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-1884-0329
Jagbir GillDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
John S GillDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada jgill@providencehealth.bc.ca.
University of British Columbia · CATufts Medical Center · USProvidence Health Care Research Institute · CA

Funding

CIHR
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe optimal induction treatment in low-immune risk kidney transplant recipients is uncertain. We therefore investigated the use and outcomes of induction immunosuppression in a low-risk cohort of patients who were well matched with their donor at HLA-A, -B, -DR, -DQB1 on the basis of serologic typing. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Our study was an observational study of first adult kidney-only transplant recipients in the United States recorded by the Organ Procurement and Transplant Network.

resultsAmong 2976 recipients, 57% were treated with T cell-depleting antibodies, 28% were treated with an IL-2 receptor antagonist, and 15% were treated without induction. There was no difference in allograft survival, death-censored graft survival, or death with function between patients treated with an IL-2 receptor antagonist and no induction therapy. In multivariable models, patients treated with T cell-depleting therapy had a similar risk of graft loss from any cause, including death (hazard ratio, 1.19; 95% confidence interval, 0.98 to 1.45), compared with patients treated with an IL-2 receptor antagonist or no induction. The findings were consistent in subgroup analyses of Black recipients, patients grouped by calculated panel reactive antibody, and donor source. The incidence of acute rejection at 1 year was low (≤5%) and did not vary between treatment groups.

conclusionsUse of induction therapy with T cell-depleting therapy or IL-2 receptor antagonists in first kidney transplant recipients who are well matched with their donor at the HLA-A, -B, -DR, -DQB1 gene loci is not associated with improved post-transplant outcomes.

Indexed as

Immunosuppression TherapyInduction ChemotherapyKidney TransplantationAdultFemaleHumansMaleMiddle AgedPatient SelectionTreatment Outcomeacute rejectionimmunosuppressionkidney transplantationorgan transplantUnited States Renal Data System

Identifiers

PMID35131930
PMCPMC8823946
OpenAlexW4210586485

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.