Evidence map›Paper›PMID 26901466›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2016

National Variation in Use of Immunosuppression for Kidney Transplantation: A Call for Evidence-Based Regimen Selection.

D A Axelrod, A S Naik, M A Schnitzler, D L Segev, V R Dharnidharka, D C Brennan, S Bae, J Chen, A Massie, K L Lentine

Abstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Effectiveness of T cell-mediated rejection therapy: A systematic review and meta-analysis.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Pooled it
  3. Review
  4. Article
  5. Article
  6. Infection Risk in Older Kidney Transplant Recipients: An Analysis in the Era of Expanded Age Limits.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  7. Article
  8. HLA-DR/DQ eplet mismatch predictsFrontiers in genetics · 2024
    Article
  9. Observational
  10. Tacrolimus induces a pro-fibrotic response in donor-derived human proximal tubule cells dependent on common variants of the CYP3A5 and ABCB1 genes.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Adequate tacrolimus exposure modulates the impact of HLA class II molecular mismatch: a validation study in an American cohort.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  19. Article
  20. Sensitization in transplantation: Assessment of risk (STAR) 2019 Working Group Meeting Report.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    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

10 authors.

D A AxelrodSection of Solid Organ Transplantation, Department of Surgery, Dartmouth Hitchcock Medical Center, Lebanon, NH.
A S NaikDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.
M A SchnitzlerSaint Louis University Center for Transplantation, Saint Louis University School of Medicine, St. Louis, MO.
D L SegevDivision of Abdominal Transplantation, Department of Surgery, Johns Hopkins University, Baltimore, MD.
V R DharnidharkaDivision of Nephrology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.
D C BrennanDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.
S BaeDivision of Abdominal Transplantation, Department of Surgery, Johns Hopkins University, Baltimore, MD.
J ChenCenter for Outcomes Research, Saint Louis University School of Medicine, St. Louis, MO.
A MassieDivision of Abdominal Transplantation, Department of Surgery, Johns Hopkins University, Baltimore, MD.
K L LentineSaint Louis University Center for Transplantation, Saint Louis University School of Medicine, St. Louis, MO.

Funding

Choosing Immune Suppression in Renal Transplantation by Efficacy and MorbidityR01DK102981 · NIDDK · WASHINGTON UNIVERSITY · PI DHARNIDHARKA, VIKAS R. · 2014 to 2018
$1.9M
NIDDK NIH HHS R01 DK102981
6 · The paper itself

Abstract

Immunosuppression management in kidney transplantation has evolved to include an increasingly diverse choice of medications. Although informed by patient and donor characteristics, choice of immunosuppression regimen varies widely across transplant programs. Using a novel database integrating national transplant registry and pharmacy fill records, immunosuppression use at 6-12 and 12-24 mo after transplant was evaluated for 22 453 patients transplanted in 249 U.S. programs in 2005-2010. Use of triple immunosuppression comprising tacrolimus, mycophenolic acid or azathioprine, and steroids varied widely (0-100% of patients per program), as did use of steroid-sparing regimens (0-77%), sirolimus-based regimens (0-100%) and cyclosporine-based regimens (0-78%). Use of triple therapy was more common in highly sensitized patients, women and recipients with dialysis duration >5 years. Sirolimus use appeared to diminish over the study period. Patient and donor characteristics explained only a limited amount of the observed variation in regimen use, whereas center choice explained 30-46% of the use of non-triple-therapy immunosuppression. The majority of patients who received triple-therapy (79%), cyclosporine-based (87.6%) and sirolimus-based (84.3%) regimens continued them in the second year after transplant. This population-based study of immunosuppression practice demonstrates substantial variation in center practice beyond that explained by differences in patient and donor characteristics.

Indexed as

Evidence-Based MedicineKidney TransplantationAdultDrug Therapy, CombinationFemaleGlomerular Filtration RateGraft RejectionGraft SurvivalHumansImmunosuppression TherapyImmunosuppressive AgentsKidney Failure, ChronicKidney Function TestsMaleMiddle AgedPostoperative ComplicationsImmunosuppressive Agentsclinical research/practicehealth services and outcomes researchimmunosuppressantimmunosuppressive regimenskidney transplantation/nephrologymaintenancesteroid

Identifiers

PMID26901466
PMCPMC5513703

What OpenQuestion holds

Textmetadata
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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.