Evidence map›Paper›PMID 39700902›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2025

Limited utility of Epstein-Barr virus (EBV) surveillance for predicting post-transplant lymphoproliferative disorders in adult EBV seropositive lung transplant recipients.

Jordan K Mah, Patrick C K Tam, Yeh-Chung Chang, Jennifer H Saullo, Arthur W Baker, Eileen K Maziarz, Julia A Messina, Beatrice Sim, Lana Abusalem, Sandrine Hanna and 7 more

Abstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

17 authors.

Jordan K MahDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA. Electronic address: jordan.mah.med@ssss.gouv.qc.ca.
Patrick C K TamDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Yeh-Chung ChangDivision of Infectious Diseases, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX USA.
Jennifer H SaulloDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Arthur W BakerDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Eileen K MaziarzDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Julia A MessinaDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Beatrice SimDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Lana AbusalemDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Sandrine HannaDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University, Durham, NC, USA.
Matthew R PipelingDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University, Durham, NC, USA.
Laurie D SnyderDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University, Durham, NC, USA.
John M ReynoldsDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University, Durham, NC, USA.
Cameron R WolfeDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Mark J LeeDivision of Microbiology, Department of Pathology, Duke University, Durham, NC, USA.
Barbara D AlexanderDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA.
Madeleine R HeldmanDivision of Infectious Diseases, Department of Medicine, Duke University, Durham, NC, USA. Electronic address: madeleine.heldman@duke.edu.

Funding

Combined Use of Statistical Process Control and Whole Genome Sequencing to Detect and Investigate Nontuberculous Mycobacterial Clusters and OutbreaksK08AI163462 · NIAID · DUKE UNIVERSITY · PI BAKER, ARTHUR W · 2021 to 2025
$942k
NIAID NIH HHS K08 AI163462
6 · The paper itself

Abstract

backgroundEBV DNAemia surveillance, with reduction of immunosuppression at certain viral load (VL) thresholds, is a common practice for mitigating progression from EBV DNAemia to post-transplant lymphoproliferative disorder (PTLD) in lung transplant recipients (LTRs). The utility of EBV surveillance in adult EBV seropositive LTRs is unknown.

methodsWe performed a retrospective cohort study of EBV seropositive adult LTRs who underwent lung transplant between 1/1/19 and 12/31/20 and received whole blood (WB) EBV PCR surveillance. We compared peak WB EBV VLs among 3 groups: 1) asymptomatic LTRs who developed PTLD, before PTLD was clinically suspected, 2) LTRs who developed PTLD, after PTLD was clinically suspected, and 3) LTRs who did not develop PTLD. We calculated the positive predictive value (PPV) of moderate-grade DNAemia (2840 to 11,360 IU/mL) and high-grade DNAemia (≥ 11,360 IU/mL) for identifying active or future PTLD.

resultsSix (2.6 %) of 229 LTRs developed PTLD. Among LTRs who developed PTLD, median peak EBV VL was significantly higher after PTLD was suspected than before clinical signs of PTLD were present (16,004 IU/mL vs. ≤568 IU/mL, p = 0.016). Median peak EBV VLs were similar between asymptomatic LTRs who later developed PTLD and LTRs who did not develop PTLD (median peak EBV VL ≤568 IU/mL vs. ≤568 IU/mL, p = 0.62). The PPVs for moderate- and high-grade DNAemia were 14.7 % and 33.3 %, respectively.

conclusionsEBV surveillance did not accurately identify EBV seropositive LTRs at risk for progressing to PTLD. EBV PCR testing in asymptomatic EBV seropositive transplant recipients may represent an opportunity for diagnostic stewardship.

Indexed as

Epstein-Barr Virus InfectionsHerpesvirus 4, HumanLung TransplantationLymphoproliferative DisordersTransplant RecipientsAdultAgedDNA, ViralFemaleHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesViral LoadYoung AdultDNA, ViralDiagnostic stewardshipEpstein–Barr virusLung transplant recipients viral PCR testingPost-transplant lymphoproliferative disorder

Identifiers

PMID39700902
PMCPMC11975427

What OpenQuestion holds

Textmetadata
LicenceTDM
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.