Evidence map›Paper›PMID 30786115›Full record

ArticlePediatric transplantation2019

Cytomegalovirus and Epstein-Barr virus infections among pediatric kidney transplant recipients at a center using universal Valganciclovir Prophylaxis.

Grant Paulsen, Pia Cumagun, Emily Mixon, Karen Fowler, Daniel Feig, Masako Shimamura

Open access · greenAbstract read
In one paragraph

Article in Pediatric transplantation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

Grant PaulsenDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.ORCID 0000-0002-8901-6513
Pia CumagunUniversity of Alabama School of Medicine, Birmingham, Alabama.
Emily MixonDivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
Karen FowlerDivision of Pediatric Infectious Diseases, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0002-9501-635X
Daniel FeigDivision of Pediatric Nephrology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0002-0017-6335
Masako ShimamuraCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
University of Alabama at Birmingham · USAlabama Department of Public Health · USCincinnati Children's Hospital Medical Center · USNationwide Children's Hospital · US

Funding

UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
UAB Infectious Diseases Training GrantT32AI052069 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHWEBKE, JANE R. · 2003 to 2018
$2.1M
Innate Immunity and Viral Renal Allograft InjuryR01AI101138 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SHIMAMURA, MASAKO · 2013 to 2017
$1.8M
NIAID NIH HHS R01 AI101138NIAID NIH HHS T32 AI052069NIDDK NIH HHS P30 DK079337NIH HHS R01AI101138
6 · The paper itself

Abstract

backgroundCMV is associated with adverse effects in renal transplant recipients. The objective of this study was to characterize the incidence and timing of CMV and EBV infections in relation to valGCV prophylaxis in a pediatric renal transplant cohort.

methodsRetrospective cohort of pediatric renal transplant patients given universal valGCV prophylaxis and universal viral surveillance was evaluated. Demographics, prophylaxis, acute rejection, and CMV and EBV infections were abstracted.

resultsA total of 92 pediatric renal allograft recipients, 2008-2013, were included. One or more viral infections developed in 77/92 (83.7%) of the patients. EBV was the most common in 62/92 (67%) patients, irrespective of valGCV (82% of episodes occurring on valGCV). CMV DNAemia occurred in 30/92 (33%) patients, 14 episodes (47%) occurring on valGCV. Incidence of breakthrough CMV on prophylaxis was 15% and was associated with persistent DNAemia (OR 7.8, CI:1.6-32.9, P < 0.02). CMV tissue-invasive disease was not seen. CMV syndrome occurred in 10% of the cohort, only in CMV D+ patients, and only one symptomatic breakthrough infection required treatment. Out of 92, 21 (23%) had simultaneous co-infections with 2-3 viruses.

conclusionsViral infections in pediatric renal transplant recipients receiving universal valGCV prophylaxis were common. EBV infections were not reduced by valGCV prophylaxis, and nearly half of CMV infections occurred on valGCV. Symptomatic CMV infection while on prophylaxis was rare. valGCV prophylaxis may prevent symptomatic CMV infection but not EBV infection, and frequent CMV surveillance in pediatric renal transplant recipients on prophylaxis may not be necessary.

Indexed as

AdolescentAntiviral AgentsChildChild, PreschoolCytomegalovirusCytomegalovirus InfectionsEpstein-Barr Virus InfectionsFemaleGanciclovirGraft RejectionHerpesvirus 4, HumanHumansImmunosuppressive AgentsIncidenceKidney TransplantationMaleAntiviral AgentsGanciclovirImmunosuppressive AgentsValganciclovirantiviral prophylaxisCMVpediatricsrenal transplantation

Identifiers

PMID30786115
PMCPMC6650320
OpenAlexW2916524009

What OpenQuestion holds

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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.