Evidence map›Paper›PMID 38361528›Full record

ArticleFrontiers in immunology2023

Viral load kinetics and the clinical consequences of cytomegalovirus in kidney transplantation.

Sabina Dobrer, Karen R Sherwood, Ishan Hirji, James Lan, John Gill, Nancy Matic, Paul A Keown

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
5.4field-weighted citation impact, top 4% 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, 14 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

7 authors at 2 institutions in 2 countries.

Sabina DobrerDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Karen R SherwoodDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Ishan HirjiGlobal Evidence and Outcomes, Takeda Development Center Americas, Inc., Lexington, MA, United States.
James LanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
John GillDepartment of Medicine, University of British Columbia, Vancouver, BC, Canada.
Nancy MaticDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Paul A KeownDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
University of British Columbia · CATakeda (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite advances in clinical management, cytomegalovirus (CMV) infection remains a serious complication and an important cause of morbidity and mortality following kidney transplantation. Here, we explore the importance of viral load kinetics as predictors of risk and potential guides to therapy to reduce transplant failure in a large longitudinal Genome Canada Transplant Consortium (GCTC) kidney transplant cohort. Methods: We examined the relationship between CMV infection rates and clinical characteristics, CMV viral load kinetics, and graft and patient outcomes in 2510 sequential kidney transplant recipients in the British Columbia Transplant Program. Transplants were performed between January 1, 2008, and December 31, 2018, were managed according to a standard protocol, and were followed until December 31, 2019, representing over 3.4 million days of care. Results: Longitudinal CMV testing was performed in 2464 patients, of whom 434 (17.6%) developed a first episode of CMV viremia at a median of 120 (range: 9-3906) days post-transplant. Of these patients, 93 (21.4%) had CMV viremia only and 341 (78.6%) had CMV viremia with clinical complications, of whom 21 (4.8%) had resulting hospitalization. A total of 279 (11.3%) patients died and 177 (7.2%) patients lost their graft during the 12 years of follow-up. Patients with CMV infection were at significantly greater risk of graft loss (p=0.0041) and death (p=0.0056) than those without. Peak viral load ranged from 2.9 to 7.0 (median: 3.5) log Conclusion: Viral load kinetics are closely related to CMV severity and to graft loss following kidney transplantation and provide a simple index of risk which may be valuable in guiding trials and treatment to prevent transplant failure.

Indexed as

Cytomegalovirus InfectionsKidney TransplantationCytomegalovirusHumansViral LoadViremiaclinical outcomesCMVcytomegaloviruskidney transplantviral load kinetics

Identifiers

PMID38361528
PMCPMC10867541
OpenAlexW4391446882

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Registered trials

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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.