Evidence map›Paper›PMID 33100098›Full record

ArticleRenal failure2020

The incidence of cytomegalovirus infection after deceased-donor kidney transplantation from hepatitis-C antibody positive donors to hepatitis-C antibody negative recipients.

Masahiko Yazawa, Tibor Fülöp, Orsolya Cseprekal, Manish Talwar, Vasanthi Balaraman, Anshul Bhalla, Ambreen Azhar, Csaba P Kovesdy, James D Eason, Miklos Z Molnar

Open access · goldAbstract read
In one paragraph

Article in Renal failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

10 authors at 5 institutions in 3 countries.

Masahiko YazawaJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Tibor FülöpDivision of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.
Orsolya CseprekalDepartment of Transplantation and Surgery, Semmelweis University, Budapest, Hungary.
Manish TalwarJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Vasanthi BalaramanJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Anshul BhallaJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Ambreen AzharJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Csaba P KovesdyDivision of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.
James D EasonJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
Miklos Z MolnarJames D. Eason Transplant Institute, Methodist University Hospital, Memphis, TN, USA.
University of Tennessee Health Science Center · USMethodist University · USMethodist University Hospital · USSemmelweis University · HUMedical University of South Carolina · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDeceased-donor kidney transplantation (KT) from hepatitis C (HCV)-infected donors into HCV-uninfected recipients (HCV D+/R-) could become standard care in the near future. However, HCV viral replication by viral transmission might lead to a higher incidence of cytomegalovirus (CMV) infection in these recipients.

methodsA national-registry-based retrospective cohort study was conducted using the Scientific Registry of Transplant Recipients (SRTR) data set. We assessed the incidence of CMV infection in HCV antibody (Ab) negative recipients receiving kidneys from HCV Ab positive (HCVAb D+/R-) and negative (HCVAb D-/R-) donors. The risk of CMV infection was analyzed by Cox regression analysis in a propensity score (PS) matched-cohort of HCVAb D+/R- (

resultsThe mean age at baseline was 54 years, 75% were male, and 55% of the patients were African American in PS-matched cohort. Compared to the HCVAb D-/R - patients, recipients with HCVAb D+/R - showed identical probability for the incidence of CMV infection (Hazard Ratio (HR) = 1.00, 95% Confidence Interval (CI): 0.82-1.22). In the sensitivity analysis, compared to the HCVAb D-/R - patients, the HCVAb D+/R - group had a significantly lower risk of CMV infection in the unadjusted analysis (HR = 0.75, 95%CI: 0.65-0.85), while this risk difference disappeared after the adjusted analysis (HR = 0.99, 95%CI: 0.87-1.14).

conclusionThe incidence of CMV infection was similar in recipients who received HCVAb D + and HCVAb D - KT. Further studies are needed to assess this association in KT from HCV nucleic acid positive donors.

Indexed as

Hepatitis CKidney TransplantationAdultCytomegalovirus InfectionsFemaleHumansIncidenceKidneyMaleMiddle AgedPostoperative ComplicationsProportional Hazards ModelsRegistriesRetrospective StudiesTissue DonorsTransplant RecipientsCytomegalovirus infectiondirect-acting antiviral agentsend-stage kidney diseasehepatitis Ckidney transplantationreal-word experience

Identifiers

PMID33100098
PMCPMC7594852
OpenAlexW3093996958

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.