Evidence map›Paper›PMID 29899574›Full record

Observational studyBone marrow transplantation2019

Pre-engraftment cytomegalovirus DNAemia in allogeneic hematopoietic stem cell transplant recipients: incidence, risk factors, and clinical outcomes.

Carlos Solano, Estela Giménez, Eliseo Albert, Eva María Mateo, Montserrat Gómez, Rosa Goterris, Ariadna Pérez, Paula Amat, Juan Carlos Hernández-Boluda, Marc Poch and 2 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Bone marrow transplantation, 2019. 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
–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

6 citing papers in PubMed.

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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

12 authors.

Carlos SolanoHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.ORCID http://orcid.org/0000-0003-3702-0817
Estela GiménezMicrobiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Eliseo AlbertMicrobiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Eva María MateoMicrobiology Department, School of Medicine, University of Valencia, Valencia, Spain.
Montserrat GómezHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Rosa GoterrisHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Ariadna PérezHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Paula AmatHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Juan Carlos Hernández-BoludaHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Marc PochHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
José Luis PiñanaHematology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
David NavarroMicrobiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain. david.navarro@uv.es.ORCID http://orcid.org/0000-0003-3010-4110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To gauge the risk of delaying initiation of prophylaxis with letermovir from the time of donor infusion to prevent CMV infection in allo-HSCT recipients we investigated the clinical outcomes of CMV DNAemia episodes occurring before engraftment, and compared to that of episodes developing after engraftment (up to day +365). A total of 197 consecutive adult patients were included. Plasma CMV DNA load was monitored by real-time PCR assays [limit of detection: 31 IU/ml]. A total of 150 out of 197 patients had CMV DNAemia (cumulative incidence of 77%; 95% CI, 73-81%), and 38 out of the 197 patients developed it before engraftment (cumulative incidence, 19%; 95% CI, 10-30.3%). Nine episodes of CMV DNAemia were detected prior to the time of donor progenitor cell infusion. A greater number of post-engraftment episodes required preemptive antiviral therapy compared with pre-engraftment episodes (62.5% vs 44.7%; P = 0.05). The cellular content of the donor progenitor cell infusion and transplant characteristics of patients did not differ between patients with pre-engraftment or post-engraftment CMV DNAemia. The cumulative incidence of overall mortality by days 100 and 365, aGvHD by day 100 and relapse by day 365 were not significantly different between patients with pre-engraftment or post-engraftment CMV DNAemia.

Indexed as

Antiviral AgentsCytomegalovirusCytomegalovirus InfectionsDNA, ViralHematopoietic Stem Cell TransplantationAdolescentAdultAgedAllograftsDisease-Free SurvivalFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesAntiviral AgentsDNA, Viral

Identifiers

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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.