Evidence map›Paper›PMID 30797790›Full record

ArticleThe Journal of infection2019

Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia.

José Luis Piñana, Estela Giménez, María Dolores Gómez, Ariadna Pérez, Eva María González, Víctor Vinuesa, Juan Carlos Hernández-Boluda, Juan Montoro, Miguel Salavert, Mar Tormo and 8 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of infection, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Cytomegalovirus Disease: Fine-Tuning Clinical Trial Enrollment and Standardization.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Delayed Onset of COVID-19 in an Immunosuppressed Patient.Infectious diseases in clinical practice (Baltimore, Md.) · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Opportunistic bacterial, viral and fungal infections of the lung.Medicine (Abingdon, England : UK ed.) · 2020
    Review
  18. Article
  19. Cytomegalovirus (CMV) Pneumonitis: Cell Tropism, Inflammation, and Immunity.International journal of molecular sciences · 2019
    Review
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

18 authors at 3 institutions in 1 country.

José Luis PiñanaHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Estela GiménezMicrobiology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
María Dolores GómezMicrobiology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Ariadna PérezHematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
Eva María GonzálezMicrobiology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Víctor VinuesaMicrobiology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
Juan Carlos Hernández-BoludaHematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
Juan MontoroHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Miguel SalavertDepartment of Infectious Diseases, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Mar TormoHematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
Paula AmatHematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
Paula MolesHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Carlos CarreteroHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Aitana Balaguer-RosellóHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Jaime SanzHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Guillermo SanzHematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Carlos SolanoHematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain; Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.
David NavarroMicrobiology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain; Department of Microbiology, School of Medicine, University of Valencia, Av. Blasco Ibáñez 17, 46010 Valencia, Spain. Electronic address: david.navarro@uv.es.
Hospital Universitari i Politècnic La Fe · ESINCLIVA Health Research Institute · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo date no definitive cut-off value for cytomegalovirus (CMV) DNA load in bronchoalveolar lavage (BAL) fluid specimens has been established to discriminate between CMV pneumonia and pulmonary CMV DNA shedding in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients.

methodsThe current retrospective study is aimed at assessing the range of CMV DNA loads quantified in BAL fluid specimens from allo-HSCT patients with pneumonia in which different microorganisms were causally involved.

resultsA total of 144 BAL specimens from 123 patients were included. CMV DNA was detected in 56 out of 144 BAL fluid specimens and the median CMV DNA load from patients in whom CMV pneumonia was unlikely or could be tentatively ruled out was 1210 (31-68, 920) IU/ml. The frequency of CMV DNA detection and median CMV DNA loads were comparable, irrespective of the attributable cause of pneumonia. Detection of CMV DNA loads in BAL fluid specimens >500 IU/ml was independently associated with pneumonia-attributable mortality.

conclusionsThe current study highlights the difficulty in establishing universal CMV DNA load thresholds in BAL fluid specimens for distinguishing between CMV pneumonia and pulmonary CMV DNA shedding, and suggests that the presence of CMV DNA in BAL fluid specimens beyond a certain level may have a deleterious impact on patient outcome.

Indexed as

Transplant RecipientsVirus SheddingAdultAgedAged, 80 and overBronchoalveolar Lavage FluidCytomegalovirusCytomegalovirus InfectionsDNA, ViralFemaleHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedPneumonia, ViralRetrospective StudiesDNA, ViralCMV DNAemiaCMV DNA in BALCMV pneumoniaCytomegalovirusPre-emptive antiviral therapy

Identifiers

PMID30797790
PMCPMC7126576
OpenAlexW2917204397

What OpenQuestion holds

Textmetadata
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.