Evidence map›Paper›PMID 31210395›Full record

Observational studyPediatric transplantation2019

Outcomes of human adenovirus infection and disease in a retrospective cohort of pediatric solid organ transplant recipients.

Craig L K Boge, Brian T Fisher, Hans Petersen, Alix E Seif, Dale R Purdy, Despoina M Galetaki, Richard L Hodinka, Ana María Cárdenas, Adriana E Kajon

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Pediatric transplantation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. 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

9 authors at 3 institutions in 1 country.

Craig L K BogeDivision of Infectious Diseases, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Brian T FisherDivision of Infectious Diseases, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Hans PetersenInfectious Disease Program, Lovelace Respiratory Research Institute, Albuquerque, New Mexico.
Alix E SeifDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Dale R PurdyCenter for Pediatric Clinical Effectiveness, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Despoina M GaletakiDivision of Infectious Diseases, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-8943-0386
Richard L HodinkaDepartment of Biomedical Sciences, Greenville Health System, University of South Carolina School of Medicine Greenville, Greenville, South Carolina.
Ana María CárdenasInfectious Disease Diagnostics Laboratory, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Adriana E KajonInfectious Disease Program, Lovelace Respiratory Research Institute, Albuquerque, New Mexico.
Children's Hospital of Philadelphia · USLovelace Respiratory Research Institute · USPrisma Health · US

Funding

NIAID NIH HHS HHSN272201000040CNIAID NIH HHS HHSN272201000040INIAID NIH HHS HHSN2722011000040CNIAID NIH HHS HHSN272201100004CNIAID NIH HHS HHSN272201100040C
6 · The paper itself

Abstract

Information about HAdV infection in SOT recipients is limited. We aimed to describe HAdV infection epidemiology and outcomes in a single-center retrospective cohort during the era of PCR availability. SOT recipients transplanted at the CHOP 2004-2013 were followed up for 180 days post-transplant. HAdV infection was defined as a positive HAdV PCR from a clinical specimen. HAdV disease was defined by organ-specific radiologic and/or laboratory abnormalities. No HAdV surveillance protocols were employed during the study period; testing was solely per clinician discretion. Progression of HAdV infection was defined as HAdV disease or ≥1-log viral load increase since a corresponding site's first positive specimen. Of the assembled 425 SOT recipients, 227 (52.6%) had ≥1 HAdV PCR. Twenty-four (10.6%) had ≥1 HAdV-positive PCR. HAdV-positive subjects were younger than uninfected subjects (2.0 years vs 6.5, P = 0.001). Infection incidence rates were highest in liver recipients (15.3%), followed by heart (8.6%), kidney (8.3%), and lung (4.2%). Four subjects (16.7%) met HAdV disease criteria at virus detection. Five subjects (20.8%) had progression of HAdV infection. All-cause mortality rates in positive and negative subjects were 0% and 3.9%, respectively. HAdV infection was infrequently detected in SOT recipients. Over one-third of HAdV-positive patients met disease criteria at detection or had infection progression, but none died. This low all-cause mortality raises questions about benefits of HAdV surveillance. Larger multicenter studies are needed to assess incidence variance by center and comparative effectiveness of therapeutic interventions.

Indexed as

Adenovirus Infections, HumanAdolescentAdultChildChild, PreschoolDisease ProgressionFemaleFollow-Up StudiesHumansIncidenceInfantMaleOrgan TransplantationRetrospective StudiesTime FactorsTransplantation, Homologousadenoviruseshumanorgan transplantationpediatrics

Identifiers

PMID31210395
PMCPMC6706289
OpenAlexW2952530576

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.