Evidence map›Paper›PMID 29181879›Full record

ArticlePediatric transplantation2018

High human herpesvirus 6 viral load in pediatric allogeneic hematopoietic stem cell transplant patients is associated with detection in end organs and high mortality.

Lena E Winestone, Rajesh Punn, John S Tamaresis, Julia Buckingham, Benjamin A Pinsky, Jesse J Waggoner, Sandhya Kharbanda

Open access · greenAbstract read
In one paragraph

Article in Pediatric transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

7 authors at 5 institutions in 2 countries.

Lena E WinestoneDivision of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID 0000-0001-9982-1594
Rajesh PunnDivision of Cardiology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
John S TamaresisDepartment of Health Research and Policy, Stanford University School of Medicine, Stanford, CA, USA.
Julia BuckinghamDivision of Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Benjamin A PinskyDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Jesse J WaggonerDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Sandhya KharbandaDivision of Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-6014-7659
Institute for Stem Cell Biology and Regenerative Medicine · INStanford Medicine · USChildren's Hospital of Philadelphia · USStanford Health Care · USStanford University · US

Funding

Pediatric Hospital Epidemiology and Outcomes Research Training ProgramT32HD060550 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI Christopher Peter Bonafide, John Chris Feudtner · 2010 to 2026
$6.8M
NICHD NIH HHS T32 HD060550
6 · The paper itself

Abstract

Human Herpes Virus 6 (HHV-6) reactivation occurs in approximately half of patients following allogeneic hematopoietic stem cell transplant (HSCT). While encephalitis and delayed engraftment are well-documented complications of HHV-6 following HSCT, the extent to which HHV-6 viremia causes disease in children is controversial. We performed a retrospective review of HHV-6 reactivation and possible manifestations in pediatric allogeneic HSCT patients at a single institution. Of 89 children and young adults who underwent allogeneic HSCT over a three-and-a-half-year period, 34 patients reactivated HHV-6 early post-transplant. Unrelated donor stem cell source and lack of antiviral prophylaxis were risk factors for the development of HHV-6 viremia. Viremia correlated with the presence of acute graft-versus-host disease, but not chronic graft-versus-host disease. We identified two subgroups within the viremic patients-a high-risk viremic and tissue-positive group that reactivated HHV-6 and had suspected end-organ disease and a low-risk viremic but asymptomatic group that reactivated HHV-6 but did not exhibit symptoms or signs of end-organ disease. Peak viral load was found to be strongly associated with mortality. Prospective studies in larger numbers of patients are needed to further investigate the role of HHV-6 in causing symptomatic end-organ disease as well as the association of viral load with mortality.

Indexed as

Viral LoadAdolescentAdultChildChild, PreschoolFemaleFollow-Up StudiesHematopoietic Stem Cell TransplantationHerpesvirus 6, HumanHumansInfantInfant, NewbornKaplan-Meier EstimateLogistic ModelsMaleRetrospective Studiesallogeneic hematopoietic stem cell transplantationend-organ diseasehuman herpesvirus-6pediatric

Identifiers

PMID29181879
PMCPMC5820136
OpenAlexW2768879109

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.