Evidence map›Paper›PMID 37515245›Full record

ArticleViruses2023

COVID-19 Disease in Pediatric Solid Organ Transplantation from Alpha to Omicron: A High Monocyte Count in the Preceding Three Months Portends a Risk for Severe Disease.

Yasmina Sirgi, Maja Stanojevic, Jaeil Ahn, Nada Yazigi, Stuart Kaufman, Khalid Khan, Bernadette Vitola, Cal Matsumoto, Alexander Kroemer, Thomas Fishbein and 1 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 1 institution in 1 country.

Yasmina SirgiDepartment of Surgery, Georgetown University Medical School, Washington, DC 20007, USA.
Maja StanojevicDepartment of Pediatrics, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Jaeil AhnDepartment of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University, Washington, DC 20007, USA.ORCID 0000-0001-7998-4759
Nada YazigiMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Stuart KaufmanMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Khalid KhanMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Bernadette VitolaMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Cal MatsumotoMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Alexander KroemerMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Thomas FishbeinMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.
Udeme D EkongMedStar Georgetown Transplant Institute, MedStar Georgetown University Hospital, Washington, DC 20007, USA.ORCID 0000-0002-3312-112X
Georgetown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importancePlanning for future resurgences in SARS-CoV-2 infection is necessary for providers who care for immunocompromised patients.

objectiveto determine factors associated with COVID-19 disease severity in immunosuppressed children.

designa case series of children with solid organ transplants diagnosed with SARS-CoV-2 infection between 15 March 2020 and 31 March 2023.

settinga single pediatric transplant center.

participantsall children with a composite transplant (liver, pancreas, intestine), isolated intestine transplant (IT), isolated liver transplant LT), or simultaneous liver kidney transplant (SLK) with a positive PCR for SARS-CoV-2. EXPOSURE: SARS-CoV-2 infection. MAIN OUTCOME AND MEASURES: We hypothesized that children on the most immunosuppression, defined by the number of immunosuppressive medications and usage of steroids, would have the most severe disease course and that differential white blood cell count in the months preceding infection would be associated with likelihood of having severe disease. The hypothesis being tested was formulated during data collection. The primary study outcome measurement was disease severity defined using WHO criteria.

results77 children (50 LT, 24 intestine, 3 SLK) were infected with SARS-CoV-2, 57.4 months from transplant (IQR 19.7-87.2). 17% were ≤1 year post transplant at infection. 55% were male, 58% were symptomatic and ~29% had severe disease. A high absolute lymphocyte count at diagnosis decreased the odds of having severe COVID-19 disease (OR 0.29; CI 0.11-0.60; CONCLUSIONS AND RELEVANCE: The significance of a high monocyte count as predictor of severe disease potentially confirms the importance of monocytic inflammasome-driven inflammation in COVID-19 pathogenesis. Our data do not support reducing immunosuppression in the setting of infection. Our observations may have important ramifications in resource management as vaccine- and infection-induced immunity wanes.

Indexed as

COVID-19Immunosuppressive AgentsOrgan TransplantationSteroidsChildChild, PreschoolFemaleGraft RejectionHumansLymphocyte CountMaleMonocytesPatient AcuityImmunosuppressive AgentsSteroidsimmunocompromised childreninflammationinnate immunityintestine transplantliver transplantlymphocyte countviral infection

Identifiers

PMID37515245
PMCPMC10383409
OpenAlexW4384526061

What Socratic 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 Socratic graph.