Evidence map›Paper›PMID 36873869›Full record

ArticleFrontiers in medicine2023

Clinical outcomes of children and adolescents with sickle cell disease and COVID-19 infection: A year in review at a metropolitan tertiary pediatric hospital.

Olufunke Y Martin, Deepika S Darbari, Stefanie Margulies, Robert S Nickel, Alexis Leonard, Barbara Speller-Brown, Brenda Martin, John R Barber, Jennifer Webb, Suvankar Majumdar and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2023. 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
3.2field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Olufunke Y MartinCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Deepika S DarbariCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Stefanie MarguliesCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Robert S NickelCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Alexis LeonardCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Barbara Speller-BrownCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Brenda MartinCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
John R BarberDepartment of Biostatistics and Study Methodology, Children's National Hospital, Washington, DC, United States.
Jennifer WebbCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Suvankar MajumdarCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Matthew P SharronGeorge Washington University School of Medicine and Health Sciences, Children's National Hospital, Washington, DC, United States.
Andrew D CampbellCenter for Cancer and Blood Disorders, Division of Hematology, Children's National Hospital, Washington, DC, United States.
Center for Cancer and Blood Disorders · USGeorge Washington University · USChildren's National · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: COVID-19 was declared a global pandemic in March 2020. Early reports were primarily in adults, and sickle cell disease (SCD) was classified as a risk factor for severe COVID-19 disease. However, there are a limited number of primarily multi-center studies reporting on the clinical course of pediatric patients with SCD and COVID-19. Methods: We conducted an observational study of all patients with SCD diagnosed with COVID-19 at our institution between March 31, 2020, and February 12, 2021. Demographic and clinical characteristics of this group were collected by retrospective chart review. Results: A total of 55 patients were studied, including 38 children and 17 adolescents. Demographics, acute COVID-19 clinical presentation, respiratory support, laboratory findings, healthcare utilization, and SCD modifying therapies were comparable between the children and adolescents. Seventy-three percent ( Conclusion: Children and adolescent patients with SCD and acute COVID-19 often present with ACS and VOC pain requiring hospital-level care. Hydroxyurea treatment appears to be protective. We observed no mortality despite variable morbidity.

Indexed as

COVID-19morbiditymortalitypediatrics–childrenSARS-CoV-2sickle cell disease (SCD)

Identifiers

PMID36873869
PMCPMC9982154
OpenAlexW4321252296

What OpenQuestion holds

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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.