Evidence map›Paper›PMID 39015498›Full record

ArticleFrontiers in oncology2024

Omicron SARS-CoV-2 infection management and outcomes in patients with hematologic disease and recipients of cell therapy.

José Luis Piñana, Lourdes Vazquez, Inmaculada Heras, Tommaso Francesco Aiello, Lucia López-Corral, Ignacio Arroyo, Eva Soler-Espejo, Irene García-Cadenas, Valentín Garcia-Gutierrez, Cristina Aroca and 20 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Trial
  2. Review
  3. Observational
  4. Review
  5. Article
  6. Review
  7. Article
  8. 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

30 authors.

José Luis PiñanaHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Lourdes VazquezHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), Salamanca, Spain.
Inmaculada HerasHematology Division, Hospital Morales Meseguer, Murcia, Spain.
Tommaso Francesco AielloInfectious Disease Division, Hospital Clinic, Barcelona, Spain.
Lucia López-CorralHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), Salamanca, Spain.
Ignacio ArroyoHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Eva Soler-EspejoHematology Division, Hospital Morales Meseguer, Murcia, Spain.
Irene García-CadenasHematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Valentín Garcia-GutierrezHematology Division, Hospital Ramon y Cajal, Madrid, Spain.
Cristina ArocaHematology Division, Hospital Morales Meseguer, Murcia, Spain.
Pedro ChoraoHematology Division, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
María T OlaveHematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Zaragoza, Spain.
Javier Lopez-JimenezHematology Division, Hospital Ramon y Cajal, Madrid, Spain.
Marina Acera GómezHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), Salamanca, Spain.
Elena ArellanoHematology Division, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Marian Cuesta-CasasHematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.
Alejandro Avendaño-PitaHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), Salamanca, Spain.
Clara González-SantillanaHematology Division, Hospital de Fuenlabrada, Madrid, Spain.
José Ángel Hernández-RivasHematology Division, Hospital Universitario Infanta Leonor, Madrid, Spain.
Alicia Roldán-PérezHematology Division, Hospital Infanta Sofia, Madrid, Spain.
Mireia Mico-CerdáHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Manuel GuerreiroHematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Zaragoza, Spain.
Julia MorellHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Paula Rodriguez-GalvezHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Jorge LabradorResearch unit, Hospital Universitario de Burgos, Burgos, Spain.
Diana CamposHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Ángel CedilloHematopoietic Stem Cell Transplantation and Cell Therapy Group (GETH-TC) office, Madrid, Spain.
Carolina Garcia VidalHematology Division, Hospital Morales Meseguer, Murcia, Spain.
Rodrigo MartinoHematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Carlos SolanoHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Scarce real-life data exists for COVID-19 management in hematologic disease (HD) patients in the Omicron era. Purpose: To assess the current clinical management and outcome of SARS-CoV-2 infection diagnosed, identify the risk factors for severe outcomes according to the HD characteristics and cell therapy procedures in a real-world setting. Methods: A retrospective observational registry led by the Spanish Transplant Group (GETH-TC) with 692 consecutive patients with HD from December 2021 to May 2023 was analyzed. Results: Nearly one-third of patients (31%) remained untreated and presented low COVID-19-related mortality (0.9%). Nirmatrelvir/ritonavir was used mainly in mild COVID-19 cases in the outpatient setting (32%) with a low mortality (1%), while treatment with remdesivir was preferentially administered in moderate-to-severe SARS-CoV-2 infection cases during hospitalization (35%) with a mortality rate of 8.6%. The hospital admission rate was 23%, while 18% developed pneumonia. COVID-19-related mortality in admitted patients was 14%. Older age, autologous hematopoietic stem cell transplantation (SCT), chimeric antigen receptor T-cell therapy, corticosteroids and incomplete vaccination were factors independently associated with COVID-19 severity and significantly related with higher rates of hospital admission and pneumonia. Incomplete vaccination status, treatment with prior anti-CD20 monoclonal antibodies, and comorbid cardiomyopathy were identified as independent risk factors for COVID-19 mortality. Conclusions: The results support that, albeit to a lower extent, COVID-19 in the Omicron era remains a significant problem in HD patients. Complete vaccination (3 doses) should be prioritized in these immunocompromised patients. The identified risk factors may help to improve COVID-19 management to decrease the rate of severe disease, ICU admissions and mortality.

Indexed as

COVID - 19hematologic diseaseimmunocompromisedrisk factorsSARS-CoV-2

Identifiers

PMID39015498
PMCPMC11250586

What OpenQuestion 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 OpenQuestion graph.