Publication:
Predictors of clinical evolution of SARS-CoV-2 infection in hematological patients: A systematic review and meta-analysis.

dc.contributor.authorCarrara, Elena
dc.contributor.authorRazzaboni, Elisa
dc.contributor.authorAzzini, Anna Maria
dc.contributor.authorDe Rui, Maria Elena
dc.contributor.authorPinho Guedes, Mariana Nunes
dc.contributor.authorGorska, Anna
dc.contributor.authorGiannella, Maddalena
dc.contributor.authorBussini, Linda
dc.contributor.authorBartoletti, Michele
dc.contributor.authorArbizzani, Federica
dc.contributor.authorPalacios-Baena, Zaira R
dc.contributor.authorCaponcello, Giulia
dc.contributor.authorMaldonado, Natalia
dc.contributor.authorRodríguez-Baño, Jesús
dc.contributor.authorVisco, Carlo
dc.contributor.authorKrampera, Mauro
dc.contributor.authorTacconelli, Evelina
dc.date.accessioned2023-05-03T14:47:15Z
dc.date.available2023-05-03T14:47:15Z
dc.date.issued2022-10-20
dc.description.abstractMain aim of this systematic review is to quantify the risk and identify predictors of clinical evolution of SARS-CoV-2 in hematological patients compared to different control populations. Two independent reviewers screened the literature assessing clinical outcomes of SARS-CoV-2 infection in adult patients with active hematological malignancies published up to June 2021. Primary outcome was COVID-19 related mortality, secondary outcomes were hospital and intensive-care admission, mechanical ventilation (MV), and thromboembolic events. Variables related to study setting, baseline patients' demographic, comorbidities, underlying hematological disease, ongoing chemotherapy, COVID-19 presentation, and treatments were extracted. A total of 67 studies including 10,061 hematological patients and 111,143 controls were included. Most of the studies were retrospective cohorts (51 studies, 76%) and only 19 (13%) provided data for a control group. A significant increased risk of clinical progression in the hematological population compared to the controls was found in terms of COVID-19 related mortality (OR, 2.12; 95% CI, 1.77-2.54), hospitalization (OR, 1.98; 95% CI, 1.15-3.43), intensive-care admission (OR, 1.77; 95% CI, 1.38-2.26), and MV (OR, 2.17; 95% CI, 1.71-2.75). The risk remained significantly higher in the subgroup analysis comparing hematological patients versus solid cancer. Meta-regression analysis of uncontrolled studies showed that older age, male sex, and hypertension were significantly related to worse clinical outcomes of COVID-19 in hematological population. Older age and hypertension were found to be associated also to thromboembolic events. In conclusion, hematological patients have a higher risk of COVID-19 clinical progression compared to both the general population and to patients with solid cancer.
dc.identifier.doi10.1002/hon.3084
dc.identifier.essn1099-1069
dc.identifier.pmcPMC9874549
dc.identifier.pmid36238977
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874549/pdf
dc.identifier.unpaywallURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874549
dc.identifier.urihttp://hdl.handle.net/10668/22039
dc.issue.number1
dc.journal.titleHematological oncology
dc.journal.titleabbreviationHematol Oncol
dc.language.isoen
dc.organizationHospital Universitario Virgen Macarena
dc.organizationHospital Universitario Virgen Macarena
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.page.number16-25
dc.pubmedtypeMeta-Analysis
dc.pubmedtypeSystematic Review
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rights.accessRightsopen access
dc.subjectCOVID-19
dc.subjectdeterminants
dc.subjecthematological malignancies
dc.subjectmortality
dc.subjectseverity
dc.subject.meshAdult
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshCOVID-19
dc.subject.meshSARS-CoV-2
dc.subject.meshRetrospective Studies
dc.subject.meshHypertension
dc.subject.meshDisease Progression
dc.subject.meshNeoplasms
dc.titlePredictors of clinical evolution of SARS-CoV-2 infection in hematological patients: A systematic review and meta-analysis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number41
dspace.entity.typePublication

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