dc.contributor.author | Romón Alonso, José Iñigo | |
dc.contributor.author | Dominguez-Garcia, Juan J. | |
dc.contributor.author | Arroyo, Jose L. | |
dc.contributor.author | Suberviola, Borja | |
dc.contributor.author | Cabezón Estevanez, Itxasne | |
dc.contributor.author | Abascal Bolado, Beatriz | |
dc.contributor.author | Baldeón, Cristina | |
dc.contributor.author | Cuesta, Amalia | |
dc.contributor.author | Portilla, Raquel | |
dc.contributor.author | Casuso, Elena | |
dc.contributor.author | Ocio San Miguel, Enrique María | |
dc.contributor.author | Briz, Montserrat | |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2022-02-01T17:28:01Z | |
dc.date.available | 2022-02-01T17:28:01Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 1471-2318 | |
dc.identifier.uri | http://hdl.handle.net/10902/23828 | |
dc.description.abstract | Background: Older patients, frequently with multiple comorbidities, have a high mortality from COVID-19 infection. Convalescent plasma (CP) is a therapeutic option for these patients. Our objective is to retrospectively evaluate the efficacy and adverse events of CP treatment in this population group.
Methods: Forty one patients over 80 years old with COVID-19 pneumonia received CP added to standard treatment, 51.2% with high anti-SARS-CoV-2 IgG titers and 48.8% with low titers. Median time between the onset of symptoms and the infusion of plasma was 7 days (IQR 4-10). A similar group of 82 patients who received only standard treatment, during a period in which CP was not available, were selected as a control group.
Results: In-hospital mortality was 26.8% for controls and 14.6% for CP patients (P = 0.131) and ICU admission was 8.5% for controls and 4.9% for CP patients (P = 0.467). Mortality tended to be lower in the high-titer group (9.5%) than in the low-titer group (20%), and in patients transfused within the first 7 days of symptom onset (10%) than in patients transfused later (19.1%), although the differences were not statistically significant (P = 0.307 and P = 0.355 respectively). There was no difference in the length of hospitalization. No significant adverse events were associated with CP treatment.
Conclusions: Convalescent plasma treatment in patients over 80 years old with COVID-19 pneumonia was well tolerated but did not present a statistically significant difference in hospital mortality, ICU admission, or length of hospitalization. The results should be interpreted with caution as only half the patients received high-titer CP and the small number of patients included in the study limits the statistical power to detect significant differences. | es_ES |
dc.format.extent | 7 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | BioMed Central | es_ES |
dc.rights | Attribution 4.0 International | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.source | BMC Geriatr
. 2021 Oct 18;21(1):566 | es_ES |
dc.subject.other | COVID-19 | es_ES |
dc.subject.other | Convalescent Plasma | es_ES |
dc.subject.other | Older Adults | es_ES |
dc.subject.other | Transfusion | es_ES |
dc.title | Convalescent plasma treatment for patients of 80 years and older with COVID-19 pneumonia | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://doi.org/10.1186/s12877-021-02447-9 | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.1186/s12877-021-02447-9 | |
dc.type.version | publishedVersion | es_ES |