|
|
|
|
LEADER |
03064nam a2200385Ia 4500 |
001 |
10.1136-jim-2021-002158 |
008 |
220706s2022 CNT 000 0 und d |
020 |
|
|
|a 17088267 (ISSN)
|
245 |
1 |
0 |
|a Timing of convalescent plasma administration and 28-day mortality in COVID-19 pneumonia
|
260 |
|
0 |
|b NLM (Medline)
|c 2022
|
856 |
|
|
|z View Fulltext in Publisher
|u https://doi.org/10.1136/jim-2021-002158
|
520 |
3 |
|
|a This is a multicenter cohort study including consecutive, hospitalized patients ≥18 years, with moderate to severe COVID-19, carried out to evaluate the relationship between the timing of convalescent plasma administration and 28-day mortality. Data were prospectively collected between May 14, 2020 and October 31, 2020. Patients were grouped according to the timing of administration of convalescent plasma as <3 days, between 3 and 7 days, and >7 days. The main outcome variable was 28-day mortality. Independent predictors of mortality were identified by logistic regression. Of 4719 patients receiving convalescent plasma, 3036 (64.3%) were in the general ward, 1171 (24.8%) in the intensive care unit (ICU), and 512 (10.8%) in the ICU on mechanical ventilation. Convalescent plasma was administered to 3113 (66%) patients within the first 3 days of hospital admission, to 1380 (29.2%) between 3 and 7 days, and to 226 after 7 days; 28-day mortality was, respectively, 18.1%, 30.4% and 38.9% (p<0.001). In the regression model, convalescent plasma administration within the first 3 days of admission was associated with reduced 28-day mortality, compared with the administration after 7 days (OR 0.40, 95% CI 0.30 to 0.53). Early convalescent plasma administration was associated to a significant decreased mortality in patients in the general ward (OR 0.45, 95% CI 0.29 to 0.69) and in the ICU (OR 0.35, 95% CI 0.19 to 0.64), but not in those requiring mechanical ventilation (OR 0.52, 95% CI 0.27 to 1.01). In conclusion, this study suggests that early administration of convalescent plasma to patients with COVID-19 pneumonia is critical to obtain therapeutic benefit. © American Federation for Medical Research 2022. No commercial re-use. See rights and permissions. Published by BMJ.
|
650 |
0 |
4 |
|a clinical trial
|
650 |
0 |
4 |
|a cohort analysis
|
650 |
0 |
4 |
|a Cohort Studies
|
650 |
0 |
4 |
|a COVID-19
|
650 |
0 |
4 |
|a human
|
650 |
0 |
4 |
|a Humans
|
650 |
0 |
4 |
|a Immunization, Passive
|
650 |
0 |
4 |
|a multicenter study
|
650 |
0 |
4 |
|a passive immunization
|
650 |
0 |
4 |
|a pneumonia
|
650 |
0 |
4 |
|a SARS-CoV-2
|
650 |
0 |
4 |
|a therapy
|
700 |
1 |
|
|a Carrera Ramos, P.M.
|e author
|
700 |
1 |
|
|a Estenssoro, E.
|e author
|
700 |
1 |
|
|a Ferrando, N.S.
|e author
|
700 |
1 |
|
|a González Martínez, V.V.
|e author
|
700 |
1 |
|
|a González, S.E.
|e author
|
700 |
1 |
|
|a Kreplak, N.
|e author
|
700 |
1 |
|
|a Pesci, S.A.
|e author
|
700 |
1 |
|
|a Regairaz, L.
|e author
|
700 |
1 |
|
|a Salazar, M.R.
|e author
|
700 |
1 |
|
|a Vidal, J.M.
|e author
|
773 |
|
|
|t Journal of investigative medicine : the official publication of the American Federation for Clinical Research
|