Selected article for: "mechanical ventilation and symptom onset"

Author: Ling, Ryan Ruiyang; Sim, Jackie Jia Lin; Tan, Felicia Liying; Tai, Bee Choo; Syn, Nicholas; Mucheli, Sharavan Sadasiv; Fan, Bingwen Eugene; Mitra, Saikat; Ramanathan, Kollengode
Title: Convalescent plasma for patients hospitalised with Coronavirus disease 2019: A meta-analysis with trial sequential analysis of randomised controlled trials
  • Cord-id: ihpc0hdj
  • Document date: 2021_10_10
  • ID: ihpc0hdj
    Snippet: Current evidence from randomised controlled trials (RCTs) and systematic reviews on the utility of convalescent plasma (CP) in patients with coronavirus disease 2019 (COVID-19) suggests a lack of benefit. We conducted an updated meta-analysis of RCTs with trial sequential analysis to investigate whether convalescent plasma is futile in reducing mortality in patients hospitalized with COVID-19. We searched six databases from 1(st) December 2019 to 1(st) August 2021 for RCTs comparing the use of C
    Document: Current evidence from randomised controlled trials (RCTs) and systematic reviews on the utility of convalescent plasma (CP) in patients with coronavirus disease 2019 (COVID-19) suggests a lack of benefit. We conducted an updated meta-analysis of RCTs with trial sequential analysis to investigate whether convalescent plasma is futile in reducing mortality in patients hospitalized with COVID-19. We searched six databases from 1(st) December 2019 to 1(st) August 2021 for RCTs comparing the use of CP with standard of care or transfusion of non-CP standard plasma in patients with COVID-19. The risk of bias was assessed using the Cochrane Risk-of-Bias 2 Tool. Random effects (DerSimonian and Laird) meta-analyses were conducted. The primary outcome was the aggregate risk for in-hospital mortality between both arms. We conducted a trial sequential analysis (TSA) based on the pooled relative risks (RRs) for in-hospital mortality. Secondary outcomes included the pooled RR for receipt of mechanical ventilation and mean difference in hospital length of stay. We included 18 RCTs (8702 CP, 7906 control). CP was not associated with a significant mortality benefit (RR: 0.95, 95%-CI: 0.86-1.04, p=0.27, high certainty). Subgroup analysis did not find any significant differences (p(interaction)=0.30) between patients who received CP within 8 days of symptom onset (RR: 0.97, 95%-CI: 0.79-1.19, p=0.80), or after 8 days (RR: 0.79, 95%-CI: 0.57-1.10, p=0.16). TSA based on a RR reduction of 10% from a baseline mortality of 20% found that CP was not effective, with the pooled effect within the boundary for futility. CP did not significantly reduce the requirement for mechanical ventilation (RR: 1.00, 95%-CI: 0.91-1.10, p=0.99, moderate certainty) or hospital length of stay (+1.32, 95%-CI: -1.86 to +4.52, p=0.42, low certainty). CP does not improve relevant clinical outcomes in patients with COVID-19, especially in severe disease. The pooled effect of mortality was within the boundary of futility, suggesting the lack of benefit of CP in patients hospitalised with COVID-19.

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