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. 2020 Nov 10;91(4):e2020175. doi: 10.23750/abm.v91i4.10681

Table 1.

Description of recent experience with convalescent plasma therapy in COVID-19.

Number Study Country Patients Indications ARDS Survival Highlights
1 Duan et al China 10 Severe
COVID 19
All 100% Prospective study (for safety)
Dose: One
Volume: 200 ml
Titers: 1: 640
Median time of illness to transfusion: 16.5 days
No Severe Adverse effect
70% undetectable viral load
Improvement in oxyhemoglobin, clinical symptoms, lymphocyte count, radiological findings
Reduction in C reactive protein
2 Shen et al China 5 Severe COVID19 All 100% Prospective study (for efficacy)
Dose: Twice
Total volume: 400 ml
Titers: 1:1000
Median time of illness to transfusion: 10-12 days
Negative viral load in 12 days
Increase in SARS-COV-2 specific ELISA and neutralizing antibody titer
Improvement in fever (80%), ARDS (80%), PaO2/FiO2 ratio
Weaning from ventilation (60%), discharge (60%)
Reduction in SOFA score
3 Zhang et al China 4 Severe COVID19 All 100% Case series
Maximum dose: 8 and 3 respectively
Maximum volume: 900 ml
Reduction in viral load
Documented RT PCR negative status after treatment at discharge
Improvement in clinical condition, lung imaging finding, and respiratory status
4 Ahn et al Korea 2 Severe COVID19 All(( 100% Case reports
Dose: 2
Volume: 500 ml
On Hydroxychloroquine as well
Measured Anti SARS – COV – 2 IgG antibody in donor plasma was: 0.586
Improvement in fever, imaging finding, respiratory parameters and clinical status
Reduction in inflammatory markers including CRP, IL -6 and Viral load
Documented negative viral RT PCR
Weaned of ventilators and discharged
5 Ye et al China 6 Moderate/SevereCOVID19 1 100% Retrospective study
Maximum doses: 3
Maximum volume: 600 ml
Improvement in symptoms and radiological findings
6 Zeng et al China 6 Severe COVID19 All 16% Retrospective study
Median dose: 2
Median volume: 300 ml
Adverse effect: None
SARS –COV-2 clearance documented in all patients (100%)
SARS –COV-2 clearance documented in all patients before death (100%)
Longer survival in patients receiving CP