Treatment of severe 2009 H1N1 infection with convalescent plasma will reduce mortality.
Patients presented with severe 2009 H1N1 infection responded poorly to antiviral agents. Meta-analysis of reports from 1918 H1N1 pandemic suggested that convalescent plasma might be an effective treatment option for patients with severe 2009 H1N1 infection.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Oseltamivir 75mg bid orally during ICU hospitalization + 500mL convalescent plasma containing \>= 1:160 of neutralizing antibody to Pandemic influenza A H1N1
Oral Oseltamivir 75mg bid during ICU hospitalization
The University of Hong Kong, Queen Mary Hospital
Hong Kong SAR, China
Death
mortality during hospitalization directly related to H1N1 2009 infection
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Complication
including pneumonia, ARDS, renal failure, heart failure and secondary infection
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Length of stay in ICU
days of stay in ICU
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Adverse events secondary to the convalescent plasma treatment
Allergic reaction (including anaphylaxis), acute renal failure, fluid overload
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Time on respiratory support
including ventilator, CPAP and BiPAP
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Change in viral load
Daily measurement of H1N1 2009 viral load
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
Change in cytokine level
daily measurement of cytokine level (serum)
Time frame: Participants are followed until death or discharge from ICU (average 2 weeks)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.