COVID-19 infection is likely to develop into a pandemic with expected accompanying high morbidity and mortality. This is also likely to apply to Norway. Through this exploratory prospective multicenter study, we wish to study the efficacy of Remdesivir in critically ill patients with detected COVID 19 who develop respiratory failure and need intubation and mechanical ventilation. Patients eligible for inclusion will be randomized to a Remdesivir treatment group or a control group (not a placebo). In addition, both groups will receive all the usual treatment offered by Norwegian intensive care units. The primary endpoint of the study is 28-day mortality. Secondary endpoints include respiratory time, intensive days, organ failure, co-infections, and follow-up after 3 months. Additional blood tests are taken for analysis of a wide range of inflammation markers, endothelial injury markers, plate activation and inoculation of COVID-19 in peripheral blood, lower respiratory tract and nasopharynx.
Humoral immunity to SARS-CoV-2 mRNA vaccination in multiple sclerosis: the relevance of time since last rituximab infusion and first experience from sporadic revaccinations
J Neurol Neurosurg Psychiatry (in press)
The COVID-19 pandemic as experienced by the spouses of home-dwelling people with dementia - a qualitative study
BMC Geriatr, 21 (1), 583
Subacute thyroiditis after vaccination against SARS-CoV-2
Tidsskr Nor Laegeforen, 141 (2021-14)