Critical illnesses associated with
coronavirus disease 2019 (COVID-19) are attributable to a hypercoagulable status. There is limited knowledge regarding the dynamic changes in
coagulation factors among
COVID-19 patients on
nafamostat mesylate, a potential therapeutic
anticoagulant for COVID-19. First, we retrospectively conducted a cluster analysis based on clinical characteristics on admission to identify latent subgroups among fifteen patients with
COVID-19 on
nafamostat mesylate at the University of Tokyo Hospital, Japan, between April 6 and May 31, 2020. Next, we delineated the characteristics of all patients as well as COVID-19-patient subgroups and compared dynamic changes in
coagulation factors among each subgroup. The subsequent dynamic changes in
fibrinogen and
D-dimer levels were presented graphically. All
COVID-19 patients were classified into three subgroups: clusters A, B, and C, representing low, intermediate, and high risk of poor outcomes, respectively. All patients were alive 30 days from symptom onset. No patient in cluster A required
mechanical ventilation; however, all patients in cluster C required
mechanical ventilation, and half of them were treated with
venovenous extracorporeal membrane oxygenation. All patients in cluster A maintained low
D-dimer levels, but some critical patients in clusters B and C showed dynamic changes in
fibrinogen and
D-dimer levels. Although the potential of
nafamostat mesylate needs to be evaluated in randomized clinical trials, admission characteristics of patients with
COVID-19 could predict subsequent coagulopathy.