Coagulation Profile of Convalescent Plasma Donors and Recipients




Pitkänen, Hanna H.; Helin, Tuukka; Khawaja, Tamim; Pietilä, Jukka-Pekka; Kajova, Mikael; Välimaa, Hanna; Vahlberg, Tero; Ihalainen, Jarkko; Vierikko, Antti; Vapalahti, Olli; Kantele, Anu; Lassila, Riitta

PublisherSAGE Publications

THOUSAND OAKS

2025

Clinical and Applied Thrombosis/Hemostasis

Clinical and Applied Thrombosis/Hemostasis

CLIN APPL THROMB-HEM

10760296251317522

31

10

1076-0296

1938-2723

DOIhttps://doi.org/10.1177/10760296251317522

https://doi.org/10.1177/10760296251317522

https://research.utu.fi/converis/portal/detail/Publication/485135055



Convalescent plasma (CP) therapy for COVID-19 infection may have favorable safety but varying efficacy, with concerns about its procoagulant impact. We investigated whether administration of CP to hospitalized patients affects their coagulation profile. Fifty-four patients randomized in a double-blinded fashion received either placebo, low-titer CP (LCP) or high-titer CP (HCP). Donor blood samples were obtained at the time of the plasmapheresis, while recipient blood samples were collected before infusion, one day post-infusion and between two and six days after infusion. Routine laboratory follow-up, coagulation biomarkers, antiphospholipid antibodies, and thrombin generation (TG) were assessed. CP donors had normal blood cell counts and coagulation profiles, without differences between LCP and HCP donors at the baseline. All CP recipients were on low-molecular-weight heparin thromboprophylaxis at the time of the infusion. Despite randomization, the HCP group had lower baseline (p = 0.004) and Day 1 platelet counts (p = 0.019) than the LCP group. Von Willebrand antigen (VWF:Ag) levels clearly exceeded normal without differences at baseline. At Day 1, LCP recipients had higher VWF:Ag (mean +/- SD 224 +/- 15%) than HCP recipients (210 +/- 8%) (p = 0.012). In all groups, overall 80% lupus anticoagulant was positive. Baseline TG variables were comparable, but again LCP recipients exhibited higher endogenous thrombin potential (ETP) (1313 +/- 535 nM.min) (p = 0.038) and peak TG (184 +/- 106 nM) (p = 0.037) than the HCP group (870 +/- 425 nM.min and 86 +/- 54 nM). Our findings show that LCP increases VWF:Ag levels and enhances TG despite the thromboprophylaxis. These results suggest that HCP induces less hypercoagulability than LCP, which may contribute to the variability in CP efficacy.


The study was funded by the Finnish Government Subsidy for Health Science Research (TYH2023238), Helsinki University Hospital grant for Coagulation Medicine (VTR, TYH2024310), The Finnish Blood Disease Research Foundation and Pulsus Foundation (Hanna Pitkänen).


Last updated on 2025-21-03 at 14:04