Convalescent plasma transfusion for immunocompromised viremic patients with COVID‐19: A retrospective multicenter study

Author:

Destremau Marjolaine1,Chaussade Hélène1ORCID,Hemar Victor1,Beguet Mathilde2,Bellecave Pantxika3,Blanchard Elodie4,Barret Amaury5,Laboure Gaelle6,Vasco‐Moynet Claire7,Lacassin Flore8,Morisse Eloïse9,Aguilar Claire10,Lafarge Xavier211,Lafon Marie‐Edith3,Bonnet Fabrice112,Issa Nahéma13ORCID,Camou Fabrice13

Affiliation:

1. CHU Bordeaux, Service de médecine interne et maladies infectieuses Bordeaux France

2. Etablissement français du sang Nouvelle Aquitaine Bordeaux France

3. CHU Bordeaux, Service de virologie Bordeaux France

4. CHU Bordeaux, Service de pneumologie Bordeaux France

5. CH Arcachon, Service de médecine interne La Teste‐de‐Buch France

6. CH Libourne, Service d'hématologie Libourne France

7. CH Libourne, Service de médecine interne et infectiologie Libourne France

8. CH Mont‐de‐Marsan, Service de médecine interne Mont‐de‐Marsan France

9. CH Pau, Service de réanimation Pau France

10. CH Périgueux, Service de maladies infectieuses Périgueux France

11. Université de Bordeaux, INSERM U1211 “Maladies Rares: Génétique et Métabolisme” Talence France

12. Université de Bordeaux, Bordeaux Population Health, INSERM U1219 Bordeaux France

13. CHU Bordeaux, Service de réanimation médicale Bordeaux France

Abstract

AbstractThis study aims to assess the safety, virological, and clinical outcomes of convalescent plasma transfusion (CPT) in immunocompromised patients hospitalized for coronavirus disease 2019 (COVID‐19). We conducted a retrospective multicenter cohort study that included all immunosuppressed patients with COVID‐19 and RNAemia from May 2020 to March 2023 treated with CPT. We included 81 patients with hematological malignancies (HM), transplants, or autoimmune diseases (69% treated with anti‐CD20). Sixty patients (74%) were vaccinated, and 14 had pre‐CPT serology >264 BAU/mL. The median delay between symptom onset and CPT was 23 days [13−31]. At D7 post‐CPT, plasma PCR was negative in 43/64 patients (67.2%), and serology became positive in 25/30 patients (82%). Post‐CPT positive serology was associated with RNAemia negativity (p < 0.001). The overall mortality rate at D28 was 26%, being higher in patients with non‐B‐cell HM (62%) than with B‐cell HM (25%) or with no HM (11%) (p = 0.02). Patients receiving anti‐CD20 without chemotherapy had the lowest mortality rate (8%). Positive RNAemia at D7 was associated with mortality at D28 in univariate analysis (HR: 3.05 [1.14−8.19]). Eight patients had adverse events, two of which were severe but transient. Our findings suggest that CPT can abolish RNAemia and ameliorate the clinical course in immunocompromised patients with COVID‐19.

Publisher

Wiley

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