Convalescent plasma treatment in severely immunosuppressed patients hospitalized with COVID-19: an observational study of 28 cases.


Journal

Infectious diseases (London, England)
ISSN: 2374-4243
Titre abrégé: Infect Dis (Lond)
Pays: England
ID NLM: 101650235

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 9 12 2021
medline: 16 2 2022
entrez: 8 12 2021
Statut: ppublish

Résumé

Immunosuppressed patients are particularly vulnerable to severe infection from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), risking prolonged viremia and symptom duration. In this study we describe clinical and virological treatment outcomes in a heterogeneous group of patients with severe immunosuppression due to various causes suffering from COVID-19 infection, who were all treated with convalescent plasma (CCP) along with standard treatment. We performed an observational, retrospective case series between May 2020 to March 2021 at three sites in Skåne, Sweden, with a population of nearly 1.4 million people. All patients hospitalized for COVID-19 who received CCP with the indication severe immunosuppression as defined by the treating physician were included in the study ( In total, 28 severely immunocompromised patients, half of which previously had been treated with rituximab, who had received in-hospital convalescent plasma treatment of COVID-19 were identified. One week after CCP treatment, 13 of 28 (46%) patients had improved clinically defined as a decrease of at least one point at the WHO-scale. Three patients had increased score points of whom two had died. For 12 patients, the WHO-scale was unchanged. As one of only few studies on CCP treatment of COVID-19 in hospitalized patients with severe immunosuppression, this study adds descriptive data. The study design prohibits conclusions on safety and efficacy, and the results should be interpreted with caution. Prospective, randomized trials are needed to investigate this further.

Sections du résumé

BACKGROUND
Immunosuppressed patients are particularly vulnerable to severe infection from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), risking prolonged viremia and symptom duration. In this study we describe clinical and virological treatment outcomes in a heterogeneous group of patients with severe immunosuppression due to various causes suffering from COVID-19 infection, who were all treated with convalescent plasma (CCP) along with standard treatment.
METHODS
We performed an observational, retrospective case series between May 2020 to March 2021 at three sites in Skåne, Sweden, with a population of nearly 1.4 million people. All patients hospitalized for COVID-19 who received CCP with the indication severe immunosuppression as defined by the treating physician were included in the study (
RESULTS
In total, 28 severely immunocompromised patients, half of which previously had been treated with rituximab, who had received in-hospital convalescent plasma treatment of COVID-19 were identified. One week after CCP treatment, 13 of 28 (46%) patients had improved clinically defined as a decrease of at least one point at the WHO-scale. Three patients had increased score points of whom two had died. For 12 patients, the WHO-scale was unchanged.
CONCLUSION
As one of only few studies on CCP treatment of COVID-19 in hospitalized patients with severe immunosuppression, this study adds descriptive data. The study design prohibits conclusions on safety and efficacy, and the results should be interpreted with caution. Prospective, randomized trials are needed to investigate this further.

Identifiants

pubmed: 34878955
doi: 10.1080/23744235.2021.2013528
pmc: PMC8726003
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

283-291

Auteurs

Oskar Ljungquist (O)

Department of Translational Medicine, Clinical Infection Medicine, Faculty of Medicine, Lund University, Malmö, Sweden.
Department of Infectious Diseases, Helsingborg Hospital, Helsingborg, Sweden.

Maria Lundgren (M)

Department of Clinical Immunology and Transfusion Medicine, Office of Medical Services, Lund, Sweden.

Elena Iliachenko (E)

Department of Clinical Immunology and Transfusion Medicine, Office of Medical Services, Lund, Sweden.

Fredrik Månsson (F)

Department of Translational Medicine, Clinical Infection Medicine, Faculty of Medicine, Lund University, Malmö, Sweden.
Skåne University Hospital, Malmö, Sweden.

Blenda Böttiger (B)

Department of Clinical Microbiology, University and Regional Laboratories, Lund, Sweden.

Mona Landin-Olsson (M)

Skåne University Hospital, Malmö, Sweden.
Department of Clinical Science, Division of Internal Medicine, Lund University, Lund, Sweden.

Christian Wikén (C)

Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Division of Infection Medicine, Lund University, Lund, Sweden.

Ebba Rosendal (E)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Anna K Överby (AK)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Byström J Wigren (BJ)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Mattias N E Forsell (MNE)

Department of Clinical Microbiology, Umeå University, Umeå, Sweden.

Jens Kjeldsen-Kragh (J)

Department of Clinical Immunology and Transfusion Medicine, Office of Medical Services, Lund, Sweden.

Magnus Rasmussen (M)

Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Division of Infection Medicine, Lund University, Lund, Sweden.

Fredrik Kahn (F)

Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Division of Infection Medicine, Lund University, Lund, Sweden.

Karin Holm (K)

Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Division of Infection Medicine, Lund University, Lund, Sweden.

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