A Report on the First 7 Sequential Patients Treated Within the C-Reactive Protein Apheresis in COVID (CACOV) Registry.


Journal

The American journal of case reports
ISSN: 1941-5923
Titre abrégé: Am J Case Rep
Pays: United States
ID NLM: 101489566

Informations de publication

Date de publication:
10 Jan 2022
Historique:
entrez: 10 1 2022
pubmed: 11 1 2022
medline: 13 1 2022
Statut: epublish

Résumé

BACKGROUND Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-induced pneumonia is a disease with high mortality and, still, no effective treatment. Excessively elevated C-reactive protein (CRP) plasma levels inversely correlate with prognosis. As CRP, via complement and macrophage activation, can cause organ damage in COVID-19, we have recently introduced selective CRP apheresis as a potentially effective treatment. Now, we report on the first patients with severe SARS-CoV-2-induced pneumonia treated within the "C-reactive protein Apheresis in COVID" (CACOV) registry. CASE REPORT Seven sequential hospitalized patients with documented COVID-19, strongly elevated CRP plasma levels, and respiratory failure were treated by selective CRP apheresis in addition to standard therapy after having given their informed consent for inclusion in the CACOV registry. We performed 2-8 CRP apheresis sessions via either peripheral or central venous access depending on clinical course and CRP plasma levels. CRP apheresis, in COVID-19, reduced CRP plasma levels by approximately 50-90%, and it was thus highly effective, feasible, and safe. Despite severe radiological lung involvement in all our patients, only 2 patients finally required intubation, and none required extracorporeal membrane oxygenation (ECMO). All 7 patients were discharged from our 2 hospitals in good clinical condition. CONCLUSIONS Selective CRP apheresis, starting early after patient admission, may be an effective treatment of SARS-CoV-2-induced pneumonia. SARS-COV-2 can cause organ damage and multiple organ failure predominantly by an excessive CRP-mediated autoimmune response of the ancient innate immune system. Further registry data and randomized trials are needed.

Identifiants

pubmed: 35007274
pii: 935263
doi: 10.12659/AJCR.935263
pmc: PMC8762613
doi:

Substances chimiques

C-Reactive Protein 9007-41-4

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e935263

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Auteurs

Christian Schumann (C)

Department of Pneumology, Thoracic Oncology, Sleep-, and Respiratory Critical Care Medicine, Clinic Association Allgaeu, Kempten, Germany.

Franz Heigl (F)

Medical Care Center Kempten-Allgaeu, Kempten, Germany.

Imanuel J Rohrbach (IJ)

Cardiovascular Center Oberallgaeu-Kempten, Clinic Association Allgaeu, Kempten, Germany.

Ahmed Sheriff (A)

Pentracor GmbH, Hennigsdorf, Germany.
Department of Gastroenterology/Infectiology/Rheumatology, Charité University Medicine Berlin, Berlin, Germany.

Lutz Wagner (L)

Department of Anesthesiology, Intensive Care and Emergency Medicine, Clinic Association Allgaeu, Kempten/Immenstadt, Germany.

Florian Wagner (F)

Department of Anesthesiology, Intensive Care and Emergency Medicine, Clinic Association Allgaeu, Kempten/Immenstadt, Germany.

Jan Torzewski (J)

Cardiovascular Center Oberallgaeu-Kempten, Clinic Association Allgaeu, Kempten, Germany.

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Classifications MeSH