Outcomes of targeted treatment in immunocompromised patients with asymptomatic or mild COVID-19: a retrospective study.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
16 09 2023
Historique:
received: 15 06 2023
accepted: 14 09 2023
medline: 18 9 2023
pubmed: 17 9 2023
entrez: 16 9 2023
Statut: epublish

Résumé

The aim of this study was to describe the outcomes of targeted COVID-19 treatments in immunocompromised patients with asymptomatic or mild COVID-19 during the period of expansion of the different Omicron subvariants in France. A retrospective monocentric observational study was performed. All immunocompromised patients aged 18 or more, with asymptomatic SARS-CoV-2 infection or mild COVID-19, and who had received a targeted treatment with sotrovimab, tixagevimab/cilgavimab, nirmatrelvir/ritonavir or remdesivir at the Bordeaux University Hospital from 1st January 2022 to 31st December 2022 were eligible. The primary outcomes of interest was defined as a composite of either (i) progression to moderate (WHO-Clinical Progression Scale at 4 or 5) or severe COVID-19 (WHO-CPS ≥ 6), or (ii) the occurrence of COVID-19-related death. The secondary outcomes of interest were the components of the primary outcome. Outcomes were collected until day 30 after targeted treatment administration or at discharge for patients still hospitalised in relation with COVID-19 at day 30. 223 immunocompromised patients received targeted treatment for asymptomatic SARS-CoV-2 infection or mild COVID-19: 114 received sotrovimab, 50 tixagevimab/cilgavimab, 49 nirmatrelvir/ritonavir, and 10 remdesivir. Among 223 treated patients, 10 (4.5%) progressed to moderate or severe disease: three patients (1.3%) progressed to moderate COVID-19 and 7 (3.1%) patients progressed to severe disease. Among them, 4 (1.8%) died of COVID-19. More than 95% of immunocompromised patients with asymptomatic SARS-CoV-2 infection or mild COVID-19 treated by targeted therapies during the Omicron subvariants era did not progress to moderate or severe disease.

Identifiants

pubmed: 37717101
doi: 10.1038/s41598-023-42727-5
pii: 10.1038/s41598-023-42727-5
pmc: PMC10505186
doi:

Substances chimiques

nirmatrelvir 7R9A5P7H32
Ritonavir O3J8G9O825

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15357

Investigateurs

Laure Barthod (L)
Pantxika Bellecave (P)
Jean-Frédéric Blanc (JF)
Elodie Blanchard (E)
Fabrice Bonnet (F)
Fabrice Camou (F)
Mathilde Carrer (M)
Charles Cazanave (C)
Faiza Chermak (F)
Lionel Couzi (L)
Amaury Daste (A)
Frédéric-Antoine Dauchy (FA)
Victor De Ledinghen (V)
Charlotte Domblides (C)
Pierre Duffau (P)
Hervé Dutronc (H)
Alexandre Duvignaud (A)
Maxime Faure (M)
Edouard Forcade (E)
Nahéma Issa (N)
Hannah Kaminski (H)
Jean-Baptise Hiriart (JB)
Marin Lahouati (M)
Julie Leitao (J)
Maëlig Lescure (M)
Estibaliz Lazaro (E)
Isabelle Maachi (I)
Didier Neau (D)
Duc Nguyen (D)
Karine Nubret (K)
Stéphane Pédeboscq (S)
Thierry Pistone (T)
Frédérique Pribat (F)
Mathilde Puges (M)
Aurélie Ruet (A)
Camille Tumiotto (C)
Marie-Anne Vandenhende (MA)
Gaétane Wirth (G)

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

M Lahouati (M)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France. marin.lahouati@chu-bordeaux.fr.
Inserm, UMR 1034, Biology of Cardiovascular Diseases, Université de Bordeaux, Pessac, France. marin.lahouati@chu-bordeaux.fr.

C Cazanave (C)

Service des maladies infectieuses et tropicales, CHU de Bordeaux, 33076, Bordeaux, France.

A Labadie (A)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.

P Gohier (P)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.

L Guirlé (L)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.

A Desclaux (A)

Service des maladies infectieuses et tropicales, CHU de Bordeaux, 33076, Bordeaux, France.

M Gigan (M)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.

D Malvy (D)

Service des maladies infectieuses et tropicales, CHU de Bordeaux, 33076, Bordeaux, France.
Inserm UMR 1219, IRD EMR 271, Bordeaux Population Health, Université de Bordeaux, 33076, Bordeaux, France.

S Pedeboscq (S)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.

F Xuereb (F)

Service de Pharmacie Clinique, Hôpital Pellegrin, Centre Hospitalo-Universitaire de Bordeaux, Place Amélie Raba Léon, 33076, Bordeaux, France.
Inserm, UMR 1034, Biology of Cardiovascular Diseases, Université de Bordeaux, Pessac, France.

A Duvignaud (A)

Service des maladies infectieuses et tropicales, CHU de Bordeaux, 33076, Bordeaux, France.
Inserm UMR 1219, IRD EMR 271, Bordeaux Population Health, Université de Bordeaux, 33076, Bordeaux, France.

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