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In-hospital mortality during the wild-type, alpha, delta, and omicron SARS-CoV-2 waves: a multinational cohort study in the EuCARE project.
Hedberg, Pontus; Parczewski, Milosz; Serwin, Karol; Marchetti, Giulia; Bai, Francesca; Ole Jensen, Björn-Erik; Pereira, Joana P V; Drobniewski, Francis; Reschreiter, Henrik; Naumovas, Daniel; Ceccherini-Silberstein, Francesca; Rubio Quintanares, Gibran Horemheb; Mwau, Matilu; Toscano, Cristina; König, Florian; Pfeifer, Nico; Zazzi, Maurizio; Fanti, Iuri; Incardona, Francesca; Cozzi-Lepri, Alessandro; Sönnerborg, Anders; Nauclér, Pontus.
Afiliación
  • Hedberg P; Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
  • Parczewski M; Department of Tropical Infectious Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
  • Serwin K; Department of Tropical Infectious Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
  • Marchetti G; Department of Health Sciences, Clinic of Infectious Diseases, ASST Santi Paolo E Carlo, University of Milan, Milan, Italy.
  • Bai F; Department of Health Sciences, Clinic of Infectious Diseases, ASST Santi Paolo E Carlo, University of Milan, Milan, Italy.
  • Ole Jensen BE; Department of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Duesseldorf, Heinrich Heine University, Duesseldorf, Germany.
  • Pereira JPV; Department of Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty and University Hospital Duesseldorf, Heinrich Heine University, Duesseldorf, Germany.
  • Drobniewski F; Department of Infectious Disease, Imperial College, London, W12 0NN, UK.
  • Reschreiter H; University Hospital Dorset, Poole Hospital, Poole, Dorset, UK.
  • Naumovas D; University Hospital Dorset, Poole Hospital, Poole, Dorset, UK.
  • Ceccherini-Silberstein F; Vilnius Santaros Klinikos Biobank, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania.
  • Rubio Quintanares GH; Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.
  • Mwau M; Virus Security Department, Paul Ehrlich Institute, Langen, Germany.
  • Toscano C; Infectious Diseases Department, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico.
  • König F; Center for Infectious and Parasitic Diseases Control Research, Kenya Medical Research Institute, Busia, Kenya.
  • Pfeifer N; Microbiology Laboratory, Centro Hospitalar de Lisboa Ocidental, Lisboa, Portugal.
  • Zazzi M; Institute for Bioinformatics and Medical Informatics and Medical Informatics (IBMI), University of Tübingen, Tübingen, Germany.
  • Fanti I; Methods in Medical Informatics Department of Computer Science, University of Tübingen, Tübingen, Germany.
  • Incardona F; Institute for Bioinformatics and Medical Informatics and Medical Informatics (IBMI), University of Tübingen, Tübingen, Germany.
  • Cozzi-Lepri A; Methods in Medical Informatics Department of Computer Science, University of Tübingen, Tübingen, Germany.
  • Sönnerborg A; Department of Medical Biotechnologies, University of Siena, Italy.
  • Nauclér P; EuResist Network GEIE, Via Guido Guinizelli, 98/100, 00152, Roma, Italy.
Lancet Reg Health Eur ; 38: 100855, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38476753
ABSTRACT

Background:

Investigating outcomes of hospitalised COVID-19 patients throughout the pandemic is crucial to understand the impact of different SARS-CoV-2 variants. We compared 28-day in-hospital mortality of Wild-type, Alpha, Delta, and Omicron variant infections. Whether the difference in risk by variant varied by age was also evaluated.

Methods:

We conducted a cohort study including patients ≥18 years, hospitalised between 2020 and 02-01 and 2022-10-15 with a SARS-CoV-2 positive test, from nine countries. Variant was classified based on sequenced viruses or from national public metadata. Mortality was compared using the cumulative incidence function and subdistribution hazard ratios (SHR) adjusted for age, sex, calendar time, and comorbidities. Results were shown age-stratified due to effect measure modification (P < 0.0001 for interaction between age and variant).

Findings:

We included 38,585

participants:

19,763 Wild-type, 6387 Alpha, 3640 Delta, and 8795 Omicron. The cumulative incidence of mortality decreased throughout the study period. Among participants ≥70 years, the adjusted SHR (95% confidence interval) for Delta vs. Omicron was 1.66 (1.29-2.13). This estimate was 1.66 (1.17-2.36) for Alpha vs. Omicron, and 1.34 (0.92-1.95) for Wild-type vs. Omicron. These were 1.21 (0.81-1.82), 1.21 (0.68-2.17), and 0.98 (0.53-1.82) among unvaccinated participants. When comparing Omicron sublineages, the aSHR for BA.1 was 1.92 (1.43-2.58) compared to BA.2 and 1.52 (1.11-2.08) compared to BA.5.

Interpretation:

The herein observed decrease in in-hospital mortality seems to reflect a combined effect of immunity from vaccinations and previous infections, although differences in virulence between SARS-CoV-2 variants may also have contributed.

Funding:

European Union's Horizon Europe Research and Innovation Programme.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Año: 2024 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Año: 2024 Tipo del documento: Article País de afiliación: Suecia