Gamberini, Lorenzo
Mazzoli, Carlo Alberto
Sintonen, Harri
Colombo, Davide
Scaramuzzo, Gaetano
Allegri, Davide
Tonetti, Tommaso
Zani, Gianluca
Capozzi, Chiara
Giampalma, Emanuela
Agnoletti, Vanni
Becherucci, Filippo
Bertellini, Elisabetta
Castelli, Andrea
Cappellini, Iacopo
Cavalli, Irene
Crimaldi, Federico
Damiani, Federica
Fusari, Maurizio
Gordini, Giovanni
Laici, Cristiana
Lanza, Maria Concetta
Leo, Mirco
Marudi, Andrea
Nardi, Giuseppe
Ottaviani, Irene
Papa, Raffaella
Potalivo, Antonella
Ranieri, Vito Marco
Russo, Emanuele
Taddei, Stefania
Volta, Carlo Alberto
Spadaro, Savino http://orcid.org/0000-0001-5027-5318
Tartaglione, Marco
Chiarini, Valentina
Buldini, Virginia
Coniglio, Carlo
Moro, Federico
Barbalace, Clara
Citino, Mario
Cilloni, Nicola
Giuntoli, Lorenzo
Bellocchio, Angela
Matteo, Emanuele
Pizzilli, Giacinto
Siniscalchi, Antonio
Tartivita, Chiara
Matteo, Francesco
Marchio, Annalisa
Bacchilega, Igor
Bernabé, Laura
Guarino, Sonia
Mosconi, Elena
Bissoni, Luca
Viola, Lorenzo
Gamberini, Emiliano
Meconi, Tommaso
Pavoni, Vittorio
Pagni, Aline
Cleta, Patrizia Pompa
Cavagnino, Marco
Malfatto, Anna
Adduci, Angelina
Pareschi, Silvia
Melegari, Gabriele
Maccieri, Jessica
Marinangeli, Elisa
Racca, Fabrizio
Verri, Marco
Falò, Giulia
Marangoni, Elisabetta
Boni, Francesco
Felloni, Giulia
Baccarini, Federico Domenico
Terzitta, Marina
Maitan, Stefano
Parise, Maddalena
Bugiani, Bernardo
Masoni, Francesca
,
Clinical trials referenced in this document:
Documents that mention this clinical trial
Quality of life of COVID-19 critically ill survivors after ICU discharge: 90 days follow-up
https://doi.org/10.1007/s11136-021-02865-7
Article History
Accepted: 28 April 2021
First Online: 12 May 2021
Declarations
:
: Harri Sintonen is the developer of the 15D and obtains royalties from its electronic versions. The other Authors have nothing to disclose.
: The study was approved by the Institutional Review Board (IRB) of the study coordinator centre (Maggiore Hospital, Bologna, Italy, approval number: 273/2020/OSS/AUSLBO) and by each institutional review committee of the participating hospitals.
: Informed consent was waived for unconscious patients, while it was acquired for conscious patients or after liberation from mechanical ventilation or at the time of follow-up. The researchers analyzed anonymized individual data.
: Not applicable.
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